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===================================================Date: Tue, 1 Feb 2011 22:05:11 -0500 Reply-To: Leanne Wilkins <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Leanne Wilkins <[log in to unmask]> Subject: Voxel Content-Type: text/plain; charset="iso-8859-1" Content-Transfer-Encoding: quoted-printable MIME-Version: 1.0 Message-ID: <[log in to unmask]> We are currently doing an ROI analysis with several different contrasts. I was wondering if there was an SPM script that would permit me to identify the top voxel activated in each ROI? I am new to SPM, I hope my question makes sense. Leanne ========================================================================Date: Wed, 2 Feb 2011 16:15:32 +1300 Reply-To: Reem Jan <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Reem Jan <[log in to unmask]> Subject: Re: Missing condition at first level - what to input in the onset tab? In-Reply-To: A<[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset="us-ascii" Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> Thank you Cyril, Michael and Donald for all the useful information you have given me regarding this. There are 6 runs/sessions and 4 conditions per subject. I have done the following. If condition A is missing from run 1 and 2 let's say.. I remove condition A from that run (in the first level model specification), and then in the contrast manager when I specify condition A's contrast I type: 0 0 0 0 0.25 0 0 0.25 0 0 0.25 0 0 0.25 0 0 And if condition A is missing only from run 2: 0.25 0 0 0 0 0.25 0 0 0.25 0 0 0.25 0 0 0.25 0 0 And I also include 6 zeros after each run for the motion regressors (which I haven't typed out here for simplicity's sake). I hope this is right? Kind regards Reem -----Original Message----- From: SPM (Statistical Parametric Mapping) [mailto:[log in to unmask]] On Behalf Of Michael Harms Sent: Wednesday, February 02, 2011 7:13 AM To: [log in to unmask] Subject: Re: [SPM] Missing condition at first level - what to input in the onset tab? Well, "reasonably" sure, although happy for someone else to chime in to the contrary. Many different contrasts can be technically valid (i.e., "estimable"). In the example in question, the contrast I proposed would test for an expected difference between the mean of condition A and B of zero, whereas in your original contrast the expected value of the contrast would not be zero under the null hypothesis of no difference between A and B. In effect, I believe that by using a factor of 6/5 on the 5 A conditions, one achieves the desired "upweighting" of the variance associated with the condition A estimate (relative to the condition B estimate). cheers, -MH On Tue, 2011-02-01 at 13:56 +0000, Cyril Pernet wrote: > Hi Michael > > r u sure? ok beta = pinv(X)*Y so we don't really care about the bias (I > was referring to nb of stimuli and variance estimation) > > for the contrast with 5A and 6B using 1/5 1/6 you average 5 sessions vs > 6 which of course works as well but you may want to somehow put this > unbalance in your contrast? I guess it's a matter of choice - note that > C is unchanged by the post multiplication by inv(X'X')X'X using my > contrast so it is still valid too .. contrast don't have to sum up to 0 > (oh yeh my full contrast wasn't right since I copied/pasted 6 times .. > but I'm sure you got the gesture). > > I actually never had this problem - was offering a possible solution but > yours seems good too - anybody out there checked this up before? > > Cyril > > > > Hi Cyril, > > Even if you don't have equal numbers, the estimated betas are themselves > > still unbiased. Thus, if you are going to compare two conditions, it > > seems to me that you still want the contrast to sum to 0. In the example > > you gave, if you wanted to compare the mean level of A to the mean level > > of B, with no estimate of A available from session 3, I think that you > > would want the following contrast: > > 1/5 -1/6 0 1/5 -1/6 0 0 -1/6 0 1/5 -1/6 0 1/5 -1/6 0 1/5 -1/6 0 > > or multiplying by 6: > > 6/5 -1 0 6/5 -1 0 0 -1 0 6/5 -1 0 6/5 -1 0 6/5 -1 0 > > (note the 0 in the "A" position of the 3rd session). > > > > cheers, > > -MH > > > >> Reem > >> > >> It doesn't really matter that in each session you don't have the same > >> number of stimuli per condition as long as across your 6 sessions you > >> end up with equal numbers (will work as well if not but it's not as good > >> because variance estimation can be biased). As for the different number > >> of conditions you can weight your contrast accordingly. Simply create 6 > >> sessions in SPM and your 2 or 3 conditions in each sessions. Let say > >> your design runs like this: > >> > >> Session 1 A B C > >> Session 2 A B > >> Session 3 B C > >> Session 4 A B C > >> Session 5 A B C > >> Session 6 A B > >> = 5*A 6*B 4*C > >> = 30/6*A 36/6*B 26/6*C (I choose to have 6 as denominator because you > >> have 6 sessions) > >> > >> Let say you want to test A - B then use a contrast [30/36 -1 0 30/36 > >> -1 0 30/36 -1 0 30/36 -1 0 30/36 -1 0 30/36 -1 0] > >> How do I end up with 30/36 and -1 --> 1/6 * 30/6 = 30/36 and -1/6 * 36/6 > >> = -1 (I use 1/6 for each session since you have 6 sessions) > >> The sum doesn't end up to 1 but the contrast should still be valid .. > >> (at least using a simple design on my machine with unbalanced design and > >> manual checking the contrast is valid - check in SPM I think it is ok) > >> > >> Good luck > >> Cyril > >> > >> > >> > >>> Dear SPMers > >>> > >>> I am trying run first level analysis on fMRI data in SPM8. > >>> > >>> The experiment design involves 6 runs/sessions, each run/session > >>> consists of 8 stimuli (48 stimuli in total). > >>> > >>> There are 3 experimental conditions spread out equally across stimuli > >>> i.e. There are 16 stimuli of each condition in total. > >>> > >>> Because the stimuli were presented at random and are event-related, I am > >>> now running into a problem because in some of the runs of 8 stimuli, > >>> there happens to be only 2 of the conditions presented and not 3. In > >>> these cases, I'm not sure what to input in the 'onsets' tab of first > >>> level model specification for the 3rd condition. > >>> > >>> Is there a way around this problem. I'd be very appreciative of some > >>> help. > >>> > >>> Kind regards > >>> Reem > >>> > >> > >> -- > >> The University of Edinburgh is a charitable body, registered in > >> Scotland, with registration number SC005336. > >> > > > > > > __________ Information from ESET NOD32 Antivirus, version of virus signature database 5838 (20110201) __________ The message was checked by ESET NOD32 Antivirus. http://www.eset.com __________ Information from ESET NOD32 Antivirus, version of virus signature database 5838 (20110201) __________ The message was checked by ESET NOD32 Antivirus. http://www.eset.com ========================================================================Date: Tue, 1 Feb 2011 22:22:52 -0500 Reply-To: "MCLAREN, Donald" <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: "MCLAREN, Donald" <[log in to unmask]> Subject: Re: Voxel Comments: To: Leanne Wilkins <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Message-ID: <[log in to unmask]> If you are doing an ROI analysis, then you don't have voxel data anymore. If you are doing a whole brain analysis and using a mask of a specific ROI (not an ROI analysis), then clicking whole brain or current cluster will give you the peak voxel. Best Regards, Donald McLaren ================D.G. McLaren, Ph.D. Postdoctoral Research Fellow, GRECC, Bedford VA Research Fellow, Department of Neurology, Massachusetts General Hospital and Harvard Medical School Office: (773) 406-2464 ====================This e-mail contains CONFIDENTIAL INFORMATION which may contain PROTECTED HEALTHCARE INFORMATION and may also be LEGALLY PRIVILEGED and which is intended only for the use of the individual or entity named above. If the reader of the e-mail is not the intended recipient or the employee or agent responsible for delivering it to the intended recipient, you are hereby notified that you are in possession of confidential and privileged information. Any unauthorized use, disclosure, copying or the taking of any action in reliance on the contents of this information is strictly prohibited and may be unlawful. If you have received this e-mail unintentionally, please immediately notify the sender via telephone at (773) 406-2464 or email. On Tue, Feb 1, 2011 at 10:05 PM, Leanne Wilkins <[log in to unmask]> wrote: > We are currently doing an ROI analysis with several different contrasts. I was wondering if there was an SPM script that would permit me to identify the top voxel activated in each ROI? > > I am new to SPM, I hope my question makes sense. > > Leanne > ========================================================================Date: Tue, 1 Feb 2011 22:23:45 -0500 Reply-To: "MCLAREN, Donald" <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: "MCLAREN, Donald" <[log in to unmask]> Subject: Re: Missing condition at first level - what to input in the onset tab? Comments: To: Reem Jan <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> The second contrast should use .2 not .25. Best Regards, Donald McLaren ================= D.G. McLaren, Ph.D. Postdoctoral Research Fellow, GRECC, Bedford VA Research Fellow, Department of Neurology, Massachusetts General Hospital and Harvard Medical School Office: (773) 406-2464 ===================== This e-mail contains CONFIDENTIAL INFORMATION which may contain PROTECTED HEALTHCARE INFORMATION and may also be LEGALLY PRIVILEGED and which is intended only for the use of the individual or entity named above. If the reader of the e-mail is not the intended recipient or the employee or agent responsible for delivering it to the intended recipient, you are hereby notified that you are in possession of confidential and privileged information. Any unauthorized use, disclosure, copying or the taking of any action in reliance on the contents of this information is strictly prohibited and may be unlawful. If you have received this e-mail unintentionally, please immediately notify the sender via telephone at (773) 406-2464 or email. On Tue, Feb 1, 2011 at 10:15 PM, Reem Jan <[log in to unmask]> wrote: > Thank you Cyril, Michael and Donald for all the useful information you > have given me regarding this. > > There are 6 runs/sessions and 4 conditions per subject. > > I have done the following. > > If condition A is missing from run 1 and 2 let's say.. I remove > condition A from that run (in the first level model specification), and > then in the contrast manager when I specify condition A's contrast I > type: > > 0 0 0 0 0.25 0 0 0.25 0 0 0.25 0 0 0.25 0 0 > > And if condition A is missing only from run 2: > > 0.25 0 0 0 0 0.25 0 0 0.25 0 0 0.25 0 0 0.25 0 0 > > And I also include 6 zeros after each run for the motion regressors > (which I haven't typed out here for simplicity's sake). > > I hope this is right? > > Kind regards > Reem > > -----Original Message----- > From: SPM (Statistical Parametric Mapping) [mailto:[log in to unmask]] > On Behalf Of Michael Harms > Sent: Wednesday, February 02, 2011 7:13 AM > To: [log in to unmask] > Subject: Re: [SPM] Missing condition at first level - what to input in > the onset tab? > > Well, "reasonably" sure, although happy for someone else to chime in to > the contrary. Many different contrasts can be technically valid (i.e., > "estimable"). In the example in question, the contrast I proposed would > test for an expected difference between the mean of condition A and B of > zero, whereas in your original contrast the expected value of the > contrast would not be zero under the null hypothesis of no difference > between A and B. > > In effect, I believe that by using a factor of 6/5 on the 5 A > conditions, one achieves the desired "upweighting" of the variance > associated with the condition A estimate (relative to the condition B > estimate). > > cheers, > -MH > > > On Tue, 2011-02-01 at 13:56 +0000, Cyril Pernet wrote: >> Hi Michael >> >> r u sure? ok beta = pinv(X)*Y so we don't really care about the bias > (I >> was referring to nb of stimuli and variance estimation) >> >> for the contrast with 5A and 6B using 1/5 1/6 you average 5 sessions > vs >> 6 which of course works as well but you may want to somehow put this >> unbalance in your contrast? I guess it's a matter of choice - note > that >> C is unchanged by the post multiplication by inv(X'X')X'X using my >> contrast so it is still valid too .. contrast don't have to sum up to > 0 >> (oh yeh my full contrast wasn't right since I copied/pasted 6 times .. > >> but I'm sure you got the gesture). >> >> I actually never had this problem - was offering a possible solution > but >> yours seems good too - anybody out there checked this up before? >> >> Cyril >> >> >> > Hi Cyril, >> > Even if you don't have equal numbers, the estimated betas are > themselves >> > still unbiased. Thus, if you are going to compare two conditions, > it >> > seems to me that you still want the contrast to sum to 0. In the > example >> > you gave, if you wanted to compare the mean level of A to the mean > level >> > of B, with no estimate of A available from session 3, I think that > you >> > would want the following contrast: >> > 1/5 -1/6 0 1/5 -1/6 0 0 -1/6 0 1/5 -1/6 0 1/5 -1/6 0 1/5 -1/6 0 >> > or multiplying by 6: >> > 6/5 -1 0 6/5 -1 0 0 -1 0 6/5 -1 0 6/5 -1 0 6/5 -1 0 >> > (note the 0 in the "A" position of the 3rd session). >> > >> > cheers, >> > -MH >> > >> >> Reem >> >> >> >> It doesn't really matter that in each session you don't have the > same >> >> number of stimuli per condition as long as across your 6 sessions > you >> >> end up with equal numbers (will work as well if not but it's not as > good >> >> because variance estimation can be biased). As for the different > number >> >> of conditions you can weight your contrast accordingly. Simply > create 6 >> >> sessions in SPM and your 2 or 3 conditions in each sessions. Let > say >> >> your design runs like this: >> >> >> >> Session 1 A B C >> >> Session 2 A B >> >> Session 3 B C >> >> Session 4 A B C >> >> Session 5 A B C >> >> Session 6 A B >> >> = 5*A 6*B 4*C >> >> = 30/6*A 36/6*B 26/6*C (I choose to have 6 as denominator because > you >> >> have 6 sessions) >> >> >> >> Let say you want to test A - B then use a contrast [30/36 -1 0 > 30/36 >> >> -1 0 30/36 -1 0 30/36 -1 0 30/36 -1 0 30/36 -1 0] >> >> How do I end up with 30/36 and -1 --> 1/6 * 30/6 = 30/36 and -1/6 > * 36/6 >> >> = -1 (I use 1/6 for each session since you have 6 sessions) >> >> The sum doesn't end up to 1 but the contrast should still be valid > .. >> >> (at least using a simple design on my machine with unbalanced > design and >> >> manual checking the contrast is valid - check in SPM I think it is > ok) >> >> >> >> Good luck >> >> Cyril >> >> >> >> >> >> >> >>> Dear SPMers >> >>> >> >>> I am trying run first level analysis on fMRI data in SPM8. >> >>> >> >>> The experiment design involves 6 runs/sessions, each run/session >> >>> consists of 8 stimuli (48 stimuli in total). >> >>> >> >>> There are 3 experimental conditions spread out equally across > stimuli >> >>> i.e. There are 16 stimuli of each condition in total. >> >>> >> >>> Because the stimuli were presented at random and are > event-related, I am >> >>> now running into a problem because in some of the runs of 8 > stimuli, >> >>> there happens to be only 2 of the conditions presented and not 3. > In >> >>> these cases, I'm not sure what to input in the 'onsets' tab of > first >> >>> level model specification for the 3rd condition. >> >>> >> >>> Is there a way around this problem. I'd be very appreciative of > some >> >>> help. >> >>> >> >>> Kind regards >> >>> Reem >> >>> >> >> >> >> -- >> >> The University of Edinburgh is a charitable body, registered in >> >> Scotland, with registration number SC005336. >> >> >> > >> > >> >> > > > __________ Information from ESET NOD32 Antivirus, version of virus > signature database 5838 (20110201) __________ > > The message was checked by ESET NOD32 Antivirus. > > http://www.eset.com > > > > __________ Information from ESET NOD32 Antivirus, version of virus > signature database 5838 (20110201) __________ > > The message was checked by ESET NOD32 Antivirus. > > http://www.eset.com > > ========================================================================Date: Wed, 2 Feb 2011 16:31:03 +1300 Reply-To: Reem Jan <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Reem Jan <[log in to unmask]> Subject: Re: Missing condition at first level - what to input in the onset tab? Comments: To: "MCLAREN, Donald" <[log in to unmask]> In-Reply-To: <[log in to unmask]> Content-Transfer-Encoding: 7bit Content-Type: text/plain; charset="us-ascii" MIME-Version: 1.0 (iPhone Mail 8C148a) Message-ID: <[log in to unmask]> Oh sorry yes I meant to change that to 0.2. Thank you Donald On 2/02/2011, at 16:23, "MCLAREN, Donald" <[log in to unmask]> wrote: > The second contrast should use .2 not .25. > > Best Regards, Donald McLaren > ================> D.G. McLaren, Ph.D. > Postdoctoral Research Fellow, GRECC, Bedford VA > Research Fellow, Department of Neurology, Massachusetts General > Hospital and Harvard Medical School > Office: (773) 406-2464 > ====================> This e-mail contains CONFIDENTIAL INFORMATION which may contain > PROTECTED HEALTHCARE INFORMATION and may also be LEGALLY PRIVILEGED > and which is intended only for the use of the individual or entity > named above. If the reader of the e-mail is not the intended recipient > or the employee or agent responsible for delivering it to the intended > recipient, you are hereby notified that you are in possession of > confidential and privileged information. Any unauthorized use, > disclosure, copying or the taking of any action in reliance on the > contents of this information is strictly prohibited and may be > unlawful. If you have received this e-mail unintentionally, please > immediately notify the sender via telephone at (773) 406-2464 or > email. > > > > On Tue, Feb 1, 2011 at 10:15 PM, Reem Jan <[log in to unmask]> wrote: >> Thank you Cyril, Michael and Donald for all the useful information you >> have given me regarding this. >> >> There are 6 runs/sessions and 4 conditions per subject. >> >> I have done the following. >> >> If condition A is missing from run 1 and 2 let's say.. I remove >> condition A from that run (in the first level model specification), and >> then in the contrast manager when I specify condition A's contrast I >> type: >> >> 0 0 0 0 0.25 0 0 0.25 0 0 0.25 0 0 0.25 0 0 >> >> And if condition A is missing only from run 2: >> >> 0.25 0 0 0 0 0.25 0 0 0.25 0 0 0.25 0 0 0.25 0 0 >> >> And I also include 6 zeros after each run for the motion regressors >> (which I haven't typed out here for simplicity's sake). >> >> I hope this is right? >> >> Kind regards >> Reem >> >> -----Original Message----- >> From: SPM (Statistical Parametric Mapping) [mailto:[log in to unmask]] >> On Behalf Of Michael Harms >> Sent: Wednesday, February 02, 2011 7:13 AM >> To: [log in to unmask] >> Subject: Re: [SPM] Missing condition at first level - what to input in >> the onset tab? >> >> Well, "reasonably" sure, although happy for someone else to chime in to >> the contrary. Many different contrasts can be technically valid (i.e., >> "estimable"). In the example in question, the contrast I proposed would >> test for an expected difference between the mean of condition A and B of >> zero, whereas in your original contrast the expected value of the >> contrast would not be zero under the null hypothesis of no difference >> between A and B. >> >> In effect, I believe that by using a factor of 6/5 on the 5 A >> conditions, one achieves the desired "upweighting" of the variance >> associated with the condition A estimate (relative to the condition B >> estimate). >> >> cheers, >> -MH >> >> >> On Tue, 2011-02-01 at 13:56 +0000, Cyril Pernet wrote: >>> Hi Michael >>> >>> r u sure? ok beta = pinv(X)*Y so we don't really care about the bias >> (I >>> was referring to nb of stimuli and variance estimation) >>> >>> for the contrast with 5A and 6B using 1/5 1/6 you average 5 sessions >> vs >>> 6 which of course works as well but you may want to somehow put this >>> unbalance in your contrast? I guess it's a matter of choice - note >> that >>> C is unchanged by the post multiplication by inv(X'X')X'X using my >>> contrast so it is still valid too .. contrast don't have to sum up to >> 0 >>> (oh yeh my full contrast wasn't right since I copied/pasted 6 times .. >> >>> but I'm sure you got the gesture). >>> >>> I actually never had this problem - was offering a possible solution >> but >>> yours seems good too - anybody out there checked this up before? >>> >>> Cyril >>> >>> >>>> Hi Cyril, >>>> Even if you don't have equal numbers, the estimated betas are >> themselves >>>> still unbiased. Thus, if you are going to compare two conditions, >> it >>>> seems to me that you still want the contrast to sum to 0. In the >> example >>>> you gave, if you wanted to compare the mean level of A to the mean >> level >>>> of B, with no estimate of A available from session 3, I think that >> you >>>> would want the following contrast: >>>> 1/5 -1/6 0 1/5 -1/6 0 0 -1/6 0 1/5 -1/6 0 1/5 -1/6 0 1/5 -1/6 0 >>>> or multiplying by 6: >>>> 6/5 -1 0 6/5 -1 0 0 -1 0 6/5 -1 0 6/5 -1 0 6/5 -1 0 >>>> (note the 0 in the "A" position of the 3rd session). >>>> >>>> cheers, >>>> -MH >>>> >>>>> Reem >>>>> >>>>> It doesn't really matter that in each session you don't have the >> same >>>>> number of stimuli per condition as long as across your 6 sessions >> you >>>>> end up with equal numbers (will work as well if not but it's not as >> good >>>>> because variance estimation can be biased). As for the different >> number >>>>> of conditions you can weight your contrast accordingly. Simply >> create 6 >>>>> sessions in SPM and your 2 or 3 conditions in each sessions. Let >> say >>>>> your design runs like this: >>>>> >>>>> Session 1 A B C >>>>> Session 2 A B >>>>> Session 3 B C >>>>> Session 4 A B C >>>>> Session 5 A B C >>>>> Session 6 A B >>>>> = 5*A 6*B 4*C >>>>> = 30/6*A 36/6*B 26/6*C (I choose to have 6 as denominator because >> you >>>>> have 6 sessions) >>>>> >>>>> Let say you want to test A - B then use a contrast [30/36 -1 0 >> 30/36 >>>>> -1 0 30/36 -1 0 30/36 -1 0 30/36 -1 0 30/36 -1 0] >>>>> How do I end up with 30/36 and -1 --> 1/6 * 30/6 = 30/36 and -1/6 >> * 36/6 >>>>> = -1 (I use 1/6 for each session since you have 6 sessions) >>>>> The sum doesn't end up to 1 but the contrast should still be valid >> .. >>>>> (at least using a simple design on my machine with unbalanced >> design and >>>>> manual checking the contrast is valid - check in SPM I think it is >> ok) >>>>> >>>>> Good luck >>>>> Cyril >>>>> >>>>> >>>>> >>>>>> Dear SPMers >>>>>> >>>>>> I am trying run first level analysis on fMRI data in SPM8. >>>>>> >>>>>> The experiment design involves 6 runs/sessions, each run/session >>>>>> consists of 8 stimuli (48 stimuli in total). >>>>>> >>>>>> There are 3 experimental conditions spread out equally across >> stimuli >>>>>> i.e. There are 16 stimuli of each condition in total. >>>>>> >>>>>> Because the stimuli were presented at random and are >> event-related, I am >>>>>> now running into a problem because in some of the runs of 8 >> stimuli, >>>>>> there happens to be only 2 of the conditions presented and not 3. >> In >>>>>> these cases, I'm not sure what to input in the 'onsets' tab of >> first >>>>>> level model specification for the 3rd condition. >>>>>> >>>>>> Is there a way around this problem. I'd be very appreciative of >> some >>>>>> help. >>>>>> >>>>>> Kind regards >>>>>> Reem >>>>>> >>>>> >>>>> -- >>>>> The University of Edinburgh is a charitable body, registered in >>>>> Scotland, with registration number SC005336. >>>>> >>>> >>>> >>> >>> >> >> >> __________ Information from ESET NOD32 Antivirus, version of virus >> signature database 5838 (20110201) __________ >> >> The message was checked by ESET NOD32 Antivirus. >> >> http://www.eset.com >> >> >> >> __________ Information from ESET NOD32 Antivirus, version of virus >> signature database 5838 (20110201) __________ >> >> The message was checked by ESET NOD32 Antivirus. >> >> http://www.eset.com >> >> ========================================================================Date: Tue, 1 Feb 2011 19:40:28 -0800 Reply-To: Michael T Rubens <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Michael T Rubens <[log in to unmask]> Subject: Re: Voxel In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/alternative; boundaryMessage-ID: <[log in to unmask]> --00221534d4cfce9be7049b446ae2 Content-Type: text/plain; charset=UTF-8 you could find the peak voxel by doing this in matlab (not spm gui): V = spm_vol('path_to_stat_image.img'); Vd = spm_read_vols(V); M = spm_vol('path_2_stat_image.img'); Md = spm_read_vols(M); mx = max(Vd(find(Md))); %thats it Cheers, Michael On Tue, Feb 1, 2011 at 7:22 PM, MCLAREN, Donald <[log in to unmask]>wrote: > If you are doing an ROI analysis, then you don't have voxel data anymore. > > If you are doing a whole brain analysis and using a mask of a specific > ROI (not an ROI analysis), then clicking whole brain or current > cluster will give you the peak voxel. > > Best Regards, Donald McLaren > ================> D.G. McLaren, Ph.D. > Postdoctoral Research Fellow, GRECC, Bedford VA > Research Fellow, Department of Neurology, Massachusetts General > Hospital and Harvard Medical School > Office: (773) 406-2464 > ====================> This e-mail contains CONFIDENTIAL INFORMATION which may contain > PROTECTED HEALTHCARE INFORMATION and may also be LEGALLY PRIVILEGED > and which is intended only for the use of the individual or entity > named above. If the reader of the e-mail is not the intended recipient > or the employee or agent responsible for delivering it to the intended > recipient, you are hereby notified that you are in possession of > confidential and privileged information. Any unauthorized use, > disclosure, copying or the taking of any action in reliance on the > contents of this information is strictly prohibited and may be > unlawful. If you have received this e-mail unintentionally, please > immediately notify the sender via telephone at (773) 406-2464 or > email. > > > > On Tue, Feb 1, 2011 at 10:05 PM, Leanne Wilkins > <[log in to unmask]> wrote: > > We are currently doing an ROI analysis with several different contrasts. > I was wondering if there was an SPM script that would permit me to identify > the top voxel activated in each ROI? > > > > I am new to SPM, I hope my question makes sense. > > > > Leanne > > > -- Research Associate Gazzaley Lab Department of Neurology University of California, San Francisco --00221534d4cfce9be7049b446ae2 Content-Type: text/html; charset=UTF-8 Content-Transfer-Encoding: quoted-printable you could find the peak voxel by doing this in matlab (not spm gui):

V = spm_vol('path_to_stat_image.img');
Vd = spm_read_vols(V);

M = spm_vol('path_2_stat_image.img');
Md = spm_read_vols(M);

mx = max(Vd(find(Md)));

%thats it

Cheers,
Michael

On Tue, Feb 1, 2011 at 7:22 PM, MCLAREN, Donald <[log in to unmask]> wrote:
If you are doing an ROI analysis, then you don't have voxel data anymore.

If you are doing a whole brain analysis and using a mask of a specific
ROI (not an ROI analysis), then clicking whole brain or current
cluster will give you the peak voxel.

Best Regards, Donald McLaren
=================
D.G. McLaren, Ph.D.
Postdoctoral Research Fellow, GRECC, Bedford VA
Research Fellow, Department of Neurology, Massachusetts General
Hospital and Harvard Medical School
Office: (773) 406-2464
=====================
This e-mail contains CONFIDENTIAL INFORMATION which may contain
PROTECTED HEALTHCARE INFORMATION and may also be LEGALLY PRIVILEGED
and which is intended only for the use of the individual or entity
named above. If the reader of the e-mail is not the intended recipient
or the employee or agent responsible for delivering it to the intended
recipient, you are hereby notified that you are in possession of
confidential and privileged information. Any unauthorized use,
disclosure, copying or the taking of any action in reliance on the
contents of this information is strictly prohibited and may be
unlawful. If you have received this e-mail unintentionally, please
immediately notify the sender via telephone at (773) 406-2464 or
email.



On Tue, Feb 1, 2011 at 10:05 PM, Leanne Wilkins
<[log in to unmask]> wrote:
> We are currently doing an ROI analysis with several different contrasts. I was wondering if there was an SPM script that would permit me to identify the top voxel activated in each ROI?
>
> I am new to SPM, I hope my question makes sense.
>
> Leanne
>



--
Research Associate
Gazzaley Lab
Department of Neurology
University of California, San Francisco
--00221534d4cfce9be7049b446ae2-- ========================================================================Date: Tue, 1 Feb 2011 19:44:24 -0800 Reply-To: Michael T Rubens <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Michael T Rubens <[log in to unmask]> Subject: Re: Voxel In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/alternative; boundaryMessage-ID: <[log in to unmask]> --000325575fded53840049b447827 Content-Type: text/plain; charset=UTF-8 whoops, 4th line should be M = spm_vol('path_2_ROI_image.img'); On Tue, Feb 1, 2011 at 7:40 PM, Michael T Rubens <[log in to unmask]>wrote: > you could find the peak voxel by doing this in matlab (not spm gui): > > V = spm_vol('path_to_stat_image.img'); > Vd = spm_read_vols(V); > > M = spm_vol('path_2_stat_image.img'); > Md = spm_read_vols(M); > > mx = max(Vd(find(Md))); > > %thats it > > Cheers, > Michael > > On Tue, Feb 1, 2011 at 7:22 PM, MCLAREN, Donald <[log in to unmask]>wrote: > >> If you are doing an ROI analysis, then you don't have voxel data anymore. >> >> If you are doing a whole brain analysis and using a mask of a specific >> ROI (not an ROI analysis), then clicking whole brain or current >> cluster will give you the peak voxel. >> >> Best Regards, Donald McLaren >> ================>> D.G. McLaren, Ph.D. >> Postdoctoral Research Fellow, GRECC, Bedford VA >> Research Fellow, Department of Neurology, Massachusetts General >> Hospital and Harvard Medical School >> Office: (773) 406-2464 >> ====================>> This e-mail contains CONFIDENTIAL INFORMATION which may contain >> PROTECTED HEALTHCARE INFORMATION and may also be LEGALLY PRIVILEGED >> and which is intended only for the use of the individual or entity >> named above. If the reader of the e-mail is not the intended recipient >> or the employee or agent responsible for delivering it to the intended >> recipient, you are hereby notified that you are in possession of >> confidential and privileged information. Any unauthorized use, >> disclosure, copying or the taking of any action in reliance on the >> contents of this information is strictly prohibited and may be >> unlawful. If you have received this e-mail unintentionally, please >> immediately notify the sender via telephone at (773) 406-2464 or >> email. >> >> >> >> On Tue, Feb 1, 2011 at 10:05 PM, Leanne Wilkins >> <[log in to unmask]> wrote: >> > We are currently doing an ROI analysis with several different contrasts. >> I was wondering if there was an SPM script that would permit me to identify >> the top voxel activated in each ROI? >> > >> > I am new to SPM, I hope my question makes sense. >> > >> > Leanne >> > >> > > > > -- > Research Associate > Gazzaley Lab > Department of Neurology > University of California, San Francisco > -- Research Associate Gazzaley Lab Department of Neurology University of California, San Francisco --000325575fded53840049b447827 Content-Type: text/html; charset=UTF-8 Content-Transfer-Encoding: quoted-printable whoops, 4th line should be


M = spm_vol('path_2_ROI_image.img');

On Tue, Feb 1, 2011 at 7:40 PM, Michael T Rubens <[log in to unmask]> wrote:
you could find the peak voxel by doing this in matlab (not spm gui):

V = spm_vol('path_to_stat_image.img');
Vd = spm_read_vols(V);

M = spm_vol('path_2_stat_image.img');
Md = spm_read_vols(M);

mx = max(Vd(find(Md)));

%thats it

Cheers,
Michael

On Tue, Feb 1, 2011 at 7:22 PM, MCLAREN, Donald <[log in to unmask]> wrote:
If you are doing an ROI analysis, then you don't have voxel data anymore.

If you are doing a whole brain analysis and using a mask of a specific
ROI (not an ROI analysis), then clicking whole brain or current
cluster will give you the peak voxel.

Best Regards, Donald McLaren
=================
D.G. McLaren, Ph.D.
Postdoctoral Research Fellow, GRECC, Bedford VA
Research Fellow, Department of Neurology, Massachusetts General
Hospital and Harvard Medical School
Office: (773) 406-2464
=====================
This e-mail contains CONFIDENTIAL INFORMATION which may contain
PROTECTED HEALTHCARE INFORMATION and may also be LEGALLY PRIVILEGED
and which is intended only for the use of the individual or entity
named above. If the reader of the e-mail is not the intended recipient
or the employee or agent responsible for delivering it to the intended
recipient, you are hereby notified that you are in possession of
confidential and privileged information. Any unauthorized use,
disclosure, copying or the taking of any action in reliance on the
contents of this information is strictly prohibited and may be
unlawful. If you have received this e-mail unintentionally, please
immediately notify the sender via telephone at (773) 406-2464 or
email.



On Tue, Feb 1, 2011 at 10:05 PM, Leanne Wilkins
<[log in to unmask]> wrote:
> We are currently doing an ROI analysis with several different contrasts. I was wondering if there was an SPM script that would permit me to identify the top voxel activated in each ROI?
>
> I am new to SPM, I hope my question makes sense.
>
> Leanne
>



--
Research Associate
Gazzaley Lab
Department of Neurology
University of California, San Francisco



--
Research Associate
Gazzaley Lab
Department of Neurology
University of California, San Francisco
--000325575fded53840049b447827-- ========================================================================Date: Wed, 2 Feb 2011 10:19:07 +0530 Reply-To: sarika cherodath <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: sarika cherodath <[log in to unmask]> Subject: Comparing conditions across runs MIME-Version: 1.0 Content-Type: multipart/alternative; boundary cf3054a5e3bbc302049b455f89 Message-ID: <[log in to unmask]> --20cf3054a5e3bbc302049b455f89 Content-Type: text/plain; charset=ISO-8859-1 Hi SPMers, How can one compare effect of two conditions in two separate runs? For eg. If run 1 = A R A R A R and so on and run 2 = B R B R B R then, how can one perform A vs. B contrast?? Will it be a problem that both A and B have same onsets?? Many thanks in advance -- Sarika Cherodath Graduate Student National Brain Research Centre Manesar, Gurgaon -122050 India --20cf3054a5e3bbc302049b455f89 Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable
Hi SPMers,

How can one compare effect of two conditions in two separate runs? For eg. If run 1 = A R A R A R and so on and run 2 = B R B R B R then, how can one perform A vs. B contrast?? Will it be a problem that both A and B have same onsets??

Many thanks in advance

--
Sarika Cherodath
Graduate Student
National Brain Research Centre
Manesar, Gurgaon -122050
India

--20cf3054a5e3bbc302049b455f89-- ========================================================================Date: Tue, 1 Feb 2011 23:02:31 -0800 Reply-To: Michael Spezio <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Michael Spezio <[log in to unmask]> Subject: Bandpass filtering with wide bands in spm8: Why is there a problem? Mime-Version: 1.0 Content-Type: multipart/alternative; boundary="=__PartFAD6F397.0__=" Message-ID: <[log in to unmask]> This is a MIME message. If you are reading this text, you may want to consider changing to a mail reader or gateway that understands how to properly handle MIME multipart messages. --=__PartFAD6F397.0__Content-Type: text/plain; charset=US-ASCII Content-Transfer-Encoding: quoted-printable Hi Vladimir, I saw in your post 041502, dated 2010-05-07, that for some reason bandpass filtering with wide bands (e.g., 0.1 to 30 Hz) elicits bad performance by the Matlab SP Toolbox and causes displays of the subsequent data to fail. Can you specify why this is occurring? It doesn't seem to make sense given that wide bandpass filters are used in signal processing routinely. Also, for the Multimodal Face tutorial, why isn't filtering done prior to downsampling? Downsampling, especially to 200 Hz or lower, should only be done after filtering out higher frequency contaminating signals, measured at a high sampling rate (500 Hz or above), to avoid aliasing from muscle signals at frequencies of 90 Hz to 200 Hz. Can you help me understand what is going on with the bandpass processing and why filtering is left out of the tutorial? Thanks so much. Best, Michael Michael L. Spezio, Ph.D. Assistant Professor of Psychology Department of Psychology Scripps College Claremont, CA [log in to unmask] 909.607.0914 and Visiting Associate Scientist Psychology & Neuroscience Division of Humanities & Social Sciences Caltech Pasadena, CA 91125 [log in to unmask] --=__PartFAD6F397.0__Content-Type: text/html; charset=US-ASCII Content-Transfer-Encoding: quoted-printable Content-Description: HTML Hi Vladimir,

I saw in your post 041502, dated 2010-05-07, that for some reason bandpass filtering with wide bands (e.g., 0.1 to 30 Hz) elicits bad performance by the Matlab SP Toolbox and causes displays of the subsequent data to fail.

Can you specify why this is occurring? It doesn't seem to make sense given that wide bandpass filters are used in signal processing routinely.

Also, for the Multimodal Face tutorial, why isn't filtering done prior to downsampling? Downsampling, especially to 200 Hz or lower, should only be done after filtering out higher frequency contaminating signals, measured at a high sampling rate (500 Hz or above), to avoid aliasing from muscle signals at frequencies of 90 Hz to 200 Hz. Can you help me understand what is going on with the bandpass processing and why filtering is left out of the tutorial?

Thanks so much.

Best,

Michael

Michael L. Spezio, Ph.D.
Assistant Professor of Psychology
Department of Psychology
Scripps College
Claremont, CA
[log in to unmask]
909.607.0914

and

Visiting Associate Scientist
Psychology & Neuroscience
Division of Humanities & Social Sciences
Caltech
Pasadena, CA 91125
[log in to unmask]

--=__PartFAD6F397.0__=-- ========================================================================Date: Wed, 2 Feb 2011 10:13:56 +0100 Reply-To: Ali Gholami <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Ali Gholami <[log in to unmask]> Subject: SPM Content-Type: text/plain; charset="UTF-8" Mime-Version: 1.0 Content-Transfer-Encoding: 7bit Message-ID: <1296638036.16391.2.camel@tb06> Hi I've installed a matlab 2010b under "/usr/local/matalab". I also extracted a SPM8 update under"/home/spm8". Now I can't see any information how to use and run SPM. My question is how to run SPM? ========================================================================Date: Wed, 2 Feb 2011 09:28:01 +0000 Reply-To: =?utf-8?B?Y3lyaWwucGVybmV0QGVkLmFjLnVr?= <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: =?utf-8?B?Y3lyaWwucGVybmV0QGVkLmFjLnVr?= <[log in to unmask]> Subject: Re: SPM Comments: To: =?utf-8?B?QWxpIEdob2xhbWk=?= <[log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/mixed; boundary="----------=_1296638927-6285-52" Content-Transfer-Encoding: binary Message-ID: <[log in to unmask]> This is a multi-part message in MIME format... ------------=_1296638927-6285-52 Received: from [192.168.0.3] (5ada724d.bb.sky.com [90.218.114.77]) (authenticated user=cpernet mech=LOGIN bits=0) by lmtp1.ucs.ed.ac.uk (8.13.8/8.13.7) with ESMTP id p129SjX0022169 (version=TLSv1/SSLv3 cipher=DHE-RSA-AES256-SHA bits%6 verify=NOT); Wed, 2 Feb 2011 09:28:46 GMT Message-Id: <[log in to unmask]> To: "=?utf-8?B?QWxpIEdob2xhbWk=?=" <[log in to unmask]>, [log in to unmask] From: "=?utf-8?B?Y3lyaWwucGVybmV0QGVkLmFjLnVr?=" <[log in to unmask]> Subject: =?utf-8?B?UmU6IFtTUE1dIFNQTQ==?Date: Wed, 02 Feb 2011 09:28:01 +0000 MIME-Version: 1.0 Content-Type: multipart/alternative; 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charset=ISO-8859-1; DelSp="Yes"; format="flowed" Content-Disposition: inline Content-Transfer-Encoding: 7bit Message-ID: <[log in to unmask]> ---------------------------------------------------------------- Este mensaje ha sido enviado desde https://webmail.unav.es ========================================================================Date: Wed, 2 Feb 2011 10:36:59 +0100 Reply-To: Ali Gholami <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Ali Gholami <[log in to unmask]> Subject: Re: SPM Comments: To: "[log in to unmask]" <[log in to unmask]> In-Reply-To: <[log in to unmask]> Content-Type: text/plain; charset="UTF-8" Mime-Version: 1.0 Content-Transfer-Encoding: 7bit Message-ID: <1296639419.16391.4.camel@tb06> Thank you Cyril for the information. Now, I get this error: >> spm ??? Error using ==> spm_check_installation>check_basic at 77 There appears to be some problem with the installation. The original spm8.zip distribution should be installed and the updates installed on top of this. Unix commands to do this are: unzip spm8.zip unzip -o spm8_updates_r????.zip -d spm8 You may need help from your local network administrator. Error in ==> spm_check_installation at 25 check_basic; Error in ==> spm at 297 spm_check_installation('basic'); Do you know the reason? Best regards Ali Gholami On Wed, 2011-02-02 at 09:28 +0000, [log in to unmask] wrote: > In matlab use the tabs File - add path - and add the SPM folder. > This way matlab knows where is SPM and can use its function. Type SPM > in the command window and the GUI will pop up. Also download the data > set. Manual is in your SPM folder in the man subfolder. > > Enjoy the best soft ever lol > > Dr Cyril Pernet > SBIRC / SINAPSE > University of Edinburgh > > ----- Reply message ----- > From: "Ali Gholami" <[log in to unmask]> > Date: Wed, Feb 2, 2011 09:13 > Subject: [SPM] SPM > To: <[log in to unmask]> > > Hi > > I've installed a matlab 2010b under "/usr/local/matalab". I also > extracted a SPM8 update under"/home/spm8". Now I can't see any > information how to use and run SPM. > > My question is how to run SPM? > > > > > > > The University of Edinburgh is a charitable body, registered in > Scotland, with registration number SC005336. ========================================================================Date: Wed, 2 Feb 2011 23:21:00 +1300 Reply-To: Reem Jan <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Reem Jan <[log in to unmask]> Subject: Re: SPM Comments: To: Ali Gholami <[log in to unmask]> In-Reply-To: <1296639419.16391.4.camel@tb06> Content-Transfer-Encoding: quoted-printable Content-Type: text/plain; charset="us-ascii" MIME-Version: 1.0 (iPhone Mail 8C148a) Message-ID: <[log in to unmask]> Hi Ali I think you may not have downloaded spm8 software and instead only downloaded the updates. You will need to download the software first then unpack the latest update and allow it to overwrite the original files. You can then set path to the spm8 folder as Cyril suggested. Cheers Reem On 2/02/2011, at 22:37, "Ali Gholami" <[log in to unmask]> wrote: > Thank you Cyril for the information. Now, I get this error: > >>> spm > ??? Error using ==> spm_check_installation>check_basic at 77 > There appears to be some problem with the installation. > The original spm8.zip distribution should be installed > and the updates installed on top of this. Unix commands > to do this are: > unzip spm8.zip > unzip -o spm8_updates_r????.zip -d spm8 > You may need help from your local network administrator. > > Error in ==> spm_check_installation at 25 > check_basic; > > Error in ==> spm at 297 > spm_check_installation('basic'); > > > > Do you know the reason? > > Best regards > Ali Gholami > > > On Wed, 2011-02-02 at 09:28 +0000, [log in to unmask] wrote: >> In matlab use the tabs File - add path - and add the SPM folder. >> This way matlab knows where is SPM and can use its function. Type SPM >> in the command window and the GUI will pop up. Also download the data >> set. Manual is in your SPM folder in the man subfolder. >> >> Enjoy the best soft ever lol >> >> Dr Cyril Pernet >> SBIRC / SINAPSE >> University of Edinburgh >> >> ----- Reply message ----- >> From: "Ali Gholami" <[log in to unmask]> >> Date: Wed, Feb 2, 2011 09:13 >> Subject: [SPM] SPM >> To: <[log in to unmask]> >> >> Hi >> >> I've installed a matlab 2010b under "/usr/local/matalab". I also >> extracted a SPM8 update under"/home/spm8". Now I can't see any >> information how to use and run SPM. >> >> My question is how to run SPM? >> >> >> >> >> >> >> The University of Edinburgh is a charitable body, registered in >> Scotland, with registration number SC005336. ========================================================================Date: Wed, 2 Feb 2011 11:25:58 +0100 Reply-To: Ali Gholami <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Ali Gholami <[log in to unmask]> Subject: Re: SPM Comments: To: Reem Jan <[log in to unmask]> In-Reply-To: <[log in to unmask]> Content-Type: text/plain; charset="UTF-8" Mime-Version: 1.0 Content-Transfer-Encoding: 7bit Message-ID: <1296642358.16391.6.camel@tb06> Hi Reem, Thank you for your answer. You are right, I just installed the updates. It was a little bit strange for me to first install the update but I couldn't find a link to "SPM" itself. Do you know where I get the SPM directly? Regards Ali On Wed, 2011-02-02 at 23:21 +1300, Reem Jan wrote: > Hi Ali > > I think you may not have downloaded spm8 software and instead only downloaded the updates. You will need to download the software first then unpack the latest update and allow it to overwrite the original files. You can then set path to the spm8 folder as Cyril suggested. > > Cheers > Reem > > On 2/02/2011, at 22:37, "Ali Gholami" <[log in to unmask]> wrote: > > > Thank you Cyril for the information. Now, I get this error: > > > >>> spm > > ??? Error using ==> spm_check_installation>check_basic at 77 > > There appears to be some problem with the installation. > > The original spm8.zip distribution should be installed > > and the updates installed on top of this. Unix commands > > to do this are: > > unzip spm8.zip > > unzip -o spm8_updates_r????.zip -d spm8 > > You may need help from your local network administrator. > > > > Error in ==> spm_check_installation at 25 > > check_basic; > > > > Error in ==> spm at 297 > > spm_check_installation('basic'); > > > > > > > > Do you know the reason? > > > > Best regards > > Ali Gholami > > > > > > On Wed, 2011-02-02 at 09:28 +0000, [log in to unmask] wrote: > >> In matlab use the tabs File - add path - and add the SPM folder. > >> This way matlab knows where is SPM and can use its function. Type SPM > >> in the command window and the GUI will pop up. Also download the data > >> set. Manual is in your SPM folder in the man subfolder. > >> > >> Enjoy the best soft ever lol > >> > >> Dr Cyril Pernet > >> SBIRC / SINAPSE > >> University of Edinburgh > >> > >> ----- Reply message ----- > >> From: "Ali Gholami" <[log in to unmask]> > >> Date: Wed, Feb 2, 2011 09:13 > >> Subject: [SPM] SPM > >> To: <[log in to unmask]> > >> > >> Hi > >> > >> I've installed a matlab 2010b under "/usr/local/matalab". I also > >> extracted a SPM8 update under"/home/spm8". Now I can't see any > >> information how to use and run SPM. > >> > >> My question is how to run SPM? > >> > >> > >> > >> > >> > >> > >> The University of Edinburgh is a charitable body, registered in > >> Scotland, with registration number SC005336. > ========================================================================Date: Wed, 2 Feb 2011 23:47:36 +1300 Reply-To: Reem Jan <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Reem Jan <[log in to unmask]> Subject: Re: SPM Comments: To: Ali Gholami <[log in to unmask]> In-Reply-To: <1296642358.16391.6.camel@tb06> Content-Transfer-Encoding: quoted-printable Content-Type: text/plain; charset="us-ascii" MIME-Version: 1.0 (iPhone Mail 8C148a) Message-ID: <[log in to unmask]> Hi Ali You can download SPM after filling out a registration form here http://www.fil.ion.ucl.ac.uk/spm/software/download.html Cheers Reem On 2/02/2011, at 23:28, "Ali Gholami" <[log in to unmask]> wrote: > Hi Reem, > > Thank you for your answer. You are right, I just installed the updates. > It was a little bit strange for me to first install the update but I > couldn't find a link to "SPM" itself. Do you know where I get the SPM > directly? > > > Regards > Ali > > > On Wed, 2011-02-02 at 23:21 +1300, Reem Jan wrote: >> Hi Ali >> >> I think you may not have downloaded spm8 software and instead only downloaded the updates. You will need to download the software first then unpack the latest update and allow it to overwrite the original files. You can then set path to the spm8 folder as Cyril suggested. >> >> Cheers >> Reem >> >> On 2/02/2011, at 22:37, "Ali Gholami" <[log in to unmask]> wrote: >> >>> Thank you Cyril for the information. Now, I get this error: >>> >>>>> spm >>> ??? Error using ==> spm_check_installation>check_basic at 77 >>> There appears to be some problem with the installation. >>> The original spm8.zip distribution should be installed >>> and the updates installed on top of this. Unix commands >>> to do this are: >>> unzip spm8.zip >>> unzip -o spm8_updates_r????.zip -d spm8 >>> You may need help from your local network administrator. >>> >>> Error in ==> spm_check_installation at 25 >>> check_basic; >>> >>> Error in ==> spm at 297 >>> spm_check_installation('basic'); >>> >>> >>> >>> Do you know the reason? >>> >>> Best regards >>> Ali Gholami >>> >>> >>> On Wed, 2011-02-02 at 09:28 +0000, [log in to unmask] wrote: >>>> In matlab use the tabs File - add path - and add the SPM folder. >>>> This way matlab knows where is SPM and can use its function. Type SPM >>>> in the command window and the GUI will pop up. Also download the data >>>> set. Manual is in your SPM folder in the man subfolder. >>>> >>>> Enjoy the best soft ever lol >>>> >>>> Dr Cyril Pernet >>>> SBIRC / SINAPSE >>>> University of Edinburgh >>>> >>>> ----- Reply message ----- >>>> From: "Ali Gholami" <[log in to unmask]> >>>> Date: Wed, Feb 2, 2011 09:13 >>>> Subject: [SPM] SPM >>>> To: <[log in to unmask]> >>>> >>>> Hi >>>> >>>> I've installed a matlab 2010b under "/usr/local/matalab". I also >>>> extracted a SPM8 update under"/home/spm8". Now I can't see any >>>> information how to use and run SPM. >>>> >>>> My question is how to run SPM? >>>> >>>> >>>> >>>> >>>> >>>> >>>> The University of Edinburgh is a charitable body, registered in >>>> Scotland, with registration number SC005336. >> ========================================================================Date: Wed, 2 Feb 2011 11:18:12 +0000 Reply-To: Vladimir Litvak <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Vladimir Litvak <[log in to unmask]> Subject: Re: Bandpass filtering with wide bands in spm8: Why is there a problem? Comments: To: Michael Spezio <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Message-ID: <[log in to unmask]> Dear Michael, On Wed, Feb 2, 2011 at 7:02 AM, Michael Spezio <[log in to unmask]> wrote: > Hi Vladimir, > > I saw in your post 041502, dated 2010-05-07, that for some reason bandpass > filtering with wide bands (e.g., 0.1 to 30 Hz) elicits bad performance by > the Matlab SP Toolbox and causes displays of the subsequent data to fail. > > Can you specify why this is occurring? It doesn't seem to make sense given > that wide bandpass filters are used in signal processing routinely. > It's not a display issue but actual data corruption issue. There are numerical stability problems that I have since also observed in high-pass filters for some combinations of filter settings and sampling rate. These problems are common for wide bandpass filters, especially for ones with low cut-off close to DC (e.g. 0.1-40 Hz). Therefore, I recommended that people use separate high-pass and low-pass in these cases. In the next SPM8 update there is a change in the code that detects automatically when a filter is unstable and gives an error so people will not have to figure it out later when their display crashes. > Also, for the Multimodal Face tutorial, why isn't filtering done prior to > downsampling? Downsampling, especially to 200 Hz or lower, should only be > done after filtering out higher frequency contaminating signals, measured at > a high sampling rate (500 Hz or above), to avoid aliasing from muscle > signals at frequencies of 90 Hz to 200 Hz. Can you help me understand what > is going on with the bandpass processing and why filtering is left out of > the tutorial? > Aliasing can occur when downsampling is done by simple decimation in the time domain (e.g. taking every other sample). SP toolbox downsampling routine is smarter than that and it pre-filters data to avoid aliasing so it is not necessary to do it explicitly. In the absence of SP toolbox we use or own routine that downsamples in the frequency domain by truncating the DFT coefficients. This way there is also no aliasing. The only problem that can occur is that if there are large DC offsets in the data, low-pass filter will cause ringing at the edges. Therefore I'd suggest to apply high-pass filtering before downsampling especially for epoched data. In the case of the faces tutorial this is not a problem because downsampling is done on continuous data (for EEG) or on baseline-corrected data (for MEG). Best, Vladimir > Thanks so much. > > Best, > > Michael > > Michael L. Spezio, Ph.D. > Assistant Professor of Psychology > Department of Psychology > Scripps College > Claremont, CA > [log in to unmask] > 909.607.0914 > > and > > Visiting Associate Scientist > Psychology & Neuroscience > Division of Humanities & Social Sciences > Caltech > Pasadena, CA 91125 > [log in to unmask] > ========================================================================Date: Wed, 2 Feb 2011 12:49:43 +0100 Reply-To: Michel Thiebaut de Schotten <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Michel Thiebaut de Schotten <[log in to unmask]> Subject: Natbrainlab Workshop Comments: To: [log in to unmask] Content-Type: text/plain; charset=iso-8859-1 Content-Transfer-Encoding: quoted-printable Mime-Version: 1.0 (Apple Message framework v1082) Message-ID: <[log in to unmask]> Dear all, The 9th Neuroanatomy and Tractography workshop will be held in London (Institute of Psychiatry) on the 23-24-25 March 2011. This workshop intends to help scientists to develop and optimise strategies for DTI datasets analysis and tractography. The number of participants is limited to 12 for allowing 1:1 tutoring. The participants will be able to work on their own datasets and receive advice from the members of the Natbrainlab (http://www.natbrainlab.com). This is also an opportunity to familiarise with fundaments of white matter anatomy and brain hodology. Wednesday 23th March VISUALIZATION OF WHITE MATTER CONNECTIONS 09:30 - 10:00 Registration 10:00 - 10:30 Brain Hodology: From post mortem dissections to diffusion MRI (M Catani) 10:30 - 11:30 Introduction to Diffusion Tensor MRI (F Dell'Acqua) 11:30 - 11:45 Coffee Break 11:45 - 12:45 Diffusion Tensor Tractography (F Dell'Acqua) 12:45 - 14:00 Lunch Break 14:00 - 15:15 DTI data formats: Management and pre-processing (M Thiebaut de Schotten) 15:15 - 15:45 Coffee Break 15:45 - 17:00 Tractography with TrackVis (M Thiebaut de Schotten) Thursday 24th March VIRTUAL IN VIVO DISSECTIONS 09:30 - 10:00 Classification of white matter connections (M Catani) 10:00 - 11:00 Association Pathways 1 (M Catani) 11:00 - 11:15 Coffee Break 11:15 - 12:30 Association Pathways 2 (S Budisavljevic) 12:30 - 14:00 Lunch Break 14:00 - 15:15 Commissural Pathways (S Forkel) 15:15 - 15:45 Coffee Break 15:45 - 17:00 Projections Pathways (S Forkel) Friday 25th March DTI TRACTOGRAPHY: CURRENT APPLICATIONS AND FUTURE DIRECTIONS 09:30 - 10:30 Beyond the limitations of tensor modeling (F Dell'Acqua) 10:30 - 10:45 Coffee Break 10:40 - 11:30 Studying Normal Anatomy with DTI Tractography (M Catani) 11:30 - 12:30 Applications to Neurological and Psychiatric Disorders (M Catani) 12:30 - 14:00 Lunch Break 14:00 - 15:15 Supervised Dissection 1 15:15 - 15:45 Coffee Break 15:45 - 16:30 Supervised Dissection 2 16:30 -17:00 Conclusions & Take Home Messages (M Catani) Michel Thiebaut de Schotten, PhD NATBRAINLABANR-CAFORPFC/ANR-HMTC CRICM-INSERM UMRS 975 Pavillon de l'Enfance et l'Adolescence 47 Bd de l'Hpital 75651 Paris Cedex 13, France www.natbrainlab.com skype: michel_thiebaut_de_schotten +33 613579133 ========================================================================Date: Wed, 2 Feb 2011 15:25:16 +0000 Reply-To: Vladimir Litvak <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Vladimir Litvak <[log in to unmask]> Subject: Re: Bandpass filtering with wide bands in spm8: Why is there a problem? Comments: To: Michael Spezio <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Message-ID: <[log in to unmask]> It's probably an SP toolbox issue, but I have never seen an example of this happening for any setting. It usually only happens for some settings. What is your sampling rate? Is your data epoched or continuous? If it's epoched perhaps your epochs are not long enough? If it's continuous I'd try changing the filter order or using an IIR filter (you can do it if you use batch interface to filtering). Or perhaps downsampling event to a slightly different rate will help. Vladimir On Wed, Feb 2, 2011 at 3:16 PM, Michael Spezio <[log in to unmask]> wrote: > Great, thanks for this very helpful response, Vladimir. > > I have noticed that even with using just highpass filtering, any setting > below 2 Hz results in the data corruption issues. If this is an issue with > the SP toolbox, then the Mathworks should be contacted to fix it. If it's a > problem with SPM8, then may there be an upgrade in the future? > > Best, > > Michael > > > Michael L. Spezio, Ph.D. > Assistant Professor of Psychology > Department of Psychology > Scripps College > Claremont, CA > [log in to unmask] > 909.607.0914 > > and > > Visiting Associate Scientist > Psychology & Neuroscience > Division of Humanities & Social Sciences > Caltech > Pasadena, CA 91125 > [log in to unmask] >>>> Vladimir Litvak <[log in to unmask]> 02/02/11 3:19 AM >>> > Dear Michael, > > On Wed, Feb 2, 2011 at 7:02 AM, Michael Spezio > <[log in to unmask]> wrote: >> Hi Vladimir, >> >> I saw in your post 041502, dated 2010-05-07, that for some reason bandpass >> filtering with wide bands (e.g., 0.1 to 30 Hz) elicits bad performance by >> the Matlab SP Toolbox and causes displays of the subsequent data to fail. >> >> Can you specify why this is occurring? It doesn't seem to make sense given >> that wide bandpass filters are used in signal processing routinely. >> > > It's not a display issue but actual data corruption issue. There are > numerical stability problems that I have since also observed in > high-pass filters for some combinations of filter settings and > sampling rate. These problems are common for wide bandpass filters, > especially for ones with low cut-off close to DC (e.g. 0.1-40 Hz). > Therefore, I recommended that people use separate high-pass and > low-pass in these cases. In the next SPM8 update there is a change in > the code that detects automatically when a filter is unstable and > gives an error so people will not have to figure it out later when > their display crashes. > >> Also, for the Multimodal Face tutorial, why isn't filtering done prior to >> downsampling? Downsampling, especially to 200 Hz or lower, should only be >> done after filtering out higher frequency contaminating signals, measured >> at >> a high sampling rate (500 Hz or above), to avoid aliasing from muscle >> signals at frequencies of 90 Hz to 200 Hz. Can you help me understand what >> is going on with the bandpass processing and why filtering is left out of >> the tutorial? >> > > Aliasing can occur when downsampling is done by simple decimation in > the time domain (e.g. taking every other sample). SP toolbox > downsampling routine is smarter than that and it pre-filters data to > avoid aliasing so it is not necessary to do it explicitly. In the > absence of SP toolbox we use or own routine that downsamples in the > frequency domain by truncating the DFT coefficients. This way there is > also no aliasing. The only problem that can occur is that if there are > large DC offsets in the data, low-pass filter will cause ringing at > the edges. Therefore I'd suggest to apply high-pass filtering before > downsampling especially for epoched data. In the case of the faces > tutorial this is not a problem because downsampling is done on > continuous data (for EEG) or on baseline-corrected data (for MEG). > > Best, > > Vladimir > >> Thanks so much. >> >> Best, >> >> Michael >> >> Michael L. Spezio, Ph.D. >> Assistant Professor of Psychology >> Department of Psychology >> Scripps College >> Claremont, CA >> [log in to unmask] >> 909.607.0914 >> >> and >> >> Visiting Associate Scientist >> Psychology & Neuroscience >> Division of Humanities & Social Sciences >> Caltech >> Pasadena, CA 91125 >> [log in to unmask] >> > ========================================================================Date: Wed, 2 Feb 2011 15:18:53 +0000 Reply-To: Gaetan Yvert <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Gaetan Yvert <[log in to unmask]> Subject: eeg source reconstruction and temporal contrast Mime-Version: 1.0 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain; charset="UTF-8" Message-ID: <[log in to unmask]> Dear SPM experts, I have used the group source reconstruction toolbox provided by SPM. It worked very well, but know it's for me to interpret my results ! I have used the both type of temporal contrast (ie gaussian window and morlet wavelet) and I founded slightly different results. I used a time windows for the inversion between 0 to 800 ms and a temporal contrast between 0 and 400 ms to highlight the different sources involved in all my process. I am working on a langage task which is known to imply broca's and wernicke's area and it is what I found ! with the gaussian window I found Broca's area and with the series of wavelet I found broca's and Wernicke's areas. both type of contrast are strongly significant even with FWE correction. And know I have to interpret it! Can I say that using a gaussian windows I highlight more continuous activation whereas using a series of wavelet I will more highlight transient activation in upper frequency band? should I refine my study and doing it in the different well known frequency band? thank you for your attention, bests regards, Gaetan Yvert ========================================================================Date: Wed, 2 Feb 2011 07:35:35 -0800 Reply-To: Michael Spezio <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Michael Spezio <[log in to unmask]> Subject: Re: Bandpass filtering with wide bands in spm8: Why is there a problem? Comments: To: [log in to unmask] Mime-Version: 1.0 Content-Type: multipart/alternative; boundary="=__PartC2EECBD7.1__=" Message-ID: <[log in to unmask]> This is a MIME message. If you are reading this text, you may want to consider changing to a mail reader or gateway that understands how to properly handle MIME multipart messages. --=__PartC2EECBD7.1__Content-Type: text/plain; charset=US-ASCII Content-Transfer-Encoding: quoted-printable Hi Vladimir, I tried the <2 Hz highpass setting for the sampling rate for the tutorial data, which is 2048 Hz. But I also tried first downsampling to 500 Hz, then applying <2 Hz filtering, and it also failed for that sampling rate. Both times, filtering was applied to continuous data rather than to epoched data. Perhaps I will try the IIR filter via the batch interface. Best, Michael Michael L. Spezio, Ph.D. Assistant Professor of Psychology Department of Psychology Scripps College Claremont, CA [log in to unmask] 909.607.0914 and Visiting Associate Scientist Psychology & Neuroscience Division of Humanities & Social Sciences Caltech Pasadena, CA 91125 [log in to unmask] >>> Vladimir Litvak 02/02/11 7:26 AM >>> It's probably an SP toolbox issue, but I have never seen an example of this happening for any setting. It usually only happens for some settings. What is your sampling rate? Is your data epoched or continuous? If it's epoched perhaps your epochs are not long enough? If it's continuous I'd try changing the filter order or using an IIR filter (you can do it if you use batch interface to filtering). Or perhaps downsampling event to a slightly different rate will help. Vladimir On Wed, Feb 2, 2011 at 3:16 PM, Michael Spezio wrote: > Great, thanks for this very helpful response, Vladimir. > > I have noticed that even with using just highpass filtering, any setting > below 2 Hz results in the data corruption issues. If this is an issue with > the SP toolbox, then the Mathworks should be contacted to fix it. If it's a > problem with SPM8, then may there be an upgrade in the future? > > Best, > > Michael > > > Michael L. Spezio, Ph.D. > Assistant Professor of Psychology > Department of Psychology > Scripps College > Claremont, CA > [log in to unmask] > 909.607.0914 > > and > > Visiting Associate Scientist > Psychology & Neuroscience > Division of Humanities & Social Sciences > Caltech > Pasadena, CA 91125 > [log in to unmask] >>>> Vladimir Litvak 02/02/11 3:19 AM >>> > Dear Michael, > > On Wed, Feb 2, 2011 at 7:02 AM, Michael Spezio > wrote: >> Hi Vladimir, >> >> I saw in your post 041502, dated 2010-05-07, that for some reason bandpass >> filtering with wide bands (e.g., 0.1 to 30 Hz) elicits bad performance by >> the Matlab SP Toolbox and causes displays of the subsequent data to fail. >> >> Can you specify why this is occurring? It doesn't seem to make sense given >> that wide bandpass filters are used in signal processing routinely. >> > > It's not a display issue but actual data corruption issue. There are > numerical stability problems that I have since also observed in > high-pass filters for some combinations of filter settings and > sampling rate. These problems are common for wide bandpass filters, > especially for ones with low cut-off close to DC (e.g. 0.1-40 Hz). > Therefore, I recommended that people use separate high-pass and > low-pass in these cases. In the next SPM8 update there is a change in > the code that detects automatically when a filter is unstable and > gives an error so people will not have to figure it out later when > their display crashes. > >> Also, for the Multimodal Face tutorial, why isn't filtering done prior to >> downsampling? Downsampling, especially to 200 Hz or lower, should only be >> done after filtering out higher frequency contaminating signals, measured >> at >> a high sampling rate (500 Hz or above), to avoid aliasing from muscle >> signals at frequencies of 90 Hz to 200 Hz. Can you help me understand what >> is going on with the bandpass processing and why filtering is left out of >> the tutorial? >> > > Aliasing can occur when downsampling is done by simple decimation in > the time domain (e.g. taking every other sample). SP toolbox > downsampling routine is smarter than that and it pre-filters data to > avoid aliasing so it is not necessary to do it explicitly. In the > absence of SP toolbox we use or own routine that downsamples in the > frequency domain by truncating the DFT coefficients. This way there is > also no aliasing. The only problem that can occur is that if there are > large DC offsets in the data, low-pass filter will cause ringing at > the edges. Therefore I'd suggest to apply high-pass filtering before > downsampling especially for epoched data. In the case of the faces > tutorial this is not a problem because downsampling is done on > continuous data (for EEG) or on baseline-corrected data (for MEG). > > Best, > > Vladimir > >> Thanks so much. >> >> Best, >> >> Michael >> >> Michael L. Spezio, Ph.D. >> Assistant Professor of Psychology >> Department of Psychology >> Scripps College >> Claremont, CA >> [log in to unmask] >> 909.607.0914 >> >> and >> >> Visiting Associate Scientist >> Psychology & Neuroscience >> Division of Humanities & Social Sciences >> Caltech >> Pasadena, CA 91125 >> [log in to unmask] >> > --=__PartC2EECBD7.1__Content-Type: text/html; charset=US-ASCII Content-Transfer-Encoding: quoted-printable Content-Description: HTML Hi Vladimir,

I tried the <2 Hz highpass setting for the sampling rate for the tutorial data, which is 2048 Hz. But I also tried first downsampling to 500 Hz, then applying <2 Hz filtering, and it also failed for that sampling rate. Both times, filtering was applied to continuous data rather than to epoched data.

Perhaps I will try the IIR filter via the batch interface.

Best,

Michael


Michael L. Spezio, Ph.D.
Assistant Professor of Psychology
Department of Psychology
Scripps College
Claremont, CA
[log in to unmask]
909.607.0914

and

Visiting Associate Scientist
Psychology & Neuroscience
Division of Humanities & Social Sciences
Caltech
Pasadena, CA 91125
[log in to unmask]

>>> Vladimir Litvak <[log in to unmask]> 02/02/11 7:26 AM >>>
It's probably an SP toolbox issue, but I have never seen an example of
this happening for any setting. It usually only happens for some
settings. What is your sampling rate? Is your data epoched or
continuous? If it's epoched perhaps your epochs are not long enough?
If it's continuous I'd try changing the filter order or using an IIR
filter (you can do it if you use batch interface to filtering). Or
perhaps downsampling event to a slightly different rate will help.

Vladimir

On Wed, Feb 2, 2011 at 3:16 PM, Michael Spezio
<[log in to unmask]> wrote:
> Great, thanks for this very helpful response, Vladimir.
>
> I have noticed that even with using just highpass filtering, any setting
> below 2 Hz results in the data corruption issues. If this is an issue with
> the SP toolbox, then the Mathworks should be contacted to fix it. If it's a
> problem with SPM8, then may there be an upgrade in the future?
>
> Best,
>
> Michael
>
>
> Michael L. Spezio, Ph.D.
> Assistant Professor of Psychology
> Department of Psychology
> Scripps College
> Claremont, CA
> [log in to unmask]
> 909.607.0914
>
> and
>
> Visiting Associate Scientist
> Psychology & Neuroscience
> Division of Humanities & Social Sciences
> Caltech
> Pasadena, CA 91125
> [log in to unmask]
>>>> Vladimir Litvak <[log in to unmask]> 02/02/11 3:19 AM >>>
> Dear Michael,
>
> On Wed, Feb 2, 2011 at 7:02 AM, Michael Spezio
> <[log in to unmask]> wrote:
>> Hi Vladimir,
>>
>> I saw in your post 041502, dated 2010-05-07, that for some reason bandpass
>> filtering with wide bands (e.g., 0.1 to 30 Hz) elicits bad performance by
>> the Matlab SP Toolbox and causes displays of the subsequent data to fail.
>>
>> Can you specify why this is occurring? It doesn't seem to make sense given
>> that wide bandpass filters are used in signal processing routinely.
>>
>
> It's not a display issue but actual data corruption issue. There are
> numerical stability problems that I have since also observed in
> high-pass filters for some combinations of filter settings and
> sampling rate. These problems are common for wide bandpass filters,
> especially for ones with low cut-off close to DC (e.g. 0.1-40 Hz).
> Therefore, I recommended that people use separate high-pass and
> low-pass in these cases. In the next SPM8 update there is a change in
> the code that detects automatically when a filter is unstable and
> gives an error so people will not have to figure it out later when
> their display crashes.
>
>> Also, for the Multimodal Face tutorial, why isn't filtering done prior to
>> downsampling? Downsampling, especially to 200 Hz or lower, should only be
>> done after filtering out higher frequency contaminating signals, measured
>> at
>> a high sampling rate (500 Hz or above), to avoid aliasing from muscle
>> signals at frequencies of 90 Hz to 200 Hz. Can you help me understand what
>> is going on with the bandpass processing and why filtering is left out of
>> the tutorial?
>>
>
> Aliasing can occur when downsampling is done by simple decimation in
> the time domain (e.g. taking every other sample). SP toolbox
> downsampling routine is smarter than that and it pre-filters data to
> avoid aliasing so it is not necessary to do it explicitly. In the
> absence of SP toolbox we use or own routine that downsamples in the
> frequency domain by truncating the DFT coefficients. This way there is
> also no aliasing. The only problem that can occur is that if there are
> large DC offsets in the data, low-pass filter will cause ringing at
> the edges. Therefore I'd suggest to apply high-pass filtering before
> downsampling especially for epoched data. In the case of the faces
> tutorial this is not a problem because downsampling is done on
> continuous data (for EEG) or on baseline-corrected data (for MEG).
>
> Best,
>
> Vladimir
>
>> Thanks so much.
>>
>> Best,
>>
>> Michael
>>
>> Michael L. Spezio, Ph.D.
>> Assistant Professor of Psychology
>> Department of Psychology
>> Scripps College
>> Claremont, CA
>> [log in to unmask]
>> 909.607.0914
>>
>> and
>>
>> Visiting Associate Scientist
>> Psychology & Neuroscience
>> Division of Humanities & Social Sciences
>> Caltech
>> Pasadena, CA 91125
>> [log in to unmask]
>>
>
--=__PartC2EECBD7.1__=-- ========================================================================Date: Wed, 2 Feb 2011 15:40:53 +0000 Reply-To: Vladimir Litvak <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Vladimir Litvak <[log in to unmask]> Subject: Re: eeg source reconstruction and temporal contrast Comments: To: Gaetan Yvert <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> Dear Gaetan, First it is very good to hear that you got sensible and significant results. It's indeed my feeling that the last version of the routines is really on the right track. Regarding interpretation, I understand that in both cases you used averaged ERP/ERF rather than epoched file as input. In this case the difference between using a Gaussian window and wavelets over your whole bandwidth is like the difference between average and RMS. So if you have some activity that changes polarity in your time window if you average over it, it can get attenuated or even average to zero. So looking at total power retains more and if you can do all your analysis just on that, perhaps that's what you should do. Averaging is just more conceptually similar and standard thing to do. Regarding limiting your analysis to a band, that's a question of whether you can justify it. Also it's perhaps something that makes more sense when looking at induced activity (i.e. inverting an epoched file). Best, Vladimir On Wed, Feb 2, 2011 at 3:18 PM, Gaetan Yvert <[log in to unmask]> wrote: > Dear SPM experts, > > I have used the group source reconstruction toolbox provided by SPM. > It worked very well, but know it's for me to interpret my results ! > > I have used the both type of temporal contrast (ie gaussian window and morlet wavelet) and I founded slightly different results. > I used a time windows for the inversion between 0 to 800 ms and a temporal contrast between 0 and 400 ms to highlight the different sources involved in all my process. > I am working on a langage task which is known to imply broca's and wernicke's area and it is what I found ! > > with the gaussian window I found Broca's area and with the series of wavelet I found broca's and Wernicke's areas. both type of contrast are strongly significant even with FWE correction. > > And know I have to interpret it! > > Can I say that using a gaussian windows I highlight more continuous activation whereas using a series of wavelet I will more highlight transient activation in upper frequency band? > > should I refine my study and doing it in the different well known frequency band? > > thank you for your attention, > > bests regards, > > Gaetan Yvert > ========================================================================Date: Wed, 2 Feb 2011 15:45:17 +0000 Reply-To: Vladimir Litvak <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Vladimir Litvak <[log in to unmask]> Subject: Re: Bandpass filtering with wide bands in spm8: Why is there a problem? Comments: To: Michael Spezio <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Message-ID: <[log in to unmask]> That's really strange and should not happen. Perhaps there is a different reason that would be hard for me to pinpoint if I can't reproduce the problem here. Vladimir On Wed, Feb 2, 2011 at 3:35 PM, Michael Spezio <[log in to unmask]> wrote: > Hi Vladimir, > > I tried the <2 Hz highpass setting for the sampling rate for the tutorial > data, which is 2048 Hz. But I also tried first downsampling to 500 Hz, then > applying <2 Hz filtering, and it also failed for that sampling rate. Both > times, filtering was applied to continuous data rather than to epoched data. > > Perhaps I will try the IIR filter via the batch interface. > > Best, > > Michael > > > Michael L. Spezio, Ph.D. > Assistant Professor of Psychology > Department of Psychology > Scripps College > Claremont, CA > [log in to unmask] > 909.607.0914 > > and > > Visiting Associate Scientist > Psychology & Neuroscience > Division of Humanities & Social Sciences > Caltech > Pasadena, CA 91125 > [log in to unmask] >>>> Vladimir Litvak <[log in to unmask]> 02/02/11 7:26 AM >>> > It's probably an SP toolbox issue, but I have never seen an example of > this happening for any setting. It usually only happens for some > settings. What is your sampling rate? Is your data epoched or > continuous? If it's epoched perhaps your epochs are not long enough? > If it's continuous I'd try changing the filter order or using an IIR > filter (you can do it if you use batch interface to filtering). Or > perhaps downsampling event to a slightly different rate will help. > > Vladimir > > On Wed, Feb 2, 2011 at 3:16 PM, Michael Spezio > <[log in to unmask]> wrote: >> Great, thanks for this very helpful response, Vladimir. >> >> I have noticed that even with using just highpass filtering, any setting >> below 2 Hz results in the data corruption issues. If this is an issue with >> the SP toolbox, then the Mathworks should be contacted to fix it. If it's >> a >> problem with SPM8, then may there be an upgrade in the future? >> >> Best, >> >> Michael >> >> >> Michael L. Spezio, Ph.D. >> Assistant Professor of Psychology >> Department of Psychology >> Scripps College >> Claremont, CA >> [log in to unmask] >> 909.607.0914 >> >> and >> >> Visiting Associate Scientist >> Psychology & Neuroscience >> Division of Humanities & Social Sciences >> Caltech >> Pasadena, CA 91125 >> [log in to unmask] >>>>> Vladimir Litvak <[log in to unmask]> 02/02/11 3:19 AM >>> >> Dear Michael, >> >> On Wed, Feb 2, 2011 at 7:02 AM, Michael Spezio >> <[log in to unmask]> wrote: >>> Hi Vladimir, >>> >>> I saw in your post 041502, dated 2010-05-07, that for some reason >>> bandpass >>> filtering with wide bands (e.g., 0.1 to 30 Hz) elicits bad performance by >>> the Matlab SP Toolbox and causes displays of the subsequent data to fail. >>> >>> Can you specify why this is occurring? It doesn't seem to make sense >>> given >>> that wide bandpass filters are used in signal processing routinely. >>> >> >> It's not a display issue but actual data corruption issue. There are >> numerical stability problems that I have since also observed in >> high-pass filters for some combinations of filter settings and >> sampling rate. These problems are common for wide bandpass filters, >> especially for ones with low cut-off close to DC (e.g. 0.1-40 Hz). >> Therefore, I recommended that people use separate high-pass and >> low-pass in these cases. In the next SPM8 update there is a change in >> the code that detects automatically when a filter is unstable and >> gives an error so people will not have to figure it out later when >> their display crashes. >> >>> Also, for the Multimodal Face tutorial, why isn't filtering done prior to >>> downsampling? Downsampling, especially to 200 Hz or lower, should only be >>> done after filtering out higher frequency contaminating signals, measured >>> at >>> a high sampling rate (500 Hz or above), to avoid aliasing from muscle >>> signals at frequencies of 90 Hz to 200 Hz. Can you help me understand >>> what >>> is going on with the bandpass processing and why filtering is left out of >>> the tutorial? >>> >> >> Aliasing can occur when downsampling is done by simple decimation in >> the time domain (e.g. taking every other sample). SP toolbox >> downsampling routine is smarter than that and it pre-filters data to >> avoid aliasing so it is not necessary to do it explicitly. In the >> absence of SP toolbox we use or own routine that downsamples in the >> frequency domain by truncating the DFT coefficients. This way there is >> also no aliasing. The only problem that can occur is that if there are >> large DC offsets in the data, low-pass filter will cause ringing at >> the edges. Therefore I'd suggest to apply high-pass filtering before >> downsampling especially for epoched data. In the case of the faces >> tutorial this is not a problem because downsampling is done on >> continuous data (for EEG) or on baseline-corrected data (for MEG). >> >> Best, >> >> Vladimir >> >>> Thanks so much. >>> >>> Best, >>> >>> Michael >>> >>> Michael L. Spezio, Ph.D. >>> Assistant Professor of Psychology >>> Department of Psychology >>> Scripps College >>> Claremont, CA >>> [log in to unmask] >>> 909.607.0914 >>> >>> and >>> >>> Visiting Associate Scientist >>> Psychology & Neuroscience >>> Division of Humanities & Social Sciences >>> Caltech >>> Pasadena, CA 91125 >>> [log in to unmask] >>> >> > ========================================================================Date: Wed, 2 Feb 2011 09:54:31 -0600 Reply-To: Shashwath Meda <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Shashwath Meda <[log in to unmask]> Subject: Art Repair batch error MIME-Version: 1.0 Content-Type: multipart/alternative; boundaryMessage-ID: <[log in to unmask]> --00235444787d264889049b4eaa18 Content-Type: text/plain; charset=ISO-8859-1 Hi All - I am in the process of batching the art_global script over multiple subjects. I seem to get the following error, can someone help. art_global(b,b1,4,0); Generated mask image is written to file ArtifactMask.img. Adaptive Mask Threshold 130533 Mapping files...: ...done Calculating globals...: ...done\n 93415 voxels were in the auto generated mask. ??? Error using ==> cd Cannot CD to (Name is nonexistent or not a directory). Error in ==> art_global at 614 cd(fileparts(P(1,:))); b = all my image files b1 = my realignment params text file Any help would be much appreciated. -- with regards, Shashwath meda *********************************************** Imaging Genetics Analyst III 515-F Light Hall Vanderbilt University Medical Center Cell: (313) 505-6847 Off: (615) 875-3086 *********************************************** --00235444787d264889049b4eaa18 Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Hi All - I am in the process of batching the art_global script over multiple subjects. I seem to get the following error, can someone help.

art_global(b,b1,4,0);
Generated mask image is written to file ArtifactMask.img.
Adaptive Mask Threshold
130533

Mapping files...: ...done
Calculating globals...: ...done\n
93415 voxels were in the auto generated mask.
??? Error using ==> cd
Cannot CD to (Name is nonexistent or not a directory).

Error in ==> art_global at 614
cd(fileparts(P(1,:)));


b = all my image files
b1 = my realignment params text file


Any help would be much appreciated.


--
with regards,

Shashwath meda

***********************************************
Imaging Genetics Analyst III
515-F Light Hall
Vanderbilt University Medical Center
Cell: (313) 505-6847
Off: (615) 875-3086

***********************************************

--00235444787d264889049b4eaa18-- ========================================================================Date: Wed, 2 Feb 2011 18:58:44 +0100 Reply-To: Jokel Meyer <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Jokel Meyer <[log in to unmask]> Subject: Advice regarding proper programming style MIME-Version: 1.0 Content-Type: multipart/alternative; boundaryMessage-ID: <[log in to unmask]> --00163628447e666edd049b5066e9 Content-Type: text/plain; charset=ISO-8859-1 Dear SPM-list! In advance I would like to apologize for this slightly off-topic post. I started extending various SPM functions and adding own scripts to facilitate my analysis of MRI data. However as the number of functions & scripts increased rapidly I start loosing overview which is due to the fact that I do not have proper education in programming. Could you recommend any online resources or books that would introduce me to some principles of "good" programming, how to best organize your function and distribute calculations between .m-files? Many thanks for your help! Jokel --00163628447e666edd049b5066e9 Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Dear SPM-list!

In advance I would like to apologize for this slightly off-topic post.
I started extending various SPM functions and adding own scripts to facilitate my analysis of MRI data. However as the number of functions & scripts increased rapidly I start loosing overview which is due to the fact that I do not have proper education in programming. Could you recommend any online resources or books that would introduce me to some principles of "good" programming, how to best organize your function and distribute calculations between .m-files?

Many thanks for your help!
Jokel
--00163628447e666edd049b5066e9-- ========================================================================Date: Wed, 2 Feb 2011 13:17:39 -0500 Reply-To: "Watson, Christopher" <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: "Watson, Christopher" <[log in to unmask]> Subject: Re: Advice regarding proper programming style Comments: To: Jokel Meyer <[log in to unmask]> In-Reply-To: <[log in to unmask]> Content-Type: text/plain; charset="us-ascii" Content-Transfer-Encoding: quoted-printable MIME-Version: 1.0 Message-ID: <[log in to unmask]> The Matlab programming fundamentals guide is pretty good. ________________________________________ From: SPM (Statistical Parametric Mapping) [[log in to unmask]] On Behalf Of Jokel Meyer [[log in to unmask]] Sent: Wednesday, February 02, 2011 12:58 PM To: [log in to unmask] Subject: [SPM] Advice regarding proper programming style Dear SPM-list! In advance I would like to apologize for this slightly off-topic post. I started extending various SPM functions and adding own scripts to facilitate my analysis of MRI data. However as the number of functions & scripts increased rapidly I start loosing overview which is due to the fact that I do not have proper education in programming. Could you recommend any online resources or books that would introduce me to some principles of "good" programming, how to best organize your function and distribute calculations between .m-files? Many thanks for your help! Jokel ========================================================================Date: Wed, 2 Feb 2011 10:28:27 -0800 Reply-To: Michael Spezio <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Michael Spezio <[log in to unmask]> Subject: Re: Advice regarding proper programming style Comments: To: [log in to unmask] Mime-Version: 1.0 Content-Type: multipart/alternative; boundary="=__Part95B99C5B.1__=" Message-ID: <[log in to unmask]> This is a MIME message. If you are reading this text, you may want to consider changing to a mail reader or gateway that understands how to properly handle MIME multipart messages. --=__Part95B99C5B.1__Content-Type: text/plain; charset=US-ASCII Content-Transfer-Encoding: quoted-printable Hi Jokel, I've found that the book by Stormy Attaway is very good for teaching programming basics to undergraduates: http://www.amazon.com/gp/product/0750687622/ref=pd_lpo_k2_dp_sr_1?pf_rd_p=486539851&pf_rd_s=lpo-top-stripe-1&pf_rd_t=201&pf_rd_i=0495073008&pf_rd_m=ATVPDKIKX0DER&pf_rd_r=1XGCACF3TPNKC80VQPXV Best, Michael Michael L. Spezio, Ph.D. Assistant Professor of Psychology Department of Psychology Scripps College Claremont, CA [log in to unmask] 909.607.0914 and Visiting Associate Scientist Psychology & Neuroscience Division of Humanities & Social Sciences Caltech Pasadena, CA 91125 [log in to unmask] >>> "Watson, Christopher" 02/02/11 10:18 AM >>> The Matlab programming fundamentals guide is pretty good. ________________________________________ From: SPM (Statistical Parametric Mapping) [[log in to unmask]] On Behalf Of Jokel Meyer [[log in to unmask]] Sent: Wednesday, February 02, 2011 12:58 PM To: [log in to unmask] Subject: [SPM] Advice regarding proper programming style Dear SPM-list! In advance I would like to apologize for this slightly off-topic post. I started extending various SPM functions and adding own scripts to facilitate my analysis of MRI data. However as the number of functions & scripts increased rapidly I start loosing overview which is due to the fact that I do not have proper education in programming. Could you recommend any online resources or books that would introduce me to some principles of "good" programming, how to best organize your function and distribute calculations between .m-files? Many thanks for your help! Jokel --=__Part95B99C5B.1__Content-Type: text/html; charset=US-ASCII Content-Transfer-Encoding: quoted-printable Content-Description: HTML Hi Jokel,

I've found that the book by Stormy Attaway is very good for teaching programming basics to undergraduates:

http://www.amazon.com/gp/product/0750687622/ref=pd_lpo_k2_dp_sr_1?pf_rd_p=486539851&pf_rd_s=lpo-top-stripe-1&pf_rd_t=201&pf_rd_i=0495073008&pf_rd_m=ATVPDKIKX0DER&pf_rd_r=1XGCACF3TPNKC80VQPXV

Best,

Michael


Michael L. Spezio, Ph.D.
Assistant Professor of Psychology
Department of Psychology
Scripps College
Claremont, CA
[log in to unmask]
909.607.0914

and

Visiting Associate Scientist
Psychology & Neuroscience
Division of Humanities & Social Sciences
Caltech
Pasadena, CA 91125
[log in to unmask]

>>> "Watson, Christopher" <[log in to unmask]> 02/02/11 10:18 AM >>>
The Matlab programming fundamentals guide is pretty good.
________________________________________
From: SPM (Statistical Parametric Mapping) [[log in to unmask]] On Behalf Of Jokel Meyer [[log in to unmask]]
Sent: Wednesday, February 02, 2011 12:58 PM
To: [log in to unmask]
Subject: [SPM] Advice regarding proper programming style

Dear SPM-list!

In advance I would like to apologize for this slightly off-topic post.
I started extending various SPM functions and adding own scripts to facilitate my analysis of MRI data. However as the number of functions & scripts increased rapidly I start loosing overview which is due to the fact that I do not have proper education in programming. Could you recommend any online resources or books that would introduce me to some principles of "good" programming, how to best organize your function and distribute calculations between .m-files?

Many thanks for your help!
Jokel
--=__Part95B99C5B.1__=-- ========================================================================Date: Wed, 2 Feb 2011 19:34:04 +0100 Reply-To: Claus Lamm <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Claus Lamm <[log in to unmask]> Organization: University of Vienna Subject: Re: Advice regarding proper programming style In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/alternative; boundary="----=_NextPart_000_00AE_01CBC310.26D0C3E0" Message-ID: <[log in to unmask]> This is a multipart message in MIME format. ------=_NextPart_000_00AE_01CBC310.26D0C3E0 Content-Type: text/plain; charset="US-ASCII" Content-Transfer-Encoding: 7bit This might be useful too: http://www.amazon.com/Matlab-Neuroscientists-Introduction-Scientific-Computi ng/dp/0123745519/ref=sr_1_1?ie=UTF8 &s=books&qid96671614&sr=1-1 From: SPM (Statistical Parametric Mapping) [mailto:[log in to unmask]] On Behalf Of Michael Spezio Sent: Mittwoch, 02. Februar 2011 19:28 To: [log in to unmask] Subject: Re: [SPM] Advice regarding proper programming style Hi Jokel, I've found that the book by Stormy Attaway is very good for teaching programming basics to undergraduates: http://www.amazon.com/gp/product/0750687622/ref=pd_lpo_k2_dp_sr_1?pf_rd_pH 6539851 &pf_rd_s=lpo-top-stripe-1&pf_rd_t 1&pf_rd_i95073008&pf_rd_m=ATVPDKIKX0D ER&pf_rd_r=1XGCACF3TPNKC80VQPXV Best, Michael Michael L. Spezio, Ph.D. Assistant Professor of Psychology Department of Psychology Scripps College Claremont, CA [log in to unmask] 909.607.0914 and Visiting Associate Scientist Psychology & Neuroscience Division of Humanities & Social Sciences Caltech Pasadena, CA 91125 [log in to unmask] >>> "Watson, Christopher" <[log in to unmask]> 02/02/11 10:18 AM >>> The Matlab programming fundamentals guide is pretty good. ________________________________________ From: SPM (Statistical Parametric Mapping) [[log in to unmask]] On Behalf Of Jokel Meyer [[log in to unmask]] Sent: Wednesday, February 02, 2011 12:58 PM To: [log in to unmask] Subject: [SPM] Advice regarding proper programming style Dear SPM-list! In advance I would like to apologize for this slightly off-topic post. I started extending various SPM functions and adding own scripts to facilitate my analysis of MRI data. However as the number of functions & scripts increased rapidly I start loosing overview which is due to the fact that I do not have proper education in programming. Could you recommend any online resources or books that would introduce me to some principles of "good" programming, how to best organize your function and distribute calculations between .m-files? Many thanks for your help! Jokel ------=_NextPart_000_00AE_01CBC310.26D0C3E0 Content-Type: text/html; charset="US-ASCII" Content-Transfer-Encoding: quoted-printable

This might be useful too:

 

http://www.amazon.com/Matlab-Neuroscientists-Introduction-Scientific-Computing/dp/0123745519/ref=sr_1_1?ie=UTF8&s=books&qid=1296671614&sr=1-1

 

 

 

From: SPM (Statistical Parametric Mapping) [mailto:[log in to unmask]] On Behalf Of Michael Spezio
Sent: Mittwoch, 02. Februar 2011 19:28
To: [log in to unmask]
Subject: Re: [SPM] Advice regarding proper programming style

 

Hi Jokel,

I've found that the book by Stormy Attaway is very good for teaching programming basics to undergraduates:

http://www.amazon.com/gp/product/0750687622/ref=pd_lpo_k2_dp_sr_1?pf_rd_p=486539851&pf_rd_s=lpo-top-stripe-1&pf_rd_t=201&pf_rd_i=0495073008&pf_rd_m=ATVPDKIKX0DER&pf_rd_r=1XGCACF3TPNKC80VQPXV

Best,

Michael

Michael L. Spezio, Ph.D.
Assistant Professor of Psychology
Department of Psychology
Scripps College
Claremont, CA
[log in to unmask]
909.607.0914

and

Visiting Associate Scientist
Psychology & Neuroscience
Division of Humanities & Social Sciences
Caltech
Pasadena, CA 91125
[log in to unmask]


>>> "Watson, Christopher" <[log in to unmask]> 02/02/11 10:18 AM >>>
The Matlab programming fundamentals guide is pretty good.
________________________________________
From: SPM (Statistical Parametric Mapping) [[log in to unmask]] On Behalf Of Jokel Meyer [[log in to unmask]]
Sent: Wednesday, February 02, 2011 12:58 PM
To: [log in to unmask]
Subject: [SPM] Advice regarding proper programming style

Dear SPM-list!

In advance I would like to apologize for this slightly off-topic post.
I started extending various SPM functions and adding own scripts to facilitate my analysis of MRI data. However as the number of functions & scripts increased rapidly I start loosing overview which is due to the fact that I do not have proper education in programming. Could you recommend any online resources or books that would introduce me to some principles of "good" programming, how to best organize your function and distribute calculations between .m-files?

Many thanks for your help!
Jokel

------=_NextPart_000_00AE_01CBC310.26D0C3E0-- ========================================================================Date: Wed, 2 Feb 2011 13:35:15 -0500 Reply-To: Jonathan Peelle <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Jonathan Peelle <[log in to unmask]> Subject: Re: covariates in multiple regression Comments: To: Sien Hu <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/alternative; boundaryMessage-ID: <[log in to unmask]> --0016e648be78fd17dc049b50e81d Content-Type: text/plain; charset=ISO-8859-1 Hi Sien What if I would like to look at the effect of only age with bmi > being controlled. Is there any way to do it in SPM? > Sure. To look at the effect of one covariate while controlling for a second, enter both in your model as covariates, but leave a 0 over the column(s) you aren't interested in in your contrast. So the columns in your design matrix might be: BMI age grand_mean and you could then use contrasts of [1 0 0] or [-1 0 0] to look for effects of BMI, with the effects of age controlled for. Hope this helps, Jonathan --0016e648be78fd17dc049b50e81d Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Hi Sien

What if I would like to look at the effect of only age with bmi
being controlled. Is there any way to do it in SPM?

Sure. To look at the effect of one covariate while controlling for a second, enter both in your model as covariates, but leave a 0 over the column(s) you aren't interested in in your contrast. So the columns in your design matrix might be:

BMI age grand_mean

and you could then use contrasts of [1 0 0] or [-1 0 0] to look for effects of BMI, with the effects of age controlled for.

Hope this helps,
Jonathan

--0016e648be78fd17dc049b50e81d-- ========================================================================Date: Wed, 2 Feb 2011 13:34:12 -0500 Reply-To: "MCLAREN, Donald" <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: "MCLAREN, Donald" <[log in to unmask]> Subject: Re: Advice regarding proper programming style Comments: To: Jokel Meyer <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Message-ID: <[log in to unmask]> MATLAB for Neuroscientists has alot of information about matlab functions. In terms of general programming, both of the mentioned sources are good. Remember that you don't need a book specifically about MATLAB as the fundamentals of programming are always the same. The only difference is the syntax. Best Regards, Donald McLaren ================D.G. McLaren, Ph.D. Postdoctoral Research Fellow, GRECC, Bedford VA Research Fellow, Department of Neurology, Massachusetts General Hospital and Harvard Medical School Office: (773) 406-2464 ====================This e-mail contains CONFIDENTIAL INFORMATION which may contain PROTECTED HEALTHCARE INFORMATION and may also be LEGALLY PRIVILEGED and which is intended only for the use of the individual or entity named above. If the reader of the e-mail is not the intended recipient or the employee or agent responsible for delivering it to the intended recipient, you are hereby notified that you are in possession of confidential and privileged information. Any unauthorized use, disclosure, copying or the taking of any action in reliance on the contents of this information is strictly prohibited and may be unlawful. If you have received this e-mail unintentionally, please immediately notify the sender via telephone at (773) 406-2464 or email. On Wed, Feb 2, 2011 at 12:58 PM, Jokel Meyer <[log in to unmask]> wrote: > Dear SPM-list! > In advance I would like to apologize for this slightly off-topic post. > I started extending various SPM functions and adding own scripts to > facilitate my analysis of MRI data. However as the number of functions & > scripts increased rapidly I start loosing overview which is due to the fact > that I do not have proper education in programming. Could you recommend any > online resources or books that would introduce me to some principles of > "good" programming, how to best organize your function and distribute > calculations between .m-files? > Many thanks for your help! > Jokel ========================================================================Date: Wed, 2 Feb 2011 22:33:08 +0000 Reply-To: Thomas Nichols <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Thomas Nichols <[log in to unmask]> Subject: PhD Studentship in Statistics of fMRI Clinical Trials Comments: To: FSL - FMRIB's Software Library <[log in to unmask]>, [log in to unmask] MIME-Version: 1.0 Content-Type: multipart/alternative; boundaryMessage-ID: <[log in to unmask]> --001636765b69bc29a3049b543b11 Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Apologies for the cross-posting. Please distribute to all interested parties. Thank you! -Tom * * *MRC CASE Studentship in Statistics - University of Warwick & GlaxoSmithKline* * * Applications are invited for a PhD studentship in Statistics at the University of Warwick, funded by a MRC Industrial CASE award with the GlaxoSmithKline's Clinical Unit Cambridge. * * *Title: *Optimal Fixed and Adaptive Designs for fMRI Clinical Trials *Supervisors:* Dr. Thomas Nichols (Warwick) and Dr. Ed Bullmore (GSK) *Funding: *Tuition fees (at UK/EU level) and tax-free stipend for a 4 year PhD. Stipend rises annually as per the UK Research Councils minimum rate (13,590 for 2010/11), and is topped-up 2,500 by the industrial sponsor. *Start Date:* October 2011 * * *Project Description:* Functional Magnetic Resonance Imaging (fMRI) is now almost 20 years old and is an indispensible tool for cognitive neuroscience. However only recently has fMRI been employed as part of drug development, as pharmaceutical companies seek to develop biomarkers that are more sensitive to disease state. By it's increased sensitivity and specificity, fMRI has the potential to reduce the time require to bring a drug to the marketplace, thus lower the cost of drug development and ultimately improve patient care. However, fMRI for clinical trials requires a different set of statistical tools than that used by conventional brain mapping: clinical trial outcomes must be precisely defined a priori, and the number of outcomes considered minimized. Further, cutting-edge type of fMRI designs, using task-free data to measure "resting state networks" presents yet new challenges for use in a clinical trial, as task-free results are intrinsically multivariate and difficult to define a priori. The goal of this project is to develop novel statistical methodology to maximize information obtained from an fMRI study while still adhering to the stringent inferential requirements of a clinical trial. The project has three broad aims. The first is to develop adaptive designs for task-based fMRI clinical trials, using initial data to customize outcomes to an unknown signal. The second is to develop optimal outcomes for the task-free (or resting-state) fMRI data. The third aim is to develop optimal outcomes from graph-theoretic measures of task-based or task-free fMRI data, understanding the impact of matrix filtering operations on the power of final summary measure. The student will obtain a unique training in statistics and neuroimaging with mentorship from leading researchers in the field. The CASE award also includes three-months of on-site research at the GSK Clinical Unit Cambridge, giving them valuable industrial experience. *Requirements:* The studentship is available to candidates with the equivalent of a first class or upper second class degree in a relevant discipline, and who meet University entry requirements (see http://www2.warwick.ac.uk/services/academicoffice/gsp/prospective). *Eligibility:* UK nationals, or EU nationals who have been resident in the UK in the last three years. Other EU nationals can only receive a fees-only award. For full deatils see http://www.mrc.ac.uk/Fundingopportunities/Applicanthandbook/Studentships/Eligibility/index.htm *To Apply: * http://www2.warwick.ac.uk/fac/sci/statistics/postgrad/research/apply (and please notify Dr. Nichols [log in to unmask] when application is submitted) * * *Deadline*: Applications are considered on rolling basis, up until 31 July 2011, but priority given to applications received before 28 February. *Inquires:* Specific questions on this project should be directed to Thomas Nichols [log in to unmask]; questions on the postgraduate application process at Warwick should be directed to Ms. Kristine Prismall [log in to unmask] *Links:* Warwick Statistics http://go.warwick.ac.uk/stats Thomas Nichols http://go.warwick.ac.uk/tenichols Ed Bullmore's academic page http://www.psychiatry.cam.ac.uk/pages/profiles/bullmore.html --001636765b69bc29a3049b543b11 Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable
Apologiesfor the cross-posting. Please distribute to all interested parties. Thank you!

-Tom


MRC CASE Studentship in Statistics - University of Warwick & GlaxoSmithKline

Applications are invited for a PhD studentship in Statistics at the University of Warwick, funded by a MRC Industrial CASE award with the GlaxoSmithKline's Clinical Unit Cambridge.

Title: Optimal Fixed and Adaptive Designs for fMRI Clinical Trials

Supervisors: Dr. Thomas Nichols (Warwick) and Dr. Ed Bullmore (GSK)

Funding: Tuition fees (at UK/EU level) and tax-free stipend for a 4 year PhD. Stipend rises annually as per the UK Research Councils minimum rate (13,590 for 2010/11), and is topped-up 2,500 by the industrial sponsor.

Start Date: October 2011

Project Description: Functional Magnetic Resonance Imaging (fMRI) is now almost 20 years old and is an indispensible tool for cognitive neuroscience. However only recently has fMRI been employed as part of drug development, as pharmaceutical companies seek to develop biomarkers that are more sensitive to disease state. By it's increased sensitivity and specificity, fMRI has the potential to reduce the time require to bring a drug to the marketplace, thus lower the cost of drug development and ultimately improve patient care. However, fMRI for clinical trials requires a different set of statistical tools than that used by conventional brain mapping: clinical trial outcomes must be precisely defined a priori, and the number of outcomes considered minimized. Further, cutting-edge type of fMRI designs, using task-free data to measure "resting state networks" presents yet new challenges for use in a clinical trial, as task-free results are intrinsically multivariate and difficult to define a priori.

The goal of this project is to develop novel statistical methodology to maximize information obtained from an fMRI study while still adhering to the stringent inferential requirements of a clinical trial. The project has three broad aims. The first is to develop adaptive designs for task-based fMRI clinical trials, using initial data to customize outcomes to an unknown signal. The second is to develop optimal outcomes for the task-free (or resting-state) fMRI data. The third aim is to develop optimal outcomes from graph-theoretic measures of task-based or task-free fMRI data, understanding the impact of matrix filtering operations on the power of final summary measure. The student will obtain a unique training in statistics and neuroimaging with mentorship from leading researchers in the field. The CASE award also includes three-months of on-site research at the GSK Clinical Unit Cambridge, giving them valuable industrial experience.

Requirements: The studentship is available to candidates with the equivalent of a first class or upper second class degree in a relevant discipline, and who meet University entry requirements (see http://www2.warwick.ac.uk/services/academicoffice/gsp/prospective).

Eligibility: UK nationals, or EU nationals who have been resident in the UK in the last three years. Other EU nationals can only receive a fees-only award. For full deatils see http://www.mrc.ac.uk/Fundingopportunities/Applicanthandbook/Studentships/Eligibility/index.htm

To Apply:http://www2.warwick.ac.uk/fac/sci/statistics/postgrad/research/apply (and please notify Dr. Nichols [log in to unmask] when application is submitted)

Deadline: Applications are considered on rolling basis, up until 31 July 2011, but priority given to applications received before 28February.

Inquires: Specific questions on this project should be directed to Thomas Nichols [log in to unmask]; questions on the postgraduate application process at Warwick should be directed to Ms. Kristine Prismall [log in to unmask]

Links:
Warwick Statistics http://go.warwick.ac.uk/stats
Thomas Nichols http://go.warwick.ac.uk/tenichols
Ed Bullmore's academic page http://www.psychiatry.cam.ac.uk/pages/profiles/bullmore.html

--001636765b69bc29a3049b543b11-- ========================================================================Date: Thu, 3 Feb 2011 09:23:36 +0100 Reply-To: Ali Gholami <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Ali Gholami <[log in to unmask]> Subject: SPM CLI Content-Type: text/plain; charset="UTF-8" Mime-Version: 1.0 Content-Transfer-Encoding: 7bit Message-ID: <1296721416.28831.4.camel@tb06> Hi Anyone knows if there's a command line mode in SPM? Best regards Ali Gholami ========================================================================Date: Thu, 3 Feb 2011 07:40:53 -0500 Reply-To: "MCLAREN, Donald" <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: "MCLAREN, Donald" <[log in to unmask]> Subject: Re: SPM CLI Comments: To: Ali Gholami <[log in to unmask]> In-Reply-To: <1296721416.28831.4.camel@tb06> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Message-ID: <[log in to unmask]ail.com> spm_jobman However, you have to setup the matlabbatch by hand first if you want to use it. Additionally, you can call each function individually from the commandline as well. Some force a GUI if the input is not correct while others will fail. On Thursday, February 3, 2011, Ali Gholami <[log in to unmask]> wrote: > Hi > > Anyone knows if there's a command line mode in SPM? > > > Best regards > Ali Gholami > -- Best Regards, Donald McLaren ================D.G. McLaren, Ph.D. Postdoctoral Research Fellow, GRECC, Bedford VA Research Fellow, Department of Neurology, Massachusetts General Hospital and Harvard Medical School Office: (773) 406-2464 ====================This e-mail contains CONFIDENTIAL INFORMATION which may contain PROTECTED HEALTHCARE INFORMATION and may also be LEGALLY PRIVILEGED and which is intended only for the use of the individual or entity named above. If the reader of the e-mail is not the intended recipient or the employee or agent responsible for delivering it to the intended recipient, you are hereby notified that you are in possession of confidential and privileged information. Any unauthorized use, disclosure, copying or the taking of any action in reliance on the contents of this information is strictly prohibited and may be unlawful. If you have received this e-mail unintentionally, please immediately notify the sender via telephone at (773) 406-2464 or email. ========================================================================Date: Thu, 3 Feb 2011 13:58:12 +0100 Reply-To: Ali Gholami <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Ali Gholami <[log in to unmask]> Subject: Re: SPM CLI Comments: To: "MCLAREN, Donald" <[log in to unmask]> In-Reply-To: <[log in to unmask]> Content-Type: text/plain; charset="UTF-8" Mime-Version: 1.0 Content-Transfer-Encoding: 7bit Message-ID: <1296737892.28831.7.camel@tb06> Thank you for the answer. Is there some documentation about installing the batch and how to use it? Best regards Ali On Thu, 2011-02-03 at 07:40 -0500, MCLAREN, Donald wrote: > spm_jobman > > However, you have to setup the matlabbatch by hand first if you want > to use it. Additionally, you can call each function individually from > the commandline as well. Some force a GUI if the input is not correct > while others will fail. > > On Thursday, February 3, 2011, Ali Gholami <[log in to unmask]> wrote: > > Hi > > > > Anyone knows if there's a command line mode in SPM? > > > > > > Best regards > > Ali Gholami > > > ========================================================================Date: Thu, 3 Feb 2011 08:05:14 -0500 Reply-To: "MCLAREN, Donald" <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: "MCLAREN, Donald" <[log in to unmask]> Subject: Re: SPM CLI Comments: To: Ali Gholami <[log in to unmask]> In-Reply-To: <1296737892.28831.7.camel@tb06> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Message-ID: <[log in to unmask]> help spm_jobman will give you a list of all of its options. spm_jobman('initcfg') is needed first in most cases, then spm_jobman('run_nogui',matlabbatch) or spm_jobman('run',matlabbatch) as for matlabbatch, I'm not sure if there is documentation for all of its possible fields. The best way to understand the matlabbatch is to make one subject with the gui and then modify the matlabbatch structure. There is even a function in spm for doing this, but I have never used it. Perhaps others might be able to point to good documentation on the matlabbatch structure. Best Regards, Donald McLaren ================D.G. McLaren, Ph.D. Postdoctoral Research Fellow, GRECC, Bedford VA Research Fellow, Department of Neurology, Massachusetts General Hospital and Harvard Medical School Office: (773) 406-2464 ====================This e-mail contains CONFIDENTIAL INFORMATION which may contain PROTECTED HEALTHCARE INFORMATION and may also be LEGALLY PRIVILEGED and which is intended only for the use of the individual or entity named above. If the reader of the e-mail is not the intended recipient or the employee or agent responsible for delivering it to the intended recipient, you are hereby notified that you are in possession of confidential and privileged information. Any unauthorized use, disclosure, copying or the taking of any action in reliance on the contents of this information is strictly prohibited and may be unlawful. If you have received this e-mail unintentionally, please immediately notify the sender via telephone at (773) 406-2464 or email. On Thu, Feb 3, 2011 at 7:58 AM, Ali Gholami <[log in to unmask]> wrote: > Thank you for the answer. Is there some documentation about installing > the batch and how to use it? > > Best regards > Ali > > > > On Thu, 2011-02-03 at 07:40 -0500, MCLAREN, Donald wrote: >> spm_jobman >> >> However, you have to setup the matlabbatch by hand first if you want >> to use it. Additionally, you can call each function individually from >> the commandline as well. Some force a GUI if the input is not correct >> while others will fail. >> >> On Thursday, February 3, 2011, Ali Gholami <[log in to unmask]> wrote: >> > Hi >> > >> > Anyone knows if there's a command line mode in SPM? >> > >> > >> > Best regards >> > Ali Gholami >> > >> > > > ========================================================================Date: Thu, 3 Feb 2011 14:25:50 +0100 Reply-To: Michael Erb <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Michael Erb <[log in to unmask]> Subject: Re: SPM CLI In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1; format=flowed Content-Transfer-Encoding: 7bit Message-ID: <[log in to unmask]> A good starting point is Part VIII of the manual, describing the Batch Interface. You can also find a file matlabbatch.man in the subdirectory matlabbatch. Michael. Am 03.02.2011 14:05, schrieb MCLAREN, Donald: > help spm_jobman will give you a list of all of its options. > spm_jobman('initcfg') is needed first in most cases, then > spm_jobman('run_nogui',matlabbatch) or spm_jobman('run',matlabbatch) > > as for matlabbatch, I'm not sure if there is documentation for all of > its possible fields. The best way to understand the matlabbatch is to > make one subject with the gui and then modify the matlabbatch > structure. There is even a function in spm for doing this, but I have > never used it. Perhaps others might be able to point to good > documentation on the matlabbatch structure. > > Best Regards, Donald McLaren > ================> D.G. McLaren, Ph.D. > Postdoctoral Research Fellow, GRECC, Bedford VA > Research Fellow, Department of Neurology, Massachusetts General > Hospital and Harvard Medical School > Office: (773) 406-2464 > ====================> This e-mail contains CONFIDENTIAL INFORMATION which may contain > PROTECTED HEALTHCARE INFORMATION and may also be LEGALLY PRIVILEGED > and which is intended only for the use of the individual or entity > named above. If the reader of the e-mail is not the intended recipient > or the employee or agent responsible for delivering it to the intended > recipient, you are hereby notified that you are in possession of > confidential and privileged information. Any unauthorized use, > disclosure, copying or the taking of any action in reliance on the > contents of this information is strictly prohibited and may be > unlawful. If you have received this e-mail unintentionally, please > immediately notify the sender via telephone at (773) 406-2464 or > email. > > > > On Thu, Feb 3, 2011 at 7:58 AM, Ali Gholami<[log in to unmask]> wrote: >> Thank you for the answer. Is there some documentation about installing >> the batch and how to use it? >> >> Best regards >> Ali >> >> >> >> On Thu, 2011-02-03 at 07:40 -0500, MCLAREN, Donald wrote: >>> spm_jobman >>> >>> However, you have to setup the matlabbatch by hand first if you want >>> to use it. Additionally, you can call each function individually from >>> the commandline as well. Some force a GUI if the input is not correct >>> while others will fail. >>> >>> On Thursday, February 3, 2011, Ali Gholami<[log in to unmask]> wrote: >>>> Hi >>>> >>>> Anyone knows if there's a command line mode in SPM? >>>> >>>> >>>> Best regards >>>> Ali Gholami >>>> >>> >> >> >> > -- <<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<< Dr. Michael Erb Sektion f. experimentelle Kernspinresonanz des ZNS Abteilung Neuroradiologie, Universitaetsklinikum Hoppe-Seyler_Str. 3, D-72076 Tuebingen Tel.: +49(0)7071/2987753 priv. +49(0)7071/61559 Fax.: +49(0)7071/294371 e-mail: <[log in to unmask]> www: http://www.medizin.uni-tuebingen.de/nrad/sektion/ <<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<< ========================================================================Date: Thu, 3 Feb 2011 14:05:51 +0000 Reply-To: Chris Rorden <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Chris Rorden <[log in to unmask]> Subject: \spm8\tpm FWHM? Mime-Version: 1.0 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain Message-ID: <[log in to unmask]> Hello- Short version: What is the FWHM smooth (if any) applied to the spm8\tpm\csf.nii, spm8\tpm\grey.nii and spm8\tpm\white.nii? The corresponding images in the spm8\apriori folder seem very smooth (8mm FWHM?), the the spm8\tpm images appear very sharp. Long version I want to make a set of alternative templates for SPM's unified normalization segmentation. The aim is to build a nice template for large stroke patient studies, and as the average age ~65 I want an age specific template. The aim is to conduct lesion-masked unified segmentation (www.pubmed.com/20542122) with an age specific template derived from a healthy aging sample. I was able to create very nice tissue probability maps from the 50 healthy controls following the instructions for SPM's newseg and DARTEL, essentially following John Ashburner's instructions here (including affine transform of the template to MNI space): http://www.fil.ion.ucl.ac.uk/~john/misc/VBMclass10.pdf Now I want to use this TPM for standard unified segmentation normalization. The question is whether I should apply any smoothing to the resulting Dartel TPM image or not. As this image is based on 50 people, to my eye it looks approximately as sharp as the images in spm8\tpm (which seg-norm uses). Should I use the mean image TPMs directly, or apply a FWHM with a small smoothing kernel? -chris ========================================================================Date: Thu, 3 Feb 2011 14:42:53 +0000 Reply-To: Duncan Astle <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Duncan Astle <[log in to unmask]> Subject: PhD Opportunity in the UK Mime-Version: 1.0 Content-Type: text/plain; charset=US-ASCII Content-Transfer-Encoding: quoted-printable Content-Disposition: inline Message-ID: <[log in to unmask]> Dear All, please forward this to anyone who might be interested. The Department ofPsychology at Royal Holloway, University of London invitesapplications for PhD studentship for the academic year 2011-12. The Department of Psychology was ranked 7thin the UKin the 2008 Research Assessment Exercise (RAE) and was ranked 4thoverall in the Guardian league tables. The department hasover thirty members of academic staff and some 25 post-graduate research (PhD)students. We offer a vibrant researchcommunity and excellent facilities including a research designated functionalimaging unit. We areseeking talented final year undergraduate or MSc students, who are interestedin developmental and/or cognitive neuroscience. The research would use 'real-time' imaging techniques (e.g. EEG and MEG) to study the neural mechanisms of memory and attention.,in typically developing children and adults. The studentship would be under the supervision of Dr. Duncan Astle, who enjoys strong research links, particularly at Royal Holloway and at Oxford. Potentialcandidates are encouraged to contact Dr. Astle to discuss potential proposals,with there being plenty of scope for students interested in executive control,working memory, visual attention and childhood development to put together anengaging research program. Thestudentship provides a stipend and also covers the full tuition fees for UK and EUstudents. Overseas applicants are alsowelcome to apply but would be required to pay the over-seas tuition fees (inthis case there may be opportunities to compete for scholarships to cover partof these fees). We encourage applications from students with good undergraduatedegrees in Psychology, or related disciplines. Contact: [log in to unmask] Many thanks, Duncan ========================================================================Date: Thu, 3 Feb 2011 17:57:33 +0100 Reply-To: Ali Gholami <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Ali Gholami <[log in to unmask]> Subject: Re: SPM CLI Comments: To: "MCLAREN, Donald" <[log in to unmask]> In-Reply-To: <[log in to unmask]> Content-Type: text/plain; charset="UTF-8" Mime-Version: 1.0 Content-Transfer-Encoding: 7bit Message-ID: <1296752253.28831.24.camel@tb06> Hi Maclaren, Thank you for your help! Still one thing I didn't understood. Do I need to install: http://sourceforge.net/projects/matlabbatch/ to have batch functionality? or just manipulating the spm_defaults.m is enough. There is a field there says: defaults.cmdline=0 and if it be turned to true, there should be no GUI running which in my case is not working. As an output when I run this command get the following error in Matlab: >> spm('defaults' , 'frmi') ??? Error using ==> spm at 481 Unknown Modality. Error in ==> spm at 426 Modality = spm('CheckModality',Modality); Best regards Ali On Thu, 2011-02-03 at 08:05 -0500, MCLAREN, Donald wrote: > help spm_jobman will give you a list of all of its options. > spm_jobman('initcfg') is needed first in most cases, then > spm_jobman('run_nogui',matlabbatch) or spm_jobman('run',matlabbatch) > > as for matlabbatch, I'm not sure if there is documentation for all of > its possible fields. The best way to understand the matlabbatch is to > make one subject with the gui and then modify the matlabbatch > structure. There is even a function in spm for doing this, but I have > never used it. Perhaps others might be able to point to good > documentation on the matlabbatch structure. > > Best Regards, Donald McLaren > ================> D.G. McLaren, Ph.D. > Postdoctoral Research Fellow, GRECC, Bedford VA > Research Fellow, Department of Neurology, Massachusetts General > Hospital and Harvard Medical School > Office: (773) 406-2464 > ====================> This e-mail contains CONFIDENTIAL INFORMATION which may contain > PROTECTED HEALTHCARE INFORMATION and may also be LEGALLY PRIVILEGED > and which is intended only for the use of the individual or entity > named above. If the reader of the e-mail is not the intended recipient > or the employee or agent responsible for delivering it to the intended > recipient, you are hereby notified that you are in possession of > confidential and privileged information. Any unauthorized use, > disclosure, copying or the taking of any action in reliance on the > contents of this information is strictly prohibited and may be > unlawful. If you have received this e-mail unintentionally, please > immediately notify the sender via telephone at (773) 406-2464 or > email. > > > > On Thu, Feb 3, 2011 at 7:58 AM, Ali Gholami <[log in to unmask]> wrote: > > Thank you for the answer. Is there some documentation about installing > > the batch and how to use it? > > > > Best regards > > Ali > > > > > > > > On Thu, 2011-02-03 at 07:40 -0500, MCLAREN, Donald wrote: > >> spm_jobman > >> > >> However, you have to setup the matlabbatch by hand first if you want > >> to use it. Additionally, you can call each function individually from > >> the commandline as well. Some force a GUI if the input is not correct > >> while others will fail. > >> > >> On Thursday, February 3, 2011, Ali Gholami <[log in to unmask]> wrote: > >> > Hi > >> > > >> > Anyone knows if there's a command line mode in SPM? > >> > > >> > > >> > Best regards > >> > Ali Gholami > >> > > >> > > > > > > ========================================================================Date: Thu, 3 Feb 2011 20:28:47 +0100 Reply-To: Michael Erb <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Michael Erb <[log in to unmask]> Subject: Re: SPM CLI MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-15; format=flowed Content-Transfer-Encoding: 7bit Message-ID: <[log in to unmask]> You don't have to install matlabbatch because it is already installed as part of spm8 ( matlabbatch subdirectory of your spm directory). try spm('defaults' , 'fmri') instead of spm('defaults' , 'frmi') Good luck, Micheal. Am 03.02.2011 17:57, schrieb Ali Gholami: > Hi Maclaren, > > Thank you for your help! Still one thing I didn't understood. Do I need > to install: http://sourceforge.net/projects/matlabbatch/ to have batch > functionality? or just manipulating the spm_defaults.m is enough. There > is a field there says: defaults.cmdline=0 and if it be turned to true, > there should be no GUI running which in my case is not working. > > As an output when I run this command get the following error in > Matlab: > >>> spm('defaults' , 'frmi') > ??? Error using ==> spm at 481 > Unknown Modality. > > Error in ==> spm at 426 > Modality = spm('CheckModality',Modality); > > > Best regards > > Ali > > > > > > > On Thu, 2011-02-03 at 08:05 -0500, MCLAREN, Donald wrote: >> help spm_jobman will give you a list of all of its options. >> spm_jobman('initcfg') is needed first in most cases, then >> spm_jobman('run_nogui',matlabbatch) or spm_jobman('run',matlabbatch) >> >> as for matlabbatch, I'm not sure if there is documentation for all of >> its possible fields. The best way to understand the matlabbatch is to >> make one subject with the gui and then modify the matlabbatch >> structure. There is even a function in spm for doing this, but I have >> never used it. Perhaps others might be able to point to good >> documentation on the matlabbatch structure. >> >> Best Regards, Donald McLaren >> ================ >> D.G. McLaren, Ph.D. >> Postdoctoral Research Fellow, GRECC, Bedford VA >> Research Fellow, Department of Neurology, Massachusetts General >> Hospital and Harvard Medical School >> Office: (773) 406-2464 >> ==================== >> This e-mail contains CONFIDENTIAL INFORMATION which may contain >> PROTECTED HEALTHCARE INFORMATION and may also be LEGALLY PRIVILEGED >> and which is intended only for the use of the individual or entity >> named above. If the reader of the e-mail is not the intended recipient >> or the employee or agent responsible for delivering it to the intended >> recipient, you are hereby notified that you are in possession of >> confidential and privileged information. Any unauthorized use, >> disclosure, copying or the taking of any action in reliance on the >> contents of this information is strictly prohibited and may be >> unlawful. If you have received this e-mail unintentionally, please >> immediately notify the sender via telephone at (773) 406-2464 or >> email. >> >> >> >> On Thu, Feb 3, 2011 at 7:58 AM, Ali Gholami<[log in to unmask]> wrote: >>> Thank you for the answer. Is there some documentation about installing >>> the batch and how to use it? >>> >>> Best regards >>> Ali >>> >>> >>> >>> On Thu, 2011-02-03 at 07:40 -0500, MCLAREN, Donald wrote: >>>> spm_jobman >>>> >>>> However, you have to setup the matlabbatch by hand first if you want >>>> to use it. Additionally, you can call each function individually from >>>> the commandline as well. Some force a GUI if the input is not correct >>>> while others will fail. >>>> >>>> On Thursday, February 3, 2011, Ali Gholami<[log in to unmask]> wrote: >>>>> Hi >>>>> >>>>> Anyone knows if there's a command line mode in SPM? >>>>> >>>>> >>>>> Best regards >>>>> Ali Gholami >>>>> >>>> >>> >>> >>> > -- <<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<< Dr. Michael Erb Sektion f. experimentelle Kernspinresonanz des ZNS Abteilung Neuroradiologie, Universitaetsklinikum Hoppe-Seyler_Str. 3, D-72076 Tuebingen Tel.: +49(0)7071/2987753 priv. +49(0)7071/61559 Fax.: +49(0)7071/294371 e-mail: <[log in to unmask]> www: http://www.medizin.uni-tuebingen.de/nrad/sektion/ <<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<< ========================================================================Date: Thu, 3 Feb 2011 14:34:31 -0500 Reply-To: Andrew Murrin <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Andrew Murrin <[log in to unmask]> Subject: Interpreting SPM Plots MIME-version: 1.0 Content-type: multipart/alternative; boundary=B_3379588477_4569921 Message-ID: <[log in to unmask]> > This message is in MIME format. Since your mail reader does not understand this format, some or all of this message may not be legible. --B_3379588477_4569921 Content-type: text/plain; charset="US-ASCII" Content-transfer-encoding: 7bit Hello! I have a couple basic questions about the plots generated by SPM: 1.) I assume that it is a log-log plot of sorts, but can anyone provide more information about how SPM actually calculates the values? 2.) For the plots at a given voxel, when using Tools > Basic Fitting, and getting the equation for the line of the format y =p1*x + p2, is p1 equal to the beta value at that voxel (and thus p2 is the error term)? Any additional insight for interpretation of plots would also be appreciated. Thanks in advance! --B_3379588477_4569921 Content-type: text/html; charset="US-ASCII" Content-transfer-encoding: quoted-printable Interpreting SPM Plots Hello!  I have a couple basic questions about the plots generated by SPM:

1.)  I assume that it is a log-log plot of sorts, but can anyone provide more information about how SPM actually calculates the values?

2.)  For the plots at a given voxel, when using Tools > Basic Fitting, and getting the equation for the line of the format y =p1*x + p2, is p1 equal to the beta value at that voxel (and thus p2 is the error term)?

Any additional insight for interpretation of plots would also be appreciated.  Thanks in advance!
--B_3379588477_4569921-- ========================================================================Date: Thu, 3 Feb 2011 14:06:24 -0600 Reply-To: Natalie Zhaoying Han <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Natalie Zhaoying Han <[log in to unmask]> Subject: Re: SPM CLI Comments: To: Ali Gholami <[log in to unmask]> In-Reply-To: <1296721416.28831.4.camel@tb06> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Message-ID: <[log in to unmask]> Hi, Ali, Here are the step-by-step using command line in SPM, based on my experience. Step 1: Save an example batch 1.1 Start regular SPM with GUI, open the Batch Editor, and set up an example job you want to do. 1.2 Click Batch Editor->File->Save Batch, this will allow you to save this job, say you give the name of test, you will have the file test.mat. This is the matlabbatch variable you will need to modify in the next step. 1.3 Then click Batch Editor ->File->Save Batch & Scripts, this will allow you to check how to change parameters, say you give the name of test, you will find two files: test.m and test_job.m. If you open test_job.m you will find all the parameters for matlabbatch structure. Step 2: Change the batch parameters and save a new matlabbatch file 2.1 Load in the test.mat: load test.mat; you will find the variable of matlabbatch. If you have multiple jobs set up before you save in 1.2, you will see matlabbatch{1}, matlabbatch{2}, .. matlabbatch{i}. Each matlabbatch{i} is called spm, and you will need to modify this variable. 2.2 To find out how to modify, you can check from test_job.m, it usually has all the information you will need to change. 2.3 Save the new spm into a new matlabbatch as matlabbatch{1}=spm; Step 3: Run the batch in command line. Here are two situation, one is you could have GUI pop-up, one is that you don't have GUI display. 3.1 With GUI: addpath /home/spm8/ spm('default','fmri'); spm_jobman('initcfg'); spm_jobman('run',matlabbatch); 3.2 without GUI you will need to change defaults.cmdline=0 to defaults.cmdline=true in the spm_defaults.m in your SPM folder. addpath /home/spm8/ spm('default','fmri'); spm_jobman('initcfg'); spm_jobman('run_nogui',matlabbatch); Step 4: enjoy the results.:-) Hope this will be helpful. Natalie Han PhD student, Electrical Engineering, Vanderbilt University http://vuiis.vanderbilt.edu/ On Thu, Feb 3, 2011 at 2:23 AM, Ali Gholami <[log in to unmask]> wrote: > Hi > > Anyone knows if there's a command line mode in SPM? > > > Best regards > Ali Gholami > ========================================================================Date: Thu, 3 Feb 2011 16:00:51 -0600 Reply-To: Michael Harms <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Michael Harms <[log in to unmask]> Subject: Re: Antw: Re: [SPM] PPI interpretation questions (with attachments) Comments: To: Darren Gitelman <[log in to unmask]> In-Reply-To: <[log in to unmask]> Content-Type: text/plain Mime-Version: 1.0 Content-Transfer-Encoding: 7bit Message-ID: <[log in to unmask]> Hello Darren, I know this thread is a bit stale, but I wanted to mention (and get it included into the thread) that betas are not simply the reciprocal of each other if you swap an "IV" with the "DV". That is not the way that the regression formulas work out. Best, -MH On Mon, 2011-01-24 at 15:20 -0600, Darren Gitelman wrote: > Dear DDW > > I am not surprised that while A to B is "significant", B to A might > not be, because the variance may differ between the areas. However, I > would be surprised if there was absolutely no result at A if you start > with B as the source. You should see some activity at A starting with > B as the source and the beta should be the reciprocal of starting with > A as the source. (When selecting the voxels defining B as the source > they should be the same voxels as the ones that came up as the target > using A as the source.) > > Unfortunately you can neither use the difference in significance nor > the values of the [reciprocal] betas to help you decide on the actual > direction of the influence. You have to decide on the direction based > on your concept or model of the brain's organization, and can then > take the PPI result as a confirmation of an influence existing (and > supporting your model) or not. > > Darren > > > On Mon, Jan 24, 2011 at 3:00 PM, D D W <[log in to unmask]> wrote: > Dear Darren & list, > > > > Exactly. You cannot use PPI to make an independent > "statistical" > > statement about the absolute direction of the influence, but > you > > shouldn't let that trouble you. This is why I brought up the > > Grabenhorst and Rolls paper because they did a nice of > showing how you > > can pick a seed (source) region but have an inference about > the > > directionality that is actually target to source (prefrontal > to > > orbitofrontal) rather than the canonical source to target. > As I said, > > PPI allows an inference about directionality because you > have > > specified the alternative model. Of course someone could > disagree with > > your model but that's ok.' > > > > I don't have much to contribute except to say that I am > flummoxed by how to interpret such a finding. For instance, > I'm sure I'm not alone in having observed a significant PPI > from source to target that is not symmetric (i.e. the target > to source PPI is non-significant). According to the line of > reasoning you outlined above, I would still be allowed to > argue, based on other evidence, that the direction of > influence is from target to source. > > To be more specific, I've run PPI analyses on 4 apriori ROIs > and found that ROI A has a significant PPI to ROI B, but not > vice versa (all at 0.05, so it's not a threshold issue). It > seems odd that I would still be allowed to conclude that the > direction of influence is from B to A. > > I understand that the directionality of the regression > doesn't buy you directionality of causal influence, but > nevertheless it seems rather odd to me that you can infer a > specific direction (based on a biological model) in the > absence of PPI in that same direction. > > If I'm missing something glaringly obvious, apologies. > > Cheers, > ddw > > > > > > > > > > > > > > -- > Darren Gitelman, MD > Northwestern University > 710 N. Lake Shore Dr., 1122 > Chicago, IL 60611 > Ph: (312) 908-8614 > Fax: (312) 908-5073 ========================================================================Date: Thu, 3 Feb 2011 16:23:21 -0600 Reply-To: Darren Gitelman <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Darren Gitelman <[log in to unmask]> Subject: Re: Antw: Re: [SPM] PPI interpretation questions (with attachments) Comments: To: Michael Harms <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/alternative; boundarye6ba3092ee99714b049b683669 Message-ID: <[log in to unmask]> --90e6ba3092ee99714b049b683669 Content-Type: text/plain; charset=ISO-8859-1 Michael You are correct. It only works out to be the reciprocal if there is no error. Thanks for the update. Darren On Thu, Feb 3, 2011 at 4:00 PM, Michael Harms <[log in to unmask]>wrote: > > Hello Darren, > I know this thread is a bit stale, but I wanted to mention (and get it > included into the thread) that betas are not simply the reciprocal of > each other if you swap an "IV" with the "DV". That is not the way that > the regression formulas work out. > > Best, > -MH > > On Mon, 2011-01-24 at 15:20 -0600, Darren Gitelman wrote: > > Dear DDW > > > > I am not surprised that while A to B is "significant", B to A might > > not be, because the variance may differ between the areas. However, I > > would be surprised if there was absolutely no result at A if you start > > with B as the source. You should see some activity at A starting with > > B as the source and the beta should be the reciprocal of starting with > > A as the source. (When selecting the voxels defining B as the source > > they should be the same voxels as the ones that came up as the target > > using A as the source.) > > > > Unfortunately you can neither use the difference in significance nor > > the values of the [reciprocal] betas to help you decide on the actual > > direction of the influence. You have to decide on the direction based > > on your concept or model of the brain's organization, and can then > > take the PPI result as a confirmation of an influence existing (and > > supporting your model) or not. > > > > Darren > > > > > > On Mon, Jan 24, 2011 at 3:00 PM, D D W <[log in to unmask]> wrote: > > Dear Darren & list, > > > > > > > Exactly. You cannot use PPI to make an independent > > "statistical" > > > statement about the absolute direction of the influence, but > > you > > > shouldn't let that trouble you. This is why I brought up the > > > Grabenhorst and Rolls paper because they did a nice of > > showing how you > > > can pick a seed (source) region but have an inference about > > the > > > directionality that is actually target to source (prefrontal > > to > > > orbitofrontal) rather than the canonical source to target. > > As I said, > > > PPI allows an inference about directionality because you > > have > > > specified the alternative model. Of course someone could > > disagree with > > > your model but that's ok.' > > > > > > > > I don't have much to contribute except to say that I am > > flummoxed by how to interpret such a finding. For instance, > > I'm sure I'm not alone in having observed a significant PPI > > from source to target that is not symmetric (i.e. the target > > to source PPI is non-significant). According to the line of > > reasoning you outlined above, I would still be allowed to > > argue, based on other evidence, that the direction of > > influence is from target to source. > > > > To be more specific, I've run PPI analyses on 4 apriori ROIs > > and found that ROI A has a significant PPI to ROI B, but not > > vice versa (all at 0.05, so it's not a threshold issue). It > > seems odd that I would still be allowed to conclude that the > > direction of influence is from B to A. > > > > I understand that the directionality of the regression > > doesn't buy you directionality of causal influence, but > > nevertheless it seems rather odd to me that you can infer a > > specific direction (based on a biological model) in the > > absence of PPI in that same direction. > > > > If I'm missing something glaringly obvious, apologies. > > > > Cheers, > > ddw > > > > > > > > > > > > > > > > > > > > > > > > > > > > -- > > Darren Gitelman, MD > > Northwestern University > > 710 N. Lake Shore Dr., 1122 > > Chicago, IL 60611 > > Ph: (312) 908-8614 > > Fax: (312) 908-5073 > > -- Darren Gitelman, MD Northwestern University 710 N. Lake Shore Dr., 1122 Chicago, IL 60611 Ph: (312) 908-8614 Fax: (312) 908-5073 --90e6ba3092ee99714b049b683669 Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Michael

You are correct. It only works out to be the reciprocal if there is no error.

Thanks for the update.

Darren

On Thu, Feb 3, 2011 at 4:00 PM, Michael Harms <[log in to unmask]> wrote:

Hello Darren,
I know this thread is a bit stale, but I wanted to mention (and get it
included into the thread) that betas are not simply the reciprocal of
each other if you swap an "IV" with the "DV". That is not the way that
the regression formulas work out.

Best,
-MH

On Mon, 2011-01-24 at 15:20 -0600, Darren Gitelman wrote:
> Dear DDW
>
> I am not surprised that while A to B is "significant", B to A might
> not be, because the variance may differ between the areas. However, I
> would be surprised if there was absolutely no result at A if you start
> with B as the source. You should see some activity at A starting with
> B as the source and the beta should be the reciprocal of starting with
> A as the source. (When selecting the voxels defining B as the source
> they should be the same voxels as the ones that came up as the target
> using A as the source.)
>
> Unfortunately you can neither use the difference in significance nor
> the values of the [reciprocal] betas to help you decide on the actual
> direction of the influence. You have to decide on the direction based
> on your concept or model of the brain's organization, and can then
> take the PPI result as a confirmation of an influence existing (and
> supporting your model) or not.
>
> Darren
>
>
> On Mon, Jan 24, 2011 at 3:00 PM, D D W <[log in to unmask]> wrote:
> Dear Darren & list,
>
>
> > Exactly. You cannot use PPI to make an independent
> "statistical"
> > statement about the absolute direction of the influence, but
> you
> > shouldn't let that trouble you. This is why I brought up the
> > Grabenhorst and Rolls paper because they did a nice of
> showing how you
> > can pick a seed (source) region but have an inference about
> the
> > directionality that is actually target to source (prefrontal
> to
> > orbitofrontal) rather than the canonical source to target.
> As I said,
> > PPI allows an inference about directionality because you
> have
> > specified the alternative model. Of course someone could
> disagree with
> > your model but that's ok.'
>
>
>
> I don't have much to contribute except to say that I am
> flummoxed by how to interpret such a finding. For instance,
> I'm sure I'm not alone in having observed a significant PPI
> from source to target that is not symmetric (i.e. the target
> to source PPI is non-significant). According to the line of
> reasoning you outlined above, I would still be allowed to
> argue, based on other evidence, that the direction of
> influence is from target to source.
>
> To be more specific, I've run PPI analyses on 4 apriori ROIs
> and found that ROI A has a significant PPI to ROI B, but not
> vice versa (all at 0.05, so it's not a threshold issue). It
> seems odd that I would still be allowed to conclude that the
> direction of influence is from B to A.
>
> I understand that the directionality of the regression
> doesn't buy you directionality of causal influence, but
> nevertheless it seems rather odd to me that you can infer a
> specific direction (based on a biological model) in the
> absence of PPI in that same direction.
>
> If I'm missing something glaringly obvious, apologies.
>
> Cheers,
> ddw
>
>
>
>
>
>
>
>
>
>
>
>
>
> --
> Darren Gitelman, MD
> Northwestern University
> 710 N. Lake Shore Dr., 1122
> Chicago, IL 60611
> Ph: (312) 908-8614
> Fax: (312) 908-5073




--
Darren Gitelman, MD
Northwestern University
710 N. Lake Shore Dr., 1122
Chicago, IL 60611
Ph: (312) 908-8614
Fax: (312) 908-5073
--90e6ba3092ee99714b049b683669-- ========================================================================Date: Thu, 3 Feb 2011 23:22:27 +0000 Reply-To: Emanuele Tinelli <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Emanuele Tinelli <[log in to unmask]> Subject: tool time course? Mime-Version: 1.0 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain Message-ID: <[log in to unmask]> hi, I wanted to know if there is a tool to obtain the values of the time course (over Y) in a group of 30 subj by placing a ROI in the same region. thanks ========================================================================Date: Fri, 4 Feb 2011 12:32:36 +1100 Reply-To: Lucy Elizabeth Vivash <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Lucy Elizabeth Vivash <[log in to unmask]> Subject: Normalising FDG-PET MIME-version: 1.0 Content-type: text/plain; charset=UTF-8 Content-transfer-encoding: 8bit Message-ID: <[log in to unmask]> Hi, I am having trouble normalising a couple of FDG-PETs. The majority of images (matrix size 128 x 128 x 56) have normalised fine. However there are a couple of images with differing matrix sizes (128 x 128 x 35, 256 x 256 x 224) which do not normalise (error message: "not enough overlap"). I have tried manually altering the matrix size to 128 x 128 x 56 to no avail. Any suggestions? Regards, Lucy Lucy Vivash MSci (Hons) PhD Student Department of Medicine Royal Melbourne Hospital 3050 Victoria Australia Ph: (03) 8344 0531 Email: [log in to unmask] ========================================================================Date: Fri, 4 Feb 2011 08:40:12 +0100 Reply-To: Christophe Phillips <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Christophe Phillips <[log in to unmask]> Subject: Re: Normalising FDG-PET Comments: To: Lucy Elizabeth Vivash <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=UTF-8; format=flowed Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> Hi Lucy, You shouldn't worry about the "matrix sizes". What is important is the original, i.e. before launching any spatial preprocessing, orientation of the image. You should check it and possibly adjust it with the 'CheckReg' function: - click on 'CheckReg' - select the PET template and your image, - check your image is overlapping the template with a "good" match (same orientation and not too far off) - if not, manually reorient your PET image (right-click on it - reorient - current image - adjust parameters as needed) and apply the parameters on the image. Then try normalising again. Note also that SPM PET template comes from H2O15 images, it could be a good idea to create your own FDG-PET template at some point. Best, Chris Le 4/02/2011 2:32, Lucy Elizabeth Vivash a écrit : > Hi, > > I am having trouble normalising a couple of FDG-PETs. The majority of > images (matrix size 128 x 128 x 56) have normalised fine. However there > are a couple of images with differing matrix sizes (128 x 128 x 35, 256 x > 256 x 224) which do not normalise (error message: "not enough overlap"). I > have tried manually altering the matrix size to 128 x 128 x 56 to no > avail. > > Any suggestions? > > Regards, > Lucy > > > > Lucy Vivash MSci (Hons) > PhD Student > Department of Medicine > Royal Melbourne Hospital > 3050 > Victoria > Australia > Ph: (03) 8344 0531 > Email: [log in to unmask] > ========================================================================Date: Fri, 4 Feb 2011 09:10:15 +0100 Reply-To: Alexander Hammers <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Alexander Hammers <[log in to unmask]> Subject: Re: Normalising FDG-PET Comments: To: Lucy Elizabeth Vivash <[log in to unmask]> In-Reply-To: <[log in to unmask]> Mime-Version: 1.0 (Apple Message framework v1082) Content-Type: multipart/mixed; boundary=Apple-Mail-39-672235824 Message-ID: <[log in to unmask]> --Apple-Mail-39-672235824 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain; charset=us-ascii Dear Lucy, Try DISPLAY: they may have funny origins or offsets and SPM then "sees" them in some corner of the matrix. You can then reorient them with the functions below the graphics window - best move them around until the crosshair shows up roughly in the position of the anterior commissure. This will likely solve the issue. If not, do get back to the list as there are some more exotic possible errors. 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wYkU3AkHJwT+aExhcoet3+i2EEp58QicZGEhCCzxF/JaM6cZAdu9wiF44MrNKt5EXnw+bHcYkhWH 9eSUrA/kaXgut3zIALF/4MxbbsXlDxC40kFv9IBL8VRwJDI5LBsO29IdVB62oj24iXVbiIPj22Hb q1shDlvRHtzEuhXi4Ph22PbqVojDVrQHN7H/AWFrGkuL8nFSAAAAAElFTkSuQmCC --Apple-Mail-39-672235824 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain; charset=windows-1252 Chair in Functional Neuroimaging Neurodis Foundation http://www.fondation-neurodis.org/ Postal Address: CERMEP Imagerie du Vivant Hpital Neurologique Pierre Wertheimer 59 Boulevard Pinel, 69003 Lyon, France Telephone +33-(0)4-72 68 86 34 Fax +33-(0)4-72 68 86 10 Email [log in to unmask];[log in to unmask] --------------------------------- Other affiliations: Visiting Reader; Honorary Consultant Neurologist Division of Neuroscience and Mental Health, Faculty of Medicine Imperial College London, UK --------------------------------- Honorary Reader in Neurology; Honorary Consultant Neurologist Department of Clinical and Experimental Epilepsy National Hospital for Neurology and Neurosurgery/ Institute of Neurology, University College London, UK On 4 Feb 2011, at 02:32, Lucy Elizabeth Vivash wrote: > Hi, > > I am having trouble normalising a couple of FDG-PETs. The majority of > images (matrix size 128 x 128 x 56) have normalised fine. However there > are a couple of images with differing matrix sizes (128 x 128 x 35, 256 x > 256 x 224) which do not normalise (error message: "not enough overlap"). I > have tried manually altering the matrix size to 128 x 128 x 56 to no > avail. > > Any suggestions? > > Regards, > Lucy > > > > Lucy Vivash MSci (Hons) > PhD Student > Department of Medicine > Royal Melbourne Hospital > 3050 > Victoria > Australia > Ph: (03) 8344 0531 > Email: [log in to unmask] --Apple-Mail-39-672235824-- ========================================================================Date: Fri, 4 Feb 2011 12:07:25 +0100 Reply-To: =?ISO-8859-1?Q?Rainer_Bgle?= <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: =?ISO-8859-1?Q?Rainer_Bgle?= <[log in to unmask]> Subject: Re: tool time course? Comments: To: Emanuele Tinelli <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/alternative; boundary cf3054a2852104e0049b72e355 Message-ID: [log in to unmask]> --20cf3054a2852104e0049b72e355 Content-Type: text/plain; charset=ISO-8859-1 Hi Emanuele, you can try to use RFXplot toolbox. http://rfxplot.sourceforge.net/ Kind regards, Rainer On Fri, Feb 4, 2011 at 12:22 AM, Emanuele Tinelli <[log in to unmask]>wrote: > hi, > I wanted to know if there is a tool to obtain the values of the time course > (over Y) in a group of 30 subj by placing a ROI in the same region. > thanks > --20cf3054a2852104e0049b72e355 Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Hi Emanuele,

you can try to use RFXplot toolbox.

http://rfxplot.sourceforge.net/

Kind regards,
Rainer

On Fri, Feb 4, 2011 at 12:22 AM, Emanuele Tinelli <[log in to unmask]> wrote:
hi,
I wanted to know if there is a tool to obtain the values of the time course (over Y) in a group of 30 subj by placing a ROI in the same region.
thanks

--20cf3054a2852104e0049b72e355-- ========================================================================Date: Fri, 4 Feb 2011 11:52:04 +0000 Reply-To: Kie Woo Nam <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Kie Woo Nam <[log in to unmask]> Subject: VBM8 - What to do after sample homogeneity check Mime-Version: 1.0 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain; charset="UTF-8" Message-ID: <[log in to unmask]> Dear SPM experts, I've run VBM8 using a customized DARTEL-template. Then, I did sample homogeneity check and identified some poor images (i.e. images with severe motion artefacts, enlarged ventricles, etc.). Among 296 images in total, I found 11 "poor" images so far, but there seem to be some more of them. Now, my question is which option I should choose between the following. (-----1-----) Start statistical analysis without those outliers (-----2-----) Start again from the beginning (i.e. re-run VBM8) without those outliers I was originally going to go for option 2 because, to my understanding, a customized DARTEL-template is made from my own images, and therefore outliers would cause bias in the template. However, I'm not sure whether this reasoning is correct. So, could anyone who understands how VBM8 works please advise me on this? I would really appreciate your help. Best wishes, Kie Woo Nam ___________________________ Kie Woo Nam, PhD student Division of Psychological Medicine Institute of Psychiatry, King's College London 16 De Crespigny Park, Denmark Hill London, SE5 8AF, UK ========================================================================Date: Fri, 4 Feb 2011 12:35:35 +0000 Reply-To: Christoph Berger <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Christoph Berger <[log in to unmask]> Subject: case study of deformations Mime-Version: 1.0 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain; charset="UTF-8" Message-ID: <[log in to unmask]> Dear SPMers, I have a question regarding a case study of morphometric abnormalities of a single subject compared to a group of probands. I have measured an t1 image from every subject and segmented every subject with the vbm8 toolbox into grey and white matter and calculated from every subject the map of the Jacobean determinates. I would like to know, whether the Jacobean from a particular subject differs from the group. I would like to use a factorial design specification (one sample t) for easy labeling and visualization of possible effects, but I do not know how. I would think of this posibility: one sample t flex fact model tests, whether a goup differs from 0. In my case, to test, whether the group differes from the particular subject I have to substract the jacobean of the particular subject from the each Jacobean in the group bevor I perform the secondlevel one sample t test over the group. Would that analysis be correct? My actual workaround is as follows: 1. I calculate with IMcalc the maps of the voxelwise standard deviations and voxelwise means of the group of probands and use that to calculate the z transformed Jacobean map of the particular proband 2. I use MRIcroN and look there for regions where the Z value is extending the significant threshold. Is there a better way to look for effects in this case study? Many thanks and kind regards, Christoph Berger ========================================================================Date: Fri, 4 Feb 2011 08:46:18 -0500 Reply-To: "MCLAREN, Donald" <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: "MCLAREN, Donald" <[log in to unmask]> Subject: Re: case study of deformations Comments: To: Christoph Berger <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> Two sample t-test with equal variance with the single subject as 1 group and the Probands as the other group. Contrast: 1 -1 or -1 1 depending on the direction of the change. A one-sample t-test against 0 won't work with Jacobians because they are centered around 1. Either a log transform or a percent change calculation for longitudinal studies is needed to change them to be centered around 0. On Friday, February 4, 2011, Christoph Berger <[log in to unmask]> wrote: > Dear SPMers, > > I have a question regarding a case study of morphometric abnormalities of a single subject compared to a group of probands. > > I have measured an t1 image from every subject and segmented every subject with the vbm8 toolbox into grey and white matter and calculated from every subject the map of the Jacobean determinates. I would like to know, whether the Jacobean from a particular subject differs from the group. > > I would like to use a factorial design specification (one sample t) for easy labeling and visualization of possible effects, but I do not know how. I would think of this posibility: one sample t flex fact model tests, whether a goup differs from 0. In my case, to test, whether the group differes from the particular subject I have to substract the jacobean of the particular subject from the each Jacobean in the group bevor I perform the secondlevel one sample t test over the group. > Would that analysis be correct? > > My actual workaround is as follows: > 1. I calculate with IMcalc the maps of the voxelwise standard deviations and voxelwise means of the group of probands and use that to calculate the z transformed Jacobean map of the particular proband > 2. I use MRIcroN and look there for regions where the Z value is extending the significant threshold. > Is there a better way to look for effects in this case study? > Many thanks and kind regards, > Christoph Berger > -- Best Regards, Donald McLaren ================= D.G. McLaren, Ph.D. Postdoctoral Research Fellow, GRECC, Bedford VA Research Fellow, Department of Neurology, Massachusetts General Hospital and Harvard Medical School Office: (773) 406-2464 ===================== This e-mail contains CONFIDENTIAL INFORMATION which may contain PROTECTED HEALTHCARE INFORMATION and may also be LEGALLY PRIVILEGED and which is intended only for the use of the individual or entity named above. If the reader of the e-mail is not the intended recipient or the employee or agent responsible for delivering it to the intended recipient, you are hereby notified that you are in possession of confidential and privileged information. Any unauthorized use, disclosure, copying or the taking of any action in reliance on the contents of this information is strictly prohibited and may be unlawful. If you have received this e-mail unintentionally, please immediately notify the sender via telephone at (773) 406-2464 or email. ========================================================================Date: Fri, 4 Feb 2011 13:47:06 +0000 Reply-To: "Stephen J. Fromm" <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: "Stephen J. Fromm" <[log in to unmask]> Subject: Re: SPM CLI Comments: To: Donald McLaren <[log in to unmask]> Mime-Version: 1.0 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain; charset="UTF-8" Message-ID: <[log in to unmask]> "There is even a function in spm for doing this, but I have never used it." What function is that? Best, S ========================================================================Date: Fri, 4 Feb 2011 16:05:46 +0100 Reply-To: michel grothe <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: michel grothe <[log in to unmask]> Subject: Re: VBM8 - What to do after sample homogeneity check Comments: To: [log in to unmask] In-Reply-To: <[log in to unmask]> Content-Type: multipart/alternative; boundary="_da845b0a-7b5d-4acf-844a-7c616bedcf1b_" MIME-Version: 1.0 Message-ID: <[log in to unmask]> --_da845b0a-7b5d-4acf-844a-7c616bedcf1b_ Content-Type: text/plain; charset="iso-8859-1" Content-Transfer-Encoding: quoted-printable If you didnt change the default settings of the toolbox, then all of your images are warped independently to the IXI-template provided by the toolbox. This is a DARTEL-compatible average template of healthy adult subjects in MNI space (see also the VBM8-manual). Thus, outliers wont affect the template and it should be safe to go for option 1 (given that you have good reasons to exclude these images, i.e. your definition of "poor" quality). BTW, it would be of interest to know the average age of the IXI-template sample, but as far as I know this information is not provided by the VBM8-manual. Maybe the author, Christian Gaser, can comment on this. Best regards, Michel > Date: Fri, 4 Feb 2011 11:52:04 +0000 > From: [log in to unmask] > Subject: [SPM] VBM8 - What to do after sample homogeneity check > To: [log in to unmask] > > Dear SPM experts, > > I've run VBM8 using a customized DARTEL-template. Then, I did sample homogeneity check and identified some poor images (i.e. images with severe motion artefacts, enlarged ventricles, etc.). Among 296 images in total, I found 11 "poor" images so far, but there seem to be some more of them. > > Now, my question is which option I should choose between the following. > > (-----1-----) Start statistical analysis without those outliers > (-----2-----) Start again from the beginning (i.e. re-run VBM8) without those outliers > > I was originally going to go for option 2 because, to my understanding, a customized DARTEL-template is made from my own images, and therefore outliers would cause bias in the template. However, I'm not sure whether this reasoning is correct. > > So, could anyone who understands how VBM8 works please advise me on this? I would really appreciate your help. > > Best wishes, > > Kie Woo Nam > > ___________________________ > Kie Woo Nam, PhD student > Division of Psychological Medicine > Institute of Psychiatry, King's College London > 16 De Crespigny Park, Denmark Hill > London, SE5 8AF, UK --_da845b0a-7b5d-4acf-844a-7c616bedcf1b_ Content-Type: text/html; charset="iso-8859-1" Content-Transfer-Encoding: quoted-printable If you didnt change the default settings of the toolbox, then all of your images are warped independently to the IXI-template provided by the toolbox. This is a DARTEL-compatible average template of healthy adult subjects in MNI space (see also the VBM8-manual). Thus, outliers wont affect the template and it should be safe to go for option 1 (given that you have good reasons to exclude these images, i.e. your definition of "poor" quality).

BTW, it would be of interest to know the average age of the IXI-template sample, but as far as I know this information is not provided by the VBM8-manual. Maybe the author, Christian Gaser, can comment on this.

Best regards,
Michel 

> Date: Fri, 4 Feb 2011 11:52:04 +0000
> From: [log in to unmask]
> Subject: [SPM] VBM8 - What to do after sample homogeneity check
> To: [log in to unmask]
>
> Dear SPM experts,
>
> I've run VBM8 using a customized DARTEL-template. Then, I did sample homogeneity check and identified some poor images (i.e. images with severe motion artefacts, enlarged ventricles, etc.). Among 296 images in total, I found 11 "poor" images so far, but there seem to be some more of them.
>
> Now, my question is which option I should choose between the following.
>
> (-----1-----) Start statistical analysis without those outliers
> (-----2-----) Start again from the beginning (i.e. re-run VBM8) without those outliers
>
> I was originally going to go for option 2 because, to my understanding, a customized DARTEL-template is made from my own images, and therefore outliers would cause bias in the template. However, I'm not sure whether this reasoning is correct.
>
> So, could anyone who understands how VBM8 works please advise me on this? I would really appreciate your help.
>
> Best wishes,
>
> Kie Woo Nam
>
> ___________________________
> Kie Woo Nam, PhD student
> Division of Psychological Medicine
> Institute of Psychiatry, King's College London
> 16 De Crespigny Park, Denmark Hill
> London, SE5 8AF, UK
--_da845b0a-7b5d-4acf-844a-7c616bedcf1b_-- ========================================================================Date: Fri, 4 Feb 2011 17:14:43 +0100 Reply-To: "Dr. Anja Ischebeck" <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: "Dr. Anja Ischebeck" <[log in to unmask]> Subject: Postdoctoral position at Graz University Austria In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/mixed; boundary="------------050203040904090002020506" Message-ID: <[log in to unmask]> --------------050203040904090002020506 Content-Type: text/plain; charset="UTF-8"; format=flowed Content-Transfer-Encoding: quoted-printable X-MIME-Autoconverted: from 8bit to quoted-printable by bofur.jiscmail.ac.uk id p14GEi9l020714 Dear SPM-List members, The Department of General Psychology (Institute of Psychology, University Graz, Austria) has an opening (starting in march 2011) for a full-time postdoctoral position for 6 years. We are looking for a candidate with a strong background in neuroimaging research. As duties also include teaching and some administration, proficiency in German is required. The University Graz is an equal opportunity employer. Please find attached the announcement (in German) for further details. A. Ischebeck ------------------------------ Univ.-Prof. Dr. Anja Ischebeck Department of General Psychology Institute of Psychology University Graz Universitätsplatz 2/DG, 8010 Graz Tel: +43 (0) 316 380-5118 E-Mail: [log in to unmask] http://psychologie.uni-graz.at/ --------------050203040904090002020506 Content-Type: application/msword; name="position_details_university_graz.doc" Content-Disposition: attachment; filename="position_details_university_graz.doc" Content-Transfer-Encoding: base64 0M8R4KGxGuEAAAAAAAAAAAAAAAAAAAAAPgADAP7/CQAGAAAAAAAAAAAAAAABAAAASQAAAAAA AAAAEAAATAAAAAEAAAD+////AAAAAEgAAAD///////////////////////////////////// //////////////////////////////////////////////////////////////////////// //////////////////////////////////////////////////////////////////////// //////////////////////////////////////////////////////////////////////// //////////////////////////////////////////////////////////////////////// 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looking images Mime-Version: 1.0 Content-Type: multipart/mixed; boundary="=__PartE5C9E9B8.0__=" Message-ID: <[log in to unmask]> This is a MIME message. If you are reading this text, you may want to consider changing to a mail reader or gateway that understands how to properly handle MIME multipart messages. --=__PartE5C9E9B8.0__Content-Type: text/plain; charset=US-ASCII Content-Transfer-Encoding: quoted-printable Content-Disposition: inline Hi, I've ran some analyses using the following steps: Realign: estimate and reslice - mean image written only Coregister: estimate - ref image is mean, and source image is individuals structural Segment Normalise:write - paramter file is segmented structural - images to write are realigned images - writing options - voxel size is [3.75x3.75x3.8] (i changed this to the size of the voxels that we used in our scanning sequence) Smoothing - 4mm All other options are left as default. Each individual person's data looks fine - but when I look at a really low threshold of the group map the BOLD signal doesn't fill the whole brain, as though my data has not been normalised correctly to the MNI brain (see image attached - overlay used is the single_subj_T1 from the canonical folder). Does anyone know what is happening and how to remedy this? Any comments/suggestions would be much appreciated. Many thanks Karen Karen Lythe PhD Wales Institute of Cognitive Neuroscience School of Psychology Cardiff University Tower Building Park Place CF10 3AT UK Tel: 029 208 70716 Email: [log in to unmask] --=__PartE5C9E9B8.0__Content-Type: application/pdf; name="spm_2011Feb04.pdf" Content-Transfer-Encoding: base64 Content-Disposition: attachment; filename="spm_2011Feb04.pdf" JVBERi0xLjIKJcfsj6IKNSAwIG9iago8PC9MZW5ndGggNiAwIFIvRmlsdGVyIC9GbGF0ZURlY29k ZT4+CnN0cmVhbQp4nM1ZyXIcRRDVETdgjlzrZsl4emrvbsJwkFcZG4xmInywHIRCHksDM9pmZItw cGfnB/gBMIYDB34Bs5458gcsBq5k7dXdo9G0HQZJtjSd/TLz1avM6qrWDsIpQVh9299rw2QnkTlP ieQoE1KmMkNDb+EFw2iQMJ7j0meHHCQbyTW0mewgmhUizZkOSiXTd02UzHhCpvZyjs5uJa/D907C wZbJIk8Zh4SCEOEvB+YyzwR8VDjzyaTCqSwKSgp0IXxch3hEDwvZX2tDtNiFhAUiBHVvJXADteAf RoKlAkksUgaZusNkvnP1ykL3TcCCqwFTBrRh9Bh1bybzw/62vU/s/ZagKTBqEWpwCnUdg+kU6Ao/ WkAMwxe5oRzPdWG8Ru3lC/bD7sGMCUVEqiwGCTmFUNmEIKkEMRXl0yquYpunBclU/utga2UsK1JB 4eON7iWTFyuZpuhDGMSPs1FmskmI5OS527UCAJgqMM/gZkv9UENnRbhtYjEQl1HkAO+o+y2CsWZL 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in to unmask]> Most demographic information about these subjects is available from http://www.brain-development.org/ . Age is not explicitly provided, although date of birth is there (but not the date of the scans). Best regards, -John On 4 February 2011 15:05, michel grothe <[log in to unmask]> wrote: > If you didnt change the default settings of the toolbox, then all of your > images are warped independently to the IXI-template provided by the toolbox. > This is a DARTEL-compatible average template of healthy adult subjects in > MNI space (see also the VBM8-manual). Thus, outliers wont affect the > template and it should be safe to go for option 1 (given that you have good > reasons to exclude these images, i.e. your definition of "poor" quality). > > BTW, it would be of interest to know the average age of the IXI-template > sample, but as far as I know this information is not provided by the > VBM8-manual. Maybe the author, Christian Gaser, can comment on this. > > Best regards, > Michel > >> Date: Fri, 4 Feb 2011 11:52:04 +0000 >> From: [log in to unmask] >> Subject: [SPM] VBM8 - What to do after sample homogeneity check >> To: [log in to unmask] >> >> Dear SPM experts, >> >> I've run VBM8 using a customized DARTEL-template. Then, I did sample >> homogeneity check and identified some poor images (i.e. images with severe >> motion artefacts, enlarged ventricles, etc.). Among 296 images in total, I >> found 11 "poor" images so far, but there seem to be some more of them. >> >> Now, my question is which option I should choose between the following. >> >> (-----1-----) Start statistical analysis without those outliers >> (-----2-----) Start again from the beginning (i.e. re-run VBM8) without >> those outliers >> >> I was originally going to go for option 2 because, to my understanding, a >> customized DARTEL-template is made from my own images, and therefore >> outliers would cause bias in the template. However, I'm not sure whether >> this reasoning is correct. >> >> So, could anyone who understands how VBM8 works please advise me on this? >> I would really appreciate your help. >> >> Best wishes, >> >> Kie Woo Nam >> >> ___________________________ >> Kie Woo Nam, PhD student >> Division of Psychological Medicine >> Institute of Psychiatry, King's College London >> 16 De Crespigny Park, Denmark Hill >> London, SE5 8AF, UK > ========================================================================Date: Fri, 4 Feb 2011 17:55:02 +0000 Reply-To: John Ashburner <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: John Ashburner <[log in to unmask]> Subject: Re: wierd looking images Comments: To: Karen Lythe <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> I'd suggest using the Check Reg button to compare the mask.img file with one of the MNI-space templates to see if they match. Also try check reg with a spatially normalised image from each of your subjects. It's possible that the grey matter masking was a bit too severe. Best regards, -John On 4 February 2011 17:17, Karen Lythe <[log in to unmask]> wrote: > Hi, > > I've ran some analyses using the following steps: > Realign: estimate and reslice > - mean image written only > Coregister: estimate > - ref image is mean, and source image is individuals structural > Segment > Normalise:write > - paramter file is segmented structural > - images to write are realigned images > - writing options - voxel size is [3.75x3.75x3.8] (i changed this to the size of the voxels that we used in our scanning sequence) > Smoothing - 4mm > > All other options are left as default. > > Each individual person's data looks fine - but when I look at a really low threshold of the group map the BOLD signal doesn't fill the whole brain, as though my data has not been normalised correctly to the MNI brain (see image attached - overlay used is the single_subj_T1 from the canonical folder). > > Does anyone know what is happening and how to remedy this? > > Any comments/suggestions would be much appreciated. > > Many thanks > Karen > > > Karen Lythe PhD > Wales Institute of Cognitive Neuroscience > School of Psychology > Cardiff University > Tower Building > Park Place > CF10 3AT > UK > > Tel: 029 208 70716 > Email: [log in to unmask] > > ========================================================================Date: Fri, 4 Feb 2011 12:30:06 -0600 Reply-To: Steffie Tomson <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Steffie Tomson <[log in to unmask]> Subject: Anatomical Regions MIME-Version: 1.0 Content-Type: multipart/alternative; boundary="----_=_NextPart_001_01CBC499.8BA602C8" Message-ID: <[log in to unmask]> This is a multi-part message in MIME format. ------_=_NextPart_001_01CBC499.8BA602C8 Content-Type: text/plain; charset="us-ascii" Content-Transfer-Encoding: quoted-printable Hi Everyone - I'd like to pull BOLD data from a set of anatomical regions. For example, I'd like to look at traces in the anterior cingulate or the left ITG. Does anyone know how to find a database of MNI-normalized anatomical regions like this? Ideally, somewhere to download individual masks for anatomical regions, or even Brodmann's areas? Thanks so much, Steffie ------_=_NextPart_001_01CBC499.8BA602C8 Content-Type: text/html; charset="us-ascii" Content-Transfer-Encoding: quoted-printable

Hi Everyone –

 

I’d like to pull BOLD data from a set of anatomical regions.  For example, I’d like to look at traces in the anterior cingulate or the left ITG.  Does anyone know how to find a database of MNI-normalized anatomical regions like this?  Ideally, somewhere to download individual masks for anatomical regions, or even Brodmann’s areas?

 

Thanks so much,

Steffie

 

------_=_NextPart_001_01CBC499.8BA602C8-- ========================================================================Date: Fri, 4 Feb 2011 10:19:39 -0800 Reply-To: Michael T Rubens <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Michael T Rubens <[log in to unmask]> Subject: Re: tool time course? Comments: To: [log in to unmask] In-Reply-To: [log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/alternative; boundarye6ba6e89aaaedfb9049b78ee59 Message-ID: <[log in to unmask]> --90e6ba6e89aaaedfb9049b78ee59 Content-Type: text/plain; charset=UTF-8 Content-Transfer-Encoding: quoted-printable Marsbar is very popular among users of spm. http://marsbar.sourceforge.net/ cheers, michael On Fri, Feb 4, 2011 at 3:07 AM, Rainer Bögle <[log in to unmask]>wrote: > Hi Emanuele, > > you can try to use RFXplot toolbox. > > http://rfxplot.sourceforge.net/ > > Kind regards, > Rainer > > On Fri, Feb 4, 2011 at 12:22 AM, Emanuele Tinelli <[log in to unmask]>wrote: > >> hi, >> I wanted to know if there is a tool to obtain the values of the time >> course (over Y) in a group of 30 subj by placing a ROI in the same region. >> thanks >> > > -- Research Associate Gazzaley Lab Department of Neurology University of California, San Francisco --90e6ba6e89aaaedfb9049b78ee59 Content-Type: text/html; charset=UTF-8 Content-Transfer-Encoding: quoted-printable Marsbar is very popular among users of spm. http://marsbar.sourceforge.net/

cheers,
michael

On Fri, Feb 4, 2011 at 3:07 AM, Rainer Bögle <[log in to unmask]> wrote:
Hi Emanuele,

you can try to use RFXplot toolbox.

http://rfxplot.sourceforge.net/

Kind regards,
Rainer

On Fri, Feb 4, 2011 at 12:22 AM, Emanuele Tinelli <[log in to unmask]> wrote:
hi,
I wanted to know if there is a tool to obtain the values of the time course (over Y) in a group of 30 subj by placing a ROI in the same region.
thanks




--
Research Associate
Gazzaley Lab
Department of Neurology
University of California, San Francisco
--90e6ba6e89aaaedfb9049b78ee59-- ========================================================================Date: Fri, 4 Feb 2011 10:38:32 -0800 Reply-To: Michael T Rubens <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Michael T Rubens <[log in to unmask]> Subject: Re: Anatomical Regions Comments: To: Steffie Tomson <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/alternative; boundarye6ba53b5283b59cd049b79329c Message-ID: <[log in to unmask]> --90e6ba53b5283b59cd049b79329c Content-Type: text/plain; charset=UTF-8 Content-Transfer-Encoding: quoted-printable WFU pickatlas http://fmri.wfubmc.edu/software/PickAtlas cheers, Michael On Fri, Feb 4, 2011 at 10:30 AM, Steffie Tomson <[log in to unmask]> wrote: > Hi Everyone – > > > > I’d like to pull BOLD data from a set of anatomical regions. For example, > I’d like to look at traces in the anterior cingulate or the left ITG. Does > anyone know how to find a database of MNI-normalized anatomical regions like > this? Ideally, somewhere to download individual masks for anatomical > regions, or even Brodmann’s areas? > > > > Thanks so much, > > Steffie > > > -- Research Associate Gazzaley Lab Department of Neurology University of California, San Francisco --90e6ba53b5283b59cd049b79329c Content-Type: text/html; charset=UTF-8 Content-Transfer-Encoding: quoted-printable WFU pickatlas

http://fmri.wfubmc.edu/software/PickAtlas

cheers,
Michael

On Fri, Feb 4, 2011 at 10:30 AM, Steffie Tomson <[log in to unmask]> wrote:

Hi Everyone –

 

I’d like to pull BOLD data from a set of anatomical regions.  For example, I’d like to look at traces in the anterior cingulate or the left ITG.  Does anyone know how to find a database of MNI-normalized anatomical regions like this?  Ideally, somewhere to download individual masks for anatomical regions, or even Brodmann’s areas?

 

Thanks so much,

Steffie

 




--
Research Associate
Gazzaley Lab
Department of Neurology
University of California, San Francisco
--90e6ba53b5283b59cd049b79329c-- ========================================================================Date: Fri, 4 Feb 2011 20:08:51 +0000 Reply-To: Ben Becker <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Ben Becker <[log in to unmask]> Subject: DARTEL-VBM: total intracranial volume in second level analysis Mime-Version: 1.0 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain; charset="UTF-8" Message-ID: <[log in to unmask]> Dear SPM-experts, I’ve computed a VBM analysis using the DARTEL-toolbox to investigate GM density differences in SPM8. The aim of the study was to investigate differences in GM density in two groups of patients. I set up the analysis according to the SPM8 manual (chapter 26 Dartel tools) using unmodulated GM images of the patients. My questions: Do I have to incorporate the individual total intracranial volume in the second-level between-group comparison as a covariate or does the analysis already account for this nuisance variable? So is it possible to analyze the date using an unpaired t-test or do I have to use the total intracranial volume as a covariate in the second-level analysis? Thanks and kind regards Ben ========================================================================Date: Fri, 4 Feb 2011 21:17:16 +0000 Reply-To: Deborah Talmi <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Deborah Talmi <[log in to unmask]> Subject: MEG source localizations and orthogonality Mime-Version: 1.0 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain; charset="UTF-8" Message-ID: <[log in to unmask]> Hi there, I ran two group source localizations of MEG data: identical but one with GS and one with MSP. I entered the nifti files to an ANCOVA. The GS gave me nice results, in line with the literature. The design matrix with MSP-localized files showed that the 4 regressors were not orthogonal, even before estimation. There were no significant voxels and the SPM was greyed out. I don't understand why the design matrix showed correlations even before estimation? If this is not an error, can I learn, from this difference between the models, something about my data? Cheers Deborah ========================================================================Date: Fri, 4 Feb 2011 17:06:41 -0500 Reply-To: John Fredy <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: John Fredy <[log in to unmask]> Subject: results visualization MIME-Version: 1.0 Content-Type: multipart/alternative; boundaryMessage-ID: [log in to unmask]> --0016e6d7843fd7b8af049b7c18f5 Content-Type: text/plain; charset=ISO-8859-1 Hello all, I will like to see the results obtained with roi analysis, using wfu_pick_atlas, in others software like MRICro or xjview, but I see that the spmT_0001.hdr contains the same data like I never do the roi analysis. Is possible see the ROI analysis in others software? Thanks John Ochoa --0016e6d7843fd7b8af049b7c18f5 Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable
Hello all,

I will like to see the results obtained with roi analysis, using wfu_pick_atlas, in others software like MRICro or xjview, but I see that the spmT_0001.hdr contains the same data like I never do the roi analysis.

Is possible see the ROI analysis in others software?

Thanks

John Ochoa
--0016e6d7843fd7b8af049b7c18f5-- ========================================================================Date: Fri, 4 Feb 2011 17:56:42 -0500 Reply-To: "MCLAREN, Donald" <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: "MCLAREN, Donald" <[log in to unmask]> Subject: Re: results visualization Comments: To: John Fredy <[log in to unmask]> In-Reply-To: [log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> Click the save button to save the thresholded maps. On Friday, February 4, 2011, John Fredy <[log in to unmask]> wrote: > Hello all, > I will like to see the results obtained with roi analysis, using wfu_pick_atlas, in others software like MRICro or xjview, but I see that the spmT_0001.hdr contains the same data like I never do the roi analysis. > > Is possible see the ROI analysis in others software? > Thanks > John Ochoa > -- Best Regards, Donald McLaren ================= D.G. McLaren, Ph.D. Postdoctoral Research Fellow, GRECC, Bedford VA Research Fellow, Department of Neurology, Massachusetts General Hospital and Harvard Medical School Office: (773) 406-2464 ===================== This e-mail contains CONFIDENTIAL INFORMATION which may contain PROTECTED HEALTHCARE INFORMATION and may also be LEGALLY PRIVILEGED and which is intended only for the use of the individual or entity named above. If the reader of the e-mail is not the intended recipient or the employee or agent responsible for delivering it to the intended recipient, you are hereby notified that you are in possession of confidential and privileged information. Any unauthorized use, disclosure, copying or the taking of any action in reliance on the contents of this information is strictly prohibited and may be unlawful. If you have received this e-mail unintentionally, please immediately notify the sender via telephone at (773) 406-2464 or email. ========================================================================Date: Sat, 5 Feb 2011 15:03:06 +0100 Reply-To: maike tahden <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: maike tahden <[log in to unmask]> Subject: Re: separate BOLD-functions per each single trial Comments: To: "MCLAREN, Donald" <[log in to unmask]>, Michael T Rubens <[log in to unmask]> In-Reply-To: <[log in to unmask]> Content-Type: text/plain; charset="utf-8" MIME-Version: 1.0 Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> Hello Mr. McLaren, hello Mr. Rubens, thank you very much for your advice! You gave me some new ideas of modelling the data and also some interesting and helpful literature. Please, excuse my late response. Thanks a lot! Best regards, Maike Tahden -------- Original-Nachricht -------- > Datum: Sun, 30 Jan 2011 16:06:03 -0800 > Von: Michael T Rubens <[log in to unmask]> > An: [log in to unmask] > Betreff: Re: [SPM] separate BOLD-functions per each single trial > Just to note, it is not uncommon to run a GLM with separate regressors for > each trial. This is how the beta series correlation method of functional > connectivity is performed. See Rissman et al. Neuroimage 2004. > > I don't think it has ever been done with using FIR as the bf though. > > cheers, > Michael > > On Sun, Jan 30, 2011 at 3:55 PM, MCLAREN, Donald > <[log in to unmask]>wrote: > > > If I understand you correctly, this is impossible. > > > > It seems like you want a separate response for each trial, this would > > require a separate set of FIR for each trial. Because of this you will > > end up with more regressors than measurements/observations. Since you > > have more predictors than measurements, the model is overspecified and > > there would be multiple solutions. > > > > On the other hand, if you assume the same shape for each individual > > event, then you could obtain a measure of the amplitude of the > > response for each trial. To do this, as Cesar stated, you want to have > > N event types in your model where N is the number of trials. > > > > Chapter 9, I believe, in Functional Magnetic Resonance Imaging by > > Jezzard et al., has a section on estimating the BOLD response and its > > limitations. Also, there were 2 papers from either 2000 or 2001 by > > Ollinger et al. on event-related designs. > > > > Hope this helps. > > > > Best Regards, Donald McLaren > > ================= > > D.G. McLaren, Ph.D. > > Postdoctoral Research Fellow, GRECC, Bedford VA > > Research Fellow, Department of Neurology, Massachusetts General > > Hospital and Harvard Medical School > > Office: (773) 406-2464 > > ===================== > > This e-mail contains CONFIDENTIAL INFORMATION which may contain > > PROTECTED HEALTHCARE INFORMATION and may also be LEGALLY PRIVILEGED > > and which is intended only for the use of the individual or entity > > named above. If the reader of the e-mail is not the intended recipient > > or the employee or agent responsible for delivering it to the intended > > recipient, you are hereby notified that you are in possession of > > confidential and privileged information. Any unauthorized use, > > disclosure, copying or the taking of any action in reliance on the > > contents of this information is strictly prohibited and may be > > unlawful. If you have received this e-mail unintentionally, please > > immediately notify the sender via telephone at (773) 406-2464 or > > email. > > > > > > > > On Sun, Jan 30, 2011 at 3:43 PM, Maike Tahden <[log in to unmask]> wrote: > > > Hello Cesar, > > > > > > thank you very much for your response! However, I don’t think I’ll > get > > the information I need, if I create a different regressor for each > event. As > > I wrote last time, I need separate BOLD-functions per each single trial > and > > till now I’ve found no way to identify these with the help of SPM, so > that > > I’m trying to model the data by myself using the Generalized Linear > Model. > > In this way I hope, to get – in whatever form – the knowledge which > > respective proportion of the signal results from the stimulus presented > 2 s > > before, to that one presented 4 s before, to that one presented 6 s > before > > and so on. But till now I don’t know how… > > > > > > Or maybe I haven’t understood your tip correctly? > > > > > > Kind regards, > > > Maike > > > > > > > > > > > > > > > > > > -------- Original-Nachricht -------- > > >> Datum: Fri, 28 Jan 2011 10:02:45 +0100 > > >> Von: Cesar Caballero <[log in to unmask]> > > >> An: [log in to unmask], [log in to unmask] > > >> Betreff: Re: [SPM] separate BOLD-functions per each single trial > > > > > >> You need to specify one condition for each trial in your model > (specify > > >> 1st-level in SPM). > > >> Set the duration of each trial equal to zero (event-related) and > define > > >> the onset for each trial. > > >> This will create a different regressor in the design matrix for each > > >> event. > > >> > > >> Then specify an F-test for the columns of the design matrix > > corresponding > > >> to the conditions you want to compare. > > >> > > >> Hope this helps, > > >> Cesar > > >> > > >> You can read chapter > > >> On Jan 27, 2011, at 10:55 PM, Maike Tahden wrote: > > >> > > >> > Hello, > > >> > > > >> > at the moment I’m writing my bachelor thesis in mathematics using > > >> fMRI-data, which come from a biological psychology group. They > employed > > a rapid > > >> event-related design so that the duration of the inter-stimulus- and > > >> inter-trial-intervals varies between 2 and 4 s. That is why the > > respective > > >> BOLD-responses probably superpose each other in a linear fashion. For > my > > >> bachelor thesis I need separate BOLD-functions per each single trial. > To > > achieve > > >> this aim, I try to model the data using the Generalized Linear Model > > (cf. > > >> first pages of Chapter 10 “Analysis of fMRI Timeseries” in > “Human Brain > > >> Function”, 2nd Edition). However, I still do not know how I get the > > >> separate functions or rather: If you fix one point at the time > series, > > how do > > >> you know which respective proportion of the signal results from the > > stimulus > > >> presented 2 s before, to that one presented 4 s before, to that one > > >> presented 6 s before and so on? > > >> > > > >> > Does anybody know the answer? > > >> > > > >> > I would be most appreciative of each advice! > > >> > > > >> > Kind regards, > > >> > Maike > > >> > > > >> > -- > > >> > GMX DSL Doppel-Flat ab 19,99 Euro/mtl.! Jetzt mit > > >> > gratis Handy-Flat! http://portal.gmx.net/de/go/dsl > > >> > > > > > > -- > > > Neu: GMX De-Mail - Einfach wie E-Mail, sicher wie ein Brief! > > > Jetzt De-Mail-Adresse reservieren: http://portal.gmx.net/de/go/demail > > > > > > > > > -- > Research Associate > Gazzaley Lab > Department of Neurology > University of California, San Francisco -- GMX DSL Doppel-Flat ab 19,99 Euro/mtl.! Jetzt mit gratis Handy-Flat! http://portal.gmx.net/de/go/dsl ========================================================================Date: Sat, 5 Feb 2011 13:31:45 -0500 Reply-To: "Watson, Christopher" <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: "Watson, Christopher" <[log in to unmask]> Subject: Re: DARTEL-VBM: total intracranial volume in second level analysis Comments: To: Ben Becker <[log in to unmask]> In-Reply-To: <[log in to unmask]> Content-Type: text/plain; charset="Windows-1252" Content-Transfer-Encoding: quoted-printable MIME-Version: 1.0 Message-ID: <[log in to unmask]> You don't *have* to include TIV. It depends on what you are looking at, your hypotheses, etc. See O'Brien et al. 2006. But yes, if you want TIV as a covariate you have to include it yourself. SPM doesn't automatically do it. ________________________________________ From: SPM (Statistical Parametric Mapping) [[log in to unmask]] On Behalf Of Ben Becker [[log in to unmask]] Sent: Friday, February 04, 2011 3:08 PM To: [log in to unmask] Subject: [SPM] DARTEL-VBM: total intracranial volume in second level analysis Dear SPM-experts, Ive computed a VBM analysis using the DARTEL-toolbox to investigate GM density differences in SPM8. The aim of the study was to investigate differences in GM density in two groups of patients. I set up the analysis according to the SPM8 manual (chapter 26 Dartel tools) using unmodulated GM images of the patients. My questions: Do I have to incorporate the individual total intracranial volume in the second-level between-group comparison as a covariate or does the analysis already account for this nuisance variable? So is it possible to analyze the date using an unpaired t-test or do I have to use the total intracranial volume as a covariate in the second-level analysis? Thanks and kind regards Ben ========================================================================Date: Sat, 5 Feb 2011 19:06:28 +0000 Reply-To: Steve Fleming <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Steve Fleming <[log in to unmask]> Subject: Re: DARTEL-VBM: total intracranial volume in second level analysis Comments: To: Chris Watson <[log in to unmask]> Mime-Version: 1.0 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain Message-ID: <[log in to unmask]> Another option is to select proportional scaling under 'Globals' when setting up the model. This converts volumes into values that are a proportion of total brain/GM volume. See here for more details (and for discussion of the relationship between different covariate approaches): http://en.wikibooks.org/wiki/SPM/VBM#Globals Best Steve ========================================================================Date: Sat, 5 Feb 2011 20:56:42 +0100 Reply-To: Alexander Hammers <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Alexander Hammers <[log in to unmask]> Subject: Re: Anatomical Regions Content-Type: multipart/alternative; boundary=Apple-Mail-108-801023220 Mime-Version: 1.0 (Apple Message framework v1082) Message-ID: <[log in to unmask]> --Apple-Mail-108-801023220 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain; charset=windows-1252 Dear Steffie, Brodmann areas are histological entities; you can therefore only really get to them via histology. There is a long-term initiative under way in Jlich, Germany to provide such maps via histological workup of ten brains and spatial transfer to MNI space - see http://www.fz-juelich.de/inm/inm-1/index.php?index=396 and papers by Zilles K, Amunts K, Eickhoff E et al. They are great but don't exist for all areas. The next best thing is to define your regions based on multiple brains. The good news is that for major sulci, there is, on average, actually a reasonable correspondence between histology and macroscopic landmarks (which you can see on MRI), see e.g. Figure 6 in Hammers A et al. Hum Brain Mapp 2007. One such atlas is our maximum probability map in MNI space (Hammers A, Allom R et al. Hum Brain Mapp 2003; since then expanded to include 83 regions and now based on 30 brains (n30r83; see Gousias IS et al. Neuroimage 2008 for the additional region definitions)), which you can get by agreeing to a one-page free academic licence (attached). There are many more atlases based on _single_ brains, including AAL (Tzourio-Mazoyer et al. 2002); our earlier segmentation of the same brain (Hammers et al. 2002); and digitalized versions based on the single Talairach hemisphere (minus cerebellum) (e.g. WFU Pickatlas). However, single brain / hemisphere atlases are by definition not representative and are therefore not likely to well represent your subject under study. This can be, and has been, quantified for AAL and PickAtlas versus the maximum probability map (Rodionov R et al.Magn Reson Imaging 2009). The most exhaustive quantification of the errors involved in single subject atlasing is in Heckemann RA et al. Neuroimage 2006. In terms of spatial overlap, for single atlases, you loose five Dice index points compared to the maxprobmap. You'd need to train a student for several months to improve that much, and by using a maximum probabilty map you get the same improvement for free :-). Obviously there are other more involved and more accurate forms of atlasing (see e.g. Heckemann RA et al. Neuroimage 2010 for one example and a review), but for working in MNI space with low-res techniques (fMRI, PET, SPECT, MEG, etc.) I think maxprobmaps are an excellent compromise. Hope this helps, ATB, A PS: If you want the n30r83 maxprobmap, just email me off-list if the licence is acceptable to you (it essentially asks to cite our work and not use it commercially). On 4 Feb 2011, at 19:38, Michael T Rubens wrote: > WFU pickatlas > > http://fmri.wfubmc.edu/software/PickAtlas > > cheers, > Michael > > On Fri, Feb 4, 2011 at 10:30 AM, Steffie Tomson <[log in to unmask]> wrote: > Hi Everyone > > > Id like to pull BOLD data from a set of anatomical regions. For example, Id like to look at traces in the anterior cingulate or the left ITG. Does anyone know how to find a database of MNI-normalized anatomical regions like this? Ideally, somewhere to download individual masks for anatomical regions, or even Brodmanns areas? > > > Thanks so much, > > Steffie > > > > > > -- > Research Associate > Gazzaley Lab > Department of Neurology > University of California, San Francisco --Apple-Mail-108-801023220 Content-Type: multipart/mixed; boundary=Apple-Mail-109-801023220 --Apple-Mail-109-801023220 Content-Transfer-Encoding: quoted-printable Content-Type: text/html; charset=iso-8859-1 Dear Steffie,


Brodmann areas are histological entities; you can therefore only really get to them via histology. There is a long-term initiative under way in Jlich, Germany to provide such maps via histological workup of ten brains and spatial transfer to MNI space - see http://www.fz-juelich.de/inm/inm-1/index.php?index=396 and papers by Zilles K, Amunts K, Eickhoff E et al.

They are great but don't exist for all areas.

The next best thing is to define your regions based on multiple brains. The good news is that for major sulci, there is, on average, actually a reasonable correspondence between histology and macroscopic landmarks (which you can see on MRI), see e.g. Figure 6 in Hammers A et al. Hum Brain Mapp 2007.

One such atlas is our maximum probability map in MNI space (Hammers A, Allom R et al. Hum Brain Mapp 2003; since then expanded to include 83 regions and now based on 30 brains (n30r83; see Gousias IS et al. Neuroimage 2008 for the additional region definitions)), which you can get by agreeing to a one-page free academic licence (attached).

There are many more atlases based on _single_ brains, including AAL (Tzourio-Mazoyer et al. 2002); our earlier segmentation of the same brain (Hammers et al. 2002); and digitalized versions based on the single Talairach hemisphere (minus cerebellum) (e.g. WFU Pickatlas). However, single brain / hemisphere atlases are by definition not representative and are therefore not likely to well represent your subject under study. This can be, and has been, quantified for AAL and PickAtlas versus the maximum probability map (Rodionov R et al.Magn Reson Imaging 2009).

The most exhaustive quantification of the errors involved in single subject atlasing is in Heckemann RA et al. Neuroimage 2006. In terms of spatial overlap, for single atlases, you loose five Dice index points compared to the maxprobmap. You'd need to train a student for several months to improve that much, and by using a maximum probabilty map you get the same improvement for free :-).

Obviously there are other more involved and more accurate forms of atlasing (see e.g. Heckemann RA et al. Neuroimage 2010 for one example and a review), but for working in MNI space with low-res techniques (fMRI, PET, SPECT, MEG, etc.) I think maxprobmaps are an excellent compromise.

Hope this helps,

ATB, A
PS: If you want the n30r83 maxprobmap, just email me off-list if the licence is acceptable to you (it essentially asks to cite our work and not use it commercially).
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On 4 Feb 2011, at 19:38, Michael T Rubens wrote:

WFU pickatlas


cheers,
Michael

On Fri, Feb 4, 2011 at 10:30 AM, Steffie Tomson <[log in to unmask]> wrote:

Hi Everyone

 

Id like to pull BOLD data from a set of anatomical regions.  For example, Id like to look at traces in the anterior cingulate or the left ITG.  Does anyone know how to find a database of MNI-normalized anatomical regions like this?  Ideally, somewhere to download individual masks for anatomical regions, or even Brodmanns areas?

 

Thanks so much,

Steffie

 



-- 
Research Associate
Gazzaley Lab
Department of Neurology
University of California, San Francisco

--Apple-Mail-109-801023220-- --Apple-Mail-108-801023220-- ========================================================================Date: Sat, 5 Feb 2011 16:41:48 -0500 Reply-To: "Watson, Christopher" <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: "Watson, Christopher" <[log in to unmask]> Subject: Re: DARTEL-VBM: total intracranial volume in second level analysis Comments: To: Steve Fleming <[log in to unmask]> In-Reply-To: <[log in to unmask]> Content-Type: text/plain; charset="us-ascii" Content-Transfer-Encoding: quoted-printable MIME-Version: 1.0 Message-ID: <[log in to unmask]> This may not always be appropriate, however. See e.g. Barnes et al (Neuroimage 2010) who found that volumes of some ROIs had a nonlinear relationship with whole brain volume. ________________________________________ From: Steve Fleming [[log in to unmask]] Sent: Saturday, February 05, 2011 2:06 PM To: [log in to unmask]; Watson, Christopher Cc: Steve Fleming Subject: Re: DARTEL-VBM: total intracranial volume in second level analysis Another option is to select proportional scaling under 'Globals' when setting up the model. This converts volumes into values that are a proportion of total brain/GM volume. See here for more details (and for discussion of the relationship between different covariate approaches): http://en.wikibooks.org/wiki/SPM/VBM#Globals Best Steve ========================================================================Date: Sat, 5 Feb 2011 17:45:43 -0600 Reply-To: Pilar Archila-Suerte <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Pilar Archila-Suerte <[log in to unmask]> Subject: Signal change in SPM MIME-Version: 1.0 Content-Type: multipart/alternative; boundaryMessage-ID: <[log in to unmask]> --0016364c794904d324049b919a8c Content-Type: text/plain; charset=UTF-8 SPM Users, Can somebody please verify this for me: Signal change for an ROI in SPM is found through the following steps: 1. Find ROI, then: "Plot -> fitted responses --> contrast --> adjusted --> plot by scan/time", am I correct? Thanks, Pilar A. --0016364c794904d324049b919a8c Content-Type: text/html; charset=UTF-8 Content-Transfer-Encoding: quoted-printable SPM Users, 
Can somebody please verify this for me: Signal change for an ROI in SPM is found through the following steps: 1. Find ROI, then: "Plot -> fitted responses --> contrast --> adjusted --> plot by scan/time", am I correct?

Thanks,

Pilar A. 
--0016364c794904d324049b919a8c-- ========================================================================Date: Sat, 5 Feb 2011 22:51:23 -0500 Reply-To: Carlton CHU <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Carlton CHU <[log in to unmask]> Subject: Re: Anatomical Regions Comments: To: Alexander Hammers <[log in to unmask]> Comments: cc: Carlton CHU <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/alternative; boundary cf300258e468f1cf049b950706 Message-ID: <[log in to unmask]> --20cf300258e468f1cf049b950706 Content-Type: text/plain; charset=windows-1252 Content-Transfer-Encoding: quoted-printable Dear Alexander: In your opinion, how does LPBA40 ( http://www.loni.ucla.edu/~shattuck/resources/lpba40/) compare with the n30r83? LPBA40 only has 56 structures, but it was constructed from 10 more subjects. It seems both n30r83 and LPBA40 have maximum probability maps. I do not want to get into the details of comparing those two templates. As a user, I just want to choose one template to mask regions in my fMRI data. Any suggestions? Best, Carlton On Sat, Feb 5, 2011 at 2:56 PM, Alexander Hammers < [log in to unmask]> wrote: > Dear Steffie, > > > Brodmann areas are histological entities; you can therefore only really get > to them via histology. There is a long-term initiative under way in Jlich, > Germany to provide such maps via histological workup of ten brains and > spatial transfer to MNI space - see > http://www.fz-juelich.de/inm/inm-1/index.php?index=396 and papers by > Zilles K, Amunts K, Eickhoff E et al. > > They are great but don't exist for all areas. > > The next best thing is to define your regions based on multiple brains. The > good news is that for major sulci, there is, on average, actually a > reasonable correspondence between histology and macroscopic landmarks (which > you can see on MRI), see e.g. Figure 6 in Hammers A et al. Hum Brain Mapp > 2007. > > One such atlas is our maximum probability map in MNI space (Hammers A, > Allom R et al. Hum Brain Mapp 2003; since then expanded to include 83 > regions and now based on 30 brains (n30r83; see Gousias IS et al. Neuroimage > 2008 for the additional region definitions)), which you can get by agreeing > to a one-page free academic licence (attached). > > There are many more atlases based on _single_ brains, including AAL > (Tzourio-Mazoyer et al. 2002); our earlier segmentation of the same brain > (Hammers et al. 2002); and digitalized versions based on the single > Talairach hemisphere (minus cerebellum) (e.g. WFU Pickatlas). However, > single brain / hemisphere atlases are by definition not representative and > are therefore not likely to well represent your subject under study. This > can be, and has been, quantified for AAL and PickAtlas versus the maximum > probability map (Rodionov R et al.Magn Reson Imaging 2009). > > The most exhaustive quantification of the errors involved in single subject > atlasing is in Heckemann RA et al. Neuroimage 2006. In terms of spatial > overlap, for single atlases, you loose five Dice index points compared to > the maxprobmap. You'd need to train a student for several months to improve > that much, and by using a maximum probabilty map you get the same > improvement for free :-). > > Obviously there are other more involved and more accurate forms of atlasing > (see e.g. Heckemann RA et al. Neuroimage 2010 for one example and a review), > but for working in MNI space with low-res techniques (fMRI, PET, SPECT, MEG, > etc.) I think maxprobmaps are an excellent compromise. > > Hope this helps, > > ATB, A > PS: If you want the n30r83 maxprobmap, just email me off-list if the > licence is acceptable to you (it essentially asks to cite our work and not > use it commercially). > > > On 4 Feb 2011, at 19:38, Michael T Rubens wrote: > > WFU pickatlas > > http://fmri.wfubmc.edu/software/PickAtlas > > cheers, > Michael > > On Fri, Feb 4, 2011 at 10:30 AM, Steffie Tomson <[log in to unmask]> > wrote: > >> Hi Everyone >> >> >> Id like to pull BOLD data from a set of anatomical regions. For example, >> Id like to look at traces in the anterior cingulate or the left ITG. Does >> anyone know how to find a database of MNI-normalized anatomical regions like >> this? Ideally, somewhere to download individual masks for anatomical >> regions, or even Brodmanns areas? >> >> >> Thanks so much, >> >> Steffie >> >> > > > > -- > Research Associate > Gazzaley Lab > Department of Neurology > University of California, San Francisco > > > > --20cf300258e468f1cf049b950706 Content-Type: text/html; charset=windows-1252 Content-Transfer-Encoding: quoted-printable Dear Alexander:

In your opinion, how does LPBA40 (http://www.loni.ucla.edu/~shattuck/resources/lpba40/) compare with then30r83? LPBA40 only has 56structures, but it was constructed from 10 more subjects. It seems both n30r83 and LPBA40 have maximum probability maps.

I do not want to get into the details of comparing those two templates. As a user,I just want to choose one template to mask regions in my fMRI data. Any suggestions?

Best,
Carlton

On Sat, Feb 5, 2011 at 2:56 PM, Alexander Hammers <[log in to unmask]> wrote:
Dear Steffie,


Brodmann areas are histological entities; you can therefore only really get to them via histology. There is a long-term initiative under way in Jlich, Germany to provide such maps via histological workup of ten brains and spatial transfer to MNI space - seehttp://www.fz-juelich.de/inm/inm-1/index.php?index=396and papers by Zilles K, Amunts K, Eickhoff E et al.

They are great but don't exist for all areas.

The next best thing is to define your regions based on multiple brains. The good news is that for major sulci, there is, on average, actually a reasonable correspondence between histology and macroscopic landmarks (which you can see on MRI), see e.g. Figure 6 in Hammers A et al. Hum Brain Mapp 2007.

One such atlas is our maximum probability map in MNI space (Hammers A, Allom R et al. Hum Brain Mapp 2003; since then expanded to include 83 regions and now based on 30 brains (n30r83; see Gousias IS et al. Neuroimage 2008 for the additional region definitions)), which you can get by agreeing to a one-page free academic licence (attached).

There are many more atlases based on _single_ brains, including AAL (Tzourio-Mazoyer et al. 2002); our earlier segmentation of the same brain (Hammers et al. 2002); and digitalized versions based on the single Talairach hemisphere (minus cerebellum) (e.g. WFU Pickatlas). However, single brain / hemisphere atlases are by definition not representative and are therefore not likely to well represent your subject under study. This can be, and has been, quantified for AAL and PickAtlas versus the maximum probability map (Rodionov R et al.Magn Reson Imaging 2009).

The most exhaustive quantification of the errors involved in single subject atlasing is in Heckemann RA et al. Neuroimage 2006. In terms of spatial overlap, for single atlases, you loose five Dice index points compared to the maxprobmap. You'd need to train a student for several months to improve that much, and by using a maximum probabilty map you get the same improvement for free :-).

Obviously there are other more involved and more accurate forms of atlasing (see e.g. Heckemann RA et al. Neuroimage 2010 for one example and a review), but for working in MNI space with low-res techniques (fMRI, PET, SPECT, MEG, etc.) I think maxprobmaps are an excellent compromise.

Hope this helps,

ATB, A
PS: If you want the n30r83 maxprobmap, just email me off-list if the licence is acceptable to you (it essentially asks to cite our work and not use it commercially).


On 4 Feb 2011, at 19:38, Michael T Rubens wrote:

WFU pickatlas


cheers,
Michael

On Fri, Feb 4, 2011 at 10:30 AM, Steffie Tomson<[log in to unmask]>wrote:

Hi Everyone


Id like to pull BOLD data from a set of anatomical regions. For example, Id like to look at traces in the anterior cingulate or the left ITG. Does anyone know how to find a database of MNI-normalized anatomical regions like this? Ideally, somewhere to download individual masks for anatomical regions, or even Brodmanns areas?


Thanks so much,

Steffie





--
Research Associate
Gazzaley Lab
Department of Neurology
University of California, San Francisco



--20cf300258e468f1cf049b950706-- ========================================================================Date: Sat, 5 Feb 2011 21:10:44 -0800 Reply-To: Michael Spezio <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Michael Spezio <[log in to unmask]> Subject: Code for saving movies made in spm eeg analyses Mime-Version: 1.0 Content-Type: multipart/alternative; boundary="=__Part022E0C44.0__=" Message-ID: <[log in to unmask]> This is a MIME message. If you are reading this text, you may want to consider changing to a mail reader or gateway that understands how to properly handle MIME multipart messages. --=__Part022E0C44.0__Content-Type: text/plain; charset=US-ASCII Content-Transfer-Encoding: quoted-printable Does anyone have experience with saving the movies that appear in the Graphics Window in SPM8's EEG analyses (e.g., the movie in EEG/MEG Source Localization)? Is there an easy way to save the scalp topographies in the Graphics Window (e.g., from Display --> M/EEG) as movies over time? Is this better accomplished in FieldTrip directly, or can this be done from within SPM8? Thanks for any guidance. Best, Michael Michael L. Spezio, Ph.D. Assistant Professor of Psychology Department of Psychology Scripps College Claremont, CA [log in to unmask] 909.607.0914 and Visiting Associate Scientist Psychology & Neuroscience Division of Humanities & Social Sciences Caltech Pasadena, CA 91125 [log in to unmask] --=__Part022E0C44.0__Content-Type: text/html; charset=US-ASCII Content-Transfer-Encoding: quoted-printable Content-Description: HTML Does anyone have experience with saving the movies that appear in the Graphics Window in SPM8's EEG analyses (e.g., the movie in EEG/MEG Source Localization)? Is there an easy way to save the scalp topographies in the Graphics Window (e.g., from Display --> M/EEG) as movies over time?

Is this better accomplished in FieldTrip directly, or can this be done from within SPM8?

Thanks for any guidance.

Best,

Michael

Michael L. Spezio, Ph.D.
Assistant Professor of Psychology
Department of Psychology
Scripps College
Claremont, CA
[log in to unmask]
909.607.0914

and

Visiting Associate Scientist
Psychology & Neuroscience
Division of Humanities & Social Sciences
Caltech
Pasadena, CA 91125
[log in to unmask]

--=__Part022E0C44.0__=-- ========================================================================Date: Sun, 6 Feb 2011 10:30:40 +0100 Reply-To: ematine tine <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: ematine tine <[log in to unmask]> Subject: Re: tool time course? In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> 2011/2/4 Michael T Rubens <[log in to unmask]>: > Marsbar is very popular among users of spm.http://marsbar.sourceforge.net/ > cheers, > michael > > On Fri, Feb 4, 2011 at 3:07 AM, Rainer Bgle <[log in to unmask]> > wrote: >> >> Hi Emanuele, >> >> you can try to use RFXplot toolbox. >> >> http://rfxplot.sourceforge.net/ >> >> Kind regards, >> Rainer >> Thanks!! ========================================================================Date: Sun, 6 Feb 2011 19:23:16 +0200 Reply-To: Panagiotis Tsiatsis <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Panagiotis Tsiatsis <[log in to unmask]> Subject: Warning in spm_eeg_convert2scalp (griddata) MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1; format=flowed Content-Transfer-Encoding: 7bit Message-ID: <[log in to unmask]> Dear All, When I am converting my CTF MEG epoched data to images, I am getting the following warning: Warning: Duplicate x-y data points detected: using average of the z values. > In griddata at 107 In spm_eeg_convert2scalp at 204 My settings are: S = []; S.n = 32; S.Fname = Concatenated_File_Name_Time; S.interpolate_bad = 1; S.modality = 'MEG'; I also have EOG channels whose chantype has been set to 'EEG' during the conversion (this of course should not interfere since I ve selected my modality to be 'MEG'). By browsing the Mathwoks forum, I suspect that this happens when nearby values get very similar (as is the case with MEG data). Anybody seen that before? Any intuitions? Thanks and best, Panagiotis -- Panagiotis S. Tsiatsis Max Planck Institute for Biological Cybernetics Cognitive NeuroImaging Group Tuebingen, Germany ========================================================================Date: Mon, 7 Feb 2011 13:31:52 +1300 Reply-To: Reem Jan <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Reem Jan <[log in to unmask]> Subject: Re: tool time course? Comments: To: =?iso-8859-1?Q?Rainer_Bgle?= <[log in to unmask]> In-Reply-To: A[log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/alternative; boundary="----_=_NextPart_001_01CBC65E.6A96BF8B" Message-ID: <[log in to unmask]> This is a multi-part message in MIME format. ------_=_NextPart_001_01CBC65E.6A96BF8B Content-Type: text/plain; charset="iso-8859-1" Content-Transfer-Encoding: quoted-printable Hi Rainer Do you know whether RFXplot toolbox can be used with SPM8? Many thanks Reem From: SPM (Statistical Parametric Mapping) [mailto:[log in to unmask]] On Behalf Of Rainer Bgle Sent: Saturday, February 05, 2011 12:07 AM To: [log in to unmask] Subject: Re: [SPM] tool time course? Hi Emanuele, you can try to use RFXplot toolbox. http://rfxplot.sourceforge.net/ Kind regards, Rainer On Fri, Feb 4, 2011 at 12:22 AM, Emanuele Tinelli <[log in to unmask]> wrote: hi, I wanted to know if there is a tool to obtain the values of the time course (over Y) in a group of 30 subj by placing a ROI in the same region. thanks __________ Information from ESET NOD32 Antivirus, version of virus signature database 5851 (20110206) __________ The message was checked by ESET NOD32 Antivirus. http://www.eset.com ------_=_NextPart_001_01CBC65E.6A96BF8B Content-Type: text/html; charset="iso-8859-1" Content-Transfer-Encoding: quoted-printable

Hi Rainer

 

Do you know whether RFXplot toolbox can be used with SPM8?

 

Many thanks

Reem

 

From: SPM (Statistical Parametric Mapping) [mailto:[log in to unmask]] On Behalf Of Rainer Bgle
Sent: Saturday, February 05, 2011 12:07 AM
To: [log in to unmask]
Subject: Re: [SPM] tool time course?

 

Hi Emanuele,

you can try to use RFXplot toolbox.

http://rfxplot.sourceforge.net/

Kind regards,
Rainer

On Fri, Feb 4, 2011 at 12:22 AM, Emanuele Tinelli <[log in to unmask]> wrote:

hi,
I wanted to know if there is a tool to obtain the values of the time course (over Y) in a group of 30 subj by placing a ROI in the same region.
thanks

 

 

__________ Information from ESET NOD32 Antivirus, version of virus signature database 5851 (20110206) __________

 

The message was checked by ESET NOD32 Antivirus.

 

http://www.eset.com



__________ Information from ESET NOD32 Antivirus, version of virus signature database 5851 (20110206) __________

The message was checked by ESET NOD32 Antivirus.

http://www.eset.com
------_=_NextPart_001_01CBC65E.6A96BF8B-- ========================================================================Date: Mon, 7 Feb 2011 03:13:12 +0000 Reply-To: Jared Stokes <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Jared Stokes <[log in to unmask]> Subject: LAB MANAGER OF FMRI LABORATORY Mime-Version: 1.0 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain; charset="UTF-8" Message-ID: <[log in to unmask]> LAB MANAGER OF FMRI LABORATORY Lab manager position available in the laboratory of Roberto Cabeza (www.cabezalab.org) at the Center for Cognitive Neuroscience of Duke University (www.mind.duke.edu). fMRI scanning is conducted at the nearby Brain Imaging and Analysis Center (www.biac.duke.edu). Duties include recruitment and neuropsychological testing of young and older participants, behavioral testing and MRI scanning, analyzing behavioral and brain imaging data, supervising and training undergraduate students, and general laboratory administration. Research topics include various forms of memory (relational, implicit, emotional) and the effects of healthy and pathological aging. The position includes opportunities for research and co-authorship of abstracts and papers. Qualifications: B.A. or equivalent with background in psychology, neuroscience, or computer science. All candidates should have excellent interpersonal and organizational skills, good computer skills, and some research experience. Experience in computer programming and familiarity with statistic are desirable. Two-year commitment is requested. Send a cover letter and a CV to [log in to unmask] Please enter “Lab Manager Position’ as the subject of the e-mail. ========================================================================Date: Mon, 7 Feb 2011 03:14:20 +0000 Reply-To: Jared Stokes <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Jared Stokes <[log in to unmask]> Subject: POSTDOCTORAL POSITION IN FMRI LABORATORY Mime-Version: 1.0 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain; charset="UTF-8" Message-ID: <[log in to unmask]> POSTDOCTORAL POSITION IN FMRI LABORATORY Postdoctoral position available in the laboratory of Roberto Cabeza (www.cabezalab.org) at the Center for Cognitive Neuroscience of Duke University (www.mind.duke.edu). fMRI scanning is conducted at the nearby Brain Imaging and Analysis Center (www.biac.duke.edu). Research will focus on the neural mechanisms of memory (e.g., relational memory, emotional memory, memory development). Within this general topic, the postdoctoral researcher will design her/his own studies. The position includes RA support and collaborations with graduate students and faculty at CCN and BIAC. The ideal candidate will have several of the following qualifications: (1) background in episodic memory research; (2) experience in fMRI methods; (3) programming skills; (4) expertise in statistics; and (5) a promising publication record. Send a statement of research interests and a CV to [log in to unmask] Please enter "Postdoctoral Position" as the subject of the e-mail. ========================================================================Date: Mon, 7 Feb 2011 13:35:14 +0800 Reply-To: han zhang <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: han zhang <[log in to unmask]> Subject: Re: SPM CLI In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/alternative; boundarye6ba5bc0bda73b76049baa98e6 Message-ID: <[log in to unmask]> --90e6ba5bc0bda73b76049baa98e6 Content-Type: text/plain; charset=ISO-8859-1 I think he means the toolkit "spm-batch". I remember it can be downloaded at SPM website. But I don't know if it still works fine for new version SPM (8?). Best, Han 2011/2/4 Stephen J. Fromm <[log in to unmask]> > "There is even a function in spm for doing this, but I have never used it." > > What function is that? > > Best, > > S > -- Han ZHANG NeuoImage Computing (NIC) group http://psychbrain.bnu.edu.cn/home/chaozhezhu/ http://publicationslist.org/han_zhang State Key Lab of Cognitive Neuroscience and Learning Beijing Normal Univ 19# Xinjiekouwai St. 100875, Beijing, China (Fax) +86-10-5880 6154 (Tel) +86-10-5880 2965 --90e6ba5bc0bda73b76049baa98e6 Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable
I think he means the toolkit"spm-batch". I remember it can be downloaded at SPM website. But I don't know if it still works finefor new version SPM (8?).
Best,
Han

2011/2/4 Stephen J. Fromm <[log in to unmask]>
"There is even a function in spm for doing this, but I have never used it."

What function is that?

Best,

S



--
Han ZHANG
NeuoImage Computing (NIC) group
http://psychbrain.bnu.edu.cn/home/chaozhezhu/
http://publicationslist.org/han_zhang
State Key Lab of Cognitive Neuroscience and Learning
Beijing Normal Univ 19# Xinjiekouwai St. 100875, Beijing, China
(Fax) +86-10-5880 6154
(Tel) +86-10-5880 2965
--90e6ba5bc0bda73b76049baa98e6-- ========================================================================Date: Mon, 7 Feb 2011 09:25:24 +0000 Reply-To: Karen Lythe <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Karen Lythe <[log in to unmask]> Subject: Re: wierd looking images Comments: To: John Ashburner <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/alternative; boundary cf3054a033c9a914049badcf42 Message-ID: <[log in to unmask]> --20cf3054a033c9a914049badcf42 Content-Type: text/plain; charset=ISO-8859-1 John, After using Check Reg it's evident that each of my subjects' normalised data and mask image is slightly smaller than the EPI template, although some to a higher degree than others. Is there a way to remedy this if it is indeed the grey matter masking that is too severe as you suggest. Best Karen On Fri, Feb 4, 2011 at 5:55 PM, John Ashburner <[log in to unmask]> wrote: > I'd suggest using the Check Reg button to compare the mask.img file > with one of the MNI-space templates to see if they match. Also try > check reg with a spatially normalised image from each of your > subjects. It's possible that the grey matter masking was a bit too > severe. > > Best regards, > -John > > On 4 February 2011 17:17, Karen Lythe <[log in to unmask]> wrote: > > Hi, > > > > I've ran some analyses using the following steps: > > Realign: estimate and reslice > > - mean image written only > > Coregister: estimate > > - ref image is mean, and source image is individuals structural > > Segment > > Normalise:write > > - paramter file is segmented structural > > - images to write are realigned images > > - writing options - voxel size is [3.75x3.75x3.8] (i changed this to the > size of the voxels that we used in our scanning sequence) > > Smoothing - 4mm > > > > All other options are left as default. > > > > Each individual person's data looks fine - but when I look at a really > low threshold of the group map the BOLD signal doesn't fill the whole brain, > as though my data has not been normalised correctly to the MNI brain (see > image attached - overlay used is the single_subj_T1 from the canonical > folder). > > > > Does anyone know what is happening and how to remedy this? > > > > Any comments/suggestions would be much appreciated. > > > > Many thanks > > Karen > > > > > > Karen Lythe PhD > > Wales Institute of Cognitive Neuroscience > > School of Psychology > > Cardiff University > > Tower Building > > Park Place > > CF10 3AT > > UK > > > > Tel: 029 208 70716 > > Email: [log in to unmask] > > > > > -- Karen Lythe, PhD School of Psychology Cardiff University Tower Building Park Place CF10 3AT Wales, UK Email: [log in to unmask] Tel: 029 208 70716 --20cf3054a033c9a914049badcf42 Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable John,

After using Check Reg it's evident that each of my subjects' normalised data and mask image is slightly smaller than the EPI template, although some to a higher degree than others.

Is there a way to remedy this if it is indeed the grey matter masking that is too severe as you suggest.

Best
Karen

On Fri, Feb 4, 2011 at 5:55 PM, John Ashburner <[log in to unmask]> wrote:
I'd suggest using the Check Reg button to compare the mask.img file
with one of the MNI-space templates to see if they match. Also try
check reg with a spatially normalised image from each of your
subjects. It's possible that the grey matter masking was a bit too
severe.

Best regards,
-John

On 4 February 2011 17:17, Karen Lythe <[log in to unmask]> wrote:
> Hi,
>
> I've ran some analyses using the following steps:
> Realign: estimate and reslice
> - mean image written only
> Coregister: estimate
> - ref image is mean, and source image is individuals structural
> Segment
> Normalise:write
> - paramter file is segmented structural
> - images to write are realigned images
> - writing options - voxel size is [3.75x3.75x3.8] (i changed this to the size of the voxels that we used in our scanning sequence)
> Smoothing - 4mm
>
> All other options are left as default.
>
> Each individual person's data looks fine - but when I look at a really low threshold of the group map the BOLD signal doesn't fill the whole brain, as though my data has not been normalised correctly to the MNI brain (see image attached - overlay used is the single_subj_T1 from the canonical folder).
>
> Does anyone know what is happening and how to remedy this?
>
> Any comments/suggestions would be much appreciated.
>
> Many thanks
> Karen
>
>
> Karen Lythe PhD
> Wales Institute of Cognitive Neuroscience
> School of Psychology
> Cardiff University
> Tower Building
> Park Place
> CF10 3AT
> UK
>
> Tel: 029 208 70716
> Email: [log in to unmask]
>
>



--
Karen Lythe, PhD
School of Psychology
Cardiff University
Tower Building
Park Place
CF10 3AT
Wales, UK
Email: [log in to unmask]
Tel: 029 208 70716
--20cf3054a033c9a914049badcf42-- ========================================================================Date: Mon, 7 Feb 2011 07:41:41 -0500 Reply-To: John Fredy <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: John Fredy <[log in to unmask]> Subject: Re: results visualization Comments: To: "MCLAREN, Donald" <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/alternative; boundaryMessage-ID: <[log in to unmask]> --001485f85aecbbed82049bb08da1 Content-Type: text/plain; charset=ISO-8859-1 Thanks! On Fri, Feb 4, 2011 at 5:56 PM, MCLAREN, Donald <[log in to unmask]>wrote: > Click the save button to save the thresholded maps. > > On Friday, February 4, 2011, John Fredy <[log in to unmask]> wrote: > > Hello all, > > I will like to see the results obtained with roi analysis, using > wfu_pick_atlas, in others software like MRICro or xjview, but I see that > the spmT_0001.hdr contains the same data like I never do the roi analysis. > > > > Is possible see the ROI analysis in others software? > > Thanks > > John Ochoa > > > > -- > > Best Regards, Donald McLaren > ================> D.G. McLaren, Ph.D. > Postdoctoral Research Fellow, GRECC, Bedford VA > Research Fellow, Department of Neurology, Massachusetts General Hospital > and > Harvard Medical School > Office: (773) 406-2464 <+17734062464> > ====================> This e-mail contains CONFIDENTIAL INFORMATION which may contain PROTECTED > HEALTHCARE INFORMATION and may also be LEGALLY PRIVILEGED and which is > intended only for the use of the individual or entity named above. If the > reader of the e-mail is not the intended recipient or the employee or agent > responsible for delivering it to the intended recipient, you are hereby > notified that you are in possession of confidential and privileged > information. Any unauthorized use, disclosure, copying or the taking of any > action in reliance on the contents of this information is strictly > prohibited and may be unlawful. If you have received this e-mail > unintentionally, please immediately notify the sender via telephone at > (773) > 406-2464 or email. > --001485f85aecbbed82049bb08da1 Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Thanks!

On Fri, Feb 4, 2011 at 5:56 PM, MCLAREN, Donald <[log in to unmask]> wrote:
Click the save button to save the thresholded maps.

On Friday, February 4, 2011, John Fredy <[log in to unmask]> wrote:
> Hello all,
> I will like to see the results obtained with roi analysis, using wfu_pick_atlas, in others software like MRICro or xjview, but I see that the spmT_0001.hdr contains the same data like I never do the roi analysis.
>
> Is possible see the ROI analysis in others software?
> Thanks
> John Ochoa
>

--

Best Regards, Donald McLaren
=================
D.G. McLaren, Ph.D.
Postdoctoral Research Fellow, GRECC, Bedford VA
Research Fellow, Department of Neurology, Massachusetts General Hospital and
Harvard Medical School
Office: (773) 406-2464
=====================
This e-mail contains CONFIDENTIAL INFORMATION which may contain PROTECTED
HEALTHCARE INFORMATION and may also be LEGALLY PRIVILEGED and which is
intended only for the use of the individual or entity named above. If the
reader of the e-mail is not the intended recipient or the employee or agent
responsible for delivering it to the intended recipient, you are hereby
notified that you are in possession of confidential and privileged
information. Any unauthorized use, disclosure, copying or the taking of any
action in reliance on the contents of this information is strictly
prohibited and may be unlawful. If you have received this e-mail
unintentionally, please immediately notify the sender via telephone at (773)
406-2464 or email.

--001485f85aecbbed82049bb08da1-- ========================================================================Date: Mon, 7 Feb 2011 12:48:45 +0000 Reply-To: Giancarlo Rossi-Fedele <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Giancarlo Rossi-Fedele <[log in to unmask]> Subject: Hi, I would need the STANDALONE SPM8 for LINUX-32 Mime-Version: 1.0 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain; charset="UTF-8" Message-ID: <[log in to unmask]> Hi, I would need the STANDALONE SPM8 for LINUX-32... Giancarlo Rossi-Fedele ========================================================================Date: Mon, 7 Feb 2011 14:15:31 +0100 Reply-To: Anders Eklund <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Anders Eklund <[log in to unmask]> Subject: Random permutation test MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1; format=flowed Content-Transfer-Encoding: 7bit Message-ID: <[log in to unmask]> Dear SPMers, I'm currently implementing a random permutation test for single subject fMRI analysis but I'm not sure of all the steps. In my opinion it is not obvious what steps that should be done in each permutation. My current algorithm looks like this Slice timing correction Motion compensation Detrending (cubic) BOLD removal (remove best linear fit between detrended time series and GLM basis functions) Estimate AR parameters from GLM residuals Apply spatial smoothing to the estimated AR parameters, to improve the estimates Apply whitening transform, to make sure the time series are white before they are permuted Iterate the whitening procedure 3-5 times, to further improve the AR estimates For each permutation (10 000) Permute the whitened timeseries Apply inverse whitening transform Smooth all the volumes For i = 1:3 ?? Detrending and BOLD removal (smoothed timeseries first iteration, then whitened smoothed timeseries) Estimate AR parameters from GLM residuals Apply whitening to smoothed time series end Detrend whitened timeseries Apply statistical analysis Save max test value End The whitening in each permutation is not necessary for the permutation approach (since the null distribution is estimated), but I want to make an as fair comparison as possible between corrected thresholds from the random permutation test and random field theory / Bonferroni correction. Would you change anything in the algorithm and why? /Anders -- -- ----------------------------------------------------------------------- Anders Eklund Phd student Medical Informatics, Department of Biomedical Engineering CMIV, Center for Medical Image Science and Visualization Tel: +46 73 6003790 mail: [log in to unmask] Fax: +46 13 101902 web: http://www.wanderineconsulting.com/ ----------------------------------------------------------------------- ========================================================================Date: Mon, 7 Feb 2011 11:53:21 -0500 Reply-To: "MCLAREN, Donald" <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: "MCLAREN, Donald" <[log in to unmask]> Subject: Re: DARTEL-VBM: total intracranial volume in second level analysis Comments: To: Ben Becker <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=windows-1252 Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> A couple of comments: (1) VBM is not the best measure of density; (2) Unmodulated images will give you a percentage of grey matter per voxel -- not necessarily density (or tissue density) (3) Since you are looking a how much tissue you have per voxel and not modulating, you are looking at a property of the tissue. Since tissue properties (like FA, MD, T2 time, etc.) are independent of brain volume, there is no need to include TBV, or TICV. (4) If you switch to modulated images, then TBV or TICV might need to be included in the model depending on how the modulation was done. See http://dbm.neuro.uni-jena.de/vbm/segmentation/modulation/ for more details. Best Regards, Donald McLaren ================= D.G. McLaren, Ph.D. Postdoctoral Research Fellow, GRECC, Bedford VA Research Fellow, Department of Neurology, Massachusetts General Hospital and Harvard Medical School Office: (773) 406-2464 ===================== This e-mail contains CONFIDENTIAL INFORMATION which may contain PROTECTED HEALTHCARE INFORMATION and may also be LEGALLY PRIVILEGED and which is intended only for the use of the individual or entity named above. If the reader of the e-mail is not the intended recipient or the employee or agent responsible for delivering it to the intended recipient, you are hereby notified that you are in possession of confidential and privileged information. Any unauthorized use, disclosure, copying or the taking of any action in reliance on the contents of this information is strictly prohibited and may be unlawful. If you have received this e-mail unintentionally, please immediately notify the sender via telephone at (773) 406-2464 or email. On Fri, Feb 4, 2011 at 3:08 PM, Ben Becker <[log in to unmask]> wrote: > Dear SPM-experts, > > Ive computed a VBM analysis using the DARTEL-toolbox to investigate GM density differences in SPM8. The aim of the study was to investigate differences in GM density in two groups of patients. I set up the analysis according to the SPM8 manual (chapter 26 Dartel tools) using unmodulated GM images of the patients. > > My questions: > Do I have to incorporate the individual total intracranial volume in the second-level between-group comparison as a covariate or does the analysis already account for this nuisance variable? So is it possible to analyze the date using an unpaired t-test or do I have to use the total intracranial volume as a covariate in the second-level analysis? > > Thanks and kind regards > > Ben > ========================================================================Date: Mon, 7 Feb 2011 18:02:25 +0000 Reply-To: Vladimir Litvak <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Vladimir Litvak <[log in to unmask]> Subject: Re: Code for saving movies made in spm eeg analyses Comments: To: Michael Spezio <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Message-ID: <[log in to unmask]> Dear Michael, There is no extensive support for making movies in SPM8 and Fieldtrip as far as I know. However, there is quite a simple generic way in Matlab to make movies from anything you can plot in a figure. Try help getframe help movie2avi In the tool invoked by 'render' button in 3D Source Reconstruction someone has already added these commands to the movie displaying code there (see around line 582 of spm_eeg_inv_visu3D_api.m). So if you write global MOVIE in the command line and then run a movie in this tool, you'll get a movie stored in the variable MOVIE and then you can save it using movie2avi. For the movie that you can generate using the 'mip' button see the code starting around line 96 of spm_eeg_invert_display.m. You can modify it in a similar way. One way to make a movie of scalp topographies via the GUI in SPM is to export your sensor data to image, open the image using CheckReg button, right click on it and choose 'Movie tool'. You can then scroll through the Z axis which is basically what you want and save it as a movie. If you want to use the plot from the reviewing tool, you'll have to write your own bit of code using spm_eeg_plotScalpData. Best, Vladimir On Sun, Feb 6, 2011 at 5:10 AM, Michael Spezio <[log in to unmask]> wrote: > Does anyone have experience with saving the movies that appear in the > Graphics Window in SPM8's EEG analyses (e.g., the movie in EEG/MEG Source > Localization)? Is there an easy way to save the scalp topographies in the > Graphics Window (e.g., from Display --> M/EEG) as movies over time? > > Is this better accomplished in FieldTrip directly, or can this be done from > within SPM8? > > Thanks for any guidance. > > Best, > > Michael > > Michael L. Spezio, Ph.D. > Assistant Professor of Psychology > Department of Psychology > Scripps College > Claremont, CA > [log in to unmask] > 909.607.0914 > > and > > Visiting Associate Scientist > Psychology & Neuroscience > Division of Humanities & Social Sciences > Caltech > Pasadena, CA 91125 > [log in to unmask] > ========================================================================Date: Mon, 7 Feb 2011 18:10:08 +0000 Reply-To: Vladimir Litvak <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Vladimir Litvak <[log in to unmask]> Subject: Re: Warning in spm_eeg_convert2scalp (griddata) Comments: To: Panagiotis Tsiatsis <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> Dear Panagiotis, Try doing: spm_eeg_load D.coor2D(D.meegchannels('MEG')) and look which of the channels have the same 2D coordinates. In principle this should not happen for CTF MEG. You can also look in 'Prepare' tool at the 2D channel layout an modify it if necessary or load a template layout from EEGtemplates. Best, Vladimir On Sun, Feb 6, 2011 at 5:23 PM, Panagiotis Tsiatsis <[log in to unmask]> wrote: > Dear All, > > When I am converting my CTF MEG epoched data to images, I am getting the > following warning: > > Warning: Duplicate x-y data points detected: using average of the z values. >> In griddata at 107 > In spm_eeg_convert2scalp at 204 > > My settings are: > > S = []; > S.n = 32; > S.Fname = Concatenated_File_Name_Time; > S.interpolate_bad = 1; > S.modality = 'MEG'; > > I also have EOG channels whose chantype has been set to 'EEG' during the > conversion (this of course should not interfere since I ve selected my > modality to be 'MEG'). > > By browsing the Mathwoks forum, I suspect that this happens when nearby > values get very similar (as is the case with MEG data). > > Anybody seen that before? Any intuitions? > > Thanks and best, > Panagiotis > > > -- > Panagiotis S. Tsiatsis > Max Planck Institute for Biological Cybernetics > Cognitive NeuroImaging Group > Tuebingen, Germany > ========================================================================Date: Mon, 7 Feb 2011 19:17:57 +0000 Reply-To: John Ashburner <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: John Ashburner <[log in to unmask]> Subject: Re: \spm8\tpm FWHM? Comments: To: Chris Rorden <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Message-ID: [log in to unmask]> The tissue probability maps used for unified segmentation should probably be a bit more blurred than the typical averages obtained via Dartel. There are a couple or main reasons for this: 1) The unified segmentation only samples the original images about every 3mm. Therefore, to prevent strange aliasing effects from sampling the tissue probability maps at frequencies lower than some of the frequenciies in the data, you may need to include some additional smoothing. I'm not sure what would be optimal here. 2) The deformation model in the unified does not have as much freedom as that of Dartel, so will not be able to warp the tissue probability maps quite as far. They may therefore need to be a bit more blurred in order to compensate for the less precise registration. All the best, -John On 3 February 2011 14:05, Chris Rorden <[log in to unmask]> wrote: > Hello- > > Short version: > What is the FWHM smooth (if any) applied to the spm8\tpm\csf.nii, spm8\tpm\grey.nii and spm8\tpm\white.nii? The corresponding images in the spm8\apriori folder seem very smooth (8mm FWHM?), the the spm8\tpm images appear very sharp. > > Long version > I want to make a set of alternative templates for SPM's unified normalization segmentation. The aim is to build a nice template for large stroke patient studies, and as the average age ~65 I want an age specific template. The aim is to conduct lesion-masked unified segmentation (www.pubmed.com/20542122) with an age specific template derived from a healthy aging sample. > I was able to create very nice tissue probability maps from the 50 healthy controls following the instructions for SPM's newseg and DARTEL, essentially following John Ashburner's instructions here (including affine transform of the template to MNI space): > http://www.fil.ion.ucl.ac.uk/~john/misc/VBMclass10.pdf > Now I want to use this TPM for standard unified segmentation normalization. The question is whether I should apply any smoothing to the resulting Dartel TPM image or not. As this image is based on 50 people, to my eye it looks approximately as sharp as the images in spm8\tpm (which seg-norm uses). Should I use the mean image TPMs directly, or apply a FWHM with a small smoothing kernel? > > -chris > ========================================================================Date: Mon, 7 Feb 2011 20:15:41 +0100 Reply-To: Carsten Stahlhut <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Carsten Stahlhut <[log in to unmask]> Subject: Code for saving movies made in spm eeg analyses Comments: To: [log in to unmask] In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/alternative; boundary cf3054a36dd4bf2f049bb60e55 Message-ID: <[log in to unmask]> --20cf3054a36dd4bf2f049bb60e55 Content-Type: text/plain; charset=ISO-8859-1 Dear Michael, In addition to Vladimir's answer you may want to download the mpgwrite package from Matlab Central http://www.mathworks.com/matlabcentral/fileexchange/309 if you want to save your movies in 'mpeg' format rather than in the '.avi' format. Hereby, you reduce the movie files quite a bit. Best, Carsten 2011/2/7 Vladimir Litvak <[log in to unmask]> Dear Michael, > > There is no extensive support for making movies in SPM8 and Fieldtrip > as far as I know. However, there is quite a simple generic way in > Matlab to make movies from anything you can plot in a figure. Try > > help getframe > help movie2avi > > In the tool invoked by 'render' button in 3D Source Reconstruction > someone has already added these commands to the movie displaying code > there (see around line 582 of spm_eeg_inv_visu3D_api.m). So if you > write > > global MOVIE > > in the command line and then run a movie in this tool, you'll get a > movie stored in the variable MOVIE and then you can save it using > movie2avi. > > For the movie that you can generate using the 'mip' button see the > code starting around line 96 of spm_eeg_invert_display.m. You can > modify it in a similar way. > > One way to make a movie of scalp topographies via the GUI in SPM is to > export your sensor data to image, open the image using CheckReg > button, right click on it and choose 'Movie tool'. You can then scroll > through the Z axis which is basically what you want and save it as a > movie. If you want to use the plot from the reviewing tool, you'll > have to write your own bit of code using spm_eeg_plotScalpData. > > Best, > > Vladimir > > > On Sun, Feb 6, 2011 at 5:10 AM, Michael Spezio > <[log in to unmask]> wrote: > > Does anyone have experience with saving the movies that appear in the > > Graphics Window in SPM8's EEG analyses (e.g., the movie in EEG/MEG Source > > Localization)? Is there an easy way to save the scalp topographies in the > > Graphics Window (e.g., from Display --> M/EEG) as movies over time? > > > > Is this better accomplished in FieldTrip directly, or can this be done > from > > within SPM8? > > > > Thanks for any guidance. > > > > Best, > > > > Michael > > > > Michael L. Spezio, Ph.D. > > Assistant Professor of Psychology > > Department of Psychology > > Scripps College > > Claremont, CA > > [log in to unmask] > > 909.607.0914 > > > > and > > > > Visiting Associate Scientist > > Psychology & Neuroscience > > Division of Humanities & Social Sciences > > Caltech > > Pasadena, CA 91125 > > [log in to unmask] > > > -- Carsten Stahlhut Section for Cognitive Systems Department of Informatics and Mathematical Modelling Richard Petersens Plads, Building 321 Technical University of Denmark DK-2800 Kongens Lyngby, Denmark --20cf3054a36dd4bf2f049bb60e55 Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable
Dear Michael,

In addition to Vladimir's answer you may want to download the mpgwrite package from Matlab Central
http://www.mathworks.com/matlabcentral/fileexchange/309
if you want to save your movies in 'mpeg' format rather than in the '.avi' format. Hereby, you reduce the movie files quite a bit.

Best,
Carsten



2011/2/7 Vladimir Litvak <[log in to unmask]>

Dear Michael,

There is no extensive support for making movies in SPM8 and Fieldtrip
as far as I know. However, there is quite a simple generic way in
Matlab to make movies from anything you can plot in a figure. Try

help getframe
help movie2avi

In the tool invoked by 'render' button in 3D Source Reconstruction
someone has already added these commands to the movie displaying code
there (see around line 582 of spm_eeg_inv_visu3D_api.m). So if you
write

global MOVIE

in the command line and then run a movie in this tool, you'll get a
movie stored in the variable MOVIE and then you can save it using
movie2avi.

For the movie that you can generate using the 'mip' button see the
code starting around line 96 of spm_eeg_invert_display.m. You can
modify it in a similar way.

One way to make a movie of scalp topographies via the GUI in SPM is to
export your sensor data to image, open the image using CheckReg
button, right click on it and choose 'Movie tool'. You can then scroll
through the Z axis which is basically what you want and save it as a
movie. If you want to use the plot from the reviewing tool, you'll
have to write your own bit of code using spm_eeg_plotScalpData.

Best,

Vladimir


On Sun, Feb 6, 2011 at 5:10 AM, Michael Spezio
<[log in to unmask]> wrote:
> Does anyone have experience with saving the movies that appear in the
> Graphics Window in SPM8's EEG analyses (e.g., the movie in EEG/MEG Source
> Localization)? Is there an easy way to save the scalp topographies in the
> Graphics Window (e.g., from Display --> M/EEG) as movies over time?
>
> Is this better accomplished in FieldTrip directly, or can this be done from
> within SPM8?
>
> Thanks for any guidance.
>
> Best,
>
> Michael
>
> Michael L. Spezio, Ph.D.
> Assistant Professor of Psychology
> Department of Psychology
> Scripps College
> Claremont, CA
> [log in to unmask]
> 909.607.0914
>
> and
>
> Visiting Associate Scientist
> Psychology & Neuroscience
> Division of Humanities & Social Sciences
> Caltech
> Pasadena, CA 91125
> [log in to unmask]
>


--
Carsten Stahlhut
Section for Cognitive Systems
Department of Informatics and Mathematical Modelling

Richard Petersens Plads, Building 321
Technical University of Denmark
DK-2800 Kongens Lyngby, Denmark
--20cf3054a36dd4bf2f049bb60e55-- ========================================================================Date: Mon, 7 Feb 2011 19:34:36 +0000 Reply-To: Sandro Shakushiya <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Sandro Shakushiya <[log in to unmask]> Subject: Error in "proportional Scaling" from Pet Study Mime-Version: 1.0 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain; charset="UTF-8" Message-ID: <[log in to unmask]> Hi When estimating the study is fine, to show the results SPM resturn this error ??? Error using ==> image Error using ==> image Image CData can not be complex. Error in ==> spm_conman at 975 hDesMtxIm = image((varargin{2}.nKX+1)*32); Error in ==> spm_conman at 944 spm_conman('ImDesMtx',xX,H. hDesMtxAx) %-Depict DesMtx Error in ==> spm_conman at 812 [F,cF] = spm_conman('Initialise','on',SPM,STATmode,n,Prompt,Mcstr,OK2chg); Error in ==> spm_getSPM at 267 [Ic,xCon] = spm_conman(SPM,'T&F',Inf,... Error in ==> spm_results_ui at 275 [SPM,xSPM] = spm_getSPM; ??? Error while evaluating uicontrol Callback. The Design of study was Paired t-test Independence: Yes Variance:Unequal Grand mean scaling: No ANCOVA:No Covariates:0 Masking Threshold Masking: Relative Threshold: 0.8 Implicit Mask: Yes Global Calculation: mean Global Normalization: Overall grand mean scaling:Yes Grand mean scaled value:50 Normalization: proportional Sandro S. Shakushiya University of São Paulo Ribeirão Preto School of Philosophy, Sciences and Literature - Department of Physics Medical Physics ========================================================================Date: Mon, 7 Feb 2011 20:03:35 +0000 Reply-To: John Ashburner <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: John Ashburner <[log in to unmask]> Subject: Re: non isotropic voxels for DARTEL anatomical template? Comments: To: kalina michalska <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> I don't think it would be so straightforward to get Dartel to handle non-isotropic voxel sizes. Usually, everything is done using isotropic voxels, so I really haven't looked into how well anisotropic voxels are handled. I suspect that there would be little or no benefit from having anisotropic voxels in the imported images anyway. Best regards, -John On 25 January 2011 21:31, kalina michalska <[log in to unmask]> wrote: > Dear SPM experts, > I would like to create an anatomical template using the DARTEL Toolbox in > SPM8. We have acquired 102 high resolution 3D T1 images in young and older > children. > I am completely new to using DARTEL. So far, I have used New Segment on each > T1 image and would like to generate a group template using the rc1 and rc2 > images from each subject. > My questions (so far!) are as follows: The voxel size of our T1 weighted > images is 1x.1x1.6mm^3.The SPM8 manual suggests that voxels should be > isotropic (p. 193, 26.1.4). Is it possible to create a template with > non-isotropic voxels or is in neccessary that they be isotropic? If so, is > there any way to make them isotropic in SPM in order to use this toolbox? Is > it okay to reslice the T1 images? > Many thanks in advance for your insights, > > Kalina > --------------------------------------------------- > Kalina J. Michalska, Ph.D. > > Postdoctoral scholar > Social Cognitive Neuroscience Lab > Department of Psychology > University of Chicago > > Phone: (773) 702-4661 > EMail: [log in to unmask] > Web: http://scnl.org > > ========================================================================Date: Mon, 7 Feb 2011 20:13:36 +0000 Reply-To: Avery Rizio <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Avery Rizio <[log in to unmask]> Subject: Using scaling Mime-Version: 1.0 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain; charset="UTF-8" Message-ID: <[log in to unmask]> I am currently scanning a project that includes an encoding and retrieval task, for both younger and older adults. I'm finding that in about half of my older adult subjects, basic trial type versus baseline contrasts show little to no activity during retrieval. Despite the fact that behavioral data indicates they are successfully performing the task, the imaging data reveals, in many cases, a complete lack of even visual activity. I've checked for several possible issues (including onset errors, or problems with the scanner), but to no avail. I reanalyzed a subject for whom there was no activity, this time with global scaling. With scaling, there was a minimal improvement, particularly with respect to visual activity. Everything that I've read has strongly advised against using scaling, but are there scenarios (such as this one) in which it acceptable? ========================================================================Date: Mon, 7 Feb 2011 20:25:47 +0000 Reply-To: "G. Sharvit" <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: "G. Sharvit" <[log in to unmask]> Subject: A problem with SPM and FIR modeling Mime-Version: 1.0 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain Message-ID: <[log in to unmask]> To the SPM experts, I am trying to set a 2nd-level factorial analysis based on contrast images taken from 1st-analysis FIR model. The software being used: SPM8 (version: 8.4010) and Matlab 7.11.0 (R2010b). In the 2nd-analysis model specification, I am using full factorial design with 2 factors: the first is 'experiment_conditions' composed of 3 levels [conditions A,B and C] and the second factor 'time_bins' composed of 32 levels [for each time bin I have]. After setting the correct order of the cells with the relevant con images from the 1st analysis I encountered a strange problem. When I first (mistakenly) set the two factors Independent value to 'Yes', the model specification batch ran and later I could estimate the model and continue the analysis. However later I realized that I need to change both my factors to be dependent so I switched the Independent value to 'No' for both factors and since this moment the model specification refuses to run. In the command window of Matlab I don't get any warnings but only the notification that the factorial design specification process is running - but this keeps forever [and there is not even generation of the SPM.mat file that I would expect in the desired folder]. Is there any solution to this strange problem? or maybe it is related to some lack of my understanding? I hope you can help me with this one, Thank you very much for your time in advance, Gil ========================================================================Date: Mon, 7 Feb 2011 20:51:38 +0000 Reply-To: Amir Tahmasebi <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Amir Tahmasebi <[log in to unmask]> Subject: POSTDOCTORAL POSITION - Neuroimaging and Brain Plasticity Mime-Version: 1.0 Content-Type: multipart/mixed; boundary="part-LiZWzTlDWILBAyw1ZNVmY89w4C3iG6ZWd5QknrWA8bCBN" Message-ID: <[log in to unmask]> --part-LiZWzTlDWILBAyw1ZNVmY89w4C3iG6ZWd5QknrWA8bCBN Content-Type: multipart/alternative; boundary="part-U6JulmCEACvjpprFCVtiSU224FE1FhCJ2ALlfn2duACAG" This is a multi-part message in MIME format. --part-U6JulmCEACvjpprFCVtiSU224FE1FhCJ2ALlfn2duACAG Content-Transfer-Encoding: quoted-printable Content-Type: text/plain; charset="UTF-8" Please see the attached file. If interested, please submit your C.V. and relevant reprints, together with a cover letter describing current research interests and future research goals, and also arrange to have three letters of reference sent independently to: Dr. Sylvain Moreno Rotman Research Institute Baycrest 3560 Bathurst Street Toronto, Ontario, M6A 2E1, Canada E-mail: [log in to unmask] ________________________________ Amir M. Tahmasebi, Ph.D. Postdoctoral Research Fellow Rotman Research Institute, University of Toronto, Toronto, Ontario CANADA ________________________________ Tel: (416) 785-2500, ext. 3130 Web: www.cs.queensu.ca/~tahmaseb --part-U6JulmCEACvjpprFCVtiSU224FE1FhCJ2ALlfn2duACAG Content-Transfer-Encoding: quoted-printable Content-Type: text/html; charset="UTF-8" --part-U6JulmCEACvjpprFCVtiSU224FE1FhCJ2ALlfn2duACAG-- --part-LiZWzTlDWILBAyw1ZNVmY89w4C3iG6ZWd5QknrWA8bCBN Content-Transfer-Encoding: base64 Content-Type: APPLICATION/PDF; name="Postdoc Fellowship - ad.pdf" JVBERi0xLjUNJeLjz9MNCjUwIDAgb2JqDTw8L0xpbmVhcml6ZWQgMS9MIDI1NDk5L08gNTIv RSAxOTkwOC9OIDEvVCAyNTE5NC9IIFsgNDgzIDE3MF0+Pg1lbmRvYmoNICAgICAgICAgICAg ICAgICAgDQo2NSAwIG9iag08PC9EZWNvZGVQYXJtczw8L0NvbHVtbnMgNC9QcmVkaWN0b3Ig MTI+Pi9GaWx0ZXIvRmxhdGVEZWNvZGUvSURbPDdDM0RGQTI4RTAyMjc4NEE4OTg0RDFFNDlC NDY3MjVBPjw4ODZEMUU1RTUyRTU1MzQxOThCODBCNDBCOEE5NDlEMT5dL0luZGV4WzUwIDMz XS9JbmZvIDQ5IDAgUi9MZW5ndGggODAvUHJldiAyNTE5NS9Sb290IDUxIDAgUi9TaXplIDgz 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Schweren <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Lizanne Schweren <[log in to unmask]> Subject: VBM in large heterogeneous dataset Mime-Version: 1.0 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain; charset="UTF-8" Message-ID: <[log in to unmask]> Dear all, I am currently integrating structural MRI data from collaborating sites from a.o. Europe and Asia, in order to create a large (±1000 subjects) dataset for VBM analyses. I have some questions regarding how to deal with such large and (morphologically) heterogeneous datasets in SPM8. Does anyone have experience segmenting brains from Asian participants? In the 'new segment' module, one can choose to warp to European (default) or Asian (or other) brains. Would it be beneficial to segment the Asian brains seperately from the European ones, and than pool all data at a later stage (e.g. in the Dartel pipeline)? And would that not conflict with the tissue probability maps that are selected by default in SPM? Second question regards Dartel (create template). Would it be beneficial to increase the number of iterations for the template, as a way to deal with the heterogeneity in the dataset? Does anyone have experience and/or specific setting recommendations in dealing with such large and heterogeneous datasets? Thanks. Lizanne ========================================================================Date: Mon, 7 Feb 2011 21:36:33 +0000 Reply-To: Lin Wang <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Lin Wang <[log in to unmask]> Subject: Re: 'NaN' in cluster level p value Mime-Version: 1.0 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain; charset="UTF-8" Message-ID: <[log in to unmask]> Dear all, I got the same problem after running the 2nd-level statistical analysis. The cluster-level p values are NaNs, and I get the following warning when I click "whole brain" to show all the clusters: Warning: Returning NaN for out of range arguments > In spm_Pcdf at 88 In spm_P_RF at 106 In spm_P at 48 In spm_list at 487 I searched the documents, but I couldn't find a clear answer for it. Could anyone help me with it? Thanks very much. Best, Lin ========================================================================Date: Tue, 8 Feb 2011 03:07:15 +0000 Reply-To: "Stephen J. Fromm" <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: "Stephen J. Fromm" <[log in to unmask]> Subject: Re: A problem with SPM and FIR modeling Comments: To: "G. Sharvit" <[log in to unmask]> Mime-Version: 1.0 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain; charset="UTF-8" Message-ID: <[log in to unmask]> I think this might be similar to a problem I had once: https://www.jiscmail.ac.uk/cgi-bin/webadmin?A2=SPM;36d6a42e.0709 ========================================================================Date: Tue, 8 Feb 2011 08:29:16 +0000 Reply-To: Tuomas Tolvanen <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Tuomas Tolvanen <[log in to unmask]> Subject: Voxel's center Mime-Version: 1.0 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain; charset="UTF-8" Message-ID: <[log in to unmask]> In voxel world, is the voxel's center same as the voxel's index? I mean that if I have voxel index=[1 1 1], does that index refer to voxel's center or corner point? Same question to mm-world. When I extract mm co-ordinates with [b xyz] = spm_read_vols(a), does those mm co-ordinates refer to desired voxel's center or corner point? br, Tuomas ========================================================================Date: Tue, 8 Feb 2011 09:45:55 +0000 Reply-To: John Ashburner <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: John Ashburner <[log in to unmask]> Subject: Re: VBM in large heterogeneous dataset Comments: To: Lizanne Schweren <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> If you use New Segment, the initial affine registration should be much more robust, so the regularisation used (for penalising unlikely shears and zooms) will have less effect. The affine registration would probably work reasonably well if you use the same form of regularisation throughout (either European or East Asian, or even disabling the regularisation). Best regards, -John On 7 February 2011 21:11, Lizanne Schweren <[log in to unmask]> wrote: > Dear all, > > I am currently integrating structural MRI data from collaborating sites from a.o. Europe and Asia, in order to create a large (1000 subjects) dataset for VBM analyses. I have some questions regarding how to deal with such large and (morphologically) heterogeneous datasets in SPM8. > > Does anyone have experience segmenting brains from Asian participants? In the 'new segment' module, one can choose to warp to European (default) or Asian (or other) brains. Would it be beneficial to segment the Asian brains seperately from the European ones, and than pool all data at a later stage (e.g. in the Dartel pipeline)? And would that not conflict with the tissue probability maps that are selected by default in SPM? > > Second question regards Dartel (create template). Would it be beneficial to increase the number of iterations for the template, as a way to deal with the heterogeneity in the dataset? Does anyone have experience and/or specific setting recommendations in dealing with such large and heterogeneous datasets? > > Thanks. Lizanne > ========================================================================Date: Tue, 8 Feb 2011 11:29:01 +0100 Reply-To: =?iso-8859-1?Q?Andr_Schmidt?= <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: =?iso-8859-1?Q?Andr_Schmidt?= <[log in to unmask]> Subject: inverse reconstruction MIME-Version: 1.0 Content-Type: multipart/alternative; boundary="----=_NextPart_000_001E_01CBC783.62799710" Message-ID: <001d01cbc77b$00b52f10$021f8d30$@[log in to unmask]> This is a multi-part message in MIME format. ------=_NextPart_000_001E_01CBC783.62799710 Content-Type: text/plain; charset="iso-8859-1" Content-Transfer-Encoding: quoted-printable Dear all Id like to imaging my eeg data. After preprocessing and forward computation, I get some problems with the inverse reconstruction. If I chose imaging, all conditions (2:deviant, std 6) and standard, this error message appeared : ??? Error using ==> fprintf Function is not defined for sparse inputs. Error in ==> spm_eeg_invert at 514 fprintf('Percent variance explained %.2f (%.2f)\n',R2,R2*VE(i)) Error in ==> spm_eeg_invert_ui at 95 D = spm_eeg_invert(D); Error in ==> spm_eeg_inv_imag_api>Inverse_Callback at 94 handles.D = spm_eeg_invert_ui(handles.D); Error in ==> spm_eeg_inv_imag_api at 53 feval(varargin{:}); % FEVAL switchyard ??? Error using ==> pause Error while evaluating uicontrol Callback Does anybody know the problem? Should I better take the Custom model and if yes which model? Thanks for help andr ------=_NextPart_000_001E_01CBC783.62799710 Content-Type: text/html; charset="iso-8859-1" Content-Transfer-Encoding: quoted-printable

Dear all

 

I’d like to imaging my eeg data. After preprocessing and forward computation, I get some problems with the inverse reconstruction.

If I chose imaging, all conditions (2:deviant, std 6)“ and standard, this error message appeared :

 

??? Error using ==> fprintf

Function is not defined for sparse inputs.

 

Error in ==> spm_eeg_invert at 514

fprintf('Percent variance explained %.2f (%.2f)\n',R2,R2*VE(i))

 

Error in ==> spm_eeg_invert_ui at 95

D = spm_eeg_invert(D);

 

Error in ==> spm_eeg_inv_imag_api>Inverse_Callback at 94

handles.D = spm_eeg_invert_ui(handles.D);

 

Error in ==> spm_eeg_inv_imag_api at 53

feval(varargin{:}); % FEVAL switchyard

??? Error using ==> pause

Error while evaluating uicontrol Callback

 

Does anybody know the problem?

 

Should I better take the Custom model and if yes which model?

 

Thanks for help

andr

 

 

------=_NextPart_000_001E_01CBC783.62799710-- ========================================================================Date: Tue, 8 Feb 2011 10:36:52 +0000 Reply-To: Vladimir Litvak <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Vladimir Litvak <[log in to unmask]> Subject: Re: inverse reconstruction Comments: To: =?ISO-8859-1?Q?Andr_Schmidt?= <[log in to unmask]> In-Reply-To: <-3958352575239621134@unknownmsgid> MIME-Version: 1.0 Content-Type: text/plain; charset=windows-1252 Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> Dear Andre, This problem should be fixed in the latest SPM update. Please make sure you have the latest version. Best, Vladimir On Tue, Feb 8, 2011 at 10:29 AM, Andr Schmidt <[log in to unmask]> wrote: > Dear all > > > > Id like to imaging my eeg data. After preprocessing and forward > computation, I get some problems with the inverse reconstruction. > > If I chose imaging, all conditions (2:deviant, std 6) and standard, this > error message appeared: > > > > ??? Error using ==> fprintf > > Function is not defined for sparse inputs. > > > > Error in ==> spm_eeg_invert at 514 > > fprintf('Percent variance explained %.2f (%.2f)\n',R2,R2*VE(i)) > > > > Error in ==> spm_eeg_invert_ui at 95 > > D = spm_eeg_invert(D); > > > > Error in ==> spm_eeg_inv_imag_api>Inverse_Callback at 94 > > handles.D = spm_eeg_invert_ui(handles.D); > > > > Error in ==> spm_eeg_inv_imag_api at 53 > > feval(varargin{:}); % FEVAL switchyard > > ??? Error using ==> pause > > Error while evaluating uicontrol Callback > > > > Does anybody know the problem? > > > > Should I better take the Custom model and if yes which model? > > > > Thanks for help > > andr > > > > ========================================================================Date: Tue, 8 Feb 2011 11:38:06 +0100 Reply-To: =?iso-8859-1?Q?Andr_Schmidt?= <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: =?iso-8859-1?Q?Andr_Schmidt?= <[log in to unmask]> Subject: inverse reconstruction MIME-Version: 1.0 Content-Type: multipart/alternative; boundary="----=_NextPart_000_0027_01CBC784.A73E4E80" Message-ID: <002601cbc77c$4579e680$d06db380$@[log in to unmask]> This is a multi-part message in MIME format. ------=_NextPart_000_0027_01CBC784.A73E4E80 Content-Type: text/plain; charset="iso-8859-1" Content-Transfer-Encoding: quoted-printable Dear all Id like to imaging my eeg data. After preprocessing and forward computation, I get some problems with the inverse reconstruction. If I chose imaging, all conditions (2:deviant, std 6) and standard, this error message appeared : ??? Error using ==> fprintf Function is not defined for sparse inputs. Error in ==> spm_eeg_invert at 514 fprintf('Percent variance explained %.2f (%.2f)\n',R2,R2*VE(i)) Error in ==> spm_eeg_invert_ui at 95 D = spm_eeg_invert(D); Error in ==> spm_eeg_inv_imag_api>Inverse_Callback at 94 handles.D = spm_eeg_invert_ui(handles.D); Error in ==> spm_eeg_inv_imag_api at 53 feval(varargin{:}); % FEVAL switchyard ??? Error using ==> pause Error while evaluating uicontrol Callback Does anybody know the problem? Should I better take the Custom model and if yes which model? Thanks for help andr ------=_NextPart_000_0027_01CBC784.A73E4E80 Content-Type: text/html; charset="iso-8859-1" Content-Transfer-Encoding: quoted-printable

Dear all

 

I’d like to imaging my eeg data. After preprocessing and forward computation,  I get some problems with the inverse reconstruction.

If I chose imaging, all conditions (2:deviant, std 6)“ and standard, this error message appeared :

 

??? Error using ==> fprintf

Function is not defined for sparse inputs.

 

Error in ==> spm_eeg_invert at 514

    fprintf('Percent variance explained %.2f (%.2f)\n',R2,R2*VE(i))

 

Error in ==> spm_eeg_invert_ui at 95

        D                            = spm_eeg_invert(D);

 

Error in ==> spm_eeg_inv_imag_api>Inverse_Callback at 94

handles.D = spm_eeg_invert_ui(handles.D);

 

Error in ==> spm_eeg_inv_imag_api at 53

        feval(varargin{:}); % FEVAL switchyard

 

??? Error using ==> pause

Error while evaluating uicontrol Callback

 

Does anybody know the problem?

 

Should I better take the Custom model and if yes which model?

 

Thanks for help

andr

 

------=_NextPart_000_0027_01CBC784.A73E4E80-- ========================================================================Date: Tue, 8 Feb 2011 10:43:08 +0000 Reply-To: John Ashburner <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: John Ashburner <[log in to unmask]> Subject: Re: Voxel's center Comments: To: Tuomas Tolvanen <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> I think of the indices as referring to the centers of the voxels. After transforming into mm coordinates, the coordinates refer to the voxel centers. Best regards, -John On 8 February 2011 08:29, Tuomas Tolvanen <[log in to unmask]> wrote: > In voxel world, is the voxel's center same as the voxel's index? I mean that if I have voxel index=[1 1 1], does that index refer to voxel's center or corner point? Same question to mm-world. When I extract mm co-ordinates with [b xyz] = spm_read_vols(a), does those mm co-ordinates refer to desired voxel's center or corner point? > > br, > > Tuomas > ========================================================================Date: Tue, 8 Feb 2011 13:12:40 +0100 Reply-To: =?ISO-8859-1?Q?Wibeke_Nordhy?= <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: =?ISO-8859-1?Q?Wibeke_Nordhy?= <[log in to unmask]> Subject: Problem using the Fieldmaps module on GE data MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1; format=flowed Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> Hello SPM-users: We've been trying to calculate B0 maps based on dual gradient echo images from our GE Signa scanner. We used the GRE sequence, with a 128 acquisition matrix reconstructed to a 256 matrix, making Re and Im images for the two echo times (4.9 ms and 7.4 ms). Then we converted these to NIfTI using either MRIcro or SPM8 before running the Fieldmaps toolbox on them. After a while, the analysis will crash and produce the following errors: ??? Error using ==> mrdivide Matrix dimensions must agree. Error in ==> pm_smooth_phasemap at 49 pm = pm_smooth_phasemap_dtj(pm,1/angvar,krnl); Error in ==> pm_make_fieldmap at 201 fm.fpm = pm_smooth_phasemap(fm.upm.*fm.mask,angvar,pxs,flags.fwhm); Error in ==> FieldMap at 1623 IP.fm = pm_make_fieldmap([IP.P{1} IP.P{2} IP.P{3} IP.P{4}],IP.uflags); Error in ==> FieldMap at 699 status=FieldMap('CreateFieldMap',IP); ??? Error while evaluating uicontrol Callback It seems that the Fieldmaps tool is geared towards Siemens scanners; have anyone used it on images from a GE scanner with good results? Any tips or ideas for us? The first error message mentions matrix dimensions. Could our problem be the difference between the acquired and reconstructed matrices? Wibeke and ystein ========================================================================Date: Tue, 8 Feb 2011 13:14:22 +0100 Reply-To: Helmut Laufs <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Helmut Laufs <[log in to unmask]> Subject: limitations of DCM (fMRI) for subcortical regions? Content-Type: multipart/alternative; boundary="_42eda7d2-88a8-477f-a898-2fbf263ed496_" MIME-Version: 1.0 Message-ID: <[log in to unmask]> --_42eda7d2-88a8-477f-a898-2fbf263ed496_ Content-Type: text/plain; charset="iso-8859-1" Content-Transfer-Encoding: quoted-printable Dear fMRI-DCMers, is there any literature or less formal knowledge about the validity of DCM for fMRI when subcortical regions are involved? I am asking because of two things 1. empirical evidence (potentially due to ROI definition issues, see similar posting on this list [DARTEL-related]) 2. work by Caroline Malherbe on functional connectivity (via sICA): http://www.imt.liu.se/minew/Intern/Onlineproceedings/ISBI_2010/pdfs/0001169.pdf where she describes that - at least in the basal ganglia - subcortical ROI time courses are a mixture of signals some of which correlate with cortical ones but others to more regional activity. Any hints greatly appreciated. Thank you. Bw, Helmut --_42eda7d2-88a8-477f-a898-2fbf263ed496_ Content-Type: text/html; charset="iso-8859-1" Content-Transfer-Encoding: quoted-printable Dear fMRI-DCMers,

is there any literature or less formal knowledge about the validity of DCM for fMRI when subcortical regions are involved?

I am asking because of two things

1. empirical evidence (potentially due to ROI definition issues, see similar posting on this list [DARTEL-related])
2. work by Caroline Malherbe on functional connectivity (via sICA):
http://www.imt.liu.se/minew/Intern/Onlineproceedings/ISBI_2010/pdfs/0001169.pdf
where she describes that - at least in the basal ganglia - subcortical ROI time courses are a mixture of signals some of which correlate with cortical ones but others to more regional activity.

Any hints greatly appreciated.

Thank you.

Bw,

Helmut

--_42eda7d2-88a8-477f-a898-2fbf263ed496_-- ========================================================================Date: Tue, 8 Feb 2011 11:53:08 -0000 Reply-To: Lorelei Howard <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Lorelei Howard <[log in to unmask]> Subject: comparing men and women Comments: cc: [log in to unmask] MIME-Version: 1.0 Content-Type: text/plain;charset=iso-8859-1 Content-Transfer-Encoding: 8bit Message-ID: <[log in to unmask]> Hi everyone, I want to compare men and women in my experiment and am finding it difficult to track down any guidance on how to do this in SPM. Does anyone have any links to useful websites/papers/texts that I could use to work out how to set up this kind of comparison in SPM? I usually use scripts to run all of my analyses so it would be even better if someone had an example script they could pass on. Also, are there any issues I should be aware of when comparing male and female brains? For example, does the difference in head size between the two groups have any detrimental influences? I would be grateful of any help or advice. Many thanks, Lorelei -- Lorelei Howard Ph.D. Student Institute of Behavioural Neuroscience Cognitive, Perceptual and Brain Sciences Department University College London 26 Bedford Way WC1H 0AP +44 (0)20 7679 8553 ========================================================================Date: Tue, 8 Feb 2011 05:19:01 -0800 Reply-To: turki sabrah <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: turki sabrah <[log in to unmask]> Subject: Conjunction analysis MIME-Version: 1.0 Content-Type: multipart/alternative; boundary="0-1483646110-1297171141=:68903" Message-ID: <[log in to unmask]> --0-1483646110-1297171141=:68903 Content-Type: text/plain; charset=iso-8859-1 Content-Transfer-Encoding: quoted-printable Dear SPM users, I have conducted two experiments and I want to carry out conjunction analysisto look at activations that are common to all subjects in these studies. Any thoughts or suggestions about which approach should I go with and why ? fixed-effect or Random-effects approach (between two studies) ? Thanks in advance Turk --0-1483646110-1297171141=:68903 Content-Type: text/html; charset=iso-8859-1 Content-Transfer-Encoding: quoted-printable
Dear SPM users,
 
I have conducted two experiments and I want to carry out conjunction analysis to look at activations that are common to all subjects in these studies. Any thoughts or suggestions about which approach should I go with and why ? fixed-effect or Random-effects approach (between two studies) ?
 
Thanks in advance
 
Turk

--0-1483646110-1297171141=:68903-- ========================================================================Date: Tue, 8 Feb 2011 22:28:52 +0800 Reply-To: Anqi Qiu <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Anqi Qiu <[log in to unmask]> Subject: Postdoctoral Fellowship on infant neurocognitive and brain development using MRI, Eyetracking, and EEG MIME-Version: 1.0 Content-Type: multipart/alternative; boundaryMessage-ID: <[log in to unmask]> --001517573e02e20efb049bc62afc Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable * * *Job description:* National University of Singapore (NUS) is a leading global university centred in Asia. It offers a global approach to education and research, with a focus on Asian perspectives and expertise. Computation functional anatomy laboratory at NUS (http://www.bioeng.nus.edu.sg/cfa) focuses on brain and cognition studies using neuroimaging techniques. Our group is leading a large-scale healthy infant neuroimaging project in Singapore. The project examines neurocognition using EEG and eye trackers and brain development using diffusion tensor imaging (DTI), resting-state fMRI, and structural MRI. We are looking for a research fellow who is interested in multi-modal MRI studies in infants for understanding normal development of brain and cognition trajectory. We offer high salary with medical and other benefits. *Requirements:* Ph. D Research background on infant brain or child cognition is preferable but necessary Knowledge in statistical analysis is necessary Good communication and writing skills in English language If you are interested in the jobs listed below, please send your CV to Dr. Anqi QIU Division of Bioengineering National University of Singapore Email: [log in to unmask] Phone: +(65) 6516 7002 --001517573e02e20efb049bc62afc Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable

Job description:

National University of Singapore (NUS) is a leading global university centred in Asia. It offers a global approach to education and research, with a focus on Asian perspectives and expertise. Computation functional anatomy laboratory at NUS (http://www.bioeng.nus.edu.sg/cfa) focuses on brain and cognition studies using neuroimaging techniques. Our group is leading a large-scale healthy infant neuroimaging project in Singapore. The project examines neurocognition using EEG and eye trackers and brain development using diffusion tensor imaging (DTI), resting-state fMRI, and structural MRI. We are looking for a research fellow who is interested in multi-modal MRI studies in infants for understanding normal development of brain and cognition trajectory. We offer high salary with medical and other benefits.

Requirements:

Ph. D

Research background on infant brain or child cognition is preferable but necessary

Knowledge in statistical analysis is necessary

Good communication and writing skills in English language

If you are interested in the jobs listed below, please send your CV to

Dr. Anqi QIU

Division of Bioengineering

National University of Singapore

Email: [log in to unmask]

Phone: +(65) 6516 7002

--001517573e02e20efb049bc62afc-- ========================================================================Date: Tue, 8 Feb 2011 09:46:25 -0500 Reply-To: "MCLAREN, Donald" <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: "MCLAREN, Donald" <[log in to unmask]> Subject: Re: Conjunction analysis Comments: To: turki sabrah <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> There are potentially several options; however, based on your wording of the word "common", I'd recommend the following: (1) Threshold each subject and make a binary image for each (imcalc: i1>0); (2) Add up all the subjects in study 1 and threshold (imcalc: X>n, where n is the number of subjects; (3) Repeat for study 2; (4) Now add study 1 and study 2 (imcalc: i1+i2.*2) This will give you regions common in all subjects in study1, study2, and study 1 and 2 combined. ------- Global Conjunction and the Conjunction Null could also be used, but there intrepretations are different from what you explicitly asked for in your email. Best Regards, Donald McLaren ================= D.G. McLaren, Ph.D. Postdoctoral Research Fellow, GRECC, Bedford VA Research Fellow, Department of Neurology, Massachusetts General Hospital and Harvard Medical School Office: (773) 406-2464 ===================== This e-mail contains CONFIDENTIAL INFORMATION which may contain PROTECTED HEALTHCARE INFORMATION and may also be LEGALLY PRIVILEGED and which is intended only for the use of the individual or entity named above. If the reader of the e-mail is not the intended recipient or the employee or agent responsible for delivering it to the intended recipient, you are hereby notified that you are in possession of confidential and privileged information. Any unauthorized use, disclosure, copying or the taking of any action in reliance on the contents of this information is strictly prohibited and may be unlawful. If you have received this e-mail unintentionally, please immediately notify the sender via telephone at (773) 406-2464 or email. On Tue, Feb 8, 2011 at 8:19 AM, turki sabrah <[log in to unmask]> wrote: > Dear SPM users, > > I have conducted two experiments and I want to carry out conjunction > analysisto look at activations that are common to all subjects in these > studies. Any thoughts or suggestions about which approach should I go with > and why ? fixed-effect or Random-effects approach (between two studies) ? > > Thanks in advance > > Turk > ========================================================================Date: Tue, 8 Feb 2011 09:46:25 -0500 Reply-To: "Watson, Christopher" <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: "Watson, Christopher" <[log in to unmask]> Subject: Re: limitations of DCM (fMRI) for subcortical regions? Comments: To: Helmut Laufs <[log in to unmask]> In-Reply-To: <[log in to unmask]> Content-Type: text/plain; charset="us-ascii" Content-Transfer-Encoding: quoted-printable MIME-Version: 1.0 Message-ID: <[log in to unmask]> This doesn't specifically discuss subcortical regions but is related to what you want: http://www.ncbi.nlm.nih.gov/pubmed/19961941 ________________________________________ From: SPM (Statistical Parametric Mapping) [[log in to unmask]] On Behalf Of Helmut Laufs [[log in to unmask]] Sent: Tuesday, February 08, 2011 7:14 AM To: [log in to unmask] Subject: [SPM] limitations of DCM (fMRI) for subcortical regions? Dear fMRI-DCMers, is there any literature or less formal knowledge about the validity of DCM for fMRI when subcortical regions are involved? I am asking because of two things 1. empirical evidence (potentially due to ROI definition issues, see similar posting on this list [DARTEL-related]) 2. work by Caroline Malherbe on functional connectivity (via sICA): http://www.imt.liu.se/minew/Intern/Onlineproceedings/ISBI_2010/pdfs/0001169.pdf where she describes that - at least in the basal ganglia - subcortical ROI time courses are a mixture of signals some of which correlate with cortical ones but others to more regional activity. Any hints greatly appreciated. Thank you. Bw, Helmut ========================================================================Date: Tue, 8 Feb 2011 10:08:19 -0500 Reply-To: "Watson, Christopher" <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: "Watson, Christopher" <[log in to unmask]> Subject: Re: comparing men and women Comments: To: Lorelei Howard <[log in to unmask]> In-Reply-To: <[log in to unmask]> Content-Type: text/plain; charset="us-ascii" Content-Transfer-Encoding: quoted-printable MIME-Version: 1.0 Message-ID: <[log in to unmask]> Are you doing fMRI? Why not just do a regular second-level analysis? RE: head size issues - I shouldn't think it makes much of a difference in fMRI analysis, but I'm sure a Pubmed or Google Scholar search of "gender covariates fmri" could help. ________________________________________ From: SPM (Statistical Parametric Mapping) [[log in to unmask]] On Behalf Of Lorelei Howard [[log in to unmask]] Sent: Tuesday, February 08, 2011 6:53 AM To: [log in to unmask] Subject: [SPM] comparing men and women Hi everyone, I want to compare men and women in my experiment and am finding it difficult to track down any guidance on how to do this in SPM. Does anyone have any links to useful websites/papers/texts that I could use to work out how to set up this kind of comparison in SPM? I usually use scripts to run all of my analyses so it would be even better if someone had an example script they could pass on. Also, are there any issues I should be aware of when comparing male and female brains? For example, does the difference in head size between the two groups have any detrimental influences? I would be grateful of any help or advice. Many thanks, Lorelei -- Lorelei Howard Ph.D. Student Institute of Behavioural Neuroscience Cognitive, Perceptual and Brain Sciences Department University College London 26 Bedford Way WC1H 0AP +44 (0)20 7679 8553 ========================================================================Date: Tue, 8 Feb 2011 16:46:05 +0200 Reply-To: Panagiotis Tsiatsis <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Panagiotis Tsiatsis <[log in to unmask]> Subject: Re: Warning in spm_eeg_convert2scalp (griddata) & spm_eeg_crop Comments: To: Vladimir Litvak <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1; format=flowed Content-Transfer-Encoding: 7bit Message-ID: <[log in to unmask]> Hello dear Vladimir and thanks for your response First of all, apologies in advance for the long e-mail; I hope that it will be at least a bit important for other users of SPM, too It seems that the problem appeared after I used spm_eeg_crop to drop my continuous CTF meg data file straight after reading it in and before applying filtering / downsampling. Without spm_eeg_crop everything works fine. [A small recap : As explained in a previous e-mail of mine, the logic behind this is that the start and the end of a continuous MEG files might be contaminated by artifacts (i.e due to subject's movement at the end of the session if she for whatever reason realized that the session is over and started moving before you press 'stop recording' ) or / and zero values because of padding added by the CTF software. All this should affect any subsequent filtering function if they are not removed (even the padding because of the sudden jump from values of order 10^-12 to zero!!!!) so I decided to crop the edges of my continuous file before continuing. ] I remember that when you send me the spm_eeg_crop file you told me that it has not been tested for continuous data but it should in principle work. I call it by using the following code : Time_Offset_in_ms = 3000; % in ms S = []; S.D = D; S.timewin = [(Time_of_First_Trial_Onset_in_ms - Time_Offset_in_ms) (Time_of_Last_Trial_Onset_in_ms + Time_Offset_in_ms)] S.freqwin = []; S.channels = 'all' D = spm_eeg_crop(S); D.save; The problem seems to appear in spm_eeg_crop when applied on a continuous file to and more specifically somewhere in the creation of the new object: Dnew = coor2D(Dnew, [], coor2D(D, chanind)); as some channels do indeed have the same coordinates : >> size(coor2D(D, chanind)') ans 337 2 >> size(unique(coor2D(D, chanind)','rows')) ans 335 2 The above number shows that spm_eeg_crop indeed puts in the coor2D matrix (or tries to put) the coordinates of all available channels. Up to now (and correct me if I am wrong) I knew that the coor2D matrix contains the coordinates of the MEGGRAD channels only. So I modified the code as follows : MEG_Channels = (D.meegchannels('MEG')); Dnew = coor2D(Dnew, [], coor2D(D, MEG_Channels)); *And indeed the conversion to images of subsequent files was executed without warnings*. So, is this a bug or am I going the wrong direction here? A couple more issues / clarifications : 1. The statistics at the end of the analysis (assuming all other equal) were slightly different depending on whether I cropped the start and the end of the continuous initial files that in many cases had large artifacts or zero values. I suppose this is because the subsequent filtering applied on the data was "smoother", in the sense that the filters did not have to compensate for the artifacts or the jumps because of the zero padding. Does this train of thought sound logical to you? 2.The cropped file (where only a few non-trial seconds from the start and from the and are missing) contains exactly the same number of events as the original continuous file. Why??? It seems that some zombie events are retained after cropping! 3. Please note that there appears to be one more problem with spm_eeg_crop and continuous data : The line Dnew = badchannels(Dnew, [], badchannels(D, chanind)); always results in an error when there are no bad channels, i.e. when isempty(D.badchannels) == 1. so i have substituted the above line with if isempty(D.badchannels) == 0 Dnew = badchannels(Dnew, [], badchannels(D, chanind)); end I suspect I should put an 'else' condition somewhere there, but of course you are the expert on this :) Thanks again and all the best, Panagiotis On 2/7/2011 8:10 PM, Vladimir Litvak wrote: > Dear Panagiotis, > > Try doing: > > spm_eeg_load > D.coor2D(D.meegchannels('MEG')) > > and look which of the channels have the same 2D coordinates. In > principle this should not happen for CTF MEG. You can also look in > 'Prepare' tool at the 2D channel layout an modify it if necessary or > load a template layout from EEGtemplates. > > Best, > > Vladimir > > On Sun, Feb 6, 2011 at 5:23 PM, Panagiotis Tsiatsis > <[log in to unmask]> wrote: >> Dear All, >> >> When I am converting my CTF MEG epoched data to images, I am getting the >> following warning: >> >> Warning: Duplicate x-y data points detected: using average of the z values. >>> In griddata at 107 >> In spm_eeg_convert2scalp at 204 >> >> My settings are: >> >> S = []; >> S.n = 32; >> S.Fname = Concatenated_File_Name_Time; >> S.interpolate_bad = 1; >> S.modality = 'MEG'; >> >> I also have EOG channels whose chantype has been set to 'EEG' during the >> conversion (this of course should not interfere since I ve selected my >> modality to be 'MEG'). >> >> By browsing the Mathwoks forum, I suspect that this happens when nearby >> values get very similar (as is the case with MEG data). >> >> Anybody seen that before? Any intuitions? >> >> Thanks and best, >> Panagiotis >> >> >> -- >> Panagiotis S. Tsiatsis >> Max Planck Institute for Biological Cybernetics >> Cognitive NeuroImaging Group >> Tuebingen, Germany >> -- Panagiotis S. Tsiatsis Max Planck Institute for Biological Cybernetics Cognitive NeuroImaging Group Tuebingen, Germany ========================================================================Date: Tue, 8 Feb 2011 11:28:50 -0500 Reply-To: David Kennedy <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: David Kennedy <[log in to unmask]> Subject: INCF Neuroinformatics Congress - Call for Abstracts MIME-Version: 1.0 Content-Type: multipart/alternative; boundary cf30433f10f7a3db049bc7d72c Message-ID: <[log in to unmask]> --20cf30433f10f7a3db049bc7d72c Content-Type: text/plain; charset=ISO-8859-1 The INCF Congress of Neuroinformatics will be held from September 4th to 6th at the Seaport Hotel in Boston, MA. They are currently collecting abstracts for poster presentations and computer demos. The annual INCF Neuroinformatics Congress provides a meeting place for researchers in all fields related to neuroinformatics, including data- and knowledge-bases of the nervous system from molecular to behavioral levels; tools for the acquisition, analysis, and visualization of nervous system data; and theoretical, computational, and simulation environments for modeling the brain. There is a current call for abstracts, deadline *April 19th, 2011*. *Submission Information:* The abstract format will be the same as in previous years, i.e. maximum one page (A4 or US letter). The abstract submission form allows for inclusion of one image and we encourage submitters to make use of this option. Accepted abstracts will be published online with Frontiers in Neuroscience and will receive a DOI (Digital Object Identifier). In order to submit an abstract, you need to visit INCF website and log in with your INCF account credentials. If you do not yet have an INCF account, please register at the INCF website before continuing. Submitted abstracts can be modified until the deadline - April 19th, 2011. To submit: http://www.neuroinformatics2011.org/abstracts * Registration Information:* All participants, including invited speakers, will be expected to cover their own expenses and registration fees. A range of housing options will be available. Registration Fees: USD Full fee early 525 Full fee late 740 Postdoc fee early 290 Postdoc fee late 460 Student fee early 155 Student fee late 250 *Early Registration closes on June 1st, 2011* *Important Dates** * Abstract submission February 4 - April 19, 2011* * Abstract decisions Mid May, 2011* * Early registration ends June 1, 2011* * Neuroinformatics 2011 Congress September 4-6, 2011 For more information, please visit http://www.neuroinformatics2011.org/ --20cf30433f10f7a3db049bc7d72c Content-Type: text/html; charset=ISO-8859-1 The INCF Congress of Neuroinformatics will be held from September 4th to 6th
at the Seaport Hotel in Boston, MA. They are currently collecting abstracts for
poster presentations and computer demos.

The annual INCF Neuroinformatics Congress provides a meeting place for
researchers in all fields related to neuroinformatics, including data- and
knowledge-bases of the nervous system from molecular to behavioral levels;
tools for the acquisition, analysis, and visualization of nervous system data; and
theoretical, computational, and simulation environments for modeling the
brain.


There is a current call for abstracts, deadline *April 19th, 2011*.

Submission Information: The abstract format will be the same as in previous
years, i.e. maximum one page (A4 or US letter). The abstract submission form
allows for inclusion of one image and we encourage submitters to make use of
this option. Accepted abstracts will be published online with Frontiers in
Neuroscience and will receive a DOI (Digital Object Identifier). In order to submit
an abstract, you need to visit INCF website and log in with your INCF account
credentials. If you do not yet have an INCF account, please register at the INCF
website before continuing. Submitted abstracts can be modified until the
deadline - April 19th, 2011.
To submit: http://www.neuroinformatics2011.org/abstracts

Registration Information:
All participants, including invited speakers, will be
expected to cover their own expenses and registration fees. A range of housing
options will be available.

Registration Fees:

USD
Full fee early
525
Full fee late
740
Postdoc fee early
290
Postdoc fee late
460
Student fee early
155
Student fee late
250
*Early Registration closes on June 1st, 2011*


Important Dates

Abstract submission
February 4 - April 19, 2011

Abstract decisions
Mid May, 2011

Early registration ends
June 1, 2011

Neuroinformatics 2011 Congress
September 4-6, 2011


For more information, please visit http://www.neuroinformatics2011.org/ --20cf30433f10f7a3db049bc7d72c-- ========================================================================Date: Tue, 8 Feb 2011 16:59:37 +0000 Reply-To: Soha Saleh <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Soha Saleh <[log in to unmask]> Subject: imcalc to do a contrast? Mime-Version: 1.0 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain; charset="UTF-8" Message-ID: <[log in to unmask]> Hi: I have 4 conditions in my experiment (A, B, C, D).. I am interested in finding the neuro activity that is higher in A than in B, and also the areas where the difference in activity between A and B, are higher than between C and D. Simply it is (A>B) - (C>D). I did each of the contrasts (A>B) and (C>D) in SPM8 and then used imcalc to subtract them to get (A>B)-(C>D). I got huge activity and T value that is very high which made me suspicious about this procedure. My questions are: Is this a valid procedure? Is there any precautions or limitations I need to be aware of? Thank you, I appreciate any assistance or advice you give. Kind regards, Soha ========================================================================Date: Tue, 8 Feb 2011 19:20:31 +0100 Reply-To: "CARLES M. FALCON FALCON" <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: "CARLES M. FALCON FALCON" <[log in to unmask]> Subject: Re: Problem using the Fieldmaps module on GE data Comments: To: Wibeke =?utf-8?b?Tm9yZGjDuHk=?= <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-version: 1.0 Content-disposition: inline Content-type: text/plain; charset=UTF-8; DelSp=Yes; format=flowed Content-transfer-encoding: quoted-printable Message-ID: <[log in to unmask]> Dear Wibeken, it could happen that voxel size of converted images was wrong due to using a different matrix for acquisition and reconstruction. Voxel size stored in dicom header could be, depending on the manufacturer, both the acquisition or the reconstruction one (one is half size the other in x and y axis). You could check if this is your problem with spm's DISPLAY tool. If brains look deformed, or the total brain size is too large (number of voxels multiplied by the voxel size), you could fix the problem by resizing your images by a factor 0.5 (probably just along x and y axis). Hope this helps Carles Wibeke Nordhøy <[log in to unmask]> ha escrit: > Hello SPM-users: > > We've been trying to calculate B0 maps based on dual gradient echo > images from our GE Signa scanner. We used the GRE sequence, with a > 128 acquisition matrix reconstructed to a 256 matrix, making Re and > Im images for the two echo times (4.9 ms and 7.4 ms). Then we > converted these to NIfTI using either MRIcro or SPM8 before running > the Fieldmaps toolbox on them. After a while, the analysis will > crash and produce the following errors: > > ??? Error using ==> mrdivide > Matrix dimensions must agree. > > Error in ==> pm_smooth_phasemap at 49 > pm = pm_smooth_phasemap_dtj(pm,1/angvar,krnl); > > Error in ==> pm_make_fieldmap at 201 > fm.fpm = pm_smooth_phasemap(fm.upm.*fm.mask,angvar,pxs,flags.fwhm); > > Error in ==> FieldMap at 1623 > IP.fm = pm_make_fieldmap([IP.P{1} IP.P{2} IP.P{3} > IP.P{4}],IP.uflags); > > Error in ==> FieldMap at 699 > status=FieldMap('CreateFieldMap',IP); > > ??? Error while evaluating uicontrol Callback > > It seems that the Fieldmaps tool is geared towards Siemens scanners; > have anyone used it on images from a GE scanner with good results? > Any tips or ideas for us? > > The first error message mentions matrix dimensions. Could our > problem be the difference between the acquired and reconstructed > matrices? > > Wibeke and Øystein > ========================================================================Date: Tue, 8 Feb 2011 10:29:21 -0800 Reply-To: Matthew Brett <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Matthew Brett <[log in to unmask]> Subject: Re: Question about ROI analysis in marsbar Comments: To: =?GB2312?Q?allen?= <[log in to unmask]> Comments: cc: [log in to unmask] In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=GB2312 Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> Hi, 2011/1/26 allen <[log in to unmask]>: > When we use Marsbar for a ROI and time course analysis, we usually use PSTH > value for time course analysis, however, there is also a "beta" value > option in the workshop, which each value represents for the beta value of > each parameter in the modeling matrix. > > My question is that, for a typical condition A (like the example I attach in > email), can I use this beta value to represent the mean activation of ROI? > If so, why the magnitude has so big difference compare to the PSTH value? Sorry to take so long to reply. I've Cc'ed the marsbar list - I think it's the one you want. Sorry if I'm being slow, but what exactly are you doing in the marsbar interface to get the PSTH and beta values in your workspace? Best, Matthew ========================================================================Date: Tue, 8 Feb 2011 13:52:48 -0500 Reply-To: Fred Sanders <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Fred Sanders <[log in to unmask]> Subject: ROI image dimensions - Marsbar MIME-Version: 1.0 Content-Type: multipart/alternative; boundaryMessage-ID: <[log in to unmask]> --000e0cd2e07ad4c051049bc9da32 Content-Type: text/plain; charset=ISO-8859-1 Hi All, I created ROI masks with Marsbar but the masks that I create all have the following image dimensions: 91x109x91. These dimensions match the image dimensions of the SPM template brains. Is there a way with Marsbar (or another script) to create ROI masks with different dimensions (say 151x188x154)? Or is there a way to easier convert the 91x109x91 images to 151x188x154? Thanks much!! Fred --000e0cd2e07ad4c051049bc9da32 Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Hi All,

I created ROI masks with Marsbar but the masks that I create all have the following image dimensions: 91x109x91. These dimensions match the image dimensions of the SPM template brains. Is there a way with Marsbar (or another script) tocreate ROI masks with different dimensions (say 151x188x154)? Or is there a way to easier convert the91x109x91 images to151x188x154?


Thanks much!!

Fred
--000e0cd2e07ad4c051049bc9da32-- ========================================================================Date: Tue, 8 Feb 2011 18:55:45 -0000 Reply-To: Lorelei Howard <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Lorelei Howard <[log in to unmask]> Subject: Re: comparing men and women Comments: To: "Watson, Christopher" <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain;charset=iso-8859-1 Content-Transfer-Encoding: 8bit Message-ID: <[log in to unmask]> Hi Chris, Thanks for the reply. Yes, I am doing fMRI. I am aware that I need to do a second level analysis... but I want to compare two groups at the second level, rather than simply running the standard second level analysis. Looking at previous papers and their methods sections has not really helped as they don't report the specifics of how to set this up in SPM. I can't find an example in the manual or any hints in the various help options and was hoping someone may give me a little more insight into how I may set it up. Thanks again, Lorelei > Are you doing fMRI? Why not just do a regular second-level analysis? > RE: head size issues - I shouldn't think it makes much of a difference in > fMRI analysis, but I'm sure a Pubmed or Google Scholar search of "gender > covariates fmri" could help. > > ________________________________________ > From: SPM (Statistical Parametric Mapping) [[log in to unmask]] On Behalf > Of Lorelei Howard [[log in to unmask]] > Sent: Tuesday, February 08, 2011 6:53 AM > To: [log in to unmask] > Subject: [SPM] comparing men and women > > Hi everyone, > > I want to compare men and women in my experiment and am finding it > difficult to track down any guidance on how to do this in SPM. > > Does anyone have any links to useful websites/papers/texts that I could > use to work out how to set up this kind of comparison in SPM? > > I usually use scripts to run all of my analyses so it would be even better > if someone had an example script they could pass on. > > Also, are there any issues I should be aware of when comparing male and > female brains? For example, does the difference in head size between the > two groups have any detrimental influences? > > I would be grateful of any help or advice. > > Many thanks, > Lorelei > > > -- > Lorelei Howard > > Ph.D. Student > > Institute of Behavioural Neuroscience > Cognitive, Perceptual and Brain Sciences Department > University College London > 26 Bedford Way > WC1H 0AP > +44 (0)20 7679 8553 > -- Lorelei Howard Ph.D. Student Institute of Behavioural Neuroscience Cognitive, Perceptual and Brain Sciences Department University College London 26 Bedford Way WC1H 0AP +44 (0)20 7679 8553 ========================================================================Date: Tue, 8 Feb 2011 14:03:34 -0500 Reply-To: Chris Watson <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Chris Watson <[log in to unmask]> Subject: Re: comparing men and women Comments: To: Lorelei Howard <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset="ISO-8859-1"; format=flowed Content-Transfer-Encoding: 7bit Message-ID: <[log in to unmask]> See Ch. 30 of the manual. Although, you'll want to do a 2-sample t-test, since you have two groups. Lorelei Howard wrote: > Hi Chris, > > Thanks for the reply. > > Yes, I am doing fMRI. > > I am aware that I need to do a second level analysis... but I want to > compare two groups at the second level, rather than simply running the > standard second level analysis. Looking at previous papers and their > methods sections has not really helped as they don't report the specifics > of how to set this up in SPM. I can't find an example in the manual or any > hints in the various help options and was hoping someone may give me a > little more insight into how I may set it up. > > Thanks again, > > Lorelei > > > >> Are you doing fMRI? Why not just do a regular second-level analysis? >> RE: head size issues - I shouldn't think it makes much of a difference in >> fMRI analysis, but I'm sure a Pubmed or Google Scholar search of "gender >> covariates fmri" could help. >> >> ________________________________________ >> From: SPM (Statistical Parametric Mapping) [[log in to unmask]] On Behalf >> Of Lorelei Howard [[log in to unmask]] >> Sent: Tuesday, February 08, 2011 6:53 AM >> To: [log in to unmask] >> Subject: [SPM] comparing men and women >> >> Hi everyone, >> >> I want to compare men and women in my experiment and am finding it >> difficult to track down any guidance on how to do this in SPM. >> >> Does anyone have any links to useful websites/papers/texts that I could >> use to work out how to set up this kind of comparison in SPM? >> >> I usually use scripts to run all of my analyses so it would be even better >> if someone had an example script they could pass on. >> >> Also, are there any issues I should be aware of when comparing male and >> female brains? For example, does the difference in head size between the >> two groups have any detrimental influences? >> >> I would be grateful of any help or advice. >> >> Many thanks, >> Lorelei >> >> >> -- >> Lorelei Howard >> >> Ph.D. Student >> >> Institute of Behavioural Neuroscience >> Cognitive, Perceptual and Brain Sciences Department >> University College London >> 26 Bedford Way >> WC1H 0AP >> +44 (0)20 7679 8553 >> >> > > > ========================================================================Date: Tue, 8 Feb 2011 19:21:45 -0000 Reply-To: Lorelei Howard <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Lorelei Howard <[log in to unmask]> Subject: Re: comparing men and women Comments: To: Chris Watson <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain;charset=iso-8859-1 Content-Transfer-Encoding: 8bit Message-ID: <[log in to unmask]> Brilliant... I had only used one-sample t-tests at the second level. Didn't even know you could change the design option to specify 2 sample t-tests etc as I hadn't been using the GUI. It makes much more sense now. Thanks again! Lorelei > See Ch. 30 of the manual. Although, you'll want to do a 2-sample t-test, > since you have two groups. > > Lorelei Howard wrote: >> Hi Chris, >> >> Thanks for the reply. >> >> Yes, I am doing fMRI. >> >> I am aware that I need to do a second level analysis... but I want to >> compare two groups at the second level, rather than simply running the >> standard second level analysis. Looking at previous papers and their >> methods sections has not really helped as they don't report the >> specifics >> of how to set this up in SPM. I can't find an example in the manual or >> any >> hints in the various help options and was hoping someone may give me a >> little more insight into how I may set it up. >> >> Thanks again, >> >> Lorelei >> >> >> >>> Are you doing fMRI? Why not just do a regular second-level analysis? >>> RE: head size issues - I shouldn't think it makes much of a difference >>> in >>> fMRI analysis, but I'm sure a Pubmed or Google Scholar search of >>> "gender >>> covariates fmri" could help. >>> >>> ________________________________________ >>> From: SPM (Statistical Parametric Mapping) [[log in to unmask]] On >>> Behalf >>> Of Lorelei Howard [[log in to unmask]] >>> Sent: Tuesday, February 08, 2011 6:53 AM >>> To: [log in to unmask] >>> Subject: [SPM] comparing men and women >>> >>> Hi everyone, >>> >>> I want to compare men and women in my experiment and am finding it >>> difficult to track down any guidance on how to do this in SPM. >>> >>> Does anyone have any links to useful websites/papers/texts that I could >>> use to work out how to set up this kind of comparison in SPM? >>> >>> I usually use scripts to run all of my analyses so it would be even >>> better >>> if someone had an example script they could pass on. >>> >>> Also, are there any issues I should be aware of when comparing male and >>> female brains? For example, does the difference in head size between >>> the >>> two groups have any detrimental influences? >>> >>> I would be grateful of any help or advice. >>> >>> Many thanks, >>> Lorelei >>> >>> >>> -- >>> Lorelei Howard >>> >>> Ph.D. Student >>> >>> Institute of Behavioural Neuroscience >>> Cognitive, Perceptual and Brain Sciences Department >>> University College London >>> 26 Bedford Way >>> WC1H 0AP >>> +44 (0)20 7679 8553 >>> >>> >> >> >> > -- Lorelei Howard Ph.D. Student Institute of Behavioural Neuroscience Cognitive, Perceptual and Brain Sciences Department University College London 26 Bedford Way WC1H 0AP +44 (0)20 7679 8553 ========================================================================Date: Tue, 8 Feb 2011 14:57:04 -0500 Reply-To: "MCLAREN, Donald" <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: "MCLAREN, Donald" <[log in to unmask]> Subject: Re: imcalc to do a contrast? Comments: To: Soha Saleh <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> Its unclear what was subtracted - single subject contrasts values or the the group level T-maps of A>B and C>D. You should not subtract T-maps nor use T-maps in second level or third level analysis. Only con images should be used. I wouldn't use imcalc as its more time consuming, but in theory will produce the same results. I'd use the contrast manager: A>B is 1 -1 0 0 (A>B) > (C>D) is 1 -1 -1 1 The enter the conimages into the second-level analysis. If D>C, then the contrast will show more than A>B. Best Regards, Donald McLaren ================= D.G. McLaren, Ph.D. Postdoctoral Research Fellow, GRECC, Bedford VA Research Fellow, Department of Neurology, Massachusetts General Hospital and Harvard Medical School Office: (773) 406-2464 ===================== This e-mail contains CONFIDENTIAL INFORMATION which may contain PROTECTED HEALTHCARE INFORMATION and may also be LEGALLY PRIVILEGED and which is intended only for the use of the individual or entity named above. If the reader of the e-mail is not the intended recipient or the employee or agent responsible for delivering it to the intended recipient, you are hereby notified that you are in possession of confidential and privileged information. Any unauthorized use, disclosure, copying or the taking of any action in reliance on the contents of this information is strictly prohibited and may be unlawful. If you have received this e-mail unintentionally, please immediately notify the sender via telephone at (773) 406-2464 or email. On Tue, Feb 8, 2011 at 11:59 AM, Soha Saleh <[log in to unmask]> wrote: > Hi: > > I have 4 conditions in my experiment (A, B, C, D).. I am interested in finding the neuro activity that is higher in A than in B, and also the areas where the difference in activity between A and B, are higher than between C and D. Simply it is (A>B) - (C>D). I did each of the contrasts (A>B) and (C>D) in SPM8 and then used imcalc to subtract them to get (A>B)-(C>D). I got huge activity and T value that is very high which made me suspicious about this procedure. > > My questions are: Is this a valid procedure? Is there any precautions or limitations I need to be aware of? > > Thank you, I appreciate any assistance or advice you give. > > Kind regards, > > Soha > ========================================================================Date: Tue, 8 Feb 2011 16:19:41 -0800 Reply-To: Matthew Brett <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Matthew Brett <[log in to unmask]> Subject: Re: ROI image dimensions - Marsbar Comments: To: Fred Sanders <[log in to unmask]> Comments: cc: [log in to unmask] In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> Hi, > I created ROI masks with Marsbar but the masks that I create all have the > following image dimensions: 91x109x91. These dimensions match the image > dimensions of the SPM template brains. Is there a way with Marsbar (or > another script) tocreate ROI masks with different dimensions (say > 151x188x154)? Or is there a way to easier convert the91x109x91 images > to151x188x154? You can set the default 'base space' for ROI images in the options menu, by choosing an image with the dimensions and voxel sizes that you want. Does that help? Best, Matthew ========================================================================Date: Wed, 9 Feb 2011 02:03:30 +0000 Reply-To: Richard Morris <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Richard Morris <[log in to unmask]> Subject: Re: SPM8 updates installing error in Mac Mime-Version: 1.0 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain; charset="UTF-8" Message-ID: <[log in to unmask]> I also installed the SPM8 4010 update on my mac (snow leopard 10.6.5) and get the same error when I try to run spm8 fmri. Is there a solution to this problem? Ta, Rich ========================================================================Date: Wed, 9 Feb 2011 00:14:26 -0200 Reply-To: Felipe Picon <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Felipe Picon <[log in to unmask]> Subject: Re: SPM8 updates installing error in Mac Comments: To: Richard Morris <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/alternative; boundaryMessage-ID: <[log in to unmask]> --0016364d2909048abf049bd008a9 Content-Type: text/plain; charset=ISO-8859-1 Hi Richard, I just received this possible solution (below), but I didn't tried it out yet. 1) reinstalled spm 8, using command line to unzip the folder rather than double clicking on the folder and using mac's archive utility to unzip. 2) re-set my path to only include matlab/spm8 not subfolders. 3) did not install the updates 4010 4) didn't keep spm in my matlab toolbox Hope this helps - Felipe Picon, MD Child and Adolescent Psychiatrist Master's Degree Student - Department of Psychiatry of Federal University of Rio Grande do Sul - UFRGS - www.ufrgs.br Adult ADHD outpatient research program - PRODAH-A - http://www6.ufrgs.br/prodah/prodah/equipe.html Hospital de Clinicas de Porto Alegre - HCPA - www.hcpa.ufrgs.br Member of the World Psychiatric Association (WPA) Early Career Psychiatrists Council Area Coordinator for the Americas - http://www.wpanet.org/detail.php?section_id"&content_id0 Web based CV: http://lattes.cnpq.br/3896757276389918 [log in to unmask] 2011/2/9 Richard Morris <[log in to unmask]> > I also installed the SPM8 4010 update on my mac (snow leopard 10.6.5) and > get the same error when I try to run spm8 fmri. Is there a solution to this > problem? > > Ta, > > Rich > - --0016364d2909048abf049bd008a9 Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable
Hi Richard,

I just received this possible solution (below), but I didn't tried it out yet.

1) reinstalled spm 8, using command line to unzip the folder rather than double clicking on the folder and using mac's archive utility to unzip.

2) re-set my path to only include matlab/spm8 not subfolders.

3) did not install the updates 4010

4) didn't keep spm in my matlab toolbox

Hope this helps

-
Felipe Picon, MD
Child and Adolescent Psychiatrist
Master's Degree Student - Department of Psychiatry of Federal University of Rio Grande do Sul - UFRGS - www.ufrgs.br
Adult ADHD outpatient research program - PRODAH-A - http://www6.ufrgs.br/prodah/prodah/equipe.html
Hospital de Clinicas de Porto Alegre - HCPA - www.hcpa.ufrgs.br
Member of the World Psychiatric Association (WPA) Early Career Psychiatrists Council
Area Coordinator for the Americas - http://www.wpanet.org/detail.php?section_id=22&content_id=120
Web based CV: http://lattes.cnpq.br/3896757276389918
[log in to unmask]

2011/2/9 Richard Morris <[log in to unmask]>
I also installed the SPM8 4010 update on my mac (snow leopard 10.6.5) and get the same error when I try to run spm8 fmri. Is there a solution to this problem?

Ta,

Rich



-
--0016364d2909048abf049bd008a9-- ========================================================================Date: Wed, 9 Feb 2011 04:44:52 +0000 Reply-To: Paul <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Paul <[log in to unmask]> Subject: Re: Non-Stationary correction in VBM 8 Comments: To: Christian Gaser <[log in to unmask]> Mime-Version: 1.0 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain Message-ID: <[log in to unmask]> Dear Christian Gaser Could you help me how to produce statistical table when using non-stationary correction function [located in "Threshold and transform spm-T maps" of newest VBM8 toolbox ] Best ========================================================================Date: Wed, 9 Feb 2011 17:05:53 +1100 Reply-To: Richard Morris <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Richard Morris <[log in to unmask]> Subject: Re: SPM8 updates installing error in Mac In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/alternative; boundary="----=_Part_149929_502318070.1297231553722" Message-ID: <[log in to unmask]> ------=_Part_149929_502318070.1297231553722 Content-Type: text/plain; charset=utf-8 Content-Transfer-Encoding: 7bit Word to the wise, regarding instructions to update SPM. If you use the Mac OS (e.g., Leopard or Snow Leopard), don't copy the update folders to your SPM directory as per Guillaume's instructions. Apple, in their divine wisdom, elected to instantiate a version of 'copy' which overwrites rather than merges common directories. So you will lose your original SPM files in any directories with a common name. I don't know what the best command to use to merge the files in terminal might be, but perhaps someone here does! Rich ----- Original Message ----- From: "Felipe Picon" <[log in to unmask]> To: "Richard Morris" <[log in to unmask]> Cc: [log in to unmask] Sent: Wednesday, 9 February, 2011 1:14:26 PM Subject: Re: [SPM] SPM8 updates installing error in Mac Hi Richard, I just received this possible solution (below), but I didn't tried it out yet. 1) reinstalled spm 8, using command line to unzip the folder rather than double clicking on the folder and using mac's archive utility to unzip. 2) re-set my path to only include matlab/spm8 not subfolders. 3) did not install the updates 4010 4) didn't keep spm in my matlab toolbox Hope this helps - Felipe Picon, MD Child and Adolescent Psychiatrist Master's Degree Student - Department of Psychiatry of Federal University of Rio Grande do Sul - UFRGS - www.ufrgs.br Adult ADHD outpatient research program - PRODAH-A - http://www6.ufrgs.br/prodah/prodah/equipe.html Hospital de Clinicas de Porto Alegre - HCPA - www.hcpa.ufrgs.br Member of the World Psychiatric Association (WPA) Early Career Psychiatrists Council Area Coordinator for the Americas - http://www.wpanet.org/detail.php?section_id"&content_id0 Web based CV: http://lattes.cnpq.br/3896757276389918 [log in to unmask] 2011/2/9 Richard Morris < [log in to unmask] > I also installed the SPM8 4010 update on my mac (snow leopard 10.6.5) and get the same error when I try to run spm8 fmri. Is there a solution to this problem? Ta, Rich - ------=_Part_149929_502318070.1297231553722 Content-Type: text/html; charset=utf-8 Content-Transfer-Encoding: quoted-printable
Word to the wise, regarding instructions to update SPM. If you use the Mac OS (e.g., Leopard or Snow Leopard), don't copy the update folders to your SPM directory as per Guillaume's instructions. Apple, in their divine wisdom, elected to instantiate a version of 'copy' which overwrites rather than merges common directories. So you will lose your original SPM files in any directories with a common name.

I don't know what the best command to use to merge the files in terminal might be, but perhaps someone here does!

Rich


From: "Felipe Picon" <[log in to unmask]>
To: "Richard Morris" <[log in to unmask]>
Cc: [log in to unmask]
Sent: Wednesday, 9 February, 2011 1:14:26 PM
Subject: Re: [SPM] SPM8 updates installing error in Mac

Hi Richard,

I just received this possible solution (below), but I didn't tried it out yet. 

1) reinstalled spm 8, using command line to unzip the folder rather than double clicking on the folder and using mac's archive utility to unzip.

2) re-set my path to only include matlab/spm8 not subfolders.

3) did not install the updates 4010

4) didn't keep spm in my matlab toolbox

Hope this helps


Felipe Picon, MD
Child and Adolescent Psychiatrist 
Master's Degree Student - Department of Psychiatry of Federal University of Rio Grande do Sul - UFRGS - www.ufrgs.br
Adult ADHD outpatient research program - PRODAH-A - http://www6.ufrgs.br/prodah/prodah/equipe.html
Hospital de Clinicas de Porto Alegre - HCPA - www.hcpa.ufrgs.br
Member of the World Psychiatric Association (WPA) Early Career Psychiatrists Council
Area Coordinator for the Americas - http://www.wpanet.org/detail.php?section_id=22&content_id=120
Web based CV: http://lattes.cnpq.br/3896757276389918
[log in to unmask]

2011/2/9 Richard Morris <[log in to unmask]>
I also installed the SPM8 4010 update on my mac (snow leopard 10.6.5) and get the same error when I try to run spm8 fmri. Is there a solution to this problem?

Ta,

Rich



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------=_Part_149929_502318070.1297231553722-- ========================================================================Date: Wed, 9 Feb 2011 01:10:11 -0500 Reply-To: "Robert L. Savoy" <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: "Robert L. Savoy" <[log in to unmask]> Subject: Hands-On SPM8 Training 2011Feb28 and 2011Mar07 in Boston; Future (New) Programs Content-Type: multipart/alternative; boundary=Apple-Mail-298--1050452246 Mime-Version: 1.0 (Apple Message framework v1081) Message-ID: <[log in to unmask]> --Apple-Mail-298--1050452246 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain; charset=windows-1252 Upcoming Courses in fMRI Experimental Design and Analysis This year we will be offering our continuing series of functional neuroimaging courses covering various conceptual and practical aspects of fMRI experimental design and analysis. In the SPM Basics and Network Analysis programs the laboratory exercises will focus on the use of SPM8, with extensive discussion of a variety of complementary software tools. Lectures and laboratory exercises will cover preprocessing, statistical modeling, visualization and anatomical labeling of data associated with a broad range of neuroimaging experimental designs. Please note that the SPM Basics and Network Analysis programs require that you bring a laptop with MATLAB installed. These courses are designed for investigators with a modest level of experience with functional MRI and basic statistics. The current schedule includes: SPM8 for Basic and Clinical Investigators - Boston, MA FEB 28 MAR 4, 2011 http://www.neurometrika.org/BasicSPM Network Analysis - Boston, MA MAR 7 MAR 11, 2011 http://www.neurometrika.org/NetworkAnalysis SPM8 for Basic and Clinical Investigators Baltimore, MD MAR 14 MAR 18, 2011 http://neurometrika.org/SPM_Basics_Baltimore SPM8 for Basic and Clinical Investigators Guangzhou, P.R. China JUL 11 JUL 15, 2011 http://www.neurometrika.org/BasicSPM *NEW OFFERING* Functional MRI in Clinical Research and Practice is a novel new course designed to give clinical investigators an intensive introduction to the issues associated with using structural and functional MRI in clinical research studies. The lectures have been specifically designed to help medically trained investigators with an interest in neuroimaging make the sometimes difficult transition from clinical training to medical research. Topics will include the basic principles of MRI measurement, techniques for stimulus presentation and response recording in high magnetic fields, basic statistical methods, individual subject experimental design and analysis techniques, group design and analysis techniques, clinical study design principles and guidelines for reporting clinical neuroimaging studies. As functional neuroimaging is enjoying an expanding role in clinical practice, coverage of current and future applications will be explored. The interactive portion of this course will include opportunities for participants to work in small groups to explore measurement, design and analysis issues associated with the use of neuroimaging as an endpoint in clinical research. Course materials will include guidance and material to facilitate subsequent self-study. Functional MRI in Clinical Research and Practice - Pittsburgh, PA JUN 13 JUN 17, 2011 http://neurometrika.org/fMRI_Clinical A complete listing of all the 2011 courses can be found at: http://www.neurometrika.org/Courses Please feel free to forward this announcement to any colleagues you think might be interested. --Apple-Mail-298--1050452246 Content-Transfer-Encoding: quoted-printable Content-Type: text/html; charset=windows-1252
Upcoming Courses in fMRI Experimental Design and Analysis

This year we will be offering our continuing series of functional
neuroimaging courses covering various conceptual and practical
aspects of fMRI experimental design and analysis.  In the SPM Basics
and Network Analysis programs the laboratory exercises will focus on
the use of SPM8, with extensive discussion of a variety of
complementary software tools. Lectures and laboratory exercises will
cover preprocessing, statistical modeling, visualization and
anatomical labeling of data associated with a broad range of
neuroimaging experimental designs. Please note that the SPM Basics
and Network Analysis programs require that you bring a laptop with
MATLAB installed. These courses are designed for investigators with
a modest level of experience with functional MRI and basic
statistics.  The current schedule includes:

SPM8 for Basic and Clinical Investigators - Boston, MA
FEB 28 MAR 4, 2011
http://www.neurometrika.org/BasicSPM

Network Analysis - Boston, MA
MAR 7 MAR 11, 2011
http://www.neurometrika.org/NetworkAnalysis

SPM8 for Basic and Clinical Investigators Baltimore, MD
MAR 14 MAR 18, 2011
http://neurometrika.org/SPM_Basics_Baltimore

SPM8 for Basic and Clinical Investigators Guangzhou, P.R. China
JUL 11 JUL 15, 2011
http://www.neurometrika.org/BasicSPM

*NEW OFFERING*

Functional MRI in Clinical Research and Practice is a novel new
course designed to give clinical investigators an intensive
introduction to the issues associated with using structural and
functional MRI in clinical research studies. The lectures have been
specifically designed to help medically trained investigators with
an interest in neuroimaging make the sometimes difficult transition
from clinical training to medical research. Topics will include the
basic principles of MRI measurement, techniques for stimulus
presentation and response recording in high magnetic fields, basic
statistical methods, individual subject experimental design and
analysis techniques, group design and analysis techniques, clinical
study design principles and guidelines for reporting clinical
neuroimaging studies. As functional neuroimaging is enjoying an
expanding role in clinical practice, coverage of current and future
applications will be explored. The interactive portion of this
course will include opportunities for participants to work in small
groups to explore measurement, design and analysis issues associated
with the use of neuroimaging as an endpoint in clinical research.
Course materials will include guidance and material to facilitate
subsequent self-study.

Functional MRI in Clinical Research and Practice - Pittsburgh, PA
JUN 13 JUN 17, 2011
http://neurometrika.org/fMRI_Clinical

A complete listing of all the 2011 courses can be found at: 
http://www.neurometrika.org/Courses
Please feel free to forward this announcement to any colleagues you
think might be interested.



--Apple-Mail-298--1050452246-- ========================================================================Date: Wed, 9 Feb 2011 10:37:44 +0100 Reply-To: Martin Jensen Dietz <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Martin Jensen Dietz <[log in to unmask]> Subject: Re: imcalc to do a contrast? Comments: To: Soha Saleh <[log in to unmask]> In-Reply-To: <[log in to unmask]> Content-Type: text/plain; charset="us-ascii" Content-Transfer-Encoding: quoted-printable MIME-Version: 1.0 Message-ID: <[log in to unmask]> Hi Soha, As an alternative to taking to the con images from a [1 -1 -1 1] contrast to a one-sample t-test, you could take your (A>B) and (C>D) con images to a paired t-test at the second level. This may seem more transparent to you. Best wishes, Martin ________________________________________ From: SPM (Statistical Parametric Mapping) [[log in to unmask]] On Behalf Of Soha Saleh [[log in to unmask]] Sent: 08 February 2011 17:59 To: [log in to unmask] Subject: [SPM] imcalc to do a contrast? Hi: I have 4 conditions in my experiment (A, B, C, D).. I am interested in finding the neuro activity that is higher in A than in B, and also the areas where the difference in activity between A and B, are higher than between C and D. Simply it is (A>B) - (C>D). I did each of the contrasts (A>B) and (C>D) in SPM8 and then used imcalc to subtract them to get (A>B)-(C>D). I got huge activity and T value that is very high which made me suspicious about this procedure. My questions are: Is this a valid procedure? Is there any precautions or limitations I need to be aware of? Thank you, I appreciate any assistance or advice you give. Kind regards, Soha ========================================================================Date: Wed, 9 Feb 2011 14:16:17 +0000 Reply-To: Tatiana Usnich <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Tatiana Usnich <[log in to unmask]> Subject: Re: Question regarding the fMRI model specification Mime-Version: 1.0 Content-Type: multipart/mixed; boundary="part-sjdkecA9iT1QtS5ApCABsAQynPWOAUQ3r2vaAA1LdSvSh" Message-ID: <[log in to unmask]> --part-sjdkecA9iT1QtS5ApCABsAQynPWOAUQ3r2vaAA1LdSvSh Content-Type: multipart/mixed; boundary="part-CauArZiIs945AXavGX1D6AdtUETknsDjOrnFmeySjA5M6" This is a multi-part message in MIME format. --part-CauArZiIs945AXavGX1D6AdtUETknsDjOrnFmeySjA5M6 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain; charset="UTF-8" Dear SPMlers, We also have the same problem. Starting to run fMRI model specification in SPM8 we are asked for a vector of onsets for one of the conditions and durations even though the conditions are specified in a .mat file. Conditions file is attached. Id really appreciate your help. Tatiana --part-CauArZiIs945AXavGX1D6AdtUETknsDjOrnFmeySjA5M6-- --part-sjdkecA9iT1QtS5ApCABsAQynPWOAUQ3r2vaAA1LdSvSh Content-Transfer-Encoding: base64 Content-Type: APPLICATION/OCTET-STREAM; name="conditions.mat" TUFUTEFCIDUuMCBNQVQtZmlsZSwgUGxhdGZvcm06IFBDV0lOLCBDcmVhdGVkIG9uOiBNb24g SnVuIDA4IDE1OjEyOjQ2IDIwMDkgICAgICAgICAgICAgICAgICAgICAgICAgICAgICAgICAg ICAgICAgICAgICAgICAgIAABSU0PAAAAjQAAAHic42NgYJBgYmBgA9IcQMzIAAGsSHx2KA0S y0vMTS0G0nxAbMGA0MeCRR+yeQJQfnFqTlp8bmouSL8DAf2caPo5YfrzgAZAxck1Jw/mEBLM 4UIzhwtuDsJBxIQLK5o5IH5qUVF+EZHu4EXTD+LnpKaVxBelFhfkA11EpDl8aOaA+EWZ6RnI BgEAet8ivw8AAABFAAAAeJzjY2BgOMDIwMAGpDmAGMgEA1YkPjuU5gTilNKixJLM/LxiqDo+ IDZgQOhnw6KfEclcJiCLZVQfVn3khicIAAAvygeuDwAAAPoDAAB4nJ1TC0yTVxj9K20RVEBW GU8R49yc4oYBhvjggLyciFAr8hqjQHlIgUJbWlpa+gB84kAmsoempup4JCRmJBsbiyhjjA0I ghnTLWOAzgGbA4OCA3H3p0tmmmUku8mX+8i95/vOd861oSgqk0VRbDIvJ8GgTIP13N7y75m+ k5crFkjEFGVD1nLqn3fsf3ln9RwevQ4nIR60fxjokoXmK0Wdm7h5WLls81GHahH8Zm+kNZzK x97zmo03aiWYdyQ3S+Rwoh8YFMAL/PaBfi2co++4zHfoQeePXSI/yyz/KyTs+oK/n/R2x8rq el30rQKUxQ+0jhqLkbgucGr0ugaKy1v2fCjQLuL7LYHPMMOnz2tz7fVtTeL/XR+1v3TVgZlg dJeEX1NVxSPFLnZ7c0Q2xpneq32bZTg2/cOgNq5oEb9vCXyOGb6BxCJO4na0JRDC7RHYeJBl PFPOBbPjHS/ZWAwUsXU+PbIkpM/c5V+M5COq4lyuvUUqWirYkw48AWwVvo27wzLwVY635pN1 OQgreGI7dlEKv+86cry/KQSRp5ivVOJqVPb7svMqdD/oag86qgZ9vM1QgtCXpMucQzSg287J 0MFCvmJD3YTO5INok65tjP/mtc2MVyXZbDj3rFKt9ETpaxFXrGsCcLDG47S0Igpz/qLeY4U8 Ex9uLNp+u7BzCycOLdlWTwxrktHFu153iZmCuW9JoV+nIvVBfNBu63QYz/gz9qenY9IhPGp+ JAtT02/GlW89At1IZ+3n4zngkbb5++Qi4HDC1Wu2IrQPbBY47RKBZOv/6XY++PTBigLcd/vo 1/B4sYlviAS80csffDkuQXHfx3GP3KQQyonjlheibCL607U+hei6F3BpyE2G+Ectd05EyCCt dmTGdMvRn/e2ZS+zCH+qj7RKxhVwYsbYeHooYeVyIWlTjxLDCk5T2FMlJkZ8ndssVHiY2v3W vlkVKg2zXr8Mq7EgmLk7zNCgc98bxwOdNDhEaEcWaBBXTpQb0yD03cfsoVNa07+b10JP+niC o1v8do2ndfhxUCsOrdfh7C2rzPWuergSOQ956bGW0Gsq1yNtx9CBVb/rEZR8r289u3RRR7sl dHQ10/FnEsFZeZNl772OaWGMqskmEOW0QJJwEFfuiKzaixeJHI4WUdj5BbfGYyEBOtq4M4mg 7XM7KRnWg0bRrrQUqAJ8kj5bkwZ3WlBOJmh7ex7OREMyj/syR2jypbvQ1J8UIXq6ybDOxzOP p4+lW8XodSJOdpYg8mZV4gIlh5tfRnBWkByVBMajoQg+f/iFhI0U4f5c/VT/qyqwtWf3nPRW I50eliXINTJaWSc1cKCNxdKCVH9zdaMWfwG+LK+K --part-sjdkecA9iT1QtS5ApCABsAQynPWOAUQ3r2vaAA1LdSvSh-- ========================================================================Date: Wed, 9 Feb 2011 10:20:06 -0500 Reply-To: "MCLAREN, Donald" <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: "MCLAREN, Donald" <[log in to unmask]> Subject: Re: Question regarding the fMRI model specification Comments: To: Tatiana Usnich <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Message-ID: <[log in to unmask]> (1) You probably have less data than time in your conditions.mat (this would make it appear that no events and it might ask for conditions; how did you specify the time in the design and how many time points are in each run? (2) Have you updated SPM with the latest updates? I just used your condition.mat file with some random files and it created a design without a problem. Best Regards, Donald McLaren ================D.G. McLaren, Ph.D. Postdoctoral Research Fellow, GRECC, Bedford VA Research Fellow, Department of Neurology, Massachusetts General Hospital and Harvard Medical School Office: (773) 406-2464 ====================This e-mail contains CONFIDENTIAL INFORMATION which may contain PROTECTED HEALTHCARE INFORMATION and may also be LEGALLY PRIVILEGED and which is intended only for the use of the individual or entity named above. If the reader of the e-mail is not the intended recipient or the employee or agent responsible for delivering it to the intended recipient, you are hereby notified that you are in possession of confidential and privileged information. Any unauthorized use, disclosure, copying or the taking of any action in reliance on the contents of this information is strictly prohibited and may be unlawful. If you have received this e-mail unintentionally, please immediately notify the sender via telephone at (773) 406-2464 or email. On Wed, Feb 9, 2011 at 9:16 AM, Tatiana Usnich <[log in to unmask]> wrote: > Dear SPMlers, > > We also have the same problem. Starting to run fMRI model specification in SPM8 we are asked for a vector of onsets for one of the conditions and durations even though the conditions are specified in a .mat file. > > Conditions file is attached. Id really appreciate your help. > > Tatiana > ========================================================================Date: Wed, 9 Feb 2011 16:53:43 +0000 Reply-To: Scott Hayes <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Scott Hayes <[log in to unmask]> Subject: Research Assistant and Postdoctoral Fellowship Positions at VA Boston Mime-Version: 1.0 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain; charset="UTF-8" Message-ID: <[log in to unmask]> We anticipate an opening for a full-time research assistant to begin in June, 2011. We are seeking applicants with previous experiences with behavioral testing and neuroimaging. The RA will assist with two primary projects, one focusing on aging and memory, and the other focusing on the elucidation of neural correlates of Posttraumatic Stress Disorder and Traumatic Brain Injury. Mieke Verfaellie and David Salat also have an opening for a postdoctoral fellow examining the neural correlates of blast-induced TBI. Additional details for both positions are available here: http://www.bu.edu/brainlab/job-openings/ ========================================================================Date: Wed, 9 Feb 2011 17:13:52 +0000 Reply-To: Scott Hayes <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Scott Hayes <[log in to unmask]> Subject: Re: Research Assistant and Postdoctoral Fellowship Positions at VA Boston Mime-Version: 1.0 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain; charset="UTF-8" Message-ID: <[log in to unmask]> Full description of RA position: Preliminary Announcement for Neuroimaging Research Assistant Position National Center for Posttraumatic Stress Disorder (Boston) The Behavioral Science Division of the National Center for PTSD, located at the VA Boston Healthcare System, anticipates an opening for a research assistant who will work on projects related to neuroimaging of posttraumatic stress disorder and memory disorders. Responsibilities for this position include: Collecting behavioral and neuroimaging data from healthy and clinical subjects, entering data and managing databases, performing statistical analyses, and assisting in the preparation of grants, manuscripts, and professional presentations. Applicants should have a B.A./B.S. (concentration in Cognitive Neuroscience/Psychology is preferred), experience working in an imaging laboratory and running functional magnetic resonance imaging (fMRI) experiments, proficiency with UNIX and MATLAB, FSL, and/or SPM, and the maturity and interpersonal sensitivity necessary for working in a clinical setting. Openings are expected for June 2011. Salary and benefits are highly competitive with similar positions at institutions in the Boston area. A two year commitment typically is required. Official job postings and formal application instructions are expected to appear in early March 2011, but potential candidates are encouraged to submit the following materials prior to formal application: 1) a letter describing their interest in a position and related career goals, 2) a resume, 3) a current transcript, and 4) at least two letters of recommendation. Materials can be sent electronically or by mail to: Andrea Carney National Center for PTSD (116B-2) VA Boston Healthcare System 150 South Huntington Ave. Boston, MA 02130-4817 [log in to unmask] Further information can be obtained via e-mail or by phone at (857) 364-4143, or visit the websites: http://www.bu.edu/traumamemorylab/ http://www.bu.edu/brainlab/ ========================================================================Date: Wed, 9 Feb 2011 17:54:43 +0000 Reply-To: Cyril Pernet <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Cyril Pernet <[log in to unmask]> Subject: spm_preproc In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1; format=flowed Content-Transfer-Encoding: 7bit Content-Disposition: inline Message-ID: <[log in to unmask]> Dear SPMers, John silly question to get my transformation matrices after segmenting ... once I run spm_prep2sn, what function shall I call to write down on the disk the transformation matrices - couldn't find out .. cheers cyril -- The University of Edinburgh is a charitable body, registered in Scotland, with registration number SC005336. ========================================================================Date: Wed, 9 Feb 2011 18:10:44 +0000 Reply-To: Mohamed Seghier <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Mohamed Seghier <[log in to unmask]> Subject: Re: spm_preproc Comments: To: Cyril Pernet <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1; format=flowed Content-Transfer-Encoding: 7bit Message-ID: <[log in to unmask]> Hi Cyril, Let's say R = spm_preproc('your anatomical image'); just run PO = spm_prep2sn(R) ; and then, all the variables that you need are: VG = PO.VG ; VF = PO.VF ; Tr = PO.Tr ; Affine = PO.Affine ; flags = PO.flags ; You can save them as an '*_seg_sn.mat' if your wish... I hope this helps, Mohamed On 09/02/2011 17:54, Cyril Pernet wrote: > Dear SPMers, John > > silly question to get my transformation matrices after segmenting ... > once I run spm_prep2sn, what function shall I call to write down on > the disk the transformation matrices - couldn't find out .. > > cheers > cyril > > > ========================================================================Date: Wed, 9 Feb 2011 11:41:10 -0800 Reply-To: kambiz rakhshan <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: kambiz rakhshan <[log in to unmask]> Subject: Vbm8 MIME-Version: 1.0 Content-Type: multipart/alternative; boundary="0-1928328450-1297280470=:17947" Message-ID: <[log in to unmask]> --0-1928328450-1297280470=:17947 Content-Type: text/plain; charset=us-ascii Dear experts, I have done a vbm analysis on 100 subjects with age range between 25-80. I used vbm8 toolbox and modulated non-linear only option to modulate the normalizad data. My specific question was to find relative volumetric loss that were not induced by total gray matter. I have two question now: 1-should one include TIV as a covariate while using non-linear modulate option? 2- in my analysis, i didn't include TIV as cov but instead age as a cov variable. Negative correlation with age reflects almost whole the brain with a very strong t value( P<0.0001,FWE).what could be the reason for that? I basically used all the default options for preprocessing. Additionally,i have removed all the potential outliers that seem to have an artifact. Any comment will be highly appreciate. Best. Kami --0-1928328450-1297280470=:17947 Content-Type: text/html; charset=us-ascii
Dear experts, I have done a vbm analysis on 100 subjects with age range between 25-80. I used vbm8 toolbox and modulated non-linear only option to modulate the normalizad data. My specific question was to find relative volumetric loss that were not induced by total gray matter. I have two question now: 1-should one include TIV as a covariate while using non-linear modulate option? 2- in my analysis, i didn't include TIV as cov but instead age as a cov variable. Negative correlation with age reflects almost whole the brain with a very strong t value( P<0.0001,FWE).what could be the reason for that? I basically used all the default options for preprocessing. Additionally,i have removed all the potential outliers that seem to have an artifact. Any comment will be highly appreciate. Best. Kami

--0-1928328450-1297280470=:17947-- ========================================================================Date: Wed, 9 Feb 2011 16:34:28 -0500 Reply-To: justine dupont <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: justine dupont <[log in to unmask]> Subject: Re: non isotropic voxels for DARTEL anatomical template? Content-Type: multipart/alternative; boundary="_350ede90-50ed-41d4-8d62-165044775448_" MIME-Version: 1.0 Message-ID: <[log in to unmask]> --_350ede90-50ed-41d4-8d62-165044775448_ Content-Type: text/plain; charset="iso-8859-1" Content-Transfer-Encoding: quoted-printable Dear John and other experts I have inherited a nice T1 dataset but the voxels are anisotropic (-0.97 x 0.97 x 1). I want to do a VBM study using these data, however according to a very recent post by John on the list, DARTEL is not appropriate for anisotropic voxels. So my question is... is it OK to use traditional VBM method (i.e. not using DARTEL) for such data? thank you very much :) Justine --_350ede90-50ed-41d4-8d62-165044775448_ Content-Type: text/html; charset="iso-8859-1" Content-Transfer-Encoding: quoted-printable Dear John and other experts 

I have inherited a nice T1 dataset but the voxels are anisotropic (-0.97 x 0.97 x 1).  I want to do a VBM study using these data, however according to a very recent post by John on the list, DARTEL is not appropriate for anisotropic voxels.  So my question is... is it OK to use traditional VBM method (i.e. not using DARTEL) for such data?

thank you very much :)

Justine


--_350ede90-50ed-41d4-8d62-165044775448_-- ========================================================================Date: Wed, 9 Feb 2011 17:37:58 -0500 Reply-To: =?ISO-8859-1?Q?Vronique_Paradis?= <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: =?ISO-8859-1?Q?Vronique_Paradis?= <[log in to unmask]> Subject: negative beta values In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/alternative; boundaryMessage-ID: <[log in to unmask]> --0016e656b59ae16c2b049be11db9 Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Bonjour our dear SPMers We have the following non-intuitive problem which can be easily stated: 1 -After making a T test on a simple condition (a beta value greater than 0) we get the coordinates of the activated regions for a given spherical region of interest. 2- We thus expect the mean beta value within those ROI to be positive. 3- We extract the beta values themselves (from the beta and SPM files in the corresponding statistical result directory) of all the voxels in the ROIs 4- When we compute means and stdev from them, we sometimes get negative mean beta values which are statistically significant when compared to their stdev. 5- How does it make sense to have both positive and negative beta values considering that we used the same spherical ROI in each cases?. 6- The other point is that when we plot the beta value for a given ROI using SPM we always get positive and much larger values. How can we make sense of all of this? No doubt that other readers have met the same problem before. Can you shed any light on this, we are still groping in the dark... Merci Pierre and Vronique --0016e656b59ae16c2b049be11db9 Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable
Bonjourour dearSPMers
We have the following non-intuitive problem which can be easily stated:
1 -After making a T test on a simple condition (a beta value greater than 0) weget the coordinates of the activated regions for a given spherical region of interest.
2- We thus expect the mean beta value within those ROI to be positive.
3- We extract the beta values themselves (from the beta and SPM files in the corresponding statistical result directory) of all the voxels in the ROIs
4- When we compute means and stdev from them,we sometimes get negative mean beta values which are statistically significant when compared to their stdev.
5- How does it make sense to have both positive and negative beta values considering that we used the same spherical ROI in each cases?.
6- The other point is that when we plot the beta value for a given ROIusing SPM we always get positive and much larger values.
How can we make sense of all of this?
No doubt that other readers have met the same problem before.
Can you shed any light on this, we are still groping in the dark...
Merci
Pierre and Vronique

--0016e656b59ae16c2b049be11db9-- ========================================================================Date: Wed, 9 Feb 2011 17:50:58 -0500 Reply-To: Jonathan Peelle <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Jonathan Peelle <[log in to unmask]> Subject: Re: Vbm8 Comments: To: kambiz rakhshan <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/alternative; boundaryMessage-ID: <[log in to unmask]> --00163630ed1965d720049be14c09 Content-Type: text/plain; charset=ISO-8859-1 Dear Kami, Dear experts, I have done a vbm analysis on 100 subjects with age range > between 25-80. I used vbm8 toolbox and modulated non-linear only option to > modulate the normalizad data. My specific question was to find relative > volumetric loss that were not induced by total gray matter. I have two > question now: 1-should one include TIV as a covariate while using non-linear > modulate option? 2- in my analysis, i didn't include TIV as cov but instead > age as a cov variable. Negative correlation with age reflects almost whole > the brain with a very strong t value( P<0.0001,FWE).what could be the reason > for that? I basically used all the default options for preprocessing. > Additionally,i have removed all the potential outliers that seem to have an > artifact. Any comment will be highly appreciate. Best. Kami > 1) I have not used the VBM8 toolbox so will let others comment on the specifics. My understanding is that most people who do the non-linear modulate option would not include TIV in the statistical model, under the assumption that the affine scaling component accurately reflects differences in TIV (Buckner et al., 2004). At the same time, if you have a sufficient number of subjects, I don't think there is any downside to including it, as there may be residual variance you can explain (i.e. affine scaling is probably not *perfectly* correlated with TIV). (I suppose one negative would be that if tissue class segmentation provides a poor estimate of TIV, or one that included systematic biases, than including this in the model might decrease sensitivity to effects of interest...). I would be very interested to hear comments from others on this approach. The most common approach when not using the VBM8 toolbox would be to modulate images (for both linear + nonlinear components) and simply try to address differences in TIV in the statistical model (Barnes et al., 2010). 2) There are multiple types of global effects which may affect your data in different ways. One of course is TIV; another is total gray matter (TGM). If you look at, for example, Good et al. (2001; Fig 3) you can see that these two measures don't always correlate. That is, generally, if you have a bigger head (TIV) you may have a bigger brain (TGM). But in the case of aging, there is also age-related GM loss, so as you age TGM decreases, but your skull doesn't shrink (thus, TIV doesn't necessarily change). (Of course, in cross-sectional studies there may be systematic effects on TIV due to nutrition or health care etc., but I'm leaving those aside for now.) Given that there are reliable decreases in GM in most areas of the brain with age, your findings are sensible. If you want to identify areas that change differently than TGM, you will need to somehow account for TGM in your analysis. An easy of doing this is to include TGM in your statistical model as a covariate (although this is not always appropriate; it really depends on what you are interested in). Hope this helps, Jonathan Barnes J, Ridgway GR, Bartlett J, Henley SMD, Lehmann M, Hobbs N, Clarkson MJ, MacManus DG, Ourselin S, Fox NC (Head size, age and gender adjustment in MRI studies: a necessary nuisance? NeuroImage 53:1244-1255.2010). Buckner RL, Head D, Parker J, Fotenos AF, Marcus D, Morris JC, Snyder AZ (A unified approach for morphometric and functional data analysis in young, old, and demented adutls using automated atlas-based head size normalization: reliability and validation against manual measurement of total intracranial volume. NeuroImage 23:724-738.2004). Good CD, Johnsrude IS, Ashburner J, Henson RNA, Friston KJ, Frackowiak RSJ (A voxel-based morphometric study of ageing in 465 normal adult human brains. NeuroImage 14:21-36.2001). --00163630ed1965d720049be14c09 Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Dear Kami,

Dear experts, I have done a vbm analysis on 100 subjects with age range between 25-80. I used vbm8 toolbox and modulated non-linear only option to modulate the normalizad data. My specific question was to find relative volumetric loss that were not induced by total gray matter. I have two question now: 1-should one include TIV as a covariate while using non-linear modulate option? 2- in my analysis, i didn't include TIV as cov but instead age as a cov variable. Negative correlation with age reflects almost whole the brain with a very strong t value( P<0.0001,FWE).what could be the reason for that? I basically used all the default options for preprocessing. Additionally,i have removed all the potential outliers that seem to have an artifact. Any comment will be highly appreciate. Best. Kami


1) I have not used the VBM8 toolbox so will let others comment on the specifics. My understanding is that most people who do the non-linear modulate option would not include TIV in the statistical model, under the assumption that the affine scaling component accurately reflects differences in TIV (Buckner et al., 2004). At the same time, if you have a sufficient number of subjects, I don't think there is any downside to including it, as there may be residual variance you can explain (i.e. affine scaling is probably not *perfectly* correlated with TIV). (I suppose one negative would be that if tissue class segmentation provides a poor estimate of TIV, or one that included systematic biases, than including this in the model might decrease sensitivity to effects of interest...). I would be very interested to hear comments from others on this approach.

The most common approach when not using the VBM8 toolbox would be to modulate images (for both linear + nonlinear components) and simply try to address differences in TIV in the statistical model (Barnes et al., 2010).


2) There are multiple types of global effects which may affect your data in different ways. One of course is TIV; another is total gray matter (TGM). If you look at, for example, Good et al. (2001; Fig 3) you can see that these two measures don't always correlate. That is, generally, if you have a bigger head (TIV) you may have a bigger brain (TGM). But in the case of aging, there is also age-related GM loss, so as you age TGM decreases, but your skull doesn't shrink (thus, TIV doesn't necessarily change). (Of course, in cross-sectional studies there may be systematic effects on TIV due to nutrition or health care etc., but I'm leaving those aside for now.) Given that there are reliable decreases in GM in most areas of the brain with age, your findings are sensible. If you want to identify areas that change differently than TGM, you will need to somehow account for TGM in your analysis. An easy of doing this is to include TGM in your statistical model as a covariate (although this is not always appropriate; it really depends on what you are interested in).

Hope this helps,

Jonathan



Barnes J, Ridgway GR, Bartlett J, Henley SMD, Lehmann M, Hobbs N, Clarkson MJ, MacManus DG, Ourselin S, Fox NC (Head size, age and gender adjustment in MRI studies: a necessary nuisance? NeuroImage 53:1244-1255.2010).


Buckner RL, Head D, Parker J, Fotenos AF, Marcus D, Morris JC, Snyder AZ (A unified approach for morphometric and functional data analysis in young, old, and demented adutls using automated atlas-based head size normalization: reliability and validation against manual measurement of total intracranial volume. NeuroImage 23:724-738.2004).


Good CD, Johnsrude IS, Ashburner J, Henson RNA, Friston KJ, Frackowiak RSJ (A voxel-based morphometric study of ageing in 465 normal adult human brains. NeuroImage 14:21-36.2001).


--00163630ed1965d720049be14c09-- ========================================================================Date: Wed, 9 Feb 2011 22:03:53 -0500 Reply-To: Jonathan Peelle <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Jonathan Peelle <[log in to unmask]> Subject: Re: negative beta values Comments: To: =?iso-8859-1?Q?Vronique_Paradis?= <[log in to unmask]> In-Reply-To: <[log in to unmask]> Mime-Version: 1.0 (Apple Message framework v1082) Content-Type: text/plain; charset=windows-1252 Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> Dear Vronique and Pierre, Please see inline responses below. I think that the answer to your question depends on the details of your analysis, so if you cannot figure this out, it would be helpful to know a bit more about the analysis you've done. > 1 -After making a T test on a simple condition (a beta value greater than 0) we get the coordinates of the activated regions for a given spherical region of interest. > 2- We thus expect the mean beta value within those ROI to be positive. I understand you to mean that you did a whole-brain analysis in SPM, identified some clusters that were significant, and then wanted to extract the parameter estimates (contrast values) for these regions. You are correct to think that if voxels show a positive effect in a t-test (e.g., a [1] contrast over a condition), that these same voxels should show positive beta values for that condition. I suspect the difference may arise in the details of how you constructed your ROIs. For example, if you create spherical ROIs around peak coordinates, there could be voxels within that sphere that do not show a significant effect in the t-test; the bigger the sphere, the more likely this is to be true. If you want to just look at the voxels that show a significant effect in your t-test, you can build such an ROI using MarsBar (http://marsbar.sourceforge.net/)that is, an ROI equivalent to an SPM cluster. So, it would be helpful to know the specifics of your analysis (single subject or group design, for example), and the details of how you constructed the ROIs. > 3- We extract the beta values themselves (from the beta and SPM files in the corresponding statistical result directory) of all the voxels in the ROIs Again, it would help to know the specificswhat files you extracted the data from, and the procedure you used to extract the values. > 4- When we compute means and stdev from them, we sometimes get negative mean beta values which are statistically significant when compared to their stdev. > 5- How does it make sense to have both positive and negative beta values considering that we used the same spherical ROI in each cases?. (I'm not sure what cases you mean here, so I may have misunderstood what you are trying to do...) > 6- The other point is that when we plot the beta value for a given ROI using SPM we always get positive and much larger values. It would be good to verify how you are plotting the beta value for an ROI in SPM. However, as indeed you would expect the beta values to be positive, it might suggest that whatever values are extracted by SPM in this way are accurate, whereas the alternate approach (that results in the negative beta values) is not accurate (or at least, not what you want to do). > How can we make sense of all of this? It's seldom easy! ;-) Good luck. Best regards, Jonathan ========================================================================Date: Thu, 10 Feb 2011 08:43:13 +0100 Reply-To: Marko Wilke <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Marko Wilke <[log in to unmask]> Subject: Re: spm_preproc Comments: To: Mohamed Seghier <[log in to unmask]> Comments: cc: cyril pernet <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1; format=flowed Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> Hi Cyril, Mohamed, > Let's say R = spm_preproc('your anatomical image'); > just run PO = spm_prep2sn(R) ; > and then, all the variables that you need are: > VG = PO.VG ; > VF = PO.VF ; > Tr = PO.Tr ; > Affine = PO.Affine ; > flags = PO.flags ; just to add another 2 cents: prep2sn is multifunctional, so if you call it without an output argument, it will save the segmentation parameters appropriately, as in % segment dataset, need to specify options beforehand results = spm_preproc(ana,opts_seg); % process generated spatial normalization parameters [po,pin] = spm_prep2sn(results); % save parameters spm_prep2sn(results); % write out segmented data (better specify these options, too :) spm_preproc_write(po,opts_write); This saved me time and some headache, hope it does for you, too. Cheers, Marko -- ____________________________________________________ PD Dr. med. Marko Wilke Facharzt fr Kinder- und Jugendmedizin Leiter, Experimentelle Pdiatrische Neurobildgebung Universitts-Kinderklinik Abt. III (Neuropdiatrie) Marko Wilke, MD, PhD Pediatrician Head, Experimental Pediatric Neuroimaging University Children's Hospital Dept. III (Pediatric Neurology) Hoppe-Seyler-Str. 1 D - 72076 Tbingen, Germany Tel. +49 7071 29-83416 Fax +49 7071 29-5473 [log in to unmask] http://www.medizin.uni-tuebingen.de/kinder/epn ____________________________________________________ ========================================================================Date: Thu, 10 Feb 2011 07:58:14 +0000 Reply-To: =?utf-8?B?Y3lyaWwucGVybmV0QGVkLmFjLnVr?= <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: =?utf-8?B?Y3lyaWwucGVybmV0QGVkLmFjLnVr?= <[log in to unmask]> Subject: Re: spm_preproc Comments: To: =?utf-8?B?TWFya28gV2lsa2U=?= <[log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/mixed; boundary="----------=_1297324745-21276-186" Content-Transfer-Encoding: binary Message-ID: <[log in to unmask]> This is a multi-part message in MIME format... ------------=_1297324745-21276-186 Received: from [192.168.0.2] (5ada7242.bb.sky.com [90.218.114.66]) (authenticated user=cpernet mech=LOGIN bits=0) by lmtp1.ucs.ed.ac.uk (8.13.8/8.13.7) with ESMTP id p1A7x4gb015293 (version=TLSv1/SSLv3 cipher=DHE-RSA-AES256-SHA bits%6 verify=NOT); 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Comments: To: justine dupont <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> It is the size of the voxels in the "imported" images that I was referring to. The actual Dartel registration is usually done using "imported" data, which are rigidly aligned versions of the GM and WM, downsampled to 1.5 mm x 1.5 mm x 1.5 mm. Your original voxel sizes should be fine. Best regards, -John On 9 February 2011 21:34, justine dupont <[log in to unmask]> wrote: > Dear John and other experts > I have inherited a nice T1 dataset but thevoxels areanisotropic (-0.97 x > 0.97 x 1). I want to do a VBM study using these data, however according to > a very recent post by John on the list, DARTEL is not appropriate > foranisotropic voxels. So my question is... is it OK to use > traditionalVBMmethod (i.e. not using DARTEL) for such data? > thank you very much :) > Justine > > ========================================================================Date: Thu, 10 Feb 2011 12:07:03 +0100 Reply-To: marco tettamanti <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: marco tettamanti <[log in to unmask]> Subject: DCM: mutual interactions between networks MIME-Version: 1.0 Content-Type: text/plain; charset="ISO-8859-1"; format=flowed content-transfer-encoding: 7bit Message-ID: <[log in to unmask]> Dear all, I don't think that this question has been addressed before: I would like to set up a DCM analysis with fMRI data to investigate the following issue: we have identified an activation in a very well known network of 4 brain regions (A,B,C,D), and we believe that, in our task, this network can be gated - depending on which one of 2 different input modalities is involved - by the activity of two other distinct networks, each including 3 brain regions (E,F,G, or H,I,J). That is, we would like to assess how network EFG interacts with network ABCD in modality 1 and how network HIJ interacts with network ABDC in modality 2, in the context of a sort of 2x2 (Modality x network-network interaction) factorial design. I presume that one could address this, by simply treating each brain region independently, and for instance by using BMS to test whether the preferred model fits the expected interaction patterns, but I think that there may be problems with the relatively large number of regions (>8). I also presume that the question could be approached by non-linear DCM, even though I think that non-linear DCM has been only used in the context of the influence of one single region on a system of interconnected regions, and not in the context of network-network interactions. Can anyone suggest a more direct way to approach this issue? Thank you and all the best, Marco -- Marco Tettamanti, Ph.D. San Raffaele Scientific Institute Via Olgettina 58 I-20132 Milano, Italy Tel. ++39-02-26434888 Fax ++39-02-26434892 Email: [log in to unmask] ----------------------------------------------------------------------------------- SOSTIENI ANCHE TU LA RICERCA DEL SAN RAFFAELE. NON C'E' CURA SENZA RICERCA. Per donazioni: ccp 42437681 intestato a Fondazione Arete' Onlus del San Raffaele. Per informazioni: tel. 02.2643.4461 - www.sanraffaele.org ========================================================================Date: Thu, 10 Feb 2011 11:14:52 +0000 Reply-To: "Pettersson-Yeo, William" <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: "Pettersson-Yeo, William" <[log in to unmask]> Subject: New Segmentation Out of Memory Error Content-Type: multipart/alternative; boundary="_000_699C0D407EF04E2B8781F618FECB9D2Ckclacuk_" MIME-Version: 1.0 Message-ID: <[log in to unmask]> --_000_699C0D407EF04E2B8781F618FECB9D2Ckclacuk_ Content-Type: text/plain; charset="us-ascii" Content-Transfer-Encoding: quoted-printable Dear SPMers, I use a MacBookPro with a 4GB hard drive and 2.53 GHz processor. When I try and run the 'New Segment' function in SPM8, I get the 'Out of Memory' error message detailed below. The structural files I'm trying to segment are approx. 80mb (bigger than what I usually work with) I have tried re-installing spm8, and have also tried changing the defaults.stats.maxmem = 2^26 to 2^31 but without success. Can anyone help? Many thanks William (Dept.of Psychosis, Institute of Psychiatry, KCL) ERROR MESSAGE: ------------------------------------------------------------------------ Running job #1 ------------------------------------------------------------------------ Running 'New Segment' Failed 'New Segment' Error using ==> unknown Out of memory. Type HELP MEMORY for your options. In file "/Users/williampettersson-yeo/Documents/spm8/toolbox/Seg/spm_preproc_write8.m" (v3172), function "affind" at line 428. In file "/Users/williampettersson-yeo/Documents/spm8/toolbox/Seg/spm_preproc_write8.m" (v3172), function "spm_preproc_write8" at line 241. In file "/Users/williampettersson-yeo/Documents/spm8/toolbox/Seg/spm_preproc_run.m" (v3859), function "run_job" at line 112. In file "/Users/williampettersson-yeo/Documents/spm8/toolbox/Seg/spm_preproc_run.m" (v3859), function "spm_preproc_run" at line 27. In file "/Users/williampettersson-yeo/Documents/spm8/toolbox/Seg/tbx_cfg_preproc8.m" (v3910), function "spm_local_preproc_run" at line 353. The following modules did not run: Failed: New Segment ??? Error using ==> spm_input at 1470 Input object cleared whilst waiting for response: Bailing out! Error in ==> spm_dcm_ui at 88 selected = spm_input(str,1,'m',Actions); ??? Error using ==> spm_dcm_ui; Error using ==> spm_input at 1470 Input object cleared whilst waiting for response: Bailing out! ??? Error while evaluating uicontrol Callback --_000_699C0D407EF04E2B8781F618FECB9D2Ckclacuk_ Content-Type: text/html; charset="us-ascii" Content-Transfer-Encoding: quoted-printable Dear SPMers,

I use a MacBookPro with a 4GB hard drive and 2.53 GHz processor.
When I try and run the 'New Segment' function in SPM8, I get the 'Out of Memory' error message detailed below.

The structural files I'm trying to segment are approx. 80mb (bigger than what I usually work with)

I have tried re-installing spm8, and have also tried changing the defaults.stats.maxmem = 2^26 to 2^31 but without success.

Can anyone help?

Many thanks
William
(Dept.of Psychosis, Institute of Psychiatry, KCL)


ERROR MESSAGE:
------------------------------------------------------------------------
Running job #1
------------------------------------------------------------------------
Running 'New Segment'
Failed  'New Segment'
Error using ==> unknown
Out of memory. Type HELP MEMORY for your options.
In file "/Users/williampettersson-yeo/Documents/spm8/toolbox/Seg/spm_preproc_write8.m" (v3172), function "affind" at line 428.
In file "/Users/williampettersson-yeo/Documents/spm8/toolbox/Seg/spm_preproc_write8.m" (v3172), function "spm_preproc_write8" at line 241.
In file "/Users/williampettersson-yeo/Documents/spm8/toolbox/Seg/spm_preproc_run.m" (v3859), function "run_job" at line 112.
In file "/Users/williampettersson-yeo/Documents/spm8/toolbox/Seg/spm_preproc_run.m" (v3859), function "spm_preproc_run" at line 27.
In file "/Users/williampettersson-yeo/Documents/spm8/toolbox/Seg/tbx_cfg_preproc8.m" (v3910), function "spm_local_preproc_run" at line 353.

The following modules did not run:
Failed: New Segment

??? Error using ==> spm_input at 1470
Input object cleared whilst waiting for response: Bailing out!

Error in ==> spm_dcm_ui at 88
    selected = spm_input(str,1,'m',Actions);

??? Error using ==> spm_dcm_ui;
Error using ==> spm_input at 1470
Input object cleared whilst waiting for response: Bailing out!

??? Error while evaluating uicontrol Callback

--_000_699C0D407EF04E2B8781F618FECB9D2Ckclacuk_-- ========================================================================Date: Thu, 10 Feb 2011 11:35:59 +0000 Reply-To: John Ashburner <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: John Ashburner <[log in to unmask]> Subject: Re: New Segmentation Out of Memory Error Comments: To: "Pettersson-Yeo, William" <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> The stats.maxmem setting won't have any effect here, as it only determines how much data is read at a time when doing the stats. I think you may simply be reaching the limit of how much a 32 bit computer can hold in memory at once for one process. This is only (2^32-1)/1024^2 Mbytes, so once you have a few deformation fields and stuff in memory, then this is easily reached. 64 bit computers don't have this limit. I'm pretty sure that much of your image is not actually brain, so maybe you could crop the data to make the file a bit smaller. Best regards, -John On 10 February 2011 11:14, Pettersson-Yeo, William <[log in to unmask]> wrote: > Dear SPMers, > I use a MacBookPro with a 4GB hard drive and 2.53 GHz processor. > When I try and run the 'New Segment' function in SPM8, I get the 'Out of > Memory' error message detailed below. > The structural files I'm trying to segment are approx. 80mb (bigger than > what I usually work with) > I have tried re-installing spm8, and have also tried changing > thedefaults.stats.maxmem = 2^26 to 2^31 but without success. > Can anyone help? > Many thanks > William > (Dept.of Psychosis, Institute of Psychiatry, KCL) > > ERROR MESSAGE: > ------------------------------------------------------------------------ > Running job #1 > ------------------------------------------------------------------------ > Running 'New Segment' > Failed 'New Segment' > Error using ==> unknown > Out of memory. Type HELP MEMORY for your options. > In file > "/Users/williampettersson-yeo/Documents/spm8/toolbox/Seg/spm_preproc_write8.m" > (v3172), function "affind" at line 428. > In file > "/Users/williampettersson-yeo/Documents/spm8/toolbox/Seg/spm_preproc_write8.m" > (v3172), function "spm_preproc_write8" at line 241. > In file > "/Users/williampettersson-yeo/Documents/spm8/toolbox/Seg/spm_preproc_run.m" > (v3859), function "run_job" at line 112. > In file > "/Users/williampettersson-yeo/Documents/spm8/toolbox/Seg/spm_preproc_run.m" > (v3859), function "spm_preproc_run" at line 27. > In file > "/Users/williampettersson-yeo/Documents/spm8/toolbox/Seg/tbx_cfg_preproc8.m" > (v3910), function "spm_local_preproc_run" at line 353. > The following modules did not run: > Failed: New Segment > ??? Error using ==> spm_input at 1470 > Input object cleared whilst waiting for response: Bailing out! > Error in ==> spm_dcm_ui at 88 > selected = spm_input(str,1,'m',Actions); > ??? Error using ==> spm_dcm_ui; > Error using ==> spm_input at 1470 > Input object cleared whilst waiting for response: Bailing out! > ??? Error while evaluating uicontrol Callback > ========================================================================Date: Thu, 10 Feb 2011 13:52:05 +0100 Reply-To: Tatiana Usnich <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Tatiana Usnich <[log in to unmask]> Subject: Re: Question regarding the fMRI model specification Comments: To: "MCLAREN, Donald" <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain;charset=UTF-8 Content-Transfer-Encoding: 8bit Message-ID: <[log in to unmask]> Thank you! There was in fact one empty cell in other conditions.mat files, that didn't work. That was most likely causing the problem. We restructured the .mat file and it works now. Best regards, Tatiana > (1) You probably have less data than time in your conditions.mat (this > would make it appear that no events and it might ask for conditions; > how did you specify the time in the design and how many time points > are in each run? > > (2) Have you updated SPM with the latest updates? > > I just used your condition.mat file with some random files and it > created a design without a problem. > > Best Regards, Donald McLaren > ================> D.G. McLaren, Ph.D. > Postdoctoral Research Fellow, GRECC, Bedford VA > Research Fellow, Department of Neurology, Massachusetts General > Hospital and Harvard Medical School > Office: (773) 406-2464 > ====================> This e-mail contains CONFIDENTIAL INFORMATION which may contain > PROTECTED HEALTHCARE INFORMATION and may also be LEGALLY PRIVILEGED > and which is intended only for the use of the individual or entity > named above. If the reader of the e-mail is not the intended recipient > or the employee or agent responsible for delivering it to the intended > recipient, you are hereby notified that you are in possession of > confidential and privileged information. Any unauthorized use, > disclosure, copying or the taking of any action in reliance on the > contents of this information is strictly prohibited and may be > unlawful. If you have received this e-mail unintentionally, please > immediately notify the sender via telephone at (773) 406-2464 or > email. > > > > On Wed, Feb 9, 2011 at 9:16 AM, Tatiana Usnich > <[log in to unmask]> wrote: >> Dear SPMlers, >> >> We also have the same problem. Starting to run fMRI model specification >> in SPM8 we are asked for a vector of onsets for one of the conditions >> and durations even though the conditions are specified in a .mat file. >> >> Conditions file is attached. Id really appreciate your help. >> >> Tatiana >> > ========================================================================Date: Thu, 10 Feb 2011 12:53:29 +0000 Reply-To: Meng-Chuan Lai <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Meng-Chuan Lai <[log in to unmask]> Subject: registration error under DARTEL and suggested smoothness Mime-Version: 1.0 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain; charset="UTF-8" Message-ID: <[log in to unmask]> Dear John and SPM users. I would like to inquire if there is any available data showing the average registration error by DARTEL? I am currently running VBM using DARTEL-processed modulated images. I found that in group comparison, the smaller extra smooth kernel I put on the modulated images (e.g. 8mm --> 4mm --> 2mm --> 1mm --> no extra smooth), the more significant clusters identified using topological FDR. Note that even with no extra smoothing, the effective smoothness of the images is about 3.8mm (voxel size is 1mm isotropic). I am not sure what smoothness should I go for so would like choose it according to the registration error by DARTEL (in mm), if there's any data available. Any idea or suggestion regarding an appropriate smoothness for DARTEL-processed modulated images with 1mm isotropic voxels when running VBM? Thanks so much. Meng-Chuan Lai ========================================================================Date: Thu, 10 Feb 2011 13:36:30 +0000 Reply-To: Neal Hinvest <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Neal Hinvest <[log in to unmask]> Subject: PhD studentship opportunity at the University of Bath, UK (Department of Psychology) MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1; format=flowed Content-Transfer-Encoding: 7bit Message-ID: <[log in to unmask]> The Department of Psychology at the University of Bath, U.K., is inviting applications for a PhD studentship. The PhD is for a fixed 3-year term and is fully funded (all tuition fees paid plus stipend). The successful candidate will start in October 2011. The project investigates internet and video-game addiction. The project is supervised by Dr. Neal Hinvest. The Department of Psychology is highly research active. The Departments has three main areas of research stength; Cognition, Affective Science and Technology Labs (CASTL), Health Psychology and Social and Cultural Psychology. For more details see http://www.bath.ac.uk/psychology/research. The successful candidate will have a 1st or 2:1 and will have relevant experience in psychology. Research experience or advanced training (e.g. Masters level degree) would be advantageous but not necessary. Experience with statistical software packages (e.g. SPSS) would be beneficial. The deadline for applications is the 15th April. Send applications to Dr. Neal Hinvest, Department of Psychology, University of Bath, Bath, BA2 7AY, U.K. Electronic applications are preferred and can be sent to [log in to unmask] -- Dr. Neal Hinvest Lecturer Department of Psychology University of Bath Bath BA2 7AY ========================================================================Date: Thu, 10 Feb 2011 15:36:47 +0100 Reply-To: Cornelia Hummel <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Cornelia Hummel <[log in to unmask]> Subject: matlab path In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/alternative; boundaryMessage-ID: [log in to unmask]> --00235444776d4c0b65049bee85bf Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Dear experts, I encounterd the following problem: I installed SPM8, ran matlab and SPM with the respetive path set, then moved the entire SPM folder to another site, changed the path in matlab, and now, when running segment, got the error message that the file "(previous folder)\spm\tpm\grey.nii" does not exist. I double checked the path setting, and cannot find why matlab still tries to read from the path that no longer exists rather than the correctly set one. (The realign and coregister procedures ran without problems.) Can anybody please help me? Thanks in advance, Cornelia -- Cornelia Hummel Voglerstrae 14 01277 Dresden --00235444776d4c0b65049bee85bf Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Dear experts,
I encounterd the following problem:
I installed SPM8, ran matlab and SPM with the respetive path set, then moved the entire SPM folder to another site, changed the path in matlab, and now, when running segment, got the error message that the file "(previous folder)\spm\tpm\grey.nii" does not exist. I double checked the path setting, and cannot find why matlab still tries to read from the path that no longer exists rather than the correctly set one. (The realign and coregister procedures ran without problems.)
Can anybody please help me?
Thanks in advance,
Cornelia


--
Cornelia Hummel
Voglerstrae 14
01277 Dresden
--00235444776d4c0b65049bee85bf-- ========================================================================Date: Thu, 10 Feb 2011 16:05:04 +0000 Reply-To: William Pettersson-Yeo <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: William Pettersson-Yeo <[log in to unmask]> Subject: Re: New Segmentation Out of Memory Error Comments: To: John Ashburner <[log in to unmask]> Mime-Version: 1.0 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain Message-ID: <[log in to unmask]> Thanks John. It turns out the problem was due to the version of Matlab I was running. Matlab2007 was only running 32bit, whilst the 2010 version is 64. Having set up with Matlab2010, the new segmentation with DARTEL import now runs without any problem, without me having to alter/crop any of the images. All the best William ========================================================================Date: Thu, 10 Feb 2011 16:47:53 +0000 Reply-To: Joachim Gross <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Joachim Gross <[log in to unmask]> Subject: Chair Position Glasgow Mime-Version: 1.0 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain; charset="UTF-8" Message-ID: <[log in to unmask]> UNIVERSITY of GLASGOW College of Medical, Veterinary and Life Sciences Institute of Neuroscience and Psychology (INP) Faculty Position in Formal Models of Cortical Networks - may be appointed at Lecturer/Senior Lecturer/Reader or Professor level Ref: M00075 Salary: Lecturer/Senior Lecturer - £31,798 - £52,556 per annum Reader/Professor – negotiable – depends on experience Applications are invited for a faculty position (up to chair level) in Formal Models of Cortical Networks from individuals with an outstanding research record. The post is designed to complement existing research strengths in the Institute for Neuroscience and Psychology and to develop a programme for studying and describing networks across the different Centres of the Institute. The Post-holder will provide research leadership in the area of cortical networks and networks in general (connectivity, information theory, graph theory). The Post-holder will be expected to raise external funds to support their research programme, to attract postdoctoral research staff and PhD students, and to contribute to research-led teaching, especially via the development of specialised content for masters and postgraduate degrees. Candidates for this post will have an exceptional international research profile, including a track record of high impact publications and substantial research funding, in the areas of network/connectivity analysis, information theory or graph theory. Informal enquiries may be made to Philippe Schyns (Director of Institute, +44 141 330 4937, [log in to unmask]) or Joachim Gross (Acting Director of Centre for Cognitive Neuroimaging (CCNi), +44 141 330 3947, [log in to unmask]). Apply online at www.glasgow.ac.uk/jobs Closing date: 12 April 2011. ========================================================================Date: Thu, 10 Feb 2011 16:59:04 +0000 Reply-To: Vy Dinh <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Vy Dinh <[log in to unmask]> Subject: SPM8 VOI Extraction: Adjusting for effects of no interest Mime-Version: 1.0 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain Message-ID: <[log in to unmask]> Dear all, Excuse me for not getting straight to the question, but I found it difficult to formulate my question otherwise. First of all, according to responses on the forum (links below), "adjusting for effects of (no) interest" removes the variances introduced by confounds in the 1st-level design matrix. SPM does this by mean-centering the data based on the betas obtained from columns that are zeroed in the F-contrast. (adjusted Y = global raw data = [sum (beta x effects of no interest)]); Therefore, if I have a design matrix with 3 conditions, motion parameters, and 1 regressor of no interest and I specified an F-contrast of 1 0 0 < right side padded with 2 zeroes (1 for regressor, 1 for constant) 0 1 0 0 0 1 .. the F-contrast will be padded with 2 zeroes as well and these columns will be accounted for during VOI extraction with adjustment (please correct me if I'm wrong). Motion parameters have often been used as an example of a regressor of no interest in these posts, but HOW DOES SPM'S ADJUSTMENT OPTION INTERPRET A COLUMN FOR DEWEIGHTING A "BAD" SCAN (WHERE BAD SCANS ARE SPECIFIED AS 1S)? Are the data associated with these scans also not included in the VOI extraction? Answers to these questions would help us understand why we are seeing slight differences between results using adjusted and non-adjusted data that do not have any confounds in the first model. Motion was addressed by adjusting the data with ArtRepair Toolbox prior to estimation. If the deweighting columns should have no effect on the VOI extraction, then mathematically speaking, the results should be the same. However, they are not. Also, some of our subjects had zero instances of 1 condition, so we had to define this condition as a zero in the Effects Of Interest F-contrast. In these cases, would specifying adjust or not adjust make a difference? Thanks, Vy Here are the links to the listserv responses regarding adjusting for regressors of no interest: https://www.jiscmail.ac.uk/cgi-bin/webadmin?A2=SPM;664c9b8.03; https://www.jiscmail.ac.uk/cgi-bin/webadmin?A2=SPM;f695a1.1004; https://www.jiscmail.ac.uk/cgi-bin/webadmin?A2=SPM;9945e539.03) ========================================================================Date: Thu, 10 Feb 2011 11:05:48 -0600 Reply-To: Darren Gitelman <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Darren Gitelman <[log in to unmask]> Subject: Re: DCM: mutual interactions between networks Comments: To: marco tettamanti <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Message-ID: <[log in to unmask]> Marco On Thu, Feb 10, 2011 at 5:07 AM, marco tettamanti <[log in to unmask]> wrote: > Dear all, > I don't think that this question has been addressed before: > > I would like to set up a DCM analysis with fMRI data to investigate the > following issue: we have identified an activation in a very well known > network of 4 brain regions (A,B,C,D), and we believe that, in our task, this > network can be gated - depending on which one of 2 different input > modalities is involved - by the activity of two other distinct networks, > each including 3 brain regions (E,F,G, or H,I,J). > That is, we would like to assess how network EFG interacts with network ABCD > in modality 1 and how network HIJ interacts with network ABDC in modality 2, > in the context of a sort of 2x2 (Modality x network-network interaction) > factorial design. > > I presume that one could address this, by simply treating each brain region > independently, and for instance by using BMS to test whether the preferred > model fits the expected interaction patterns, but I think that there may be > problems with the relatively large number of regions (>8). You can deal with this by setting up the DCM file from the command line. If you set up a simpler DCM using the GUI you will see what fields you need. The 8 region limitation is mostly due to the gui (and memory). > I also presume that the question could be approached by non-linear DCM, even > though I think that non-linear DCM has been only used in the context of the > influence of one single region on a system of interconnected regions, and > not in the context of network-network interactions. I'm not sure how you could use a non-linear DCM in this scenario. You can't really setup a small DCM network as an input, per se. The two "subnetworks" would just be connected into the larger 4 region network perhaps through a common area. This would be through an intrinsic connection. DCM only accepts as inputs the condition-type vectors that it extracts from an SPM.mat file. You would also need other actual inputs into each of the subnetworks in order to drive overall system activity. Non-linear DCM's can be used to modulate an intrinsic connection, so perhaps you are thinking of using the 3 region subnetworks to modulate an external input into the 4 region network? However, I don't think you can modulate an input as DCM is currently set up, and you would still need to drive the subnetworks in some way. Darren > > Can anyone suggest a more direct way to approach this issue? > > Thank you and all the best, > Marco > > -- > Marco Tettamanti, Ph.D. > San Raffaele Scientific Institute > Via Olgettina 58 > I-20132 Milano, Italy > Tel. ++39-02-26434888 > Fax ++39-02-26434892 > Email: [log in to unmask] > > ----------------------------------------------------------------------------------- > SOSTIENI ANCHE TU LA RICERCA DEL SAN RAFFAELE. > NON C'E' CURA SENZA RICERCA. > Per donazioni: ccp 42437681 intestato a Fondazione Arete' Onlus del San > Raffaele. > Per informazioni: tel. 02.2643.4461 - www.sanraffaele.org > -- Darren Gitelman, MD Northwestern University 710 N. Lake Shore Dr., 1122 Chicago, IL 60611 Ph: (312) 908-8614 Fax: (312) 908-5073 ========================================================================Date: Thu, 10 Feb 2011 17:29:41 +0000 Reply-To: Tom Johnstone <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Tom Johnstone <[log in to unmask]> Subject: University of Reading International Studentship Comments: To: "[log in to unmask] [log in to unmask]" <[log in to unmask]>, [log in to unmask] MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Message-ID: <[log in to unmask]> Opportunity for PhD Studentship at the Centre for Integrative Neuroscience & Neurodynamics (CINN). The Faculties of Sciences & Life Sciences at the University of Reading are jointly holding a studentship competition for International Students (defined as non-EU/EEA). We encourage applications from candidates wishing to complete a PhD in the Cognitive, Affective or Social Neurosciences at the CINN. Each studentship will provide a subsistence grant (normal UK research council rate) as well as the University tuition fee (full-time international at Reading) for 3 Academic Years. Candidates should possess a 1st class Honours degree or equivalent in Psychology, Neuroscience or a related discipline. An MSc with Distinction or progress towards such an MSc would be an advantage. Applications will be judged in a 2-stage procedure. In the first step, the School of Psychology & Clinical Language Sciences will select the strongest 2 submissions to the school. These will then be submitted to the Faculty Deans, who will select the highest quality candidates who have strong research plans for a topic compatible with the University's Research Strategy. The Centre for Integrative Neuroscience and Neurodynamics ( http://www.reading.ac.uk/cinn/ ) occupies a dedicated wing in the School of Psychology & CLS building at the University of Reading. It houses a 3T Siemens Trio research-dedicated MRI scanner and high-density EEG laboratory. These facilities are complemented by high resolution stimulus display systems with integrated high-speed eye tracking, MRI compatible EEG and TMS systems. Research at CINN involves the neural mechanisms underpinning complex cognitive and affective behaviours, with particular strengths in affective neuroscience and the neural mechanisms of perception and action. Interested candidates should send an email with a brief statement of research interests and a CV, including details of nationality to: Tom Johnstone Centre for Integrative Neuroscience & Neurodynamics School of Psychology and CLS [log in to unmask] http://www.personal.reading.ac.uk/~sxs07itj/index.html Closing date: Friday the 25th of February. ========================================================================Date: Thu, 10 Feb 2011 18:12:34 +0000 Reply-To: John Ashburner <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: John Ashburner <[log in to unmask]> Subject: Re: registration error under DARTEL and suggested smoothness Comments: To: Meng-Chuan Lai <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=windows-1252 Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> Without knowing the ground truth (which probably does not exist anyway), it is difficult to say what the average registration error is. The closest we have are comparisons of various registration algorithms in terms of how well they can propagate manually defined regions. I suspect that the manually defined regions used for the validations may not be so accurate, but they will probably be accurate enough to compare among models. There is a validation of what was in the SPM5 implementation (with the original Unified Segmentation) within: Evaluation of 14 nonlinear deformation algorithms applied to human brain MRI registration Original Research Article NeuroImage, Volume 46, Issue 3, 1 July 2009, Pages 786-802 Arno Klein, Jesper Andersson, Babak A. Ardekani, John Ashburner, Brian Avants, Ming-Chang Chiang, Gary E. Christensen, D. Louis Collins, James Gee, Pierre Hellier, Joo Hyun Song, Mark Jenkinson, Claude Lepage, Daniel Rueckert, Paul Thompson, Tom Vercauteren, Roger P. Woods, J. John Mann, Ramin V. Parsey For a validation of the SPM8 implementation (with the New Segment), see: Diffeomorphic registration using geodesic shooting and GaussNewton optimisation NeuroImage, In Press, Corrected Proof, Available online 7 January 2011 John Ashburner, Karl J. Friston Best regards, -John On 10 February 2011 12:53, Meng-Chuan Lai <[log in to unmask]> wrote: > Dear John and SPM users. > > I would like to inquire if there is any available data showing the average registration error by DARTEL? > > I am currently running VBM using DARTEL-processed modulated images. I found that in group comparison, the smaller extra smooth kernel I put on the modulated images (e.g. 8mm --> 4mm --> 2mm --> 1mm --> no extra smooth), the more significant clusters identified using topological FDR. Note that even with no extra smoothing, the effective smoothness of the images is about 3.8mm (voxel size is 1mm isotropic). I am not sure what smoothness should I go for so would like choose it according to the registration error by DARTEL (in mm), if there's any data available. Any idea or suggestion regarding an appropriate smoothness for DARTEL-processed modulated images with 1mm isotropic voxels when running VBM? > > Thanks so much. > > Meng-Chuan Lai > ========================================================================Date: Thu, 10 Feb 2011 18:17:56 +0000 Reply-To: John Ashburner <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: John Ashburner <[log in to unmask]> Subject: Re: matlab path Comments: To: Cornelia Hummel <[log in to unmask]> In-Reply-To: [log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Message-ID: [log in to unmask]> Are you trying to run a batch file? If so, the location of the tissue probability maps will be defined by that file. Best regards, -John On 10 February 2011 14:36, Cornelia Hummel <[log in to unmask]> wrote: > Dear experts, > I encounterd the following problem: > I installed SPM8, ran matlab and SPM with the respetive path set, then moved > the entire SPM folder to another site, changed the path in matlab, and now, > when running segment, got the error message that the file "(previous > folder)\spm\tpm\grey.nii" does not exist. I double checked the path setting, > and cannot find why matlab still tries to read from the path that no longer > exists rather than the correctly set one. (The realign and coregister > procedures ran without problems.) > Can anybody please help me? > Thanks in advance, > Cornelia > > > -- > Cornelia Hummel > Voglerstrae 14 > 01277 Dresden > ========================================================================Date: Thu, 10 Feb 2011 13:27:21 -0500 Reply-To: Giulia Dormal <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Giulia Dormal <[log in to unmask]> Subject: SPM8 fMRI model specification MIME-Version: 1.0 Content-Type: multipart/mixed; boundaryMessage-ID: <[log in to unmask]> --00504502c86877f759049bf1bb7b Content-Type: multipart/alternative; boundary --00504502c86877f751049bf1bb79 Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Dear SPMers, I am trying to run an fMRI model specification batch (in attached), for a single run of a block design containing 3 conditions + baseline. I have specified the different conditions in seconds. When I run the batch, I systematically get this error message in matlab window: Failed 'fMRI model specification' Cell contents reference from a non-cell array object. In file "C:\Program Files\spm8\spm8\spm_Ce.m" (v3527), function "spm_Ce" at line 54. In file "C:\Program Files\spm8\spm8\spm_fmri_spm_ui.m" (v3691), function "spm_fmri_spm_ui" at line 345. In file "C:\Program Files\spm8\spm8\config\spm_run_fmri_spec.m"(v3757), function "spm_run_fmri_spec" at line 301. I would very much appreciate your help! Giulia ---------- Forwarded message ---------- From: Giulia Dormal <[log in to unmask]> Date: 2011/2/10 Subject: To: "giulia.dormal" <[log in to unmask]> -- Giulia Dormal, PhD Student IPSY/IoNS - Universit Catholique de Louvain CERNEC - Universit de Montral (001) 514 343 61 11 #1715 -- Giulia Dormal, PhD Student IPSY/IoNS - Universit Catholique de Louvain CERNEC - Universit de Montral (001) 514 343 61 11 #1715 --00504502c86877f751049bf1bb79 Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Dear SPMers,

I am trying to run an fMRI model specification batch (in attached), for a single run of a block design containing 3 conditions + baseline. I have specified the different conditions in seconds. When I run the batch, I systematically get this error message in matlab window:
Failed 'fMRI model specification'
Cell contents reference from a non-cell array object.
In file "C:\Program Files\spm8\spm8\spm_Ce.m" (v3527), function "spm_Ce" at line 54.
In file "C:\Program Files\spm8\spm8\spm_fmri_spm_ui.m" (v3691),
function "spm_fmri_spm_ui" at line 345.
In file "C:\Program Files\spm8\spm8\config\spm_run_fmri_spec.m"(v3757), function "spm_run_fmri_spec" at line 301.

I would very much appreciate your help!

Giulia



---------- Forwarded message ----------
From: Giulia Dormal <[log in to unmask]>
Date: 2011/2/10
Subject:
To: "giulia.dormal" <[log in to unmask]>


--
Giulia Dormal, PhD Student
IPSY/IoNS - Universit Catholique de Louvain
CERNEC - Universit de Montral
(001) 514 343 61 11 #1715



--
Giulia Dormal, PhD Student
IPSY/IoNS - Universit Catholique de Louvain
CERNEC - Universit de Montral
(001) 514 343 61 11 #1715


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Subject: regressors of no interest in first level model MIME-Version: 1.0 Content-Type: multipart/alternative; boundaryMessage-ID: [log in to unmask]> --0016364ef8feb97f88049bf20402 Content-Type: text/plain; charset=ISO-8859-1 Hi all, I hope you can help me with a question regarding modelling regressors of no interest in a first level model. I assumed it is better to model all time intervals, including the periods of certain ''conditions'' you are not interested in (for example, an instruction period before a specific event), to reduce variance in the signal during the conditions that you will use for further analysis that is actually caused by conditions of no interest. However, now I was told that in doing so, one would reduce the degree of orthogonality of each regressor with respect to the constant regressor. Now I do not know what is the best option: model every condition or only the ones you will use for further analysis. I hope someone can advise me on this! Thanks, Maaike --0016364ef8feb97f88049bf20402 Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable
Hi all,
I hope you can help me with a question regarding modelling regressors of no interest in a first level model.
I assumed it is better to model all time intervals, including the periods of certain ''conditions''you are not interested in (for example, an instruction period before a specific event), to reduce variancein the signal during the conditions that you will use for further analysis that is actually caused by conditions of no interest.
However, nowI was told that in doing so,one wouldreduce the degree oforthogonality of each regressor with respect to theconstant regressor.
Now I do not know what is the best option: model every condition or only the ones you will use for further analysis. I hopesomeone can advise me on this!
Thanks,
Maaike
--0016364ef8feb97f88049bf20402-- ========================================================================Date: Thu, 10 Feb 2011 14:13:51 -0500 Reply-To: "MCLAREN, Donald" <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: "MCLAREN, Donald" <[log in to unmask]> Subject: Re: regressors of no interest in first level model Comments: To: maaike rive <[log in to unmask]> In-Reply-To: [log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> If you know that the activity is changing from baseline, then you should model it if you can. Otherwise, the condition of interest will be with respective to the constant+instruction. The problem can arise though, that the instruction is too close to the condition of interest or is not properly randomized, then it becomes hard to estimate the effects of each. For example, if the instruction is for 1s followed by your condition, then its hard to separate the two events, especially if the instruction is always the same before that type of condition. Its not the orthogonality with the constant, its the lack of orthogonality/collinearity of each of the condtions that becomes an issue. Best Regards, Donald McLaren ================= D.G. McLaren, Ph.D. Postdoctoral Research Fellow, GRECC, Bedford VA Research Fellow, Department of Neurology, Massachusetts General Hospital and Harvard Medical School Office: (773) 406-2464 ===================== This e-mail contains CONFIDENTIAL INFORMATION which may contain PROTECTED HEALTHCARE INFORMATION and may also be LEGALLY PRIVILEGED and which is intended only for the use of the individual or entity named above. If the reader of the e-mail is not the intended recipient or the employee or agent responsible for delivering it to the intended recipient, you are hereby notified that you are in possession of confidential and privileged information. Any unauthorized use, disclosure, copying or the taking of any action in reliance on the contents of this information is strictly prohibited and may be unlawful. If you have received this e-mail unintentionally, please immediately notify the sender via telephone at (773) 406-2464 or email. On Thu, Feb 10, 2011 at 1:47 PM, maaike rive <[log in to unmask]> wrote: > Hi all, > > I hope you can help me with a question regarding modelling regressors of no > interest in a first level model. > I assumed it is better to model all time intervals, including the periods of > certain ''conditions''you are not interested in (for example, an > instruction period before a specific event), to reduce variancein the > signal during the conditions that you will use for further analysis that is > actually caused by conditions of no interest. > > However, nowI was told that in doing so,one wouldreduce the degree > oforthogonality of each regressor with respect to theconstant regressor. > > Now I do not know what is the best option: model every condition or only the > ones you will use for further analysis. I hopesomeone can advise me on > this! > > Thanks, > > Maaike > > > ========================================================================Date: Thu, 10 Feb 2011 19:38:43 +0000 Reply-To: Meng-Chuan Lai <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Meng-Chuan Lai <[log in to unmask]> Subject: Re: registration error under DARTEL and suggested smoothness Comments: To: John Ashburner <[log in to unmask]> Mime-Version: 1.0 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain; charset="UTF-8" Message-ID: <[log in to unmask]> Dear John, Thank you for the very valuable information. With these in mind, practically, if to run VBM and we expect to find regional differences in small areas in the brain such as hypothalamus, ventral striatum or amygdala, what would be the lowest effective smoothness for DARTEL-processed modulated images with 1mm isotropic voxels, that the registration error should have been taken care of by such smoothness? Thank you! best regards, Meng-chuan Lai ========================================================================Date: Thu, 10 Feb 2011 20:42:47 +0000 Reply-To: John Ashburner <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: John Ashburner <[log in to unmask]> Subject: Re: registration error under DARTEL and suggested smoothness Comments: To: Meng-Chuan Lai <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> These regions tend to be pretty well aligned, so you probably need a bit less than you would for the cortex. However, you may need to use some smoothing to suppress some of the aliasing effects that occur. These depend on the resolution of your original scans. At a rough guess, I'd suggest that somewhere between about 4mm and 8mm could be reasonable, although I don't have any evidence to back this up. Best regards, -John On 10 February 2011 19:38, Meng-Chuan Lai <[log in to unmask]> wrote: > Dear John, > > Thank you for the very valuable information. > > With these in mind, practically, if to run VBM and we expect to find regional differences in small areas in the brain such as hypothalamus, ventral striatum or amygdala, what would be the lowest effective smoothness for DARTEL-processed modulated images with 1mm isotropic voxels, that the registration error should have been taken care of by such smoothness? > > Thank you! > > best regards, > Meng-chuan Lai > ========================================================================Date: Thu, 10 Feb 2011 16:31:01 -0500 Reply-To: "Claire (Jung Eun) Han" <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: "Claire (Jung Eun) Han" <[log in to unmask]> Subject: Question regarding FIR and contrasts MIME-Version: 1.0 Content-Type: multipart/alternative; boundaryMessage-ID: [log in to unmask]> --000e0cd4cd4455ea25049bf44c95 Content-Type: text/plain; charset=ISO-8859-1 Hello, There are two conditions A and B I would like to compare. In fMRI model specification, I chose to use the Finite Impulse Response such that my design has 9 three-second-bins for each condition. I would like to compare the two conditions in each time bin...is it possible to do this at once? Which of the t- or f-test should I be using and what should I put for contrasts? Thanks a lot, Claire --000e0cd4cd4455ea25049bf44c95 Content-Type: text/html; charset=ISO-8859-1 Hello,

There are two conditions A and B I would like to compare.

In fMRI model specification, I chose to use the Finite Impulse Response such that my design has 9 three-second-bins for each condition.

I would like to compare the two conditions in each time bin...is it possible to do this at once? Which of the t- or f-test should I be using and what should I put for contrasts?

Thanks a lot,
Claire
--000e0cd4cd4455ea25049bf44c95-- ========================================================================Date: Thu, 10 Feb 2011 21:39:29 +0000 Reply-To: Meng-Chuan Lai <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Meng-Chuan Lai <[log in to unmask]> Subject: Re: registration error under DARTEL and suggested smoothness Comments: To: John Ashburner <[log in to unmask]> Mime-Version: 1.0 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain; charset="UTF-8" Message-ID: <[log in to unmask]> Hi John, Thanks so much. For the 4-8mm you suggested, do you mean the smoothing applied with FWHM or the effective smoothness in the data itself? I have tried a 2mm kernel which gives an effective smoothness of 5.5mm in the data itself, and it seems to pick up quite a few reasonable regions. Would you suspect this to be valid? Thanks so much for the prompt answers! best, Meng-chuan ========================================================================Date: Thu, 10 Feb 2011 17:31:16 -0500 Reply-To: Zipporah Nussbaum <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Zipporah Nussbaum <[log in to unmask]> Subject: Postdoctoral Fellowship in Cognitive Neuroscience of Memory MIME-Version: 1.0 Content-Type: text/plain; charset=windows-1252; format=flowed Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> The Rotman Research Institute of Baycrest, affiliated with the University of Toronto is offering a postdoctoral fellowship in cognitive neuroscience of memory in the laboratory of Dr. Bradley Buchsbaum. The post-doctoral fellow will collaborate in CIHR-funded research investigating the neural basis of human memory, especially short-term and episodic memory. Projects will involve the use of fMRI and MEG to study how memories are stored and represented in the brain, using both univariate and multivariate pattern recognition methods. Candidates should have interest and expertise in some of the following topics: - Cognitive neuroscience of working memory - Aging and memory - Functional neuroimaging (fMRI and MEG) - Multivariate pattern recognition applied to neuroimaging data The Rotman Institute is fully equipped for cognitive neuroscience research, with a _3 T MRI, _151 -channel CTF MEG, several EEG systems. We seek a candidate with a strong background in memory research, good computing skills, and experience with functional neuroimaging. Toronto is consistently ranked as one of the most livable cities in the world, as well as the most multicultural. It is an excellent place to work for those interested in cross-linguistic research, as native speaker populations can be found for dozens of world languages. Applicants should have a recent Ph.D. or M.D. degree, and the potential for successfully obtaining external funding. The postdoctoral position carries a term of 2 years and is potentially renewable. Bursaries are in line with the fellowship scales of the Canadian Institutes of Health Research (CIHR) and include an allowance for travel and research expenses. A minimum of 80% of each fellows time will be devoted to research and related activities. Start date is negotiable, but ideally in the spring or summer of 2011. Applicants should submit a C.V. and relevant reprints, together with a cover letter describing current research interests and future research goals, and also arrange to have three letters of reference sent independently to: Bradley Buchsbaum, Ph.D. Rotman Research Institute, Baycrest 3560 Bathurst Street, Toronto, Ontario, M6A 2E1, Canada [log in to unmask] For more information on the institute, see http://www.rotman-baycrest.on.ca/ The Rotman Research Institute welcomes applications from all qualified individuals, including members of visible groups, minorities, women, aboriginal persons, and persons with disabilities. All qualified candidates are encouraged to apply; however, Canadians and permanent residents will be given priority. ========================================================================Date: Thu, 10 Feb 2011 22:58:01 +0000 Reply-To: Courtney Kastner <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Courtney Kastner <[log in to unmask]> Subject: Extracting ROIs in SPM8 Mime-Version: 1.0 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain; charset="UTF-8" Message-ID: <[log in to unmask]> I'm using SPM8 and its functions to analyze data collected from a test with two conditions of rotation and baseline in math-gifted and average students. The end goal of my project is to extract regions of interest from the fMRI data. Is it absolutely necessary to create a design matrix and define a contrast, or is there another easier but still effective way to do this? ========================================================================Date: Fri, 11 Feb 2011 01:17:50 +0000 Reply-To: Matt Johnson <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Matt Johnson <[log in to unmask]> Subject: Standard error calculation in spm_contrasts.m - r4010 Mime-Version: 1.0 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain; charset="UTF-8" Message-ID: <[log in to unmask]> Hi SPMers. We have been doing some comparisons between different fMRI data processing methods recently, including sanity checks on the stats returned by SPM vs FSL vs done by hand. While evaluating a T-contrast (on a simple second-level one-sample T-test model), I noticed that the T-statistics returned by SPM8 r4010 were different than those returned by the equivalent FSL model or by simply running a T-test in the Matlab command window (with FSL, Matlab, and earlier SPMs being identical, within reasonable rounding error). Upon further investigation, I see that the difference arises from line 178 of spm_contrasts.m, where the parameter estimate is divided by standard error to yield the T-statistic. The line is now: Z=cB./(SE+exp(-8)*max(SE)); whereas previously it did not contain the (+exp(-8)*max(SE)) bit. I believe this is the change referred to thus in the release notes: "Problems with using SPM to test for between-subject effects in contrasts based on source reconstructed MEEG data have been finessed by lower bounding the standard error of a t-test that forces very low variance and effect-size voxels to shrink to 0. This is hidden (in spm_contrasts.m) because it will not affect normal SPMs (where the scaling of the data is roughly uniform over the image)." While the difference induced by this change is small, I think it may not be entirely inconsequential for some users. For instance, in my sample analysis, it changes the max T in the results from a "true" value of 18.37 to a value of 17.91. For smaller Ts, the change is less drastic, but it still equates to about 35 fewer voxels in the output passing an uncorrected p<.001 threshold, or about 600 fewer passing an uncorrected p<.05 threshold. This probably makes no difference for most analyses, but it might be a bit more than rounding error for those who are sticklers about precision. Of course in our local copy we can just change that line back if we want our SPM Ts to agree with the others, but I thought I'd pass this along just as an FYI to others, and/or in case the folks at the FIL might want to tweak the line in question a bit further (e.g., to only apply the standard error correction when it is needed). Cheers, Matt ========================================================================Date: Fri, 11 Feb 2011 11:00:10 +0100 Reply-To: marco tettamanti <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: marco tettamanti <[log in to unmask]> Subject: Re: DCM: mutual interactions between networks Comments: To: Darren Gitelman <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset="ISO-8859-1"; format=flowed content-transfer-encoding: 7bit Message-ID: <[log in to unmask]> Dear Darren, thank you for your useful comments! On 02/10/2011 06:05 PM, Darren Gitelman wrote: > You can deal with this by setting up the DCM file from the command > line. If you set up a simpler DCM using the GUI you will see what > fields you need. The 8 region limitation is mostly due to the gui (and > memory). I was not aware of this possibility and it is good to know. On the other hand, I would like to stick to the "relevant model space" principle as much as possible, whereby I am much more interested in network-network than in within-networks dynamics. But as you are pointing out, it may not be possible to study such modulations with DCM, at least in its current implementation. > I'm not sure how you could use a non-linear DCM in this scenario. You > can't really setup a small DCM network as an input, per se. The two > "subnetworks" would just be connected into the larger 4 region network > perhaps through a common area. This would be through an intrinsic > connection. DCM only accepts as inputs the condition-type vectors that > it extracts from an SPM.mat file. You would also need other actual > inputs into each of the subnetworks in order to drive overall system > activity. Non-linear DCM's can be used to modulate an intrinsic > connection, so perhaps you are thinking of using the 3 region > subnetworks to modulate an external input into the 4 region network? > However, I don't think you can modulate an input as DCM is currently > set up, and you would still need to drive the subnetworks in some way. One possibility I was wondering about is whether it would be possible to constrain the within-network interactions, by modelling each netwtork as a single VOI, i.e. extracting one VOI for network 1 based on a mask including the activations of areas A,B,C,D, one VOI for network 2 including areas E,F,G and one VOI for network 3 including areas H,I,J, and then study modality-dependent bilinear modulations between networks in a simple model including these three VOIs. Does this make any sense? Or do such multi-regional VOIs violate the biophysical assumptions or any other assumptions in DCM? Thank you again, Marco -- Marco Tettamanti, Ph.D. San Raffaele Scientific Institute Via Olgettina 58 I-20132 Milano, Italy Tel. ++39-02-26434888 Fax ++39-02-26434892 Email: [log in to unmask] ----------------------------------------------------------------------------------- SOSTIENI ANCHE TU LA RICERCA DEL SAN RAFFAELE. NON C'E' CURA SENZA RICERCA. Per donazioni: ccp 42437681 intestato a Fondazione Arete' Onlus del San Raffaele. Per informazioni: tel. 02.2643.4461 - www.sanraffaele.org ========================================================================Date: Fri, 11 Feb 2011 11:34:07 +0000 Reply-To: John Ashburner <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: John Ashburner <[log in to unmask]> Subject: Re: registration error under DARTEL and suggested smoothness Comments: To: Meng-Chuan Lai <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Message-ID: [log in to unmask]> It's really a matter of empiricism (although I don't actually know how to check these things properly using the SPM analysis framework), but my best guess is that between 4 and 8 mm of additional smoothing would work reasonably well. As I say, that is just a guess, and I have no idea at all really. Best regards, -John On 10 February 2011 21:39, Meng-Chuan Lai <[log in to unmask]> wrote: > Hi John, > > Thanks so much. For the 4-8mm you suggested, do you mean the smoothing applied with FWHM or the effective smoothness in the data itself? > > I have tried a 2mm kernel which gives an effective smoothness of 5.5mm in the data itself, and it seems to pick up quite a few reasonable regions. Would you suspect this to be valid? > > Thanks so much for the prompt answers! > > best, > Meng-chuan > > ========================================================================Date: Fri, 11 Feb 2011 13:30:57 +0100 Reply-To: Marko Wilke <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Marko Wilke <[log in to unmask]> Subject: Re: matlab path Comments: To: John Ashburner <[log in to unmask]> In-Reply-To: [log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1; format=flowed Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> Hello, just to mention another instance where this bugged me some time ago: if you segmented data on another machine (or before moving spm), the location of the priors used is hardcoded in the resulting seg_sn-files. Therefore, if you want to use them to normalize an image later-on, this may also result in the error you mentioned. You can check that if you load the file and check po.VG(1) and see which GM prior that refers to. Hope this helps, Marko John Ashburner wrote: > Are you trying to run a batch file? If so, the location of the tissue > probability maps will be defined by that file. > > Best regards, > -John > > On 10 February 2011 14:36, Cornelia Hummel<[log in to unmask]> wrote: >> Dear experts, >> I encounterd the following problem: >> I installed SPM8, ran matlab and SPM with the respetive path set, then moved >> the entire SPM folder to another site, changed the path in matlab, and now, >> when running segment, got the error message that the file "(previous >> folder)\spm\tpm\grey.nii" does not exist. I double checked the path setting, >> and cannot find why matlab still tries to read from the path that no longer >> exists rather than the correctly set one. (The realign and coregister >> procedures ran without problems.) >> Can anybody please help me? >> Thanks in advance, >> Cornelia >> >> >> -- >> Cornelia Hummel >> Voglerstrae 14 >> 01277 Dresden >> > -- ____________________________________________________ PD Dr. med. Marko Wilke Facharzt fr Kinder- und Jugendmedizin Leiter, Experimentelle Pdiatrische Neurobildgebung Universitts-Kinderklinik Abt. III (Neuropdiatrie) Marko Wilke, MD, PhD Pediatrician Head, Experimental Pediatric Neuroimaging University Children's Hospital Dept. III (Pediatric Neurology) Hoppe-Seyler-Str. 1 D - 72076 Tbingen, Germany Tel. +49 7071 29-83416 Fax +49 7071 29-5473 [log in to unmask] http://www.medizin.uni-tuebingen.de/kinder/epn ____________________________________________________ ========================================================================Date: Fri, 11 Feb 2011 14:21:51 +0000 Reply-To: Lena Palaniyappan <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Lena Palaniyappan <[log in to unmask]> Subject: VBM ROI Marsbar query Content-Type: text/html; charset="iso-8859-1" Content-Transfer-Encoding: quoted-printable MIME-Version: 1.0 Message-ID: <[log in to unmask]> VBM ROI Marsbar query Hi all

I am trying to calculate the volume of grey matter within a ROI defined using Marsbar (originally the binary ROI was obtained from the ‘activated’ cluster when doing a VBM analysis) in a set of 90 scans. When I extract the mean ‘time series’ value using Marsbar for each image using standard marsbar functions, I presume what I get in structural scans is the Mean VBM ‘density’. If I need the volume, I should multiply the density by total number of voxels within the mask (the mask is 1X1X1 isotropic). Is this a correct assumption?

I undertook a ‘modulated VBM’  - hope the assumptions still hold true

Cheers
Lena
 

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========================================================================Date: Fri, 11 Feb 2011 09:51:12 -0500 Reply-To: Jonathan Peelle <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Jonathan Peelle <[log in to unmask]> Subject: Re: VBM ROI Marsbar query In-Reply-To: <[log in to unmask]> Content-Type: text/plain; charset=windows-1252 Mime-Version: 1.0 (Apple Message framework v1082) Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> Hi Lena > I am trying to calculate the volume of grey matter within a ROI defined using Marsbar (originally the binary ROI was obtained from the activated cluster when doing a VBM analysis) in a set of 90 scans. When I extract the mean time series value using Marsbar for each image using standard marsbar functions, I presume what I get in structural scans is the Mean VBM density. If I need the volume, I should multiply the density by total number of voxels within the mask (the mask is 1X1X1 isotropic). Is this a correct assumption? In the modulated images, each voxel value basically represents the gray matter volume for a voxel. So, typically, this is what you would usefor example, the average values in an ROI would represent average gray matter volume within that ROI. The density/volume issue can be a bit tricky and relates to the modulated/unmodulated analyses, but in most cases the modulated analysis (as you've done) is what people want. Hope this helps! Jonathan ========================================================================Date: Fri, 11 Feb 2011 09:25:34 -0800 Reply-To: Hoameng Ung <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Hoameng Ung <[log in to unmask]> Subject: Research Assistant position at Stanford University MIME-Version: 1.0 Content-Type: multipart/alternative; boundary cf3054a48fc6ab4c049c04fe03 Message-ID: <[log in to unmask]> --20cf3054a48fc6ab4c049c04fe03 Content-Type: text/plain; charset=ISO-8859-1 *Stanford University Social Science Research Assistant* Job ID: 41512 Job Location: School of Medicine Job Category : Social Science Research Salary : 1A3 Date Posted : Feb 9, 2011 The Stanford Systems Neuroscience and Pain Lab is recruiting a full-time Social Science Research Assistant (SSRA) to assist with ongoing and new NIH funded research related to neuroimaging and pain. These studies involve structural and functional imaging in healthy individuals and patients with chronic pain, functional imaging of the cervical spinal cord, and using fMRI as a biofeedback tool (real-time fMRI neurofeedback) for pain modulation. The research assistant will work directly with postdoctoral research fellows, principal investigators, and fellow research assistants in a large, collaborative environment. This position will span multiple projects, requiring the applicant to be comfortable working in a variety of settings, prioritizing goals, and working with multiple lab members. The SSRA will assist neuroimaging research, operation of MRI scanner and other study equipment, and data pre-processing and analysis. Assistance at the scanner will include operating scanner and stimuli computers, assisting with participant set-up, and transferring and organizing data. The SSRA will also assist with implementation and maintenance of analysis software and serve as technical support for lab personnel regarding software and analyses. Familiarity with SPM (preferred), AFNI, FSL neuroimaging analysis programs is preferred. Some programming experience (eg Matlab) is preferred. The SSRA will be responsible for maintenance of psychophysical testing equipment and communication with technical support as necessary. Must be self-motivated, independent, and able to work in a fast-paced, changing environment. Applicant may also be responsible for some recruitment, scheduling, and participant procedures. The applicant must have strong interpersonal skills, be organized and detail-oriented, and able to work independently with minimal supervision. Required: Proficient with MS office, including Word and Excel. Ability to multi-task and work independently. Strong organizational skills. Familiarity with neuroscience and computer programming. A two year college degree or equivalent experience. Desired: Previous experience working with MRI scanners, MRI and fMRI processing, and neuroimaging analysis highly desirable. Knowledge of programming (eg Matlab) and statistical analyses. Comfort with multiple operating systems, including Linux. Previous experience with software packages such as SPM, FSL, and AFNI. A four-year degree desired. --20cf3054a48fc6ab4c049c04fe03 Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable

Stanford University Social Science Research Assistant

Job ID:41512

Job Location: School of Medicine

Job Category:Social Science Research

Salary:1A3

Date Posted:Feb 9, 2011

The Stanford Systems Neuroscience and Pain Lab is recruiting a full-time Social Science Research Assistant (SSRA) to assist with ongoing and new NIH funded research related to neuroimaging and pain. These studies involve structural and functional imaging in healthy individuals and patients with chronic pain, functional imaging of the cervical spinal cord, and using fMRI as a biofeedback tool (real-time fMRI neurofeedback) for pain modulation. The research assistant will work directly with postdoctoral research fellows, principal investigators, and fellow research assistants in a large, collaborative environment. This position will span multiple projects, requiring the applicant to be comfortable working in a variety of settings, prioritizing goals, and working with multiple lab members.

The SSRA will assist neuroimaging research, operation of MRI scanner and other study equipment, and data pre-processing and analysis. Assistance at the scanner will include operating scanner and stimuli computers, assisting with participant set-up, and transferring and organizing data. The SSRA will also assist with implementation and maintenance of analysis software and serve as technical support for lab personnel regarding software and analyses. Familiarity with SPM (preferred), AFNI, FSL neuroimaging analysis programs is preferred. Some programming experience (eg Matlab) is preferred. The SSRA will be responsible for maintenance of psychophysical testing equipment and communication with technical support as necessary. Must be self-motivated, independent, and able to work in a fast-paced, changing environment. Applicant may also be responsible for some recruitment, scheduling, and participant procedures. The applicant must have strong interpersonal skills, be organized and detail-oriented, and able to work independently with minimal supervision.

Required:
Proficient with MS office, including Word and Excel. Ability to multi-task and work independently. Strong organizational skills. Familiarity with neuroscience and computer programming. A two year college degree or equivalent experience.

Desired:
Previous experience working with MRI scanners, MRI and fMRI processing, and neuroimaging analysis highly desirable. Knowledge of programming (eg Matlab) and statistical analyses. Comfort with multiple operating systems, including Linux. Previous experience with software packages such as SPM, FSL, and AFNI. A four-year degree desired.

--20cf3054a48fc6ab4c049c04fe03-- ========================================================================Date: Fri, 11 Feb 2011 10:13:49 -0800 Reply-To: "Jiang, Zhiguo" <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: "Jiang, Zhiguo" <[log in to unmask]> Subject: naive quesiton about mapping between images in different space Content-Type: multipart/related; boundary="_004_D8D86424FFCFA144BDA7076B5BDF7BFC03163E9D05EMGMB6admedct_"; type="multipart/alternative" MIME-Version: 1.0 Message-ID: <[log in to unmask]> --_004_D8D86424FFCFA144BDA7076B5BDF7BFC03163E9D05EMGMB6admedct_ Content-Type: multipart/alternative; boundary="_000_D8D86424FFCFA144BDA7076B5BDF7BFC03163E9D05EMGMB6admedct_" --_000_D8D86424FFCFA144BDA7076B5BDF7BFC03163E9D05EMGMB6admedct_ Content-Type: text/plain; charset="us-ascii" Content-Transfer-Encoding: quoted-printable In spm_reslice.m , it states % Assuming that image1 has a transformation matrix M1, and image2 has a % transformation matrix M2, the mapping from image1 to image2 is: M2\M1 % (ie. from the coordinate system of image1 into millimeters, followed % by a mapping from millimeters into the space of image2). So to map a x0,y0,z0 in image1 space to image2, isn't the composite matrix M1\M2 instead of M2\M1... ? Beause we need to bring x0,y0,z0 to mm then do an inverse of M2 to image 2 ... Not sure where I got it wrong... Thanks, Tony ------------------------------------------------------------------------------------------------------------------------------ [cid:image001.jpg@01CBC9D4.606E1D30] Tony Jiang,Ph.D.|Research Scholar|University of California, Los Angeles Peter V. Ueberroth Building, Rm 2338C2|10945 Le Conte Avenue. Los Angeles,CA 90095 Tel: (310)206-1423|Email: [log in to unmask] ________________________________ IMPORTANT WARNING: This email (and any attachments) is only intended for the use of the person or entity to which it is addressed, and may contain information that is privileged and confidential. You, the recipient, are obligated to maintain it in a safe, secure and confidential manner. Unauthorized redisclosure or failure to maintain confidentiality may subject you to federal and state penalties. If you are not the intended recipient, please immediately notify us by return email, and delete this message from your computer. --_000_D8D86424FFCFA144BDA7076B5BDF7BFC03163E9D05EMGMB6admedct_ Content-Type: text/html; charset="us-ascii" Content-Transfer-Encoding: quoted-printable

In spm_reslice.m , it states

 

% Assuming that image1 has a transformation matrix M1, and image2 has a

% transformation matrix M2, the mapping from image1 to image2 is: M2\M1

% (ie. from the coordinate system of image1 into millimeters, followed

% by a mapping from millimeters into the space of image2).

 

 

 

So to map a x0,y0,z0 in image1 space to image2, isn’t the composite matrix

 

M1\M2 instead of M2\M1… ?

 

Beause  we need to bring x0,y0,z0 to mm then do an inverse of M2 to image 2 …

 

Not sure where I got it wrong…

 

 

Thanks,

 

Tony

 

------------------------------------------------------------------------------------------------------------------------------

logo

Tony Jiang,Ph.D.|Research Scholar|University of California, Los Angeles
Peter V. Ueberroth Building, Rm 2338C2|10945 Le Conte Avenue. Los Angeles,CA 90095

Tel: (310)206-1423|Email: [log in to unmask]

 

 

 



IMPORTANT WARNING: This email (and any attachments) is only intended for the use of the person or entity to which it is addressed, and may contain information that is privileged and confidential. You, the recipient, are obligated to maintain it in a safe, secure and confidential manner. Unauthorized redisclosure or failure to maintain confidentiality may subject you to federal and state penalties. If you are not the intended recipient, please immediately notify us by return email, and delete this message from your computer.
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IHGvaU/d5ee17S5rOz731N3yy1vy91b8rGD4t1mDWLqL7Grra2dtFaQ+Zje0cIOGYDgElj3PGM4P A1pQcE+bdtydtrsibUnpslZfIs+LtVtrxbOx09/NtbC1SMNtdQ0z/NO4V1VhuYL26gkZFTSi480p qzlK/wAumw5taKOyX49Tjq6TIVWKHKnBHQjg0ADMWOSck9SetGwCUAFADvMbbsydvXGTjPrjpSGN piCgBVYocqSCOhHBpAJTAcXYqEydo5AzwPw6UhiKxQ5UkEdCODQICSxyeSeSTTASgAoAKACgAoAK ACgAoAKACgAoAKACgAoAKACgAoAKACgAoAKACgAoAKACgAoAKACgAoAKACgAoAKACgAoAKACgAoA KACgAoAKACgAoAKACgAoAKACgAoAKACgAoAKACgAoAKAP//Z --_004_D8D86424FFCFA144BDA7076B5BDF7BFC03163E9D05EMGMB6admedct_-- ========================================================================Date: Fri, 11 Feb 2011 11:10:54 -0800 Reply-To: "Jiang, Zhiguo" <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: "Jiang, Zhiguo" <[log in to unmask]> Subject: Ignore my previous question Content-Type: multipart/related; boundary="_004_D8D86424FFCFA144BDA7076B5BDF7BFC03163E9D20EMGMB6admedct_"; type="multipart/alternative" MIME-Version: 1.0 Message-ID: <[log in to unmask]> --_004_D8D86424FFCFA144BDA7076B5BDF7BFC03163E9D20EMGMB6admedct_ Content-Type: multipart/alternative; boundary="_000_D8D86424FFCFA144BDA7076B5BDF7BFC03163E9D20EMGMB6admedct_" --_000_D8D86424FFCFA144BDA7076B5BDF7BFC03163E9D20EMGMB6admedct_ Content-Type: text/plain; charset="us-ascii" Content-Transfer-Encoding: quoted-printable I mistakenly read '\' as '/' Tony ------------------------------------------------------------------------------------------------------------------------------ [cid:image001.jpg@01CBC9DC.596C77E0] Tony Jiang,Ph.D.|Research Scholar|University of California, Los Angeles Peter V. Ueberroth Building, Rm 2338C2|10945 Le Conte Avenue. Los Angeles,CA 90095 Tel: (310)206-1423|Email: [log in to unmask] ________________________________ IMPORTANT WARNING: This email (and any attachments) is only intended for the use of the person or entity to which it is addressed, and may contain information that is privileged and confidential. You, the recipient, are obligated to maintain it in a safe, secure and confidential manner. Unauthorized redisclosure or failure to maintain confidentiality may subject you to federal and state penalties. If you are not the intended recipient, please immediately notify us by return email, and delete this message from your computer. --_000_D8D86424FFCFA144BDA7076B5BDF7BFC03163E9D20EMGMB6admedct_ Content-Type: text/html; charset="us-ascii" Content-Transfer-Encoding: quoted-printable

I mistakenly read ‘\’ as ‘/’

 

 

Tony

 

 

 

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Tony Jiang,Ph.D.|Research Scholar|University of California, Los Angeles
Peter V. Ueberroth Building, Rm 2338C2|10945 Le Conte Avenue. Los Angeles,CA 90095

Tel: (310)206-1423|Email: [log in to unmask]

 

 

 



IMPORTANT WARNING: This email (and any attachments) is only intended for the use of the person or entity to which it is addressed, and may contain information that is privileged and confidential. You, the recipient, are obligated to maintain it in a safe, secure and confidential manner. Unauthorized redisclosure or failure to maintain confidentiality may subject you to federal and state penalties. If you are not the intended recipient, please immediately notify us by return email, and delete this message from your computer.
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IHGvaU/d5ee17S5rOz731N3yy1vy91b8rGD4t1mDWLqL7Grra2dtFaQ+Zje0cIOGYDgElj3PGM4P A1pQcE+bdtydtrsibUnpslZfIs+LtVtrxbOx09/NtbC1SMNtdQ0z/NO4V1VhuYL26gkZFTSi480p qzlK/wAumw5taKOyX49Tjq6TIVWKHKnBHQjg0ADMWOSck9SetGwCUAFADvMbbsydvXGTjPrjpSGN piCgBVYocqSCOhHBpAJTAcXYqEydo5AzwPw6UhiKxQ5UkEdCODQICSxyeSeSTTASgAoAKACgAoAK ACgAoAKACgAoAKACgAoAKACgAoAKACgAoAKACgAoAKACgAoAKACgAoAKACgAoAKACgAoAKACgAoA KACgAoAKACgAoAKACgAoAKACgAoAKACgAoAKACgAoAKAP//Z --_004_D8D86424FFCFA144BDA7076B5BDF7BFC03163E9D20EMGMB6admedct_-- ========================================================================Date: Fri, 11 Feb 2011 19:56:43 +0000 Reply-To: Hauke Hillebrandt <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Hauke Hillebrandt <[log in to unmask]> Subject: Modelling time derivative: valid to use t-contrasts? Mime-Version: 1.0 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain Message-ID: <[log in to unmask]> Dear SPM Users, in my fMRI model specification I model the time derivative and then I use t-contrasts on the 1st and 2nd level of my analysis to get the activation maps. Now I read in the SPM manual on page 66 that this might not be okay: "The informed basis set requires an SPMF for inference. T-contrasts over just the canonical are perfectly valid but assume constant delay/dispersion." am I right that this means that I have to use f-contrasts exclusively on the 1st and 2nd level of my analysis (+the flexible factorial design option) if I model the time derivative and that I cannot use t-tests at all in this case? Best wishes, Hauke ========================================================================Date: Fri, 11 Feb 2011 16:07:58 -0500 Reply-To: Jason Steffener <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Jason Steffener <[log in to unmask]> Subject: Re: Modelling time derivative: valid to use t-contrasts? Comments: To: Hauke Hillebrandt <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/alternative; boundaryMessage-ID: [log in to unmask]> --001636c5b6bbba64f8049c081780 Content-Type: text/plain; charset=ISO-8859-1 Dear Hauke, The use of a t-test across the two regressors means that you are testing a specific relationship between the two regressors. e.g your design is: [canonical derivative] and your contrast is: [1 1] Then you are "assuming" that the canonical and derivative have equal weight. The F-test allows you to test any arbitrary relationship between the canonical and derivative regressors. I hope this helps, Jason. On Fri, Feb 11, 2011 at 2:56 PM, Hauke Hillebrandt < [log in to unmask]> wrote: > Dear SPM Users, > > in my fMRI model specification I model the time derivative and then I use > t-contrasts on the 1st and 2nd level of my analysis to get the activation > maps. Now I read in the SPM manual on page 66 that this might not be okay: > > "The informed basis set requires an SPMF for inference. T-contrasts over > just the canonical are > perfectly valid but assume constant delay/dispersion." > > am I right that this means that I have to use f-contrasts exclusively on > the 1st and 2nd level of my analysis (+the flexible factorial design option) > if I model the time derivative and that I cannot use t-tests at all in this > case? > > Best wishes, > > Hauke > -- Jason Steffener, Ph.D. Department of Neurology Columbia University http://www.cogneurosci.org/steffener.html --001636c5b6bbba64f8049c081780 Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Dear Hauke,
The use of a t-test across the two regressors means that you are testing a specific relationship between the two regressors.
e.g your design is:
[canonical derivative]
and your contrast is:
[1 1]
Then you are "assuming" that the canonical and derivative have equal weight.
The F-test allows you to test any arbitrary relationship between the canonical and derivative regressors.


I hope this helps,
Jason.


On Fri, Feb 11, 2011 at 2:56 PM, Hauke Hillebrandt <[log in to unmask]> wrote:
Dear SPM Users,

in my fMRI model specification I model the time derivative and then I use t-contrasts on the 1st and 2nd level of my analysis to get the activation maps. Now I read in the SPM manual on page 66 that this might not be okay:

"The informed basis set requires an SPMF for inference. T-contrasts over just the canonical are
perfectly valid but assume constant delay/dispersion."

am I right that this means that I have to use f-contrasts exclusively on the 1st and 2nd level of my analysis (+the flexible factorial design option) if I model the time derivative and that I cannot use t-tests at all in this case?

Best wishes,

Hauke



--
Jason Steffener, Ph.D.
Department of Neurology
Columbia University
http://www.cogneurosci.org/steffener.html
--001636c5b6bbba64f8049c081780-- ========================================================================Date: Fri, 11 Feb 2011 14:03:33 -0800 Reply-To: Manish Dalwani <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Manish Dalwani <[log in to unmask]> Subject: Why should I use SPM8 vs SPM5? MIME-Version: 1.0 Content-Type: multipart/alternative; boundary="0-466683208-1297461813=:75525" Message-ID: <[log in to unmask]> --0-466683208-1297461813=:75525 Content-Type: text/plain; charset=iso-8859-1 Content-Transfer-Encoding: quoted-printable Hello SPM'ers, Can experts please advice on why I should switch from SPM8 from SPM5? Regards,Manish DalwaniSr. PRADept. of PsychiatryUniversity of Colorado --0-466683208-1297461813=:75525 Content-Type: text/html; charset=iso-8859-1 Content-Transfer-Encoding: quoted-printable
Hello SPM'ers, 

Can experts please advice on why I should switch from SPM8 from SPM5?

Regards,
Manish Dalwani
Sr. PRA
Dept. of Psychiatry
University of Colorado

--0-466683208-1297461813=:75525-- ========================================================================Date: Fri, 11 Feb 2011 14:33:49 -0800 Reply-To: Michael T Rubens <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Michael T Rubens <[log in to unmask]> Subject: Re: Modelling time derivative: valid to use t-contrasts? Comments: To: Hauke Hillebrandt <[log in to unmask]> In-Reply-To: [log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/alternative; boundary cf30549f638ad175049c094c9f Message-ID: <[log in to unmask]> --20cf30549f638ad175049c094c9f Content-Type: text/plain; charset=UTF-8 I think this is a good question Hauke. If I understand you correctly, you'd want to do a comparison of 2 conditions, each with an informed basis set. i.e., [A-hrf A-tderiv B-hrf B-tderiv] [ 1 1 -1 -1 ] to my understanding that makes sense, but i'd like to hear other opinions. Cheers, Michael On Fri, Feb 11, 2011 at 1:07 PM, Jason Steffener <[log in to unmask]>wrote: > Dear Hauke, > The use of a t-test across the two regressors means that you are testing a > specific relationship between the two regressors. > e.g your design is: > [canonical derivative] > and your contrast is: > [1 1] > Then you are "assuming" that the canonical and derivative have equal > weight. > The F-test allows you to test any arbitrary relationship between the > canonical and derivative regressors. > > > I hope this helps, > Jason. > > > > On Fri, Feb 11, 2011 at 2:56 PM, Hauke Hillebrandt < > [log in to unmask]> wrote: > >> Dear SPM Users, >> >> in my fMRI model specification I model the time derivative and then I use >> t-contrasts on the 1st and 2nd level of my analysis to get the activation >> maps. Now I read in the SPM manual on page 66 that this might not be okay: >> >> "The informed basis set requires an SPMF for inference. T-contrasts over >> just the canonical are >> perfectly valid but assume constant delay/dispersion." >> >> am I right that this means that I have to use f-contrasts exclusively on >> the 1st and 2nd level of my analysis (+the flexible factorial design option) >> if I model the time derivative and that I cannot use t-tests at all in this >> case? >> >> Best wishes, >> >> Hauke >> > > > > -- > Jason Steffener, Ph.D. > Department of Neurology > Columbia University > http://www.cogneurosci.org/steffener.html > -- Research Associate Gazzaley Lab Department of Neurology University of California, San Francisco --20cf30549f638ad175049c094c9f Content-Type: text/html; charset=UTF-8 Content-Transfer-Encoding: quoted-printable I think this is a good question Hauke. If I understand you correctly, you'd want to do a comparison of 2 conditions, each with an informed basis set. i.e.,

[A-hrf A-tderiv  B-hrf B-tderiv]

[   1        1         -1       -1   ]

to my understanding that makes sense, but i'd like to hear other opinions.

Cheers,
Michael

On Fri, Feb 11, 2011 at 1:07 PM, Jason Steffener <[log in to unmask]> wrote:
Dear Hauke,
The use of a t-test across the two regressors means that you are testing a specific relationship between the two regressors.
e.g your design is:
[canonical derivative]
and your contrast is:
[1 1]
Then you are "assuming" that the canonical and derivative have equal weight.
The F-test allows you to test any arbitrary relationship between the canonical and derivative regressors.


I hope this helps,
Jason.



On Fri, Feb 11, 2011 at 2:56 PM, Hauke Hillebrandt <[log in to unmask]> wrote:
Dear SPM Users,

in my fMRI model specification I model the time derivative and then I use t-contrasts on the 1st and 2nd level of my analysis to get the activation maps. Now I read in the SPM manual on page 66 that this might not be okay:

"The informed basis set requires an SPMF for inference. T-contrasts over just the canonical are
perfectly valid but assume constant delay/dispersion."

am I right that this means that I have to use f-contrasts exclusively on the 1st and 2nd level of my analysis (+the flexible factorial design option) if I model the time derivative and that I cannot use t-tests at all in this case?

Best wishes,

Hauke



--
Jason Steffener, Ph.D.
Department of Neurology
Columbia University
http://www.cogneurosci.org/steffener.html



--
Research Associate
Gazzaley Lab
Department of Neurology
University of California, San Francisco
--20cf30549f638ad175049c094c9f-- ========================================================================Date: Fri, 11 Feb 2011 18:44:08 -0500 Reply-To: "MCLAREN, Donald" <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: "MCLAREN, Donald" <[log in to unmask]> Subject: Re: Why should I use SPM8 vs SPM5? Comments: To: Manish Dalwani <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Message-ID: <[log in to unmask]> Switching from 5 to 8 as newer algorithms and bug fixes are employed. The newer algorithms address concerns of the field such as registration accuracy. Also, only 8 is really supported. Can't think of any reason to go back to 5. On Friday, February 11, 2011, Manish Dalwani <[log in to unmask]> wrote: > Hello SPM'ers, > Can experts please advice on why I should switch from SPM8 from SPM5? > Regards,Manish DalwaniSr. PRADept. of PsychiatryUniversity of Colorado > -- Best Regards, Donald McLaren ================D.G. McLaren, Ph.D. Postdoctoral Research Fellow, GRECC, Bedford VA Research Fellow, Department of Neurology, Massachusetts General Hospital and Harvard Medical School Office: (773) 406-2464 ====================This e-mail contains CONFIDENTIAL INFORMATION which may contain PROTECTED HEALTHCARE INFORMATION and may also be LEGALLY PRIVILEGED and which is intended only for the use of the individual or entity named above. If the reader of the e-mail is not the intended recipient or the employee or agent responsible for delivering it to the intended recipient, you are hereby notified that you are in possession of confidential and privileged information. Any unauthorized use, disclosure, copying or the taking of any action in reliance on the contents of this information is strictly prohibited and may be unlawful. If you have received this e-mail unintentionally, please immediately notify the sender via telephone at (773) 406-2464 or email. ========================================================================Date: Fri, 11 Feb 2011 20:52:23 -0500 Reply-To: Jonathan Peelle <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Jonathan Peelle <[log in to unmask]> Subject: Re: Modelling time derivative: valid to use t-contrasts? In-Reply-To: <[log in to unmask]> Content-Type: text/plain; charset=windows-1252 Mime-Version: 1.0 (Apple Message framework v1082) Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> What we usually want to know when doing fMRI analyses is whether a region is "active" or not. When modeling with just a canonical HRF, this is fairly simple, as a positive parameter estimate (beta value) means that there was a response that matched the canonical HRF, which we can fairly safely interpret as "activation" (i.e., increase in signal that is time-locked to some stimulus category at about the time we expect). The tricky thing about interpreting any other type of basis set is how it relates to "activation" (assuming this is what we're interested in). In general, the effect of the derivatives is really only interpretable in relation to a reliable positive loading on the canonical HRF. I.e., if you have an HRF-like shape, the derivatives can tell you about how the observed response differs from canonical. But you could imagine a situation in which you have a significant weighting on a derivative, but not on the canonical. In these situations it's quite difficult to interpret the result. Getting back to the point at hand, if you model conditions A and B with [Ahrf Atemp_deriv Bhrf Btemp_deriv] then the contrast [1 1 0 0] will give you the effect of the *average* of the canonical and temporal derivative. But this is sort of a meaningless measure; it would give the same result for something that is really well-explained by the canonical only, really well-explained by the temporal derivative only, or explained by equal contributions from the two. The most straightforward way to assess "activation" would be to just look at the canonical HRF: [1 0 0 0] Or, if you want to look for "informed" effects, use an F test: [1 0 0 0 0 1 0 0] see Chapter 30 in the SPM manual, for example (Face Group Data). For comparing across groups, the same logic holds: the most straightforward way to assess "activation" would be to just compare the canonical HRFs: [1 0 -1 0] and if you wanted to compare more, you could use an F test: [1 0 -1 0 0 1 0 -1] but you still run into non-straightforward interpretations, because a significant F value doesn't tell you (a) in which direction the effect is, or (b) whether the difference is on the canonical HRF or the derivative. The following papers are very helpfulsurely moreso than my attempt above. :) Henson, R.N.A., Price, C.J., Rugg, M.D., Turner, R., Friston, K.J., 2002. Detecting latency differences in event-related BOLD responses: Application to words versus nonwords and initial versus repeated face presentations. NeuroImage 15, 83-97. Calhoun, V.D., Stevens, M.C., Pearlson, G.D., Kiehl, K.A., 2004. fMRI analysis with the general linear model: removal of latency-induced amplitude bias by incorporation of hemodynamic derivative terms. NeuroImage 22, 252-257. Hope this helps, Jonathan -- Dr. Jonathan Peelle Department of Neurology University of Pennsylvania 3 West Gates 3400 Spruce Street Philadelphia, PA 19104 USA http://jonathanpeelle.net/ On Feb 11, 2011, at 5:33 PM, Michael T Rubens wrote: > I think this is a good question Hauke. If I understand you correctly, you'd want to do a comparison of 2 conditions, each with an informed basis set. i.e., > > [A-hrf A-tderiv B-hrf B-tderiv] > > [ 1 1 -1 -1 ] > > to my understanding that makes sense, but i'd like to hear other opinions. > > Cheers, > Michael > > On Fri, Feb 11, 2011 at 1:07 PM, Jason Steffener <[log in to unmask]> wrote: > Dear Hauke, > The use of a t-test across the two regressors means that you are testing a specific relationship between the two regressors. > e.g your design is: > [canonical derivative] > and your contrast is: > [1 1] > Then you are "assuming" that the canonical and derivative have equal weight. > The F-test allows you to test any arbitrary relationship between the canonical and derivative regressors. > > > I hope this helps, > Jason. > > > > On Fri, Feb 11, 2011 at 2:56 PM, Hauke Hillebrandt <[log in to unmask]> wrote: > Dear SPM Users, > > in my fMRI model specification I model the time derivative and then I use t-contrasts on the 1st and 2nd level of my analysis to get the activation maps. Now I read in the SPM manual on page 66 that this might not be okay: > > "The informed basis set requires an SPMF for inference. T-contrasts over just the canonical are > perfectly valid but assume constant delay/dispersion." > > am I right that this means that I have to use f-contrasts exclusively on the 1st and 2nd level of my analysis (+the flexible factorial design option) if I model the time derivative and that I cannot use t-tests at all in this case? > > Best wishes, > > Hauke > ========================================================================Date: Sat, 12 Feb 2011 11:20:32 +0800 Reply-To: Xinian Zuo <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Xinian Zuo <[log in to unmask]> Subject: Opening positions Comments: To: fsl <[log in to unmask]>, [log in to unmask] Comments: cc: ZANG Yu-Feng <[log in to unmask]>, Xuchu Weng <[log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/alternative; boundary cf305644d323d10c049c0d4c9c Message-ID: <[log in to unmask]> --20cf305644d323d10c049c0d4c9c Content-Type: text/plain; charset=ISO-8859-1 Opening positions (postdoc, research assistant, or professorship) for collaborative projects from the Center for Human Brain Research, Hangzhou Normal University (Professor WENG Xuchu, [log in to unmask]), Key Laboratory of Cognitive Neuroscience and Learning, Beijing Normal University (Professor ZANG Yufeng, [log in to unmask]), and Institute of Psychology, Chinese Academy of Science (Professor ZUO Xi-Nian, [log in to unmask]). Any applicant with relevant neuroimaging background is welcome, including neuroscience, medicine, psychology, biology, physics, mathematics, computer and information science, and so on. Salary and compensation are almost the best in China. Please send your CV to any of the three e-mail addresses listed above if you are interested in these jobs. -- Xi-Nian Zuo, Ph.D of Applied Mathematics (http://lfcd.psych.ac.cn) --20cf305644d323d10c049c0d4c9c Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Opening positions (postdoc, research assistant, or professorship) for collaborative projects from the Center for Human Brain Research, Hangzhou Normal University (Professor WENG Xuchu, [log in to unmask]), Key Laboratory of Cognitive Neuroscience and Learning, Beijing Normal University (Professor ZANG Yufeng, [log in to unmask]), and Institute of Psychology, Chinese Academy of Science (Professor ZUO Xi-Nian, [log in to unmask]). Any applicant with relevant neuroimaging background is welcome, including neuroscience, medicine, psychology, biology, physics, mathematics, computer and information science, and so on. Salary and compensation are almost the best in China.

Please send your CV to any of the three e-mail addresses listed above if you are interested in these jobs.
--
Xi-Nian Zuo, Ph.D of Applied Mathematics (http://lfcd.psych.ac.cn)



--20cf305644d323d10c049c0d4c9c-- ========================================================================Date: Fri, 11 Feb 2011 22:57:17 -0500 Reply-To: hekmatyar <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: hekmatyar <[log in to unmask]> Subject: Re: coregistration problem In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset="us-ascii" Content-Transfer-Encoding: 7bit Message-ID: <[log in to unmask]> Hi All I try to co register mean functional (EPI) to anatomical (T2 weighted) using spm99, it does coregister, but not good, kind of distorted and did not do properly. When I tried to use spm8, after co-registration, it puts one of my coronal view into saggital plane, it completely screws up. I even tried mutual information selection, it did not work.I am wondering that what might be causing the orientation swap. Please let me know. Thanks Khan Hekmatyar BioImaging Research Center University of Georgia Athens, GA-30606 ========================================================================Date: Sat, 12 Feb 2011 11:54:42 +0100 Reply-To: Lin Wang <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Lin Wang <[log in to unmask]> Subject: Re: 'NaN' in cluster level p value In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/alternative; boundaryMessage-ID: <[log in to unmask]> --0016e644c79c5d9991049c13a4c9 Content-Type: text/plain; charset=ISO-8859-1 Dear all, I realized that I incorrectly took the SPM[T] values for the 2nd-level statistical analysis, which leads to the NaNs. Now I know I should use the contrast images for the group analysis. But I still don't get it why the use of SPM[T] values will give me NaNs in the statistical results... Best, Lin 2011/2/7 Lin Wang <[log in to unmask]> > Dear all, > > I got the same problem after running the 2nd-level statistical analysis. > The cluster-level p values are NaNs, and I get the following warning when I > click "whole brain" to show all the clusters: > > Warning: Returning NaN for out of range arguments > > In spm_Pcdf at 88 > In spm_P_RF at 106 > In spm_P at 48 > In spm_list at 487 > > I searched the documents, but I couldn't find a clear answer for it. Could > anyone help me with it? > > Thanks very much. > > Best, > Lin > > --0016e644c79c5d9991049c13a4c9 Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Dear all,

I realized that I incorrectly took the SPM[T] values for the 2nd-level statistical analysis, which leads to the NaNs.

Now I know I should use the contrast images for the group analysis. But I still don't get it why the use of SPM[T] values will give me NaNs in the statistical results...

Best,
Lin

2011/2/7 Lin Wang <[log in to unmask]>
Dear all,

I got the same problem after running the 2nd-level statistical analysis. The cluster-level p values are NaNs, and I get the following warning when I click "whole brain" to show all the clusters:

Warning: Returning NaN for out of range arguments
> In spm_Pcdf at 88
In spm_P_RF at 106
In spm_P at 48
In spm_list at 487

I searched the documents, but I couldn't find a clear answer for it. Could anyone help me with it?

Thanks very much.

Best,
Lin


--0016e644c79c5d9991049c13a4c9-- ========================================================================Date: Sat, 12 Feb 2011 17:43:10 +0000 Reply-To: "Stephen J. Fromm" <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: "Stephen J. Fromm" <[log in to unmask]> Subject: spm_api_bmc.m: typo in help comments? Mime-Version: 1.0 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain; charset="UTF-8" Message-ID: <[log in to unmask]> The beginning of SPM8: spm_api_bmc.m reads: function out=spm_api_bmc(F,N,exp_r,xp,family) % API to select and compare DCMs using Bayesian model comparison % FORMAT out=spm_api_bmc(F,N,alpha,exp_r,xp) % % INPUT: % F - Matrix/Vector of log model evidences % N - vector of model names % alpha - vector of model probabilities % exp_r - expectation of the posterior p(r|y) % xp - exceedance probabilities % % OUTPUT: % out - conditional probability of DCMs (when using fixed effect method) %__________________________________________________________________________ % Copyright (C) 2008 Wellcome Trust Centre for Neuroimaging The actual function prototype and the one in the help under FORMAT don't seem to match. ========================================================================Date: Sat, 12 Feb 2011 17:47:13 +0000 Reply-To: "Stephen J. Fromm" <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: "Stephen J. Fromm" <[log in to unmask]> Subject: DCM theory: def'n of exceedance prob.? Mime-Version: 1.0 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain; charset="UTF-8" Message-ID: <[log in to unmask]> Equation (16) of Stephan et al., "Bayesian model selection for group studies" (2009, NeuroImage) is: -------------------------------------------------- For all j in {1, 2, ..., K | j=/=k}: phi_k = p(r_k > r_j | y; alpha). -------------------------------------------------- This doesn't make sense to me as written. I would assume it's something like -------------------------------------------------- phi_k = p(r_k > r_j for all j=/=k | y; alpha). -------------------------------------------------- ========================================================================Date: Sun, 13 Feb 2011 04:27:28 +0000 Reply-To: Yang Hu <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Yang Hu <[log in to unmask]> Subject: about ROI signal value Mime-Version: 1.0 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain; charset="UTF-8" Message-ID: <[log in to unmask]> Dear Experts, Based on whole-brain analysis via SPM8 (1st- and 2nd-level analysis), I want to extract signal value from atlas-based ROIs (e.g. amygdala) in four experimental conditions, compared with rest condition respectively, by AFNI rather than MarsBar. Specific steps are listed as follows: 1. Mask generation: by WFU pickatlas, an file of ROI in amygdala (named as "amy.nii") was generated 2. File conversion: by AFNI command "3dcopy", the "amy.nii" was converted to "amy+orig.BRIK/HEAD", which could be recognized by AFNI 3. ROI calculation: by AFNI command "3dmaskave", the average value within the ROI mask (amygdala) of each subject (sbj**) in certain condition (con_000*) could be obtained; Specifically, the full command is like that "3dmaskave -quiet -mask amy+orig sbj**_con_000*.hdr". The file "sbj**_con_000*.hdr" was generated after 1st-level analysis via SPM8. So I just wonder the meaning of ROI value obtained through those steps mentioned above. Whether does the value mean percent signal change (PSC), contrast value (CV), or parameter estimates (PE) ? And what's the difference between the three terms (namely PSC, CV, PE) always used in ROI analysis? Thanks a lot for your help and comment! Yang Hu ICN, ECNU, Shanghai, China ========================================================================Date: Sun, 13 Feb 2011 09:40:33 +0000 Reply-To: William Sohn <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: William Sohn <[log in to unmask]> Subject: MEG data conversion Mime-Version: 1.0 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain; charset="UTF-8" Message-ID: <[log in to unmask]> Dear SPM community, I have some MEG data and I want to run analysis using SPM. The data format is a bin cue format but I can export data into a text format. Data is arranged where channels are in columns. I was wondering how I can convert this into a format where I can read in SPM. Thank you, -William Sohn ========================================================================Date: Sun, 13 Feb 2011 17:59:34 +0800 Reply-To: Brahim HAMADICHAREF <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Brahim HAMADICHAREF <[log in to unmask]> Subject: Re: MEG data conversion Comments: To: [log in to unmask] In-Reply-To: <[log in to unmask]> Content-Type: multipart/alternative; boundary="_33766111-2257-41d1-9795-31c473c69fcf_" MIME-Version: 1.0 Message-ID: <[log in to unmask]> --_33766111-2257-41d1-9795-31c473c69fcf_ Content-Type: text/plain; charset="gb2312" Content-Transfer-Encoding: 8bit Maybe by using biosig to import the data and save it into a standardand known format by SPM ... GDF for e.g. although I am not sure whatSPM8 recognize ... Brahim > Date: Sun, 13 Feb 2011 09:40:33 +0000 > From: [log in to unmask] > Subject: [SPM] MEG data conversion > To: [log in to unmask] > > Dear SPM community, > > I have some MEG data and I want to run analysis using SPM. The data format is a bin cue format but I can export data into a text format. Data is arranged where channels are in columns. > > I was wondering how I can convert this into a format where I can read in SPM. > > Thank you, > > -William Sohn --_33766111-2257-41d1-9795-31c473c69fcf_ Content-Type: text/html; charset="gb2312" Content-Transfer-Encoding: 8bit Maybe by using biosig to import the data and save it into a standard
and known format by SPM ... GDF for e.g. although I am not sure what
SPM8 recognize ... 

Brahim  


> Date: Sun, 13 Feb 2011 09:40:33 +0000
> From: [log in to unmask]
> Subject: [SPM] MEG data conversion
> To: [log in to unmask]
>
> Dear SPM community,
>
> I have some MEG data and I want to run analysis using SPM. The data format is a bin cue format but I can export data into a text format. Data is arranged where channels are in columns.
>
> I was wondering how I can convert this into a format where I can read in SPM.
>
> Thank you,
>
> -William Sohn
--_33766111-2257-41d1-9795-31c473c69fcf_-- ========================================================================Date: Sun, 13 Feb 2011 11:45:19 +0000 Reply-To: Vladimir Litvak <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Vladimir Litvak <[log in to unmask]> Subject: Re: MEG data conversion Comments: To: William Sohn <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> Dear William, In SPM manual you can find 'Converting arbitrary data' section which explains what you should do. There is also an example script mentioned there. This will be sufficient to convert your channel data. However, you also need your sensor locations and for this you will need the data in their original format. For some analyses you might manage without, but it depends on what exactly you want to do. Best, Vladimir On Sun, Feb 13, 2011 at 9:40 AM, William Sohn <[log in to unmask]> wrote: > Dear SPM community, > > I have some MEG data and I want to run analysis using SPM. The data format is a bin cue format but I can export data into a text format. Data is arranged where channels are in columns. > > I was wondering how I can convert this into a format where I can read in SPM. > > Thank you, > > -William Sohn > ========================================================================Date: Sun, 13 Feb 2011 12:00:23 +0000 Reply-To: Viridiana Mazzola <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Viridiana Mazzola <[log in to unmask]> Subject: extract ROI at the edge of the cerebellum Mime-Version: 1.0 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain; charset="UTF-8" Message-ID: <[log in to unmask]> Dear all, I am trying to extract a ROI at the edge of the cerebellum following the Brett's FAQ instructions. 1 . I rename the ROI my_roi.mat, then I write in matlab the command: roi_filename = 'my_roi.mat'; my_roi = maroi(roi_filename); my_roi = spm_hold(my_roi, 0); % set NN resampling saveroi(my_roi, roi_filename); 2. then I rerun the extraction of my_roi, but this error appears: Fetching data : 1/1 Error in ==> maroi.getdata at 30 if nargin < 2 ??? Output argument "vXYZ" (and maybe others) not assigned during call to "[log in to unmask] (getdata)". Error in ==> maroi.get_marsy at 76 [y vals vXYZ mat] = getdata(o, VY); Error in ==> marsbar at 985 marsY = get_marsy(o{:}, VY, sumfunc, 'v'); Error in ==> spm at 964 evalin('base',CBs{v-1}) ??? Error while evaluating uicontrol Callback => Where am I wrong? Thank you for your attention! Viridiana NeuroLab IPRA ========================================================================Date: Sun, 13 Feb 2011 12:42:14 +0000 Reply-To: Klaas Enno Stephan <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Klaas Enno Stephan <[log in to unmask]> Subject: Re: DCM theory: def'n of exceedance prob.? Comments: To: "Stephen J. Fromm" <[log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/alternative; boundary="0-994732579-1297600934=:1208" Message-ID: <[log in to unmask]> --0-994732579-1297600934=:1208 Content-Type: text/plain; charset=utf-8 Content-Transfer-Encoding: quoted-printable Dear Stephen, I am sorry if my mathematical notation confused you (the convention I grew up with is that existential and universal quantifiers precede set-theoretic statements). The equation means exactly what you express in your reformulation. Best wishes, Klaas ________________________________ Von: Stephen J. Fromm <[log in to unmask]> An: [log in to unmask] Gesendet: Samstag, den 12. Februar 2011, 18:47:13 Uhr Betreff: [SPM] DCM theory: def'n of exceedance prob.? Equation (16) of Stephan et al., "Bayesian model selection for group studies" (2009, NeuroImage) is: -------------------------------------------------- For all j in {1, 2, ..., K | j=/=k}: phi_k = p(r_k > r_j | y; alpha). -------------------------------------------------- This doesn't make sense to me as written. I would assume it's something like -------------------------------------------------- phi_k = p(r_k > r_j for all j=/=k | y; alpha). -------------------------------------------------- --0-994732579-1297600934=:1208 Content-Type: text/html; charset=utf-8 Content-Transfer-Encoding: quoted-printable
Dear Stephen,

I am sorry if my mathematical notation confused you (the convention I grew up with is that existential and universal quantifiers precede set-theoretic statements).  The equation means exactly what you express in your reformulation. 

Best wishes,
Klaas



Von: Stephen J. Fromm <[log in to unmask]>
An: [log in to unmask]
Gesendet: Samstag, den 12. Februar 2011, 18:47:13 Uhr
Betreff: [SPM] DCM theory: def'n of exceedance prob.?

Equation (16) of Stephan et al., "Bayesian model selection for group studies" (2009, NeuroImage) is:

--------------------------------------------------

For all j in {1, 2, ..., K | j=/=k}:

phi_k = p(r_k > r_j | y; alpha).

--------------------------------------------------

This doesn't make sense to me as written.  I would assume it's something like

--------------------------------------------------

phi_k = p(r_k > r_j  for all j=/=k | y; alpha).

--------------------------------------------------

--0-994732579-1297600934=:1208-- ========================================================================Date: Sun, 13 Feb 2011 08:38:39 -0500 Reply-To: "Fromm, Stephen (NIH/NIMH) [C]" <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: "Fromm, Stephen (NIH/NIMH) [C]" <[log in to unmask]> Subject: Re: DCM theory: def'n of exceedance prob.? Comments: To: Klaas Enno Stephan <[log in to unmask]> In-Reply-To: <[log in to unmask]> Content-Type: text/plain; charset="iso-8859-1" Content-Transfer-Encoding: quoted-printable MIME-Version: 1.0 Message-ID: <[log in to unmask]> Klaas, Thanks for your timely response! Very interesting paper. Cheers, Stephen J. Fromm, PhD Contractor, NIMH/MAP (301) 451--9265 ________________________________ From: Klaas Enno Stephan [[log in to unmask]] Sent: Sunday, February 13, 2011 7:42 AM To: Fromm, Stephen (NIH/NIMH) [C]; [log in to unmask] Subject: RE: [SPM] DCM theory: def'n of exceedance prob.? Dear Stephen, I am sorry if my mathematical notation confused you (the convention I grew up with is that existential and universal quantifiers precede set-theoretic statements). The equation means exactly what you express in your reformulation. Best wishes, Klaas ________________________________ Von: Stephen J. Fromm <[log in to unmask]> An: [log in to unmask] Gesendet: Samstag, den 12. Februar 2011, 18:47:13 Uhr Betreff: [SPM] DCM theory: def'n of exceedance prob.? Equation (16) of Stephan et al., "Bayesian model selection for group studies" (2009, NeuroImage) is: -------------------------------------------------- For all j in {1, 2, ..., K | j=/=k}: phi_k = p(r_k > r_j | y; alpha). -------------------------------------------------- This doesn't make sense to me as written. I would assume it's something like -------------------------------------------------- phi_k = p(r_k > r_j for all j=/=k | y; alpha). -------------------------------------------------- ========================================================================Date: Sun, 13 Feb 2011 14:39:21 +0000 Reply-To: Klaas Enno Stephan <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Klaas Enno Stephan <[log in to unmask]> Subject: Re: DCM theory: def'n of exceedance prob.? Comments: To: "Fromm, Stephen (NIH/NIMH) [C]" <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/alternative; boundary="0-1462288926-1297607961=:62528" Message-ID: <[log in to unmask]> --0-1462288926-1297607961=:62528 Content-Type: text/plain; charset=utf-8 Content-Transfer-Encoding: quoted-printable Thank you, Stephen. To prevent any further confusion, let me point out that there is a typo in Eq. A.3 in the appendix. The log's are missing for the first two terms on the right hand side, i.e. the equation should read: KL[q(theta)|p(theta|m)] = 0.5*log(det(C_theta)) - 0.5*log(det(C_theta|y)) + ... There is an erratum at this address: http://www.sciencedirect.com/science?_ob=ArticleURL&_udi=B6WNP-4WNWRT0-1&_user=10&_coverDate=10%2F15%2F2009&_rdoc=1&_fmt=high&_orig=browse&_origin=browse&_zone=rslt_list_item&_cdi=6968&_sort=d&_docanchor=&view=c&_ct=1&_refLink=Y&_acct=C000050221&_version=1&_urlVersion=0&_userid=10&md5=9790004e41680cc8dbdadb633ac5d207&searchtype=a Best wishes, Klaas ________________________________ Von: "Fromm, Stephen (NIH/NIMH) [C]" <[log in to unmask]> An: [log in to unmask] Gesendet: Sonntag, den 13. Februar 2011, 14:38:39 Uhr Betreff: Re: [SPM] DCM theory: def'n of exceedance prob.? Klaas, Thanks for your timely response! Very interesting paper. Cheers, Stephen J. Fromm, PhD Contractor, NIMH/MAP (301) 451--9265 ________________________________ From: Klaas Enno Stephan [[log in to unmask]] Sent: Sunday, February 13, 2011 7:42 AM To: Fromm, Stephen (NIH/NIMH) [C]; [log in to unmask] Subject: RE: [SPM] DCM theory: def'n of exceedance prob.? Dear Stephen, I am sorry if my mathematical notation confused you (the convention I grew up with is that existential and universal quantifiers precede set-theoretic statements). The equation means exactly what you express in your reformulation. Best wishes, Klaas ________________________________ Von: Stephen J. Fromm <[log in to unmask]> An: [log in to unmask] Gesendet: Samstag, den 12. Februar 2011, 18:47:13 Uhr Betreff: [SPM] DCM theory: def'n of exceedance prob.? Equation (16) of Stephan et al., "Bayesian model selection for group studies" (2009, NeuroImage) is: -------------------------------------------------- For all j in {1, 2, ..., K | j=/=k}: phi_k = p(r_k > r_j | y; alpha). -------------------------------------------------- This doesn't make sense to me as written. I would assume it's something like -------------------------------------------------- phi_k = p(r_k > r_j for all j=/=k | y; alpha). -------------------------------------------------- --0-1462288926-1297607961=:62528 Content-Type: text/html; charset=utf-8 Content-Transfer-Encoding: quoted-printable
Thank you, Stephen.

To prevent any further confusion, let me point out that there is a typo in Eq. A.3 in the appendix.  The log's are missing for the first two terms on the right hand side, i.e. the equation should read:

KL[q(theta)|p(theta|m)] = 0.5*log(det(C_theta)) - 0.5*log(det(C_theta|y)) + ...

There is an erratum at this address:
http://www.sciencedirect.com/science?_ob=ArticleURL&_udi=B6WNP-4WNWRT0-1&_user=10&_coverDate=10%2F15%2F2009&_rdoc=1&_fmt=high&_orig=browse&_origin=browse&_zone=rslt_list_item&_cdi=6968&_sort=d&_docanchor=&view=c&_ct=1&_refLink=Y&_acct=C000050221&_version=1&_urlVersion=0&_userid=10&md5=9790004e41680cc8dbdadb633ac5d207&searchtype=a

Best wishes,
Klaas




Von: "Fromm, Stephen (NIH/NIMH) [C]" <[log in to unmask]>
An: [log in to unmask]
Gesendet: Sonntag, den 13. Februar 2011, 14:38:39 Uhr
Betreff: Re: [SPM] DCM theory: def'n of exceedance prob.?

Klaas,

Thanks for your timely response!  Very interesting paper.

Cheers,

Stephen J. Fromm, PhD
Contractor, NIMH/MAP
(301) 451--9265

________________________________
From: Klaas Enno Stephan [[log in to unmask]]
Sent: Sunday, February 13, 2011 7:42 AM
To: Fromm, Stephen (NIH/NIMH) [C]; [log in to unmask]
Subject: RE: [SPM] DCM theory: def'n of exceedance prob.?

Dear Stephen,

I am sorry if my mathematical notation confused you (the convention I grew up with is that existential and universal quantifiers precede set-theoretic statements).  The equation means exactly what you express in your reformulation.

Best wishes,
Klaas


________________________________
Von: Stephen J. Fromm <[log in to unmask]>
An: [log in to unmask]
Gesendet: Samstag, den 12. Februar 2011, 18:47:13 Uhr
Betreff: [SPM] DCM theory: def'n of exceedance prob.?

Equation (16) of Stephan et al., "Bayesian model selection for group studies" (2009, NeuroImage) is:

--------------------------------------------------

For all j in {1, 2, ..., K | j=/=k}:

phi_k = p(r_k > r_j | y; alpha).

--------------------------------------------------

This doesn't make sense to me as written.  I would assume it's something like

--------------------------------------------------

phi_k = p(r_k > r_j  for all j=/=k | y; alpha).

--------------------------------------------------

--0-1462288926-1297607961=:62528-- ========================================================================Date: Sun, 13 Feb 2011 15:34:23 -0500 Reply-To: Jason Steffener <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Jason Steffener <[log in to unmask]> Subject: Re: Modelling time derivative: valid to use t-contrasts? In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/alternative; boundaryMessage-ID: <[log in to unmask]> --001636c5b6bb4e352c049c2fdb0c Content-Type: text/plain; charset=windows-1252 Content-Transfer-Encoding: quoted-printable Hello. I completely agree with everything that Johnathan has said. I also want to suggest reading my own paper. I combine many of the ideas behind the Henson and Calhoun papers and provide a method for bringing the derivative info to the group level. I hope this helps for at least providing another view of some of the issues at hand. Also, all the steps discussed in the paper have accompanying code which I provide a link to in the paper and below. Steffener, J., Tabert, M., Reuben, A., Stern, Y. Investigating hemodynamic response variability at the group level using basis functions (2010) NeuroImage, 49 (3), pp. 2113-2122. http://cumc.columbia.edu/dept/sergievsky/cnd/steffener.html Jason. On Fri, Feb 11, 2011 at 8:52 PM, Jonathan Peelle <[log in to unmask]> wrote: > What we usually want to know when doing fMRI analyses is whether a region > is "active" or not. When modeling with just a canonical HRF, this is fairly > simple, as a positive parameter estimate (beta value) means that there was a > response that matched the canonical HRF, which we can fairly safely > interpret as "activation" (i.e., increase in signal that is time-locked to > some stimulus category at about the time we expect). > > The tricky thing about interpreting any other type of basis set is how it > relates to "activation" (assuming this is what we're interested in). In > general, the effect of the derivatives is really only interpretable in > relation to a reliable positive loading on the canonical HRF. I.e., if you > have an HRF-like shape, the derivatives can tell you about how the observed > response differs from canonical. But you could imagine a situation in which > you have a significant weighting on a derivative, but not on the canonical. > In these situations it's quite difficult to interpret the result. > > Getting back to the point at hand, if you model conditions A and B with > > [Ahrf Atemp_deriv Bhrf Btemp_deriv] > > then the contrast > > [1 1 0 0] > > will give you the effect of the *average* of the canonical and temporal > derivative. But this is sort of a meaningless measure; it would give the > same result for something that is really well-explained by the canonical > only, really well-explained by the temporal derivative only, or explained by > equal contributions from the two. The most straightforward way to assess > "activation" would be to just look at the canonical HRF: > > [1 0 0 0] > > Or, if you want to look for "informed" effects, use an F test: > > [1 0 0 0 > 0 1 0 0] > > see Chapter 30 in the SPM manual, for example (Face Group Data). > > For comparing across groups, the same logic holds: the most straightforward > way to assess "activation" would be to just compare the canonical HRFs: > > [1 0 -1 0] > > and if you wanted to compare more, you could use an F test: > > [1 0 -1 0 > 0 1 0 -1] > > but you still run into non-straightforward interpretations, because a > significant F value doesn't tell you (a) in which direction the effect is, > or (b) whether the difference is on the canonical HRF or the derivative. > > The following papers are very helpfulsurely moreso than my attempt above. > :) > > Henson, R.N.A., Price, C.J., Rugg, M.D., Turner, R., Friston, K.J., 2002. > Detecting latency differences in event-related BOLD responses: Application > to words versus nonwords and initial versus repeated face presentations. > NeuroImage 15, 83-97. > > Calhoun, V.D., Stevens, M.C., Pearlson, G.D., Kiehl, K.A., 2004. fMRI > analysis with the general linear model: removal of latency-induced amplitude > bias by incorporation of hemodynamic derivative terms. NeuroImage 22, > 252-257. > > > Hope this helps, > Jonathan > > -- > Dr. Jonathan Peelle > Department of Neurology > University of Pennsylvania > 3 West Gates > 3400 Spruce Street > Philadelphia, PA 19104 > USA > http://jonathanpeelle.net/ > > > On Feb 11, 2011, at 5:33 PM, Michael T Rubens wrote: > > > I think this is a good question Hauke. If I understand you correctly, > you'd want to do a comparison of 2 conditions, each with an informed basis > set. i.e., > > > > [A-hrf A-tderiv B-hrf B-tderiv] > > > > [ 1 1 -1 -1 ] > > > > to my understanding that makes sense, but i'd like to hear other > opinions. > > > > Cheers, > > Michael > > > > On Fri, Feb 11, 2011 at 1:07 PM, Jason Steffener <[log in to unmask]> > wrote: > > Dear Hauke, > > The use of a t-test across the two regressors means that you are testing > a specific relationship between the two regressors. > > e.g your design is: > > [canonical derivative] > > and your contrast is: > > [1 1] > > Then you are "assuming" that the canonical and derivative have equal > weight. > > The F-test allows you to test any arbitrary relationship between the > canonical and derivative regressors. > > > > > > I hope this helps, > > Jason. > > > > > > > > On Fri, Feb 11, 2011 at 2:56 PM, Hauke Hillebrandt < > [log in to unmask]> wrote: > > Dear SPM Users, > > > > in my fMRI model specification I model the time derivative and then I use > t-contrasts on the 1st and 2nd level of my analysis to get the activation > maps. Now I read in the SPM manual on page 66 that this might not be okay: > > > > "The informed basis set requires an SPMF for inference. T-contrasts over > just the canonical are > > perfectly valid but assume constant delay/dispersion." > > > > am I right that this means that I have to use f-contrasts exclusively on > the 1st and 2nd level of my analysis (+the flexible factorial design option) > if I model the time derivative and that I cannot use t-tests at all in this > case? > > > > Best wishes, > > > > Hauke > > > -- Jason Steffener, Ph.D. Department of Neurology Columbia University http://www.cogneurosci.org/steffener.html --001636c5b6bb4e352c049c2fdb0c Content-Type: text/html; charset=windows-1252 Content-Transfer-Encoding: quoted-printable Hello.
I completely agree with everything that Johnathan has said. I also want to suggest reading my own paper. I combine many of the ideas behind the Henson and Calhoun papers and provide a method for bringing the derivative info to the group level. I hope this helps for at least providing another view of some of the issues at hand. Also, all the steps discussed in the paper have accompanying code which I provide a link to in the paper and below.

Steffener, J., Tabert, M., Reuben, A., Stern, Y.
Investigating hemodynamic response variability at the group level using basis functions
(2010) NeuroImage, 49 (3), pp. 2113-2122.

http://cumc.columbia.edu/dept/sergievsky/cnd/steffener.html

Jason.


On Fri, Feb 11, 2011 at 8:52 PM, Jonathan Peelle <[log in to unmask]> wrote:
What we usually want to know when doing fMRI analyses is whether a region is "active" or not. When modeling with just a canonical HRF, this is fairly simple, as a positive parameter estimate (beta value) means that there was a response that matched the canonical HRF, which we can fairly safely interpret as "activation" (i.e., increase in signal that is time-locked to some stimulus category at about the time we expect).

The tricky thing about interpreting any other type of basis set is how it relates to "activation" (assuming this is what we're interested in). In general, the effect of the derivatives is really only interpretable in relation to a reliable positive loading on the canonical HRF. I.e., if you have an HRF-like shape, the derivatives can tell you about how the observed response differs from canonical. But you could imagine a situation in which you have a significant weighting on a derivative, but not on the canonical. In these situations it's quite difficult to interpret the result.

Getting back to the point at hand, if you model conditions A and B with

[Ahrf Atemp_deriv Bhrf Btemp_deriv]

then the contrast

[1 1 0 0]

will give you the effect of the *average* of the canonical and temporal derivative. But this is sort of a meaningless measure; it would give the same result for something that is really well-explained by the canonical only, really well-explained by the temporal derivative only, or explained by equal contributions from the two. The most straightforward way to assess "activation" would be to just look at the canonical HRF:

[1 0 0 0]

Or, if you want to look for "informed" effects, use an F test:

[1 0 0 0
0 1 0 0]

see Chapter 30 in the SPM manual, for example (Face Group Data).

For comparing across groups, the same logic holds: the most straightforward way to assess "activation" would be to just compare the canonical HRFs:

[1 0 -1 0]

and if you wanted to compare more, you could use an F test:

[1 0 -1 0
0 1 0 -1]

but you still run into non-straightforward interpretations, because a significant F value doesn't tell you (a) in which direction the effect is, or (b) whether the difference is on the canonical HRF or the derivative.

The following papers are very helpfulsurely moreso than my attempt above. :)

Henson, R.N.A., Price, C.J., Rugg, M.D., Turner, R., Friston, K.J., 2002. Detecting latency differences in event-related BOLD responses: Application to words versus nonwords and initial versus repeated face presentations. NeuroImage 15, 83-97.

Calhoun, V.D., Stevens, M.C., Pearlson, G.D., Kiehl, K.A., 2004. fMRI analysis with the general linear model: removal of latency-induced amplitude bias by incorporation of hemodynamic derivative terms. NeuroImage 22, 252-257.


Hope this helps,
Jonathan

--
Dr. Jonathan Peelle
Department of Neurology
University of Pennsylvania
3 West Gates
3400 Spruce Street
Philadelphia, PA 19104
USA
http://jonathanpeelle.net/


On Feb 11, 2011, at 5:33 PM, Michael T Rubens wrote:

> I think this is a good question Hauke. If I understand you correctly, you'd want to do a comparison of 2 conditions, each with an informed basis set. i.e.,
>
> [A-hrf A-tderiv B-hrf B-tderiv]
>
> [ 1 1 -1 -1 ]
>
> to my understanding that makes sense, but i'd like to hear other opinions.
>
> Cheers,
> Michael
>
> On Fri, Feb 11, 2011 at 1:07 PM, Jason Steffener <[log in to unmask]> wrote:
> Dear Hauke,
> The use of a t-test across the two regressors means that you are testing a specific relationship between the two regressors.
> e.g your design is:
> [canonical derivative]
> and your contrast is:
> [1 1]
> Then you are "assuming" that the canonical and derivative have equal weight.
> The F-test allows you to test any arbitrary relationship between the canonical and derivative regressors.
>
>
> I hope this helps,
> Jason.
>
>
>
> On Fri, Feb 11, 2011 at 2:56 PM, Hauke Hillebrandt <[log in to unmask]> wrote:
> Dear SPM Users,
>
> in my fMRI model specification I model the time derivative and then I use t-contrasts on the 1st and 2nd level of my analysis to get the activation maps. Now I read in the SPM manual on page 66 that this might not be okay:
>
> "The informed basis set requires an SPMF for inference. T-contrasts over just the canonical are
> perfectly valid but assume constant delay/dispersion."
>
> am I right that this means that I have to use f-contrasts exclusively on the 1st and 2nd level of my analysis (+the flexible factorial design option) if I model the time derivative and that I cannot use t-tests at all in this case?
>
> Best wishes,
>
> Hauke
>



--
Jason Steffener, Ph.D.
Department of Neurology
Columbia University
http://www.cogneurosci.org/steffener.html
--001636c5b6bb4e352c049c2fdb0c-- ========================================================================Date: Sun, 13 Feb 2011 20:58:37 +0000 Reply-To: eleftherios garyfallidis <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: eleftherios garyfallidis <[log in to unmask]> Subject: First Official Dipy Release :-) Content-Type: multipart/alternative; boundary="_000_84A2B00B70D30141AFE47C6D0CA17777390DB30FWSR21mrccbsuloc_" MIME-Version: 1.0 Message-ID: <[log in to unmask]> --_000_84A2B00B70D30141AFE47C6D0CA17777390DB30FWSR21mrccbsuloc_ Content-Type: text/plain; charset="iso-8859-1" Content-Transfer-Encoding: quoted-printable ======================= Announcing Dipy 0.5.0 ======================= Dipy is a fast growing python toolbox for analysis of diffusion MR imaging. Just from its first official release dipy provides a great amount of utilities to facilitate diffusion MRI research. Here are just a few of them. - Reconstruction algorithms e.g. GQI, DTI - Tractography generation algorithms e.g. EuDX - Intelligent downsampling of tracks - Ultra fast tractography clustering - Resampling datasets with anisotropic voxels to isotropic - Visualizing multiple brains simultaneously - Finding track correspondence between different brains - Warping tractographies into another space e.g. MNI space - Reading many different file formats e.g. Trackvis or Nifti - Dealing with huge tractographies without memory restrictions - Playing with datasets interactively without storing on disk * Website http://www.dipy.org * Docs http://www.dipy.org/documentation.html * Tutorials http://www.dipy.org/examples_index.html * Downloads http://pypi.python.org/pypi/dipy * Code https://github.com/Garyfallidis/dipy * Mailing List http://mail.scipy.org/mailman/listinfo/nipy-devel * Bugs/Issues/Requests https://github.com/Garyfallidis/dipy/issues Be happy to inform us for any problems or join in and contribute with your code. Best wishes, Dipy Developers --_000_84A2B00B70D30141AFE47C6D0CA17777390DB30FWSR21mrccbsuloc_ Content-Type: text/html; charset="iso-8859-1" Content-Transfer-Encoding: quoted-printable
=======================
Announcing Dipy 0.5.0
=======================

Dipy is a fast growing python toolbox for analysis of diffusion MR imaging.

Just from its first official release dipy provides a great amount of utilities to facilitate diffusion MRI research. Here are just a few of them.

- Reconstruction algorithms e.g. GQI, DTI
- Tractography generation algorithms e.g. EuDX
- Intelligent downsampling of tracks
- Ultra fast tractography clustering
- Resampling datasets with anisotropic voxels to isotropic

- Visualizing multiple brains simultaneously
- Finding track correspondence between different brains
- Warping tractographies into another space e.g. MNI space
- Reading many different file formats e.g. Trackvis or Nifti

- Dealing with huge tractographies without memory restrictions
- Playing with datasets interactively without storing on disk

* Website
http://www.dipy.org

* Docs
http://www.dipy.org/documentation.html

* Tutorials
http://www.dipy.org/examples_index.html

* Downloads
http://pypi.python.org/pypi/dipy

* Code
https://github.com/Garyfallidis/dipy

* Mailing List
http://mail.scipy.org/mailman/listinfo/nipy-devel

* Bugs/Issues/Requests
https://github.com/Garyfallidis/dipy/issues

Be happy to inform us for any problems or join in and contribute with your code.

Best wishes,
Dipy Developers
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unmask]> Dear Vladimir & list, I can successfully change the channel type using spm_eeg_prep. According to the manual chantype is able to do the same job. However chantype doesn't seem to allow any (0/1) flags ? Best wishes Martin ========================================================================Date: Mon, 14 Feb 2011 11:15:52 +0000 Reply-To: John Ashburner <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: John Ashburner <[log in to unmask]> Subject: Re: naive quesiton about mapping between images in different space Comments: To: "Jiang, Zhiguo" <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/related; boundaryMessage-ID: <[log in to unmask]> --0015175cb154c389f2049c3c2bf3 Content-Type: multipart/alternative; boundary --0015175cb154c389eb049c3c2bf2 Content-Type: text/plain; charset=windows-1252 Content-Transfer-Encoding: quoted-printable Multiplying by M1 maps from voxels in image1 to mm space. Then multiplying this by the inverse of M2 will map from mm space to voxels in image2. Note that if we want to generate a resliced version of image1 that is aligned with image2, we need the mapping from image2 to image1. This is because reslicing an image usually involves scanning through the voxels image that we wish to create, and then figuring out where the values should be read from in the original. Best regards, -John On 11 February 2011 18:13, Jiang, Zhiguo <[log in to unmask]>wrote: > In spm_reslice.m , it states > > > > % Assuming that image1 has a transformation matrix M1, and image2 has a > > % transformation matrix M2, the mapping from image1 to image2 is: M2\M1 > > % (ie. from the coordinate system of image1 into millimeters, followed > > % by a mapping from millimeters into the space of image2). > > > > > > > > So to map a x0,y0,z0 in image1 space to image2, isnt the composite matrix > > > > M1\M2 instead of M2\M1 ? > > > > Beause we need to bring x0,y0,z0 to mm then do an inverse of M2 to image 2 > > > > > Not sure where I got it wrong > > > > > > Thanks, > > > > Tony > > > > > ------------------------------------------------------------------------------------------------------------------------------ > > [image: logo] > > Tony Jiang,Ph.D.|Research Scholar|University of California, Los Angeles > Peter V. Ueberroth Building, Rm 2338C2|10945 Le Conte Avenue. Los > Angeles,CA 90095 > > Tel: (310)206-1423|Email: [log in to unmask] > > > > > > > > ------------------------------ > IMPORTANT WARNING: This email (and any attachments) is only intended for > the use of the person or entity to which it is addressed, and may contain > information that is privileged and confidential. You, the recipient, are > obligated to maintain it in a safe, secure and confidential manner. > Unauthorized redisclosure or failure to maintain confidentiality may subject > you to federal and state penalties. If you are not the intended recipient, > please immediately notify us by return email, and delete this message from > your computer. > --0015175cb154c389eb049c3c2bf2 Content-Type: text/html; charset=windows-1252 Content-Transfer-Encoding: quoted-printable Multiplying by M1 maps from voxels in image1 to mm space. Then multiplying this by the inverse of M2 will map from mm space to voxels in image2.

Note that if we want to generate a resliced version of image1 that is aligned with image2, we need the mapping from image2 to image1. This is because reslicing an image usually involves scanning through the voxels image that we wish to create, and then figuring out where the values should be read from in the original.

Best regards,
-John

On 11 February 2011 18:13, Jiang, Zhiguo <[log in to unmask]> wrote:

In spm_reslice.m , it states

% Assuming that image1 has a transformation matrix M1, and image2 has a

% transformation matrix M2, the mapping from image1 to image2 is: M2\M1

% (ie. from the coordinate system of image1 into millimeters, followed

% by a mapping from millimeters into the space of image2).

So to map a x0,y0,z0 in image1 space to image2, isnt the composite matrix

M1\M2 instead of M2\M1 ?

Beause we need to bring x0,y0,z0 to mm then do an inverse of M2 to image 2

Not sure where I got it wrong

Thanks,

Tony

------------------------------------------------------------------------------------------------------------------------------

logo

Tony Jiang,Ph.D.|Research Scholar|University of California, Los Angeles
Peter V. Ueberroth Building, Rm 2338C2|10945 Le Conte Avenue. Los Angeles,CA 90095

Tel: (310)206-1423|Email: [log in to unmask]



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Vladimir On Mon, Feb 14, 2011 at 9:30 AM, Martin Dietz <[log in to unmask]> wrote: > Dear Vladimir & list, > > I can successfully change the channel type using spm_eeg_prep. According to the manual chantype is able to do the same job. However chantype doesn't seem to allow any (0/1) flags ? > > Best wishes > Martin > ========================================================================Date: Mon, 14 Feb 2011 12:56:17 +0100 Reply-To: Martin Jensen Dietz <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Martin Jensen Dietz <[log in to unmask]> Subject: Re: M/EEG chantype Comments: To: Vladimir Litvak <[log in to unmask]> In-Reply-To: <[log in to unmask]> Content-Type: text/plain; charset="us-ascii" Content-Transfer-Encoding: quoted-printable MIME-Version: 1.0 Message-ID: <[log in to unmask]> Hi Vladimir, Thanks. I erroneously assumed a flag based on the example in section 12.7.4 Martin On Feb 14, 2011, at 12:34 PM, Vladimir Litvak wrote: > Dear Martin, > > The syntax of chantype is something like: > > D = chantype(D, 1:10, 'EEG'); > > I don't see where you expect 0/1 flags to be. > > Vladimir > > On Mon, Feb 14, 2011 at 9:30 AM, Martin Dietz <[log in to unmask]> wrote: >> Dear Vladimir & list, >> >> I can successfully change the channel type using spm_eeg_prep. According to the manual chantype is able to do the same job. However chantype doesn't seem to allow any (0/1) flags ? >> >> Best wishes >> Martin >> ========================================================================Date: Mon, 14 Feb 2011 12:29:18 +0000 Reply-To: Vladimir Litvak <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Vladimir Litvak <[log in to unmask]> Subject: Re: Question about lead field matrix Comments: To: [log in to unmask] Comments: cc: Robert Oostenveld <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> Dear Carsten On Fri, Feb 11, 2011 at 11:56 PM, Carsten Stahlhut <[log in to unmask]> wrote: > Dear Vladimir, > > I have approx three questions (or issues) that I hope you can help me out > with. > > Do you know what the units are for the lead field matrix and the source > estimates in SPM8? These are two different questions. > If you apply one of the EEG imaging methods (as I understood it) then the > source estimates should be current density i.e. the unit should be something > like A/m^2 or uA/mm^2 depending on the scaling of the EEG data and lead > field matrix. > And then the units of the lead field should be something like m^2 * Ohm ( = > m^2 / S ). In theory the forward computation done by the 'forward' toolbox should be unit-blind so the units of the lead field should depend on units of the head model (mm in SPM). In practice this might not be the case. We recently found a difference in scaling between 'single shell' and other MEG models. This will be fixed in the next update. There might be something similar also for EEG. SPM is not sensitive to it but it's still something worth looking into. > Does this also holds for SPM8 or do there exist any type of scaling of the > lead field matrix such as a normalization of the columns or something like > that? > Yes, there are several scaling and normalization steps so the units of the output images are not related to original physical units but are normalize to the total power across sources and conditions. > The second question is related to the lead field matrix as well. If I > compare two different head models a BEM and 3-spheres model then they seem > to be on two very different scales - is that really the case? Or am I > missing an important step? Of course it is two very different head model > assumptions so they should be quite different but I'm a bit surprised that > there exists a scaling factor of 100 between the largest element in the BEM > gain matrix and the 3-spheres gain matrix. See above. > What I just did was to load the mat-files with the gain-matrices and used > the imagesc-function to show the amplitudes of the two lead field matrices. > > The 28th Jul 2010 you sent an answer to a post regarding head models and you > here mentioned that FEM head models from SimBio might be an option in the > very nice MEEGTool. I was wondering what the status is on integrating the > SimBio FEM implementation with SPM, as I'm very interested to try out the > FEM head models. I guess there is no reason that I will try to write the > code my self if the option is almost done and will be part of the MEEGTool. > I am aware of some efforts to integrate SimBio support in the forward toolbox. Even if this is done I don't expect it to become one of the standard options in SPM because SimBio runs only on a particular Unix platform (I'm not even sure it's LINUX) and I suspect has very lengthy computing time. But if you compute a gain matrix for the canonical mesh in SimBio you can just replace the mat file generated by SPM with your file and it will be used by spm_eeg_invert. If there is inconsistency in units, it shouldn't be a problem. There is also a possibility to use another BEM implementation OpenMEEG (http://www-sop.inria.fr/athena/software/OpenMEEG/). That's something that works and I tested it last year, but found it impractical for most users again because of difficulties with installation and long computation time (about 24 h for normal mesh). The differences in the lead fields with our BEM were only for a small number of vertices close to the surface. But I can give you the glue code for this if you want. Best, Vladimir > Best, > Carsten > > > ========================================================================Date: Mon, 14 Feb 2011 12:44:58 +0000 Reply-To: John Ashburner <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: John Ashburner <[log in to unmask]> Subject: Re: How to do the coregistration between the functional MRI images with a high resolution anatomical head image Comments: To: Linling Li <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=GB2312 Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> It's not really about right or wrong. The important thing is whether it works for your data. This will depend on many factors, but the amount of spatial distortion in your fMRI will be one of these. Best regards, -John 2011/2/14 Linling Li <[log in to unmask]>: > Dear all, > > > > I have two kinds of anatomical images of each subject, one is regular T2 > image which has low resolution, and the other one is 3D T1 structural image > (3DHead) which has very high resolution. And I do the preprocessing as > follow: > > > > 1. Realignment(Estimate&Write) -> Data to input: all fMRI images; > > > > 2. Coregistration(Estimate) -> Reference Image: mean fMRI image > produced after last step > > Source Image: T2 anatomical image > > So, the T2 anatomical image could be registered to functional images during > this step; > > > > 3. Coregistration(Estimate) -> Reference Image: T2 anatomical image > > Source Image: 3DHead image > > Here, the 3DHead image could be registered to T2 image which has been > already registered to functional images. Therefore, we have finished the > coregistration between 3DHead image and functional images with the help of > T2 anatomical image. Since the large resolution difference between3DHead > image and functional image, We think this coregistration method is more > proper; > > > > 4. Segmentation -> Data: 3DHead image > > > > 5. Normalise(write) -> Parameter file: 3DHead_seg_sn.mat > > Images to write: all the realigned functional images > > > > Would this be right? > > > > Any suggestion would be appreciated and thank you all in advance! > > > 2011-02-14 > ________________________________ > > > Linling Li > Research Centre for Neural Engineering > -------------------------------------- > Phone: +86-755-86392232 > Email: [log in to unmask] > Shenzhen Institutes of Advanced Technology, > Chinese Academy of Sciences. ========================================================================Date: Mon, 14 Feb 2011 15:38:19 +0100 Reply-To: workshop-networks <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: workshop-networks <[log in to unmask]> Subject: workshop "networks in the human brain" MIME-Version: 1.0 Content-Type: text/plain; charset=utf-8 Content-Transfer-Encoding: 7bit Message-ID: <499626810.8000.1297694299153.JavaMail.root@zimbra> Dear all, please do not try to register anymore for our workshop "networks in the human brain" to be held at the Max-Planck- Institute in Leipzig, March 7-8. 2011. We are booked up ! Thank you for your interest, Gabriele Lohmann, Dirk Goldhahn, Robert Turner ========================================================================Date: Mon, 14 Feb 2011 09:44:47 -0500 Reply-To: justine dupont <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: justine dupont <[log in to unmask]> Subject: dartel misregistration - or not? Content-Type: multipart/mixed; boundary="_eb62bde8-154a-4a7d-9fd9-b2bc8bfd8e0e_" MIME-Version: 1.0 Message-ID: <[log in to unmask]> --_eb62bde8-154a-4a7d-9fd9-b2bc8bfd8e0e_ Content-Type: multipart/alternative; boundary="_df7cf205-f75b-40c4-8a56-9204a9a37eab_" --_df7cf205-f75b-40c4-8a56-9204a9a37eab_ Content-Type: text/plain; charset="iso-8859-1" Content-Transfer-Encoding: quoted-printable Dear experts I have run a DARTEL analysis and comparing the DARTEL template and the regular T1 canonical brain I get the result attached. I was surprised that the two images are so different in shape. My sample is 45 young healthy adults, roughly equal numbers of males and females. Eyeballing the original scans there are no 'outliers' or anomalies. Likewise there were no obvious anomalies looking at the various stages of preprocessing. So I am not sure whether something has gone wrong, or whether my sample, for some reason, had genuinely small brains, compared to the canonical T1, or perhaps whether there is some other explanation. Thank you Justine --_df7cf205-f75b-40c4-8a56-9204a9a37eab_ Content-Type: text/html; charset="iso-8859-1" Content-Transfer-Encoding: quoted-printable Dear experts

I have run a DARTEL analysis and comparing the DARTEL template and the regular T1 canonical brain I get the result attached.  I was surprised that the two images are so different in shape.  My sample is 45 young healthy adults, roughly equal numbers of males and females.  Eyeballing the original scans there are no 'outliers' or anomalies.  Likewise there were no obvious anomalies looking at the various stages of preprocessing.

So I am not sure whether something has gone wrong, or whether my sample, for some reason, had genuinely small brains, compared to the canonical T1, or perhaps whether there is some other explanation.

Thank you

Justine

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0jNkLtD/ACAbgyafia3vtQvNMsbbTre8td0lxdJdyMkEiqu1Y2wjgktIHAI/5Ze2R1HkR/8AP1D+ T/8AxNHkR/8AP1D+T/8AxNAHm+naJq+oy77o3FnqNvYW9k94JHBlVZbmKZlkK5JZNsq/7XlMcgc9 T4Xs/sGjNbC3+zol7d+XFs2BUNxIVwOw2kEdsYrf8iP/AJ+ofyf/AOJo8iP/AJ+ofyf/AOJoAIP9 Tc/9cx/6GtFPAjihm/fxuXQKAob+8D3HtRQB/9k --_eb62bde8-154a-4a7d-9fd9-b2bc8bfd8e0e_-- ========================================================================Date: Mon, 14 Feb 2011 09:56:02 -0500 Reply-To: "MCLAREN, Donald" <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: "MCLAREN, Donald" <[log in to unmask]> Subject: Re: dartel misregistration - or not? Comments: To: justine dupont <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> DARTEL typically produces a smaller template compared to the T1 canonical brain in MNI. In SPM8, you should select the option to warp to MNI space as well. If your using SPM5, there is a program under resources at brainmap.wisc.edu to warp to MNI space. If you selected the warp to MNI space, I am surprised with the misregistration. On Monday, February 14, 2011, justine dupont <[log in to unmask]> wrote: > > > > > > Dear experts > > I have run a DARTEL analysis and comparing the DARTEL template and the regular T1 canonical brain I get the result attached. I was surprised that the two images are so different in shape. My sample is 45 young healthy adults, roughly equal numbers of males and females. Eyeballing the original scans there are no 'outliers' or anomalies. Likewise there were no obvious anomalies looking at the various stages of preprocessing. > > So I am not sure whether something has gone wrong, or whether my sample, for some reason, had genuinely small brains, compared to the canonical T1, or perhaps whether there is some other explanation. > > Thank you > > Justine > > > -- Best Regards, Donald McLaren ================= D.G. McLaren, Ph.D. Postdoctoral Research Fellow, GRECC, Bedford VA Research Fellow, Department of Neurology, Massachusetts General Hospital and Harvard Medical School Office: (773) 406-2464 ===================== This e-mail contains CONFIDENTIAL INFORMATION which may contain PROTECTED HEALTHCARE INFORMATION and may also be LEGALLY PRIVILEGED and which is intended only for the use of the individual or entity named above. If the reader of the e-mail is not the intended recipient or the employee or agent responsible for delivering it to the intended recipient, you are hereby notified that you are in possession of confidential and privileged information. Any unauthorized use, disclosure, copying or the taking of any action in reliance on the contents of this information is strictly prohibited and may be unlawful. If you have received this e-mail unintentionally, please immediately notify the sender via telephone at (773) 406-2464 or email. ========================================================================Date: Mon, 14 Feb 2011 14:59:34 +0000 Reply-To: John Ashburner <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: John Ashburner <[log in to unmask]> Subject: Re: dartel misregistration - or not? Comments: To: justine dupont <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> The single subject brain is just that of a single individual, who has been affine aligned to MNI space. The Dartel template is the average in both shape and size of your population of subjects. Unless those subjects have extremely large brains, then it is unlikely that their average will match with MNI space. If you use the option to normalise to MNI space (in the Dartel toolbox of SPM8), then an additional affine registration step is done, which aligns your population average to MNI space. It only uses an affine registration because the official MNI space has only been defined using affine registered brains. Best regards, -John On 14 February 2011 14:44, justine dupont <[log in to unmask]> wrote: > Dear experts > > I have run a DARTEL analysis and comparing the DARTEL template and the > regular T1 canonical brain I get the result attached. I was surprised that > the two images are so different in shape. My sample is 45 young healthy > adults, roughly equal numbers of males and females. Eyeballing the original > scans there are no 'outliers' or anomalies. Likewise there were no obvious > anomalies looking at the various stages of preprocessing. > > So I am not sure whether something has gone wrong, or whether my sample, for > some reason, had genuinely small brains, compared to the canonical T1, or > perhaps whether there is some other explanation. > > Thank you > > Justine > > ========================================================================Date: Mon, 14 Feb 2011 10:08:08 -0500 Reply-To: Hekmatyar <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Hekmatyar <[log in to unmask]> Subject: Re: Orientation swap In-Reply-To: <499626810.8000.1297694299153.JavaMail.root@zimbra> MIME-Version: 1.0 Content-Type: multipart/mixed; boundary="----=_NextPart_000_01BD_01CBCC2F.14974BE0" Message-ID: <[log in to unmask]> ------=_NextPart_000_01BD_01CBCC2F.14974BE0 Content-Type: text/plain; charset="utf-8" Content-Transfer-Encoding: quoted-printable Hello All Could you please suggest me why the orientation of the images were swapped after co-registraton (snapshot of coregistration)? 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8n5QwmUbAJa8ie3irg0X6pXGqg5Ie57wCIBZMoZgxnqI4ThFb3OCxbLJWERiREKDDfOtLLdvPMLG xE3sG6JULad9ec5/dWo2pxtjbR6HO0LEbZwneNZ1WMc0z1vmxrbW5jZK9I7DPng+nuMkztfHMjxE RDK71k/LrX1wE7q1iMXwzKC2E0T+wI2wtbW1tbW1tbW19TfL1+fnguCqHG2xBXe5fJYVkYiNE/jf u80kIZ/f+rgAAAAASUVORK5CYII ------=_NextPart_000_01BD_01CBCC2F.14974BE0-- ========================================================================Date: Mon, 14 Feb 2011 15:18:52 +0000 Reply-To: John Ashburner <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: John Ashburner <[log in to unmask]> Subject: Re: Orientation swap Comments: To: Hekmatyar <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Message-ID: <[log in to unmask]> I'm not sure that any orientation has been swapped. The images are simply displayed in a way that uses the orientation images in the headers. If you show one of the images with eg the Display button, then the orientation in which the image is displayed will be determined by the orientation encoded in your image headers. As these do not appear to be human brains, I would perhaps suggest changing the values in the "Separation" option. When estimating the parameters, the algorithm only looks at the image every few mm (to save time). In the case of these images, every few mm is likely to mean that most of the information is unused. I notice that the joint histograms are very noisy. This should be fixed by using more of the data. Best regards, -John On 14 February 2011 15:08, Hekmatyar <[log in to unmask]> wrote: > Hello All > Could you please suggest me why the orientation of the images were swapped after co-registraton (snapshot of coregistration)? Thanks > > Hekmatyar > BIRC > UGA > > ========================================================================Date: Mon, 14 Feb 2011 10:11:58 -0500 Reply-To: Alexandre Gramfort <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Alexandre Gramfort <[log in to unmask]> Subject: Re: Question about lead field matrix Comments: To: Vladimir Litvak <[log in to unmask]> Comments: cc: Sharing information on OpenMEEG <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Message-ID: [log in to unmask]> Hi Vladimir, > There is also a possibility to use another BEM implementation OpenMEEG > (http://www-sop.inria.fr/athena/software/OpenMEEG/). That's something > that works and I tested it last year, but found it impractical for > most users again because of difficulties with installation we're working on this. New windows 64, linux 64 and Mac OS X installers will be available shortly with the 2.1 release that adds speed improvements using the adjoint approach. > and long > computation time (about 24 h for normal mesh). we will be presenting at HBM this year our improvements using the adjoint approach that brings computation on the SPM canonical mesh to 1h40 on a Linux 64 with 8 cores machine (3h45 with non-adjoint method). > The differences in the > lead fields with our BEM were only for a small number of vertices > close to the surface. That is the whole point of the symmetric BEM. Give precision for dipoles close to the inner skull (sources on top of gyri). Note that OpenMEEG features also lead fields computation for EIT and Internal Potential calculation (see. "Forward field computation with OpenMEEG" Alexandre Gramfort, Thodore Papadopoulo, Emmanuel Olivi, and M. Clerc to appear in the special issue: "Academic Software Applications for Electromagnetic Brain Mapping Using MEG and EEG") Best, Alex and the OpenMEEG developers. -- Alexandre Gramfort, PhD [log in to unmask] Dept. of Radiology MGH Martinos Center / Harvard Medical School http://www-sop.inria.fr/members/Alexandre.Gramfort/ ========================================================================Date: Mon, 14 Feb 2011 11:31:56 -0500 Reply-To: "MCLAREN, Donald" <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: "MCLAREN, Donald" <[log in to unmask]> Subject: Re: about ROI signal value Comments: To: Yang Hu <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> These are CV as they come from the contrasts. Contrasts are simply a linear combination (addition or subtraction) of the PE or beta images. PSC requires dividing by the constant term. I always use the CV and I also use the above AFNI commands. The one cautionary note is that AFNI/SPM have the L and R on opposite sides, so you want to make sure your extracting from the correct voxels. Additionally, you don't need step 2 as AFNI can read .nii files. Best Regards, Donald McLaren ================= D.G. McLaren, Ph.D. Postdoctoral Research Fellow, GRECC, Bedford VA Research Fellow, Department of Neurology, Massachusetts General Hospital and Harvard Medical School Office: (773) 406-2464 ===================== This e-mail contains CONFIDENTIAL INFORMATION which may contain PROTECTED HEALTHCARE INFORMATION and may also be LEGALLY PRIVILEGED and which is intended only for the use of the individual or entity named above. If the reader of the e-mail is not the intended recipient or the employee or agent responsible for delivering it to the intended recipient, you are hereby notified that you are in possession of confidential and privileged information. Any unauthorized use, disclosure, copying or the taking of any action in reliance on the contents of this information is strictly prohibited and may be unlawful. If you have received this e-mail unintentionally, please immediately notify the sender via telephone at (773) 406-2464 or email. On Sat, Feb 12, 2011 at 11:27 PM, Yang Hu <[log in to unmask]> wrote: > Dear Experts, > > Based on whole-brain analysis via SPM8 (1st- and 2nd-level analysis), I want to extract signal value from atlas-based ROIs (e.g. amygdala) in four experimental conditions, compared with rest condition respectively, by AFNI rather than MarsBar. Specific steps are listed as follows: > > 1. Mask generation: by WFU pickatlas, an file of ROI in amygdala (named as "amy.nii") was generated > 2. File conversion: by AFNI command "3dcopy", the "amy.nii" was converted to "amy+orig.BRIK/HEAD", which could be recognized by AFNI > 3. ROI calculation: by AFNI command "3dmaskave", the average value within the ROI mask (amygdala) of each subject (sbj**) in certain condition (con_000*) could be obtained; Specifically, the full command is like that "3dmaskave -quiet -mask amy+orig sbj**_con_000*.hdr". The file "sbj**_con_000*.hdr" was generated after 1st-level analysis via SPM8. > > So I just wonder the meaning of ROI value obtained through those steps mentioned above. Whether does the value mean percent signal change (PSC), contrast value (CV), or parameter estimates (PE) ? And what's the difference between the three terms (namely PSC, CV, PE) always used in ROI analysis? > > Thanks a lot for your help and comment! > > Yang Hu > > ICN, ECNU, Shanghai, China > ========================================================================Date: Mon, 14 Feb 2011 11:35:04 -0500 Reply-To: Hekmatyar <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Hekmatyar <[log in to unmask]> Subject: Re: Orientation swap Comments: To: John Ashburner <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/mixed; boundary="----=_NextPart_000_023B_01CBCC3B.393DA870" Message-ID: <[log in to unmask]> ------=_NextPart_000_023B_01CBCC3B.393DA870 Content-Type: text/plain; charset="us-ascii" Content-Transfer-Encoding: 7bit Thanks Dr. John I will check that, The orientation of anatomical before coregistration is same as orientation in the functional. I have attached some snapshots of display and checkreg. Those are from rat brains, I will try changing separation values as well. Thanks Hek -----Original Message----- From: SPM (Statistical Parametric Mapping) [mailto:[log in to unmask]] On Behalf Of John Ashburner Sent: Monday, February 14, 2011 10:19 AM To: [log in to unmask] Subject: Re: [SPM] Orientation swap I'm not sure that any orientation has been swapped. The images are simply displayed in a way that uses the orientation images in the headers. If you show one of the images with eg the Display button, then the orientation in which the image is displayed will be determined by the orientation encoded in your image headers. As these do not appear to be human brains, I would perhaps suggest changing the values in the "Separation" option. When estimating the parameters, the algorithm only looks at the image every few mm (to save time). In the case of these images, every few mm is likely to mean that most of the information is unused. I notice that the joint histograms are very noisy. This should be fixed by using more of the data. Best regards, -John On 14 February 2011 15:08, Hekmatyar <[log in to unmask]> wrote: > Hello All > Could you please suggest me why the orientation of the images were swapped after co-registraton (snapshot of coregistration)? 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Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Message-ID: [log in to unmask]> A couple other things to check: (1) That the voxel sizes are on the same scale between scans; (2) Use a smaller smoothing kernel as well. (3) Set the voxel size to the actual size, rather than multiplying by 10 or 20. (4) Make sure the origin is the same in both images. Best Regards, Donald McLaren ================= D.G. McLaren, Ph.D. Postdoctoral Research Fellow, GRECC, Bedford VA Research Fellow, Department of Neurology, Massachusetts General Hospital and Harvard Medical School Office: (773) 406-2464 ===================== This e-mail contains CONFIDENTIAL INFORMATION which may contain PROTECTED HEALTHCARE INFORMATION and may also be LEGALLY PRIVILEGED and which is intended only for the use of the individual or entity named above. If the reader of the e-mail is not the intended recipient or the employee or agent responsible for delivering it to the intended recipient, you are hereby notified that you are in possession of confidential and privileged information. Any unauthorized use, disclosure, copying or the taking of any action in reliance on the contents of this information is strictly prohibited and may be unlawful. If you have received this e-mail unintentionally, please immediately notify the sender via telephone at (773) 406-2464 or email. On Mon, Feb 14, 2011 at 11:35 AM, Hekmatyar <[log in to unmask]> wrote: > Thanks Dr. John > I will check that, The orientation of anatomical before coregistration is > same as orientation in the functional. I have attached some snapshots of > display and checkreg. > Those are from rat brains, I will try changing separation values as well. > Thanks > Hek > > -----Original Message----- > From: SPM (Statistical Parametric Mapping) [mailto:[log in to unmask]] On > Behalf Of John Ashburner > Sent: Monday, February 14, 2011 10:19 AM > To: [log in to unmask] > Subject: Re: [SPM] Orientation swap > > I'm not sure that any orientation has been swapped. The images are > simply displayed in a way that uses the orientation images in the > headers. If you show one of the images with eg the Display button, > then the orientation in which the image is displayed will be > determined by the orientation encoded in your image headers. > > As these do not appear to be human brains, I would perhaps suggest > changing the values in the "Separation" option. When estimating the > parameters, the algorithm only looks at the image every few mm (to > save time). In the case of these images, every few mm is likely to > mean that most of the information is unused. I notice that the joint > histograms are very noisy. This should be fixed by using more of the > data. > > Best regards, > -John > > On 14 February 2011 15:08, Hekmatyar <[log in to unmask]> wrote: >> Hello All >> Could you please suggest me why the orientation of the images were swapped > after co-registraton (snapshot of coregistration)? Thanks >> >> Hekmatyar >> BIRC >> UGA >> >> > ========================================================================Date: Mon, 14 Feb 2011 13:02:36 -0500 Reply-To: "Claire (Jung Eun) Han" <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: "Claire (Jung Eun) Han" <[log in to unmask]> Subject: Putting a non-zero value for the time derivative MIME-Version: 1.0 Content-Type: multipart/alternative; boundaryMessage-ID: <[log in to unmask]> --000e0cd2e6e258a66c049c41da0a Content-Type: text/plain; charset=ISO-8859-1 Hello, What does the result mean if I put a non-zero value for the time derivative (e.g. putting '1' for both hrf and the time derivative)? Thanks in advance, Claire --000e0cd2e6e258a66c049c41da0a Content-Type: text/html; charset=ISO-8859-1 Hello,

What does the result mean if I put a non-zero value for the time derivative (e.g. putting '1' for both hrf and the time derivative)?

Thanks in advance,
Claire
--000e0cd2e6e258a66c049c41da0a-- ========================================================================Date: Mon, 14 Feb 2011 12:20:10 -0600 Reply-To: Steffie Tomson <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Steffie Tomson <[log in to unmask]> Subject: Resizing mask MIME-Version: 1.0 Content-Type: multipart/alternative; boundary="----_=_NextPart_001_01CBCC73.D0E75523" Message-ID: <[log in to unmask]> This is a multi-part message in MIME format. ------_=_NextPart_001_01CBCC73.D0E75523 Content-Type: text/plain; charset="US-ASCII" Content-Transfer-Encoding: quoted-printable Hi Everyone - probably a silly question, but how do I resize a mask? I have masks from the AAL atlas that are 181x217x181 and I need them in the 46x56x34 size. Conceptually it should be a simple interpolation, but is there a function that does this? Thanks again, Steffie ------_=_NextPart_001_01CBCC73.D0E75523 Content-Type: text/html; charset="US-ASCII" Content-Transfer-Encoding: quoted-printable

Hi Everyone – probably a silly question, but how do I resize a mask?  I have masks from the AAL atlas that are 181x217x181 and I need them in the 46x56x34 size.  Conceptually it should be a simple interpolation, but is there a function that does this?

 

Thanks again,

Steffie

 

------_=_NextPart_001_01CBCC73.D0E75523-- ========================================================================Date: Mon, 14 Feb 2011 18:37:57 +0000 Reply-To: John Ashburner <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: John Ashburner <[log in to unmask]> Subject: Re: Resizing mask Comments: To: Steffie Tomson <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=windows-1252 Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> You can reslice the mask to match some other image using either the realign (reslice only) or coregister (reslice only) options. Best regards, -John On 14 February 2011 18:20, Steffie Tomson <[log in to unmask]> wrote: > Hi Everyone probably a silly question, but how do I resize a mask? I have > masks from the AAL atlas that are 181x217x181 and I need them in the > 46x56x34 size. Conceptually it should be a simple interpolation, but is > there a function that does this? > > > > Thanks again, > > Steffie > > ========================================================================Date: Mon, 14 Feb 2011 13:52:37 -0500 Reply-To: "MCLAREN, Donald" <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: "MCLAREN, Donald" <[log in to unmask]> Subject: Re: Putting a non-zero value for the time derivative Comments: To: "Claire (Jung Eun) Han" <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Message-ID: <[log in to unmask]> It means that you would average the weight of the HRF and the derivative. This is completelly uninformative as you would get the same answer for when the the time derivative is 0 and HRF is 1 or when the canonical HRF is 0 and time derivative is 1, which are clearly very different in their interpretation. There been several posts this week on this topic. Best Regards, Donald McLaren ================D.G. McLaren, Ph.D. Postdoctoral Research Fellow, GRECC, Bedford VA Research Fellow, Department of Neurology, Massachusetts General Hospital and Harvard Medical School Office: (773) 406-2464 ====================This e-mail contains CONFIDENTIAL INFORMATION which may contain PROTECTED HEALTHCARE INFORMATION and may also be LEGALLY PRIVILEGED and which is intended only for the use of the individual or entity named above. If the reader of the e-mail is not the intended recipient or the employee or agent responsible for delivering it to the intended recipient, you are hereby notified that you are in possession of confidential and privileged information. Any unauthorized use, disclosure, copying or the taking of any action in reliance on the contents of this information is strictly prohibited and may be unlawful. If you have received this e-mail unintentionally, please immediately notify the sender via telephone at (773) 406-2464 or email. On Mon, Feb 14, 2011 at 1:02 PM, Claire (Jung Eun) Han <[log in to unmask]> wrote: > Hello, > > What does the result mean if I put a non-zero value for the time derivative > (e.g. putting '1' for both hrf and the time derivative)? > > Thanks in advance, > Claire > ========================================================================Date: Mon, 14 Feb 2011 17:16:57 -0500 Reply-To: cliff <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: cliff <[log in to unmask]> Subject: spm_create_vol &&& spm_write_vol MIME-Version: 1.0 Content-Type: multipart/alternative; boundaryMessage-ID: <[log in to unmask]> --000e0cd5d004f9ac20049c456771 Content-Type: text/plain; charset=ISO-8859-1 Hi, all, I thought before that "spm_create_vol " is used to create the ".hdr" files of the images. However, today I found that "spm_write_vol" can produce both of the ".hdr" and ".img" files. then, what is the "spm_create_vol " exactly used for? Thanks~ --000e0cd5d004f9ac20049c456771 Content-Type: text/html; charset=ISO-8859-1 Hi, all,
I thought before that "spm_create_vol " is used to create the ".hdr" files of the images.
However, today I found that "spm_write_vol" can produce both of the ".hdr" and ".img" files.

then, what is the "spm_create_vol " exactly used for?

Thanks~
--000e0cd5d004f9ac20049c456771-- ========================================================================Date: Mon, 14 Feb 2011 22:32:05 +0000 Reply-To: John Ashburner <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: John Ashburner <[log in to unmask]> Subject: Re: spm_create_vol &&& spm_write_vol Comments: To: cliff <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Message-ID: <[log in to unmask]> spm_write_vol calls spm_create_vol. Sometimes, for example in the fMRI stats, we may wish to create headers but only write out a slice of data at a time (as there is not enough memory to hold all the images). best regards, -John On 14 February 2011 22:16, cliff <[log in to unmask]> wrote: > Hi, all, > I thought before that "spm_create_vol " is used to create the ".hdr" files > of the images. > However, today I found that "spm_write_vol" can produce both of the ".hdr" > and ".img" files. > > then, what is the "spm_create_vol " exactly used for? > > Thanks~ > ========================================================================Date: Mon, 14 Feb 2011 17:20:56 -0800 Reply-To: Matthew Brett <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Matthew Brett <[log in to unmask]> Subject: Re: extract ROI at the edge of the cerebellum Comments: To: Viridiana Mazzola <[log in to unmask]> Comments: cc: [log in to unmask] In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> Hi, On Sun, Feb 13, 2011 at 4:00 AM, Viridiana Mazzola <[log in to unmask]> wrote: > Dear all, > I am trying to extract a ROI at the edge of the cerebellum following the Brett's FAQ instructions. > > 1 . I rename the ROI my_roi.mat, then I write in matlab the command: > roi_filename = 'my_roi.mat'; > my_roi = maroi(roi_filename); > my_roi = spm_hold(my_roi, 0); % set NN resampling > saveroi(my_roi, roi_filename); > > 2. then I rerun the extraction of my_roi, but this error appears: > Fetching data : 1/1 Error in ==> maroi.getdata at 30 > if nargin < 2 > ??? Output argument "vXYZ" (and maybe others) not assigned during call to Could you have a try of the fixes suggested here and let us know they work? http://marsbar.sourceforge.net/faq.html#why-do-i-get-a-no-valid-data-for-roi-warning-when-extracting-data The marsbar is the best list for these questions - I've Cc'ed it... Best, Matthew ========================================================================Date: Mon, 14 Feb 2011 20:25:30 -0500 Reply-To: MP <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: MP <[log in to unmask]> Subject: Re: EEG significant clusters outside the MIP glass brain Comments: To: [log in to unmask] In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/mixed; boundarye6ba476b13485c07049c480aa2 Message-ID: <[log in to unmask]> --90e6ba476b13485c07049c480aa2 Content-Type: multipart/alternative; boundarye6ba476b13485bfb049c480aa0 --90e6ba476b13485bfb049c480aa0 Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Hello Vladimir, I tried to use the inner skull mask as you suggested to avoid getting significant cluster outside the glass brain, but it is drastically changing the results. Attached the figures of results with and without applying the mask. Could you please tell me if I am doing something wrong here? P.S. I include the iskull mask as an implicit mask in the flexible factorial design. Thanks - Muhammad On Fri, Dec 31, 2010 at 12:03 AM, <[log in to unmask]> wrote: > Dear Muhammad, > > Threshold masking will not necessarily work. It depends whether the values > outside the brain are really low. You can use an explicit inner skull mask. > There should be one in EEGTemplates as far as I remember or you can make > your own. > > You can either re-run your stats or use small volume correction for inner > skull but the latter will not fix the graphics. > > Best, > > Vladimir > > Sent from my BlackBerry smartphone from orange > ------------------------------ > *From: * MP <[log in to unmask]> > *Sender: * "SPM (Statistical Parametric Mapping)" <[log in to unmask]> > *Date: *Thu, 30 Dec 2010 21:33:40 -0500 > *To: *<[log in to unmask]> > *ReplyTo: * MP <[log in to unmask]> > *Subject: *[SPM] EEG significant clusters outside the MIP glass brain > > Hello all, > > I am doing EEG analysis using SPM8 and while viewing the results, I see > that some of the significant clusters appear outside the brain. I understand > that it could be due to smoothing of the images, but is there a way to > restrict these clusters inside the MIP? I think Threshold masking may be the > way to go, but I am not sure what threshold value to use? > > If indeed threshold masking is the way to go, would I need to re-do all the > analyses? > > Any help would be much appreciated. > > Thanks > - Muhammad > --90e6ba476b13485bfb049c480aa0 Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Hello Vladimir,

I tried to use the inner skull mask as you suggested to avoid getting significant cluster outside the glass brain, but it is drastically changing the results. Attached the figures of results with and without applying the mask. Could you please tell me if I am doing something wrong here?

P.S. I include the iskull mask as an implicit mask in the flexible factorial design.

Thanks
- Muhammad

On Fri, Dec 31, 2010 at 12:03 AM, <[log in to unmask]> wrote:
Dear Muhammad,

Threshold masking will not necessarily work. It depends whether the values outside the brain are really low. You can use an explicit inner skull mask. There should be one in EEGTemplates as far as I remember or you can make your own.

You can either re-run your stats or use small volume correction for inner skull but the latter will not fix the graphics.

Best,

Vladimir

Sent from my BlackBerry smartphone from orange


From: MP <[log in to unmask]>
Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]>
Date: Thu, 30 Dec 2010 21:33:40 -0500
ReplyTo: MP <[log in to unmask]>
Subject: [SPM] EEG significant clusters outside the MIP glass brain

Hello all,

I am doing EEG analysis using SPM8 and while viewing the results, I see that some of the significant clusters appear outside the brain. I understand that it could be due to smoothing of the images, but is there a way to restrict these clusters inside the MIP? I think Threshold masking may be the way to go, but I am not sure what threshold value to use?

If indeed threshold masking is the way to go, would I need to re-do all the analyses?

Any help would be much appreciated.

Thanks
- Muhammad

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ZKEljdyGw6yEFvulWU5AIKsCMVXHhi6+xfYVubGC08vySltaMhWPGCq5cheOOnFAHSp/q1+gopVG FA9BRQAtFFFABRRRQAUUUUAFFFFABRRRQAUUUUAFFFFABRRRQAUUUUAFFFFABRRRQAUUUUAFFFFA BRRRQAUUUUAFFFFABRRRQAUUUUAFFFFABRRRQAUUUUAFFFFABRRRQAUUUUAFFFFABRRRQAUUUUAF FFFABRRRQAUUUUAFFFFABRRRQAUUUUAFFFFAGfp1reW99q0tzcebDc3ay2qby3lRiGJCuD9350ds Dj5s9Sa0KKKACiiigAooooAKKKKACiiigAooooAKKKKACiiigAooooAKKKKACiiigAooooAKKKKA CiiigAooooAKKKKACiiigAooooAKKKKACiiigAooooAKKKKACiiigAooooAKKKKACiiigAooooAK KKKACiiigAooooAKKKKACiiigAooooAKKKKACiiigAooooAKKKKACiiigD//2Q=--90e6ba476b13485c07049c480aa2-- ========================================================================Date: Mon, 14 Feb 2011 21:04:16 -0500 Reply-To: cliff <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: cliff <[log in to unmask]> Subject: Re: spm_create_vol &&& spm_write_vol Comments: To: John Ashburner <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/alternative; boundaryMessage-ID: <[log in to unmask]> --000e0cd5d004ec29fe049c48948b Content-Type: text/plain; charset=ISO-8859-1 Thanks~~ Does that mean if I use "spm_create_vol" to create headers followed by "spm_write_vol" (if it is necessary), then the headers created by "spm_create_vol" will be overwrited? On Mon, Feb 14, 2011 at 5:32 PM, John Ashburner <[log in to unmask]>wrote: > spm_write_vol calls spm_create_vol. Sometimes, for example in the > fMRI stats, we may wish to create headers but only write out a slice > of data at a time (as there is not enough memory to hold all the > images). > > best regards, > -John > > On 14 February 2011 22:16, cliff <[log in to unmask]> wrote: > > Hi, all, > > I thought before that "spm_create_vol " is used to create the ".hdr" > files > > of the images. > > However, today I found that "spm_write_vol" can produce both of the > ".hdr" > > and ".img" files. > > > > then, what is the "spm_create_vol " exactly used for? > > > > Thanks~ > > > -- Sincerely, Senhua Zhu --000e0cd5d004ec29fe049c48948b Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable
Thanks~~
Does that mean if I use "spm_create_vol" to create headers followed by "spm_write_vol" (if it is necessary), then the headers created by "spm_create_vol" will be overwrited?

On Mon, Feb 14, 2011 at 5:32 PM, John Ashburner <[log in to unmask]> wrote:
spm_write_vol calls spm_create_vol. Sometimes, for example in the
fMRI stats, we may wish to create headers but only write out a slice
of data at a time (as there is not enough memory to hold all the
images).

best regards,
-John

On 14 February 2011 22:16, cliff <[log in to unmask]> wrote:
> Hi, all,
> I thought before that "spm_create_vol " is used to create the ".hdr" files
> of the images.
> However, today I found that "spm_write_vol" can produce both of the ".hdr"
> and ".img" files.
>
> then, what is the "spm_create_vol " exactly used for?
>
> Thanks~
>



--
Sincerely,
Senhua Zhu


--000e0cd5d004ec29fe049c48948b-- ========================================================================Date: Mon, 14 Feb 2011 18:09:10 -0800 Reply-To: Michael T Rubens <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Michael T Rubens <[log in to unmask]> Subject: Re: EEG significant clusters outside the MIP glass brain Comments: To: MP <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/alternative; boundaryMessage-ID: <[log in to unmask]> --00248c6a5726382f06049c48a80a Content-Type: text/plain; charset=UTF-8 Content-Transfer-Encoding: quoted-printable that is not right, the results should change due to the mask. Why don't you just run the analysis and mask out the resulting stat map. You're obviously not interested in anything off the brain (i.e., noise) anyway, so its valid. Cheers, Michael On Mon, Feb 14, 2011 at 5:25 PM, MP <[log in to unmask]> wrote: > Hello Vladimir, > > I tried to use the inner skull mask as you suggested to avoid getting > significant cluster outside the glass brain, but it is drastically changing > the results. Attached the figures of results with and without applying the > mask. Could you please tell me if I am doing something wrong here? > > P.S. I include the iskull mask as an implicit mask in the flexible > factorial design. > > Thanks > - Muhammad > > > On Fri, Dec 31, 2010 at 12:03 AM, <[log in to unmask]> wrote: > >> Dear Muhammad, >> >> Threshold masking will not necessarily work. It depends whether the values >> outside the brain are really low. You can use an explicit inner skull mask. >> There should be one in EEGTemplates as far as I remember or you can make >> your own. >> >> You can either re-run your stats or use small volume correction for inner >> skull but the latter will not fix the graphics. >> >> Best, >> >> Vladimir >> >> Sent from my BlackBerry® smartphone from orange >> ------------------------------ >> *From: * MP <[log in to unmask]> >> *Sender: * "SPM (Statistical Parametric Mapping)" <[log in to unmask]> >> *Date: *Thu, 30 Dec 2010 21:33:40 -0500 >> *To: *<[log in to unmask]> >> *ReplyTo: * MP <[log in to unmask]> >> *Subject: *[SPM] EEG significant clusters outside the MIP glass brain >> >> Hello all, >> >> I am doing EEG analysis using SPM8 and while viewing the results, I see >> that some of the significant clusters appear outside the brain. I understand >> that it could be due to smoothing of the images, but is there a way to >> restrict these clusters inside the MIP? I think Threshold masking may be the >> way to go, but I am not sure what threshold value to use? >> >> If indeed threshold masking is the way to go, would I need to re-do all >> the analyses? >> >> Any help would be much appreciated. >> >> Thanks >> - Muhammad >> > > -- Research Associate Gazzaley Lab Department of Neurology University of California, San Francisco --00248c6a5726382f06049c48a80a Content-Type: text/html; charset=UTF-8 Content-Transfer-Encoding: quoted-printable that is not right, the results should change due to the mask. Why don't you just run the analysis and mask out the resulting stat map. You're obviously not interested in anything off the brain (i.e., noise) anyway, so its valid.

Cheers,
Michael

On Mon, Feb 14, 2011 at 5:25 PM, MP <[log in to unmask]> wrote:
Hello Vladimir,

I tried to use the inner skull mask as you suggested to avoid getting significant cluster outside the glass brain, but it is drastically changing the results. Attached the figures of results with and without applying the mask. Could you please tell me if I am doing something wrong here?

P.S. I include the iskull mask as an implicit mask in the flexible factorial design.

Thanks
- Muhammad  


On Fri, Dec 31, 2010 at 12:03 AM, <[log in to unmask]> wrote:
Dear Muhammad,

Threshold masking will not necessarily work. It depends whether the values outside the brain are really low. You can use an explicit inner skull mask. There should be one in EEGTemplates as far as I remember or you can make your own.

You can either re-run your stats or use small volume correction for inner skull but the latter will not fix the graphics.

Best,

Vladimir

Sent from my BlackBerry® smartphone from orange


From: MP <[log in to unmask]>
Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]>
Date: Thu, 30 Dec 2010 21:33:40 -0500
ReplyTo: MP <[log in to unmask]>
Subject: [SPM] EEG significant clusters outside the MIP glass brain

Hello all,

I am doing EEG analysis using SPM8 and while viewing the results, I see that some of the significant clusters appear outside the brain. I understand that it could be due to smoothing of the images, but is there a way to restrict these clusters inside the MIP? I think Threshold masking may be the way to go, but I am not sure what threshold value to use?

If indeed threshold masking is the way to go, would I need to re-do all the analyses?

Any help would be much appreciated.

Thanks
- Muhammad 




--
Research Associate
Gazzaley Lab
Department of Neurology
University of California, San Francisco
--00248c6a5726382f06049c48a80a-- ========================================================================Date: Mon, 14 Feb 2011 21:27:10 -0500 Reply-To: MP <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: MP <[log in to unmask]> Subject: Re: EEG significant clusters outside the MIP glass brain Comments: To: Michael T Rubens <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/mixed; boundarye6ba6e8f6ed086e6049c48e60a Message-ID: <[log in to unmask]> --90e6ba6e8f6ed086e6049c48e60a Content-Type: multipart/alternative; boundarye6ba6e8f6ed086de049c48e608 --90e6ba6e8f6ed086de049c48e608 Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Thanks Michael, but even then the results ARE very different when I use the "inclusive" iskull.nii mask on stat map. See attached. What do you think is going on? On Mon, Feb 14, 2011 at 9:09 PM, Michael T Rubens <[log in to unmask]>wrote: > that is not right, the results should change due to the mask. Why don't you > just run the analysis and mask out the resulting stat map. You're obviously > not interested in anything off the brain (i.e., noise) anyway, so its valid. > > Cheers, > Michael > > > On Mon, Feb 14, 2011 at 5:25 PM, MP <[log in to unmask]> wrote: > >> Hello Vladimir, >> >> I tried to use the inner skull mask as you suggested to avoid getting >> significant cluster outside the glass brain, but it is drastically changing >> the results. Attached the figures of results with and without applying the >> mask. Could you please tell me if I am doing something wrong here? >> >> P.S. I include the iskull mask as an implicit mask in the flexible >> factorial design. >> >> Thanks >> - Muhammad >> >> >> On Fri, Dec 31, 2010 at 12:03 AM, <[log in to unmask]> wrote: >> >>> Dear Muhammad, >>> >>> Threshold masking will not necessarily work. It depends whether the >>> values outside the brain are really low. You can use an explicit inner skull >>> mask. There should be one in EEGTemplates as far as I remember or you can >>> make your own. >>> >>> You can either re-run your stats or use small volume correction for inner >>> skull but the latter will not fix the graphics. >>> >>> Best, >>> >>> Vladimir >>> >>> Sent from my BlackBerry smartphone from orange >>> ------------------------------ >>> *From: * MP <[log in to unmask]> >>> *Sender: * "SPM (Statistical Parametric Mapping)" <[log in to unmask]> >>> *Date: *Thu, 30 Dec 2010 21:33:40 -0500 >>> *To: *<[log in to unmask]> >>> *ReplyTo: * MP <[log in to unmask]> >>> *Subject: *[SPM] EEG significant clusters outside the MIP glass brain >>> >>> Hello all, >>> >>> I am doing EEG analysis using SPM8 and while viewing the results, I see >>> that some of the significant clusters appear outside the brain. I understand >>> that it could be due to smoothing of the images, but is there a way to >>> restrict these clusters inside the MIP? I think Threshold masking may be the >>> way to go, but I am not sure what threshold value to use? >>> >>> If indeed threshold masking is the way to go, would I need to re-do all >>> the analyses? >>> >>> Any help would be much appreciated. >>> >>> Thanks >>> - Muhammad >>> >> >> > > > -- > Research Associate > Gazzaley Lab > Department of Neurology > University of California, San Francisco > --90e6ba6e8f6ed086de049c48e608 Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Thanks Michael, but even then the results ARE very different when I use the "inclusive" iskull.nii mask on stat map. See attached.

What do you think is going on?

On Mon, Feb 14, 2011 at 9:09 PM, Michael T Rubens <[log in to unmask]> wrote:
that is not right, the results should change due to the mask. Why don't you just run the analysis and mask out the resulting stat map. You're obviously not interested in anything off the brain (i.e., noise) anyway, so its valid.

Cheers,
Michael


On Mon, Feb 14, 2011 at 5:25 PM, MP <[log in to unmask]> wrote:
Hello Vladimir,

I tried to use the inner skull mask as you suggested to avoid getting significant cluster outside the glass brain, but it is drastically changing the results. Attached the figures of results with and without applying the mask. Could you please tell me if I am doing something wrong here?

P.S. I include the iskull mask as an implicit mask in the flexible factorial design.

Thanks
- Muhammad


On Fri, Dec 31, 2010 at 12:03 AM, <[log in to unmask]> wrote:
Dear Muhammad,

Threshold masking will not necessarily work. It depends whether the values outside the brain are really low. You can use an explicit inner skull mask. There should be one in EEGTemplates as far as I remember or you can make your own.

You can either re-run your stats or use small volume correction for inner skull but the latter will not fix the graphics.

Best,

Vladimir

Sent from my BlackBerry smartphone from orange


From: MP <[log in to unmask]>
Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]>
Date: Thu, 30 Dec 2010 21:33:40 -0500
ReplyTo: MP <[log in to unmask]>
Subject: [SPM] EEG significant clusters outside the MIP glass brain

Hello all,

I am doing EEG analysis using SPM8 and while viewing the results, I see that some of the significant clusters appear outside the brain. I understand that it could be due to smoothing of the images, but is there a way to restrict these clusters inside the MIP? I think Threshold masking may be the way to go, but I am not sure what threshold value to use?

If indeed threshold masking is the way to go, would I need to re-do all the analyses?

Any help would be much appreciated.

Thanks
- Muhammad




--
Research Associate
Gazzaley Lab
Department of Neurology
University of California, San Francisco

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(Statistical Parametric Mapping)" <[log in to unmask]> From: Michael T Rubens <[log in to unmask]> Subject: Re: EEG significant clusters outside the MIP glass brain Comments: To: MP <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/alternative; boundary cf3054ac0b0f9a2b049c491673 Message-ID: <[log in to unmask]> --20cf3054ac0b0f9a2b049c491673 Content-Type: text/plain; charset=UTF-8 Content-Transfer-Encoding: quoted-printable no idea, did you look at the mask to see what it looks like? what kind of threshold/correction are you using? if you're using a cluster based threshold like friston's cluster fdr then it could be that off brain stuff is inflating clusters that don't pass correction with the mask. Cheers, Michael On Mon, Feb 14, 2011 at 6:27 PM, MP <[log in to unmask]> wrote: > Thanks Michael, but even then the results ARE very different when I use the > "inclusive" iskull.nii mask on stat map. See attached. > > What do you think is going on? > > On Mon, Feb 14, 2011 at 9:09 PM, Michael T Rubens <[log in to unmask]>wrote: > >> that is not right, the results should change due to the mask. Why don't >> you just run the analysis and mask out the resulting stat map. You're >> obviously not interested in anything off the brain (i.e., noise) anyway, so >> its valid. >> >> Cheers, >> Michael >> >> >> On Mon, Feb 14, 2011 at 5:25 PM, MP <[log in to unmask]> wrote: >> >>> Hello Vladimir, >>> >>> I tried to use the inner skull mask as you suggested to avoid getting >>> significant cluster outside the glass brain, but it is drastically changing >>> the results. Attached the figures of results with and without applying the >>> mask. Could you please tell me if I am doing something wrong here? >>> >>> P.S. I include the iskull mask as an implicit mask in the flexible >>> factorial design. >>> >>> Thanks >>> - Muhammad >>> >>> >>> On Fri, Dec 31, 2010 at 12:03 AM, <[log in to unmask]> wrote: >>> >>>> Dear Muhammad, >>>> >>>> Threshold masking will not necessarily work. It depends whether the >>>> values outside the brain are really low. You can use an explicit inner skull >>>> mask. There should be one in EEGTemplates as far as I remember or you can >>>> make your own. >>>> >>>> You can either re-run your stats or use small volume correction for >>>> inner skull but the latter will not fix the graphics. >>>> >>>> Best, >>>> >>>> Vladimir >>>> >>>> Sent from my BlackBerry® smartphone from orange >>>> ------------------------------ >>>> *From: * MP <[log in to unmask]> >>>> *Sender: * "SPM (Statistical Parametric Mapping)" <[log in to unmask]> >>>> *Date: *Thu, 30 Dec 2010 21:33:40 -0500 >>>> *To: *<[log in to unmask]> >>>> *ReplyTo: * MP <[log in to unmask]> >>>> *Subject: *[SPM] EEG significant clusters outside the MIP glass brain >>>> >>>> Hello all, >>>> >>>> I am doing EEG analysis using SPM8 and while viewing the results, I see >>>> that some of the significant clusters appear outside the brain. I understand >>>> that it could be due to smoothing of the images, but is there a way to >>>> restrict these clusters inside the MIP? I think Threshold masking may be the >>>> way to go, but I am not sure what threshold value to use? >>>> >>>> If indeed threshold masking is the way to go, would I need to re-do all >>>> the analyses? >>>> >>>> Any help would be much appreciated. >>>> >>>> Thanks >>>> - Muhammad >>>> >>> >>> >> >> >> -- >> Research Associate >> Gazzaley Lab >> Department of Neurology >> University of California, San Francisco >> > > -- Research Associate Gazzaley Lab Department of Neurology University of California, San Francisco --20cf3054ac0b0f9a2b049c491673 Content-Type: text/html; charset=UTF-8 Content-Transfer-Encoding: quoted-printable no idea, did you look at the mask to see what it looks like?

what kind of threshold/correction are you using? if you're using a cluster based threshold like friston's cluster fdr then it could be that off brain stuff is inflating clusters that don't pass correction with the mask.

Cheers,
Michael

On Mon, Feb 14, 2011 at 6:27 PM, MP <[log in to unmask]> wrote:
Thanks Michael, but even then the results ARE very different when I use the "inclusive" iskull.nii  mask on stat map. See attached.

What do you think is going on?

On Mon, Feb 14, 2011 at 9:09 PM, Michael T Rubens <[log in to unmask]> wrote:
that is not right, the results should change due to the mask. Why don't you just run the analysis and mask out the resulting stat map. You're obviously not interested in anything off the brain (i.e., noise) anyway, so its valid.

Cheers,
Michael


On Mon, Feb 14, 2011 at 5:25 PM, MP <[log in to unmask]> wrote:
Hello Vladimir,

I tried to use the inner skull mask as you suggested to avoid getting significant cluster outside the glass brain, but it is drastically changing the results. Attached the figures of results with and without applying the mask. Could you please tell me if I am doing something wrong here?

P.S. I include the iskull mask as an implicit mask in the flexible factorial design.

Thanks
- Muhammad  


On Fri, Dec 31, 2010 at 12:03 AM, <[log in to unmask]> wrote:
Dear Muhammad,

Threshold masking will not necessarily work. It depends whether the values outside the brain are really low. You can use an explicit inner skull mask. There should be one in EEGTemplates as far as I remember or you can make your own.

You can either re-run your stats or use small volume correction for inner skull but the latter will not fix the graphics.

Best,

Vladimir

Sent from my BlackBerry® smartphone from orange


From: MP <[log in to unmask]>
Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]>
Date: Thu, 30 Dec 2010 21:33:40 -0500
ReplyTo: MP <[log in to unmask]>
Subject: [SPM] EEG significant clusters outside the MIP glass brain

Hello all,

I am doing EEG analysis using SPM8 and while viewing the results, I see that some of the significant clusters appear outside the brain. I understand that it could be due to smoothing of the images, but is there a way to restrict these clusters inside the MIP? I think Threshold masking may be the way to go, but I am not sure what threshold value to use?

If indeed threshold masking is the way to go, would I need to re-do all the analyses?

Any help would be much appreciated.

Thanks
- Muhammad 




--
Research Associate
Gazzaley Lab
Department of Neurology
University of California, San Francisco




--
Research Associate
Gazzaley Lab
Department of Neurology
University of California, San Francisco
--20cf3054ac0b0f9a2b049c491673-- ========================================================================Date: Mon, 14 Feb 2011 21:52:53 -0500 Reply-To: MP <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: MP <[log in to unmask]> Subject: Re: EEG significant clusters outside the MIP glass brain Comments: To: Michael T Rubens <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/alternative; boundarye6ba476b13bf211e049c494270 Message-ID: <[log in to unmask]> --90e6ba476b13bf211e049c494270 Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable hi Michael, The mask looks fine to me. Could it be due to different dimensions of the mask and the stat map? - M On Mon, Feb 14, 2011 at 9:39 PM, Michael T Rubens <[log in to unmask]>wrote: > no idea, did you look at the mask to see what it looks like? > > what kind of threshold/correction are you using? if you're using a cluster > based threshold like friston's cluster fdr then it could be that off brain > stuff is inflating clusters that don't pass correction with the mask. > > Cheers, > Michael > > > On Mon, Feb 14, 2011 at 6:27 PM, MP <[log in to unmask]> wrote: > >> Thanks Michael, but even then the results ARE very different when I use >> the "inclusive" iskull.nii mask on stat map. See attached. >> >> What do you think is going on? >> >> On Mon, Feb 14, 2011 at 9:09 PM, Michael T Rubens <[log in to unmask]>wrote: >> >>> that is not right, the results should change due to the mask. Why don't >>> you just run the analysis and mask out the resulting stat map. You're >>> obviously not interested in anything off the brain (i.e., noise) anyway, so >>> its valid. >>> >>> Cheers, >>> Michael >>> >>> >>> On Mon, Feb 14, 2011 at 5:25 PM, MP <[log in to unmask]> wrote: >>> >>>> Hello Vladimir, >>>> >>>> I tried to use the inner skull mask as you suggested to avoid getting >>>> significant cluster outside the glass brain, but it is drastically changing >>>> the results. Attached the figures of results with and without applying the >>>> mask. Could you please tell me if I am doing something wrong here? >>>> >>>> P.S. I include the iskull mask as an implicit mask in the flexible >>>> factorial design. >>>> >>>> Thanks >>>> - Muhammad >>>> >>>> >>>> On Fri, Dec 31, 2010 at 12:03 AM, <[log in to unmask]> wrote: >>>> >>>>> Dear Muhammad, >>>>> >>>>> Threshold masking will not necessarily work. It depends whether the >>>>> values outside the brain are really low. You can use an explicit inner skull >>>>> mask. There should be one in EEGTemplates as far as I remember or you can >>>>> make your own. >>>>> >>>>> You can either re-run your stats or use small volume correction for >>>>> inner skull but the latter will not fix the graphics. >>>>> >>>>> Best, >>>>> >>>>> Vladimir >>>>> >>>>> Sent from my BlackBerry smartphone from orange >>>>> ------------------------------ >>>>> *From: * MP <[log in to unmask]> >>>>> *Sender: * "SPM (Statistical Parametric Mapping)" <[log in to unmask]> >>>>> >>>>> *Date: *Thu, 30 Dec 2010 21:33:40 -0500 >>>>> *To: *<[log in to unmask]> >>>>> *ReplyTo: * MP <[log in to unmask]> >>>>> *Subject: *[SPM] EEG significant clusters outside the MIP glass brain >>>>> >>>>> Hello all, >>>>> >>>>> I am doing EEG analysis using SPM8 and while viewing the results, I see >>>>> that some of the significant clusters appear outside the brain. I understand >>>>> that it could be due to smoothing of the images, but is there a way to >>>>> restrict these clusters inside the MIP? I think Threshold masking may be the >>>>> way to go, but I am not sure what threshold value to use? >>>>> >>>>> If indeed threshold masking is the way to go, would I need to re-do all >>>>> the analyses? >>>>> >>>>> Any help would be much appreciated. >>>>> >>>>> Thanks >>>>> - Muhammad >>>>> >>>> >>>> >>> >>> >>> -- >>> Research Associate >>> Gazzaley Lab >>> Department of Neurology >>> University of California, San Francisco >>> >> >> > > > -- > Research Associate > Gazzaley Lab > Department of Neurology > University of California, San Francisco > --90e6ba476b13bf211e049c494270 Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable hi Michael,

The mask looks fine to me. Could it be due to different dimensions of the mask and the stat map?

- M

On Mon, Feb 14, 2011 at 9:39 PM, Michael T Rubens <[log in to unmask]> wrote:
no idea, did you look at the mask to see what it looks like?

what kind of threshold/correction are you using? if you're using a cluster based threshold like friston's cluster fdr then it could be that off brain stuff is inflating clusters that don't pass correction with the mask.

Cheers,
Michael


On Mon, Feb 14, 2011 at 6:27 PM, MP <[log in to unmask]> wrote:
Thanks Michael, but even then the results ARE very different when I use the "inclusive" iskull.nii mask on stat map. See attached.

What do you think is going on?

On Mon, Feb 14, 2011 at 9:09 PM, Michael T Rubens <[log in to unmask]> wrote:
that is not right, the results should change due to the mask. Why don't you just run the analysis and mask out the resulting stat map. You're obviously not interested in anything off the brain (i.e., noise) anyway, so its valid.

Cheers,
Michael


On Mon, Feb 14, 2011 at 5:25 PM, MP <[log in to unmask]> wrote:
Hello Vladimir,

I tried to use the inner skull mask as you suggested to avoid getting significant cluster outside the glass brain, but it is drastically changing the results. Attached the figures of results with and without applying the mask. Could you please tell me if I am doing something wrong here?

P.S. I include the iskull mask as an implicit mask in the flexible factorial design.

Thanks
- Muhammad


On Fri, Dec 31, 2010 at 12:03 AM, <[log in to unmask]> wrote:
Dear Muhammad,

Threshold masking will not necessarily work. It depends whether the values outside the brain are really low. You can use an explicit inner skull mask. There should be one in EEGTemplates as far as I remember or you can make your own.

You can either re-run your stats or use small volume correction for inner skull but the latter will not fix the graphics.

Best,

Vladimir

Sent from my BlackBerry smartphone from orange


From: MP <[log in to unmask]>
Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]>
Date: Thu, 30 Dec 2010 21:33:40 -0500
ReplyTo: MP <[log in to unmask]>
Subject: [SPM] EEG significant clusters outside the MIP glass brain

Hello all,

I am doing EEG analysis using SPM8 and while viewing the results, I see that some of the significant clusters appear outside the brain. I understand that it could be due to smoothing of the images, but is there a way to restrict these clusters inside the MIP? I think Threshold masking may be the way to go, but I am not sure what threshold value to use?

If indeed threshold masking is the way to go, would I need to re-do all the analyses?

Any help would be much appreciated.

Thanks
- Muhammad




--
Research Associate
Gazzaley Lab
Department of Neurology
University of California, San Francisco




--
Research Associate
Gazzaley Lab
Department of Neurology
University of California, San Francisco

--90e6ba476b13bf211e049c494270-- ========================================================================Date: Tue, 15 Feb 2011 08:43:31 +0000 Reply-To: John Ashburner <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: John Ashburner <[log in to unmask]> Subject: Re: spm_create_vol &&& spm_write_vol Comments: To: cliff <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> If spm_create_vol provides a different set of information about headers from what was in spm_create_vol, then the header will contain the most recent information. Best regards, -John On 15 February 2011 02:04, cliff <[log in to unmask]> wrote: > Thanks~~ > > Does that mean if I use "spm_create_vol" to create headers followed by > "spm_write_vol" (if it is necessary), then the headers created by > "spm_create_vol" will be overwrited? > > On Mon, Feb 14, 2011 at 5:32 PM, John Ashburner <[log in to unmask]> > wrote: >> >> spm_write_vol calls spm_create_vol. Sometimes, for example in the >> fMRI stats, we may wish to create headers but only write out a slice >> of data at a time (as there is not enough memory to hold all the >> images). >> >> best regards, >> -John >> >> On 14 February 2011 22:16, cliff <[log in to unmask]> wrote: >> > Hi, all, >> > I thought before that "spm_create_vol " is used to create the ".hdr" >> > files >> > of the images. >> > However, today I found that "spm_write_vol" can produce both of the >> > ".hdr" >> > and ".img" files. >> > >> > then, what is the "spm_create_vol " exactly used for? >> > >> > Thanks~ >> > > > > > -- > Sincerely, > Senhua Zhu > > > ========================================================================Date: Tue, 15 Feb 2011 12:09:03 +0100 Reply-To: vgarcia <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: vgarcia <[log in to unmask]> Subject: Paired t-test + Covariate MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1; format=flowed Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> Dear List, Our design is a paired t-test (13 subjects) with a covariate (its value is the same in both images of the same subject). We would like to test the hypothesis of zero regression slope against the alternative of a positive slope with the following contrast (value 1 in the column of the covariate): zeros(1,13) 1 0 0 But the contrast is invalid. What are we doing wrong? Thanks a million Vernica ========================================================================Date: Tue, 15 Feb 2011 11:20:54 +0000 Reply-To: Vladimir Litvak <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Vladimir Litvak <[log in to unmask]> Subject: Re: EEG significant clusters outside the MIP glass brain Comments: To: MP <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> Dear Muhammad, It looks like the analysis you are doing is at the sensor level, but you use a brain mask. This does not make sense. In your original message you said that you are getting clusters outside the brain so I assumed that you are talking about source images. If you are doing sensor level analysis and you smooth your images you can possibly get clusters extending outside the scalp. To avoid that you can generate a mask using Other/Mask Images. You should provide an original unsmoothed image as input. Best, Vladimir On Tue, Feb 15, 2011 at 2:52 AM, MP <[log in to unmask]> wrote: > hi Michael, > The mask looks fine to me. Could it be due to different dimensions of the > mask and the stat map? > - M > > On Mon, Feb 14, 2011 at 9:39 PM, Michael T Rubens <[log in to unmask]> > wrote: >> >> no idea, did you look at the mask to see what it looks like? >> >> what kind of threshold/correction are you using? if you're using a cluster >> based threshold like friston's cluster fdr then it could be that off brain >> stuff is inflating clusters that don't pass correction with the mask. >> >> Cheers, >> Michael >> >> On Mon, Feb 14, 2011 at 6:27 PM, MP <[log in to unmask]> wrote: >>> >>> Thanks Michael, but even then the results ARE very different when I use >>> the "inclusive" iskull.nii mask on stat map. See attached. >>> What do you think is going on? >>> >>> On Mon, Feb 14, 2011 at 9:09 PM, Michael T Rubens <[log in to unmask]> >>> wrote: >>>> >>>> that is not right, the results should change due to the mask. Why don't >>>> you just run the analysis and mask out the resulting stat map. You're >>>> obviously not interested in anything off the brain (i.e., noise) anyway, so >>>> its valid. >>>> >>>> Cheers, >>>> Michael >>>> >>>> On Mon, Feb 14, 2011 at 5:25 PM, MP <[log in to unmask]> wrote: >>>>> >>>>> Hello Vladimir, >>>>> I tried to use the inner skull mask as you suggested to avoid getting >>>>> significant cluster outside the glass brain, but it is drastically changing >>>>> the results. Attached the figures of results with and without applying the >>>>> mask. Could you please tell me if I am doing something wrong here? >>>>> P.S. I include the iskull mask as an implicit mask in the flexible >>>>> factorial design. >>>>> Thanks >>>>> - Muhammad >>>>> >>>>> On Fri, Dec 31, 2010 at 12:03 AM, <[log in to unmask]> wrote: >>>>>> >>>>>> Dear Muhammad, >>>>>> >>>>>> Threshold masking will not necessarily work. It depends whether the >>>>>> values outside the brain are really low. You can use an explicit inner skull >>>>>> mask. There should be one in EEGTemplates as far as I remember or you can >>>>>> make your own. >>>>>> >>>>>> You can either re-run your stats or use small volume correction for >>>>>> inner skull but the latter will not fix the graphics. >>>>>> >>>>>> Best, >>>>>> >>>>>> Vladimir >>>>>> >>>>>> Sent from my BlackBerry smartphone from orange >>>>>> >>>>>> ________________________________ >>>>>> From: MP <[log in to unmask]> >>>>>> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> >>>>>> Date: Thu, 30 Dec 2010 21:33:40 -0500 >>>>>> To: <[log in to unmask]> >>>>>> ReplyTo: MP <[log in to unmask]> >>>>>> Subject: [SPM] EEG significant clusters outside the MIP glass brain >>>>>> Hello all, >>>>>> I am doing EEG analysis using SPM8 and while viewing the results, I >>>>>> see that some of the significant clusters appear outside the brain. I >>>>>> understand that it could be due to smoothing of the images, but is there a >>>>>> way to restrict these clusters inside the MIP? I think Threshold masking may >>>>>> be the way to go, but I am not sure what threshold value to use? >>>>>> If indeed threshold masking is the way to go, would I need to re-do >>>>>> all the analyses? >>>>>> Any help would be much appreciated. >>>>>> Thanks >>>>>> - Muhammad >>>> >>>> >>>> >>>> -- >>>> Research Associate >>>> Gazzaley Lab >>>> Department of Neurology >>>> University of California, San Francisco >>> >> >> >> >> -- >> Research Associate >> Gazzaley Lab >> Department of Neurology >> University of California, San Francisco > > ========================================================================Date: Tue, 15 Feb 2011 11:29:30 +0000 Reply-To: Vladimir Litvak <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Vladimir Litvak <[log in to unmask]> Subject: Re: Question about lead field matrix Comments: To: Carsten Stahlhut <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Message-ID: [log in to unmask]> Dear Carsten, I actually see now that the option to use OpenMEEG is already in the code of the present version 4010. If you look in spm_eeg_inv_forward around line 88, you'll find it there. It's just not in the GUI, which is easy to fix by adding 'OpenMEEG BEM' to the list in spm_eeg_inv_forward_ui. I'm sure Alexandre will be glad to help you with installation. I suspect on LINUX it's more straightforward than on Windows. Best, Vladimir On Mon, Feb 14, 2011 at 9:58 PM, Carsten Stahlhut <[log in to unmask]> wrote: > Dear Vladimir, > > Thanks for clarifying the issue with the physical units - that confirmed a > little suspicion on my that it would probably be better for me to leave out > the units in some plots that I did of reconstructed sources. > > Yes, indeed the platform is also one my concerns - however, I think it > should work with Linux. > Regarding the computation time - my impression is that it is very fast > compared to other FEM implementations and almost just as fast as computing > BEM solutions. I guess the reason why I suddenly found the SimBio's FEM head > model very appealing was that in one of their recent papers (see e.g. the > attached paper page 1926), they claim that with a grid of 2 * 2 * 2 mm^3 > they can build a FEM with 71 electrodes in less than 22 min and less than 38 > min for a sensor configuration of 258 electrodes! That's quite an > improvement. > All of this is performed just on a Linux-workstation - Intel Core 2 Duo > E6600 processor (2.4 GHz) with 4 GB memory. > > Thanks for bringing the OpenMEEG software to my attention. I think that's a > really good alternative. Yes, that would be really great if I would send me > your code for using the OpenMEEG BEM implementation. > > Best, > Carsten > > > > > 2011/2/14 Vladimir Litvak <[log in to unmask]> >> >> Dear Carsten >> >> On Fri, Feb 11, 2011 at 11:56 PM, Carsten Stahlhut <[log in to unmask]> wrote: >> > Dear Vladimir, >> > >> > I have approx three questions (or issues) that I hope you can help me >> > out >> > with. >> > >> > Do you know what the units are for the lead field matrix and the source >> > estimates in SPM8? >> >> These are two different questions. >> >> > If you apply one of the EEG imaging methods (as I understood it) then >> > the >> > source estimates should be current density i.e. the unit should be >> > something >> > like A/m^2 or uA/mm^2 depending on the scaling of the EEG data and lead >> > field matrix. >> > And then the units of the lead field should be something like m^2 * Ohm >> > ( = >> > m^2 / S ). >> >> In theory the forward computation done by the 'forward' toolbox should >> be unit-blind so the units of the lead field should depend on units of >> the head model (mm in SPM). In practice this might not be the case. We >> recently found a difference in scaling between 'single shell' and >> other MEG models. This will be fixed in the next update. There might >> be something similar also for EEG. SPM is not sensitive to it but it's >> still something worth looking into. >> >> > Does this also holds for SPM8 or do there exist any type of scaling of >> > the >> > lead field matrix such as a normalization of the columns or something >> > like >> > that? >> > >> >> Yes, there are several scaling and normalization steps so the units of >> the output images are not related to original physical units but are >> normalize to the total power across sources and conditions. >> >> > The second question is related to the lead field matrix as well. If I >> > compare two different head models a BEM and 3-spheres model then they >> > seem >> > to be on two very different scales - is that really the case? Or am I >> > missing an important step? Of course it is two very different head model >> > assumptions so they should be quite different but I'm a bit surprised >> > that >> > there exists a scaling factor of 100 between the largest element in the >> > BEM >> > gain matrix and the 3-spheres gain matrix. >> >> See above. >> >> > What I just did was to load the mat-files with the gain-matrices and >> > used >> > the imagesc-function to show the amplitudes of the two lead field >> > matrices. >> > >> > The 28th Jul 2010 you sent an answer to a post regarding head models and >> > you >> > here mentioned that FEM head models from SimBio might be an option in >> > the >> > very nice MEEGTool. I was wondering what the status is on integrating >> > the >> > SimBio FEM implementation with SPM, as I'm very interested to try out >> > the >> > FEM head models. I guess there is no reason that I will try to write the >> > code my self if the option is almost done and will be part of the >> > MEEGTool. >> > >> >> I am aware of some efforts to integrate SimBio support in the forward >> toolbox. Even if this is done I don't expect it to become one of the >> standard options in SPM because SimBio runs only on a particular Unix >> platform (I'm not even sure it's LINUX) and I suspect has very lengthy >> computing time. But if you compute a gain matrix for the canonical >> mesh in SimBio you can just replace the mat file generated by SPM with >> your file and it will be used by spm_eeg_invert. If there is >> inconsistency in units, it shouldn't be a problem. >> >> There is also a possibility to use another BEM implementation OpenMEEG >> (http://www-sop.inria.fr/athena/software/OpenMEEG/). That's something >> that works and I tested it last year, but found it impractical for >> most users again because of difficulties with installation and long >> computation time (about 24 h for normal mesh). The differences in the >> lead fields with our BEM were only for a small number of vertices >> close to the surface. But I can give you the glue code for this if you >> want. >> >> Best, >> >> Vladimir >> >> >> >> >> > Best, >> > Carsten >> > >> > >> > > > > > -- > Carsten Stahlhut > Section for Cognitive Systems > Department of Informatics and Mathematical Modelling > > Richard Petersens Plads, Building 321 > Technical University of Denmark > DK-2800 Kongens Lyngby, Denmark > ========================================================================Date: Tue, 15 Feb 2011 12:59:06 +0000 Reply-To: "B. de Haan" <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: "B. de Haan" <[log in to unmask]> Subject: Lesion analysis workshop Tuebingen 27th of May 2011 Mime-Version: 1.0 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain; charset="UTF-8" Message-ID: <[log in to unmask]> We would like to announce a lesion analysis workshop on the 27th of May 2011 in Tuebingen. The workshop will provide an overview on the background, rationale and methods of modern lesion analysis as well as a demonstration of their practical application. At the end of the workshop, participants should be able to independently conduct modern lesion analyses. Further information including program and registration form can be found on: http://homepages.uni-tuebingen.de/karnath/LesionAnalysisWorkshop2011/LesionAnalysisWorkshopHome.html ========================================================================Date: Tue, 15 Feb 2011 14:07:20 +0000 Reply-To: Joseph Whittaker <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Joseph Whittaker <[log in to unmask]> Subject: Normalization after New Segment MIME-Version: 1.0 Content-Type: multipart/alternative; boundaryMessage-ID: <[log in to unmask]> --001636c59ab9c984c4049c52ae52 Content-Type: text/plain; charset=ISO-8859-1 Dear SPM experts, I have some structural images that will not segment properly using the default segment option in SPM8, however the New Segment option available in the tools does work. The only problem is that it does not output a parameter file that can be used in the normalization procedure. Has anyone found away around this problem? Perhaps I could copy the relevant parameters from the seg8.mat file (produced by New Segment) to the seg_sn.mat file (produced by default Segment) as a sort of work around, or maybe just change the seg8.mat file into an acceptable format. Any advice or information would be appreciated. Thanks. Regards joe -- Joseph Whittaker, M.Sc Ph.D Student G.803 Neuroscience and Psychiatry Unit Stopford Building University of Manchester Oxford Road Manchester, UK Tel: 0161 275 1729 --001636c59ab9c984c4049c52ae52 Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable
Dear SPM experts,

I have some structural images that will not segment properly using the default segment option in SPM8, however the New Segment option available in the tools does work. The only problem is that it does not output a parameter file that can be used in the normalization procedure. Has anyone found away around this problem? Perhaps I could copy the relevant parameters from the seg8.mat file (produced by New Segment) to the seg_sn.mat file (produced by default Segment) as a sort of work around, or maybe just change the seg8.mat file into an acceptable format. Any advice or information would be appreciated. Thanks.

Regards

joe
--
Joseph Whittaker, M.Sc
Ph.D Student
G.803 Neuroscience and Psychiatry Unit
Stopford Building
University of Manchester
Oxford Road
Manchester, UK
Tel: 0161 275 1729
--001636c59ab9c984c4049c52ae52-- ========================================================================Date: Tue, 15 Feb 2011 14:42:35 +0000 Reply-To: John Ashburner <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: John Ashburner <[log in to unmask]> Subject: Re: Normalization after New Segment Comments: To: Joseph Whittaker <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Message-ID: [log in to unmask]> The new segment algorithm can be set up to generate a deformation field, which can be used for spatially normalising images. You'll see these options down the bottom of the new segment UI. The deformation fields can be used to warp images via the Deformations Utility, although it may not be so friendly for those who don't know what a composition is. Best regards, -John On 15 February 2011 14:07, Joseph Whittaker <[log in to unmask]> wrote: > > Dear SPM experts, > > I have some structural images that will not segment properly using the > default segment option in SPM8, however the New Segment option available in > the tools does work. The only problem is that it does not output a parameter > file that can be used in the normalization procedure. Has anyone found away > around this problem? Perhaps I could copy the relevant parameters from the > seg8.mat file (produced by New Segment) to the seg_sn.mat file (produced by > default Segment) as a sort of work around, or maybe just change the seg8.mat > file into an acceptable format. Any advice or information would be > appreciated. Thanks. > > Regards > > joe > -- > Joseph Whittaker, M.Sc > Ph.D Student > G.803 Neuroscience and Psychiatry Unit > Stopford Building > University of Manchester > Oxford Road > Manchester, UK > Tel: 0161 275 1729 > ========================================================================Date: Tue, 15 Feb 2011 16:42:06 +0100 Reply-To: vgarcia <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: vgarcia <[log in to unmask]> Subject: Re: Paired t-test + Covariate In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/alternative; boundary="------------080802090806010109080809" Message-ID: <[log in to unmask]> This is a multi-part message in MIME format. --------------080802090806010109080809 Content-Type: text/plain; charset=ISO-8859-1; format=flowed Content-Transfer-Encoding: quoted-printable X-MIME-Autoconverted: from 8bit to quoted-printable by bifur.jiscmail.ac.uk id p1FFjeGB011923 Dear List Our design matrix is the following one: Thanks a lot, Vernica On 14 February 2011 15:08, vgarcia<[log in to unmask]> wrote: > Dear List, > > Our design is a paired t-test (13 subjects) with a covariate (its value > is the same in both images of the same subject). We would like to test > the hypothesis of zero regression slope against the alternative of a > positive slope with the following contrast (value 1 in the column of the > covariate): > > zeros(1,13) 1 0 0 > > But the contrast is invalid. What are we doing wrong? > > Thanks a million > > Vernica > > > > --------------080802090806010109080809 Content-Type: multipart/related; boundary="------------060905000103080704000403" --------------060905000103080704000403 Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: 7bit
Dear List

Our design matrix is the following one:




Thanks a lot,

Verónica


On 14 February 2011 15:08, vgarcia <[log in to unmask]> wrote:
[log in to unmask]" type="cite">Dear List,

Our design is a paired t-test (13 subjects) with a covariate (its value
is the same in both images of the same subject). We would like to test
the hypothesis of zero regression slope against the alternative of a
positive slope with the following contrast (value 1 in the column of the
covariate):

zeros(1,13) 1 0 0

But the contrast is invalid. What are we doing wrong?

Thanks a million

Verónica





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<[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/related; boundary cf3054a28506dee0049c54307c Message-ID: <[log in to unmask]> --20cf3054a28506dee0049c54307c Content-Type: multipart/alternative; boundary cf3054a28506deda049c54307b --20cf3054a28506deda049c54307b Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Veronica, A couple of points: (1) Conditions should be set to equal variance, you have them set to unequal; (2) This is not a valid contrast, however, there are two ways around this depending on your question: (a) You want to know where you covariate correlates to the average value of condition1 and condition2; form a new contrast at the single subject level for the average of condition1 and condition 2 (1/2 1/2) and then then use a one-sample t-test with your covariate. (b) You want to know where the covariate correlates with the difference in condition 1 and condition2; form a new contrast at the single subject level for condition1-condition2 (1 -1) and then then a one-sample t-test with your covariate. Best Regards, Donald McLaren ================= D.G. McLaren, Ph.D. Postdoctoral Research Fellow, GRECC, Bedford VA Research Fellow, Department of Neurology, Massachusetts General Hospital and Harvard Medical School Office: (773) 406-2464 ===================== This e-mail contains CONFIDENTIAL INFORMATION which may contain PROTECTED HEALTHCARE INFORMATION and may also be LEGALLY PRIVILEGED and which is intended only for the use of the individual or entity named above. If the reader of the e-mail is not the intended recipient or the employee or agent responsible for delivering it to the intended recipient, you are hereby notified that you are in possession of confidential and privileged information. Any unauthorized use, disclosure, copying or the taking of any action in reliance on the contents of this information is strictly prohibited and may be unlawful. If you have received this e-mail unintentionally, please immediately notify the sender via telephone at (773) 406-2464 or email. On Tue, Feb 15, 2011 at 10:42 AM, vgarcia <[log in to unmask]> wrote: > Dear List > > Our design matrix is the following one: > > > > Thanks a lot, > > Vernica > > > On 14 February 2011 15:08, vgarcia <[log in to unmask]> <[log in to unmask]> wrote: > > Dear List, > > Our design is a paired t-test (13 subjects) with a covariate (its value > is the same in both images of the same subject). We would like to test > the hypothesis of zero regression slope against the alternative of a > positive slope with the following contrast (value 1 in the column of the > covariate): > > zeros(1,13) 1 0 0 > > But the contrast is invalid. What are we doing wrong? > > Thanks a million > > Vernica > > > > > > --20cf3054a28506deda049c54307b Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Veronica,

A couple of points:
(1) Conditions should be set to equal variance, you have them set to unequal;
(2) This is not a valid contrast, however, there are two ways around this depending on your question:
(a) You want to know where you covariate correlates to the average value of condition1 and condition2; form a new contrast at the single subject level for the average of condition1 and condition 2 (1/2 1/2) and then then use a one-sample t-test with your covariate.
(b) You want to know where the covariate correlates with the difference in condition 1 and condition2; form a new contrast at the single subject level for condition1-condition2 (1 -1) and then then a one-sample t-test with your covariate.

Best Regards, Donald McLaren
=================
D.G. McLaren, Ph.D.
Postdoctoral Research Fellow, GRECC, Bedford VA
Research Fellow, Department of Neurology, Massachusetts General Hospital and Harvard Medical School
Office: (773) 406-2464
=====================
This e-mail contains CONFIDENTIAL INFORMATION which may contain PROTECTED HEALTHCARE INFORMATION and may also be LEGALLY PRIVILEGED and which is intended only for the use of the individual or entity named above. If the reader of the e-mail is not the intended recipient or the employee or agent responsible for delivering it to the intended recipient, you are hereby notified that you are in possession of confidential and privileged information. Any unauthorized use, disclosure, copying or the taking of any action in reliance on the contents of this information is strictly prohibited and may be unlawful. If you have received this e-mail unintentionally, please immediately notify the sender via telephone at (773) 406-2464 or email.


On Tue, Feb 15, 2011 at 10:42 AM, vgarcia <[log in to unmask]> wrote:
Dear List

Our design matrix is the following one:




Thanks a lot,

Vernica


On 14 February 2011 15:08, vgarcia <[log in to unmask]> wrote:
Dear List,

Our design is a paired t-test (13 subjects) with a covariate (its value
is the same in both images of the same subject). We would like to test
the hypothesis of zero regression slope against the alternative of a
positive slope with the following contrast (value 1 in the column of the
covariate):

zeros(1,13) 1 0 0

But the contrast is invalid. What are we doing wrong?

Thanks a million

Vernica






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5llZ/sSFr2URN4prbU4rt7Sx27ePqj3zTrtbKvNOp9xY89KkasQe2nGv4JZLuXU187T/ij8Nxbrf 9r4ak0CbTuO5RsH27p7NPONbo6VjR+ZdmiZwinsFtxRrU7EwiS8W21o6Gv91r/UiLrXiGlpXEMdj z6uuIPbeHjxXu9MmZWy0d91S5PRbrPUobtQDaP/eAY24XbC0mSsaq+ea+L7AETcTlnP6puGlfaEd 3xcMws2EFdU/xdqjL7Tj+4IRuJ8AAFGQeQCAKMg8AEAUZB4AIAoyDwAQBZkHAIiCzAMAREHmAQCi IPMAAFGQeQCAKMg8AEAUZB4AIAoyDwAQBZkHAIiCzAMARPH/AZwx0Q9AabJoAAAAAElFTkSuQmCC --20cf3054a28506dee0049c54307c-- ========================================================================Date: Tue, 15 Feb 2011 08:36:13 -0800 Reply-To: Jose Soares <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Jose Soares <[log in to unmask]> Subject: fMRI-EEG Post-Doc Open Position MIME-Version: 1.0 Content-Type: multipart/alternative; boundary="0-1499706008-1297787773=:89678" Message-ID: <[log in to unmask]> --0-1499706008-1297787773=:89678 Content-Type: text/plain; charset=iso-8859-1 Content-Transfer-Encoding: quoted-printable Hi all, there is an open position to fMRI-EEG, http://www.eracareers.pt/opportunities/index.aspx?task=global&jobId=22187 Best, Jose --0-1499706008-1297787773=:89678 Content-Type: text/html; charset=iso-8859-1 Content-Transfer-Encoding: quoted-printable
Hi all, 

there is an open position to fMRI-EEG,


Best, 

Jose

  --0-1499706008-1297787773=:89678-- ========================================================================Date: Tue, 15 Feb 2011 09:03:39 -0800 Reply-To: "Jiang, Zhiguo" <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: "Jiang, Zhiguo" <[log in to unmask]> Subject: AR(1) Content-Type: multipart/related; boundary="_004_D8D86424FFCFA144BDA7076B5BDF7BFC03163E9ECEEMGMB6admedct_"; type="multipart/alternative" MIME-Version: 1.0 Message-ID: <[log in to unmask]> --_004_D8D86424FFCFA144BDA7076B5BDF7BFC03163E9ECEEMGMB6admedct_ Content-Type: multipart/alternative; boundary="_000_D8D86424FFCFA144BDA7076B5BDF7BFC03163E9ECEEMGMB6admedct_" --_000_D8D86424FFCFA144BDA7076B5BDF7BFC03163E9ECEEMGMB6admedct_ Content-Type: text/plain; charset="us-ascii" Content-Transfer-Encoding: quoted-printable Can someone point me to some useful example/scripts/tutorial on how SPM take care of the serial correlations. It seems to me that SPM uses 0.2 as a default AR coefficient. (but in Statistical Parametric Maping book, p. 122. It says SPM uses a 1/e as coefficient). I am trying to figure out how to get the whitening matrix SPM uses without running SPM8 model specification. I tracked it down to spm_Ce.m and spm_Q.m but I got stuck on these codes Q = spm_Q(a,v); dQda = spm_diff('spm_Q',a,v,1); C{1} = Q - dQda{1}*a; C{2} = Q + dQda{1}*a; Any comments? Thanks, Tony ------------------------------------------------------------------------------------------------------------------------------ [cid:image001.jpg@01CBCCEF.04F7F480] Tony Jiang,Ph.D.|Research Scholar|University of California, Los Angeles Peter V. Ueberroth Building, Rm 2338C2|10945 Le Conte Avenue. Los Angeles,CA 90095 Tel: (310)206-1423|Email: [log in to unmask] ________________________________ IMPORTANT WARNING: This email (and any attachments) is only intended for the use of the person or entity to which it is addressed, and may contain information that is privileged and confidential. You, the recipient, are obligated to maintain it in a safe, secure and confidential manner. Unauthorized redisclosure or failure to maintain confidentiality may subject you to federal and state penalties. If you are not the intended recipient, please immediately notify us by return email, and delete this message from your computer. --_000_D8D86424FFCFA144BDA7076B5BDF7BFC03163E9ECEEMGMB6admedct_ Content-Type: text/html; charset="us-ascii" Content-Transfer-Encoding: quoted-printable

Can someone point me to some useful example/scripts/tutorial on how SPM take care of the serial correlations.

 

It seems to me that SPM uses 0.2 as a default AR coefficient.  (but in Statistical Parametric Maping book, p. 122. It says SPM uses a 1/e as coefficient).

I am trying to figure out how to get the whitening matrix SPM uses without running SPM8 model specification.  I  tracked it down to

spm_Ce.m and spm_Q.m but I got stuck on these codes

 

Q    = spm_Q(a,v);

        dQda = spm_diff('spm_Q',a,v,1);

        C{1} = Q - dQda{1}*a;

        C{2} = Q + dQda{1}*a;

 

 

Any comments?

 

Thanks,

 

Tony

 

------------------------------------------------------------------------------------------------------------------------------

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Tony Jiang,Ph.D.|Research Scholar|University of California, Los Angeles
Peter V. Ueberroth Building, Rm 2338C2|10945 Le Conte Avenue. Los Angeles,CA 90095

Tel: (310)206-1423|Email: [log in to unmask]

 

 

 



IMPORTANT WARNING: This email (and any attachments) is only intended for the use of the person or entity to which it is addressed, and may contain information that is privileged and confidential. You, the recipient, are obligated to maintain it in a safe, secure and confidential manner. Unauthorized redisclosure or failure to maintain confidentiality may subject you to federal and state penalties. If you are not the intended recipient, please immediately notify us by return email, and delete this message from your computer.
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--20cf3054a163abc1b8049c5581a3 Content-Type: text/plain; charset=ISO-8859-1 Dear John (and other knowledgeable types), I used the deformation file (e.g., Y_p1_T1.nii) from Seg8 to normalise a functional MRI timeseries. That worked fine - the anatomical images that I additionally warped in this way look great - but I now cannot do anything with the timeseries. It is now almost 4Gb in size. I appreciate that using DARTEL to warp fMRI data can result in massive files which are problematic (and thus a work around is to apply the warp to contrast images), but I didn't expect the segment deformation field to do the same. Does this sound about right for a timeseries with 465 volumes (voxel dim 2.5 x 2.5 x 3; matrix 96x96; numslices = 42)? Or have I made a mistake somewhere? so I'm supposing my inability to use the warped timeseries is a memory issue - I am running a 64-bit machine with 8Gb memory (I can see all this being used in the task manager so doesn't seem to be a matlab version problem) but maybe this file is just way too big for the SPM platform.....???? I could crop the image, etc I suppose but maybe the biggest problem is the shear number of volumes. Thanks in advance for your thoughts Richard On Thu, Feb 10, 2011 at 4:05 PM, William Pettersson-Yeo < [log in to unmask]> wrote: > Thanks John. > > It turns out the problem was due to the version of Matlab I was running. > > Matlab2007 was only running 32bit, whilst the 2010 version is 64. > > Having set up with Matlab2010, the new segmentation with DARTEL import now > runs without any problem, without me having to alter/crop any of the images. > > All the best > William > --20cf3054a163abc1b8049c5581a3 Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable
Dear John (and other knowledgeable types),
I used the deformation file (e.g., Y_p1_T1.nii) from Seg8 to normalise a functional MRI timeseries. That worked fine - the anatomical imagesthat Iadditionally warped in thisway look great - but I now cannot do anything with the timeseries.
It is now almost 4Gb in size. I appreciate that using DARTEL to warp fMRI data can result in massive files which are problematic (and thus a work around is to apply the warp to contrast images), but I didn't expect the segment deformation field to do the same.
Does this sound about right for a timeseries with 465 volumes (voxel dim 2.5 x 2.5 x 3; matrix 96x96; numslices = 42)? Or have I made a mistake somewhere?
so I'm supposing my inability to use the warped timeseries is a memory issue- I am running a 64-bit machine with 8Gb memory (I can see all this being used in the task manager so doesn't seem to be a matlab version problem) but maybe this file is just way too big for the SPM platform.....???? I could crop the image, etc I suppose but maybe the biggest problem is the shear number of volumes.
Thanks in advance for your thoughts
Richard

On Thu, Feb 10, 2011 at 4:05 PM, William Pettersson-Yeo <[log in to unmask]> wrote:
Thanks John.

It turns out the problem was due to the version of Matlab I was running.

Matlab2007 was only running 32bit, whilst the 2010 version is 64.

Having set up with Matlab2010, the new segmentation with DARTEL import now runs without any problem, without me having to alter/crop any of the images.

All the best
William

--20cf3054a163abc1b8049c5581a3-- ========================================================================Date: Tue, 15 Feb 2011 17:42:49 +0000 Reply-To: John Ashburner <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: John Ashburner <[log in to unmask]> Subject: Re: New Segmentation Out of Memory Error Comments: To: Richard Binney <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> You may wish to change the voxel sizes and bounding box in order to obtain slightly lower resolution versions (other than the default 1.5mm isotropic with a large bounding box). See the email I sent out recently. Best regards, -John On 15 February 2011 17:29, Richard Binney <[log in to unmask]> wrote: > Dear John (and other knowledgeable types), > > I used the deformation file (e.g., Y_p1_T1.nii) from Seg8 to normalise a > functional MRI timeseries. That worked fine - the anatomical imagesthat > Iadditionally warped in thisway look great - but I now cannot do anything > with the timeseries. > > It is now almost 4Gb in size. I appreciate that using DARTEL to warp fMRI > data can result in massive files which are problematic (and thus a work > around is to apply the warp to contrast images), but I didn't expect the > segment deformation field to do the same. > > Does this sound about right for a timeseries with 465 volumes (voxel dim 2.5 > x 2.5 x 3; matrix 96x96; numslices = 42)? Or have I made a mistake > somewhere? > > so I'm supposing my inability to use the warped timeseries is a memory > issue- I am running a 64-bit machine with 8Gb memory (I can see all this > being used in the task manager so doesn't seem to be a matlab version > problem) but maybe this file is just way too big for the SPM > platform.....???? I could crop the image, etc I suppose but maybe the > biggest problem is the shear number of volumes. > > Thanks in advance for your thoughts > > Richard > > On Thu, Feb 10, 2011 at 4:05 PM, William Pettersson-Yeo > <[log in to unmask]> wrote: >> >> Thanks John. >> >> It turns out the problem was due to the version of Matlab I was running. >> >> Matlab2007 was only running 32bit, whilst the 2010 version is 64. >> >> Having set up with Matlab2010, the new segmentation with DARTEL import now >> runs without any problem, without me having to alter/crop any of the images. >> >> All the best >> William > > ========================================================================Date: Tue, 15 Feb 2011 17:36:09 -0500 Reply-To: Jonathan Peelle <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Jonathan Peelle <[log in to unmask]> Subject: Re: Question regarding FIR and contrasts Comments: To: "Claire (Jung Eun) Han" <[log in to unmask]> In-Reply-To: [log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/alternative; boundaryMessage-ID: <[log in to unmask]> --0016363b959676d552049c59ca34 Content-Type: text/plain; charset=ISO-8859-1 Hi Claire > There are two conditions A and B I would like to compare. > > In fMRI model specification, I chose to use the Finite Impulse Response > such that my design has 9 three-second-bins for each condition. > > I would like to compare the two conditions in each time bin...is it > possible to do this at once? Which of the t- or f-test should I be using and > what should I put for contrasts? > Two ways to compare A and B in your design are: 1) Use an F test, where each row of the F test compares A vs. B at one time point. For example: 1 0 0 0 0 0 0 0 0 -1 0 0 0 0 0 0 0 0 0 1 0 0 0 0 0 0 0 0 -1 0 0 0 0 0 0 0 0 0 1 0 0 0 0 0 0 0 0 -1 0 0 0 0 0 0 . . . 0 0 0 0 0 0 0 0 1 0 0 0 0 0 0 0 0 -1 or alternatively, use some Matlab functions: [eye(9) 0-eye(9)] The trick is that if you get a significant difference, you don't know which time bin caused it, or which direction the difference was in (A>B or B>A), so you would need to investigate further to find out (e.g., plotting effects for each region). 2) A simpler approach is to simply look at the total "area under the curve" for each condition in a t-test. This effectively discards the timing information: [1 1 1 1 1 1 1 1 1 -1 -1 -1 -1 -1 -1 -1 -1 -1] for example would give you the sum of condition A compared to the sum of condition B (i.e., A > B). Alternatively you could write this [ones(1,9) ones(1,9)*-1]. Because this is a t-test it can give you information about directionality. However, you lose the temporal detail, which may be one of the reasons to choose an FIR model in the first place. Ultimately it will depend on what you are most interested in. There is some discussion of FIR models in Chapter 30 of the SPM manual (Face Group fMRI Data), which may also be of interest. Hope this helps, Jonathan -- Dr. Jonathan Peelle Department of Neurology University of Pennsylvania 3 West Gates 3400 Spruce Street Philadelphia, PA 19104 USA http://jonathanpeelle.net/ --0016363b959676d552049c59ca34 Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Hi Claire
There are two conditions A and B I would like to compare.

In fMRI model specification, I chose to use the Finite Impulse Response such that my design has 9 three-second-bins for each condition.

I would like to compare the two conditions in each time bin...is it possible to do this at once? Which of the t- or f-test should I be using and what should I put for contrasts?

Two ways to compare A and B in your design are:

1) Use an F test, where each row of the F test compares A vs. B at one time point. For example:

1 0 0 0 0 0 0 0 0 -1 0 0 0 0 0 0 0 0
0 1 0 0 0 0 0 0 0 0 -1 0 0 0 0 0 0 0
0 0 1 0 0 0 0 0 0 0 0 -1 0 0 0 0 0 0
.
.
.
0 0 0 0 0 0 0 0 1 0 0 0 0 0 0 0 0 -1

or alternatively, use some Matlab functions:

[eye(9) 0-eye(9)]

The trick is that if you get a significant difference, you don't know which time bin caused it, or which direction the difference was in (A>B or B>A), so you would need to investigate further to find out (e.g., plotting effects for each region).

2) A simpler approach is to simply look at the total "area under the curve" for each condition in a t-test. This effectively discards the timing information:

[1 1 1 1 1 1 1 1 1 -1 -1 -1 -1 -1 -1 -1 -1 -1]

for example would give you the sum of condition A compared to the sum of condition B (i.e., A > B). Alternatively you could write this [ones(1,9) ones(1,9)*-1]. Because this is a t-test it can give you information about directionality. However, you lose the temporal detail, which may be one of the reasons to choose an FIR model in the first place.

Ultimately it will depend on what you are most interested in. There is some discussion of FIR models in Chapter 30 of the SPM manual (Face Group fMRI Data), which may also be of interest.

Hope this helps,
Jonathan


--
Dr. Jonathan Peelle
Department of Neurology
University of Pennsylvania
3 West Gates
3400 Spruce Street
Philadelphia, PA 19104
USA
http://jonathanpeelle.net/

--0016363b959676d552049c59ca34-- ========================================================================Date: Tue, 15 Feb 2011 18:58:35 -0800 Reply-To: Michael T Rubens <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Michael T Rubens <[log in to unmask]> Subject: Fwd: Urge your Representative to Oppose Science Funding Cuts Comments: To: [log in to unmask], Gazz Lab <[log in to unmask]> In-Reply-To: <12.37.01488.7160B5D4@dc1bhmta04> MIME-Version: 1.0 Content-Type: multipart/alternative; boundarye6ba6e8e7cc867ec049c5d7622 Message-ID: <[log in to unmask]> --90e6ba6e8e7cc867ec049c5d7622 Content-Type: text/plain; charset=UTF-8 Content-Transfer-Encoding: quoted-printable ---------- Forwarded message ---------- From: Society for Neuroscience <[log in to unmask]> Date: Tue, Feb 15, 2011 at 2:55 PM Subject: Urge your Representative to Oppose Science Funding Cuts To: Michael Rubens <[log in to unmask]> [image: Society for Neuroscience banner graphic] Urge Your Representative to Oppose $2.4 Billion in Proposed Cuts for NIH and NSF SfN urges members to contact their representatives *today* to support National Institutes of Health (NIH) and National Science Foundation (NSF) funding. The House of Representatives is set to debate and vote *this week*on legislation to reduce FY2011 funding for science, including a $1.6 billion cut for NIH and a $826 million cut for NSF. Such cuts, proposed by the House Republican leadership, would reduce the NIH and NSF budgets to FY2008 levels. Contact your representatives *now* through the SfN Legislative Action Centerand ask them to *oppose cuts* that will delay treatments, eliminate jobs, and jeopardize America’s standing as a global leader in scientific discovery. House votes are expected Thursday – contact your member of Congresstoday! * Please urge five colleagues to add their voices* in opposition to cuts that will hurt science and hurt America. Society for Neuroscience | 1121 14th St NW | Suite 1010 | Washington | DC | 20005 This message was sent to: [log in to unmask] as part of an established business relationship with the Society for Neuroscience. You were added to the system August 5, 2010. For more information click here[log in to unmask]&cid=963dd964631f5b9b1df45416d6fa1fbc> . -- Research Associate Gazzaley Lab Department of Neurology University of California, San Francisco --90e6ba6e8e7cc867ec049c5d7622 Content-Type: text/html; charset=UTF-8 Content-Transfer-Encoding: quoted-printable

---------- Forwarded message ----------
From: Society for Neuroscience <[log in to unmask]>
Date: Tue, Feb 15, 2011 at 2:55 PM
Subject: Urge your Representative to Oppose Science Funding Cuts
To: Michael Rubens <[log in to unmask]>


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Urge Your Representative to Oppose $2.4 Billion in
Proposed Cuts for NIH and NSF

SfN urges members to contact their representatives today to support National Institutes of Health (NIH) and National Science Foundation (NSF) funding. The House of Representatives is set to debate and vote this week on legislation to reduce FY2011 funding for science, including a $1.6 billion cut for NIH and a $826 million cut for NSF. Such cuts, proposed by the House Republican leadership, would reduce the NIH and NSF budgets to FY2008 levels.

Contact your representatives now through the SfN Legislative Action Center and ask them to oppose cuts that will delay treatments, eliminate jobs, and jeopardize America’s standing as a global leader in scientific discovery.

House votes are expected Thursday – contact your member of Congress today! Please urge five colleagues to add their voices in opposition to cuts that will hurt science and hurt America.

 

 

 

 

 

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--
Research Associate
Gazzaley Lab
Department of Neurology
University of California, San Francisco
--90e6ba6e8e7cc867ec049c5d7622-- ========================================================================Date: Wed, 16 Feb 2011 14:57:13 +0000 Reply-To: Vladimir Litvak <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Vladimir Litvak <[log in to unmask]> Subject: Re: Warning in spm_eeg_convert2scalp (griddata) & spm_eeg_crop Comments: To: Panagiotis Tsiatsis <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> Dear Panagiotis, Sorry for the late reply. I only now found time to look into it more carefully. On Tue, Feb 8, 2011 at 2:46 PM, Panagiotis Tsiatsis <[log in to unmask]> wrote: > Hello dear Vladimir and thanks for your response > > First of all, apologies in advance for the long e-mail; I hope that it will > be at least a bit important for other users of SPM, too > > It seems that the problem appeared after I used spm_eeg_crop to drop my > continuous CTF meg data file straight after reading it in and before > applying filtering / downsampling. Without spm_eeg_crop everything works > fine. > > [A small recap : > As explained in a previous e-mail of mine, the logic behind this is that the > start and the end of a continuous MEG files might be contaminated by > artifacts (i.e due to subject's movement at the end of the session if she > for whatever reason realized that the session is over and started moving > before you press 'stop recording' ) or / and zero values because of > padding added by the CTF software. All this should affect any subsequent > filtering function if they are not removed (even the padding because of the > sudden jump from values of order 10^-12 to zero!!!!) so I decided to crop > the edges of my continuous file before continuing. ] > > I remember that when you send me the spm_eeg_crop file you told me that it > has not been tested for continuous data but it should in principle work. > > I call it by using the following code : > > Time_Offset_in_ms = 3000; % in ms > S = []; > S.D = D; > S.timewin = [(Time_of_First_Trial_Onset_in_ms - > Time_Offset_in_ms) (Time_of_Last_Trial_Onset_in_ms + Time_Offset_in_ms)] > S.freqwin = []; > S.channels = 'all' > > D = spm_eeg_crop(S); > D.save; > > > The problem seems to appear in spm_eeg_crop when applied on a continuous > file to and more specifically somewhere in the creation of the new object: > > Dnew = coor2D(Dnew, [], coor2D(D, chanind)); > > as some channels do indeed have the same coordinates : > >>> size(coor2D(D, chanind)') > > ans = > > 337 2 > >>> size(unique(coor2D(D, chanind)','rows')) > > ans = > > 335 2 > > > The above number shows that spm_eeg_crop indeed puts in the coor2D matrix > (or tries to put) the coordinates of all available channels. Up to now (and > correct me if I am wrong) I knew that the coor2D matrix contains the > coordinates of the MEGGRAD channels only. So I modified the code as follows > : > > MEG_Channels = (D.meegchannels('MEG')); > Dnew = coor2D(Dnew, [], coor2D(D, MEG_Channels)); > > > *And indeed the conversion to images of subsequent files was executed > without warnings*. So, is this a bug or am I going the wrong direction here? > I tried this on my CTF dataset and I don't get identical 2D coordinates. So this is something that happens for your data and I'm not sure why. If you send me an example I can look. In general this code should work as it is because 2D coordinates are defined for all channels (for non-scalp channels these are just points on a square grid). > A couple more issues / clarifications : > > 1. The statistics at the end of the analysis (assuming all other equal) were > slightly different depending on whether I cropped the start and the end of > the continuous initial files that in many cases had large artifacts or zero > values. I suppose this is because the subsequent filtering applied on the > data was "smoother", in the sense that the filters did not have to > compensate for the artifacts or the jumps because of the zero padding. Does > this train of thought sound logical to you? Yes that's a reasonable explanation, although how reasonable it is depends on how far your trials were from the edges and how low was your high-pass cutoff. It's not that the filters 'compensate' for something it's just that due to filtering artefacts from the edges can contaminate data slightly away from the edges. > > 2.The cropped file (where only a few non-trial seconds from the start and > from the and are missing) contains exactly the same number of events as the > original continuous file. Why??? It seems that some zombie events are > retained after cropping! > > That's indeed a bug, due to the fact that I wasn't planning this function to be used on continuous data. I now fixed it and it'll be in the next update. > 3. Please note that there appears to be one more problem with spm_eeg_crop > and continuous data : > > The line Dnew = badchannels(Dnew, [], badchannels(D, chanind)); always > results in an error when there are no bad channels, i.e. when > isempty(D.badchannels) == 1. so i have substituted the above line with > > if isempty(D.badchannels) == 0 > Dnew = badchannels(Dnew, [], badchannels(D, chanind)); > end > I can't reproduce this problem either. The code should work also for no bad channels because badchannels(D, chanind) always returns a vector of 0/1 Best, Vladimir > > I suspect I should put an 'else' condition somewhere there, but of course > you are the expert on this :) > > Thanks again and all the best, > Panagiotis > > On 2/7/2011 8:10 PM, Vladimir Litvak wrote: >> >> Dear Panagiotis, >> >> Try doing: >> >> spm_eeg_load >> D.coor2D(D.meegchannels('MEG')) >> >> and look which of the channels have the same 2D coordinates. In >> principle this should not happen for CTF MEG. You can also look in >> 'Prepare' tool at the 2D channel layout an modify it if necessary or >> load a template layout from EEGtemplates. >> >> Best, >> >> Vladimir >> >> On Sun, Feb 6, 2011 at 5:23 PM, Panagiotis Tsiatsis >> <[log in to unmask]> wrote: >>> >>> Dear All, >>> >>> When I am converting my CTF MEG epoched data to images, I am getting the >>> following warning: >>> >>> Warning: Duplicate x-y data points detected: using average of the z >>> values. >>>> >>>> In griddata at 107 >>> >>> In spm_eeg_convert2scalp at 204 >>> >>> My settings are: >>> >>> S = []; >>> S.n = 32; >>> S.Fname = Concatenated_File_Name_Time; >>> S.interpolate_bad = 1; >>> S.modality = 'MEG'; >>> >>> I also have EOG channels whose chantype has been set to 'EEG' during the >>> conversion (this of course should not interfere since I ve selected my >>> modality to be 'MEG'). >>> >>> By browsing the Mathwoks forum, I suspect that this happens when nearby >>> values get very similar (as is the case with MEG data). >>> >>> Anybody seen that before? Any intuitions? >>> >>> Thanks and best, >>> Panagiotis >>> >>> >>> -- >>> Panagiotis S. Tsiatsis >>> Max Planck Institute for Biological Cybernetics >>> Cognitive NeuroImaging Group >>> Tuebingen, Germany >>> > > > -- > Panagiotis S. Tsiatsis > Max Planck Institute for Biological Cybernetics > Cognitive NeuroImaging Group > Tuebingen, Germany > > ========================================================================Date: Wed, 16 Feb 2011 15:39:18 +0000 Reply-To: Richard Binney <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Richard Binney <[log in to unmask]> Subject: Re: New Segmentation Out of Memory Error Comments: To: John Ashburner <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/alternative; boundary cf3054962583e57b049c681574 Message-ID: <[log in to unmask]> --20cf3054962583e57b049c681574 Content-Type: text/plain; charset=ISO-8859-1 Ah, yes. I couldn't find the email you were refferring to, but I've done it and it makes a huge difference. Pretty obvious really. One more thing, John (or anybody else for that matter) - is there now a way in which one can easily create an inverse of the DARTEL normalise-to-MNI deformation composition (so from MNI --> study average --> individual subject space)? Is it possible (i.e., is there script) to have this (forward and/or backwards) written out for each subject or, alternatively, to have the affine template-to-TPM transform outputted such that one can combine it with a flow field, and subsequently inverse the composition using the deformations tool? All the best, Richard On Tue, Feb 15, 2011 at 5:42 PM, John Ashburner <[log in to unmask]>wrote: > You may wish to change the voxel sizes and bounding box in order to > obtain slightly lower resolution versions (other than the default > 1.5mm isotropic with a large bounding box). See the email I sent out > recently. > > Best regards, > -John > > On 15 February 2011 17:29, Richard Binney <[log in to unmask]> > wrote: > > Dear John (and other knowledgeable types), > > > > I used the deformation file (e.g., Y_p1_T1.nii) from Seg8 to normalise a > > functional MRI timeseries. That worked fine - the anatomical images that > > I additionally warped in this way look great - but I now cannot do > anything > > with the timeseries. > > > > It is now almost 4Gb in size. I appreciate that using DARTEL to warp fMRI > > data can result in massive files which are problematic (and thus a work > > around is to apply the warp to contrast images), but I didn't expect the > > segment deformation field to do the same. > > > > Does this sound about right for a timeseries with 465 volumes (voxel dim > 2.5 > > x 2.5 x 3; matrix 96x96; numslices = 42)? Or have I made a mistake > > somewhere? > > > > so I'm supposing my inability to use the warped timeseries is a memory > > issue - I am running a 64-bit machine with 8Gb memory (I can see all this > > being used in the task manager so doesn't seem to be a matlab version > > problem) but maybe this file is just way too big for the SPM > > platform.....???? I could crop the image, etc I suppose but maybe the > > biggest problem is the shear number of volumes. > > > > Thanks in advance for your thoughts > > > > Richard > > > > On Thu, Feb 10, 2011 at 4:05 PM, William Pettersson-Yeo > > <[log in to unmask]> wrote: > >> > >> Thanks John. > >> > >> It turns out the problem was due to the version of Matlab I was running. > >> > >> Matlab2007 was only running 32bit, whilst the 2010 version is 64. > >> > >> Having set up with Matlab2010, the new segmentation with DARTEL import > now > >> runs without any problem, without me having to alter/crop any of the > images. > >> > >> All the best > >> William > > > > > --20cf3054962583e57b049c681574 Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable
Ah, yes. I couldn't find the email you were refferring to,butI've done it and it makes a huge difference. Pretty obvious really.
One more thing, John (or anybody else for that matter)- is there now a way in which one can easilycreate an inverseof theDARTEL normalise-to-MNI deformation composition (so from MNI --> study average --> individual subject space)? Is it possible (i.e., is there script)to have this (forward and/or backwards)written out for each subject or, alternatively, to have the affine template-to-TPMtransform outputtedsuch that one can combine it witha flow field, and subsequently inversethe composition using the deformations tool?
All the best,
Richard

On Tue, Feb 15, 2011 at 5:42 PM, John Ashburner <[log in to unmask]> wrote:
You may wish to change the voxel sizes and bounding box in order to
obtain slightly lower resolution versions (other than the default
1.5mm isotropic with a large bounding box). See the email I sent out
recently.

Best regards,
-John

On 15 February 2011 17:29, Richard Binney <[log in to unmask]> wrote:
> Dear John (and other knowledgeable types),
>
> I used the deformation file (e.g., Y_p1_T1.nii) from Seg8 to normalise a
> functional MRI timeseries. That worked fine - the anatomical imagesthat
> Iadditionally warped in thisway look great - but I now cannot do anything
> with the timeseries.
>
> It is now almost 4Gb in size. I appreciate that using DARTEL to warp fMRI
> data can result in massive files which are problematic (and thus a work
> around is to apply the warp to contrast images), but I didn't expect the
> segment deformation field to do the same.
>
> Does this sound about right for a timeseries with 465 volumes (voxel dim 2.5
> x 2.5 x 3; matrix 96x96; numslices = 42)? Or have I made a mistake
> somewhere?
>
> so I'm supposing my inability to use the warped timeseries is a memory
> issue- I am running a 64-bit machine with 8Gb memory (I can see all this
> being used in the task manager so doesn't seem to be a matlab version
> problem) but maybe this file is just way too big for the SPM
> platform.....???? I could crop the image, etc I suppose but maybe the
> biggest problem is the shear number of volumes.
>
> Thanks in advance for your thoughts
>
> Richard
>
> On Thu, Feb 10, 2011 at 4:05 PM, William Pettersson-Yeo
> <[log in to unmask]> wrote:
>>
>> Thanks John.
>>
>> It turns out the problem was due to the version of Matlab I was running.
>>
>> Matlab2007 was only running 32bit, whilst the 2010 version is 64.
>>
>> Having set up with Matlab2010, the new segmentation with DARTEL import now
>> runs without any problem, without me having to alter/crop any of the images.
>>
>> All the best
>> William
>
>

--20cf3054962583e57b049c681574-- ========================================================================Date: Wed, 16 Feb 2011 15:44:35 +0000 Reply-To: Richard Binney <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Richard Binney <[log in to unmask]> Subject: Re: New Segmentation Out of Memory Error Comments: To: John Ashburner <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/alternative; boundary cf305641c971f168049c6828fc Message-ID: <[log in to unmask]> --20cf305641c971f168049c6828fc Content-Type: text/plain; charset=ISO-8859-1 ......I've just spotted that running normalise-to-mni now spits out a 'Template_6_2mni.mat' file. I don't recall seeing this before - would this happen to be the affine transform I spoke of? R On Wed, Feb 16, 2011 at 3:39 PM, Richard Binney < [log in to unmask]> wrote: > Ah, yes. I couldn't find the email you were refferring to, but I've done it > and it makes a huge difference. Pretty obvious really. > > One more thing, John (or anybody else for that matter) - is there now a way > in which one can easily create an inverse of the DARTEL normalise-to-MNI > deformation composition (so from MNI --> study average --> individual > subject space)? Is it possible (i.e., is there script) to have this (forward > and/or backwards) written out for each subject or, alternatively, to have > the affine template-to-TPM transform outputted such that one can combine it > with a flow field, and subsequently inverse the composition using the > deformations tool? > > All the best, > > Richard > > On Tue, Feb 15, 2011 at 5:42 PM, John Ashburner <[log in to unmask]>wrote: > >> You may wish to change the voxel sizes and bounding box in order to >> obtain slightly lower resolution versions (other than the default >> 1.5mm isotropic with a large bounding box). See the email I sent out >> recently. >> >> Best regards, >> -John >> >> On 15 February 2011 17:29, Richard Binney <[log in to unmask]> >> wrote: >> > Dear John (and other knowledgeable types), >> > >> > I used the deformation file (e.g., Y_p1_T1.nii) from Seg8 to normalise a >> > functional MRI timeseries. That worked fine - the anatomical images that >> > I additionally warped in this way look great - but I now cannot do >> anything >> > with the timeseries. >> > >> > It is now almost 4Gb in size. I appreciate that using DARTEL to warp >> fMRI >> > data can result in massive files which are problematic (and thus a work >> > around is to apply the warp to contrast images), but I didn't expect the >> > segment deformation field to do the same. >> > >> > Does this sound about right for a timeseries with 465 volumes (voxel dim >> 2.5 >> > x 2.5 x 3; matrix 96x96; numslices = 42)? Or have I made a mistake >> > somewhere? >> > >> > so I'm supposing my inability to use the warped timeseries is a memory >> > issue - I am running a 64-bit machine with 8Gb memory (I can see all >> this >> > being used in the task manager so doesn't seem to be a matlab version >> > problem) but maybe this file is just way too big for the SPM >> > platform.....???? I could crop the image, etc I suppose but maybe the >> > biggest problem is the shear number of volumes. >> > >> > Thanks in advance for your thoughts >> > >> > Richard >> > >> > On Thu, Feb 10, 2011 at 4:05 PM, William Pettersson-Yeo >> > <[log in to unmask]> wrote: >> >> >> >> Thanks John. >> >> >> >> It turns out the problem was due to the version of Matlab I was >> running. >> >> >> >> Matlab2007 was only running 32bit, whilst the 2010 version is 64. >> >> >> >> Having set up with Matlab2010, the new segmentation with DARTEL import >> now >> >> runs without any problem, without me having to alter/crop any of the >> images. >> >> >> >> All the best >> >> William >> > >> > >> > > --20cf305641c971f168049c6828fc Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable
......I've just spotted that running normalise-to-mni now spits out a 'Template_6_2mni.mat' file. I don't recall seeing this before -would this happen to be the affine transform I spoke of?
R

On Wed, Feb 16, 2011 at 3:39 PM, Richard Binney <[log in to unmask]> wrote:
Ah, yes. I couldn't find the email you were refferring to,butI've done it and it makes a huge difference. Pretty obvious really.
One more thing, John (or anybody else for that matter)- is there now a way in which one can easilycreate an inverseof theDARTEL normalise-to-MNI deformation composition (so from MNI --> study average --> individual subject space)? Is it possible (i.e., is there script)to have this (forward and/or backwards)written out for each subject or, alternatively, to have the affine template-to-TPMtransform outputtedsuch that one can combine it witha flow field, and subsequently inversethe composition using the deformations tool?
All the best,
Richard

On Tue, Feb 15, 2011 at 5:42 PM, John Ashburner <[log in to unmask]> wrote:
You may wish to change the voxel sizes and bounding box in order to
obtain slightly lower resolution versions (other than the default
1.5mm isotropic with a large bounding box). See the email I sent out
recently.

Best regards,
-John

On 15 February 2011 17:29, Richard Binney <[log in to unmask]> wrote:
> Dear John (and other knowledgeable types),
>
> I used the deformation file (e.g., Y_p1_T1.nii) from Seg8 to normalise a
> functional MRI timeseries. That worked fine - the anatomical imagesthat
> Iadditionally warped in thisway look great - but I now cannot do anything
> with the timeseries.
>
> It is now almost 4Gb in size. I appreciate that using DARTEL to warp fMRI
> data can result in massive files which are problematic (and thus a work
> around is to apply the warp to contrast images), but I didn't expect the
> segment deformation field to do the same.
>
> Does this sound about right for a timeseries with 465 volumes (voxel dim 2.5
> x 2.5 x 3; matrix 96x96; numslices = 42)? Or have I made a mistake
> somewhere?
>
> so I'm supposing my inability to use the warped timeseries is a memory
> issue- I am running a 64-bit machine with 8Gb memory (I can see all this
> being used in the task manager so doesn't seem to be a matlab version
> problem) but maybe this file is just way too big for the SPM
> platform.....???? I could crop the image, etc I suppose but maybe the
> biggest problem is the shear number of volumes.
>
> Thanks in advance for your thoughts
>
> Richard
>
> On Thu, Feb 10, 2011 at 4:05 PM, William Pettersson-Yeo
> <[log in to unmask]> wrote:
>>
>> Thanks John.
>>
>> It turns out the problem was due to the version of Matlab I was running.
>>
>> Matlab2007 was only running 32bit, whilst the 2010 version is 64.
>>
>> Having set up with Matlab2010, the new segmentation with DARTEL import now
>> runs without any problem, without me having to alter/crop any of the images.
>>
>> All the best
>> William
>
>


--20cf305641c971f168049c6828fc-- ========================================================================Date: Wed, 16 Feb 2011 15:58:16 +0000 Reply-To: John Ashburner <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: John Ashburner <[log in to unmask]> Subject: Re: New Segmentation Out of Memory Error Comments: To: Richard Binney <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> This file does indeed contain an affine transform, and is generated when the affine registration between population average and MNI space is estimated. There's no script to do what you're after yet, but if the demand is high enough I could introduce the option. Can I ask how you plan to use the transforms? Best regards, -John On 16 February 2011 15:44, Richard Binney <[log in to unmask]> wrote: > ......I've just spotted that running normalise-to-mni now spits out a > 'Template_6_2mni.mat' file. I don't recall seeing this before -would this > happen to be the affine transform I spoke of? > > R > > On Wed, Feb 16, 2011 at 3:39 PM, Richard Binney > <[log in to unmask]> wrote: >> >> Ah, yes. I couldn't find the email you were refferring to,butI've done >> it and it makes a huge difference. Pretty obvious really. >> >> One more thing, John (or anybody else for that matter)- is there now a >> way in which one can easilycreate an inverseof theDARTEL normalise-to-MNI >> deformation composition (so from MNI --> study average --> individual >> subject space)? Is it possible (i.e., is there script)to have this (forward >> and/or backwards)written out for each subject or, alternatively, to have >> the affine template-to-TPMtransform outputtedsuch that one can combine it >> witha flow field, and subsequently inversethe composition using the >> deformations tool? >> >> All the best, >> >> Richard >> >> On Tue, Feb 15, 2011 at 5:42 PM, John Ashburner <[log in to unmask]> >> wrote: >>> >>> You may wish to change the voxel sizes and bounding box in order to >>> obtain slightly lower resolution versions (other than the default >>> 1.5mm isotropic with a large bounding box). See the email I sent out >>> recently. >>> >>> Best regards, >>> -John >>> >>> On 15 February 2011 17:29, Richard Binney <[log in to unmask]> >>> wrote: >>> > Dear John (and other knowledgeable types), >>> > >>> > I used the deformation file (e.g., Y_p1_T1.nii) from Seg8 to normalise >>> > a >>> > functional MRI timeseries. That worked fine - the anatomical >>> > imagesthat >>> > Iadditionally warped in thisway look great - but I now cannot do >>> > anything >>> > with the timeseries. >>> > >>> > It is now almost 4Gb in size. I appreciate that using DARTEL to warp >>> > fMRI >>> > data can result in massive files which are problematic (and thus a work >>> > around is to apply the warp to contrast images), but I didn't expect >>> > the >>> > segment deformation field to do the same. >>> > >>> > Does this sound about right for a timeseries with 465 volumes (voxel >>> > dim 2.5 >>> > x 2.5 x 3; matrix 96x96; numslices = 42)? Or have I made a mistake >>> > somewhere? >>> > >>> > so I'm supposing my inability to use the warped timeseries is a memory >>> > issue- I am running a 64-bit machine with 8Gb memory (I can see all >>> > this >>> > being used in the task manager so doesn't seem to be a matlab version >>> > problem) but maybe this file is just way too big for the SPM >>> > platform.....???? I could crop the image, etc I suppose but maybe the >>> > biggest problem is the shear number of volumes. >>> > >>> > Thanks in advance for your thoughts >>> > >>> > Richard >>> > >>> > On Thu, Feb 10, 2011 at 4:05 PM, William Pettersson-Yeo >>> > <[log in to unmask]> wrote: >>> >> >>> >> Thanks John. >>> >> >>> >> It turns out the problem was due to the version of Matlab I was >>> >> running. >>> >> >>> >> Matlab2007 was only running 32bit, whilst the 2010 version is 64. >>> >> >>> >> Having set up with Matlab2010, the new segmentation with DARTEL import >>> >> now >>> >> runs without any problem, without me having to alter/crop any of the >>> >> images. >>> >> >>> >> All the best >>> >> William >>> > >>> > >> > > ========================================================================Date: Wed, 16 Feb 2011 17:48:33 +0100 Reply-To: michel grothe <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: michel grothe <[log in to unmask]> Subject: Re: New Segmentation Out of Memory Error Comments: To: [log in to unmask] In-Reply-To: <[log in to unmask]> Content-Type: multipart/alternative; boundary="_fd2415e3-e3d7-48dc-a0ca-d5dba1603bcc_" MIME-Version: 1.0 Message-ID: <[log in to unmask]> --_fd2415e3-e3d7-48dc-a0ca-d5dba1603bcc_ Content-Type: text/plain; charset="iso-8859-1" Content-Transfer-Encoding: quoted-printable Hi, I havent seen such a file in my version of SPM8 (the penultimate update, run on win32). Is it possible that this file is just generated during estimation of the affine transform and not stored permanently on disk? Or does it come with the latest update? It would be very helpful to have such a file, mainly for the reasons Richard mentioned, i.e. use it to compose the complete transform 'native->DARTEL-mean->MNI'. The inverse of such a composition could be used to warp Atlas-labels in MNI space to native space. Best regards, Michel > Date: Wed, 16 Feb 2011 15:58:16 +0000 > From: [log in to unmask] > Subject: Re: [SPM] New Segmentation Out of Memory Error > To: [log in to unmask] > > This file does indeed contain an affine transform, and is generated > when the affine registration between population average and MNI space > is estimated. > > There's no script to do what you're after yet, but if the demand is > high enough I could introduce the option. Can I ask how you plan to > use the transforms? > > Best regards, > -John > > > On 16 February 2011 15:44, Richard Binney <[log in to unmask]> wrote: > > ......I've just spotted that running normalise-to-mni now spits out a > > 'Template_6_2mni.mat' file. I don't recall seeing this before - would this > > happen to be the affine transform I spoke of? > > > > R > > > > On Wed, Feb 16, 2011 at 3:39 PM, Richard Binney > > <[log in to unmask]> wrote: > >> > >> Ah, yes. I couldn't find the email you were refferring to, but I've done > >> it and it makes a huge difference. Pretty obvious really. > >> > >> One more thing, John (or anybody else for that matter) - is there now a > >> way in which one can easily create an inverse of the DARTEL normalise-to-MNI > >> deformation composition (so from MNI --> study average --> individual > >> subject space)? Is it possible (i.e., is there script) to have this (forward > >> and/or backwards) written out for each subject or, alternatively, to have > >> the affine template-to-TPM transform outputted such that one can combine it > >> with a flow field, and subsequently inverse the composition using the > >> deformations tool? > >> > >> All the best, > >> > >> Richard > >> > >> On Tue, Feb 15, 2011 at 5:42 PM, John Ashburner <[log in to unmask]> > >> wrote: > >>> > >>> You may wish to change the voxel sizes and bounding box in order to > >>> obtain slightly lower resolution versions (other than the default > >>> 1.5mm isotropic with a large bounding box). See the email I sent out > >>> recently. > >>> > >>> Best regards, > >>> -John > >>> > >>> On 15 February 2011 17:29, Richard Binney <[log in to unmask]> > >>> wrote: > >>> > Dear John (and other knowledgeable types), > >>> > > >>> > I used the deformation file (e.g., Y_p1_T1.nii) from Seg8 to normalise > >>> > a > >>> > functional MRI timeseries. That worked fine - the anatomical > >>> > images that > >>> > I additionally warped in this way look great - but I now cannot do > >>> > anything > >>> > with the timeseries. > >>> > > >>> > It is now almost 4Gb in size. I appreciate that using DARTEL to warp > >>> > fMRI > >>> > data can result in massive files which are problematic (and thus a work > >>> > around is to apply the warp to contrast images), but I didn't expect > >>> > the > >>> > segment deformation field to do the same. > >>> > > >>> > Does this sound about right for a timeseries with 465 volumes (voxel > >>> > dim 2.5 > >>> > x 2.5 x 3; matrix 96x96; numslices = 42)? Or have I made a mistake > >>> > somewhere? > >>> > > >>> > so I'm supposing my inability to use the warped timeseries is a memory > >>> > issue - I am running a 64-bit machine with 8Gb memory (I can see all > >>> > this > >>> > being used in the task manager so doesn't seem to be a matlab version > >>> > problem) but maybe this file is just way too big for the SPM > >>> > platform.....???? I could crop the image, etc I suppose but maybe the > >>> > biggest problem is the shear number of volumes. > >>> > > >>> > Thanks in advance for your thoughts > >>> > > >>> > Richard > >>> > > >>> > On Thu, Feb 10, 2011 at 4:05 PM, William Pettersson-Yeo > >>> > <[log in to unmask]> wrote: > >>> >> > >>> >> Thanks John. > >>> >> > >>> >> It turns out the problem was due to the version of Matlab I was > >>> >> running. > >>> >> > >>> >> Matlab2007 was only running 32bit, whilst the 2010 version is 64. > >>> >> > >>> >> Having set up with Matlab2010, the new segmentation with DARTEL import > >>> >> now > >>> >> runs without any problem, without me having to alter/crop any of the > >>> >> images. > >>> >> > >>> >> All the best > >>> >> William > >>> > > >>> > > >> > > > > --_fd2415e3-e3d7-48dc-a0ca-d5dba1603bcc_ Content-Type: text/html; charset="iso-8859-1" Content-Transfer-Encoding: quoted-printable Hi,
I havent seen such a file in my version of SPM8 (the penultimate update, run on win32). Is it possible that this file is just generated during estimation of the affine transform and not stored permanently on disk? Or does it come with the latest update?
It would be very helpful to have such a file, mainly for the reasons Richard mentioned, i.e. use it to compose the complete transform 'native->DARTEL-mean->MNI'. The inverse of such a composition could be used to warp Atlas-labels in MNI space to native space.

Best regards,
Michel
 

> Date: Wed, 16 Feb 2011 15:58:16 +0000
> From: [log in to unmask]
> Subject: Re: [SPM] New Segmentation Out of Memory Error
> To: [log in to unmask]
>
> This file does indeed contain an affine transform, and is generated
> when the affine registration between population average and MNI space
> is estimated.
>
> There's no script to do what you're after yet, but if the demand is
> high enough I could introduce the option. Can I ask how you plan to
> use the transforms?
>
> Best regards,
> -John
>
>
> On 16 February 2011 15:44, Richard Binney <[log in to unmask]> wrote:
> > ......I've just spotted that running normalise-to-mni now spits out a
> > 'Template_6_2mni.mat' file. I don't recall seeing this before - would this
> > happen to be the affine transform I spoke of?
> >
> > R
> >
> > On Wed, Feb 16, 2011 at 3:39 PM, Richard Binney
> > <[log in to unmask]> wrote:
> >>
> >> Ah, yes. I couldn't find the email you were refferring to, but I've done
> >> it and it makes a huge difference. Pretty obvious really.
> >>
> >> One more thing, John (or anybody else for that matter) - is there now a
> >> way in which one can easily create an inverse of the DARTEL normalise-to-MNI
> >> deformation composition (so from MNI --> study average --> individual
> >> subject space)? Is it possible (i.e., is there script) to have this (forward
> >> and/or backwards) written out for each subject or, alternatively, to have
> >> the affine template-to-TPM transform outputted such that one can combine it
> >> with a flow field, and subsequently inverse the composition using the
> >> deformations tool?
> >>
> >> All the best,
> >>
> >> Richard
> >>
> >> On Tue, Feb 15, 2011 at 5:42 PM, John Ashburner <[log in to unmask]>
> >> wrote:
> >>>
> >>> You may wish to change the voxel sizes and bounding box in order to
> >>> obtain slightly lower resolution versions (other than the default
> >>> 1.5mm isotropic with a large bounding box).  See the email I sent out
> >>> recently.
> >>>
> >>> Best regards,
> >>> -John
> >>>
> >>> On 15 February 2011 17:29, Richard Binney <[log in to unmask]>
> >>> wrote:
> >>> > Dear John (and other knowledgeable types),
> >>> >
> >>> > I used the deformation file (e.g., Y_p1_T1.nii) from Seg8 to normalise
> >>> > a
> >>> > functional MRI timeseries. That worked fine - the anatomical
> >>> > images that
> >>> > I additionally warped in this way look great - but I now cannot do
> >>> > anything
> >>> > with the timeseries.
> >>> >
> >>> > It is now almost 4Gb in size. I appreciate that using DARTEL to warp
> >>> > fMRI
> >>> > data can result in massive files which are problematic (and thus a work
> >>> > around is to apply the warp to contrast images), but I didn't expect
> >>> > the
> >>> > segment deformation field to do the same.
> >>> >
> >>> > Does this sound about right for a timeseries with 465 volumes (voxel
> >>> > dim 2.5
> >>> > x 2.5 x 3; matrix 96x96; numslices = 42)? Or have I made a mistake
> >>> > somewhere?
> >>> >
> >>> > so I'm supposing my inability to use the warped timeseries is a memory
> >>> > issue - I am running a 64-bit machine with 8Gb memory (I can see all
> >>> > this
> >>> > being used in the task manager so doesn't seem to be a matlab version
> >>> > problem) but maybe this file is just way too big for the SPM
> >>> > platform.....???? I could crop the image, etc I suppose but maybe the
> >>> > biggest problem is the shear number of volumes.
> >>> >
> >>> > Thanks in advance for your thoughts
> >>> >
> >>> > Richard
> >>> >
> >>> > On Thu, Feb 10, 2011 at 4:05 PM, William Pettersson-Yeo
> >>> > <[log in to unmask]> wrote:
> >>> >>
> >>> >> Thanks John.
> >>> >>
> >>> >> It turns out the problem was due to the version of Matlab I was
> >>> >> running.
> >>> >>
> >>> >> Matlab2007 was only running 32bit, whilst the 2010 version is 64.
> >>> >>
> >>> >> Having set up with Matlab2010, the new segmentation with DARTEL import
> >>> >> now
> >>> >> runs without any problem, without me having to alter/crop any of the
> >>> >> images.
> >>> >>
> >>> >> All the best
> >>> >> William
> >>> >
> >>> >
> >>
> >
> >
--_fd2415e3-e3d7-48dc-a0ca-d5dba1603bcc_-- ========================================================================Date: Wed, 16 Feb 2011 17:10:35 +0000 Reply-To: Richard Binney <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Richard Binney <[log in to unmask]> Subject: Fwd: [SPM] New Segmentation Out of Memory Error In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/alternative; boundarye6ba6e85e6fd0d09049c695bdd Message-ID: <[log in to unmask]> --90e6ba6e85e6fd0d09049c695bdd Content-Type: text/plain; charset=ISO-8859-1 ---------- Forwarded message ---------- From: Richard Binney <[log in to unmask]> Date: Wed, Feb 16, 2011 at 5:10 PM Subject: Re: [SPM] New Segmentation Out of Memory Error To: John Ashburner <[log in to unmask]> Hi John, Thanks for the quick response. So for example - I may have ROIs defined on the basis of coordinates taken from functional data or probabilistic anatomical maps in MNI space. Say I wanted to use these ROIs for DWI tractography which is of course performed in the native diffusion space, and so I would require a transform from the MNI space to the T1 - which would of course have been coreg'd to the diffusion dataset prior to any transform estimation (alternatively I could use the b0 image but the T1 or multispectral classification is better). I can easily do this with the other normalisation methods (e.g., segment and new segment), however, for interpreting the tractography maps (say in averaging to get group maps) I require the best possible inter-subject registration available to me. I believe that is where DARTEL comes in. So I would need an MNI-to-native option in DARTEL or a file containing the affine transform that I can combine with the DARTEL flowfield and subsequently invert using the deformations utility (I can't use the current .mat file in 'deformations', can I?). I had previously thought I would need this option for performing functional connectivity (etc) analyses seeded from ROIs defined on the basis of standard group-level (in MNI) GLM analyses. This was because I had been performing fixed effects (1st level) analyses in subject space and normalising the contrast images and I ideally wanted to use the same transform in the forward and backwards direction of course. I was doing this because I found that normalising the whole time-series with DARTEL resulted in enormous files that SPM couldn't deal with at the stage of the GLM. I've now of course (quite embarrasingly) realised with your help, that changing the voxel size and bounding box size circumvents this issue. This may remain an issue for people who find themselves with datasets larger than mine. Other people may know of other potential applications beyond DWI tractography...... Any thoughts? Kind regards, Richard On Wed, Feb 16, 2011 at 3:58 PM, John Ashburner <[log in to unmask]>wrote: > This file does indeed contain an affine transform, and is generated > when the affine registration between population average and MNI space > is estimated. > > There's no script to do what you're after yet, but if the demand is > high enough I could introduce the option. Can I ask how you plan to > use the transforms? > > Best regards, > -John > > > On 16 February 2011 15:44, Richard Binney <[log in to unmask]> > wrote: > > ......I've just spotted that running normalise-to-mni now spits out a > > 'Template_6_2mni.mat' file. I don't recall seeing this before - would > this > > happen to be the affine transform I spoke of? > > > > R > > > > On Wed, Feb 16, 2011 at 3:39 PM, Richard Binney > > <[log in to unmask]> wrote: > >> > >> Ah, yes. I couldn't find the email you were refferring to, but I've done > >> it and it makes a huge difference. Pretty obvious really. > >> > >> One more thing, John (or anybody else for that matter) - is there now a > >> way in which one can easily create an inverse of the DARTEL > normalise-to-MNI > >> deformation composition (so from MNI --> study average --> individual > >> subject space)? Is it possible (i.e., is there script) to have this > (forward > >> and/or backwards) written out for each subject or, alternatively, to > have > >> the affine template-to-TPM transform outputted such that one can combine > it > >> with a flow field, and subsequently inverse the composition using the > >> deformations tool? > >> > >> All the best, > >> > >> Richard > >> > >> On Tue, Feb 15, 2011 at 5:42 PM, John Ashburner <[log in to unmask]> > >> wrote: > >>> > >>> You may wish to change the voxel sizes and bounding box in order to > >>> obtain slightly lower resolution versions (other than the default > >>> 1.5mm isotropic with a large bounding box). See the email I sent out > >>> recently. > >>> > >>> Best regards, > >>> -John > >>> > >>> On 15 February 2011 17:29, Richard Binney < > [log in to unmask]> > >>> wrote: > >>> > Dear John (and other knowledgeable types), > >>> > > >>> > I used the deformation file (e.g., Y_p1_T1.nii) from Seg8 to > normalise > >>> > a > >>> > functional MRI timeseries. That worked fine - the anatomical > >>> > images that > >>> > I additionally warped in this way look great - but I now cannot do > >>> > anything > >>> > with the timeseries. > >>> > > >>> > It is now almost 4Gb in size. I appreciate that using DARTEL to warp > >>> > fMRI > >>> > data can result in massive files which are problematic (and thus a > work > >>> > around is to apply the warp to contrast images), but I didn't expect > >>> > the > >>> > segment deformation field to do the same. > >>> > > >>> > Does this sound about right for a timeseries with 465 volumes (voxel > >>> > dim 2.5 > >>> > x 2.5 x 3; matrix 96x96; numslices = 42)? Or have I made a mistake > >>> > somewhere? > >>> > > >>> > so I'm supposing my inability to use the warped timeseries is a > memory > >>> > issue - I am running a 64-bit machine with 8Gb memory (I can see all > >>> > this > >>> > being used in the task manager so doesn't seem to be a matlab version > >>> > problem) but maybe this file is just way too big for the SPM > >>> > platform.....???? I could crop the image, etc I suppose but maybe the > >>> > biggest problem is the shear number of volumes. > >>> > > >>> > Thanks in advance for your thoughts > >>> > > >>> > Richard > >>> > > >>> > On Thu, Feb 10, 2011 at 4:05 PM, William Pettersson-Yeo > >>> > <[log in to unmask]> wrote: > >>> >> > >>> >> Thanks John. > >>> >> > >>> >> It turns out the problem was due to the version of Matlab I was > >>> >> running. > >>> >> > >>> >> Matlab2007 was only running 32bit, whilst the 2010 version is 64. > >>> >> > >>> >> Having set up with Matlab2010, the new segmentation with DARTEL > import > >>> >> now > >>> >> runs without any problem, without me having to alter/crop any of the > >>> >> images. > >>> >> > >>> >> All the best > >>> >> William > >>> > > >>> > > >> > > > > > --90e6ba6e85e6fd0d09049c695bdd Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable

---------- Forwarded message ----------
From: Richard Binney <[log in to unmask]>
Date: Wed, Feb 16, 2011 at 5:10 PM
Subject: Re: [SPM] New Segmentation Out of Memory Error
To: John Ashburner <[log in to unmask]>


Hi John,
Thanks for the quick response.
So for example - I may have ROIs definedon the basis of coordinates taken fromfunctional data or probabilistic anatomical maps in MNI space. Say I wanted to use theseROIs for DWI tractographywhich is of course performed in the native diffusion space, and so I would require a transform from the MNI space to the T1 - which would of coursehave been coreg'd to the diffusion dataset prior to any transform estimation (alternatively I could use the b0 image but the T1 or multispectral classification is better). I can easilydo this with the other normalisation methods (e.g., segment and new segment), however, for interpreting the tractography maps (say in averaging to get group maps) I require the best possible inter-subject registration available to me. I believe that is where DARTEL comes in.
So I would need an MNI-to-native option in DARTEL or a file containing the affine transform that I can combine with the DARTEL flowfield and subsequently invert using the deformations utility (I can't use the current .mat file in 'deformations', can I?).
I had previously thought I would need this option for performing functional connectivity (etc) analyses seeded from ROIs defined on the basis of standard group-level (in MNI) GLM analyses.This was because I had been performing fixed effects (1st level) analyses in subject space andnormalising the contrast images and I ideally wanted to use the same transform in the forward and backwards direction of course. I was doing this because I found that normalising the whole time-series with DARTEL resulted in enormous files that SPM couldn't deal with at the stage of the GLM. I've now of course (quite embarrasingly) realised with your help, that changing the voxel size and bounding box size circumvents this issue. This may remain an issue for people who find themselves with datasets larger than mine.
Other people mayknow ofother potential applications beyond DWI tractography......
Any thoughts?
Kind regards,
Richard
On Wed, Feb 16, 2011 at 3:58 PM, John Ashburner <[log in to unmask]> wrote:
This file does indeed contain an affine transform, and is generated
when the affine registration between population average and MNI space
is estimated.

There's no script to do what you're after yet, but if the demand is
high enough I could introduce the option. Can I ask how you plan to
use the transforms?

Best regards,
-John


On 16 February 2011 15:44, Richard Binney <[log in to unmask]> wrote:
> ......I've just spotted that running normalise-to-mni now spits out a
> 'Template_6_2mni.mat' file. I don't recall seeing this before -would this
> happen to be the affine transform I spoke of?
>
> R
>
> On Wed, Feb 16, 2011 at 3:39 PM, Richard Binney
> <[log in to unmask]> wrote:
>>
>> Ah, yes. I couldn't find the email you were refferring to,butI've done
>> it and it makes a huge difference. Pretty obvious really.
>>
>> One more thing, John (or anybody else for that matter)- is there now a
>> way in which one can easilycreate an inverseof theDARTEL normalise-to-MNI
>> deformation composition (so from MNI --> study average --> individual
>> subject space)? Is it possible (i.e., is there script)to have this (forward
>> and/or backwards)written out for each subject or, alternatively, to have
>> the affine template-to-TPMtransform outputtedsuch that one can combine it
>> witha flow field, and subsequently inversethe composition using the
>> deformations tool?
>>
>> All the best,
>>
>> Richard
>>
>> On Tue, Feb 15, 2011 at 5:42 PM, John Ashburner <[log in to unmask]>
>> wrote:
>>>
>>> You may wish to change the voxel sizes and bounding box in order to
>>> obtain slightly lower resolution versions (other than the default
>>> 1.5mm isotropic with a large bounding box). See the email I sent out
>>> recently.
>>>
>>> Best regards,
>>> -John
>>>
>>> On 15 February 2011 17:29, Richard Binney <[log in to unmask]>
>>> wrote:
>>> > Dear John (and other knowledgeable types),
>>> >
>>> > I used the deformation file (e.g., Y_p1_T1.nii) from Seg8 to normalise
>>> > a
>>> > functional MRI timeseries. That worked fine - the anatomical
>>> > imagesthat
>>> > Iadditionally warped in thisway look great - but I now cannot do
>>> > anything
>>> > with the timeseries.
>>> >
>>> > It is now almost 4Gb in size. I appreciate that using DARTEL to warp
>>> > fMRI
>>> > data can result in massive files which are problematic (and thus a work
>>> > around is to apply the warp to contrast images), but I didn't expect
>>> > the
>>> > segment deformation field to do the same.
>>> >
>>> > Does this sound about right for a timeseries with 465 volumes (voxel
>>> > dim 2.5
>>> > x 2.5 x 3; matrix 96x96; numslices = 42)? Or have I made a mistake
>>> > somewhere?
>>> >
>>> > so I'm supposing my inability to use the warped timeseries is a memory
>>> > issue- I am running a 64-bit machine with 8Gb memory (I can see all
>>> > this
>>> > being used in the task manager so doesn't seem to be a matlab version
>>> > problem) but maybe this file is just way too big for the SPM
>>> > platform.....???? I could crop the image, etc I suppose but maybe the
>>> > biggest problem is the shear number of volumes.
>>> >
>>> > Thanks in advance for your thoughts
>>> >
>>> > Richard
>>> >
>>> > On Thu, Feb 10, 2011 at 4:05 PM, William Pettersson-Yeo
>>> > <[log in to unmask]> wrote:
>>> >>
>>> >> Thanks John.
>>> >>
>>> >> It turns out the problem was due to the version of Matlab I was
>>> >> running.
>>> >>
>>> >> Matlab2007 was only running 32bit, whilst the 2010 version is 64.
>>> >>
>>> >> Having set up with Matlab2010, the new segmentation with DARTEL import
>>> >> now
>>> >> runs without any problem, without me having to alter/crop any of the
>>> >> images.
>>> >>
>>> >> All the best
>>> >> William
>>> >
>>> >
>>
>
>


--90e6ba6e85e6fd0d09049c695bdd-- ========================================================================Date: Wed, 16 Feb 2011 17:15:28 +0000 Reply-To: Richard Binney <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Richard Binney <[log in to unmask]> Subject: Re: New Segmentation Out of Memory Error In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/alternative; boundarye6ba6e8b88716639049c696db4 Message-ID: <[log in to unmask]> --90e6ba6e8b88716639049c696db4 Content-Type: text/plain; charset=ISO-8859-1 Dear Michel, I updated my SPM8 yesterday - today is the first time I have seen this file. I ran DARTEL's normalise-to-MNI in the usual way and this file was stored to disk permanently. Richard On Wed, Feb 16, 2011 at 5:10 PM, Richard Binney < [log in to unmask]> wrote: > > > ---------- Forwarded message ---------- > From: Richard Binney <[log in to unmask]> > Date: Wed, Feb 16, 2011 at 5:10 PM > Subject: Re: [SPM] New Segmentation Out of Memory Error > To: John Ashburner <[log in to unmask]> > > > Hi John, > > Thanks for the quick response. > > So for example - I may have ROIs defined on the basis of coordinates taken > from functional data or probabilistic anatomical maps in MNI space. Say I > wanted to use these ROIs for DWI tractography which is of course performed > in the native diffusion space, and so I would require a transform from the > MNI space to the T1 - which would of course have been coreg'd to the > diffusion dataset prior to any transform estimation (alternatively I could > use the b0 image but the T1 or multispectral classification is better). I > can easily do this with the other normalisation methods (e.g., segment and > new segment), however, for interpreting the tractography maps (say in > averaging to get group maps) I require the best possible inter-subject > registration available to me. I believe that is where DARTEL comes in. > > So I would need an MNI-to-native option in DARTEL or a file containing the > affine transform that I can combine with the DARTEL flowfield and > subsequently invert using the deformations utility (I can't use the current > .mat file in 'deformations', can I?). > > I had previously thought I would need this option for performing functional > connectivity (etc) analyses seeded from ROIs defined on the basis of > standard group-level (in MNI) GLM analyses. This was because I had been > performing fixed effects (1st level) analyses in subject space > and normalising the contrast images and I ideally wanted to use the same > transform in the forward and backwards direction of course. I was doing this > because I found that normalising the whole time-series with DARTEL resulted > in enormous files that SPM couldn't deal with at the stage of the GLM. I've > now of course (quite embarrasingly) realised with your help, that changing > the voxel size and bounding box size circumvents this issue. This may remain > an issue for people who find themselves with datasets larger than mine. > > Other people may know of other potential applications beyond DWI > tractography...... > > Any thoughts? > > Kind regards, > > Richard > > On Wed, Feb 16, 2011 at 3:58 PM, John Ashburner <[log in to unmask]>wrote: > >> This file does indeed contain an affine transform, and is generated >> when the affine registration between population average and MNI space >> is estimated. >> >> There's no script to do what you're after yet, but if the demand is >> high enough I could introduce the option. Can I ask how you plan to >> use the transforms? >> >> Best regards, >> -John >> >> >> On 16 February 2011 15:44, Richard Binney <[log in to unmask]> >> wrote: >> > ......I've just spotted that running normalise-to-mni now spits out a >> > 'Template_6_2mni.mat' file. I don't recall seeing this before - would >> this >> > happen to be the affine transform I spoke of? >> > >> > R >> > >> > On Wed, Feb 16, 2011 at 3:39 PM, Richard Binney >> > <[log in to unmask]> wrote: >> >> >> >> Ah, yes. I couldn't find the email you were refferring to, but I've >> done >> >> it and it makes a huge difference. Pretty obvious really. >> >> >> >> One more thing, John (or anybody else for that matter) - is there now a >> >> way in which one can easily create an inverse of the DARTEL >> normalise-to-MNI >> >> deformation composition (so from MNI --> study average --> individual >> >> subject space)? Is it possible (i.e., is there script) to have this >> (forward >> >> and/or backwards) written out for each subject or, alternatively, to >> have >> >> the affine template-to-TPM transform outputted such that one can >> combine it >> >> with a flow field, and subsequently inverse the composition using the >> >> deformations tool? >> >> >> >> All the best, >> >> >> >> Richard >> >> >> >> On Tue, Feb 15, 2011 at 5:42 PM, John Ashburner <[log in to unmask]> >> >> wrote: >> >>> >> >>> You may wish to change the voxel sizes and bounding box in order to >> >>> obtain slightly lower resolution versions (other than the default >> >>> 1.5mm isotropic with a large bounding box). See the email I sent out >> >>> recently. >> >>> >> >>> Best regards, >> >>> -John >> >>> >> >>> On 15 February 2011 17:29, Richard Binney < >> [log in to unmask]> >> >>> wrote: >> >>> > Dear John (and other knowledgeable types), >> >>> > >> >>> > I used the deformation file (e.g., Y_p1_T1.nii) from Seg8 to >> normalise >> >>> > a >> >>> > functional MRI timeseries. That worked fine - the anatomical >> >>> > images that >> >>> > I additionally warped in this way look great - but I now cannot do >> >>> > anything >> >>> > with the timeseries. >> >>> > >> >>> > It is now almost 4Gb in size. I appreciate that using DARTEL to warp >> >>> > fMRI >> >>> > data can result in massive files which are problematic (and thus a >> work >> >>> > around is to apply the warp to contrast images), but I didn't expect >> >>> > the >> >>> > segment deformation field to do the same. >> >>> > >> >>> > Does this sound about right for a timeseries with 465 volumes (voxel >> >>> > dim 2.5 >> >>> > x 2.5 x 3; matrix 96x96; numslices = 42)? Or have I made a mistake >> >>> > somewhere? >> >>> > >> >>> > so I'm supposing my inability to use the warped timeseries is a >> memory >> >>> > issue - I am running a 64-bit machine with 8Gb memory (I can see all >> >>> > this >> >>> > being used in the task manager so doesn't seem to be a matlab >> version >> >>> > problem) but maybe this file is just way too big for the SPM >> >>> > platform.....???? I could crop the image, etc I suppose but maybe >> the >> >>> > biggest problem is the shear number of volumes. >> >>> > >> >>> > Thanks in advance for your thoughts >> >>> > >> >>> > Richard >> >>> > >> >>> > On Thu, Feb 10, 2011 at 4:05 PM, William Pettersson-Yeo >> >>> > <[log in to unmask]> wrote: >> >>> >> >> >>> >> Thanks John. >> >>> >> >> >>> >> It turns out the problem was due to the version of Matlab I was >> >>> >> running. >> >>> >> >> >>> >> Matlab2007 was only running 32bit, whilst the 2010 version is 64. >> >>> >> >> >>> >> Having set up with Matlab2010, the new segmentation with DARTEL >> import >> >>> >> now >> >>> >> runs without any problem, without me having to alter/crop any of >> the >> >>> >> images. >> >>> >> >> >>> >> All the best >> >>> >> William >> >>> > >> >>> > >> >> >> > >> > >> > > > --90e6ba6e8b88716639049c696db4 Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable
Dear Michel,
I updated my SPM8 yesterday - today is the first time I have seen this file. I ran DARTEL's normalise-to-MNI in the usual way andthis filewas stored to disk permanently.
Richard

On Wed, Feb 16, 2011 at 5:10 PM, Richard Binney <[log in to unmask]> wrote:


---------- Forwarded message ----------
From: Richard Binney <[log in to unmask]>
Date: Wed, Feb 16, 2011 at 5:10 PM
Subject: Re: [SPM] New Segmentation Out of Memory Error
To: John Ashburner <[log in to unmask]>


Hi John,
Thanks for the quick response.
So for example - I may have ROIs definedon the basis of coordinates taken fromfunctional data or probabilistic anatomical maps in MNI space. Say I wanted to use theseROIs for DWI tractographywhich is of course performed in the native diffusion space, and so I would require a transform from the MNI space to the T1 - which would of coursehave been coreg'd to the diffusion dataset prior to any transform estimation (alternatively I could use the b0 image but the T1 or multispectral classification is better). I can easilydo this with the other normalisation methods (e.g., segment and new segment), however, for interpreting the tractography maps (say in averaging to get group maps) I require the best possible inter-subject registration available to me. I believe that is where DARTEL comes in.
So I would need an MNI-to-native option in DARTEL or a file containing the affine transform that I can combine with the DARTEL flowfield and subsequently invert using the deformations utility (I can't use the current .mat file in 'deformations', can I?).
I had previously thought I would need this option for performing functional connectivity (etc) analyses seeded from ROIs defined on the basis of standard group-level (in MNI) GLM analyses.This was because I had been performing fixed effects (1st level) analyses in subject space andnormalising the contrast images and I ideally wanted to use the same transform in the forward and backwards direction of course. I was doing this because I found that normalising the whole time-series with DARTEL resulted in enormous files that SPM couldn't deal with at the stage of the GLM. I've now of course (quite embarrasingly) realised with your help, that changing the voxel size and bounding box size circumvents this issue. This may remain an issue for people who find themselves with datasets larger than mine.
Other people mayknow ofother potential applications beyond DWI tractography......
Any thoughts?
Kind regards,
Richard
On Wed, Feb 16, 2011 at 3:58 PM, John Ashburner <[log in to unmask]> wrote:
This file does indeed contain an affine transform, and is generated
when the affine registration between population average and MNI space
is estimated.

There's no script to do what you're after yet, but if the demand is
high enough I could introduce the option. Can I ask how you plan to
use the transforms?

Best regards,
-John


On 16 February 2011 15:44, Richard Binney <[log in to unmask]> wrote:
> ......I've just spotted that running normalise-to-mni now spits out a
> 'Template_6_2mni.mat' file. I don't recall seeing this before -would this
> happen to be the affine transform I spoke of?
>
> R
>
> On Wed, Feb 16, 2011 at 3:39 PM, Richard Binney
> <[log in to unmask]> wrote:
>>
>> Ah, yes. I couldn't find the email you were refferring to,butI've done
>> it and it makes a huge difference. Pretty obvious really.
>>
>> One more thing, John (or anybody else for that matter)- is there now a
>> way in which one can easilycreate an inverseof theDARTEL normalise-to-MNI
>> deformation composition (so from MNI --> study average --> individual
>> subject space)? Is it possible (i.e., is there script)to have this (forward
>> and/or backwards)written out for each subject or, alternatively, to have
>> the affine template-to-TPMtransform outputtedsuch that one can combine it
>> witha flow field, and subsequently inversethe composition using the
>> deformations tool?
>>
>> All the best,
>>
>> Richard
>>
>> On Tue, Feb 15, 2011 at 5:42 PM, John Ashburner <[log in to unmask]>
>> wrote:
>>>
>>> You may wish to change the voxel sizes and bounding box in order to
>>> obtain slightly lower resolution versions (other than the default
>>> 1.5mm isotropic with a large bounding box). See the email I sent out
>>> recently.
>>>
>>> Best regards,
>>> -John
>>>
>>> On 15 February 2011 17:29, Richard Binney <[log in to unmask]>
>>> wrote:
>>> > Dear John (and other knowledgeable types),
>>> >
>>> > I used the deformation file (e.g., Y_p1_T1.nii) from Seg8 to normalise
>>> > a
>>> > functional MRI timeseries. That worked fine - the anatomical
>>> > imagesthat
>>> > Iadditionally warped in thisway look great - but I now cannot do
>>> > anything
>>> > with the timeseries.
>>> >
>>> > It is now almost 4Gb in size. I appreciate that using DARTEL to warp
>>> > fMRI
>>> > data can result in massive files which are problematic (and thus a work
>>> > around is to apply the warp to contrast images), but I didn't expect
>>> > the
>>> > segment deformation field to do the same.
>>> >
>>> > Does this sound about right for a timeseries with 465 volumes (voxel
>>> > dim 2.5
>>> > x 2.5 x 3; matrix 96x96; numslices = 42)? Or have I made a mistake
>>> > somewhere?
>>> >
>>> > so I'm supposing my inability to use the warped timeseries is a memory
>>> > issue- I am running a 64-bit machine with 8Gb memory (I can see all
>>> > this
>>> > being used in the task manager so doesn't seem to be a matlab version
>>> > problem) but maybe this file is just way too big for the SPM
>>> > platform.....???? I could crop the image, etc I suppose but maybe the
>>> > biggest problem is the shear number of volumes.
>>> >
>>> > Thanks in advance for your thoughts
>>> >
>>> > Richard
>>> >
>>> > On Thu, Feb 10, 2011 at 4:05 PM, William Pettersson-Yeo
>>> > <[log in to unmask]> wrote:
>>> >>
>>> >> Thanks John.
>>> >>
>>> >> It turns out the problem was due to the version of Matlab I was
>>> >> running.
>>> >>
>>> >> Matlab2007 was only running 32bit, whilst the 2010 version is 64.
>>> >>
>>> >> Having set up with Matlab2010, the new segmentation with DARTEL import
>>> >> now
>>> >> runs without any problem, without me having to alter/crop any of the
>>> >> images.
>>> >>
>>> >> All the best
>>> >> William
>>> >
>>> >
>>
>
>



--90e6ba6e8b88716639049c696db4-- ========================================================================Date: Wed, 16 Feb 2011 17:16:00 +0000 Reply-To: John Ashburner <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: John Ashburner <[log in to unmask]> Subject: Re: New Segmentation Out of Memory Error Comments: To: michel grothe <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> > I havent seen such a file in my version of SPM8 (the penultimate update, > run on win32). Is it possible that this file is just generated during > estimation of the affine transform and not stored permanently on disk? Or > does it come with the latest update? This change occurred in SPM8 r3727, so should be in the current updates, which are to r4010. > It would be very helpful to have such a file, mainly for the reasons Richard > mentioned, i.e. use it to compose the complete transform > 'native->DARTEL-mean->MNI'. The inverse of such a composition could be used > to warp Atlas-labels in MNI space to native space. There's no easy way to use the file yet, but I'll try to code something up for a future version of SPM8. Best regards, -John >> Date: Wed, 16 Feb 2011 15:58:16 +0000 >> From: [log in to unmask] >> Subject: Re: [SPM] New Segmentation Out of Memory Error >> To: [log in to unmask] >> >> This file does indeed contain an affine transform, and is generated >> when the affine registration between population average and MNI space >> is estimated. >> >> There's no script to do what you're after yet, but if the demand is >> high enough I could introduce the option. Can I ask how you plan to >> use the transforms? >> >> Best regards, >> -John >> >> >> On 16 February 2011 15:44, Richard Binney <[log in to unmask]> >> wrote: >> > ......I've just spotted that running normalise-to-mni now spits out a >> > 'Template_6_2mni.mat' file. I don't recall seeing this before -would >> > this >> > happen to be the affine transform I spoke of? >> > >> > R >> > >> > On Wed, Feb 16, 2011 at 3:39 PM, Richard Binney >> > <[log in to unmask]> wrote: >> >> >> >> Ah, yes. I couldn't find the email you were refferring to,butI've >> >> done >> >> it and it makes a huge difference. Pretty obvious really. >> >> >> >> One more thing, John (or anybody else for that matter)- is there now a >> >> way in which one can easilycreate an inverseof theDARTEL >> >> normalise-to-MNI >> >> deformation composition (so from MNI --> study average --> individual >> >> subject space)? Is it possible (i.e., is there script)to have this >> >> (forward >> >> and/or backwards)written out for each subject or, alternatively, to >> >> have >> >> the affine template-to-TPMtransform outputtedsuch that one can >> >> combine it >> >> witha flow field, and subsequently inversethe composition using the >> >> deformations tool? >> >> >> >> All the best, >> >> >> >> Richard >> >> >> >> On Tue, Feb 15, 2011 at 5:42 PM, John Ashburner <[log in to unmask]> >> >> wrote: >> >>> >> >>> You may wish to change the voxel sizes and bounding box in order to >> >>> obtain slightly lower resolution versions (other than the default >> >>> 1.5mm isotropic with a large bounding box). See the email I sent out >> >>> recently. >> >>> >> >>> Best regards, >> >>> -John >> >>> >> >>> On 15 February 2011 17:29, Richard Binney >> >>> <[log in to unmask]> >> >>> wrote: >> >>> > Dear John (and other knowledgeable types), >> >>> > >> >>> > I used the deformation file (e.g., Y_p1_T1.nii) from Seg8 to >> >>> > normalise >> >>> > a >> >>> > functional MRI timeseries. That worked fine - the anatomical >> >>> > imagesthat >> >>> > Iadditionally warped in thisway look great - but I now cannot do >> >>> > anything >> >>> > with the timeseries. >> >>> > >> >>> > It is now almost 4Gb in size. I appreciate that using DARTEL to warp >> >>> > fMRI >> >>> > data can result in massive files which are problematic (and thus a >> >>> > work >> >>> > around is to apply the warp to contrast images), but I didn't expect >> >>> > the >> >>> > segment deformation field to do the same. >> >>> > >> >>> > Does this sound about right for a timeseries with 465 volumes (voxel >> >>> > dim 2.5 >> >>> > x 2.5 x 3; matrix 96x96; numslices = 42)? Or have I made a mistake >> >>> > somewhere? >> >>> > >> >>> > so I'm supposing my inability to use the warped timeseries is a >> >>> > memory >> >>> > issue- I am running a 64-bit machine with 8Gb memory (I can see all >> >>> > this >> >>> > being used in the task manager so doesn't seem to be a matlab >> >>> > version >> >>> > problem) but maybe this file is just way too big for the SPM >> >>> > platform.....???? I could crop the image, etc I suppose but maybe >> >>> > the >> >>> > biggest problem is the shear number of volumes. >> >>> > >> >>> > Thanks in advance for your thoughts >> >>> > >> >>> > Richard >> >>> > >> >>> > On Thu, Feb 10, 2011 at 4:05 PM, William Pettersson-Yeo >> >>> > <[log in to unmask]> wrote: >> >>> >> >> >>> >> Thanks John. >> >>> >> >> >>> >> It turns out the problem was due to the version of Matlab I was >> >>> >> running. >> >>> >> >> >>> >> Matlab2007 was only running 32bit, whilst the 2010 version is 64. >> >>> >> >> >>> >> Having set up with Matlab2010, the new segmentation with DARTEL >> >>> >> import >> >>> >> now >> >>> >> runs without any problem, without me having to alter/crop any of >> >>> >> the >> >>> >> images. >> >>> >> >> >>> >> All the best >> >>> >> William >> >>> > >> >>> > >> >> >> > >> > > ========================================================================Date: Wed, 16 Feb 2011 11:24:12 -0600 Reply-To: Prabhakaran Vivek <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Prabhakaran Vivek <[log in to unmask]> Subject: Postdoctoral position in neuroimaging applications in translational and clinical research MIME-Version: 1.0 Content-Type: text/plain; charset="iso-8859-1" Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> PhDs and/or MDs who are U.S. Citizens or Permanent Residents interested in postdoctoral traineeships in the Computation and Informatics in Biology and Medicine (CIBM) Training Program, funded by the NLM Grant 5T15LM007359 are asked to apply. The postdoctoral traineeship is for a one- to two-year period. One is to begin by June, 2011, and the other to begin Summer 2011 or later. (The last year is contingent on renewal of the NLM Grant supporting the CIBM Training Program.) These traineeships are designed for cross-disciplinary training - the candidate will have a secondary mentor in addition to the primary mentor (one from computational / informatics areas, and the other from biological areas). If interested in a postdoctoral position in neuroimaging applications in translational and clinical research, please email a CV to Vivek Prabhakaran M.D., Ph.D., Director of Functional Neuroimaging in Radiology. Vivek Prabhakaran M.D., Ph.D. Assistant Professor, Director of Functional Neuroimaging in Radiology UWHealth UW Hospital and Clinics University of Wisconsin-Madison Department of Radiology HealthEmotions Research Institute 600 Highland Avenue 6001 Research Park Blvd rm 1003 Madison, WI 53792 Madison, WI 53719 Office: 608-265-5269 Office: 608-232-3342 ========================================================================Date: Wed, 16 Feb 2011 13:51:45 -0500 Reply-To: cliff <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: cliff <[log in to unmask]> Subject: T1 & functional image reorigin MIME-Version: 1.0 Content-Type: multipart/alternative; boundaryMessage-ID: <[log in to unmask]> --000e0cd6a8ccc443dd049c6ac5ce Content-Type: text/plain; charset=ISO-8859-1 Now I always use SPM99's Head-edit funtion to do these stuff (set the origin first and then apply to images). In this way, the new origin can be read correctly both in SPM99 and SPM8. However, it is quite a boring job. Is there any independent funtion in SPM that I can use to reorigin images in a modified batch way? Or is there any assistant toolbox I can use? Thanks! --000e0cd6a8ccc443dd049c6ac5ce Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable
Now I always use SPM99's Head-edit funtion to do these stuff (set the origin first and then apply toimages).
In this way, the new origin can be read correctly both in SPM99 and SPM8.
However, it is quite a boring job.
Is there any independent funtion in SPM that I can use to reorigin images in a modified batch way?
Or is there any assistant toolbox I can use?
Thanks!
--000e0cd6a8ccc443dd049c6ac5ce-- ========================================================================Date: Wed, 16 Feb 2011 20:45:14 +0100 Reply-To: michel grothe <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: michel grothe <[log in to unmask]> Subject: Re: New Segmentation Out of Memory Error Comments: To: [log in to unmask] In-Reply-To: <[log in to unmask]> Content-Type: multipart/alternative; boundary="_d114b127-7ddd-48ec-b028-6c3509a53daf_" MIME-Version: 1.0 Message-ID: <[log in to unmask]> --_d114b127-7ddd-48ec-b028-6c3509a53daf_ Content-Type: text/plain; charset="iso-8859-1" Content-Transfer-Encoding: quoted-printable Thanks, this would be great. Meanwhile, I have some questions regarding a possible work-around: Would it be OK to use an affine transform calculated with the Normalise-Button to approximate the affine transform from 'DARTEL-Normalise to MNI' in order to be able to generate the mentioned composition 'native->DARTEL->MNI'. Does the affine alignment step in 'DARTEL-Normalise to MNI' register the DARTEL-GM template to the GM-apriori map (or the GM map in TPM.nii,1?) or does it also use the respective WM-maps? How much does the affine alignment in 'DARTEL-Normalise to MNI' differ from the one in 'Normalise', when registering DARTEL-GM to GM-apriori map (or TPM.nii,1) and setting non-linear iterations to 0? Thanks again for your help. Best regards, Michel > Date: Wed, 16 Feb 2011 17:16:00 +0000 > From: [log in to unmask] > Subject: Re: [SPM] New Segmentation Out of Memory Error > To: [log in to unmask] > > > I havent seen such a file in my version of SPM8 (the penultimate update, > > run on win32). Is it possible that this file is just generated during > > estimation of the affine transform and not stored permanently on disk? Or > > does it come with the latest update? > > This change occurred in SPM8 r3727, so should be in the current > updates, which are to r4010. > > > > It would be very helpful to have such a file, mainly for the reasons Richard > > mentioned, i.e. use it to compose the complete transform > > 'native->DARTEL-mean->MNI'. The inverse of such a composition could be used > > to warp Atlas-labels in MNI space to native space. > > There's no easy way to use the file yet, but I'll try to code > something up for a future version of SPM8. > > Best regards, > -John > > > >> Date: Wed, 16 Feb 2011 15:58:16 +0000 > >> From: [log in to unmask] > >> Subject: Re: [SPM] New Segmentation Out of Memory Error > >> To: [log in to unmask] > >> > >> This file does indeed contain an affine transform, and is generated > >> when the affine registration between population average and MNI space > >> is estimated. > >> > >> There's no script to do what you're after yet, but if the demand is > >> high enough I could introduce the option. Can I ask how you plan to > >> use the transforms? > >> > >> Best regards, > >> -John > >> > >> > >> On 16 February 2011 15:44, Richard Binney <[log in to unmask]> > >> wrote: > >> > ......I've just spotted that running normalise-to-mni now spits out a > >> > 'Template_6_2mni.mat' file. I don't recall seeing this before - would > >> > this > >> > happen to be the affine transform I spoke of? > >> > > >> > R > >> > > >> > On Wed, Feb 16, 2011 at 3:39 PM, Richard Binney > >> > <[log in to unmask]> wrote: > >> >> > >> >> Ah, yes. I couldn't find the email you were refferring to, but I've > >> >> done > >> >> it and it makes a huge difference. Pretty obvious really. > >> >> > >> >> One more thing, John (or anybody else for that matter) - is there now a > >> >> way in which one can easily create an inverse of the DARTEL > >> >> normalise-to-MNI > >> >> deformation composition (so from MNI --> study average --> individual > >> >> subject space)? Is it possible (i.e., is there script) to have this > >> >> (forward > >> >> and/or backwards) written out for each subject or, alternatively, to > >> >> have > >> >> the affine template-to-TPM transform outputted such that one can > >> >> combine it > >> >> with a flow field, and subsequently inverse the composition using the > >> >> deformations tool? > >> >> > >> >> All the best, > >> >> > >> >> Richard > >> >> > >> >> On Tue, Feb 15, 2011 at 5:42 PM, John Ashburner <[log in to unmask]> > >> >> wrote: > >> >>> > >> >>> You may wish to change the voxel sizes and bounding box in order to > >> >>> obtain slightly lower resolution versions (other than the default > >> >>> 1.5mm isotropic with a large bounding box). See the email I sent out > >> >>> recently. > >> >>> > >> >>> Best regards, > >> >>> -John > >> >>> > >> >>> On 15 February 2011 17:29, Richard Binney > >> >>> <[log in to unmask]> > >> >>> wrote: > >> >>> > Dear John (and other knowledgeable types), > >> >>> > > >> >>> > I used the deformation file (e.g., Y_p1_T1.nii) from Seg8 to > >> >>> > normalise > >> >>> > a > >> >>> > functional MRI timeseries. That worked fine - the anatomical > >> >>> > images that > >> >>> > I additionally warped in this way look great - but I now cannot do > >> >>> > anything > >> >>> > with the timeseries. > >> >>> > > >> >>> > It is now almost 4Gb in size. I appreciate that using DARTEL to warp > >> >>> > fMRI > >> >>> > data can result in massive files which are problematic (and thus a > >> >>> > work > >> >>> > around is to apply the warp to contrast images), but I didn't expect > >> >>> > the > >> >>> > segment deformation field to do the same. > >> >>> > > >> >>> > Does this sound about right for a timeseries with 465 volumes (voxel > >> >>> > dim 2.5 > >> >>> > x 2.5 x 3; matrix 96x96; numslices = 42)? Or have I made a mistake > >> >>> > somewhere? > >> >>> > > >> >>> > so I'm supposing my inability to use the warped timeseries is a > >> >>> > memory > >> >>> > issue - I am running a 64-bit machine with 8Gb memory (I can see all > >> >>> > this > >> >>> > being used in the task manager so doesn't seem to be a matlab > >> >>> > version > >> >>> > problem) but maybe this file is just way too big for the SPM > >> >>> > platform.....???? I could crop the image, etc I suppose but maybe > >> >>> > the > >> >>> > biggest problem is the shear number of volumes. > >> >>> > > >> >>> > Thanks in advance for your thoughts > >> >>> > > >> >>> > Richard > >> >>> > > >> >>> > On Thu, Feb 10, 2011 at 4:05 PM, William Pettersson-Yeo > >> >>> > <[log in to unmask]> wrote: > >> >>> >> > >> >>> >> Thanks John. > >> >>> >> > >> >>> >> It turns out the problem was due to the version of Matlab I was > >> >>> >> running. > >> >>> >> > >> >>> >> Matlab2007 was only running 32bit, whilst the 2010 version is 64. > >> >>> >> > >> >>> >> Having set up with Matlab2010, the new segmentation with DARTEL > >> >>> >> import > >> >>> >> now > >> >>> >> runs without any problem, without me having to alter/crop any of > >> >>> >> the > >> >>> >> images. > >> >>> >> > >> >>> >> All the best > >> >>> >> William > >> >>> > > >> >>> > > >> >> > >> > > >> > > > --_d114b127-7ddd-48ec-b028-6c3509a53daf_ Content-Type: text/html; charset="iso-8859-1" Content-Transfer-Encoding: quoted-printable Thanks, this would be great.

Meanwhile, I have some questions regarding a possible work-around:

Would it be OK to use an affine transform calculated with the Normalise-Button to approximate the affine transform from 'DARTEL-Normalise to MNI' in order to be able to generate the mentioned composition 'native->DARTEL->MNI'. Does the affine alignment step in 'DARTEL-Normalise to MNI' register the DARTEL-GM template to the GM-apriori map (or the GM map in TPM.nii,1?) or does it also use the respective WM-maps?
How much does the affine alignment in 'DARTEL-Normalise to MNI' differ from the one in 'Normalise', when registering DARTEL-GM to GM-apriori map (or TPM.nii,1) and setting non-linear iterations to 0?

Thanks again for your help.
Best regards,
Michel

> Date: Wed, 16 Feb 2011 17:16:00 +0000
> From: [log in to unmask]
> Subject: Re: [SPM] New Segmentation Out of Memory Error
> To: [log in to unmask]
>
> > I havent seen such a file in my version of SPM8 (the penultimate update,
> > run on win32). Is it possible that this file is just generated during
> > estimation of the affine transform and not stored permanently on disk? Or
> > does it come with the latest update?
>
> This change occurred in SPM8 r3727, so should be in the current
> updates, which are to r4010.
>
>
> > It would be very helpful to have such a file, mainly for the reasons Richard
> > mentioned, i.e. use it to compose the complete transform
> > 'native->DARTEL-mean->MNI'. The inverse of such a composition could be used
> > to warp Atlas-labels in MNI space to native space.
>
> There's no easy way to use the file yet, but I'll try to code
> something up for a future version of SPM8.
>
> Best regards,
> -John
>
>
> >> Date: Wed, 16 Feb 2011 15:58:16 +0000
> >> From: [log in to unmask]
> >> Subject: Re: [SPM] New Segmentation Out of Memory Error
> >> To: [log in to unmask]
> >>
> >> This file does indeed contain an affine transform, and is generated
> >> when the affine registration between population average and MNI space
> >> is estimated.
> >>
> >> There's no script to do what you're after yet, but if the demand is
> >> high enough I could introduce the option. Can I ask how you plan to
> >> use the transforms?
> >>
> >> Best regards,
> >> -John
> >>
> >>
> >> On 16 February 2011 15:44, Richard Binney <[log in to unmask]>
> >> wrote:
> >> > ......I've just spotted that running normalise-to-mni now spits out a
> >> > 'Template_6_2mni.mat' file. I don't recall seeing this before - would
> >> > this
> >> > happen to be the affine transform I spoke of?
> >> >
> >> > R
> >> >
> >> > On Wed, Feb 16, 2011 at 3:39 PM, Richard Binney
> >> > <[log in to unmask]> wrote:
> >> >>
> >> >> Ah, yes. I couldn't find the email you were refferring to, but I've
> >> >> done
> >> >> it and it makes a huge difference. Pretty obvious really.
> >> >>
> >> >> One more thing, John (or anybody else for that matter) - is there now a
> >> >> way in which one can easily create an inverse of the DARTEL
> >> >> normalise-to-MNI
> >> >> deformation composition (so from MNI --> study average --> individual
> >> >> subject space)? Is it possible (i.e., is there script) to have this
> >> >> (forward
> >> >> and/or backwards) written out for each subject or, alternatively, to
> >> >> have
> >> >> the affine template-to-TPM transform outputted such that one can
> >> >> combine it
> >> >> with a flow field, and subsequently inverse the composition using the
> >> >> deformations tool?
> >> >>
> >> >> All the best,
> >> >>
> >> >> Richard
> >> >>
> >> >> On Tue, Feb 15, 2011 at 5:42 PM, John Ashburner <[log in to unmask]>
> >> >> wrote:
> >> >>>
> >> >>> You may wish to change the voxel sizes and bounding box in order to
> >> >>> obtain slightly lower resolution versions (other than the default
> >> >>> 1.5mm isotropic with a large bounding box).  See the email I sent out
> >> >>> recently.
> >> >>>
> >> >>> Best regards,
> >> >>> -John
> >> >>>
> >> >>> On 15 February 2011 17:29, Richard Binney
> >> >>> <[log in to unmask]>
> >> >>> wrote:
> >> >>> > Dear John (and other knowledgeable types),
> >> >>> >
> >> >>> > I used the deformation file (e.g., Y_p1_T1.nii) from Seg8 to
> >> >>> > normalise
> >> >>> > a
> >> >>> > functional MRI timeseries. That worked fine - the anatomical
> >> >>> > images that
> >> >>> > I additionally warped in this way look great - but I now cannot do
> >> >>> > anything
> >> >>> > with the timeseries.
> >> >>> >
> >> >>> > It is now almost 4Gb in size. I appreciate that using DARTEL to warp
> >> >>> > fMRI
> >> >>> > data can result in massive files which are problematic (and thus a
> >> >>> > work
> >> >>> > around is to apply the warp to contrast images), but I didn't expect
> >> >>> > the
> >> >>> > segment deformation field to do the same.
> >> >>> >
> >> >>> > Does this sound about right for a timeseries with 465 volumes (voxel
> >> >>> > dim 2.5
> >> >>> > x 2.5 x 3; matrix 96x96; numslices = 42)? Or have I made a mistake
> >> >>> > somewhere?
> >> >>> >
> >> >>> > so I'm supposing my inability to use the warped timeseries is a
> >> >>> > memory
> >> >>> > issue - I am running a 64-bit machine with 8Gb memory (I can see all
> >> >>> > this
> >> >>> > being used in the task manager so doesn't seem to be a matlab
> >> >>> > version
> >> >>> > problem) but maybe this file is just way too big for the SPM
> >> >>> > platform.....???? I could crop the image, etc I suppose but maybe
> >> >>> > the
> >> >>> > biggest problem is the shear number of volumes.
> >> >>> >
> >> >>> > Thanks in advance for your thoughts
> >> >>> >
> >> >>> > Richard
> >> >>> >
> >> >>> > On Thu, Feb 10, 2011 at 4:05 PM, William Pettersson-Yeo
> >> >>> > <[log in to unmask]> wrote:
> >> >>> >>
> >> >>> >> Thanks John.
> >> >>> >>
> >> >>> >> It turns out the problem was due to the version of Matlab I was
> >> >>> >> running.
> >> >>> >>
> >> >>> >> Matlab2007 was only running 32bit, whilst the 2010 version is 64.
> >> >>> >>
> >> >>> >> Having set up with Matlab2010, the new segmentation with DARTEL
> >> >>> >> import
> >> >>> >> now
> >> >>> >> runs without any problem, without me having to alter/crop any of
> >> >>> >> the
> >> >>> >> images.
> >> >>> >>
> >> >>> >> All the best
> >> >>> >> William
> >> >>> >
> >> >>> >
> >> >>
> >> >
> >> >
> >
--_d114b127-7ddd-48ec-b028-6c3509a53daf_-- ========================================================================Date: Wed, 16 Feb 2011 19:47:46 +0000 Reply-To: John Ashburner <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: John Ashburner <[log in to unmask]> Subject: Re: T1 & functional image reorigin Comments: To: cliff <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> If all subjects have similar positioning in the scanner, then you can use Display to adjust the positioning of one scan of one subject, and then select all scans of all subjects when you actually do the reorienting. I had no idea that anyone was still seriously using SPM99. It's really just a museum piece now. Although it may have some archaeological interest, it probably isn't so great for doing science. Best regards, -John On 16 February 2011 18:51, cliff <[log in to unmask]> wrote: > Now I always use SPM99's Head-edit funtion to do these stuff (set the origin > first and then apply toimages). > In this way, the new origin can be read correctly both in SPM99 and SPM8. > However, it is quite a boring job. > > Is there any independent funtion in SPM that I can use to reorigin images in > a modified batch way? > Or is there any assistant toolbox I can use? > > Thanks! ========================================================================Date: Wed, 16 Feb 2011 22:59:07 +0100 Reply-To: SPM-Workshop Hannover <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: SPM-Workshop Hannover <[log in to unmask]> Subject: SPM-Workshop Hannover (Germany) MIME-Version: 1.0 Content-Type: multipart/alternative; boundaryMessage-ID: <[log in to unmask]> --001636c5b4d8d76261049c6d6369 Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable SPM-Workshop (German) Hannover, Germany May 11-13, 2011 Hands-on workshop for new users at Hannover Medical School in Germany focussing on the practical use of SPM8. This three-day course is designed for researchers with little or no experience in the analysis of functional imaging data. The course will be held in German. The aim of this workshop is to explain the basic principles of fMRI analysis with SPM and Matlab, and to apply this knowledge right away. All steps of data analysis in SPM8 will be covered, from importing the raw data, logfile extraction, preprocessing, 1st and 2nd level analysis to results inspection, extraction and visualization. For more information please visit www.spmworkshop-hannover.de or mail to [log in to unmask] -- *SPM-Workshop Hannover* ...learn how to do it! Email: [log in to unmask] Web: www.spmworkshop-hannover.de --001636c5b4d8d76261049c6d6369 Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable SPM-Workshop (German)
Hannover, Germany
May 11-13, 2011

Hands-on workshop for new users at Hannover Medical School in Germany focussing on the practical use of SPM8. This three-day course is designed for researchers with little or no experience in the analysis of functional imaging data. The course will be held in German.

The aim of this workshop is to explain the basic principles of fMRI analysis with SPM and Matlab, and to apply this knowledge right away. All steps of data analysis in SPM8 will be covered, from importing the raw data, logfile extraction, preprocessing, 1st and 2nd level analysis to results inspection, extraction and visualization.

For more information please visit www.spmworkshop-hannover.de or mail to [log in to unmask]


--

SPM-Workshop Hannover
...learn how to do it!

Email: [log in to unmask]
Web: www.spmworkshop-hannover.de


--001636c5b4d8d76261049c6d6369-- ========================================================================Date: Wed, 16 Feb 2011 14:34:00 -0800 Reply-To: kambiz rakhshan <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: kambiz rakhshan <[log in to unmask]> Subject: DARTEL template in MNI space MIME-Version: 1.0 Content-Type: multipart/alternative; boundary="0-778413605-1297895640=:53278" Message-ID: <[log in to unmask]> --0-778413605-1297895640=:53278 Content-Type: text/plain; charset=iso-8859-1 Content-Transfer-Encoding: quoted-printable Dear all, I am wondering how to use spm_get_space to affine normalize theDARTEL template in MNI space? Shall one use *Template_6 as P and *_2mni.mat as M? Isn't it possible to use normalize_write function instead? My second question concerns the use of suitable maskafter applying normalize to MNI function for fMRI data to get ride of potentialaliasing effects.Is it better to use normalized template of dartel as an explicitmask (while doing second level analysis) or to apply the deformation to thefirst level subject-specific mask and then multiply with the smoothed normalized images created by normalize toMNI function? Thanks in advance /Kami --0-778413605-1297895640=:53278 Content-Type: text/html; charset=iso-8859-1 Content-Transfer-Encoding: quoted-printable
Dear all,
 
I am wondering how to use spm_get_space to affine normalize the DARTEL template in MNI space? Shall one use *Template_6 as P and *_2mni.mat as M?
Isn't it possible to use normalize_write function instead?
 
My second question concerns the use of suitable mask after applying normalize to MNI function for fMRI data to get ride of potential aliasing effects.Is it better to use normalized template of dartel as an explicit mask (while doing second level analysis) or to apply the deformation to the first level subject-specific mask and then multiply with the smoothed normalized images created  by normalize to MNI function? 
 
Thanks in advance
/Kami
 

--0-778413605-1297895640=:53278-- ========================================================================Date: Wed, 16 Feb 2011 20:02:00 -0500 Reply-To: James Bursley <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: James Bursley <[log in to unmask]> Subject: VOI Batch Module Content-Type: text/plain; charset=us-ascii Content-Transfer-Encoding: quoted-printable Mime-Version: 1.0 (Apple Message framework v1082) Message-ID: <[log in to unmask]> Hi SPMers, I'm having some trouble using the Volume of Interest batch module. I'm trying to extract a sphere from a single-subject .mat file, and I want to adjust the extraction to an F-contrast I've run for that subject. When I enter a '1' as the parameter for "Adjust data," though, to select that contrast, I get this error: Error with file beta_0001.img Failed 'Volume of Interest' Error using --> spm_sample_vol Cant open image file. In file "/usr/local/analysistools/fmritools/matlab/toolbox/spm8/spm_get_data.m" (v3950), function "spm_get_data" at line 44. In file "/usr/local/analysistools/fmritools/matlab/toolbox/spm8/spm_regions.m" (v3812), function "spm_regions" at line 147. In file "/usr/local/analysistools/fmritools/matlab/toolbox/spm8/config/spm_run_voi.m" (v3780), function "spm_run_voi" at line 68. Any idea what's going on? Thanks very much! James========================================================================Date: Thu, 17 Feb 2011 02:21:17 +0000 Reply-To: James Bursley <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: James Bursley <[log in to unmask]> Subject: Re: VOI Batch Module Mime-Version: 1.0 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain Message-ID: <[log in to unmask]> Two other pieces of information regarding this problem: 1. No errors come up when I extract a VOI using the GUI; I only encounter this error when using the batch script. 2. The error only appears when "Adjust data" is set to something other than '0', i.e., when data IS being adjusted. Otherwise, the batch runs fine. ========================================================================Date: Thu, 17 Feb 2011 02:41:30 +0000 Reply-To: Toni Pitcher <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Toni Pitcher <[log in to unmask]> Subject: multiple conditions/regressors in SPM8 batch Mime-Version: 1.0 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain; charset="UTF-8" Message-ID: <[log in to unmask]> Hi All I have just converted to SPM8 and have constructed a batch template for processing fMRI model specification, estimation, contrast manager and results report for chosen study, whereby each subject has 4 sessions. After assigning dependencies etc and using the 'save and script' option, the following was produced. % List of open inputs % fMRI model specification: Directory - cfg_files % fMRI model specification: Scans - cfg_files % fMRI model specification: Scans - cfg_files % fMRI model specification: Scans - cfg_files % fMRI model specification: Scans - cfg_files nrun = X; % enter the number of runs here jobfile = {'/Users/stats_job.m'}; jobs = repmat(jobfile, 1, nrun); inputs = cell(5, nrun); for crun = 1:nrun inputs{1, crun} = MATLAB_CODE_TO_FILL_INPUT; % fMRI model specification: Directory - cfg_files inputs{2, crun} = MATLAB_CODE_TO_FILL_INPUT; % fMRI model specification: Scans - cfg_files inputs{3, crun} = MATLAB_CODE_TO_FILL_INPUT; % fMRI model specification: Scans - cfg_files inputs{4, crun} = MATLAB_CODE_TO_FILL_INPUT; % fMRI model specification: Scans - cfg_files inputs{5, crun} = MATLAB_CODE_TO_FILL_INPUT; % fMRI model specification: Scans - cfg_files end spm('defaults', 'FMRI'); spm_jobman('serial', jobs, '', inputs{:}); Required inputs being directory and scans for each of the 4 sessions. What I would also like to do is specify multiple conditions and multiple regressors files for each session. I would like to do this in a script so that the batch template can be applied across subjects. These are not listed as required inputs (<-X) in the batch, so am unsure how to specify. Thanks Toni ========================================================================Date: Thu, 17 Feb 2011 09:32:54 +0000 Reply-To: Rik Henson <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Rik Henson <[log in to unmask]> Subject: Research Assistant Position in Cambridge Content-Type: multipart/alternative; boundary="_000_3822A22C3FB6974099045A8DB62D39F93919E5D1WSR21mrccbsuloc_" MIME-Version: 1.0 Message-ID: <[log in to unmask]> --_000_3822A22C3FB6974099045A8DB62D39F93919E5D1WSR21mrccbsuloc_ Content-Type: text/plain; charset="iso-8859-1" Content-Transfer-Encoding: quoted-printable Dear colleagues - Please see Research Assistant position available below: MRC Cognition and Brain Sciences Unit - Cambridge Research Assistant Ref: IRC14207 The MRC Cognition and Brain Sciences Unit (CBSU) is an internationally renowned research institute with state-of-the-art cognitive neuroscience facilities, including on-site fMRI, MEG, and EEG laboratories, and neuropsychological patient panel and large panel of healthy volunteers. Applications are invited for a Research Assistant to provide scientific support for Dr Richard Henson's MRC programme on the systems neuroscience of human memory and perception, particularly for acquiring behavioural, EEG/MEG and/or fMRI data during cognitive experiments on volunteers. You will be highly motivated and proactive, with a degree in psychology or a related discipline. Experience in scientific research, particularly with human volunteers, is important, as is familiarity with computer programming and statistics. Experience with EEG, MEG or MRI acquisition and/or analysis would be an advantage. Good communication skills plus the ability to work as part of a large, multi-disciplinary team are essential. The starting salary will be in the range of 20,074 - 27,271 per annum, depending upon qualifications and experience. We offer a flexible pay and reward policy, 30 days annual leave entitlement, and an optional MRC final salary Pension Scheme. On site car and bicycle parking is available. Applications are handled by the RCUK Shared Services Centre; to apply please visit our job board at https://ext.ssc.rcuk.ac.uk and complete an online application form. If you are unable to apply online please contact us on 01793 867003 quoting reference IRC14207. Closing date: 21st March 2011 This position is subject to pre-employment screening The Medical Research Council is an Equal Opportunities Employer ------------------------------------------------------- Dr Richard Henson Assistant Director, Neuroimaging MRC Cognition & Brain Sciences Unit 15 Chaucer Road Cambridge, CB2 7EF, UK Office: +44 (0)1223 355 294 x522 Mob: +44 (0)794 1377 345 Fax: +44 (0)1223 359 062 http://www.mrc-cbu.cam.ac.uk/people/rik.henson ------------------------------------------------------- --_000_3822A22C3FB6974099045A8DB62D39F93919E5D1WSR21mrccbsuloc_ Content-Type: text/html; charset="iso-8859-1" Content-Transfer-Encoding: quoted-printable
 
Dear colleagues –
 
Please see Research Assistant position available below:
 
 
MRC Cognition and Brain Sciences Unit – Cambridge
Research Assistant
 
Ref: IRC14207
 
The MRC Cognition and Brain Sciences Unit (CBSU) is an internationally renowned research institute with state-of-the-art cognitive neuroscience facilities, including on-site fMRI, MEG, and EEG laboratories, and neuropsychological patient panel and large panel of healthy volunteers. Applications are invited for a Research Assistant to provide scientific support for Dr Richard Henson’s MRC programme on the systems neuroscience of human memory and perception, particularly for acquiring behavioural, EEG/MEG and/or fMRI data during cognitive experiments on volunteers.
You will be highly motivated and proactive, with a degree in psychology or a related discipline. Experience in scientific research, particularly with human volunteers, is important, as is familiarity with computer programming and statistics. Experience with EEG, MEG or MRI acquisition and/or analysis would be an advantage.  Good communication skills plus the ability to work as part of a large, multi-disciplinary team are essential.
 
The starting salary will be in the range of 20,074 - 27,271 per annum, depending upon qualifications and experience.   We offer a flexible pay and reward policy, 30 days annual leave entitlement, and an optional MRC final salary Pension Scheme.  On site car and bicycle parking is available.
 
Applications are handled by the RCUK Shared Services Centre; to apply please visit our job board at https://ext.ssc.rcuk.ac.uk and complete an online application form. If you are unable to apply online please contact us on 01793 867003 quoting reference IRC14207.
 
Closing date: 21st March 2011
 
This position is subject to pre-employment screening
The Medical Research Council is an Equal Opportunities Employer
 
 
-------------------------------------------------------
                 Dr Richard Henson
          Assistant Director, Neuroimaging
         MRC Cognition & Brain Sciences Unit
                 15 Chaucer Road
              Cambridge, CB2 7EF, UK
 
          Office: +44 (0)1223 355 294 x522
             Mob: +44 (0)794 1377 345
             Fax: +44 (0)1223 359 062
 
-------------------------------------------------------
 
 
 
--_000_3822A22C3FB6974099045A8DB62D39F93919E5D1WSR21mrccbsuloc_-- ========================================================================Date: Thu, 17 Feb 2011 11:49:09 +0100 Reply-To: Michael Erb <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Michael Erb <[log in to unmask]> Subject: Re: multiple conditions/regressors in SPM8 batch Comments: To: Toni Pitcher <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=UTF-8; format=flowed Content-Transfer-Encoding: 7bit Message-ID: <[log in to unmask]> Hi Toni, if you right click on the 'multiple conditions' or 'multiple regressors' in the batch editor, you can apply 'Clear Value' to get the <-X. Michael. Am 17.02.2011 03:41, schrieb Toni Pitcher: > Hi All > > I have just converted to SPM8 and have constructed a batch template for processing fMRI model specification, estimation, contrast manager and results report for chosen study, whereby each subject has 4 sessions. > > After assigning dependencies etc and using the 'save and script' option, the following was produced. > > % List of open inputs > % fMRI model specification: Directory - cfg_files > % fMRI model specification: Scans - cfg_files > % fMRI model specification: Scans - cfg_files > % fMRI model specification: Scans - cfg_files > % fMRI model specification: Scans - cfg_files > nrun = X; % enter the number of runs here > jobfile = {'/Users/stats_job.m'}; > jobs = repmat(jobfile, 1, nrun); > inputs = cell(5, nrun); > for crun = 1:nrun > inputs{1, crun} = MATLAB_CODE_TO_FILL_INPUT; % fMRI model specification: Directory - cfg_files > inputs{2, crun} = MATLAB_CODE_TO_FILL_INPUT; % fMRI model specification: Scans - cfg_files > inputs{3, crun} = MATLAB_CODE_TO_FILL_INPUT; % fMRI model specification: Scans - cfg_files > inputs{4, crun} = MATLAB_CODE_TO_FILL_INPUT; % fMRI model specification: Scans - cfg_files > inputs{5, crun} = MATLAB_CODE_TO_FILL_INPUT; % fMRI model specification: Scans - cfg_files > end > spm('defaults', 'FMRI'); > spm_jobman('serial', jobs, '', inputs{:}); > > > Required inputs being directory and scans for each of the 4 sessions. > > What I would also like to do is specify multiple conditions and multiple regressors files for each session. I would like to do this in a script so that the batch template can be applied across subjects. These are not listed as required inputs (<-X) in the batch, so am unsure how to specify. > > > > Thanks > > Toni > -- <<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<< Dr. Michael Erb Sektion f. experimentelle Kernspinresonanz des ZNS Abteilung Neuroradiologie, Universitaetsklinikum Hoppe-Seyler_Str. 3, D-72076 Tuebingen Tel.: +49(0)7071/2987753 priv. +49(0)7071/61559 Fax.: +49(0)7071/294371 e-mail: <[log in to unmask]> www: http://www.medizin.uni-tuebingen.de/nrad/sektion/ <<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<<< ========================================================================Date: Thu, 17 Feb 2011 13:11:05 +0000 Reply-To: John Ashburner <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: John Ashburner <[log in to unmask]> Subject: Re: DARTEL template in MNI space Comments: To: kambiz rakhshan <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/alternative; boundaryMessage-ID: <[log in to unmask]> --00163630f77d500ad5049c7a214f Content-Type: text/plain; charset=ISO-8859-1 > I am wondering how to use spm_get_space to affine normalize the DARTEL > template in MNI space? Shall one use *Template_6 as P and *_2mni.mat as M? > Isn't it possible to use normalize_write function instead? > You could write the matrix in *_2mni.mat into the header of the Template_6.nii image. The spm_get_space function would do that. > My second question concerns the use of suitable mask after applying > normalize to MNI function for fMRI data to get ride of potential aliasing > effects.Is it better to use normalized template of dartel as an > explicit mask (while doing second level analysis) or to apply the > deformation to the first level subject-specific mask and then multiply with > the smoothed normalized images created by normalize to MNI function? > These are not really aliasing effects. It's the effect of missing data in the images, where SPM tries to guess about what values should be there. Usually, these regions contain zeros, which cause even greater artifacts after smoothing, as some subjects' scans will have data, whereas others have zeros. Because this seems to be a concern for so many, I'll have a go at including a fix for the data so that those voxels with very little signal are set to zero. Best regards, -John --00163630f77d500ad5049c7a214f Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable
I am wondering how to use spm_get_space to affine normalize theDARTEL template in MNI space? Shall one use *Template_6 as P and *_2mni.mat as M?
Isn't it possible to use normalize_write function instead?

You could write the matrix in *_2mni.mat into the header of the Template_6.nii image. The spm_get_space function would do that.

My second question concerns the use of suitable maskafter applying normalize to MNI function for fMRI data to get ride of potentialaliasing effects.Is it better to use normalized template of dartel as an explicitmask (while doing second level analysis) or to apply the deformation to thefirst level subject-specific mask and then multiply with the smoothed normalized images created by normalize toMNI function?

These are not really aliasing effects. It's the effect of missing data in the images, where SPM tries to guess about what values should be there. Usually, these regions contain zeros, which cause even greater artifacts after smoothing, as some subjects' scans will have data, whereas others have zeros.

Because this seems to be a concern for so many, I'll have a go at including a fix for the data so that those voxels with very little signal are set to zero.

Best regards,
-John
--00163630f77d500ad5049c7a214f-- ========================================================================Date: Thu, 17 Feb 2011 13:54:19 +0000 Reply-To: Vladimir Litvak <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Vladimir Litvak <[log in to unmask]> Subject: Re: methodological question Comments: To: Pierre Larigneux <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Message-ID: <[log in to unmask]> Dear Gaetan, You should contrast similar things so if you have 20 ms activation time window you should compare it to a 20 ms baseline time window. You can indeed generate multiple windows from the baseline and put them all in the same design matrix as in your option (3). You could also compare your activation windows to each other across trials/subjects, then you could talk about sources being more strongly activated at time A vs. time B. Note that for these comparisons you need to specify all the time windows together (separated by ';' ) when you export to images. Best, Vladimir On Thu, Feb 17, 2011 at 11:42 AM, Pierre Larigneux <[log in to unmask]> wrote: > Dear Vladimir, > > I changed my methodology. I do not work anymore on the amplitude. > I come back to you to have some advise about the way I should look onto my > data. > > Now, to bring to light the region activated by my task I do a paired t-test > between 20 ms time windows post stimulus against baseline. > I reconstruct the sources on the global time window -200 to 600 ms and I use > gaussian windows as contrast. > > I am wondering about the most proper way to do it, I have got three main > ideas: > > 1. contrasting my 20 ms time windows against the global mean on the baseline > -200 to 0. > 2. constrating my 20 ms time windows against the mean energy of ten (or a > bit less) 20 ms time windows on the baseline. > 3. constrating my 20 ms time windows against each 20 ms time windows in a > big design matrix. > > I do not know what is the best way to do it. I tried the different things > and it gave me really close results in the localisation of the activity. > it change mainly the T of the statistics from significant to very > significant. > > Thanks for your attention, > > bests regards, > > Gaetan Yvert ========================================================================Date: Thu, 17 Feb 2011 15:02:45 +0000 Reply-To: Nick Davis <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Nick Davis <[log in to unmask]> Organization: Bangor University Subject: Creating an "average" structural image MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1; format=flowed Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> Hello SPM nerds. I would like to project my activation blobs onto some kind of average image of the brains of the subjects in my experiment. I can't see a way to create this average image in SPM8, so is there another method I could use? Thanks! Nick -- [log in to unmask] -- Gall y neges e-bost hon, ac unrhyw atodiadau a anfonwyd gyda hi, gynnwys deunydd cyfrinachol ac wedi eu bwriadu i'w defnyddio'n unig gan y sawl y cawsant eu cyfeirio ato (atynt). Os ydych wedi derbyn y neges e-bost hon trwy gamgymeriad, rhowch wybod i'r anfonwr ar unwaith a dilwch y neges. Os na fwriadwyd anfon y neges atoch chi, rhaid i chi beidio defnyddio, cadw neu ddatgelu unrhyw wybodaeth a gynhwysir ynddi. Mae unrhyw farn neu safbwynt yn eiddo i'r sawl a'i hanfonodd yn unig ac nid yw o anghenraid yn cynrychioli barn Prifysgol Bangor. Nid yw Prifysgol Bangor yn gwarantu bod y neges e-bost hon neu unrhyw atodiadau yn rhydd rhag firysau neu 100% yn ddiogel. Oni bai fod hyn wedi ei ddatgan yn uniongyrchol yn nhestun yr e-bost, nid bwriad y neges e-bost hon yw ffurfio contract rhwymol - mae rhestr o lofnodwyr awdurdodedig ar gael o Swyddfa Cyllid Prifysgol Bangor. www.bangor.ac.uk This email and any attachments may contain confidential material and is solely for the use of the intended recipient(s). If you have received this email in error, please notify the sender immediately and delete this email. If you are not the intended recipient(s), you must not use, retain or disclose any information contained in this email. Any views or opinions are solely those of the sender and do not necessarily represent those of the Bangor University. Bangor University does not guarantee that this email or any attachments are free from viruses or 100% secure. Unless expressly stated in the body of the text of the email, this email is not intended to form a binding contract - a list of authorised signatories is available from the Bangor University Finance Office. www.bangor.ac.uk ========================================================================Date: Thu, 17 Feb 2011 15:19:16 +0000 Reply-To: Michael O'Sullivan <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Michael O'Sullivan <[log in to unmask]> Subject: Re: Creating an "average" structural image Comments: To: Nick Davis <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/alternative; boundary="=_alternative 0054298F8025783A_=" Message-ID: <[log in to unmask]> This is a multipart message in MIME format. --=_alternative 0054298F8025783A_Content-Type: text/plain; charset="ISO-8859-1" Content-Transfer-Encoding: quoted-printable Dear Nick Assuming they are all in the same space.... you should be able to just add them all up with ImCalc. You will probably need to smooth the final sum/average to make it look nicer. If the results are in MNI space an alternative is to use one of the canonical images. Mike From: Nick Davis <[log in to unmask]> To: [log in to unmask] Date: 17/02/2011 15:13 Subject: [SPM] Creating an "average" structural image Sent by: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> Hello SPM nerds. I would like to project my activation blobs onto some kind of average image of the brains of the subjects in my experiment. I can't see a way to create this average image in SPM8, so is there another method I could use? Thanks! Nick -- [log in to unmask] -- Gall y neges e-bost hon, ac unrhyw atodiadau a anfonwyd gyda hi, gynnwys deunydd cyfrinachol ac wedi eu bwriadu i'w defnyddio'n unig gan y sawl y cawsant eu cyfeirio ato (atynt). Os ydych wedi derbyn y neges e-bost hon trwy gamgymeriad, rhowch wybod i'r anfonwr ar unwaith a dilwch y neges. Os na fwriadwyd anfon y neges atoch chi, rhaid i chi beidio defnyddio, cadw neu ddatgelu unrhyw wybodaeth a gynhwysir ynddi. Mae unrhyw farn neu safbwynt yn eiddo i'r sawl a'i hanfonodd yn unig ac nid yw o anghenraid yn cynrychioli barn Prifysgol Bangor. Nid yw Prifysgol Bangor yn gwarantu bod y neges e-bost hon neu unrhyw atodiadau yn rhydd rhag firysau neu 100% yn ddiogel. Oni bai fod hyn wedi ei ddatgan yn uniongyrchol yn nhestun yr e-bost, nid bwriad y neges e-bost hon yw ffurfio contract rhwymol - mae rhestr o lofnodwyr awdurdodedig ar gael o Swyddfa Cyllid Prifysgol Bangor. www.bangor.ac.uk This email and any attachments may contain confidential material and is solely for the use of the intended recipient(s). If you have received this email in error, please notify the sender immediately and delete this email. If you are not the intended recipient(s), you must not use, retain or disclose any information contained in this email. Any views or opinions are solely those of the sender and do not necessarily represent those of the Bangor University. Bangor University does not guarantee that this email or any attachments are free from viruses or 100% secure. Unless expressly stated in the body of the text of the email, this email is not intended to form a binding contract - a list of authorised signatories is available from the Bangor University Finance Office. www.bangor.ac.uk --=_alternative 0054298F8025783A_Content-Type: text/html; charset="ISO-8859-1" Content-Transfer-Encoding: quoted-printable Dear Nick
Assuming they are all in the same space.... you should be able to just add them all up with ImCalc. You will probably need to smooth the final sum/average to make it look nicer. If the results are in MNI space an alternative is to use one of the canonical images.

Mike





From:        Nick Davis <[log in to unmask]>
To:        [log in to unmask]
Date:        17/02/2011 15:13
Subject:        [SPM] Creating an "average" structural image
Sent by:        "SPM (Statistical Parametric Mapping)" <[log in to unmask]>




Hello SPM nerds.

I would like to project my activation blobs onto some kind of average
image of the brains of the subjects in my experiment. I can't see a way
to create this average image in SPM8, so is there another method I could
use?

Thanks!
Nick



--
         [log in to unmask]

--
Gall y neges e-bost hon, ac unrhyw atodiadau a anfonwyd gyda hi,
gynnwys deunydd cyfrinachol ac wedi eu bwriadu i'w defnyddio'n unig
gan y sawl y cawsant eu cyfeirio ato (atynt). Os ydych wedi derbyn y
neges e-bost hon trwy gamgymeriad, rhowch wybod i'r anfonwr ar
unwaith a dilwch y neges. Os na fwriadwyd anfon y neges atoch chi,
rhaid i chi beidio defnyddio, cadw neu ddatgelu unrhyw wybodaeth a
gynhwysir ynddi. Mae unrhyw farn neu safbwynt yn eiddo i'r sawl a'i
hanfonodd yn unig  ac nid yw o anghenraid yn cynrychioli barn
Prifysgol Bangor. Nid yw Prifysgol Bangor yn gwarantu
bod y neges e-bost hon neu unrhyw atodiadau yn rhydd rhag firysau neu
100% yn ddiogel. Oni bai fod hyn wedi ei ddatgan yn uniongyrchol yn
nhestun yr e-bost, nid bwriad y neges e-bost hon yw ffurfio contract
rhwymol - mae rhestr o lofnodwyr awdurdodedig ar gael o Swyddfa
Cyllid Prifysgol Bangor.  
www.bangor.ac.uk

This email and any attachments may contain confidential material and
is solely for the use of the intended recipient(s).  If you have
received this email in error, please notify the sender immediately
and delete this email.  If you are not the intended recipient(s), you
must not use, retain or disclose any information contained in this
email.  Any views or opinions are solely those of the sender and do
not necessarily represent those of the Bangor University.
Bangor University does not guarantee that this email or
any attachments are free from viruses or 100% secure.  Unless
expressly stated in the body of the text of the email, this email is
not intended to form a binding contract - a list of authorised
signatories is available from the Bangor University Finance
Office.  
www.bangor.ac.uk

--=_alternative 0054298F8025783A_=-- ========================================================================Date: Thu, 17 Feb 2011 15:43:36 +0000 Reply-To: John Ashburner <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: John Ashburner <[log in to unmask]> Subject: Re: Creating an "average" structural image Comments: To: Nick Davis <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Message-ID: [log in to unmask]> Creating an average is just the same as fitting a GLM through the data, where the design matrix is simply a column of ones. Therefore, you could just use the stats options. Best regards, John On 17 February 2011 15:02, Nick Davis <[log in to unmask]> wrote: > Hello SPM nerds. > > I would like to project my activation blobs onto some kind of average image > of the brains of the subjects in my experiment. I can't see a way to create > this average image in SPM8, so is there another method I could use? > > Thanks! > Nick > > > > -- > [log in to unmask] > > -- > Gall y neges e-bost hon, ac unrhyw atodiadau a anfonwyd gyda hi, > gynnwys deunydd cyfrinachol ac wedi eu bwriadu i'w defnyddio'n unig > gan y sawl y cawsant eu cyfeirio ato (atynt). Os ydych wedi derbyn y > neges e-bost hon trwy gamgymeriad, rhowch wybod i'r anfonwr ar > unwaith a dilwch y neges. Os na fwriadwyd anfon y neges atoch chi, > rhaid i chi beidio defnyddio, cadw neu ddatgelu unrhyw wybodaeth a > gynhwysir ynddi. Mae unrhyw farn neu safbwynt yn eiddo i'r sawl a'i > hanfonodd yn unig ac nid yw o anghenraid yn cynrychioli barn > Prifysgol Bangor. Nid yw Prifysgol Bangor yn gwarantu > bod y neges e-bost hon neu unrhyw atodiadau yn rhydd rhag firysau neu > 100% yn ddiogel. Oni bai fod hyn wedi ei ddatgan yn uniongyrchol yn > nhestun yr e-bost, nid bwriad y neges e-bost hon yw ffurfio contract > rhwymol - mae rhestr o lofnodwyr awdurdodedig ar gael o Swyddfa > Cyllid Prifysgol Bangor. www.bangor.ac.uk > > This email and any attachments may contain confidential material and > is solely for the use of the intended recipient(s). If you have > received this email in error, please notify the sender immediately > and delete this email. If you are not the intended recipient(s), you > must not use, retain or disclose any information contained in this > email. Any views or opinions are solely those of the sender and do > not necessarily represent those of the Bangor University. > Bangor University does not guarantee that this email or > any attachments are free from viruses or 100% secure. Unless > expressly stated in the body of the text of the email, this email is > not intended to form a binding contract - a list of authorised > signatories is available from the Bangor University Finance > Office. www.bangor.ac.uk > ========================================================================Date: Thu, 17 Feb 2011 16:56:40 +0100 Reply-To: claus lamm <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: claus lamm <[log in to unmask]> Subject: Re: Creating an "average" structural image Comments: To: Nick Davis <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1; format=flowed Content-Transfer-Encoding: 7bit Message-ID: <[log in to unmask]> On 2/17/2011 4:02 PM, Nick Davis wrote: > Hello SPM nerds. > > I would like to project my activation blobs onto some kind of average > image of the brains of the subjects in my experiment. I can't see a > way to create this average image in SPM8, so is there another method I > could use? > > Thanks! > Nick > > > you could also use imcalc - mean(X) after loading all the individual normalized images as input ========================================================================Date: Thu, 17 Feb 2011 16:33:07 +0000 Reply-To: John Ashburner <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: John Ashburner <[log in to unmask]> Subject: Re: New Segmentation Out of Memory Error Comments: To: michel grothe <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> The best possible workaround would be the following. In principle, if you have scans from other subjects that have additional information (eg structure label images etc), then you can align these scans to the population average images, using Dartel. Once you have done this, the information can be warped so that it overlays on your individuals' scans via a procedure described towards the end of the "Using Dartel" chapter of the SPM8 manual. Alternatively, you could create a copy of the MNI-space image of labels, and tweak the matrix in its header, so that it is in alignment with the population average. This is untested, but I think you'd set the matrix to M3*inv(M2)*M1, where: M1 = voxel-to-world matrix of your MNI-space labels M2 = voxel-to-world matrix of the population average space Template_6 M3 = matrix in the Template_6_2mni.mat If this works, you should be able to use one of the options in the Dartel toolbox (or the Deformations Utility) to warp the data on to your original scans. Best regards, -John On 16 February 2011 19:45, michel grothe <[log in to unmask]> wrote: > Thanks, this would be great. > > Meanwhile, I have some questions regarding a possible work-around: > > Would it be OK to use an affine transform calculated with the > Normalise-Button to approximate the affine transform from 'DARTEL-Normalise > to MNI' in order to be able to generate the mentioned composition > 'native->DARTEL->MNI'. Does the affine alignment step in 'DARTEL-Normalise > to MNI' register the DARTEL-GM template to the GM-apriori map (or the GM map > in TPM.nii,1?) or does it also use the respective WM-maps? > How much does the affine alignment in 'DARTEL-Normalise to MNI' differ from > the one in 'Normalise', when registering DARTEL-GM to GM-apriori map (or > TPM.nii,1) and setting non-linear iterations to 0? > > Thanks again for your help. > Best regards, > Michel > >> Date: Wed, 16 Feb 2011 17:16:00 +0000 >> From: [log in to unmask] >> Subject: Re: [SPM] New Segmentation Out of Memory Error >> To: [log in to unmask] >> >> > I havent seen such a file in my version of SPM8 (the penultimate >> > update, >> > run on win32). Is it possible that this file is just generated during >> > estimation of the affine transform and not stored permanently on disk? >> > Or >> > does it come with the latest update? >> >> This change occurred in SPM8 r3727, so should be in the current >> updates, which are to r4010. >> >> >> > It would be very helpful to have such a file, mainly for the reasons >> > Richard >> > mentioned, i.e. use it to compose the complete transform >> > 'native->DARTEL-mean->MNI'. The inverse of such a composition could be >> > used >> > to warp Atlas-labels in MNI space to native space. >> >> There's no easy way to use the file yet, but I'll try to code >> something up for a future version of SPM8. >> >> Best regards, >> -John >> >> >> >> Date: Wed, 16 Feb 2011 15:58:16 +0000 >> >> From: [log in to unmask] >> >> Subject: Re: [SPM] New Segmentation Out of Memory Error >> >> To: [log in to unmask] >> >> >> >> This file does indeed contain an affine transform, and is generated >> >> when the affine registration between population average and MNI space >> >> is estimated. >> >> >> >> There's no script to do what you're after yet, but if the demand is >> >> high enough I could introduce the option. Can I ask how you plan to >> >> use the transforms? >> >> >> >> Best regards, >> >> -John >> >> >> >> >> >> On 16 February 2011 15:44, Richard Binney >> >> <[log in to unmask]> >> >> wrote: >> >> > ......I've just spotted that running normalise-to-mni now spits out a >> >> > 'Template_6_2mni.mat' file. I don't recall seeing this before -would >> >> > this >> >> > happen to be the affine transform I spoke of? >> >> > >> >> > R >> >> > >> >> > On Wed, Feb 16, 2011 at 3:39 PM, Richard Binney >> >> > <[log in to unmask]> wrote: >> >> >> >> >> >> Ah, yes. I couldn't find the email you were refferring to,butI've >> >> >> done >> >> >> it and it makes a huge difference. Pretty obvious really. >> >> >> >> >> >> One more thing, John (or anybody else for that matter)- is there >> >> >> now a >> >> >> way in which one can easilycreate an inverseof theDARTEL >> >> >> normalise-to-MNI >> >> >> deformation composition (so from MNI --> study average --> >> >> >> individual >> >> >> subject space)? Is it possible (i.e., is there script)to have this >> >> >> (forward >> >> >> and/or backwards)written out for each subject or, alternatively, to >> >> >> have >> >> >> the affine template-to-TPMtransform outputtedsuch that one can >> >> >> combine it >> >> >> witha flow field, and subsequently inversethe composition using >> >> >> the >> >> >> deformations tool? >> >> >> >> >> >> All the best, >> >> >> >> >> >> Richard >> >> >> >> >> >> On Tue, Feb 15, 2011 at 5:42 PM, John Ashburner >> >> >> <[log in to unmask]> >> >> >> wrote: >> >> >>> >> >> >>> You may wish to change the voxel sizes and bounding box in order to >> >> >>> obtain slightly lower resolution versions (other than the default >> >> >>> 1.5mm isotropic with a large bounding box). See the email I sent >> >> >>> out >> >> >>> recently. >> >> >>> >> >> >>> Best regards, >> >> >>> -John >> >> >>> >> >> >>> On 15 February 2011 17:29, Richard Binney >> >> >>> <[log in to unmask]> >> >> >>> wrote: >> >> >>> > Dear John (and other knowledgeable types), >> >> >>> > >> >> >>> > I used the deformation file (e.g., Y_p1_T1.nii) from Seg8 to >> >> >>> > normalise >> >> >>> > a >> >> >>> > functional MRI timeseries. That worked fine - the anatomical >> >> >>> > imagesthat >> >> >>> > Iadditionally warped in thisway look great - but I now cannot >> >> >>> > do >> >> >>> > anything >> >> >>> > with the timeseries. >> >> >>> > >> >> >>> > It is now almost 4Gb in size. I appreciate that using DARTEL to >> >> >>> > warp >> >> >>> > fMRI >> >> >>> > data can result in massive files which are problematic (and thus >> >> >>> > a >> >> >>> > work >> >> >>> > around is to apply the warp to contrast images), but I didn't >> >> >>> > expect >> >> >>> > the >> >> >>> > segment deformation field to do the same. >> >> >>> > >> >> >>> > Does this sound about right for a timeseries with 465 volumes >> >> >>> > (voxel >> >> >>> > dim 2.5 >> >> >>> > x 2.5 x 3; matrix 96x96; numslices = 42)? Or have I made a >> >> >>> > mistake >> >> >>> > somewhere? >> >> >>> > >> >> >>> > so I'm supposing my inability to use the warped timeseries is a >> >> >>> > memory >> >> >>> > issue- I am running a 64-bit machine with 8Gb memory (I can see >> >> >>> > all >> >> >>> > this >> >> >>> > being used in the task manager so doesn't seem to be a matlab >> >> >>> > version >> >> >>> > problem) but maybe this file is just way too big for the SPM >> >> >>> > platform.....???? I could crop the image, etc I suppose but maybe >> >> >>> > the >> >> >>> > biggest problem is the shear number of volumes. >> >> >>> > >> >> >>> > Thanks in advance for your thoughts >> >> >>> > >> >> >>> > Richard >> >> >>> > >> >> >>> > On Thu, Feb 10, 2011 at 4:05 PM, William Pettersson-Yeo >> >> >>> > <[log in to unmask]> wrote: >> >> >>> >> >> >> >>> >> Thanks John. >> >> >>> >> >> >> >>> >> It turns out the problem was due to the version of Matlab I was >> >> >>> >> running. >> >> >>> >> >> >> >>> >> Matlab2007 was only running 32bit, whilst the 2010 version is >> >> >>> >> 64. >> >> >>> >> >> >> >>> >> Having set up with Matlab2010, the new segmentation with DARTEL >> >> >>> >> import >> >> >>> >> now >> >> >>> >> runs without any problem, without me having to alter/crop any of >> >> >>> >> the >> >> >>> >> images. >> >> >>> >> >> >> >>> >> All the best >> >> >>> >> William >> >> >>> > >> >> >>> > >> >> >> >> >> > >> >> > >> > > ========================================================================Date: Thu, 17 Feb 2011 17:55:36 +0100 Reply-To: Christian Doeller <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Christian Doeller <[log in to unmask]> Subject: PhD Student and Postdoctoral Researcher Positions in Neuroimaging, Donders Institute, Nijmegen MIME-Version: 1.0 Content-Type: multipart/alternative; boundaryMessage-ID: <[log in to unmask]> --001485f92356386899049c7d4470 Content-Type: text/plain; charset=windows-1252 Content-Transfer-Encoding: quoted-printable PhD Student and Postdoctoral Researcher Positions in Neuroimaging (1,0 fte) *Donders Institute, Centre for Cognitive Neuroimaging* *Vacancy number: 30.03.11* *Closing date: 15 March 2011* *Job description* The newly established PI group of Dr Christian Doeller at the Donders Institute for Brain, Cognition and Behaviour seeks highly talented and dedicated postdoctoral researchers and PhD students to work on an exciting project funded by a recently awarded ERC Starting Grant. The goal of this project is to gain understanding of how the human brain maps space and forms episodic memories. Our specific aim is to infer the fine-scale properties of neural systems in humans by building on models from single-cell electrophysiology (see Doeller et al., Evidence for Grid Cells in a Human Memory Network, Nature 2010, 463, 657-661). The techniques involve combinations of functional magnetic resonance imaging (fMRI, including 7T high-field scanning), virtual reality technologies, psychophysics and advanced tools for neuroimaging data analysis. *Requirements* As a candidate you should have a Masters degree or equivalent (for the PhD student positions) or a PhD degree (for the postdoctoral positions) in a field related to cognitive neuroscience, e.g. experimental psychology, cognitive science, biology, neuroscience or related disciplines. Excellent candidates with a background in quantitative disciplines such as mathematics, physics or engineering who are interested in neuroscience are also encouraged to apply. Selection criteria for the postdoctoral positions will consider the record of published research, familiarity with neuroimaging techniques and programming skills (Matlab). For the PhD student positions, familiarity with neuroimaging techniques and good programming skills (Matlab) are desirable. Proficiency in oral and written English is required. You are expected to work in an interdisciplinary environment, sharing technical know-how and ideas. *Organization* The Donders Institute for Brain, Cognition and Behaviour consists of the Centre for Cognition, the Centre for Cognitive Neuroimaging, and the Centre for Neuroscience. The mission of the Centre for Cognitive Neuroimaging is to conduct cutting-edge fundamental research in cognitive neuroscience. Much of the rapid progress in this field is being driven by the development of complex neuroimaging techniques for measuring activity in the human working brain - an area in which the Centre plays a leading role. The research themes cover central cognitive functions, such as perception, action, control, decision making, attention, memory, language, learning and plasticity. The Centre also aims to establish how the different brain areas coordinate their activity with very high temporal precision to enable human and animal cognition. The internationally renowned centre currently hosts more than 100 PhD students and postdoctoral researchers from more than 20 nationalities, offering a stimulating and multidisciplinary research environment. The centre is equipped with three MRI scanners (7T, 3T, 1.5T), a 275-channel MEG system, an EEG-TMS laboratory, several (MR-compatible) EEG systems, and high-performance computational facilities. English is the lingua franca at the centre. Website: http://www.ru.nl/donders *Conditions of employment* Employment: 1,0 fte PhD student: The starting salary is 2,042 per month and will increase to 2,612 per month in the fourth year. Postdoctoral researcher: Depending on experience, the gross salary will be between 3,195 and 4,374. *Additional conditions of employment* Duration of the PhD-student contracts: 4 years. Duration of the postdoctoral contracts: 3 years (extension possible). In addition to the gross monthly salary, you will receive two yearly 8% bonuses (holiday and end-of-year). *Other Information* You should submit your application in a single PDF file, including an application letter, a statement of research interests, your CV, and the names of two persons who can provide references. *Additional Information* Dr Christian Doeller, Principal Investigator Telephone: +31 24 3610983 E-mail: [log in to unmask] *Application* You can apply for the job (mention the vacancy number 30.03.11) *before 15 March 2011* by sending your application -preferably by email- to: Radboud University Nijmegen, P&O department PO Box 7005, 6503 GM NIJMEGEN, NL Telephone: +31 24 3611173 E-mail: [log in to unmask] --001485f92356386899049c7d4470 Content-Type: text/html; charset=windows-1252 Content-Transfer-Encoding: quoted-printable

PhD Student and Postdoctoral Researcher Positions in Neuroimaging (1,0 fte)


Donders Institute, Centre for Cognitive Neuroimaging
Vacancy number: 30.03.11
Closing date: 15 March 2011

Job description
The newly established PI group of Dr Christian Doeller at the Donders Institute for Brain, Cognition and Behaviour seeks highly talented and dedicated postdoctoral researchers and PhD students to work on an exciting project funded by a recently awarded ERC Starting Grant.

The goal of this project is to gain understanding of how the human brain maps space and forms episodic memories. Our specific aim is to infer the fine-scale properties of neural systems in humans by building on models from single-cell electrophysiology (see Doeller et al., Evidence for Grid Cells in a Human Memory Network, Nature 2010, 463, 657-661).

The techniques involve combinations of functional magnetic resonance imaging (fMRI, including 7T high-field scanning), virtual reality technologies, psychophysics and advanced tools for neuroimaging data analysis.

Requirements
As a candidate you should have a Masters degree or equivalent (for the PhD student positions) or a PhD degree (for the postdoctoral positions) in a field related to cognitive neuroscience, e.g. experimental psychology, cognitive science, biology, neuroscience or related disciplines. Excellent candidates with a background in quantitative disciplines such as mathematics, physics or engineering who are interested in neuroscience are also encouraged to apply.

Selection criteria for the postdoctoral positions will consider the record of published research, familiarity with neuroimaging techniques and programming skills (Matlab). For the PhD student positions, familiarity with neuroimaging techniques and good programming skills (Matlab) are desirable.

Proficiency in oral and written English is required. You are expected to work in an interdisciplinary environment, sharing technical know-how and ideas.

Organization
The Donders Institute for Brain, Cognition and Behaviour consists of the Centre for Cognition, the Centre for Cognitive Neuroimaging, and the Centre for Neuroscience.

The mission of the Centre for Cognitive Neuroimaging is to conduct cutting-edge fundamental research in cognitive neuroscience. Much of the rapid progress in this field is being driven by the development of complex neuroimaging techniques for measuring activity in the human working brain - an area in which the Centre plays a leading role. The research themes cover central cognitive functions, such as perception, action, control, decision making, attention, memory, language, learning and plasticity. The Centre also aims to establish how the different brain areas coordinate their activity with very high temporal precision to enable human and animal cognition. The internationally renowned centre currently hosts more than 100 PhD students and postdoctoral researchers from more than 20 nationalities, offering a stimulating and multidisciplinary research environment. The centre is equipped with three MRI scanners (7T, 3T, 1.5T), a 275-channel MEG system, an EEG-TMS laboratory, several (MR-compatible) EEG systems, and high-performance computational facilities. English is the lingua franca at the centre.
Website:http://www.ru.nl/donders

Conditions of employment
Employment: 1,0 fte
PhD student: The starting salary is 2,042 per month and will increase to 2,612 per month in the fourth year.
Postdoctoral researcher: Depending on experience, the gross salary will be between 3,195 and 4,374.

Additional conditions of employment
Duration of the PhD-student contracts: 4 years.
Duration of the postdoctoral contracts: 3 years (extension possible).

In addition to the gross monthly salary, you will receive two yearly 8% bonuses (holiday and end-of-year).

Other Information
You should submit your application in a single PDF file, including an application letter, a statement of research interests, your CV, and the names of two persons who can provide references.

Additional Information
Dr Christian Doeller, Principal Investigator
Telephone: +31 24 3610983
E-mail:[log in to unmask]

Application
You can apply for the job (mention the vacancy number 30.03.11)before 15 March 2011by sending your application -preferably by email- to:

Radboud University Nijmegen, P&O department
PO Box 7005, 6503 GM NIJMEGEN, NL
Telephone: +31 24 3611173
E-mail:[log in to unmask]

--001485f92356386899049c7d4470-- ========================================================================Date: Thu, 17 Feb 2011 16:49:21 +0000 Reply-To: Vy Dinh <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Vy Dinh <[log in to unmask]> Subject: Re: VOI Batch Module Comments: To: James Bursley <[log in to unmask]> In-Reply-To: <[log in to unmask]> Content-Type: text/plain; charset="us-ascii" Content-Transfer-Encoding: quoted-printable MIME-Version: 1.0 Message-ID: <[log in to unmask]> Hi James, I think that this issue may have been discussed on the forums before. When you specify the adjust step, you set this field to the index for your F-contrast, which means that the F-contrast needed to be specified at the first level model or that your index was wrong. Since you mentioned that there were not any errors when you did this via the GUI, the latter may be the issue. Hope that helps. Vy T.U. Dinh Research Assistant, Neurological Sciences Rush University Medical Center Phone: (312) 563-3853 Fax: (312) 563-4660 Email: [log in to unmask] ________________________________________ From: SPM (Statistical Parametric Mapping) [[log in to unmask]] on behalf of James Bursley [[log in to unmask]] Sent: Wednesday, February 16, 2011 8:21 PM To: [log in to unmask] Subject: Re: [SPM] VOI Batch Module Two other pieces of information regarding this problem: 1. No errors come up when I extract a VOI using the GUI; I only encounter this error when using the batch script. 2. The error only appears when "Adjust data" is set to something other than '0', i.e., when data IS being adjusted. Otherwise, the batch runs fine. ========================================================================Date: Thu, 17 Feb 2011 11:28:46 -0800 Reply-To: Siddharth Srivastava <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Siddharth Srivastava <[log in to unmask]> Subject: help with spm_snbasis code MIME-Version: 1.0 Content-Type: multipart/alternative; boundaryaec53f944ffb757a049c7f67ac Message-ID: <[log in to unmask]> --bcaec53f944ffb757a049c7f67ac Content-Type: text/plain; charset=ISO-8859-1 Hi everyone, I have been reading source for spm_snbasis and spm_brainwarp to get a better understanding of the underlying math, and I came across these lines in spm_snbasis (spm99 source, line no 82-85): s1 = 3*prod(k); s2 = s1 + prod(size(VG))*4; T = zeros(s2,1); T(s1+(1:4:prod(size(VG))*4)) = 1; I wanted to know why T is initialized the way it is by the last line of the source snippet? Also, what does the multiplication by 4 imply? thanks, sid. --bcaec53f944ffb757a049c7f67ac Content-Type: text/html; charset=ISO-8859-1 Hi everyone,

I have been reading source for spm_snbasis and spm_brainwarp to get a better understanding of the
underlying math, and I came across these lines in spm_snbasis (spm99 source, line no 82-85):

s1 = 3*prod(k);
s2 = s1 + prod(size(VG))*4;
T = zeros(s2,1);
T(s1+(1:4:prod(size(VG))*4)) = 1;

I wanted to know why T is initialized the way it is by the last line of the source snippet? Also, what does
the multiplication by 4 imply?

thanks,
sid.


--bcaec53f944ffb757a049c7f67ac-- ========================================================================Date: Thu, 17 Feb 2011 20:08:30 +0000 Reply-To: John Ashburner <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: John Ashburner <[log in to unmask]> Subject: Re: help with spm_snbasis code Comments: To: Siddharth Srivastava <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Message-ID: <[log in to unmask]> There are additional parameters that model linear intensity gradients in the x, y and z directions. The parameters would essentially be coefficients for a linear combination if template1 template1.*x template1.*y template1.*z template2 template2.*x template2.*y template2.*z ... Best regards, -John On 17 February 2011 19:28, Siddharth Srivastava <[log in to unmask]> wrote: > Hi everyone, > > I have been reading source for spm_snbasis and spm_brainwarp to get a better > understanding of the > underlying math, and I came across these lines in spm_snbasis (spm99 source, > line no 82-85): > > s1 = 3*prod(k); > s2 = s1 + prod(size(VG))*4; > T = zeros(s2,1); > T(s1+(1:4:prod(size(VG))*4)) = 1; > > I wanted to know why T is initialized the way it is by the last line of the > source snippet? Also, what does > the multiplication by 4 imply? > > thanks, > sid. > > > ========================================================================Date: Thu, 17 Feb 2011 15:38:34 -0500 Reply-To: [log in to unmask] Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Jake Thompson <[log in to unmask]> Subject: How to display mutltiple spm results for one subject with multiple t-contrasts with batch editor? In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/alternative; boundary="--------MB_8CD9CF9C7F2EC49_D14_23BBC_webmail-d011.sysops.aol.com" Message-ID: <[log in to unmask]> This is a multi-part message in MIME format. ----------MB_8CD9CF9C7F2EC49_D14_23BBC_webmail-d011.sysops.aol.com Content-Transfer-Encoding: quoted-printable Content-Type: text/plain; charset="us-ascii" How to display mutltiple spm results for one subject with multiple t-contrasts with batch editor? I am only able to display the results from the last T-contrasts, but I want to display the results for all the t-contrasts I pu tinto the batch editor. ----------MB_8CD9CF9C7F2EC49_D14_23BBC_webmail-d011.sysops.aol.com Content-Transfer-Encoding: quoted-printable Content-Type: text/html; charset="us-ascii"
How to display mutltiple spm results for one subject with multiple t-contrasts with batch editor? I am only able to display the results from the last T-contrasts, but I want to display the results for all the t-contrasts I pu tinto the batch editor.
----------MB_8CD9CF9C7F2EC49_D14_23BBC_webmail-d011.sysops.aol.com-- ========================================================================Date: Fri, 18 Feb 2011 00:10:35 +0100 Reply-To: Saemann Philipp <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Saemann Philipp <[log in to unmask]> Subject: sensitivity of DARTEL Mime-Version: 1.0 Content-Type: text/plain; charset="us-ascii" Message-ID: <[log in to unmask]> Dear SPMers, in a recent paper by Pereira et al. on Resgistration accuracy for VBM studies, NeuroImage 2010;49:2205-15 DARTEL as implemented in SPM5 is presented as very insensitive to focal GM changes - in their work, they used a small Alzheimer Disease sample to to (amongmany other analyses) check the sensitivity to detect hippocampal atrophy. However, sensitivity and regional specificity were completely regained when three preprocessing steps were performed: 1. skull stripping, 2. bias correction, and 3., "fine tuned BET". > Has anybody made similar observations on insensitivity of DARTEL? > Is the SPM Bias correction (default parameters) really so non-optimal? > Is it the order of steps (first skull stripping, then bias correction) the crucial difference? > Is DARTEL in SPM8 in combination with the "New Segment" function more sensitive? I think for VBM where DARTEL has (my perception) repeatedly been recommended as excellent/best registration tool, it would be very useful if also the preprocessing/optimizations can be performed within SPM. - It is somewhat strange that extra preprocessing steps seem necessary outside SPM. I am very interested in comments/opinions here, thanks, Philipp Max Planck Institute of Psychiatry NMR Research Group Kraepelinstr. 2-10 80804 Munich Mail: [log in to unmask] Phone: 0049-89-30622-413 ========================================================================Date: Thu, 17 Feb 2011 18:53:01 -0500 Reply-To: Lisa Pan <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Lisa Pan <[log in to unmask]> Subject: SVC correction MIME-Version: 1.0 Content-Type: multipart/alternative; boundaryMessage-ID: <[log in to unmask]> --001485f1dbbc0e0ec4049c831997 Content-Type: text/plain; charset=ISO-8859-1 Does anyone know what exactly the SVC option in SPM5 is doing? You can select and area to SVC correct and then you can also choose FWE or FDR, but you do not have to. If you just do SVC, what is it calculating? Thank you for any information. Lisa -- Become a Friend! http://FriendsofPineRidgeReservation.org --001485f1dbbc0e0ec4049c831997 Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable
Does anyone know what exactly the SVC option in SPM5 is doing? You can select and area to SVC correct and then you can also choose FWE or FDR, but you do not have to. If you just do SVC, what is it calculating?
Thank you for any information.
--001485f1dbbc0e0ec4049c831997-- ========================================================================Date: Fri, 18 Feb 2011 00:09:00 +0000 Reply-To: Anup Bidesi <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Anup Bidesi <[log in to unmask]> Subject: VBM results question Content-Type: multipart/mixed; boundary="_008_006C97B7E36B0340BBD2B31E976738F306CF72B7swmsmail2swmedo_" MIME-Version: 1.0 Message-ID: <[log in to unmask]> --_008_006C97B7E36B0340BBD2B31E976738F306CF72B7swmsmail2swmedo_ Content-Type: multipart/alternative; boundary="_000_006C97B7E36B0340BBD2B31E976738F306CF72B7swmsmail2swmedo_" --_000_006C97B7E36B0340BBD2B31E976738F306CF72B7swmsmail2swmedo_ Content-Type: text/plain; charset="iso-8859-1" Content-Transfer-Encoding: quoted-printable Hello SPM'ers, I have question about VBM data results (from 10, Normals and 19, Schizophrenic subjects) upon segmenting them using VBM8 w/Dartel normalization and looking at the stats using non-parametric SnPM toolbox. For the GM/WM Segmentaion: I've used VBM8's Estimate & Write option and set all other parameters to defaults in extended options (with modulated normalized "non-linear only" selected) and later smoothed the data using a 12 mm kernel using SPM8, to obtain the the processed data as sm0wrp1/p2/p3 associated with GM/WM/CSF segmentation, To compare both groups: design/set-up, estimation/compute and Results were done using SnPM. I've downloaded SnPM for SPM8 (see Readme.txt file attached from snpm folder), however while loading up SnPM in SPM8 it is stated as version SnPM5. In the SnPM Set-up following parameters were used: 2 Groups: Two Sample T test; 1scan/subject, Subject index specified as: AAA...(for Normals)...BBB...(for SZ subjs.) ; Selected Yes, for # Perms. Use approx. test? and Specified no. of Permutions as 1000 to begin with to 10,000; Variance smoothing of 10 mm, specified Yes, for Collect supra-Threshold stats?; with "No" for Define the thresh now? , No global normalisation and grand mean scaling; specified Absolute Threshold masking of 0.15. For Analysis mask specified:Smooth modulated sample subject scan (sm0wrp1....img) with 1000 & 10,000 permutations and also tried canonical "avg_152T1_GM.hdr/.img" with 5000 permutations as Gray matter masks. Upon looking up for GM differences between 2 groups with these SnPM settings, estimate and looking up results specifying "+ve" for effects (since looking for NC>SZ) Selecting to "Write filtered statistic img"; specifying P for "Results for which img? T/P" and then specifying FDR-corrected p value threshold of 0.05 and saved the outputs attached. There GM differences between both groups did not survive corrected threshold at 0.05 threshold, but showed meaningful differences using 10,000 permutations with smoothed modulated subject GM segmented scan as analysis mask and for 5000 permutations with avg_152T1_GM .img as GM mask. Upon looking the filtered_statistic image from both the tests using xjview, the clusters seem to contain considerable WM voxels (upto 40-50%) while looking for GM differences between groups ? why do they appear and how can these WM voxels be cleaned out from the results ? Thanks for all your help! Anup Research Associate Dept. of Psychiatry, UT Southwestern Medical Center ________________________________ UT Southwestern Medical Center The future of medicine, today. --_000_006C97B7E36B0340BBD2B31E976738F306CF72B7swmsmail2swmedo_ Content-Type: text/html; charset="iso-8859-1" Content-Transfer-Encoding: quoted-printable
Hello SPM'ers,

I have question about VBM data results (from 10, Normals and 19, Schizophrenic subjects) upon segmenting them using VBM8 w/Dartel normalization and looking at the stats using non-parametric SnPM toolbox.

For the GM/WM Segmentaion: I've used VBM8's Estimate & Write option
and set all other parameters to defaults in extended options (with modulated normalized "non-linear only" selected) and later smoothed the data using a 12 mm kernel using SPM8, to obtain the the processed data as sm0wrp1/p2/p3 associated with GM/WM/CSF segmentation,  To compare both groups: design/set-up, estimation/compute and Results were done using SnPM. I've downloaded SnPM for SPM8 (see Readme.txt file attached from snpm folder), however while loading up SnPM in SPM8 it is stated as version SnPM5.

In the SnPM Set-up following parameters were used: 2 Groups: Two Sample T test; 1scan/subject, Subject index specified as: AAA...(for Normals)...BBB...(for SZ subjs.) ;

Selected Yes, for # Perms. Use approx. test? and Specified no. of Permutions as 1000 to begin with to 10,000;
Variance smoothing of 10 mm,  specified Yes, for Collect supra-Threshold stats?; with "No" for Define the thresh now? ,
No global normalisation and grand mean scaling; specified Absolute Threshold masking of 0.15.
For Analysis mask
specified:Smooth modulated sample subject scan (sm0wrp1....img) with 1000 & 10,000 permutations and also tried canonical "avg_152T1_GM.hdr/.img" with 5000 permutations as Gray matter masks.

Upon looking up for GM differences between 2 groups with these SnPM settings, estimate and looking up results
specifying "+ve" for effects (since looking for NC>SZ)

Selecting to "Write filtered statistic img"; specifying P for "Results for which img? T/P"
and then specifying FDR-corrected p value threshold of 0.05 and saved the outputs attached.
There GM differences between both groups did not survive corrected threshold at 0.05 threshold, but showed meaningful differences using 10,000 permutations with smoothed modulated subject GM segmented scan as analysis mask and for 5000 permutations with avg_152T1_GM .img as GM mask.

Upon looking the filtered_statistic image from both the tests using xjview, the clusters seem to contain considerable WM voxels (upto 40-50%) while looking for GM differences between groups ? why do they appear and how can these WM voxels be cleaned out from the results ?

Thanks for all your help!

Anup

Research Associate
Dept. of Psychiatry,
UT Southwestern Medical Center




UT Southwestern Medical Center
The future of medicine, today.
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ICBUaG9tYXMgTmljaG9scywgRGVwYXJ0bWVudCBvZiBTdGF0aXN0aWNzICYgV2Fyd2ljayBNYW51 ZmFjdHVyaW5nCiAgIEdyb3VwLCBVbml2ZXJpc3R5IG9mIFdhcndpY2sKCiUgJElkICQKCgoKCgoK Cgo --_008_006C97B7E36B0340BBD2B31E976738F306CF72B7swmsmail2swmedo_-- ========================================================================Date: Fri, 18 Feb 2011 00:10:48 +0000 Reply-To: John Ashburner <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: John Ashburner <[log in to unmask]> Subject: Re: sensitivity of DARTEL Comments: To: Saemann Philipp <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Message-ID: <[log in to unmask]> > in a recent paper by Pereira et al. on Resgistration accuracy for VBM > studies, NeuroImage 2010;49:2205-15 DARTEL as implemented > in SPM5 is presented as very insensitive to focal GM changes - in their > work, they used a small Alzheimer Disease sample to > to (amongmany other analyses) check the sensitivity to detect hippocampal > atrophy. > > However, sensitivity and regional specificity were completely regained when > three preprocessing steps were performed: > 1. skull stripping, 2. bias correction, and 3., "fine tuned BET". The limited set of tissue probability maps mean that SPM5 segmentation doesn't handle separating bone from CSF very well for some data, so skull stripping could be of some benefit. This is usually of less importance for SPM8 though, although there are still occasional scans that cause problems if there are strange artifacts in the background (from strange preprocessing done to the data) or if the subject is very heavily built (with lots of tissue outside the skull). The optimal amount of bias correction will depend on the data used. If the scans contain a lot of artifact, then lots of bias correction is needed. If there is no bias artifact, then the best results should result when no bias correction is done. If the data are heavily corrupted, the default amount of correction may not be great enough. In these cases, it is relatively easy to decrease the amount of regularisation used within the segmentation algorithm, rather than bias correcting the data first. > >> Has anybody made similar observations on insensitivity of DARTEL? >> Is the SPM Bias correction (default parameters) really so non-optimal? >> Is it the order of steps (first skull stripping, then bias correction) > the crucial difference? >> Is DARTEL in SPM8 in combination with the "New Segment" function more > sensitive? I'd be slightly curious about feedback too, although I no longer care that much about the accuracy of results from SPM5, as it is now six years out of date. > > I think for VBM where DARTEL has (my perception) repeatedly been > recommended as excellent/best registration tool, > it would be very useful if also the preprocessing/optimizations can be > performed within SPM. - It is somewhat > strange that extra preprocessing steps seem necessary outside SPM. All I can say is that the evaluations done for the paper by Klein et al show that Dartel and a number of other approaches achieved better alignment (as judged via manual segmentations) than the other spatial normalisation procedures available within SPM. More accurate alignment should translate into more accurate interpetation of results in terms of localising volumetric differences. This may not necessarily translate into smaller p values, as systematic mis-registration could potentially cause significant differences to occur. Best regards, -John ========================================================================Date: Thu, 17 Feb 2011 17:05:35 -0800 Reply-To: Siddharth Srivastava <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Siddharth Srivastava <[log in to unmask]> Subject: Re: help with spm_snbasis code Comments: To: John Ashburner <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/alternative; boundaryaec53f944f8ec7fa049c841ce9 Message-ID: [log in to unmask]> --bcaec53f944f8ec7fa049c841ce9 Content-Type: text/plain; charset=ISO-8859-1 Hi John, Thanks for the reply. regarding my other question, what does the multiplication by 4 do? I am guessing that a constant term will also be modeled (3 + 1 paramater sets for this, constant term = 1), can you please verify if I am thinking correctly about this initialization strategy? thanks again, sid. On Thu, Feb 17, 2011 at 12:08 PM, John Ashburner <[log in to unmask]>wrote: > There are additional parameters that model linear intensity gradients > in the x, y and z directions. The parameters would essentially be > coefficients for a linear combination if > > template1 template1.*x template1.*y template1.*z template2 > template2.*x template2.*y template2.*z ... > > Best regards, > -John > > On 17 February 2011 19:28, Siddharth Srivastava <[log in to unmask]> wrote: > > Hi everyone, > > > > I have been reading source for spm_snbasis and spm_brainwarp to get a > better > > understanding of the > > underlying math, and I came across these lines in spm_snbasis (spm99 > source, > > line no 82-85): > > > > s1 = 3*prod(k); > > s2 = s1 + prod(size(VG))*4; > > T = zeros(s2,1); > > T(s1+(1:4:prod(size(VG))*4)) = 1; > > > > I wanted to know why T is initialized the way it is by the last line of > the > > source snippet? Also, what does > > the multiplication by 4 imply? > > > > thanks, > > sid. > > > > > > > --bcaec53f944f8ec7fa049c841ce9 Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Hi John,
Thanks for the reply. regarding my other question, what does the
multiplication by 4 do? I am guessing that a constant term will also
be modeled (3 + 1 paramater sets for this, constant term = 1), can you
please verify if I am thinking correctly about this initialization strategy?
thanks again,
sid.

On Thu, Feb 17, 2011 at 12:08 PM, John Ashburner <[log in to unmask]> wrote:
There are additional parameters that model linear intensity gradients
in the x, y and z directions. The parameters would essentially be
coefficients for a linear combination if

template1 template1.*x template1.*y template1.*z template2
template2.*x template2.*y template2.*z ...

Best regards,
-John

On 17 February 2011 19:28, Siddharth Srivastava <[log in to unmask]> wrote:
> Hi everyone,
>
> I have been reading source for spm_snbasis and spm_brainwarp to get a better
> understanding of the
> underlying math, and I came across these lines in spm_snbasis (spm99 source,
> line no 82-85):
>
> s1 = 3*prod(k);
> s2 = s1 + prod(size(VG))*4;
> T = zeros(s2,1);
> T(s1+(1:4:prod(size(VG))*4)) = 1;
>
> I wanted to know why T is initialized the way it is by the last line of the
> source snippet? Also, what does
> the multiplication by 4 imply?
>
> thanks,
> sid.
>
>
>

--bcaec53f944f8ec7fa049c841ce9-- ========================================================================Date: Fri, 18 Feb 2011 02:45:09 +0100 Reply-To: michel grothe <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: michel grothe <[log in to unmask]> Subject: Re: sensitivity of DARTEL Comments: To: [log in to unmask] In-Reply-To: <[log in to unmask]> Content-Type: multipart/alternative; boundary="_0d0961c3-b624-4bbe-adc0-9979ff4c2b23_" MIME-Version: 1.0 Message-ID: <[log in to unmask]> --_0d0961c3-b624-4bbe-adc0-9979ff4c2b23_ Content-Type: text/plain; charset="iso-8859-1" Content-Transfer-Encoding: quoted-printable Dear Philipp and others, with my own data, or more exactly with the OASIS database (not skull-stripped), Ive made similar observations, i.e. SPM8-new-segmentation (or "normal" SPM5-unified-segmentation)+DARTEL VBM failed to detect significant hippocampus atrophy for most parts of the hippocampus in AD and MCI. While the effects seemed to be consistent with the literature for most parts of the cortex (atrophy in PCC, ACC, temporoparietal areas and relative sparing of somoatosensory areas and the cerebellum in AD), effects in the MTL were restricted to the amygdala and anterior parts of the hippocampus. However, VBM procedures rely on a mixture of accurate segmentation AND normalisation to a common space and I think the error here may rather lie in inaccurate segmentaion than in the DARTEL normalisation. Repeating the analysis with "Gaser"-segmented images (VBM8) and exactly the same DARTEL-settings revealed "perfect" (i.e. expected or more consistent with the literature) results for the MTL and the rest of the cortex. A possible explanation for this observation is that registration accuracy (using tissue-priors based on a normal population) and hence segmentation accuracy of the unified approaches in spm5/8 decreases with increasing atrophy. Although the detailed tissue information in "New-segment" normally leads to convincingly improved segmentation results and the high-dimensional warping in DARTEL is capable to model large deformations, it might still be necessary to adjust the tissue priors when dealing with groups that differ strongly from the anatomy of the normal population. The tissue prior-free approach of the VBM8-toolbox produced much more "realistic" results when comparing a large cohort of healthy elderly and AD patients (the OASIS database). Would be interesting to hear about the experiences of the rest of the SPM/VBM-community. Best regards, Michel > Date: Fri, 18 Feb 2011 00:10:35 +0100 > From: [log in to unmask] > Subject: [SPM] sensitivity of DARTEL > To: [log in to unmask] > > Dear SPMers, > > in a recent paper by Pereira et al. on Resgistration accuracy for VBM > studies, NeuroImage 2010;49:2205-15 DARTEL as implemented > in SPM5 is presented as very insensitive to focal GM changes - in their > work, they used a small Alzheimer Disease sample to > to (amongmany other analyses) check the sensitivity to detect hippocampal > atrophy. > > However, sensitivity and regional specificity were completely regained when > three preprocessing steps were performed: > 1. skull stripping, 2. bias correction, and 3., "fine tuned BET". > > > Has anybody made similar observations on insensitivity of DARTEL? > > Is the SPM Bias correction (default parameters) really so non-optimal? > > Is it the order of steps (first skull stripping, then bias correction) > the crucial difference? > > Is DARTEL in SPM8 in combination with the "New Segment" function more > sensitive? > > I think for VBM where DARTEL has (my perception) repeatedly been > recommended as excellent/best registration tool, > it would be very useful if also the preprocessing/optimizations can be > performed within SPM. - It is somewhat > strange that extra preprocessing steps seem necessary outside SPM. > > I am very interested in comments/opinions here, > thanks, > Philipp > Max Planck Institute of Psychiatry > NMR Research Group > Kraepelinstr. 2-10 > 80804 Munich > Mail: [log in to unmask] > Phone: 0049-89-30622-413 --_0d0961c3-b624-4bbe-adc0-9979ff4c2b23_ Content-Type: text/html; charset="iso-8859-1" Content-Transfer-Encoding: quoted-printable Dear Philipp and others,

with my own data, or more exactly with the OASIS database (not skull-stripped), Ive made similar observations, i.e. SPM8-new-segmentation (or "normal" SPM5-unified-segmentation)+DARTEL VBM failed to detect significant hippocampus atrophy for most parts of the hippocampus in AD and MCI. While the effects seemed to be consistent with the literature for most parts of the cortex (atrophy in PCC, ACC, temporoparietal areas and relative sparing of somoatosensory areas and the cerebellum in AD), effects in the MTL were restricted to the amygdala and anterior parts of the hippocampus.
However, VBM procedures rely on a mixture of accurate segmentation AND normalisation to a common space and I think the error here may rather lie in inaccurate segmentaion than in the DARTEL normalisation. Repeating the analysis with "Gaser"-segmented images (VBM8) and exactly the same DARTEL-settings revealed "perfect" (i.e. expected or more consistent with the literature) results for the MTL and the rest of the cortex.
A possible explanation for this observation is that registration accuracy (using tissue-priors based on a normal population) and hence segmentation accuracy of the unified approaches in spm5/8 decreases with increasing atrophy. Although the detailed tissue information in "New-segment" normally leads to convincingly improved segmentation results and the high-dimensional warping in DARTEL is capable to model large deformations, it might still be necessary to adjust the tissue priors when dealing with groups that differ strongly from the anatomy of the normal population. The tissue prior-free approach of the VBM8-toolbox produced much more "realistic" results when comparing a large cohort of healthy elderly and AD patients (the OASIS database).

Would be interesting to hear about the experiences of the rest of the SPM/VBM-community.

Best regards,
Michel

> Date: Fri, 18 Feb 2011 00:10:35 +0100
> From: [log in to unmask]
> Subject: [SPM] sensitivity of DARTEL
> To: [log in to unmask]
>
> Dear SPMers,
>
> in a recent paper by Pereira et al. on Resgistration accuracy for VBM
> studies, NeuroImage 2010;49:2205-15 DARTEL as implemented
> in SPM5 is presented as very insensitive to focal GM changes - in their
> work, they used a small Alzheimer Disease sample to
> to (amongmany other analyses) check the sensitivity to detect hippocampal
> atrophy.
>
> However, sensitivity and regional specificity were completely regained when
> three preprocessing steps were performed:
> 1. skull stripping, 2. bias correction, and 3., "fine tuned BET".
>
> > Has anybody made similar observations on insensitivity of DARTEL?
> > Is the SPM Bias correction (default parameters) really so non-optimal?
> > Is it the order of steps (first skull stripping, then bias correction)
> the crucial difference?
> > Is DARTEL in SPM8 in combination with the "New Segment" function more
> sensitive?
>
> I think for VBM where DARTEL has (my perception) repeatedly been
> recommended as excellent/best registration tool,
> it would be very useful if also the preprocessing/optimizations can be
> performed within SPM. - It is somewhat
> strange that extra preprocessing steps seem necessary outside SPM.
>
> I am very interested in comments/opinions here,
> thanks,
> Philipp
> Max Planck Institute of Psychiatry
> NMR Research Group
> Kraepelinstr. 2-10
> 80804 Munich
> Mail: [log in to unmask]
> Phone: 0049-89-30622-413
--_0d0961c3-b624-4bbe-adc0-9979ff4c2b23_-- ========================================================================Date: Fri, 18 Feb 2011 10:59:22 +0900 Reply-To: HwangArum <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: HwangArum <[log in to unmask]> Subject: Asking "interaction analysis" in spm !! :D Comments: To: [log in to unmask], [log in to unmask], [log in to unmask] Content-Type: multipart/alternative; boundary="_d7c4f5ac-ffad-4f6f-88e1-ca978ece01e9_" MIME-Version: 1.0 Message-ID: <[log in to unmask]> --_d7c4f5ac-ffad-4f6f-88e1-ca978ece01e9_ Content-Type: text/plain; charset="ks_c_5601-1987" Content-Transfer-Encoding: quoted-printable X-MIME-Autoconverted: from 8bit to quoted-printable by bofur.jiscmail.ac.uk id p1I1xMRT025734 We conducted 2x2 within-subject design in fMRI study. Each subjects performed two different kinds of tasks A, B in two different contexts X, Y (e.g., X[A-B]-Y[A-B]). Is it allowed to make an interaction analysis (e.g., [XA-XB]-[YA-YB]) with two-sample t-test in within-subject design (using spm)? For example, put [XA-XB] con image into one group and put [YA-YB] con image into another group. If yes, indepence option should be set as yes(default) or should be changed into no? Best regards, Arum Hwang --_d7c4f5ac-ffad-4f6f-88e1-ca978ece01e9_ Content-Type: text/html; charset="ks_c_5601-1987" Content-Transfer-Encoding: quoted-printable X-MIME-Autoconverted: from 8bit to quoted-printable by bofur.jiscmail.ac.uk id p1I1xMRT025734

We conducted 2x2 within-subject design in fMRI study. Each subjects performed two different kinds of tasks A, B in two different contexts X, Y (e.g., X[A-B]-Y[A-B]).

 

Is it allowed to make an interaction analysis (e.g., [XA-XB]-[YA-YB]) with two-sample t-test in within-subject design (using spm)?

 

For example, put [XA-XB] con image into one group and put [YA-YB] con image into another group. If yes, indepence option should be set as yes(default) or should be changed into no?

 

 

Best regards, Arum Hwang

--_d7c4f5ac-ffad-4f6f-88e1-ca978ece01e9_-- ========================================================================Date: Thu, 17 Feb 2011 21:25:03 -0500 Reply-To: "MCLAREN, Donald" <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: "MCLAREN, Donald" <[log in to unmask]> Subject: Re: Asking "interaction analysis" in spm !! :D Comments: To: HwangArum <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=windows-1252 Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> You need to use a paired t-test. On Thursday, February 17, 2011, HwangArum <[log in to unmask]> wrote: > > > > > > We conducted 2x2 within-subject design in fMRI study. Each subjects performed two different kinds of tasks A, B in two different contexts X, Y (e.g., X[A-B]-Y[A-B]). > > Is it allowed to make an interaction analysis (e.g., [XA-XB]-[YA-YB]) with two-sample t-test in within-subject design (using spm)? > > For example, put [XA-XB] con image into one group and put [YA-YB] con image into another group. If yes, indepence option should be set as yes(default) or should be changed into no? > > > Best regards, Arum Hwang > -- Best Regards, Donald McLaren ================= D.G. McLaren, Ph.D. Postdoctoral Research Fellow, GRECC, Bedford VA Research Fellow, Department of Neurology, Massachusetts General Hospital and Harvard Medical School Office: (773) 406-2464 ===================== This e-mail contains CONFIDENTIAL INFORMATION which may contain PROTECTED HEALTHCARE INFORMATION and may also be LEGALLY PRIVILEGED and which is intended only for the use of the individual or entity named above. If the reader of the e-mail is not the intended recipient or the employee or agent responsible for delivering it to the intended recipient, you are hereby notified that you are in possession of confidential and privileged information. Any unauthorized use, disclosure, copying or the taking of any action in reliance on the contents of this information is strictly prohibited and may be unlawful. If you have received this e-mail unintentionally, please immediately notify the sender via telephone at (773) 406-2464 or email. ========================================================================Date: Fri, 18 Feb 2011 02:18:46 +0000 Reply-To: chihiro <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: chihiro <[log in to unmask]> Subject: HELP!with VBM (estimation error) Mime-Version: 1.0 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain Message-ID: <[log in to unmask]> During my data processing, I encountered some problems. I used VBM to analyze. First, I used the DARTEL tool for VBM following the DARTEL manual and got the smwc images. In the statistical analysis, I tried to find the differences between a patient and 20 age matched healthy controls with two-sample t-test (one group was a patient, and the other group was the healthy individuals). I could do the design specification but when I did model estimation, the following error was occured. Running job #1 ------------------------------------------------------------------------ Running 'Factorial design specification' Mapping files : ...done Design configuration : ...done Saving SPM configuration : ...SPM.mat saved Design reporting : ...done Done Done 'Factorial design specification' Done ------------------------------------------------------------------------ Running job #2 ------------------------------------------------------------------------ Running 'Model estimation' SPM8: spm_spm (v3468) 10:39:13 - 18/02/2011 ======================================================================== Initialising parameters : ...done Plane 121/121, block 1/1 : ...done Temporal non-sphericity (over voxels) : ...ReML estimation ReML Iteration 1 : ...0.000000e+00 [+4.25] SPM8: spm_spm (v3468) 10:39:28 - 18/02/2011 ======================================================================== Initialising parameters : ...computingFailed 'Model estimation' Index exceeds matrix dimensions. In file "/Applications/MATLAB_R2009b.app/toolbox/matlab/sparfun/spdiags.m" (???), function "spdiags" at line 114. In file "/Applications/spm8/spm_spm.m" (v3468), function "spm_spm" at line 427. In file "/Applications/spm8/spm_spm.m" (v3468), function "spm_spm" at line 878. In file "/Applications/spm8/config/spm_run_fmri_est.m" (v3327), function "spm_run_fmri_est" at line 53. The following modules did not run: Failed: Model estimation I uses the MAC OS X 10.6.6, the MATLAB 7.9.0.529 (R2009b), and the SPM 8. I appreciate if you can help me! ========================================================================Date: Thu, 17 Feb 2011 21:53:22 -0500 Reply-To: "MCLAREN, Donald" <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: "MCLAREN, Donald" <[log in to unmask]> Subject: Re: HELP!with VBM (estimation error) Comments: To: chihiro <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> Set the variance to equal. On Thursday, February 17, 2011, chihiro <[log in to unmask]> wrote: > During my data processing, I encountered some problems. > > I used VBM to analyze. > First, I used the DARTEL tool for VBM following the DARTEL manual and got the smwc images. > > In the statistical analysis, I tried to find the differences > between a patient and 20 age matched healthy controls with two-sample t-test (one group was a patient, and > the other group was the healthy individuals). > > I could do the design specification but when I did model estimation, the following error was occured. > > Running job #1 > ------------------------------------------------------------------------ > Running 'Factorial design specification' > Mapping files : ...done > Design configuration : ...done > Saving SPM configuration : ...SPM.mat saved > Design reporting : ...done > Done > Done 'Factorial design specification' > Done > > > > ------------------------------------------------------------------------ > Running job #2 > ------------------------------------------------------------------------ > Running 'Model estimation' > > SPM8: spm_spm (v3468) 10:39:13 - 18/02/2011 > ======================================================================== > Initialising parameters : ...done > Plane 121/121, block 1/1 : ...done > Temporal non-sphericity (over voxels) : ...ReML estimation > ReML Iteration 1 : ...0.000000e+00 [+4.25] > > SPM8: spm_spm (v3468) 10:39:28 - 18/02/2011 > ======================================================================== > Initialising parameters : ...computingFailed 'Model estimation' > Index exceeds matrix dimensions. > In file "/Applications/MATLAB_R2009b.app/toolbox/matlab/sparfun/spdiags.m" (???), function "spdiags" at line 114. > In file "/Applications/spm8/spm_spm.m" (v3468), function "spm_spm" at line 427. > In file "/Applications/spm8/spm_spm.m" (v3468), function "spm_spm" at line 878. > In file "/Applications/spm8/config/spm_run_fmri_est.m" (v3327), function "spm_run_fmri_est" at line 53. > > The following modules did not run: > Failed: Model estimation > > > > I uses the MAC OS X 10.6.6, > the MATLAB 7.9.0.529 (R2009b), > and the SPM 8. > > I appreciate if you can help me! > -- Best Regards, Donald McLaren ================= D.G. McLaren, Ph.D. Postdoctoral Research Fellow, GRECC, Bedford VA Research Fellow, Department of Neurology, Massachusetts General Hospital and Harvard Medical School Office: (773) 406-2464 ===================== This e-mail contains CONFIDENTIAL INFORMATION which may contain PROTECTED HEALTHCARE INFORMATION and may also be LEGALLY PRIVILEGED and which is intended only for the use of the individual or entity named above. If the reader of the e-mail is not the intended recipient or the employee or agent responsible for delivering it to the intended recipient, you are hereby notified that you are in possession of confidential and privileged information. Any unauthorized use, disclosure, copying or the taking of any action in reliance on the contents of this information is strictly prohibited and may be unlawful. If you have received this e-mail unintentionally, please immediately notify the sender via telephone at (773) 406-2464 or email. ========================================================================Date: Thu, 17 Feb 2011 22:10:06 -0500 Reply-To: John Fredy <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: John Fredy <[log in to unmask]> Subject: vbm8 for single subject MIME-Version: 1.0 Content-Type: multipart/alternative; boundaryMessage-ID: <[log in to unmask]> --0016e6d7843fdfb662049c85d9f5 Content-Type: text/plain; charset=ISO-8859-1 Hello all, Is possible use the vbm8 toolbox for compare a single subject against the template Thanks in advance --0016e6d7843fdfb662049c85d9f5 Content-Type: text/html; charset=ISO-8859-1 Hello all,

Is possible use the vbm8 toolbox for compare a single subject against the template

Thanks in advance
--0016e6d7843fdfb662049c85d9f5-- ========================================================================Date: Fri, 18 Feb 2011 03:32:16 +0000 Reply-To: Nero Evero <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Nero Evero <[log in to unmask]> Subject: MATLAB Out of Memory error Mime-Version: 1.0 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain; charset="UTF-8" Message-ID: <[log in to unmask]> Hello All, We are trying to run a fixed effects analysis using SPM8 on a Windows 7 32-bit OS with 4GM of RAM. We have 120 subjects/sessions with a total of 6600 scans (55/session). The analysis stops during the parameter estimation and gives the following erroe message: Initialising parameters : ...done Output images : ...initialised Plane 1/46 , block 1/3 : ...estimation??? Out of memory. Type HELP MEMORY for your options. Error in ==> spm_spm at 715 CY = CY + Y*Y'; Error in ==> spm_getSPM at 233 SPM = spm_spm(SPM); Error in ==> spm_results_ui at 277 [SPM,xSPM] = spm_getSPM; ??? Error while evaluating uicontrol Callback I tried adding more memory to SPM (i.e. by changing defaults.stats.maxmem to about 2GB), but I still received the error. Looking through the archives it seems like the common solution is to change to a 64-bit OS, but I wanted to know if there was any other possible solutions? Thanks in adavance. Nero ========================================================================Date: Thu, 17 Feb 2011 23:46:29 -0500 Reply-To: Jonathan Peelle <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Jonathan Peelle <[log in to unmask]> Subject: Re: vbm8 for single subject Comments: To: John Fredy <[log in to unmask]> In-Reply-To: <[log in to unmask]> Mime-Version: 1.0 (Apple Message framework v1082) Content-Type: text/plain; charset=windows-1252 Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> Hi John > Is possible use the vbm8 toolbox for compare a single subject against the template You can't get any sort of statistics out of comparing a single subject against a template because you have no variance. The best you could do is a simple subtraction but this woudn't be particularly informative I don't think. To look at a single participant you really need a sample with which to compare theme.g., 1 patient vs. 20 age- and sex-matched controls. Jonathan -- Dr. Jonathan Peelle Department of Neurology University of Pennsylvania 3 West Gates 3400 Spruce Street Philadelphia, PA 19104 USA http://jonathanpeelle.net/ ========================================================================Date: Fri, 18 Feb 2011 08:44:01 +0100 Reply-To: Lucas Eggert <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Lucas Eggert <[log in to unmask]> Subject: TIV as nuisance factor for unmodulated data in a VBM-analysis MIME-Version: 1.0 Content-Type: multipart/signed; protocol="application/pkcs7-signature"; micalg=sha1; boundary="------------ms040708000206040902000902" Message-ID: <[log in to unmask]> This is a cryptographically signed message in MIME format. --------------ms040708000206040902000902 Content-Type: multipart/alternative; boundary="------------020304020908000302080105" This is a multi-part message in MIME format. --------------020304020908000302080105 Content-Type: text/plain; charset=ISO-8859-15; format=flowed Content-Transfer-Encoding: quoted-printable Dear Dr. Gaser, Dear List, at the moment I am unsure about whether correcting for total brain volume (TIV) in a VBM analysis of unmodulated gray matter segments (density) does make sense or not. On Dr. Gaser's homepage --- I have the feeling --- there are two slightly opposite statements: statement (a) (please refer below) clearly states that TIV should not be used as a nuisacne factor with unmodulated data. On the other hand, I read statement (b) (please see below) as correcting unmodulated data for TIV gives me relative density after correcting for TIV, which seems to make more sense to me. Which procedure is the more valid one, or for which kind of question would I use which procedure respectively? Thanks for any help in advance. Best regards, Lucas Eggert ****************** STATEMENT (a): http://dbm.neuro.uni-jena.de/vbm/vbm2-for-spm2/calculate-raw-volumes/ "The use of raw volumes as nuisance or globals is only recommended for modulated data. These data are corrected for size changes due to spatial normalization and are thought to be in raw (un-normalized) space. In contrast, un-modulated data are yet corrected for differences in size due to spatial normalization to a reference brain and there is no need to correct for these differences again." STATEMENT (b): http://dbm.neuro.uni-jena.de/vbm/segmentation/modulation/ Interpretation If we follow the commonly used terms "volume" for modulated data and "density" (or concentration) for unmodulated data and concentrate on GM there are many possible ways to correct or not correct for different brain size: *No modulation:* *Correction * *Interpretation* nothing relative density globals "localised" relative density after correcting for total GM or TIV (multiplicative effects) AnCova "localised" relative density that can not be explained by total GM or TIV (additive effects) -- Lucas Eggert, M.Sc. Institute of Cognitive Science University of Osnabrueck Albrechtstrasse 28 D-49076 Osnabrueck Germany Phone: +49-541-969-44-28 Website: http://www.cogsci.uni-osnabrueck.de/~leggert/ --------------020304020908000302080105 Content-Type: text/html; charset=ISO-8859-15 Content-Transfer-Encoding: quoted-printable Dear Dr. Gaser,
Dear List,

at the moment I am unsure about whether correcting for total brain volume (TIV) in
a VBM analysis of unmodulated gray matter segments (density) does make sense or not.

On Dr. Gaser's homepage --- I have the feeling --- there are two slightly opposite statements:
statement (a) (please refer below) clearly states that TIV should not be used as a nuisacne factor with unmodulated data.

On the other hand, I read statement (b) (please see below) as correcting unmodulated data for TIV gives me relative
density after correcting for TIV, which seems to make more sense to me.

Which procedure is the more valid one, or for which kind of question would I use which procedure respectively?

Thanks for any help in advance.

Best regards,
Lucas Eggert

******************

STATEMENT (a):
http://dbm.neuro.uni-jena.de/vbm/vbm2-for-spm2/calculate-raw-volumes/

"The use of raw volumes as nuisance or globals is only recommended for modulated data.
These data are corrected for size changes due to spatial normalization and are thought
to be in raw (un-normalized) space. In contrast, un-modulated data are yet corrected
for differences in size due to spatial normalization to a reference brain and there
is no need to correct for these differences again."

STATEMENT (b):
http://dbm.neuro.uni-jena.de/vbm/segmentation/modulation/

Interpretation

If we follow the commonly used terms “volume” for modulated data and “density” (or concentration)
for unmodulated data and concentrate on GM there are many possible ways to correct or not correct for different brain size:

No modulation:

Correction Interpretation
nothing relative density
globals “localised” relative density after correcting for total GM or TIV (multiplicative effects)
AnCova “localised” relative density that can not be explained by total GM or TIV (additive effects)


-- 
Lucas Eggert, M.Sc.
Institute of Cognitive Science
University of Osnabrueck
Albrechtstrasse 28 
D-49076 Osnabrueck
Germany

Phone:	   +49-541-969-44-28
Website:   http://www.cogsci.uni-osnabrueck.de/~leggert/ 




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pBN0KICnvTKrQnX8UlznbSKASYlDK5jaoT/i3bcoHL3JqNV4iECw7lOcKADPGSOisZ3NPXp1 CQhKgjYVUQ9pUavpy7ehgtuigdHBIIV9hg5/Plow3nFRAAAAAAAA --------------ms040708000206040902000902-- ========================================================================Date: Fri, 18 Feb 2011 12:04:06 +0100 Reply-To: Cesar Caballero <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Cesar Caballero <[log in to unmask]> Subject: is possible to register to another image than first one in realignment In-Reply-To: <[log in to unmask]> MIME-version: 1.0 Content-transfer-encoding: 7BIT Content-type: text/plain; CHARSET=US-ASCII Message-ID: <[log in to unmask]> Hello all, In realignment, there are two options: register to mean or register to first. Is there any way to do realignment to a different image that is not the first one in SPM 8? Thanks very much, Cesar ========================================================================Date: Fri, 18 Feb 2011 11:21:44 +0000 Reply-To: John Ashburner <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: John Ashburner <[log in to unmask]> Subject: Re: is possible to register to another image than first one in realignment Comments: To: Cesar Caballero <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Message-ID: <[log in to unmask]> You could select the images in a different order. There is no temporal information used by the realignment. Best regards, -John On 18 February 2011 11:04, Cesar Caballero <[log in to unmask]> wrote: > Hello all, > > In realignment, there are two options: register to mean or register to first. > Is there any way to do realignment to a different image that is not the first one in SPM 8? > > Thanks very much, > Cesar > ========================================================================Date: Fri, 18 Feb 2011 12:48:50 +0100 Reply-To: Cesar Caballero <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Cesar Caballero <[log in to unmask]> Subject: Re: is possible to register to another image than first one in realignment Comments: To: John Ashburner <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-version: 1.0 Content-transfer-encoding: 7BIT Content-type: text/plain; CHARSET=US-ASCII Message-ID: <[log in to unmask]> Hello John, Thanks very much for your answer, I was wondering about the temporal information of the realignment parameters for the analysis. What would it be the effect if I select the scans on different order? Best wishes, Cesar On Feb 18, 2011, at 12:21 PM, John Ashburner wrote: > You could select the images in a different order. There is no > temporal information used by the realignment. > > Best regards, > -John > > On 18 February 2011 11:04, Cesar Caballero > <[log in to unmask]> wrote: >> Hello all, >> >> In realignment, there are two options: register to mean or register to first. >> Is there any way to do realignment to a different image that is not the first one in SPM 8? >> >> Thanks very much, >> Cesar >> ========================================================================Date: Fri, 18 Feb 2011 11:51:34 +0000 Reply-To: John Ashburner <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: John Ashburner <[log in to unmask]> Subject: Re: is possible to register to another image than first one in realignment Comments: To: Cesar Caballero <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> All scans would be aligned to the first image you select. Best regards, -John On 18 February 2011 11:48, Cesar Caballero <[log in to unmask]> wrote: > Hello John, > > Thanks very much for your answer, > I was wondering about the temporal information of the realignment parameters for the analysis. > What would it be the effect if I select the scans on different order? > > Best wishes, > Cesar > > On Feb 18, 2011, at 12:21 PM, John Ashburner wrote: > >> You could select the images in a different order. There is no >> temporal information used by the realignment. >> >> Best regards, >> -John >> >> On 18 February 2011 11:04, Cesar Caballero >> <[log in to unmask]> wrote: >>> Hello all, >>> >>> In realignment, there are two options: register to mean or register to first. >>> Is there any way to do realignment to a different image that is not the first one in SPM 8? >>> >>> Thanks very much, >>> Cesar >>> > > ========================================================================Date: Fri, 18 Feb 2011 13:00:17 +0100 Reply-To: jmrabanal <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: jmrabanal <[log in to unmask]> Subject: CURSO DE NEUROIMAGEN AVANZADA MIME-Version: 1.0 Content-Type: text/plain; charset=UTF-8 Content-Transfer-Encoding: quoted-printable Message-ID: <8244675c248d4ae58ca01f7da700c7ee@localhost> V CURSO DE NEUROIMAGEN AVANZADA EN NEUROCIENCIA COGNITIVA Y PSIQUIATRÍA. INSCRIPCIÓN NO PRESENCIAL: Teléfono: 93 248 38 71 E-mail: •[log in to unmask] INSCRIPCIÓN PRESENCIAL: Escola de Postgrau • Servei atenció a l’usuari • Edifici U Planta 1 Campus UAB • Bellaterra (Cerdanyola del Vallès) IMPORTE MATRICULA: PRECIO: 375 Euros LUGAR DE REALIZACIÓN DEL CURSO: Parc de Recerca Biomèdica de Barcelona (PRBB) • Sala Xipre 1ª planta C/ Doctor Aiguader, 88 • 08003 BARCELONA • PLAZO DE INSCRIPCIÓN: Del 10 de Diciembre 2010 al 20 de Marzo 2011 El curso se impartirá en castellano. Este curso de postgrado es una introducción a las técnicas y los diseños experimentales de neuroimagen que se utilizan en la investigación en neurociencia cognitiva y psiquiatría, orientado fundamentalmente hacia la resonancia magnética estructural y funcional. En este curso se abordan los fundamentos físicos y biológicos de dichas técnicas, se adentra en los procedimientos de pre y postprocesado y en la descripción de los paradigmas empleados en la investigación básica en neurociencia cognitiva y en la investigación clínica en psiquiatría. ¿a quién va dirigido? A clínicos e investigadores que provienen de disciplinas como la psiquiatría, la neurología, la psicología, la neurorradiología y la medicina nuclear. El curso se estructura en cuatro módulos: Módulo 1: “Fundamentos de neuroimagen”, está dedicado a los conceptos fundamentales de las principales técnicas avanzadas de neuroimagen, con énfasis en la resonancia magnética estructural y funcional. Nuevas aplicaciones de la resonancia magnética como la espectroscopia protónica y la imaginería por tensores de difusión reciben también especial atención. Se exponen asimismo las bases biológicas de la RM funcional. Módulo 2: “Paradigmas experimentales en RM funcional”, aborda los fundamentos de los diseños experimentales en RM funcional. Se estudian los principales paradigmas experimentales empleados en neurociencia cognitiva (atención, memoria, percepción, emoción y mixtos), tras una exposición de los correspondientes circuitos anatómico-funcionales implicados. Módulo 3: “Post-procesado en neuroimagen”, está dedicado a los procedimientos empleados en el pre-procesamiento (realineamiento espacial, normalización estereotáxica, corregistro y suavizado espacial) y post-procesamiento funcional (específicamente Voxel-based morphometry “VBM”). Se exponen los fundamentos de la estadística inferencial y las principales técnicas estadísticas empleados en post-procesado de neuroimagen (la t de Student, el análisis correlacional, el análisis de Fourier y el modelo lineal general). Se estudian asimismo análisis de regiones de interés. Módulo 4: “Neuroimagen en los trastornos psiquiátricos”, está dedicado a la exposición de las contribuciones que las técnicas de neuroimagen han aportado al conocimiento de la neurobiología de los trastornos mentales, específicamente, en los trastornos de ansiedad, la esquizofrenia, el trastorno obsesivo compulsivo y el trastorno por déficit de atención e hiperactividad. ========================================================================Date: Fri, 18 Feb 2011 07:15:33 -0500 Reply-To: John Fredy <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: John Fredy <[log in to unmask]> Subject: Re: vbm8 for single subject Comments: To: Jonathan Peelle <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/alternative; boundaryMessage-ID: <[log in to unmask]> --0016e6d58dac861487049c8d78d3 Content-Type: text/plain; charset=windows-1252 Content-Transfer-Encoding: quoted-printable Thanks! On Thu, Feb 17, 2011 at 11:46 PM, Jonathan Peelle <[log in to unmask]> wrote: > Hi John > > > Is possible use the vbm8 toolbox for compare a single subject against the > template > > You can't get any sort of statistics out of comparing a single subject > against a template because you have no variance. The best you could do is a > simple subtraction but this woudn't be particularly informative I don't > think. To look at a single participant you really need a sample with which > to compare theme.g., 1 patient vs. 20 age- and sex-matched controls. > > Jonathan > > > > -- > Dr. Jonathan Peelle > Department of Neurology > University of Pennsylvania > 3 West Gates > 3400 Spruce Street > Philadelphia, PA 19104 > USA > http://jonathanpeelle.net/ > > > > --0016e6d58dac861487049c8d78d3 Content-Type: text/html; charset=windows-1252 Content-Transfer-Encoding: quoted-printable Thanks!

On Thu, Feb 17, 2011 at 11:46 PM, Jonathan Peelle <[log in to unmask]> wrote:
Hi John

> Is possible use the vbm8 toolbox for compare a single subject against the template

You can't get any sort of statistics out of comparing a single subject against a template because you have no variance. The best you could do is a simple subtraction but this woudn't be particularly informative I don't think. To look at a single participant you really need a sample with which to compare theme.g., 1 patient vs. 20 age- and sex-matched controls.

Jonathan



--
Dr. Jonathan Peelle
Department of Neurology
University of Pennsylvania
3 West Gates
3400 Spruce Street
Philadelphia, PA 19104
USA
http://jonathanpeelle.net/




--0016e6d58dac861487049c8d78d3-- ========================================================================Date: Fri, 18 Feb 2011 12:15:01 +0000 Reply-To: " " <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: " " <[log in to unmask]> Subject: SPM error Mime-Version: 1.0 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain; charset="UTF-8" Message-ID: <[log in to unmask]> Hi all, I repeatedly get this error when trying to convert/filter/downsample my MEG data, although not every time... ??? Error using ==> mat2file Cant open file. Error in ==> file_array.subsasgn>subfun at 132 mat2file(sobj,dat,va{:}); Error in ==> file_array.subsasgn at 70 subfun(sobj,double(dat),args{:}); Error in ==> meeg.subsasgn at 29 this.data.y = subsasgn(this.data.y, subs, dat); Error in ==> spm_eeg_downsample at 124 Dnew(blkchan,:,1)=Dtemp(:,1:nsamples_new,1); Error in ==> spm at 961 evalin('base',CBs{v-1}) ??? Error while evaluating uicontrol Callback I've been told it's generally to do with permissions but I have got full permission/access etc to the data and the folders in which the data is in and there is plenty of room on my hard drive. The other issue is that the error is inconsistent in that sometimes when I repeat the same step having got the error, it will then work, sometimes not. Does anyone know of any other reason that I might be getting this error? Kind regards, Holly ========================================================================Date: Fri, 18 Feb 2011 12:30:02 +0000 Reply-To: Vladimir Litvak <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Vladimir Litvak <[log in to unmask]> Subject: Re: SPM error Comments: To: " " <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> Hi Holly, This has to do with the backup process that runs on your PC. Disable it (from the toolbar tray) before doing SPM analysis. Vladimir On Fri, Feb 18, 2011 at 12:15 PM, <[log in to unmask]> wrote: > Hi all, > > I repeatedly get this error when trying to convert/filter/downsample my MEG data, although not every time... > > ??? Error using ==> mat2file > Cant open file. > > Error in ==> file_array.subsasgn>subfun at 132 > mat2file(sobj,dat,va{:}); > > Error in ==> file_array.subsasgn at 70 > subfun(sobj,double(dat),args{:}); > > Error in ==> meeg.subsasgn at 29 > this.data.y = subsasgn(this.data.y, subs, dat); > > Error in ==> spm_eeg_downsample at 124 > Dnew(blkchan,:,1)=Dtemp(:,1:nsamples_new,1); > > Error in ==> spm at 961 > evalin('base',CBs{v-1}) > > ??? Error while evaluating uicontrol Callback > > I've been told it's generally to do with permissions but I have got full permission/access etc to the data and the folders in which the data is in and there is plenty of room on my hard drive. > > The other issue is that the error is inconsistent in that sometimes when I repeat the same step having got the error, it will then work, sometimes not. > > Does anyone know of any other reason that I might be getting this error? > > Kind regards, > > Holly > ========================================================================Date: Fri, 18 Feb 2011 13:51:47 +0000 Reply-To: Stephen Smith <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Stephen Smith <[log in to unmask]> Subject: Announcement: The 2011 FSL & FreeSurfer Course Content-Type: multipart/alternative; boundary=Apple-Mail-198--245155489 Mime-Version: 1.0 (Apple Message framework v1082) Message-ID: <[log in to unmask]> --Apple-Mail-198--245155489 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain; charset=us-ascii With kind permission from Karl and John: ---------------------------- We are pleased to announce the 2011 FSL & FreeSurfer Course, to be held in Montreal, Canada. It will run immediately before the Human Brain Mapping conference, which will be in Quebec City, a short plane/train/road journey from Montreal. The intensive course covers both the theory and practice of functional and structural brain image analysis. Background concepts and the practicalities of analyses are taught in detailed lectures; these are interleaved with hands-on practical sessions where attendees learn how to carry out analysis for themselves on real data, with one computer provided for every two attendees. After completing the course, attendees should be able to analyse their own FMRI and MRI data sets. The course lasts 5 days, from June 20-24. Numbers of attendees are strictly limited and are available on a first-come-first-served basis. For full information and to register for the course, please go to: http://www.fmrib.ox.ac.uk/fslcourse/montreal2011.html Regards, course organisers. --------------------------------------------------------------------------- Stephen M. Smith, Professor of Biomedical Engineering Associate Director, Oxford University FMRIB Centre FMRIB, JR Hospital, Headington, Oxford OX3 9DU, UK +44 (0) 1865 222726 (fax 222717) [log in to unmask] http://www.fmrib.ox.ac.uk/~steve --------------------------------------------------------------------------- --Apple-Mail-198--245155489 Content-Transfer-Encoding: quoted-printable Content-Type: text/html; charset=us-ascii
With kind permission from Karl and John:
----------------------------

We are pleased to announce the 2011 FSL & FreeSurfer Course, to be held in Montreal, Canada. It will run immediately before the Human Brain Mapping conference, which will be in Quebec City, a short plane/train/road journey from Montreal.

The intensive course covers both the theory and practice of functional and structural brain image analysis. Background concepts and the practicalities of analyses are taught in detailed lectures; these are interleaved with hands-on practical sessions where attendees learn how to carry out analysis for themselves on real data, with one computer provided for every two attendees. After completing the course, attendees should be able to analyse their own FMRI and MRI data sets.

The course lasts 5 days, from June 20-24.

Numbers of attendees are strictly limited and are available on a first-come-first-served basis.

For full information and to register for the course, please go to:

http://www.fmrib.ox.ac.uk/fslcourse/montreal2011.html

Regards, course organisers.


---------------------------------------------------------------------------
Stephen M. Smith, Professor of Biomedical Engineering
Associate Director,  Oxford University FMRIB Centre

FMRIB, JR Hospital, Headington, Oxford  OX3 9DU, UK
+44 (0) 1865 222726  (fax 222717)
[log in to unmask]    http://www.fmrib.ox.ac.uk/~steve
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--Apple-Mail-198--245155489-- ========================================================================Date: Fri, 18 Feb 2011 09:03:32 -0500 Reply-To: Fred Sanders <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Fred Sanders <[log in to unmask]> Subject: DCM and global signal MIME-Version: 1.0 Content-Type: multipart/alternative; boundary cf30433ef2b1ed73049c8efa9c Message-ID: <[log in to unmask]> --20cf30433ef2b1ed73049c8efa9c Content-Type: text/plain; charset=ISO-8859-1 I recently used DCM (in SPM8) to model the connectivity between 2 brain regions. A reviewer was concerned that DCM contains a regressor for global signal and that including this regressor could introduce artificial anti-correlations. I would greatly appreciate it if someone could help me understand this. I did not think DCM used a regressor for global signal - was this done in prior versions of DCM? Or is this referring to the constant term from the first level analysis? Also, how could that introduce anti-correlations? Any thoughts? Thanks!! --20cf30433ef2b1ed73049c8efa9c Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable I recently used DCM (in SPM8) to model the connectivity between 2 brain regions. A reviewer was concerned that DCM contains a regressor for global signal and that including this regressor could introduceartificialanti-correlations. I would greatly appreciate it if someone could help me understand this. I did not think DCM used a regressor for global signal - was this done in prior versions of DCM? Or is this referring to the constant term from the first level analysis? Also, how could that introduce anti-correlations?

Any thoughts?


Thanks!!
--20cf30433ef2b1ed73049c8efa9c-- ========================================================================Date: Fri, 18 Feb 2011 14:56:05 +0000 Reply-To: Ghazal Mohades <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Ghazal Mohades <[log in to unmask]> Subject: Interpret pediatric fMRI Mime-Version: 1.0 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain; charset="UTF-8" Message-ID: <[log in to unmask]> Dear colleagues fro the mailing list I understood that there had been a few of you having the same question as mine, however I couldn't get an exact answer to it. I am using TOM template to create a group specific template based on the data from NIH study (that I suppose works the best for a group of 42 8-11 year old children). and I used that template in normalization step during preprocessing. it goes without saying that there is no meaningful dependence or relation between this template and the known template for adults (e.g. MNI template) and it makes the interpretation of the activation spots quite tricky!! since I cannot use the coordinates given by SPM and look them up in available brain atlases to find the anatomical point for activation. (as these atlases are all based on adults brains) sop how can I report about the anatomical point of activation. i am not very good at anatomy too look at the activity and guess the name of that point. even if I was that wouldn't be scientifically accepted I suppose Thanks in advance for your help regrds Ghazal Mohades PhD student VUB Brussels ========================================================================Date: Fri, 18 Feb 2011 10:01:07 -0500 Reply-To: Deepika Nandiraju <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Deepika Nandiraju <[log in to unmask]> Subject: how to save realignment output MIME-Version: 1.0 Content-Type: multipart/alternative; boundaryMessage-ID: <[log in to unmask]> --0016e646a53aabad9a049c8fc8fa Content-Type: text/plain; charset=ISO-8859-1 Hi everybody, I have a quick question regarding realignment of fMRI data. " Is there an easy way to save the realignment output plot when batching other than copying the r* text file into excel an doing it ourselves?" Thank you very much. Best Regards, Deepika. --0016e646a53aabad9a049c8fc8fa Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable
Hi everybody,
I have a quick question regarding realignment of fMRI data.
" Is there an easy way to save the realignment output plot when batching other than copying the r* text file into excel an doing it ourselves?"
Thank you very much.
Best Regards,
Deepika.
--0016e646a53aabad9a049c8fc8fa-- ========================================================================Date: Fri, 18 Feb 2011 16:14:49 +0100 Reply-To: Marko Wilke <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Marko Wilke <[log in to unmask]> Subject: Re: how to save realignment output Comments: To: Deepika Nandiraju <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1; format=flowed Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> Hi Deepika, > I have a quick question regarding realignment of fMRI data. > " Is there an easy way to save the realignment output plot when batching > other than copying the r* text file into excel an doing it ourselves?" I dimly remember I already saw a code snippet on the list for this purpose, but if you cannot find it, this may help: % === Start === filt = ['^rp_*','.*\.txt$']; b = spm_select([Inf],'any','Select realignment parameters',[],pwd,filt); scaleme = [-3 3]; mydata = pwd; for i = 1:size(b,1) [p nm e v] = spm_fileparts(b(i,:)); printfig = figure; set(printfig, 'Name', ['Motion parameters: subject ' num2str(i) ], 'Visible', 'on'); loadmot = load(deblank(b(i,:))); subplot(2,1,1); plot(loadmot(:,1:3)); grid on; % ylim(scaleme); % enable to always scale between fixed values title(['Motion parameters: shifts (top, in mm) and rotations (bottom, in dg)'], 'interpreter', 'none'); subplot(2,1,2); plot(loadmot(:,4:6)*180/pi); grid on; % ylim(scaleme); title(['Data from ' p], 'interpreter', 'none'); mydate = date; motname = [mydata filesep 'motion_sub_' sprintf('%02.0f', i) '_' mydate '.png']; print(printfig, '-dpng', '-noui', '-r100', motname); close(printfig) end; % === End === Watch out for linebreaks before pasting it into the Matlab window. Cheers, Marko -- ____________________________________________________ PD Dr. med. Marko Wilke Facharzt fr Kinder- und Jugendmedizin Leiter, Experimentelle Pdiatrische Neurobildgebung Universitts-Kinderklinik Abt. III (Neuropdiatrie) Marko Wilke, MD, PhD Pediatrician Head, Experimental Pediatric Neuroimaging University Children's Hospital Dept. III (Pediatric Neurology) Hoppe-Seyler-Str. 1 D - 72076 Tbingen, Germany Tel. +49 7071 29-83416 Fax +49 7071 29-5473 [log in to unmask] http://www.medizin.uni-tuebingen.de/kinder/epn ____________________________________________________ ========================================================================Date: Fri, 18 Feb 2011 10:24:56 -0500 Reply-To: Xin Di <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Xin Di <[log in to unmask]> Subject: mis-registration of subject's anatomical and functional images MIME-Version: 1.0 Content-Type: multipart/mixed; boundary cf3054a15f008c72049c901f1b Message-ID: <[log in to unmask]> --20cf3054a15f008c72049c901f1b Content-Type: multipart/alternative; boundary cf3054a15f008c5d049c901f19 --20cf3054a15f008c5d049c901f19 Content-Type: text/plain; charset=ISO-8859-1 Dear Experts, I tried to coregister subject's functional images to it's own T1 image, but they did not registered very well (please see attached). I also tried to run skull strip to the anatomical image and reorient the functional images, but the results were still not good. Can any one kindly give me some suggestions on how to do next? Thank you very much! Sincerely, -- Xin Di, PhD Postdoctoral Researcher Department of Radiology University of Medicine and Dentistry of New Jersey 30 Bergen Street, ADMC 582 Newark, NJ 07101 --20cf3054a15f008c5d049c901f19 Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Dear Experts,

I tried to coregister subject's functional images to it's own T1 image, but they did not registered very well (please see attached). I also tried to run skull strip to the anatomical image and reorient the functional images, but the results were still not good. Can any one kindly give me some suggestions on how to do next? Thank you very much!

Sincerely,

--
Xin Di, PhD

Postdoctoral Researcher
Department of Radiology
University of Medicine and Dentistry of New Jersey
30 Bergen Street, ADMC 582
Newark, NJ 07101

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ooooAKKKKACiiigAooooAKKKKACiiigAooooAKKKKACiiigAooooAKKKKACiiigAooooAKKKKACi iigAooooAKKKKACiiigAooooAKKKKACiiigAooooAKKKKACiiigAooooAKKKKACiiigAooooAKKK KACiiigAooooAKKKKACiiigAooooAKKKKACiiigAooooAKKKKACiiigAooooAKKKKACiiigAoooo AKKKKACiiigAooooAKKKKACiiigAooooAKKKKACiiigAooooAKKKKACiiigAooooAKKKKACiiigA ooooAKKKKACiiigAooooAKKKKACiiigAooooAKKKKACiiigAooooAKKKKACiiigAooooAKKKKACi iigAooooAKKKKACiiigAooooAKKKKACiiigAooooAKKKKACiiigAooooAKKKKACiiigAooooAKKK KACiiigAooooAKKKKACiiigAooooAKKKKACiiigAooooAKKKKACiiigAooooAKKKKACiiigAoooo AKKKKACiiigAooooAKKKKACiiigAooooAKKKKACiiigAooooAKKKKACiiigAooooAKKKKACiiigA ooooAKKKKACiiigAooooAKKKKACiiigAooooAKKKKACiiigAooooAKKKKACiiigAooooAKKKKACi iigAooooA//Z --20cf3054a15f008c72049c901f1b-- ========================================================================Date: Fri, 18 Feb 2011 16:39:19 +0100 Reply-To: Michel Thiebaut de Schotten <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Michel Thiebaut de Schotten <[log in to unmask]> Subject: International School of Clinical Neuroanatomy on the Frontal Lobes. Comments: To: [log in to unmask] Content-Type: text/plain; charset=iso-8859-1 Content-Transfer-Encoding: quoted-printable Mime-Version: 1.0 (Apple Message framework v1082) Message-ID: <[log in to unmask]> We're pleased to invite you to attend to the first meeting of the INTERNATIONAL SCHOOL OF CLINICAL NEUROANATOMY to be held May 25-27, 2011 in Palermo, Sicily. The meeting is dedicated to the clinical neuroanatomy of the Frontal Lobes. Keynote speakers include Donald Stuss, Michael Petrides, Geraint Rees, Michael Kopelman, Mark Richardson and Marco Catani Topics cover comparative anatomy, cytoarchitectonic maps, connectional anatomy, executive functions, intra-operative mapping, consciousness, fronto-temporal dementia, motor neuron disease, traumatic brain injury, memory and confabulation, neuropsychological testing, virtual tractography dissections and epilepsy. A hands-on workshop on diffusion tensor imaging tractography will be run in parallel. Deadline for registration and abstract submission is 15 April 2011. For further information please visit our website http://www.isocn.eu We look forward to seeing you in Sicily! On behalf of the program committee. Michel Michel Thiebaut de Schotten, PhD NATBRAINLAB ANR-CAFORPFC/ANR-HMTC CRICM-INSERM UMRS 975 Pavillon de l'Enfance et l'Adolescence 47 Bd de l'Hpital 75651 Paris Cedex 13, France www.natbrainlab.com skype: michel_thiebaut_de_schotten +33 613579133 ========================================================================Date: Fri, 18 Feb 2011 16:57:24 +0100 Reply-To: Marko Wilke <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Marko Wilke <[log in to unmask]> Subject: Re: Interpret pediatric fMRI Comments: To: Ghazal Mohades <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=UTF-8; format=flowed Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> Hi Ghazal, > fro the mailing list I understood that there had been a few of you having the same question as mine, however I couldn't get an exact answer to it. That may be because there is no exact answer :) > I am using TOM template to create a group specific template based on the data from NIH study (that I suppose works the best for a group of 42 8-11 year old children). and I used that template in normalization step during preprocessing. it goes without saying that there is no meaningful dependence or relation between this template and the known template for adults (e.g. MNI template) and it makes the interpretation of the activation spots quite tricky!! since I cannot use the coordinates given by SPM and look them up in available brain atlases to find the anatomical point for activation. (as these atlases are all based on adults brains) I agree: the whole point of using a custom template is to be have more appropriate reference data for your group under study. When using such a template, you bring the images into (in SPM's case) MNI space, but they are not necessarily in alignment with the templates that were used to generate automatic lookup-helper-applications (although they may not be very far off, either). Note that this issue is by no means one of the TOM approach but will apply to each and every study using customized templates. I see that the famous Good et al paper (NI 2001) has been cited about 1500 times, and if all of them used the there-described approach to creating a custom template... you get my point. > sop how can I report about the anatomical point of activation. i am not very good at anatomy too look at the activity and guess the name of that point. even if I was that wouldn't be scientifically accepted I suppose I agree that guessing is not a good idea but I do not see why it should not be scientifically acceptable to use your eyes. Actually, I think that it may be less scientific to feed a long row of numbers into an algorithm and take the results at face value without checking at least some of them, using common sense and an anatomy textbook. The good thing is that the images may speak for themselves, so including representative slice that allow the reader to assess the localization goes a long way (you should still be able to name the structures involved, though :). I have written long paragraphs in a number of revisions, not all of them successful, trying to convey may unwillingness to include a table of activation foci, because, yes, this makes meta-analyses harder. But it is a compromise, and somehting's got to give. Cheers, Marko -- ____________________________________________________ PD Dr. med. Marko Wilke Facharzt für Kinder- und Jugendmedizin Leiter, Experimentelle Pädiatrische Neurobildgebung Universitäts-Kinderklinik Abt. III (Neuropädiatrie) Marko Wilke, MD, PhD Pediatrician Head, Experimental Pediatric Neuroimaging University Children's Hospital Dept. III (Pediatric Neurology) Hoppe-Seyler-Str. 1 D - 72076 Tübingen, Germany Tel. +49 7071 29-83416 Fax +49 7071 29-5473 [log in to unmask] http://www.medizin.uni-tuebingen.de/kinder/epn ____________________________________________________ ========================================================================Date: Fri, 18 Feb 2011 16:00:12 +0000 Reply-To: John Ashburner <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: John Ashburner <[log in to unmask]> Subject: Re: mis-registration of subject's anatomical and functional images Comments: To: Xin Di <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Message-ID: <[log in to unmask]> Are you sure these two scans are from the same subject? One brain looks much bigger than the other. Maybe the voxel sizes in the headers are wrong. Best regards, -John On 18 February 2011 15:24, Xin Di <[log in to unmask]> wrote: > Dear Experts, > > I tried to coregister subject's functional images to it's own T1 image, but > they did not registered very well (please see attached). I also tried to run > skull strip to the anatomical image and reorient the functional images, but > the results were still not good. Can any one kindly give me some suggestions > on how to do next? Thank you very much! > > Sincerely, > > -- > Xin Di, PhD > > Postdoctoral Researcher > Department of Radiology > University of Medicine and Dentistry of New Jersey > 30 Bergen Street, ADMC 582 > Newark, NJ 07101 > > ========================================================================Date: Fri, 18 Feb 2011 11:25:23 -0500 Reply-To: Xin Di <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Xin Di <[log in to unmask]> Subject: Re: mis-registration of subject's anatomical and functional images In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/alternative; boundaryMessage-ID: <[log in to unmask]> --00221532ccd02f4158049c90f736 Content-Type: text/plain; charset=ISO-8859-1 Dear John, Thank you for your reply! I am pretty sure that they are from the same subject. The functional images might be transformed into 4D nii image by other software (AFNI or FSL). Does it cause the problem? Thank you! Sincerely, On Fri, Feb 18, 2011 at 11:00 AM, John Ashburner <[log in to unmask]>wrote: > Are you sure these two scans are from the same subject? One brain > looks much bigger than the other. Maybe the voxel sizes in the > headers are wrong. > > Best regards, > -John > > On 18 February 2011 15:24, Xin Di <[log in to unmask]> wrote: > > Dear Experts, > > > > I tried to coregister subject's functional images to it's own T1 image, > but > > they did not registered very well (please see attached). I also tried to > run > > skull strip to the anatomical image and reorient the functional images, > but > > the results were still not good. Can any one kindly give me some > suggestions > > on how to do next? Thank you very much! > > > > Sincerely, > > > > -- > > Xin Di, PhD > > > > Postdoctoral Researcher > > Department of Radiology > > University of Medicine and Dentistry of New Jersey > > 30 Bergen Street, ADMC 582 > > Newark, NJ 07101 > > > > > -- Xin Di, PhD Postdoctoral Researcher Department of Radiology University of Medicine and Dentistry of New Jersey 30 Bergen Street, ADMC 582 Newark, NJ 07101 --00221532ccd02f4158049c90f736 Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Dear John,

Thank you for your reply! I am pretty sure that they are from the same subject. The functional images might be transformed into 4D nii image by other software (AFNI or FSL). Does it cause the problem? Thank you!

Sincerely,


On Fri, Feb 18, 2011 at 11:00 AM, John Ashburner <[log in to unmask]> wrote:
Are you sure these two scans are from the same subject? One brain
looks much bigger than the other. Maybe the voxel sizes in the
headers are wrong.

Best regards,
-John

On 18 February 2011 15:24, Xin Di <[log in to unmask]> wrote:
> Dear Experts,
>
> I tried to coregister subject's functional images to it's own T1 image, but
> they did not registered very well (please see attached). I also tried to run
> skull strip to the anatomical image and reorient the functional images, but
> the results were still not good. Can any one kindly give me some suggestions
> on how to do next? Thank you very much!
>
> Sincerely,
>
> --
> Xin Di, PhD
>
> Postdoctoral Researcher
> Department of Radiology
> University of Medicine and Dentistry of New Jersey
> 30 Bergen Street, ADMC 582
> Newark, NJ 07101
>
>



--
Xin Di, PhD

Postdoctoral Researcher
Department of Radiology
University of Medicine and Dentistry of New Jersey
30 Bergen Street, ADMC 582
Newark, NJ 07101

--00221532ccd02f4158049c90f736-- ========================================================================Date: Fri, 18 Feb 2011 18:26:09 +0100 Reply-To: Javier Navas <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Javier Navas <[log in to unmask]> Subject: Parametric or categorical design MIME-Version: 1.0 Content-Type: multipart/alternative; boundaryMessage-ID: <[log in to unmask]> --00235440bd494e9ac7049c91cf71 Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Hi SPMers! I have some doubts in the analyses of fMRI data: What is the difference between the Parametric or categorical design?? and, regarding the contrast specification? And, in case you use temporal derivatives of the canonical HRF how should Ill be the contrast for a single task? thank you all!! -- /**********************************************************\ Francisco Javier Navas Snchez Laboratorio de Imagen Mdica U.M.C.E. Hospital General Universitario Gregorio Maran Dr Esquerdo 46, 28007 Madrid, Spain Phone : (+34) 91 426 50 67 Fax: (+34) 91 426 5108 e-mail:[log in to unmask] http://image.hggm.es --00235440bd494e9ac7049c91cf71 Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Hi SPMers!
I have some doubts in the analyses of fMRI data:

What is the difference between the Parametric or categorical design?? and, regarding the contrast specification?

And, in case you use temporal derivatives of the canonical HRF how should Ill be the contrast for a single task?

thank you all!!

--
/**********************************************************\
Francisco Javier Navas Snchez
Laboratorio de Imagen Mdica U.M.C.E.
Hospital General Universitario Gregorio Maran
Dr Esquerdo 46, 28007 Madrid, Spain
Phone : (+34) 91 426 50 67 Fax: (+34) 91 426 5108
e-mail:[log in to unmask] http://image.hggm.es
--00235440bd494e9ac7049c91cf71-- ========================================================================Date: Fri, 18 Feb 2011 12:51:27 -0500 Reply-To: "MCLAREN, Donald" <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: "MCLAREN, Donald" <[log in to unmask]> Subject: Re: Parametric or categorical design Comments: To: Javier Navas <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> It could be fundamentally different or it could just be in the analysis. Categorical data has no assumption about the relationship between values or conditions; whereas parametric designs assume a relationship. However, parametric designs can also be modelled like categorical data, but not vice versa. When I've done a parametric design, I've treated it like categorical data so that I don't have to assume any apriori relationship and can define the relationship from the data. If you model something parametrically, there is one column for it. Most people just look at the canonical HRF term. If you want to incorporate the derivative terms, I'd read the earlier posts from this week or last week by Jason Steffener. Best Regards, Donald McLaren ================= D.G. McLaren, Ph.D. Postdoctoral Research Fellow, GRECC, Bedford VA Research Fellow, Department of Neurology, Massachusetts General Hospital and Harvard Medical School Office: (773) 406-2464 ===================== This e-mail contains CONFIDENTIAL INFORMATION which may contain PROTECTED HEALTHCARE INFORMATION and may also be LEGALLY PRIVILEGED and which is intended only for the use of the individual or entity named above. If the reader of the e-mail is not the intended recipient or the employee or agent responsible for delivering it to the intended recipient, you are hereby notified that you are in possession of confidential and privileged information. Any unauthorized use, disclosure, copying or the taking of any action in reliance on the contents of this information is strictly prohibited and may be unlawful. If you have received this e-mail unintentionally, please immediately notify the sender via telephone at (773) 406-2464 or email. On Fri, Feb 18, 2011 at 12:26 PM, Javier Navas <[log in to unmask]> wrote: > Hi SPMers! > I have some doubts in the analyses of fMRI data: > > What is the difference between the Parametric or categorical design?? and, > regarding the contrast specification? > > And, in case you use temporal derivatives of the canonical HRF how should > Ill be the contrast for a single task? > > thank you all!! > > -- > /**********************************************************\ > Francisco Javier Navas Snchez > Laboratorio de Imagen Mdica U.M.C.E. > Hospital General Universitario Gregorio Maran > Dr Esquerdo 46, 28007 Madrid, Spain > Phone : (+34) 91 426 50 67 Fax: (+34) 91 426 5108 > e-mail:[log in to unmask] http://image.hggm.es > ========================================================================Date: Fri, 18 Feb 2011 17:58:01 +0000 Reply-To: Chris Filo Gorgolewski <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Chris Filo Gorgolewski <[log in to unmask]> Subject: Neuroimaging Data Processing Workshop 23-24 March 2011, Edinburgh, UK Comments: To: nipy-devel <[log in to unmask]>, [log in to unmask], [log in to unmask], [log in to unmask], freesurfer <[log in to unmask]>, FSL - FMRIB's Software Library <[log in to unmask]> Comments: cc: dtc-edinburgh <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=UTF-8 Message-ID: <[log in to unmask]> Dear all, I am delighted to invite you to a Neuroimaging Data Processing Workshop which will be held on 23-24th of March 2011 at University of Edinburgh, UK. During the workshop we will cover neuroimaging data analysis and management with reusable, scalable and reproducible processing workflows that combine different software packages (such as SPM, FSL, and FreeSurfer) using NiPyPE framework. The workshop will also feature talks and demos covering data management, encapsulation and visualization using PyXNAT and the Connectome Library and Viewer. More details can be found at the workshop website: http://nipype.blogspot.com Best regards, Chris Gorgolewski ========================================================================Date: Fri, 18 Feb 2011 18:29:02 +0000 Reply-To: Todd Hare <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Todd Hare <[log in to unmask]> Subject: Job Ad: Postdoctoral and PhD positions in decision-making SNS lab, University of Zurich Mime-Version: 1.0 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain Message-ID: <[log in to unmask]> Applications are invited for both PhD and postdoctoral positions at the Laboratory for Social and Neural Systems Research at the University of Zurich under the direction of Prof. Todd Hare. The projects will focus on the neurobiology and causal mechanisms of value computation and decision-making in different contexts using functional magnetic resonance imaging (fMRI) and transcranial magnetic stimulation (TMS). We are looking for candidates familiar with fMRI, TMS, neuroeconomics, and/or computational modeling approaches to decision-making. The successful candidate will join a friendly and multi-disciplinary research environment with a research-dedicated 3T scanner, TMS, TCDS, and EEG facilities and a large laboratory for conducting behavioral experiments. For details, please see www.sns.uzh.ch. The working language in the laboratory is English, but knowledge of German would be beneficial. Employment can begin immediately but is negotiable. For postdoctoral positions, initial appointment will be for 1 year with the possibility of renewal for at least two additional years. Salaries will follow Swiss National Science Foundation guidelines. Applications, including CV, names and email addresses or letter of reference from two referees, a brief statement of research experience related to the mentioned requirements and research papers should be submitted electronically to Prof. Todd Hare: [log in to unmask] The application deadline is April 1, 2011. The University of Zurich is an equal opportunity employer, and as such welcomes applications from women and minority candidates. ========================================================================Date: Fri, 18 Feb 2011 11:44:21 -0800 Reply-To: Dennis Thompson <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Dennis Thompson <[log in to unmask]> Subject: Re: MATLAB Out of Memory error Comments: To: Nero Evero <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/alternative; boundaryMessage-ID: <[log in to unmask]> --0023547c902391b159049c93bd39 Content-Type: text/plain; charset=ISO-8859-1 Window 32 bit limits you to 2 GB of memory by default . There are some tricks to boost that to 3GB as outlined by Matlab in this link http://www.mathworks.com/help/techdoc/matlab_prog/brh72ex-49.html#brh72ex-67 Here at the IRC we do all our processing on 64 bit linux computers. Have not had a "Out of memory error" in years. On Thu, Feb 17, 2011 at 7:32 PM, Nero Evero <[log in to unmask]> wrote: > Hello All, > > We are trying to run a fixed effects analysis using SPM8 on a Windows 7 > 32-bit OS with 4GM of RAM. We have 120 subjects/sessions with a total of > 6600 scans (55/session). The analysis stops during the parameter estimation > and gives the following erroe message: > > Initialising parameters : ...done > Output images : ...initialised > Plane 1/46 , block 1/3 : ...estimation??? > Out of memory. Type HELP MEMORY for your options. > > Error in ==> spm_spm at 715 > CY = CY + Y*Y'; > > Error in ==> spm_getSPM at 233 > SPM = spm_spm(SPM); > > Error in ==> spm_results_ui at 277 > [SPM,xSPM] = spm_getSPM; > > ??? Error while evaluating uicontrol Callback > > I tried adding more memory to SPM (i.e. by changing defaults.stats.maxmem > to about 2GB), but I still received the error. Looking through the archives > it seems like the common solution is to change to a 64-bit OS, but I wanted > to know if there was any other possible solutions? Thanks in adavance. > > Nero > --0023547c902391b159049c93bd39 Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable
Window 32 bit limits you to 2 GB of memory by default . There are some tricks to boost that to 3GB as outlined by Matlab in this link

http://www.mathworks.com/help/techdoc/matlab_prog/brh72ex-49.html#brh72ex-67


Here at the IRC we do all our processing on 64 bit linux computers. Have not had a "Out of memory error" in years.



On Thu, Feb 17, 2011 at 7:32 PM, Nero Evero <[log in to unmask]> wrote:
Hello All,

We are trying to run a fixed effects analysis using SPM8 on a Windows 7 32-bit OS with 4GM of RAM. We have 120 subjects/sessions with a total of 6600 scans (55/session). The analysis stops during the parameter estimation and gives the following erroe message:

Initialising parameters : ...done
Output images : ...initialised
Plane 1/46 , block 1/3 : ...estimation??? Out of memory. Type HELP MEMORY for your options.

Error in ==> spm_spm at 715
CY = CY + Y*Y';

Error in ==> spm_getSPM at 233
SPM = spm_spm(SPM);

Error in ==> spm_results_ui at 277
[SPM,xSPM] = spm_getSPM;

??? Error while evaluating uicontrol Callback

I tried adding more memory to SPM (i.e. by changing defaults.stats.maxmem to about 2GB), but I still received the error. Looking through the archives it seems like the common solution is to change to a 64-bit OS, but I wanted to know if there was any other possible solutions? Thanks in adavance.

Nero

--0023547c902391b159049c93bd39-- ========================================================================Date: Sat, 19 Feb 2011 13:38:33 +0000 Reply-To: Richard Binney <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Richard Binney <[log in to unmask]> Subject: acceptable high pass filtering MIME-Version: 1.0 Content-Type: multipart/alternative; boundary cf3043478e322880049ca2bff3 Message-ID: <[log in to unmask]> --20cf3043478e322880049ca2bff3 Content-Type: text/plain; charset=ISO-8859-1 Dear all, Somrthing has recently been said to me that has made me think, and I want to get my head around this a bit more..... At what point does high pass filtering becomes ineffective? It has not been a concern for me in the past, but recently it has been suggested to me that a rule of thumb is to set the high pass filter at a minimum of 1.5 x your longest SOA. That seems reasonable if this is equal to or less than 128secs. I say that because I beleive that this is the optimum filter setting to remove low-freq noise associated with cardiac/respiratory noise. But what if you use a filter at a lower frequency (e.g., 260secs)? It has been said to me that this would be OK. But aren't you running a risk of alliasing signal of interest at frequencies lower than 0.01Hz with cardiac/respiratory noise etc? IF this is an acceptable risk with a filter of say 260secs, at what point does it becomes unacceptable and the filter becomes ineffective? Eg., Say you had an enomrous longest SOA of 800 secs, you might want to use a filter set at 1000secs (0.001Hz) just to be sure. would this filter be effectively redundant? What other factors might speak to this? Jittered SOAs for example? Using a range of SOAs would of course spread the signal of interest across frequencies increasing sensitivity. Does this have an effect of reducing the risk of alliasing with low-freq noise or are you still losing some of your signal in the <0.1Hz frequencies (either due to noise or a 128 sec filter)? In what manner should this inform your high-pass filter? Should you be concerned with the longest SOA or the mean SOA (fundamental frequency) of your signal? Thanks in advance for your help, Richard --20cf3043478e322880049ca2bff3 Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable
Dear all,
Somrthing has recently been said to me that has made me think, and I want to get my head around this a bit more.....
At what point does high pass filtering becomes ineffective? It has not been a concern for me in the past, but recently it has been suggested to me thata rule of thumb is toset the high pass filter at a minimum of1.5 x your longest SOA. That seems reasonable if this is equal to orless than 128secs. I say that because I beleive that this is the optimum filter setting to remove low-freq noise associated with cardiac/respiratory noise. But what if you use a filter at a lower frequency (e.g., 260secs)? It has been said to me that this would be OK. But aren't you running a risk of alliasing signal of interest at frequencies lower than 0.01Hz with cardiac/respiratory noise etc? IF this is an acceptable risk with a filter of say 260secs, at what point does it becomes unacceptable and the filter becomes ineffective? Eg., Say you had an enomrous longest SOA of 800 secs, you might want to use a filter set at 1000secs(0.001Hz)just to be sure. would this filter be effectively redundant?
What other factors might speak to this? Jittered SOAs for example? Using a range of SOAs would of course spread the signal of interest across frequencies increasing sensitivity. Does this have an effect of reducing the risk of alliasing with low-freq noise or are you still losing some of your signal in the <0.1Hz frequencies (either due to noise or a 128 sec filter)? In what manner should this inform your high-pass filter? Should you be concerned with the longest SOA or the mean SOA (fundamental frequency) of your signal?
Thanks in advance for your help,
Richard
--20cf3043478e322880049ca2bff3-- ========================================================================Date: Sat, 19 Feb 2011 17:43:29 +0000 Reply-To: Klaas Enno Stephan <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Klaas Enno Stephan <[log in to unmask]> Subject: Re: DCM and global signal Comments: To: Fred Sanders <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/alternative; boundary="0-588276456-1298137409=:8431" Message-ID: <[log in to unmask]> --0-588276456-1298137409=:8431 Content-Type: text/plain; charset=utf-8 Content-Transfer-Encoding: quoted-printable Dear Fred, This reviewer seems to be referring to the problem of artificial anti-correlations in the context of global signal regression for resting state fMRI data (i.e., resting state data are sometimes orthogonalized to the global mean brain signal using the global signal as a confound regressor in a GLM, prior to the actual functional connectivity analyses). For details, see this paper by Murphy et al.: http://www.ncbi.nlm.nih.gov/pubmed/18976716 This is not an issue for DCM. DCM for fMRI is only informed about local signals (i.e., those from your regions of interest) and does not consider anything related to global brain signal (unless you manually construct an input that reflects global brain signal). Best wishes Klaas ________________________________ Von: Fred Sanders <[log in to unmask]> An: [log in to unmask] Gesendet: Freitag, den 18. Februar 2011, 15:03:32 Uhr Betreff: [SPM] DCM and global signal I recently used DCM (in SPM8) to model the connectivity between 2 brain regions. A reviewer was concerned that DCM contains a regressor for global signal and that including this regressor could introduce artificial anti-correlations. I would greatly appreciate it if someone could help me understand this. I did not think DCM used a regressor for global signal - was this done in prior versions of DCM? Or is this referring to the constant term from the first level analysis? Also, how could that introduce anti-correlations? Any thoughts? Thanks!! --0-588276456-1298137409=:8431 Content-Type: text/html; charset=utf-8 Content-Transfer-Encoding: quoted-printable
Dear Fred,

This reviewer seems to be referring to the problem of artificial anti-correlations in the context of global signal regression for resting state fMRI data (i.e., resting state data are sometimes orthogonalized to the global mean brain signal using the global signal as a confound regressor in a GLM, prior to the actual functional connectivity analyses).  For details, see this paper by Murphy et al.:
http://www.ncbi.nlm.nih.gov/pubmed/18976716

This is not an issue for DCM.  DCM for fMRI is only informed about local signals (i.e., those from your regions of interest) and does not consider anything related to global brain signal (unless you manually construct an input that reflects global brain signal).

Best wishes
Klaas





Von: Fred Sanders <[log in to unmask]>
An: [log in to unmask]
Gesendet: Freitag, den 18. Februar 2011, 15:03:32 Uhr
Betreff: [SPM] DCM and global signal

I recently used DCM (in SPM8) to model the connectivity between 2 brain regions. A reviewer was concerned that DCM contains a regressor for global signal and that including this regressor could introduce artificial anti-correlations.  I would greatly appreciate it if someone could help me understand this.  I did not think DCM used a regressor for global signal - was this done in prior versions of DCM?  Or is this referring to the constant term from the first level analysis? Also, how could that introduce anti-correlations?  

Any thoughts?


Thanks!!

--0-588276456-1298137409=:8431-- ========================================================================Date: Sun, 20 Feb 2011 02:10:46 +0000 Reply-To: Jerome Courtemanche <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Jerome Courtemanche <[log in to unmask]> Subject: SPM to Fieldtrip for ICA Mime-Version: 1.0 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain; charset="UTF-8" Message-ID: <[log in to unmask]> Hi Gurus, Here is the commands and error command. Any help greatly appreciated. D=spm_eeg_load raw=D.ftraw; D.ftraw(0); cfg=[];cfg.channel='MEG'; ic_data = ft_componentanalysis(cfg,raw); cfg.viewmode='component'; cfg.continuous='yes'; cfg.blocksize=30; cfg.channels=[1:10]; ft_databrowser(cfg,ic_data) ??? Error using ==> fetch_header at 38 trial definition is not internally consistent Error in ==> ft_databrowser at 135 hdr = fetch_header(data); ========================================================================Date: Sat, 19 Feb 2011 22:50:38 -0500 Reply-To: MP <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: MP <[log in to unmask]> Subject: SPM EEG Pre processing: Not sure if everything looks OK MIME-Version: 1.0 Content-Type: multipart/mixed; boundary cf305496b5866b64049caea6ca Message-ID: <[log in to unmask]> --20cf305496b5866b64049caea6ca Content-Type: multipart/alternative; boundary cf305496b5866b56049caea6c8 --20cf305496b5866b56049caea6c8 Content-Type: text/plain; charset=ISO-8859-1 Hi all, I am doing the TF analysis on EEG data and I see some worrisome "spots" in my rescaled TF, which translate as sharp "dips" in the waveform of averaged TF over 12-20Hz when I convert TF into image. I know that these spots could be from the noise (since it is a single subject data), but I am worried that they will influence the statistics. I have attached the ERP waveform (-200 to 2000ms), its TF representation (4-20Hz, -198-2000ms), rescaled TF (using Log rescaling, baseline=-148 to 0), and the waveform when TF is averaged over 12-20Hz range. Is it possible that since these dips are random they will not influence the results in the scalp-space considerably? Is there anything I can do to minimize these dips, like lowpass filter the ERP before doing TF? thanks for your help in advance - Muhammad --20cf305496b5866b56049caea6c8 Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Hi all,

I am doing the TF analysis on EEG data and I see some worrisome "spots" in my rescaled TF, which translate as sharp "dips" in the waveform of averaged TF over 12-20Hz when I convert TF into image. I know that these spots could be from the noise (since it is a single subject data), but I am worried that they will influence the statistics.

I have attached the ERP waveform (-200 to 2000ms), its TF representation (4-20Hz, -198-2000ms), rescaled TF (using Log rescaling, baseline=-148 to 0), and the waveform when TF is averaged over 12-20Hz range.

Is it possible that since these dips are random they will not influence the results in the scalp-space considerably? Is there anything I can do to minimize these dips, like lowpass filter the ERP before doing TF?

thanks for your help in advance

- Muhammad
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========================================================================Date: Sun, 20 Feb 2011 08:49:56 -0500 Reply-To: Steven Liu <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Steven Liu <[log in to unmask]> Subject: Conjunction analysis bug in SPM8 ? MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Message-ID: <[log in to unmask]> Dear Experts: In SPM software, using the minimum of two T maps as their conjunction without doing this for posive and negative activations separately! If within the same regions, the voxels are activated from map X, but deactivated from map Y, they are NOT conjunctive, right ? But using SPM, these voxels may be considered as conjunctive if the minimum (negative values in this case because they are always smaller than positives no matter how big or how small their absolute values ) are significant! Why we do not do positive and negative voxels separately so that we just compare voxels in the same direction (positive or negative) ?? Thank you! Steven ========================================================================Date: Sun, 20 Feb 2011 14:26:49 -0500 Reply-To: John Fredy <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: John Fredy <[log in to unmask]> Subject: medial temporal lobe roi mask MIME-Version: 1.0 Content-Type: multipart/alternative; boundaryMessage-ID: <[log in to unmask]> --0016e6d7e01e8b7aa3049cbbba86 Content-Type: text/plain; charset=ISO-8859-1 Hello all, I am using a memory encoding paradigm and I use the wfu pickatlas for roi definition but the mask seems that only covers gray matter (I use the broadmman areas 34, 35, 36 and hippocampus), and I lose too many voxels that appears active when no use roi. Exists any mask that cover all the medial temporal lobe region including white matter? Thanks in advance John Ochoa Universidad de Antioquia --0016e6d7e01e8b7aa3049cbbba86 Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Hello all,

I am using a memory encoding paradigm and I use the wfu pickatlas for roi definition but the mask seems that only covers gray matter (I use the broadmman areas 34, 35, 36 and hippocampus), and I lose too many voxels that appears active when no use roi. Exists any mask that cover all the medial temporal lobe region including white matter?

Thanks in advance

John Ochoa
Universidad de Antioquia
--0016e6d7e01e8b7aa3049cbbba86-- ========================================================================Date: Sun, 20 Feb 2011 14:20:37 -0800 Reply-To: Vladimir Bogdanov <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Vladimir Bogdanov <[log in to unmask]> Subject: Check Reg Figures SPM8 - size and arrangement MIME-Version: 1.0 Content-Type: multipart/mixed; boundary="0-1068215501-1298240437=:67343" Message-ID: <[log in to unmask]> --0-1068215501-1298240437=:67343 Content-Type: text/plain; charset=iso-8859-1 Content-Transfer-Encoding: quoted-printable Dear SPM experts, By default the size of the images in Check Reg figure does not allow to see well anatomical details (see screen1 in attachment). This can be changed manually (screen2), but those changes take time. Is there a simple way do it fast? Is it possible to change SPM settings somewhere to make the figure in the same way (different from default) every time we call Check Reg? Thank you in advance for your help, Vladimir Volodymyr Bogdanov, PhD Headache Research Unit GIGA - Neurosciences University of Liege CHU T4 +1, Sart Tilman Av de l'Hpital 1 4000 Liege, Belgium --0-1068215501-1298240437=:67343 Content-Type: image/jpeg; name="screen1.jpg" Content-Transfer-Encoding: base64 Content-Disposition: attachment; filename="screen1.jpg" /9j/4AAQSkZJRgABAQEAeAB4AAD/2wBDAAIBAQIBAQICAgICAgICAwUDAwMD AwYEBAMFBwYHBwcGBwcICQsJCAgKCAcHCg0KCgsMDAwMBwkODw0MDgsMDAz/ 2wBDAQICAgMDAwYDAwYMCAcIDAwMDAwMDAwMDAwMDAwMDAwMDAwMDAwMDAwM DAwMDAwMDAwMDAwMDAwMDAwMDAwMDAz/wAARCAHCAyADASIAAhEBAxEB/8QA HwAAAQUBAQEBAQEAAAAAAAAAAAECAwQFBgcICQoL/8QAtRAAAgEDAwIEAwUF BAQAAAF9AQIDAAQRBRIhMUEGE1FhByJxFDKBkaEII0KxwRVS0fAkM2JyggkK FhcYGRolJicoKSo0NTY3ODk6Q0RFRkdISUpTVFVWV1hZWmNkZWZnaGlqc3R1 dnd4eXqDhIWGh4iJipKTlJWWl5iZmqKjpKWmp6ipqrKztLW2t7i5usLDxMXG x8jJytLT1NXW19jZ2uHi4+Tl5ufo6erx8vP09fb3+Pn6/8QAHwEAAwEBAQEB AQEBAQAAAAAAAAECAwQFBgcICQoL/8QAtREAAgECBAQDBAcFBAQAAQJ3AAEC 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wpPwZ/0KPhj/AMFcH/xNH/Ck/Bn/AEKPhj/wVwf/ABNFFAB/wpPwZ/0KPhj/ AMFcH/xNH/Ck/Bn/AEKPhj/wVwf/ABNFFAMP+FJ+DP8AoUfDH/grg/8AiaP+ FJ+DP+hR8Mf+CuD/AOJoooAP+FJ+DP8AoUfDH/grg/8AiaP+FJ+DP+hR8Mf+ CuD/AOJoopAy34f+GHhrwprSahpfh7Q9NvxG1uLm1sIoZhE5Vmj3qoO0tGhI zglFPYV0FFFZ1Ny4/CFFFFQMKKKKACiiigAooooAKKKKACiiigAooooAKKKK ACiiigAqd5nuYNsjNIsI2RhjkIuN2B6DJJx6k+tFFVEmRHsHoPyo2D0H5UUV fQkNg9B+VGweg/Kiiop7IEGweg/KjYPQflRRVoaDYPQflTZVAQ8Dof5GiikD P//Z --0-1068215501-1298240437=:67343-- ========================================================================Date: Sun, 20 Feb 2011 22:27:16 +0000 Reply-To: Vladimir Litvak <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Vladimir Litvak <[log in to unmask]> Subject: Re: SPM EEG Pre processing: Not sure if everything looks OK Comments: To: MP <[log in to unmask]> In-Reply-To: <[log in to unmask]> Mime-Version: 1.0 (iPad Mail 8C148) Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Message-ID: <-101706040748529818@unknownmsgid> Dear Muhammad, The way one would usually do TF analysis is to apply TF to an epoched file, then average the result and then rescale. If you apply TF to an ERP which is quite noisy you'll get basically single trial TF which is noisy as well. Filtering will not help since you will either remove your frequency range of interest or not affect it. Best, Vladimir On 20 Feb 2011, at 03:51, MP <[log in to unmask]> wrote: > Hi all, > > I am doing the TF analysis on EEG data and I see some worrisome "spots" in my rescaled TF, which translate as sharp "dips" in the waveform of averaged TF over 12-20Hz when I convert TF into image. I know that these spots could be from the noise (since it is a single subject data), but I am worried that they will influence the statistics. > > I have attached the ERP waveform (-200 to 2000ms), its TF representation (4-20Hz, -198-2000ms), rescaled TF (using Log rescaling, baseline=-148 to 0), and the waveform when TF is averaged over 12-20Hz range. > > Is it possible that since these dips are random they will not influence the results in the scalp-space considerably? Is there anything I can do to minimize these dips, like lowpass filter the ERP before doing TF? > > thanks for your help in advance > > - Muhammad > > > > ========================================================================Date: Sun, 20 Feb 2011 15:53:22 -0800 Reply-To: Michael T Rubens <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Michael T Rubens <[log in to unmask]> Subject: Re: medial temporal lobe roi mask Comments: To: John Fredy <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/alternative; boundary cf30549f63930a26049cbf7571 Message-ID: <[log in to unmask]> --20cf30549f63930a26049cbf7571 Content-Type: text/plain; charset=UTF-8 try AAL, they have Hipp and Parahipp. Talarach deamon may have them too.or you can take your BA mask and dilate it. Cheers, Michael On Sun, Feb 20, 2011 at 11:26 AM, John Fredy <[log in to unmask]> wrote: > Hello all, > > I am using a memory encoding paradigm and I use the wfu pickatlas for roi > definition but the mask seems that only covers gray matter (I use the > broadmman areas 34, 35, 36 and hippocampus), and I lose too many voxels that > appears active when no use roi. Exists any mask that cover all the medial > temporal lobe region including white matter? > > Thanks in advance > > John Ochoa > Universidad de Antioquia > -- Research Associate Gazzaley Lab Department of Neurology University of California, San Francisco --20cf30549f63930a26049cbf7571 Content-Type: text/html; charset=UTF-8 Content-Transfer-Encoding: quoted-printable try AAL, they have Hipp and Parahipp. Talarach deamon may have them too.or you can take your BA mask and dilate it.

Cheers,
Michael

On Sun, Feb 20, 2011 at 11:26 AM, John Fredy <[log in to unmask]> wrote:
Hello all,

I am using a memory encoding paradigm and I use the wfu pickatlas for roi definition but the mask seems that only covers gray matter (I use the broadmman areas 34, 35, 36 and hippocampus), and I lose too many voxels that appears active when no use roi. Exists any mask that cover all the medial temporal lobe region including white matter?

Thanks in advance

John Ochoa
Universidad de Antioquia



--
Research Associate
Gazzaley Lab
Department of Neurology
University of California, San Francisco
--20cf30549f63930a26049cbf7571-- ========================================================================Date: Mon, 21 Feb 2011 00:22:19 +0000 Reply-To: Anna McCarrey <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Anna McCarrey <[log in to unmask]> Subject: Reporting stats Mime-Version: 1.0 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain; charset="UTF-8" Message-ID: <[log in to unmask]> Hi all, I have a 2x2 flexible factorial design in fMRI and wish to report main effects and the interaction. When I run the F contrast for Main effect of Group and click whole brain analysis, many voxel clusters appear. So I must follow up with t-tests to understand in which the direction the groups differ. Do I write this as: Group1 had significantly more voxel activation in the (e.g.) amygdala region than Group2 (t(64) = etc. and then report the t and p values? If there are many voxel clusters, what's the best way to set a minimum threshold? Lastly, when I run the Group x Condition interaction, no suprathreshold clusters appear - with no F statistic, how do I formally report this? Many thanks in advance. Anna ========================================================================Date: Mon, 21 Feb 2011 03:35:30 +0000 Reply-To: G Elliott Wimmer <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: G Elliott Wimmer <[log in to unmask]> Subject: Re: medial temporal lobe roi mask Mime-Version: 1.0 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain Message-ID: <[log in to unmask]> Hi, Regarding the AAL template (which is most likely what you have already seen in the WFU pickatlas), I too have noticed that the AAL hippocampus definition tries to only cover grey matter. This exclusion leads to gaps and holes in the mask that I think you are referring to. Given the anatomical variability between subjects in the hippocampus, it appears to me that the AAL mask attempts to be far too precise; moreover, it is not left-right symmetric. In the past, I have used AFNI's 'draw dataset' function to correct these problems with the AAL mask and used the resulting modified mask to define ROIs. Alternatively, I've seen probabilistic anatomical masks that I think were used in FSL, and that may be worth checking out. Best Regards, G Elliott Wimmer Dept. of Psychology Columbia University ========================================================================Date: Mon, 21 Feb 2011 11:02:28 +0000 Reply-To: Vladimir Litvak <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Vladimir Litvak <[log in to unmask]> Subject: Re: SPM to Fieldtrip for ICA Comments: To: Jerome Courtemanche <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> Dear Jerome, Since you are getting the error not in SPM but in Fieldtrip on data that has already been processed by a Fieldtrip function I suggest that you ask this question on the Fieldtrip mailing list. Just note that you don't need the D.ftraw(0) line. You could try raw=D.ftraw(0) , but that probably wouldn't help in this case. Vladimir On Sun, Feb 20, 2011 at 2:10 AM, Jerome Courtemanche <[log in to unmask]> wrote: > Hi Gurus, > > Here is the commands and error command. Any help greatly appreciated. > > D=spm_eeg_load > raw=D.ftraw; > D.ftraw(0); > cfg=[];cfg.channel='MEG'; > ic_data = ft_componentanalysis(cfg,raw); > cfg.viewmode='component'; > cfg.continuous='yes'; > cfg.blocksize=30; > cfg.channels=[1:10]; > ft_databrowser(cfg,ic_data) > > ??? Error using ==> fetch_header at 38 > trial definition is not internally consistent > > Error in ==> ft_databrowser at 135 > hdr = fetch_header(data); > ========================================================================Date: Mon, 21 Feb 2011 11:29:52 +0000 Reply-To: Poornima Kumar <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Poornima Kumar <[log in to unmask]> Subject: Realignment parameters Mime-Version: 1.0 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain Message-ID: <[log in to unmask]> Hi I have searched through the archives for info on acceptable threshold for movement in our analysis, but with no luck. Can any one suggest if we use the realignment parameters as covariates in 1st level, what is the maximum movement (translation, rotation....) that is removed by these steps? For example, if a participant has moved say 8mm and 12deg in one block, can we include the participant in the analysis, assuming that using motion regressors in 1st level has taken care of this? Any advice on this will be very helpful! Thanks Poornima ========================================================================Date: Mon, 21 Feb 2011 07:50:09 -0500 Reply-To: John Fredy <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: John Fredy Subject: Re: medial temporal lobe roi mask Comments: To: G Elliott Wimmer <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/alternative; boundaryMessage-ID: <[log in to unmask]> --001636c598d9d2363d049cca4dfb Content-Type: text/plain; charset=ISO-8859-1 Thanks Alexander, Michael and Elliot for the reply, I will see the AAL atlas and the maxprobmap more deeply. I am in the beggining in fmri in the hippocampus for epilepsy patients, so, I will have time to explore more and more in working with roi analysis. Best wishes from Antioquia On Sun, Feb 20, 2011 at 10:35 PM, G Elliott Wimmer <[log in to unmask]>wrote: > Hi, > > Regarding the AAL template (which is most likely what you have already seen > in the WFU pickatlas), I too have noticed that the AAL hippocampus > definition tries to only cover grey matter. This exclusion leads to gaps and > holes in the mask that I think you are referring to. > > Given the anatomical variability between subjects in the hippocampus, it > appears to me that the AAL mask attempts to be far too precise; moreover, it > is not left-right symmetric. In the past, I have used AFNI's 'draw dataset' > function to correct these problems with the AAL mask and used the resulting > modified mask to define ROIs. > > Alternatively, I've seen probabilistic anatomical masks that I think were > used in FSL, and that may be worth checking out. > > Best Regards, > > G Elliott Wimmer > > Dept. of Psychology > Columbia University > --001636c598d9d2363d049cca4dfb Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable
Thanks Alexander, Michael and Elliot for the reply, I will see the AAL atlas and the maxprobmap more deeply. I am in the beggining in fmri in the hippocampus for
epilepsy patients, so, I will have time to explore more and more in working with roianalysis.

Best wishes from Antioquia

On Sun, Feb 20, 2011 at 10:35 PM, G Elliott Wimmer <[log in to unmask]> wrote:
Hi,

Regarding the AAL template (which is most likely what you have already seen in the WFU pickatlas), I too have noticed that the AAL hippocampus definition tries to only cover grey matter. This exclusion leads to gaps and holes in the mask that I think you are referring to.

Given the anatomical variability between subjects in the hippocampus, it appears to me that the AAL mask attempts to be far too precise; moreover, it is not left-right symmetric. In the past, I have used AFNI's 'draw dataset' function to correct these problems with the AAL mask and used the resulting modified mask to define ROIs.

Alternatively, I've seen probabilistic anatomical masks that I think were used in FSL, and that may be worth checking out.

Best Regards,

G Elliott Wimmer

Dept. of Psychology
Columbia University

--001636c598d9d2363d049cca4dfb-- ========================================================================Date: Mon, 21 Feb 2011 13:16:01 +0000 Reply-To: Joseph Whittaker <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Joseph Whittaker <[log in to unmask]> Subject: SPM functions for BMS MIME-Version: 1.0 Content-Type: multipart/alternative; boundaryMessage-ID: <[log in to unmask]> --0016e65a09c0517a27049ccaaab5 Content-Type: text/plain; charset=ISO-8859-1 Dear DCMers I am doing BMS with families of models, which is easy using the DCM GUI in SPM8, but I like to write a script to speed up the process. This is because I will be doing it multiple times and would like to save the results into one file. Is there anyone who has done anything similar who can tell me what the relevant functions are and how they relate to one another? Thank you. Regards Joe -- Joseph Whittaker, M.Sc Ph.D Student G.803 Neuroscience and Psychiatry Unit Stopford Building University of Manchester Oxford Road Manchester, UK --0016e65a09c0517a27049ccaaab5 Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable
Dear DCMers

I am doing BMS with families of models, which is easy using the DCM GUI in SPM8, but I like to write a script to speed up the process. This is because I will be doing it multiple times and would like to save the results into one file.

Is there anyone who has done anything similar who can tell me what the relevant functions are and how they relate to one another? Thank you.

Regards

Joe

--
Joseph Whittaker, M.Sc
Ph.D Student
G.803 Neuroscience and Psychiatry Unit
Stopford Building
University of Manchester
Oxford Road
Manchester, UK
--0016e65a09c0517a27049ccaaab5-- ========================================================================Date: Mon, 21 Feb 2011 14:16:56 +0100 Reply-To: Marko Wilke <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Marko Wilke <[log in to unmask]> Subject: Re: Realignment parameters Comments: To: Poornima Kumar <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1; format=flowed Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> Hi Poornima, > I have searched through the archives for info on acceptable threshold for movement in our analysis, but with no luck. This is because no-one really knows for sure. There is a rule of thumb that "motion exceeding one voxel size" may be bad, but then again, cannot see that from the realignment parameters as you will have to combine translations and rotations. See the toolbox by Paul Mazaika for an approach that does that for you. There also likely is no fixed number as I guess it would depend on your data, paradigm, sequence... > Can any one suggest if we use the realignment parameters as covariates in 1st level, what is the maximum movement (translation, rotation....) that is removed by these steps? This question I believe cannot be answered, as you do not remove motion, but the additional variance associated with it. See Friston et al., 1996, or Johnstone et al., 2006, for some hints. > For example, if a participant has moved say 8mm and 12deg in one block, can we include the participant in the analysis, assuming that using motion regressors in 1st level has taken care of this? I am used to working with children, but 8 mm and 12 degrees is massive motion even in my book. I would not expect the realignment parameters to "take care" of this. Cheers, Marko -- ____________________________________________________ PD Dr. med. Marko Wilke Facharzt fr Kinder- und Jugendmedizin Leiter, Experimentelle Pdiatrische Neurobildgebung Universitts-Kinderklinik Abt. III (Neuropdiatrie) Marko Wilke, MD, PhD Pediatrician Head, Experimental Pediatric Neuroimaging University Children's Hospital Dept. III (Pediatric Neurology) Hoppe-Seyler-Str. 1 D - 72076 Tbingen, Germany Tel. +49 7071 29-83416 Fax +49 7071 29-5473 [log in to unmask] http://www.medizin.uni-tuebingen.de/kinder/epn ____________________________________________________ ========================================================================Date: Mon, 21 Feb 2011 16:07:40 +0000 Reply-To: "Veena A. Nair" <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: "Veena A. Nair" <[log in to unmask]> Subject: PostDoctoral Job Announcement - University of Wisconsin-Madison Mime-Version: 1.0 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain; charset="UTF-8" Message-ID: <[log in to unmask]> Hello All, posting this on behalf of the neuroimaging lab at UW-Madison: "postdoctoral traineeships in the Computation and Informatics in Biology and Medicine (CIBM) Training Program, funded by the NLM Grant 5T15LM007359" see complete announcement below:- ------------------------------------------------------------------------------------------------------------------ PostDoctoral Job Announcement University of Wisconsin-Madison University of Wisconsin-Madison HERI & WIMR Radiology are currently recruiting a post-doctoral fellow or research associate interested in characterizing brain abnormalities affecting cognitive, affective & sensory processes, in psychiatric, neurological (Stroke, Epilepsy) and neurosurgical populations(Tumor and Vascular lesions). The individual will have access to a state-of the-art 3T MRI, 19 HD-EEG machines as part of World's largest Sleep Center, TMS, neurophysiology bioinstrumentation at HERI as well as state-of the-art MRI and PET systems in Radiology, WIMR, and at the Waismann Center Keck Lab. The fellow will work as part of a multidisciplinary team of Psychologists, Neuroscientists, Neurologists, Psychiatrists, Neuroradiologists, Engineers & Medical Physicists integrating findings from a broad spectrum of approaches including: - resting state functional MRI - task-based functional MRI - DTI, MRS, Perfusion imaging, HYPR-VIPR MRA - Cortical Thinning, VBM - Brain-Computer Interface - Multimodal approach: Awake EEG/ERP and Sleep EEG, PET, TMS Minimum qualifications for a successful candidate include - Must be a US Citizen or Permanent Resident to apply. - completed MD and/or PhD in Cognitive neuroscience/psychology, Statistics, Computer Science, Engineering, or Medical Physics or other equivalent background - significant prior neuroimaging experience with functional MRI/EEG/TMS, strong skills in usage of one or more common functional neuroimaging (FSL, SPM, AFNI), programming experience in Matlab, C/C++ or similar platform are all plusses, but not required. postdoctoral traineeships in the Computation and Informatics in Biology and Medicine (CIBM) Training Program, funded by the NLM Grant 5T15LM007359. The postdoctoral traineeship is for a one- to -two-year period. One is to begin by June, 2011, and the other to begin Summer 2011 or later. (The last year is contingent on renewal of the NLM Grant supporting the CIBM Training Program.) These traineeships are designed for cross-disciplinary training - the candidate will have a secondary mentor in addition to the primary mentor (one from computational / informatics areas, and the other from biological areas). How to apply: Please email CV and 3 references to [log in to unmask] Vivek Prabhakaran M.D., Ph.D. (Stanford Neurosciences, 2001) Assistant Professor, Director of Functional Neuroimaging in Radiology Board-Certified Neurologist, Radiologist, & Neuroradiologist (Johns Hopkins,2008) University of Wisconsin Health Hospital and Clinics Department of Radiology 600 Highland Avenue Madison, WI 53792 Office: 608-265-5269 Office: 608-232-3343 Feel free to contact with any questions prior to applying for the position. For more information about HERI & WIMR Radiology, please visit us at http://healthemotions.org// or http://ntp.neuroscience.wisc.edu/faculty/prabhakaran.html http://www.radiology.wisc.edu/research/neuroimagingLab/index.php ========================================================================Date: Mon, 21 Feb 2011 16:27:39 +0000 Reply-To: Molly Crockett <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Molly Crockett <[log in to unmask]> Subject: ArtRepair and Realign-Unwarp Mime-Version: 1.0 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain Message-ID: <[log in to unmask]> Hello, I'm looking into using the ArtRepair toolbox to deal with motion-related artifacts in a couple of subjects. My study is a repeated-measures pharmacological design, and I don't want to have to exclude subjects that only moved in one of the sessions. I see from the ArtRepair documentation that detecting and repairing bad volumes should take place after realignment. On my non-moving subjects, I've used the Realign & Unwarp procedure, and I'd like to keep things consistent across subjects. Is it reasonable to use ArtRepair on images that have been realigned & unwarped? Or is ArtRepair only valid for use on images that have been realigned without unwarping? Thanks, Molly ========================================================================Date: Mon, 21 Feb 2011 11:39:14 -0500 Reply-To: "MCLAREN, Donald" <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: "MCLAREN, Donald" <[log in to unmask]> Subject: Re: Realignment parameters Comments: To: Marko Wilke <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> Additionally, You could exclude TR-to-TR motion that is excessive, by adding a column of a single 1 in the design matrix for each bad point, but again there is no standard for a bad point. We've used .75mm translation and 1 degree rotation. In summary, if you have 5 bad points, then you will have 5 columns added to your design matrix. As a side note to the above procedure, the question arises as to how many bad points are allowable in a single session. We have excluded runs that have greater than 10-15% bad points. Finally, neither motion correction nor motion parameters can correct for within TR motion, so data inspection is also necessary to make sure there is no motion artifacts. We usually check the ResMS, spmT, and beta images. One can also inspect the raw EPI data for artifacts as well. Best Regards, Donald McLaren ================= D.G. McLaren, Ph.D. Postdoctoral Research Fellow, GRECC, Bedford VA Research Fellow, Department of Neurology, Massachusetts General Hospital and Harvard Medical School Office: (773) 406-2464 ===================== This e-mail contains CONFIDENTIAL INFORMATION which may contain PROTECTED HEALTHCARE INFORMATION and may also be LEGALLY PRIVILEGED and which is intended only for the use of the individual or entity named above. If the reader of the e-mail is not the intended recipient or the employee or agent responsible for delivering it to the intended recipient, you are hereby notified that you are in possession of confidential and privileged information. Any unauthorized use, disclosure, copying or the taking of any action in reliance on the contents of this information is strictly prohibited and may be unlawful. If you have received this e-mail unintentionally, please immediately notify the sender via telephone at (773) 406-2464 or email. On Mon, Feb 21, 2011 at 8:16 AM, Marko Wilke <[log in to unmask]> wrote: > Hi Poornima, > >> I have searched through the archives for info on acceptable threshold for >> movement in our analysis, but with no luck. > > This is because no-one really knows for sure. There is a rule of thumb that > "motion exceeding one voxel size" may be bad, but then again, cannot see > that from the realignment parameters as you will have to combine > translations and rotations. See the toolbox by Paul Mazaika for an approach > that does that for you. There also likely is no fixed number as I guess it > would depend on your data, paradigm, sequence... > >> Can any one suggest if we use the realignment parameters as covariates in >> 1st level, what is the maximum movement (translation, rotation....) that is >> removed by these steps? > > This question I believe cannot be answered, as you do not remove motion, but > the additional variance associated with it. See Friston et al., 1996, or > Johnstone et al., 2006, for some hints. > >> For example, if a participant has moved say 8mm and 12deg in one block, >> can we include the participant in the analysis, assuming that using motion >> regressors in 1st level has taken care of this? > > I am used to working with children, but 8 mm and 12 degrees is massive > motion even in my book. I would not expect the realignment parameters to > "take care" of this. > > Cheers, > Marko > -- > ____________________________________________________ > PD Dr. med. Marko Wilke > Facharzt fr Kinder- und Jugendmedizin > Leiter, Experimentelle Pdiatrische Neurobildgebung > Universitts-Kinderklinik > Abt. III (Neuropdiatrie) > > > Marko Wilke, MD, PhD > Pediatrician > Head, Experimental Pediatric Neuroimaging > University Children's Hospital > Dept. III (Pediatric Neurology) > > > Hoppe-Seyler-Str. 1 > D - 72076 Tbingen, Germany > Tel. +49 7071 29-83416 > Fax +49 7071 29-5473 > [log in to unmask] > > http://www.medizin.uni-tuebingen.de/kinder/epn > ____________________________________________________ > ========================================================================Date: Mon, 21 Feb 2011 11:47:22 -0500 Reply-To: "MCLAREN, Donald" <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: "MCLAREN, Donald" <[log in to unmask]> Subject: Re: Reporting stats Comments: To: Anna McCarrey <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> (1) The main effect of group is inflated in your model. To test the main effect of group properly, you need to average your conditions and then compute a model using the averages. If you only have two groups, I'd skip the F-test and just do the T-test. (2) If you have more than 2 groups, you need to do post-hoc t-tests. I would say that the had greater activation rather than more voxel as more voxel seems to imply extent, which isn't being tested. (3) For the interaction, make sure you have subject in your model and in the design matrix. If you still get no significant results, you can say that the interaction was not statistically significant or no voxels passed the significance threshold. (4) There are a number of ways to determine thresholds. Personally, I like using AlphaSim in AFNI if possible. For exploratory analysis, you can lower the voxel extent criteria a bit. In general, most studies use p<0.001. Best Regards, Donald McLaren ================= D.G. McLaren, Ph.D. Postdoctoral Research Fellow, GRECC, Bedford VA Research Fellow, Department of Neurology, Massachusetts General Hospital and Harvard Medical School Office: (773) 406-2464 ===================== This e-mail contains CONFIDENTIAL INFORMATION which may contain PROTECTED HEALTHCARE INFORMATION and may also be LEGALLY PRIVILEGED and which is intended only for the use of the individual or entity named above. If the reader of the e-mail is not the intended recipient or the employee or agent responsible for delivering it to the intended recipient, you are hereby notified that you are in possession of confidential and privileged information. Any unauthorized use, disclosure, copying or the taking of any action in reliance on the contents of this information is strictly prohibited and may be unlawful. If you have received this e-mail unintentionally, please immediately notify the sender via telephone at (773) 406-2464 or email. On Sun, Feb 20, 2011 at 7:22 PM, Anna McCarrey <[log in to unmask]> wrote: > Hi all, > > I have a 2x2 flexible factorial design in fMRI and wish to report main effects and the interaction. > > When I run the F contrast for Main effect of Group and click whole brain analysis, many voxel clusters appear. So I must follow up with t-tests to understand in which the direction the groups differ. Do I write this as: Group1 had significantly more voxel activation in the (e.g.) amygdala region than Group2 (t(64) = etc. and then report the t and p values? > If there are many voxel clusters, what's the best way to set a minimum threshold? > > Lastly, when I run the Group x Condition interaction, no suprathreshold clusters appear - with no F statistic, how do I formally report this? > > Many thanks in advance. > > Anna > ========================================================================Date: Mon, 21 Feb 2011 18:22:01 +0100 Reply-To: Alexander Hammers <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Alexander Hammers <[log in to unmask]> Subject: Re: Anatomical Regions Comments: To: Carlton CHU <[log in to unmask]> Comments: cc: "Prof. Dr. Robert Turner" <[log in to unmask]> In-Reply-To: <[log in to unmask]> Mime-Version: 1.0 (Apple Message framework v1082) Content-Type: multipart/alternative; boundary=Apple-Mail-7-26658180 Message-ID: <[log in to unmask]> --Apple-Mail-7-26658180 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain; charset=windows-1252 Dear Carlton, Thanks and sorry about the delay in getting back to you. I don't think there is a right or wrong in the choice of probabilistic or maximum probability resources - as long of course as you avoid population inferences based on single brains or hemispheres ;-). Re: numbers: For healthy controls, there is probably not that much to be gained after averaging of say 15-20 or so datasets in MNI space. The boundaries of the Jlich maps at n=10 can be a bit rough; visually the maxprobmaps didn't change that much after about n=15 (Figure 1 in Hammers, Allom et al. 2003). This will depend a bit on the region, too - compare the more or less invariant basal ganglia (Ahsan et al. 2007) with a cortical region, e.g. the inferior frontal gyrus (Hammers, Chen et al. 2007; Amunts K et al. 1999). After that many datasets, there is also increasingly less (but still some) gain from multi-atlas propagation and label fusion in individual space (Fig. 5 in Heckemann RA et al. 2006; see also Aljabar P et al. 2009). However, large atlas sets may be more important with very large age ranges and/or pathology; well-done intermediate propagations steps (Wolz R et al., LEAP, NI 2010) are another option for anatomically segmenting individual MRIs. I need to stop expanding to Simon Warfield's STAPLE, Louis Collins' work, etc., because you wanted a pragmatic answer and not a review on atlasing! Pragmatically I would check out the regions you are interested in (are they available?), and compare the protocols and distributions for those. One major difference between the Loni and our maps is the number of people drawing and checking the regions; one would expect systematic differences but I haven't checked. Depending on your research question cytoarchitectonic fields may be more important (in which case the Jlich maps are for you), or macroscopic landmarks (in which case LONI's or our maps may be more appropriate). Bob Turner sent me a mail off-list after the recent discussion and correctly pointed out that in vivo cytoarchitectonic mapping is possible in principle, too (e.g. Geyer S et al. Frontiers in Human Neuroscience, in press) - the examples for the moment are mainly V1 / Brodmann 17 and some other primary areas at 7T, but SNR keeps increasing. Then there's of course also folding, connectivity, etc. etc. (Fischl, Behrens,...). Happy mapping, and I hope the brief comments above are useful. WBW, Alexander ----------------------------- Alexander Hammers, MD PhD Chair in Functional Neuroimaging Neurodis Foundation http://www.fondation-neurodis.org/ Postal Address: CERMEP Imagerie du Vivant Hpital Neurologique Pierre Wertheimer 59 Boulevard Pinel, 69003 Lyon, France Telephone +33-(0)4-72 68 86 34 Fax +33-(0)4-72 68 86 10 Email [log in to unmask];[log in to unmask] --------------------------------- Other affiliations: Visiting Reader; Honorary Consultant Neurologist Division of Neuroscience and Mental Health, Faculty of Medicine Imperial College London, UK --------------------------------- Honorary Reader in Neurology; Honorary Consultant Neurologist Department of Clinical and Experimental Epilepsy National Hospital for Neurology and Neurosurgery/ Institute of Neurology, University College London, UK On 6 Feb 2011, at 04:51, Carlton CHU wrote: > Dear Alexander: > > In your opinion, how does LPBA40 (http://www.loni.ucla.edu/~shattuck/resources/lpba40/) compare with the n30r83? LPBA40 only has 56 structures, but it was constructed from 10 more subjects. It seems both n30r83 and LPBA40 have maximum probability maps. > > I do not want to get into the details of comparing those two templates. As a user, I just want to choose one template to mask regions in my fMRI data. Any suggestions? > > Best, > Carlton > > On Sat, Feb 5, 2011 at 2:56 PM, Alexander Hammers <[log in to unmask]> wrote: > Dear Steffie, > > > Brodmann areas are histological entities; you can therefore only really get to them via histology. There is a long-term initiative under way in Jlich, Germany to provide such maps via histological workup of ten brains and spatial transfer to MNI space - see http://www.fz-juelich.de/inm/inm-1/index.php?index=396 and papers by Zilles K, Amunts K, Eickhoff E et al. > > They are great but don't exist for all areas. > > The next best thing is to define your regions based on multiple brains. The good news is that for major sulci, there is, on average, actually a reasonable correspondence between histology and macroscopic landmarks (which you can see on MRI), see e.g. Figure 6 in Hammers A et al. Hum Brain Mapp 2007. > > One such atlas is our maximum probability map in MNI space (Hammers A, Allom R et al. Hum Brain Mapp 2003; since then expanded to include 83 regions and now based on 30 brains (n30r83; see Gousias IS et al. Neuroimage 2008 for the additional region definitions)), which you can get by agreeing to a one-page free academic licence (attached). > > There are many more atlases based on _single_ brains, including AAL (Tzourio-Mazoyer et al. 2002); our earlier segmentation of the same brain (Hammers et al. 2002); and digitalized versions based on the single Talairach hemisphere (minus cerebellum) (e.g. WFU Pickatlas). However, single brain / hemisphere atlases are by definition not representative and are therefore not likely to well represent your subject under study. This can be, and has been, quantified for AAL and PickAtlas versus the maximum probability map (Rodionov R et al.Magn Reson Imaging 2009). > > The most exhaustive quantification of the errors involved in single subject atlasing is in Heckemann RA et al. Neuroimage 2006. In terms of spatial overlap, for single atlases, you loose five Dice index points compared to the maxprobmap. You'd need to train a student for several months to improve that much, and by using a maximum probabilty map you get the same improvement for free :-). > > Obviously there are other more involved and more accurate forms of atlasing (see e.g. Heckemann RA et al. Neuroimage 2010 for one example and a review), but for working in MNI space with low-res techniques (fMRI, PET, SPECT, MEG, etc.) I think maxprobmaps are an excellent compromise. > > Hope this helps, > > ATB, A > PS: If you want the n30r83 maxprobmap, just email me off-list if the licence is acceptable to you (it essentially asks to cite our work and not use it commercially). > > > On 4 Feb 2011, at 19:38, Michael T Rubens wrote: > >> WFU pickatlas >> >> http://fmri.wfubmc.edu/software/PickAtlas >> >> cheers, >> Michael >> >> On Fri, Feb 4, 2011 at 10:30 AM, Steffie Tomson <[log in to unmask]> wrote: >> Hi Everyone >> >> >> Id like to pull BOLD data from a set of anatomical regions. For example, Id like to look at traces in the anterior cingulate or the left ITG. Does anyone know how to find a database of MNI-normalized anatomical regions like this? Ideally, somewhere to download individual masks for anatomical regions, or even Brodmanns areas? >> >> >> Thanks so much, >> >> Steffie >> >> >> >> >> >> -- >> Research Associate >> Gazzaley Lab >> Department of Neurology >> University of California, San Francisco > > > > --Apple-Mail-7-26658180 Content-Type: multipart/related; type="text/html"; boundary=Apple-Mail-8-26658180 --Apple-Mail-8-26658180 Content-Transfer-Encoding: quoted-printable Content-Type: text/html; charset=windows-1252 Dear Carlton,


Thanks and sorry about the delay in getting back to you.

I don't think there is a right or wrong in the choice of probabilistic or maximum probability resources - as long of course as you avoid population inferences based on single brains or hemispheres ;-).

Re: numbers: For healthy controls, there is probably not that much to be gained after averaging of say 15-20 or so datasets in MNI space. The boundaries of the Jlich maps at n=10 can be a bit rough; visually the maxprobmaps didn't change that much after about n=15 (Figure 1 in Hammers, Allom et al. 2003). This will depend a bit on the region, too - compare the more or less invariant basal ganglia (Ahsan et al. 2007) with a cortical region, e.g. the inferior frontal gyrus (Hammers, Chen et al. 2007; Amunts K et al. 1999). After that many datasets, there is also increasingly less (but still some) gain from multi-atlas propagation and label fusion in individual space (Fig. 5 in Heckemann RA et al. 2006; see also Aljabar P et al. 2009). However, large atlas sets may be more important with very large age ranges and/or pathology; well-done intermediate propagations steps (Wolz R et al., LEAP, NI 2010) are another option for anatomically segmenting individual MRIs. I need to stop expanding to Simon Warfield's STAPLE,  Louis Collins' work, etc., because you wanted a pragmatic answer and not a review on atlasing!

Pragmatically I would check out the regions you are interested in (are they available?), and compare the protocols and distributions for those. One major difference between the Loni and our maps is the number of people drawing and checking the regions; one would expect systematic differences but I haven't checked. Depending on your research question cytoarchitectonic fields may be more important (in which case the Jlich maps are for you), or macroscopic landmarks (in which case LONI's or our maps may be more appropriate).

Bob Turner sent me a mail off-list after the recent discussion and correctly pointed out that in vivo cytoarchitectonic mapping is possible in principle, too (e.g. Geyer S et al. Frontiers in Human Neuroscience, in press) - the examples for the moment are mainly V1 / Brodmann 17 and some other primary areas at 7T, but SNR keeps increasing.

Then there's of course also folding, connectivity, etc. etc. (Fischl, Behrens,...).

Happy mapping, and I hope the brief comments above are useful.

WBW,

Alexander



-----------------------------
Alexander Hammers, MD PhD





Chair in Functional Neuroimaging
Neurodis Foundation
http://www.fondation-neurodis.org/
Postal Address:
CERMEP Imagerie du Vivant
Hpital Neurologique Pierre Wertheimer
59 Boulevard Pinel, 69003 Lyon, France

Telephone +33-(0)4-72 68 86 34
Fax +33-(0)4-72 68 86 10
Email [log in to unmask];[log in to unmask]
---------------------------------
Other affiliations:

Visiting Reader; Honorary Consultant Neurologist
Division of Neuroscience and Mental Health, Faculty of Medicine
Imperial College London, UK
---------------------------------
Honorary Reader in Neurology; Honorary Consultant Neurologist
Department of Clinical and Experimental Epilepsy
National Hospital for Neurology and Neurosurgery/ Institute of Neurology, University College London, UK




On 6 Feb 2011, at 04:51, Carlton CHU wrote:

Dear Alexander:

In your opinion, how does LPBA40 (http://www.loni.ucla.edu/~shattuck/resources/lpba40/) compare with the n30r83? LPBA40 only has 56 structures, but it was constructed from 10 more subjects. It seems both n30r83 and LPBA40 have maximum probability maps. 

I do not want to get into the details of comparing those two templates. As a user, I just want to choose one template to mask regions in my fMRI data. Any suggestions?

Best,
Carlton

On Sat, Feb 5, 2011 at 2:56 PM, Alexander Hammers <[log in to unmask]> wrote:
Dear Steffie,


Brodmann areas are histological entities; you can therefore only really get to them via histology. There is a long-term initiative under way in Jlich, Germany to provide such maps via histological workup of ten brains and spatial transfer to MNI space - see http://www.fz-juelich.de/inm/inm-1/index.php?index=396 and papers by Zilles K, Amunts K, Eickhoff E et al.

They are great but don't exist for all areas.

The next best thing is to define your regions based on multiple brains. The good news is that for major sulci, there is, on average, actually a reasonable correspondence between histology and macroscopic landmarks (which you can see on MRI), see e.g. Figure 6 in Hammers A et al. Hum Brain Mapp 2007.

One such atlas is our maximum probability map in MNI space (Hammers A, Allom R et al. Hum Brain Mapp 2003; since then expanded to include 83 regions and now based on 30 brains (n30r83; see Gousias IS et al. Neuroimage 2008 for the additional region definitions)), which you can get by agreeing to a one-page free academic licence (attached).

There are many more atlases based on _single_ brains, including AAL (Tzourio-Mazoyer et al. 2002); our earlier segmentation of the same brain (Hammers et al. 2002); and digitalized versions based on the single Talairach hemisphere (minus cerebellum) (e.g. WFU Pickatlas). However, single brain / hemisphere atlases are by definition not representative and are therefore not likely to well represent your subject under study. This can be, and has been, quantified for AAL and PickAtlas versus the maximum probability map (Rodionov R et al.Magn Reson Imaging 2009).

The most exhaustive quantification of the errors involved in single subject atlasing is in Heckemann RA et al. Neuroimage 2006. In terms of spatial overlap, for single atlases, you loose five Dice index points compared to the maxprobmap. You'd need to train a student for several months to improve that much, and by using a maximum probabilty map you get the same improvement for free :-).

Obviously there are other more involved and more accurate forms of atlasing (see e.g. Heckemann RA et al. Neuroimage 2010 for one example and a review), but for working in MNI space with low-res techniques (fMRI, PET, SPECT, MEG, etc.) I think maxprobmaps are an excellent compromise.

Hope this helps,

ATB, A
PS: If you want the n30r83 maxprobmap, just email me off-list if the licence is acceptable to you (it essentially asks to cite our work and not use it commercially).


On 4 Feb 2011, at 19:38, Michael T Rubens wrote:

WFU pickatlas


cheers,
Michael

On Fri, Feb 4, 2011 at 10:30 AM, Steffie Tomson <[log in to unmask]> wrote:

Hi Everyone

 

Id like to pull BOLD data from a set of anatomical regions.  For example, Id like to look at traces in the anterior cingulate or the left ITG.  Does anyone know how to find a database of MNI-normalized anatomical regions like this?  Ideally, somewhere to download individual masks for anatomical regions, or even Brodmanns areas?

 

Thanks so much,

Steffie

 



-- 
Research Associate
Gazzaley Lab
Department of Neurology
University of California, San Francisco




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Just a comment on two of the points made - 1. I don't think the AAL mask is trying to be "too precise", rather the contrary: I've just measured the AAL hippocampi and they weigh in at a hefty ~7,500mm^3. Ok, they're in Colin Holmes / MNI space which is about 35% (Ashburner et al. 1997) to 46% (Hammers, Allom et al. 2003) bigger than average, but still they're big - as partly explained by the protocol (Tzourio-Mazoyer et al. 2002). For comparison, our protocol (Niemann K et al. 2000) yields volumes of about 2100mm^3 in native space and 3300mm^3 in MNI space (Hammers, Allom et al. 2003); they are the volumes that went into the maxprobmap in MNI space recently discussed here. There are reviews/overviews of protocols and differences (e.g. Konrad C et al. 2009). If a "GM only" mask bothers you, you can always get rid of the "holes" with simple morphological operations - e.g. by smoothing say with a 4mm kernel and then thresholding back. Obviously if you loose many voxels, your activation may not be in the hippocampus at all - which might also be interesting. 2. "moreover, it's not left-right symmetric": Well, why would it be? The physiological R>L asymmetry is well known (e.g. Pedraza O et al. 2004), certainly depends a bit on protocols, but should probably be around 5-12%; personally I use its detection as a rough indicator of the quality/plausability of a delineation protocol. In the case of AAL, it's present but a bit small at 1.5% (remember this is an atlas based on a _single_subject_). Ignoring the physiological asymmetry is in my view dangerous, especially when clinical decisions are at stake, as for example in epilepsy surgery (see Hammers et al. NI 2007 for a discussion with example). The only instance when hippocampi would be expected to be symmetrical is when only _one_hemisphere_ is available and then mirrored, as in the Talairach atlas (and derivatives). But of course that carries no information about physiological asymmetry. Hope this helps, Best wishes, Alexander ----------------------------- Alexander Hammers, MD PhD Chair in Functional Neuroimaging Neurodis Foundation http://www.fondation-neurodis.org/ Postal Address: CERMEP Imagerie du Vivant Hpital Neurologique Pierre Wertheimer 59 Boulevard Pinel, 69003 Lyon, France Telephone +33-(0)4-72 68 86 34 Fax +33-(0)4-72 68 86 10 Email [log in to unmask];[log in to unmask] --------------------------------- Other affiliations: Visiting Reader; Honorary Consultant Neurologist Division of Neuroscience and Mental Health, Faculty of Medicine Imperial College London, UK --------------------------------- Honorary Reader in Neurology; Honorary Consultant Neurologist Department of Clinical and Experimental Epilepsy National Hospital for Neurology and Neurosurgery/ Institute of Neurology, University College London, UK On 21 Feb 2011, at 13:50, John Fredy wrote: > Thanks Alexander, Michael and Elliot for the reply, I will see the AAL atlas and the maxprobmap more deeply. I am in the beggining in fmri in the hippocampus for > epilepsy patients, so, I will have time to explore more and more in working with roi analysis. > > Best wishes from Antioquia > > On Sun, Feb 20, 2011 at 10:35 PM, G Elliott Wimmer <[log in to unmask]> wrote: > Hi, > > Regarding the AAL template (which is most likely what you have already seen in the WFU pickatlas), I too have noticed that the AAL hippocampus definition tries to only cover grey matter. This exclusion leads to gaps and holes in the mask that I think you are referring to. > > Given the anatomical variability between subjects in the hippocampus, it appears to me that the AAL mask attempts to be far too precise; moreover, it is not left-right symmetric. In the past, I have used AFNI's 'draw dataset' function to correct these problems with the AAL mask and used the resulting modified mask to define ROIs. > > Alternatively, I've seen probabilistic anatomical masks that I think were used in FSL, and that may be worth checking out. > > Best Regards, > > G Elliott Wimmer > > Dept. of Psychology > Columbia University > --Apple-Mail-10-26904456 Content-Type: multipart/related; type="text/html"; boundary=Apple-Mail-11-26904457 --Apple-Mail-11-26904457 Content-Transfer-Encoding: quoted-printable Content-Type: text/html; charset=windows-1252 Dear John, Elliott,


Thanks. Just a comment on two of the points made  - 

1. I don't think the AAL mask is trying to be "too precise", rather the contrary: I've just measured the AAL hippocampi and they weigh in at a hefty ~7,500mm^3. Ok, they're in Colin Holmes / MNI space which is about 35% (Ashburner et al. 1997) to 46% (Hammers, Allom et al. 2003) bigger than average, but still they're big - as partly explained by the protocol (Tzourio-Mazoyer et al. 2002). For comparison, our protocol (Niemann K et al. 2000) yields volumes of about 2100mm^3 in native space and 3300mm^3 in MNI space (Hammers, Allom et al. 2003); they are the volumes that went into the maxprobmap in MNI space recently discussed here. There are reviews/overviews of protocols and differences (e.g. Konrad C et al. 2009).

If a "GM only" mask bothers you, you can always get rid of the "holes" with simple morphological operations - e.g. by smoothing say with a 4mm kernel and then thresholding back. Obviously if you loose many voxels, your activation may not be in the hippocampus at all - which might also be interesting.


2. "moreover, it's not left-right symmetric": Well, why would it be? The physiological R>L asymmetry is well known (e.g. Pedraza O et al. 2004), certainly depends a bit on protocols, but should probably be around 5-12%; personally I use its detection as a rough indicator of the quality/plausability of a delineation protocol. In the case of AAL, it's present but a bit small at 1.5% (remember this is an atlas based on a _single_subject_). Ignoring the physiological asymmetry is in my view dangerous, especially when clinical decisions are at stake, as for example in epilepsy surgery (see Hammers et al. NI 2007 for a discussion with example).
The only instance when hippocampi would be expected to be symmetrical is when only _one_hemisphere_ is available and then mirrored, as in the Talairach atlas (and derivatives). But of course that carries no information about physiological asymmetry.

Hope this helps,

Best wishes,

Alexander





-----------------------------
Alexander Hammers, MD PhD





Chair in Functional Neuroimaging
Neurodis Foundation
http://www.fondation-neurodis.org/
Postal Address:
CERMEP Imagerie du Vivant
Hpital Neurologique Pierre Wertheimer
59 Boulevard Pinel, 69003 Lyon, France

Telephone +33-(0)4-72 68 86 34
Fax +33-(0)4-72 68 86 10
Email [log in to unmask];[log in to unmask]
---------------------------------
Other affiliations:

Visiting Reader; Honorary Consultant Neurologist
Division of Neuroscience and Mental Health, Faculty of Medicine
Imperial College London, UK
---------------------------------
Honorary Reader in Neurology; Honorary Consultant Neurologist
Department of Clinical and Experimental Epilepsy
National Hospital for Neurology and Neurosurgery/ Institute of Neurology, University College London, UK




On 21 Feb 2011, at 13:50, John Fredy wrote:

Thanks Alexander, Michael and Elliot for the reply, I will see the AAL atlas and the  maxprobmap more deeply. I am in the beggining in fmri in the hippocampus for 
epilepsy patients, so, I will have time to explore more and more in working with roi analysis.

Best wishes from Antioquia

On Sun, Feb 20, 2011 at 10:35 PM, G Elliott Wimmer <[log in to unmask]> wrote:
Hi,

Regarding the AAL template (which is most likely what you have already seen in the WFU pickatlas), I too have noticed that the AAL hippocampus definition tries to only cover grey matter. This exclusion leads to gaps and holes in the mask that I think you are referring to.

Given the anatomical variability between subjects in the hippocampus, it appears to me that the AAL mask attempts to be far too precise; moreover, it is not left-right symmetric.  In the past, I have used AFNI's 'draw dataset' function to correct these problems with the AAL mask and used the resulting modified mask to define ROIs.

Alternatively, I've seen probabilistic anatomical masks that I think were used in FSL, and that may be worth checking out.

Best Regards,

G Elliott Wimmer

Dept. of Psychology
Columbia University


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wYkU3AkHJwT+aExhcoet3+i2EEp58QicZGEhCCzxF/JaM6cZAdu9wiF44MrNKt5EXnw+bHcYkhWH 9eSUrA/kaXgut3zIALF/4MxbbsXlDxC40kFv9IBL8VRwJDI5LBsO29IdVB62oj24iXVbiIPj22Hb q1shDlvRHtzEuhXi4Ph22PbqVojDVrQHN7H/AWFrGkuL8nFSAAAAAElFTkSuQmCC --Apple-Mail-11-26904457-- --Apple-Mail-10-26904456-- ========================================================================Date: Mon, 21 Feb 2011 19:28:23 +0000 Reply-To: G Elliott Wimmer <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: G Elliott Wimmer <[log in to unmask]> Subject: Re: medial temporal lobe roi mask Mime-Version: 1.0 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain Message-ID: <[log in to unmask]> Hi, That is very useful information! Regarding hippocampal lateralization, I think an asymmetry may not be known broadly enough in the imaging community (after checking, I now see it in a recent dataset, at approx. 2.5%). This may particularly be an issue to consider when researchers are using atlas-based ROIs, as sometimes they want (and assume) equal numbers of voxels in left/right ROIs. (Also, I should have qualified my answer by noting that these aspects of the AAL may be concerns if you are considering an fMRI study of a population.) However, I would quibble about the AAL hippocampus definition, as it does seem, to me at least, to be more *precisely* defined than the rest of the atlas, with respect to excluding white matter. (e.g., compared to frontal regions - unless the atlas brain has a huge amount of grey matter!) If this is the case - and it may not be - there is probably a good reason for it, but nevertheless it may be something to think about when using such this ROI. ========================================================================Date: Mon, 21 Feb 2011 21:29:36 +0100 Reply-To: Andrea Cherubini <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Andrea Cherubini <[log in to unmask]> Subject: Research Assistant and Postdoctoral Fellowship Positions Content-Type: multipart/alternative; boundary=Apple-Mail-2-37912977 Mime-Version: 1.0 (Apple Message framework v1082) Message-ID: <[log in to unmask]> --Apple-Mail-2-37912977 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain; charset=us-ascii Postdoctoral/Research Assistant positions in medical neuroimaging with a particular focus on magnetic resonance imaging (MRI) are available in the Neuroimaging Laboratory, Magna Grecia University/CNR, Catanzaro, Italy. One position for a period of five years, four positions for a period of one year, with possible extension to a second year. Research in the host laboratory focuses on the development and application of quantitative MRI methods, including advanced image processing and mathematical modeling. Current projects in the laboratory include the development of methods for acquisition, processing and analysis of images from multiple modalities with applications toward the elucidation of structure, function and physiology at the tissue level, with particular focus on the brain. The laboratory is staffed by physicians, psychologists, physicists and others focused on translational use of MRI. Anticipated activities entail the further development, implementation, validation and maintenance of imaging techniques as well as large-scale image data processing and analysis. Candidates are expected to actively participate in translational studies applying the above methodology to patients affected by neurodegenerative disorders. Candidates are expected to have an advanced degree in any field related to neuroscience (physics, mathematics, informatics, engineering, neurology, radiology, or psychology). Candidates with documented experience in medical research are preferred. Experience in scientific programming related to medical imaging is a plus. Fluency in English language is essential. Applicants are requested to submit their curriculum vitae along with two letters of recommendation as attachments to email. Andrea Cherubini Neuroimaging Laboratory National Research Council University Magna Grecia Germaneto (Catanzaro) Italy Tel: +39 0984 9801768 Fax: +39 0984 9801791 For enquiries please e-mail: [log in to unmask] --Apple-Mail-2-37912977 Content-Transfer-Encoding: quoted-printable Content-Type: text/html; charset=us-ascii Postdoctoral/Research Assistant positions in medical neuroimaging with a particular focus on magnetic resonance imaging (MRI) are available in the Neuroimaging Laboratory, Magna Grecia University/CNR, Catanzaro, Italy. One position for a period of five years, four positions for a period of one year, with possible extension to a second year.

Research in the host laboratory focuses on the development and application of quantitative MRI methods, including advanced image processing and mathematical modeling. Current projects in the laboratory include the development of methods for acquisition, processing and analysis of images from multiple modalities with applications toward the elucidation of structure, function and physiology at the tissue level, with particular focus on the brain. The laboratory is staffed by physicians, psychologists, physicists and others focused on translational use of MRI. Anticipated activities entail the further development, implementation, validation and maintenance of imaging techniques as well as large-scale image data processing and analysis. Candidates are expected to actively participate in translational studies applying the above methodology to patients affected by neurodegenerative disorders.

Candidates are expected to have an advanced degree in any field related to neuroscience (physics, mathematics, informatics, engineering, neurology, radiology, or psychology). Candidates with documented experience in medical research are preferred. Experience in scientific programming related to medical imaging is a plus. Fluency in English language is essential.

Applicants are requested to submit their curriculum vitae along with two letters of recommendation as attachments to email.

Andrea Cherubini
Neuroimaging Laboratory
National Research Council
University Magna Grecia
Germaneto (Catanzaro)
Italy

Tel: +39 0984 9801768
Fax: +39 0984 9801791

For enquiries please e-mail: [log in to unmask] --Apple-Mail-2-37912977-- ========================================================================Date: Mon, 21 Feb 2011 16:40:59 -0500 Reply-To: Jonathan Peelle <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Jonathan Peelle <[log in to unmask]> Subject: Re: TIV as nuisance factor for unmodulated data in a VBM-analysis Comments: To: Lucas Eggert <[log in to unmask]> In-Reply-To: <[log in to unmask]> Mime-Version: 1.0 (Apple Message framework v1082) Content-Type: text/plain; charset=windows-1252 Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> Hi Lucas > at the moment I am unsure about whether correcting for total brain volume (TIV) in > a VBM analysis of unmodulated gray matter segments (density) does make sense or not. > > On Dr. Gaser's homepage --- I have the feeling --- there are two slightly opposite statements: > statement (a) (please refer below) clearly states that TIV should not be used as a nuisacne factor with unmodulated data. > > On the other hand, I read statement (b) (please see below) as correcting unmodulated data for TIV gives me relative > density after correcting for TIV, which seems to make more sense to me. > > Which procedure is the more valid one, or for which kind of question would I use which procedure respectively? One important issue that you bring up is the use of modulated gray matter (GM) images and what an analysis using these images would tell you. I think the prevailing view on this is as follows: if normalization were perfect, and there was no modulation, then all GM images would be perfectly aligned. Because we haven't modulated to account for changes in size, the images will be identical. Thus, any differences we see in an unmodulated analysis are likely due to errors in registration. So the first issue, i think, is to make sure that unmodulated images are answering the question you want to answer. I think that the most common view of TIV and unmodulated analyses is that unmodulated GM images represent a property of the tissue, which (unlike its volume) should not depend on head size. Thus, the advice you came across not to include TIV in an unmodulated analysis. [One thing I wonder about the above interpretation of unmodulated analyses, though, is the application to patients with various types of neurodegenerative disease. If there are small pockets of damage (e.g. spongiform encephalopathies), then I would think that an unmodulated analysis might pick this up. Which is to say, I think there may be things other than registration differences that may lead to differences in unmodulated analyses. However, I would be very interested to hear from someone who has had some experience with this.] So, as to your specific question, if you don't have a reason to think that what you are looking at (e.g. tissue density) would be impacted by head size, then I wouldn't think there is a good reason to include TIV. (Although you may want to do some exploratory analyses, preferably in another group of subjects, and include itthen you could see empirically what variance in density, if any, was accounted for by TIV, which might be informative for you, and others.) :) Best regards, Jonathan -- Dr. Jonathan Peelle Department of Neurology University of Pennsylvania 3 West Gates 3400 Spruce Street Philadelphia, PA 19104 USA http://jonathanpeelle.net/ ========================================================================Date: Mon, 21 Feb 2011 18:06:31 -0600 Reply-To: Erik Kastman <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Erik Kastman <[log in to unmask]> Subject: Research Specialist Position - University of Wisconsin, Madison Comments: To: [log in to unmask] Content-Type: multipart/alternative; boundary=Apple-Mail-4-50927819 Mime-Version: 1.0 (Apple Message framework v1082) Message-ID: <[log in to unmask]> --Apple-Mail-4-50927819 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain; charset=us-ascii The Wisconsin Alzheimer's Disease Research Center NeuroImaging group is seeking a talented Masters or Bachelors level research specialist to join our functional and structural brain imaging team. We focus on neuroimaging research studies in early Alzheimer's disease and other dementias, with a focus on memory and other co-occuring cognitive changes. We are looking for someone to assist with image processing, multi-modal data analysis, documentation, scripting and management of a wide range of modalities, including fMRI, DTI, ASL, FDG PET and PiB PET data. Familiarity and skill with image analysis and imaging software is a plus. Further details and contact information can be found here: http://www.ohr.wisc.edu/pvl/pv_066683.html If interested, please send resume and cover letter referring to Position Vacancy Listing #66683 to Amy Hawley at [log in to unmask] Erik Kastman brainmap.wisc.edu --Apple-Mail-4-50927819 Content-Transfer-Encoding: quoted-printable Content-Type: text/html; charset=us-ascii
The Wisconsin Alzheimer's Disease Research Center NeuroImaging group is seeking a talented Masters or Bachelors level research specialist to join our functional and structural brain imaging team.  We focus on neuroimaging research studies in early Alzheimer's disease and other dementias, with a focus on memory and other co-occuring cognitive changes.  

We are looking for someone to assist with image processing, multi-modal data analysis, documentation, scripting and management of a wide range of modalities, including fMRI, DTI, ASL, FDG PET and PiB PET data. Familiarity and skill with image analysis and imaging software is a plus.

Further details and contact information can be found here:  http://www.ohr.wisc.edu/pvl/pv_066683.html   

If interested, please send resume and cover letter referring to Position Vacancy Listing #66683 to Amy Hawley at [log in to unmask]

Erik Kastman

--Apple-Mail-4-50927819-- ========================================================================Date: Tue, 22 Feb 2011 11:46:58 +0000 Reply-To: tony han <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: tony han <[log in to unmask]> Subject: bandpass filter in REST toolbox Content-Type: multipart/alternative; boundary="_79ec0d2c-25d8-4464-aa26-c8a8eb8dcd08_" MIME-Version: 1.0 Message-ID: <[log in to unmask]> --_79ec0d2c-25d8-4464-aa26-c8a8eb8dcd08_ Content-Type: text/plain; charset="iso-8859-1" Content-Transfer-Encoding: quoted-printable Dear REST developers, Sorry for the simple question but when I try to bandpass my dataset, the error occurs as follows: >> rest_bandpass('C:\Program Files\MATLAB71\work\FunImgNormalizedSmoothed\sub1', 3, 0.08, 0.009, 'No', 'C:\Program Files\MATLAB71\work\Masks\mask001.img'); Ideal rectangular filter: "C:\Program Files\MATLAB71\work\FunImgNormalizedSmoothed\sub1" Read 3D EPI functional images: "C:\Program Files\MATLAB71\work\FunImgNormalizedSmoothed\sub1".??? Error using ==> rest_ReadNiftiImage Meet error while reading data. Please restart MATLAB, this problem may be solved. Error in ==> rest_readfile at 61 [Outdata,Header]= rest_ReadNiftiImage(imageIN,volumeIndex); Error in ==> rest_to4d at 41 [theOneTimePoint, VoxelSize, Header] = rest_readfile(theFilename); Error in ==> rest_bandpass at 39 [AllVolume,vsize,theImgFileList, Header] =rest_to4d(ADataDir); What's the problem? And how can I solve it? Thanks. Tony --_79ec0d2c-25d8-4464-aa26-c8a8eb8dcd08_ Content-Type: text/html; charset="iso-8859-1" Content-Transfer-Encoding: quoted-printable Dear REST developers,

    Sorry for the simple question but when I try to bandpass my dataset, the error occurs as follows:

>> rest_bandpass('C:\Program Files\MATLAB71\work\FunImgNormalizedSmoothed\sub1', 3, 0.08, 0.009, 'No', 'C:\Program Files\MATLAB71\work\Masks\mask001.img');

Ideal rectangular filter:    "C:\Program Files\MATLAB71\work\FunImgNormalizedSmoothed\sub1"
     Read 3D EPI functional images: "C:\Program Files\MATLAB71\work\FunImgNormalizedSmoothed\sub1".??? Error using ==> rest_ReadNiftiImage
Meet error while reading data. Please restart MATLAB, this problem may be solved.

Error in ==> rest_readfile at 61
            [Outdata,Header]= rest_ReadNiftiImage(imageIN,volumeIndex);

Error in ==> rest_to4d at 41
        [theOneTimePoint, VoxelSize, Header] = rest_readfile(theFilename);

Error in ==> rest_bandpass at 39
    [AllVolume,vsize,theImgFileList, Header] =rest_to4d(ADataDir);


What's the problem? And how can I solve it? Thanks.

Tony
--_79ec0d2c-25d8-4464-aa26-c8a8eb8dcd08_-- ========================================================================Date: Tue, 22 Feb 2011 11:48:38 +0000 Reply-To: Richard Binney <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Richard Binney <[log in to unmask]> Subject: acceptable high pass filtering MIME-Version: 1.0 Content-Type: multipart/alternative; boundaryMessage-ID: <[log in to unmask]> --0016e6d447daaea4f7049cdd8f85 Content-Type: text/plain; charset=ISO-8859-1 Dear all, Something has recently been said to me that has made me think, and I want to get my head around this a bit more..... At what point does high pass filtering becomes ineffective? It has not been a concern for me in the past, but recently it has been suggested to me that a rule of thumb is to set the high pass filter at a minimum of 1.5 x your longest SOA. That seems reasonable if this is equal to or less than 128secs. I say that because I beleive that this is the optimum filter setting to remove low-freq noise associated with cardiac/respiratory noise, etc. But what if you use a filter at a lower frequency (e.g., 260secs)? It has been said to me that this would be OK. But aren't you running a risk of alliasing signal of interest at frequencies lower than 0.01Hz with cardiac/respiratory noise etc? IF this is an acceptable risk with a filter of say 260secs, at what point does it becomes unacceptable and the filter becomes ineffective? Eg., Say you had an enomrous longest SOA of 800 secs, you might want to use a filter set at 1000secs (0.001Hz) just to be sure. would this filter be effectively redundant? What other factors might speak to this? Jittered SOAs for example? Using a range of SOAs would of course spread the signal of interest across frequencies increasing sensitivity. Does this have an effect of reducing the risk of alliasing with low-freq noise or are you still losing a significant proprotion of your signal in the <0.1Hz frequencies (either due to noise or a 128 sec filter)? In what manner should this inform your high-pass filter? Should you be concerned with the longest SOA or the mean SOA (fundamental frequency) of your signal? Thanks in advance for your help, Richard --0016e6d447daaea4f7049cdd8f85 Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Dear all,

Something has recently been said to me that has made me think, and I want to get my head around this a bit more.....

At what point does high pass filtering becomes ineffective? It has not been a concern for me in the past, but recently it has been suggested to me that a rule of thumb is to set the high pass filter at a minimum of 1.5 x your longest SOA. That seems reasonable if this is equal to or less than 128secs. I say that because I beleive that this is the optimum filter setting to remove low-freq noise associated with cardiac/respiratory noise, etc. But what if you use a filter at a lower frequency (e.g., 260secs)? It has been said to me that this would be OK. But aren't you running a risk of alliasing signal of interest at frequencies lower than 0.01Hz with cardiac/respiratory noise etc? IF this is an acceptable risk with a filter of say 260secs, at what point does it becomes unacceptable and the filter becomes ineffective? Eg., Say you had an enomrous longest SOA of 800 secs, you might want to use a filter set at 1000secs (0.001Hz) just to be sure. would this filter be effectively redundant?

What other factors might speak to this? Jittered SOAs for example? Using a range of SOAs would of course spread the signal of interest across frequencies increasing sensitivity. Does this have an effect of reducing the risk of alliasing with low-freq noise or are you still losinga significant proprotion ofyour signal in the <0.1Hz frequencies (either due to noise or a 128 sec filter)? In what manner should this inform your high-pass filter? Should you be concerned with the longest SOA or the mean SOA (fundamental frequency) of your signal?

Thanks in advance for your help,

Richard --0016e6d447daaea4f7049cdd8f85-- ========================================================================Date: Tue, 22 Feb 2011 19:54:22 +0800 Reply-To: YAN Chao-Gan <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: YAN Chao-Gan <[log in to unmask]> Subject: Re: bandpass filter in REST toolbox Comments: To: tony han <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/alternative; boundary cf30549fcd20a463049cdda4f6 Message-ID: <[log in to unmask]> --20cf30549fcd20a463049cdda4f6 Content-Type: text/plain; charset=ISO-8859-1 Dear Tony, What's you operation system? Usually, run "rest_Fix_Read_Write_Error" right after you started MATLAB, then this problem would be fixed. Further questions about REST are also welcomed to the REST forum: www.restfmri.net Best wishes! YAN Chao-Gan On Tue, Feb 22, 2011 at 7:46 PM, tony han <[log in to unmask]> wrote: > Dear REST developers, > > Sorry for the simple question but when I try to bandpass my dataset, > the error occurs as follows: > > >> rest_bandpass('C:\Program > Files\MATLAB71\work\FunImgNormalizedSmoothed\sub1', 3, 0.08, 0.009, 'No', > 'C:\Program Files\MATLAB71\work\Masks\mask001.img'); > > Ideal rectangular filter: "C:\Program > Files\MATLAB71\work\FunImgNormalizedSmoothed\sub1" > Read 3D EPI functional images: "C:\Program > Files\MATLAB71\work\FunImgNormalizedSmoothed\sub1".??? Error using ==> > rest_ReadNiftiImage > Meet error while reading data. Please restart MATLAB, this problem may be > solved. > > Error in ==> rest_readfile at 61 > [Outdata,Header]= rest_ReadNiftiImage(imageIN,volumeIndex); > > Error in ==> rest_to4d at 41 > [theOneTimePoint, VoxelSize, Header] = rest_readfile(theFilename); > > Error in ==> rest_bandpass at 39 > [AllVolume,vsize,theImgFileList, Header] =rest_to4d(ADataDir); > > > What's the problem? And how can I solve it? Thanks. > > Tony > -- YAN Chao-Gan, Ph.D. Candidate State Key Laboratory of Cognitive Neuroscience and Learning Beijing Normal University Beijing, China, 100875 Phone: +86-10-58801023 [log in to unmask] http://www.restfmri.net/forum/yanchaogan --20cf30549fcd20a463049cdda4f6 Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Dear Tony,
What's you operation system?
Usually, run "rest_Fix_Read_Write_Error" right after you started MATLAB, then this problem would be fixed.
Further questions about REST are also welcomed to the REST forum: www.restfmri.net
Best wishes!
YAN Chao-Gan

On Tue, Feb 22, 2011 at 7:46 PM, tony han <[log in to unmask]> wrote:
Dear REST developers,

Sorry for the simple question but when I try to bandpass my dataset, the error occurs as follows:

>> rest_bandpass('C:\Program Files\MATLAB71\work\FunImgNormalizedSmoothed\sub1', 3, 0.08, 0.009, 'No', 'C:\Program Files\MATLAB71\work\Masks\mask001.img');

Ideal rectangular filter: "C:\Program Files\MATLAB71\work\FunImgNormalizedSmoothed\sub1"
Read 3D EPI functional images: "C:\Program Files\MATLAB71\work\FunImgNormalizedSmoothed\sub1".??? Error using ==> rest_ReadNiftiImage
Meet error while reading data. Please restart MATLAB, this problem may be solved.

Error in ==> rest_readfile at 61
[Outdata,Header]= rest_ReadNiftiImage(imageIN,volumeIndex);

Error in ==> rest_to4d at 41
[theOneTimePoint, VoxelSize, Header] = rest_readfile(theFilename);

Error in ==> rest_bandpass at 39
[AllVolume,vsize,theImgFileList, Header] =rest_to4d(ADataDir);


What's the problem? And how can I solve it? Thanks.

Tony



--
YAN Chao-Gan, Ph.D. Candidate
State Key Laboratory of Cognitive Neuroscience and Learning
Beijing Normal University
Beijing, China, 100875
Phone: +86-10-58801023
[log in to unmask]
http://www.restfmri.net/forum/yanchaogan
--20cf30549fcd20a463049cdda4f6-- ========================================================================Date: Tue, 22 Feb 2011 14:39:31 +0000 Reply-To: John Ashburner <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: John Ashburner <[log in to unmask]> Subject: Re: Check Reg Figures SPM8 - size and arrangement Comments: To: Vladimir Bogdanov <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> There are no default settings that could be changed to make SPM do what you would like it to do. However, the beauty of having SPM in MATLAB is that it is relatively easy to tweak the code to make it do exactly what you want. Best regards, -John On 20 February 2011 22:20, Vladimir Bogdanov <[log in to unmask]> wrote: > Dear SPM experts, > > By default the size of the images in Check Reg figure does not allow to see well anatomical details (see screen1 in attachment). This can be changed manually (screen2), but those changes take time. > > Is there a simple way do it fast? Is it possible to change SPM settings somewhere to make the figure in the same way (different from default) every time we call Check Reg? > > Thank you in advance for your help, > Vladimir > > Volodymyr Bogdanov, PhD > > Headache Research Unit > GIGA - Neurosciences > University of Liege > CHU T4 +1, Sart Tilman > Av de l'Hpital 1 > 4000 Liege, Belgium > > > ========================================================================Date: Tue, 22 Feb 2011 06:58:14 -0800 Reply-To: Vladimir Bogdanov <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Vladimir Bogdanov <[log in to unmask]> Subject: Re: Check Reg Figures SPM8 - size and arrangement Comments: To: John Ashburner <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=iso-8859-1 Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> Dear John, Thank you for your response! Where is the part of the code responsible for this located? The SPM script is huge and I am only a beginner. :) Sincerely yours, Vladimir --- On Tue, 2/22/11, John Ashburner <[log in to unmask]> wrote: > From: John Ashburner <[log in to unmask]> > Subject: Re: [SPM] Check Reg Figures SPM8 - size and arrangement > To: [log in to unmask] > Date: Tuesday, February 22, 2011, 3:39 PM > There are no default settings that > could be changed to make SPM do > what you would like it to do. However, the beauty of > having SPM in > MATLAB is that it is relatively easy to tweak the code to > make it do > exactly what you want. > > Best regards, > -John > > On 20 February 2011 22:20, Vladimir Bogdanov <[log in to unmask]> > wrote: > > Dear SPM experts, > > > > By default the size of the images in Check Reg figure > does not allow to see well anatomical details (see screen1 > in attachment). This can be changed manually (screen2), but > those changes take time. > > > > Is there a simple way do it fast? Is it possible to > change SPM settings somewhere to make the figure in the same > way (different from default) every time we call Check Reg? > > > > Thank you in advance for your help, > > Vladimir > > > > Volodymyr Bogdanov, PhD > > > > Headache Research Unit > > GIGA - Neurosciences > > University of Liege > > CHU T4 +1, Sart Tilman > > Av de l'Hpital 1 > > 4000 Liege, Belgium > > > > > > > ========================================================================Date: Tue, 22 Feb 2011 15:08:49 +0000 Reply-To: John Ashburner <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: John Ashburner <[log in to unmask]> Subject: Re: Check Reg Figures SPM8 - size and arrangement Comments: To: Vladimir Bogdanov <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> When you run Check Reg, Display or any of the other routines calling spm_orthviews.m, there is a data structure saved as a global variable. So if you call spm_check_registration and type the following, you should get access to various pieces of information that could be useful.... global st st.vols{1} Some of the fields you see refer to the positions of the axes on the screen. You'd need to modify these. Best regards, -John On 22 February 2011 14:58, Vladimir Bogdanov <[log in to unmask]> wrote: > Dear John, > > Thank you for your response! Where is the part of the code responsible for this located? The SPM script is huge and I am only a beginner. :) > > Sincerely yours, > Vladimir > > > --- On Tue, 2/22/11, John Ashburner <[log in to unmask]> wrote: > >> From: John Ashburner <[log in to unmask]> >> Subject: Re: [SPM] Check Reg Figures SPM8 - size and arrangement >> To: [log in to unmask] >> Date: Tuesday, February 22, 2011, 3:39 PM >> There are no default settings that >> could be changed to make SPM do >> what you would like it to do. However, the beauty of >> having SPM in >> MATLAB is that it is relatively easy to tweak the code to >> make it do >> exactly what you want. >> >> Best regards, >> -John >> >> On 20 February 2011 22:20, Vladimir Bogdanov <[log in to unmask]> >> wrote: >> > Dear SPM experts, >> > >> > By default the size of the images in Check Reg figure >> does not allow to see well anatomical details (see screen1 >> in attachment). This can be changed manually (screen2), but >> those changes take time. >> > >> > Is there a simple way do it fast? Is it possible to >> change SPM settings somewhere to make the figure in the same >> way (different from default) every time we call Check Reg? >> > >> > Thank you in advance for your help, >> > Vladimir >> > >> > Volodymyr Bogdanov, PhD >> > >> > Headache Research Unit >> > GIGA - Neurosciences >> > University of Liege >> > CHU T4 +1, Sart Tilman >> > Av de l'Hpital 1 >> > 4000 Liege, Belgium >> > >> > >> > >> > > > > ========================================================================Date: Tue, 22 Feb 2011 16:16:14 +0000 Reply-To: Jonas Persson <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Jonas Persson <[log in to unmask]> Subject: Regarding scanner sequences Mime-Version: 1.0 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain; charset="UTF-8" Message-ID: <[log in to unmask]> Hello, I have a couple of questions regarding settings of scanner sequences and how it affects subsequent data processing in SPM. 1. If we scan, say, coronally or saggitally during our T1-sequence and acquire our functional data with an axial EPI-sequence, will this create a problem later in SPM for example with the normalisation process? I.e. is it recommended to always acquire all the data in the same direction? 2. A follow-up question: If i scan during the same paradigm with the same EPI-sequence, but collecting the slices in different directions (i.e. coronally vs. axially) should I then expect any differences in the data acquired? (other than the slice gaps obviously appearing at different places) 3. We use an EPI-sequence at our lab with a TR=3, which collects all slices as fast as possible and then rests during the reminder of the TR. I guess this should be good for minimizing the time differences between slices, but could this create a problem for an event related paradigm? So far we have only used traditional block designs. Thank you for any reply! Best regards, Jonas ========================================================================Date: Tue, 22 Feb 2011 16:39:32 +0000 Reply-To: John Ashburner <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: John Ashburner <[log in to unmask]> Subject: Re: Regarding scanner sequences Comments: To: Jonas Persson <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Message-ID: [log in to unmask]> > 1. If we scan, say, coronally or saggitally during our T1-sequence and acquire our functional data with an axial EPI-sequence, will this create a problem later in SPM for example with the normalisation process? I.e. is it recommended to always acquire all the data in the same direction? This should be fine, providing the orientation information in the image headers is correct. If you used the DICOM conversion routines in SPM, then this should be the case. > > 2. A follow-up question: If i scan during the same paradigm with the same EPI-sequence, but collecting the slices in different directions (i.e. coronally vs. axially) should I then expect any differences in the data acquired? (other than the slice gaps obviously appearing at different places) The distortion and dropout in the data is likely to differ, depending on whether the phase-encoding direction is the same or not. There may be other effects, but the easiest way to discover them would be to try it. > > 3. We use an EPI-sequence at our lab with a TR=3, which collects all slices as fast as possible and then rests during the reminder of the TR. I guess this should be good for minimizing the time differences between slices, but could this create a problem for an event related paradigm? So far we have only used traditional block designs. I can't really comment on this as it's not my area. Best regards, -John ========================================================================Date: Tue, 22 Feb 2011 09:24:50 -0800 Reply-To: Manish Dalwani <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Manish Dalwani <[log in to unmask]> Subject: SPM8 batchscripts? MIME-Version: 1.0 Content-Type: multipart/alternative; boundary="0-151767339-1298395490=:7828" Message-ID: <[log in to unmask]> --0-151767339-1298395490=:7828 Content-Type: text/plain; charset=us-ascii Hello SPM'ers Is there a model preprocessing SPM8 batchscript? ...that you can modify as per your preprocessing plans! If so, where can I find it? Regards,Manish DalwaniSr. PRADept. of PsychiatryUniversity of Colorado --0-151767339-1298395490=:7828 Content-Type: text/html; charset=us-ascii
Hello SPM'ers

Is there a model preprocessing SPM8 batchscript? ...that you can modify as per your preprocessing plans! If so, where can I find it?

Regards,
Manish Dalwani
Sr. PRA
Dept. of Psychiatry
University of Colorado

--0-151767339-1298395490=:7828-- ========================================================================Date: Tue, 22 Feb 2011 13:56:23 -0600 Reply-To: Pamela LaMontagne <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Pamela LaMontagne <[log in to unmask]> Subject: modelling assumed & unassumed hrf together MIME-Version: 1.0 Content-Type: multipart/alternative; boundaryMessage-ID: <[log in to unmask]> --0016e6dab4dfff0f36049ce45f78 Content-Type: text/plain; charset=ISO-8859-1 I have a mixed-design study with blocks representing a task-set (2 tasks) and events representing different trial-types (2 trial types/task) within the block. Based on Visscher 2003 I am interested in modeling the assumed hrf function with the blocks and an unassumed hrf function for the trials. I know that the unassumed response can be modeled using FIR. However, how do I model these in the same model specification? The current in-house program I am using allows for conditions to be specified with an assumed or unassumed response within the same design matrix but I would prefer to switch over to SPM8. How is this implemented in SPM? Is there a toolbox that can do this? Thanks, Pamela LaMontagne Post Doctoral Fellow Washington University St. Louis --0016e6dab4dfff0f36049ce45f78 Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable
I have a mixed-design study with blocks representing a task-set (2 tasks) and events representing different trial-types (2 trial types/task) within the block. Based on Visscher 2003 I am interested in modeling the assumed hrf function with the blocks and an unassumed hrf function for the trials. I know that the unassumed response can be modeled using FIR. However, how do I model these in the same model specification? The current in-house program I am using allows for conditions to be specified with an assumed or unassumed response within the same design matrix but I would prefer to switch over to SPM8.

How is this implemented in SPM? Is there a toolbox that can do this?

Thanks,

Pamela LaMontagne
Post Doctoral Fellow
Washington University St. Louis
--0016e6dab4dfff0f36049ce45f78-- ========================================================================Date: Wed, 23 Feb 2011 04:16:00 +0800 Reply-To: [log in to unmask] Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Kuo Bo-Cheng <[log in to unmask]> Subject: Re: SPM EEG Pre processing: Not sure if everything looks OK Comments: To: Vladimir Litvak <[log in to unmask]> In-Reply-To: <-101706040748529818@unknownmsgid> MIME-Version: 1.0 Content-Type: text/plain; charset=UTF-8; DelSp="Yes"; format="flowed" Content-Disposition: inline Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> Dear Vladmir, Can we rescale single trial TF before average? Many thanks! Bo-Cheng 引述 Vladimir Litvak <[log in to unmask]>: > Dear Muhammad, > > The way one would usually do TF analysis is to apply TF to an epoched > file, then average the result and then rescale. If you apply TF to an > ERP which is quite noisy you'll get basically single trial TF which is > noisy as well. > > Filtering will not help since you will either remove your frequency > range of interest or not affect it. > > Best, > > Vladimir > > > On 20 Feb 2011, at 03:51, MP <[log in to unmask]> wrote: > >> Hi all, >> >> I am doing the TF analysis on EEG data and I see some worrisome >> "spots" in my rescaled TF, which translate as sharp "dips" in the >> waveform of averaged TF over 12-20Hz when I convert TF into image. >> I know that these spots could be from the noise (since it is a >> single subject data), but I am worried that they will influence the >> statistics. >> >> I have attached the ERP waveform (-200 to 2000ms), its TF >> representation (4-20Hz, -198-2000ms), rescaled TF (using Log >> rescaling, baseline=-148 to 0), and the waveform when TF is >> averaged over 12-20Hz range. >> >> Is it possible that since these dips are random they will not >> influence the results in the scalp-space considerably? Is there >> anything I can do to minimize these dips, like lowpass filter the >> ERP before doing TF? >> >> thanks for your help in advance >> >> - Muhammad >> >> >> >> > ========================================================================Date: Tue, 22 Feb 2011 21:05:13 +0000 Reply-To: Vladimir Litvak <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Vladimir Litvak <[log in to unmask]> Subject: Re: SPM EEG Pre processing: Not sure if everything looks OK Comments: To: "[log in to unmask]" <[log in to unmask]> In-Reply-To: <[log in to unmask]> Mime-Version: 1.0 (iPad Mail 8C148) Content-Type: text/plain; charset=UTF-8 Content-Transfer-Encoding: quoted-printable Message-ID: <-3545688754431432339@unknownmsgid> Dear Bo-Cheng, Technically, yes. The question is whether this is something that makes sense. Average of rescaled data and rescaled average are usually not the same thing. Vladimir On 22 Feb 2011, at 20:16, "[log in to unmask]" <[log in to unmask]> wrote: > Dear Vladmir, > > Can we rescale single trial TF before average? > Many thanks! > > Bo-Cheng > > > 引述 Vladimir Litvak <[log in to unmask]>: > >> Dear Muhammad, >> >> The way one would usually do TF analysis is to apply TF to an epoched >> file, then average the result and then rescale. If you apply TF to an >> ERP which is quite noisy you'll get basically single trial TF which is >> noisy as well. >> >> Filtering will not help since you will either remove your frequency >> range of interest or not affect it. >> >> Best, >> >> Vladimir >> >> >> On 20 Feb 2011, at 03:51, MP <[log in to unmask]> wrote: >> >>> Hi all, >>> >>> I am doing the TF analysis on EEG data and I see some worrisome "spots" in my rescaled TF, which translate as sharp "dips" in the waveform of averaged TF over 12-20Hz when I convert TF into image. I know that these spots could be from the noise (since it is a single subject data), but I am worried that they will influence the statistics. >>> >>> I have attached the ERP waveform (-200 to 2000ms), its TF representation (4-20Hz, -198-2000ms), rescaled TF (using Log rescaling, baseline=-148 to 0), and the waveform when TF is averaged over 12-20Hz range. >>> >>> Is it possible that since these dips are random they will not influence the results in the scalp-space considerably? Is there anything I can do to minimize these dips, like lowpass filter the ERP before doing TF? >>> >>> thanks for your help in advance >>> >>> - Muhammad >>> >>> >>> >>> >> > > ========================================================================Date: Tue, 22 Feb 2011 15:21:45 -0800 Reply-To: J S Lee <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: J S Lee <[log in to unmask]> Subject: Can't find driving effects for PPI analysis MIME-Version: 1.0 Content-Type: multipart/alternative; boundary="----=_NextPart_000_2B18_01CBD2A4.37747680" Message-ID: <[log in to unmask]> This is a multi-part message in MIME format. ------=_NextPart_000_2B18_01CBD2A4.37747680 Content-Type: text/plain; charset="iso-8859-1" Content-Transfer-Encoding: 7bit Dear list, I conducted a PPI analysis in an experiment with 6 conditions. To replicate a previous study's PPI analysis, I was interested in connectivity differences between 5 of the conditions compared to the control (6th) condition, so extracted my VOI (using an all effects of interest contrast), then created a PPI model with a [1 1 1 1 1 -1] weighting for the psychological context regressor. I get a reasonable replication of the same PPI effects from the previous study, so the results are sensible. However, in that previous study, there were not enough trials of each of the 5 conditions to realistically analyze them separately, which is why I collapsed across them. In this study, there are many more trials, so I was hoping to look at which of the 5 conditions were driving the original PPI results. I was given hope when the initial PPI replicated in this new study. However, when I create separate PPI models for each condition versus control (e.g., context regressors using [1 0 0 0 0 -1] for model 1, [0 1 0 0 0 -1] for model 2, etc.), NONE of these analyses show the same pattern as the 1 1 1 1 1 -1 model does. Mostly there are no significant (or anywhere near significant) results, and those random speckles that do show up at low threshold are not in the same places. Is it theoretically possible that 5 conditions vs 1 other can produce a PPI, but that none of those conditions singly vs the 1 other can do that? Or must there be an error? I have checked the microtime onset files to make the context is specified correctly, and made sure everything matches up in terms of specifying the conditions. Everything about the models looks fine to me. I know the 5 conditions vs 1 is a bit unbalanced, but it replicates the previous study (in which the 5 vs 1 were equal in terms of number of trials), and I understand that when creating the context variable one does NOT sum the vector to zero the way one would in defining a contrast for a regional activation analysis. Many thanks in advance for any thoughts, Jamie Lee

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------=_NextPart_000_2B18_01CBD2A4.37747680 Content-Type: text/html Content-Transfer-Encoding: 7bit Dear list,

I conducted a PPI analysis in an experiment with 6 conditions. To replicate a previous study's PPI analysis, I was interested in connectivity differences between 5 of the conditions compared to the control (6th) condition, so extracted my VOI (using an all effects of interest contrast), then created a PPI model with a [1 1 1 1 1 -1] weighting for the psychological context regressor. I get a reasonable replication of the same PPI effects from the previous study, so the results are sensible.

However, in that previous study, there were not enough trials of each of the 5 conditions to realistically analyze them separately, which is why I collapsed across them. In this study, there are many more trials, so I was hoping to look at which of the 5 conditions were driving the original PPI results. I was given hope when the initial PPI replicated in this new study. However, when I create separate PPI models for each condition versus control (e.g., context regressors using [1 0 0 0 0 -1] for model 1, [0 1 0 0 0 -1] for model 2, etc.), NONE of these analyses show the same pattern as the 1 1 1 1 1 -1 model does. Mostly there are no significant (or anywhere near significant) results, and those random speckles that do show up at low threshold are not in the same places.

Is it theoretically possible that 5 conditions vs 1 other can produce a PPI, but that none of those conditions singly vs the 1 other can do that? Or must there be an error? I have checked the microtime onset files to make the context is specified correctly, and made sure everything matches up in terms of specifying the conditions. Everything about the models looks fine to me. I know the 5 conditions vs 1 is a bit unbalanced, but it replicates the previous study (in which the 5 vs 1 were equal in terms of number of trials), and I understand that when creating the context variable one does NOT sum the vector to zero the way one would in defining a contrast for a regional activation analysis.

Many thanks in advance for any thoughts,
Jamie Lee

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------=_NextPart_000_2B18_01CBD2A4.37747680-- ========================================================================Date: Tue, 22 Feb 2011 18:52:25 -0500 Reply-To: "MCLAREN, Donald" <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: "MCLAREN, Donald" <[log in to unmask]> Subject: Re: Can't find driving effects for PPI analysis Comments: To: J S Lee <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Message-ID: [log in to unmask]> Are you using SPM8? The issue of summing was fixed in one of the later releases of SPM5, so if you have an older version, that could explain some of the issue. You could check to make sure that negative aspects of the SPM.xX.X for the PPI term are the same for all subjects. You could plot them. Are you using the same adjustment for all models? Are you using exactly the same voxels for all models? Best Regards, Donald McLaren ================= D.G. McLaren, Ph.D. Postdoctoral Research Fellow, GRECC, Bedford VA Research Fellow, Department of Neurology, Massachusetts General Hospital and Harvard Medical School Office: (773) 406-2464 ===================== This e-mail contains CONFIDENTIAL INFORMATION which may contain PROTECTED HEALTHCARE INFORMATION and may also be LEGALLY PRIVILEGED and which is intended only for the use of the individual or entity named above. If the reader of the e-mail is not the intended recipient or the employee or agent responsible for delivering it to the intended recipient, you are hereby notified that you are in possession of confidential and privileged information. Any unauthorized use, disclosure, copying or the taking of any action in reliance on the contents of this information is strictly prohibited and may be unlawful. If you have received this e-mail unintentionally, please immediately notify the sender via telephone at (773) 406-2464 or email. On Tue, Feb 22, 2011 at 6:21 PM, J S Lee <[log in to unmask]> wrote: > Dear list, > > I conducted a PPI analysis in an experiment with 6 conditions. To replicate > a previous study's PPI analysis, I was interested in connectivity > differences between 5 of the conditions compared to the control (6th) > condition, so extracted my VOI (using an all effects of interest contrast), > then created a PPI model with a [1 1 1 1 1 -1] weighting for the > psychological context regressor. I get a reasonable replication of the same > PPI effects from the previous study, so the results are sensible. > > However, in that previous study, there were not enough trials of each of the > 5 conditions to realistically analyze them separately, which is why I > collapsed across them. In this study, there are many more trials, so I was > hoping to look at which of the 5 conditions were driving the original PPI > results. I was given hope when the initial PPI replicated in this new study. > However, when I create separate PPI models for each condition versus control > (e.g., context regressors using [1 0 0 0 0 -1] for model 1, [0 1 0 0 0 -1] > for model 2, etc.), NONE of these analyses show the same pattern as the 1 1 > 1 1 1 -1 model does. Mostly there are no significant (or anywhere near > significant) results, and those random speckles that do show up at low > threshold are not in the same places. > > Is it theoretically possible that 5 conditions vs 1 other can produce a PPI, > but that none of those conditions singly vs the 1 other can do that? Or must > there be an error? I have checked the microtime onset files to make the > context is specified correctly, and made sure everything matches up in terms > of specifying the conditions. Everything about the models looks fine to me. > I know the 5 conditions vs 1 is a bit unbalanced, but it replicates the > previous study (in which the 5 vs 1 were equal in terms of number of > trials), and I understand that when creating the context variable one does > NOT sum the vector to zero the way one would in defining a contrast for a > regional activation analysis. > > Many thanks in advance for any thoughts, > Jamie Lee > > _______________________________________________________________ > Get the Free email that has everyone talking at http://www.mail2world.com > Unlimited Email Storage POP3 Calendar SMS Translator Much More! ========================================================================Date: Wed, 23 Feb 2011 01:29:50 +0000 Reply-To: Dashjamts Jargal <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Dashjamts Jargal <[log in to unmask]> Subject: DARTEL modulation versus no modulation: accuracy? Mime-Version: 1.0 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain; charset="UTF-8" Message-ID: <[log in to unmask]> Dear all, I am trying to examine the diagnositc performance in DARTEL-based VBM. My unmodulated data show larger relevant difference areas and have higher diagnostic accuracy than the modulated. What could explain such result? Why the unmodulated demonstrated much more affected areas than the modulated? Is the following correct according to the definition of how modulation works: "perfectly registered unmodulated data should show no difference between the groups"?Does it mean that unmodulated data have some compound of registration failures? What areas in the brain are more prone to DARTEL-registration failures? Thank you in advance for your consideration. ========================================================================Date: Wed, 23 Feb 2011 08:15:40 +0100 Reply-To: Lucas Eggert <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Lucas Eggert <[log in to unmask]> Subject: Re: TIV as nuisance factor for unmodulated data in a VBM-analysis Comments: To: Jonathan Peelle <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/signed; protocol="application/pkcs7-signature"; micalg=sha1; boundary="------------ms040108020106000704050504" Message-ID: <[log in to unmask]> This is a cryptographically signed message in MIME format. --------------ms040108020106000704050504 Content-Type: text/plain; charset=windows-1252; format=flowed Content-Transfer-Encoding: quoted-printable Hi Jonathan, thanks very much for your response. I guess for now, I will rather go for unmodulated images without correcting for globals; and I will definitely do some tests to see what difference the correction for TIV would make. All the best, Lucas > Hi Lucas > >> at the moment I am unsure about whether correcting for total brain volume (TIV) in >> a VBM analysis of unmodulated gray matter segments (density) does make sense or not. >> >> On Dr. Gaser's homepage --- I have the feeling --- there are two slightly opposite statements: >> statement (a) (please refer below) clearly states that TIV should not be used as a nuisacne factor with unmodulated data. >> >> On the other hand, I read statement (b) (please see below) as correcting unmodulated data for TIV gives me relative >> density after correcting for TIV, which seems to make more sense to me. >> >> Which procedure is the more valid one, or for which kind of question would I use which procedure respectively? > > One important issue that you bring up is the use of modulated gray matter (GM) images and what an analysis using these images would tell you. I think the prevailing view on this is as follows: if normalization were perfect, and there was no modulation, then all GM images would be perfectly aligned. Because we haven't modulated to account for changes in size, the images will be identical. Thus, any differences we see in an unmodulated analysis are likely due to errors in registration. So the first issue, i think, is to make sure that unmodulated images are answering the question you want to answer. > > I think that the most common view of TIV and unmodulated analyses is that unmodulated GM images represent a property of the tissue, which (unlike its volume) should not depend on head size. Thus, the advice you came across not to include TIV in an unmodulated analysis. > > [One thing I wonder about the above interpretation of unmodulated analyses, though, is the application to patients with various types of neurodegenerative disease. If there are small pockets of damage (e.g. spongiform encephalopathies), then I would think that an unmodulated analysis might pick this up. Which is to say, I think there may be things other than registration differences that may lead to differences in unmodulated analyses. However, I would be very interested to hear from someone who has had some experience with this.] > > So, as to your specific question, if you don't have a reason to think that what you are looking at (e.g. tissue density) would be impacted by head size, then I wouldn't think there is a good reason to include TIV. (Although you may want to do some exploratory analyses, preferably in another group of subjects, and include itthen you could see empirically what variance in density, if any, was accounted for by TIV, which might be informative for you, and others.) :) > > Best regards, > Jonathan > > > > -- Lucas Eggert, M.Sc. Institute of Cognitive Science University of Osnabrueck Albrechtstrasse 28 D-49076 Osnabrueck Germany Phone: +49-541-969-44-28 Website: http://www.cogsci.uni-osnabrueck.de/~leggert/ --------------ms040108020106000704050504 Content-Type: application/pkcs7-signature; name="smime.p7s" Content-Transfer-Encoding: base64 Content-Disposition: attachment; filename="smime.p7s" Content-Description: S/MIME Cryptographic Signature MIAGCSqGSIb3DQEHAqCAMIACAQExCzAJBgUrDgMCGgUAMIAGCSqGSIb3DQEHAQAAoIIUEzCC BCEwggMJoAMCAQICAgDHMA0GCSqGSIb3DQEBBQUAMHExCzAJBgNVBAYTAkRFMRwwGgYDVQQK ExNEZXV0c2NoZSBUZWxla29tIEFHMR8wHQYDVQQLExZULVRlbGVTZWMgVHJ1c3QgQ2VudGVy MSMwIQYDVQQDExpEZXV0c2NoZSBUZWxla29tIFJvb3QgQ0EgMjAeFw0wNjEyMTkxMDI5MDBa Fw0xOTA2MzAyMzU5MDBaMFoxCzAJBgNVBAYTAkRFMRMwEQYDVQQKEwpERk4tVmVyZWluMRAw DgYDVQQLEwdERk4tUEtJMSQwIgYDVQQDExtERk4tVmVyZWluIFBDQSBHbG9iYWwgLSBHMDEw ggEiMA0GCSqGSIb3DQEBAQUAA4IBDwAwggEKAoIBAQDpm8NnhfkNrvWNVMOWUDU9YuluTO2U 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"/Applications/MATLAB_R2008a/spm8/tpm/grey.nii" does not exist. In file "/Applications/spm8/spm_vol.m" (v2237), function "subfunc" at line 111. In file "/Applications/spm8/spm_vol.m" (v2237), function "subfunc1" at line 84. In file "/Applications/spm8/spm_vol.m" (v2237), function "subfunc2" at line 70. In file "/Applications/spm8/spm_vol.m" (v2237), function "spm_vol" at line 54. In file "/Applications/spm8/spm_preproc.m" (v1143), function "spm_preproc" at line 66. In file "/Applications/spm8/config/spm_run_preproc.m" (v2312), function "spm_run_preproc" at line 19. No executable modules, but still unresolved dependencies or incomplete module inputs. The following modules did not run: Failed: Segment Skipped: Normalise: Write Skipped: Smooth If i treat my images step by step, nothing goes wrong and I can get to the end of it. Does any one have an idea where this problem could be coming from? -- *Marine* --90e6ba3fccf3b65375049cef7647 Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Hello,

I made a batch for spatial pre processing and it stops every time during segmentation with this message:
Running 'Segment'
Failed 'Segment'
Error using ==> spm_vol>subfunc at 111
File "/Applications/MATLAB_R2008a/spm8/tpm/grey.nii" does not exist.
In file "/Applications/spm8/spm_vol.m" (v2237), function "subfunc" at line 111.
In file "/Applications/spm8/spm_vol.m" (v2237), function "subfunc1" at line 84.
In file "/Applications/spm8/spm_vol.m" (v2237), function "subfunc2" at line 70.
In file "/Applications/spm8/spm_vol.m" (v2237), function "spm_vol" at line 54.
In file "/Applications/spm8/spm_preproc.m" (v1143), function "spm_preproc" at line 66.
In file "/Applications/spm8/config/spm_run_preproc.m" (v2312), function "spm_run_preproc" at line 19.

No executable modules, but still unresolved dependencies or incomplete module inputs.
The following modules did not run:
Failed: Segment
Skipped: Normalise: Write
Skipped: Smooth

If i treat my images step by step, nothing goes wrong and I can get to the end of it. Does any one have an idea where this problem could be coming from?

--
Marine
--90e6ba3fccf3b65375049cef7647-- ========================================================================Date: Wed, 23 Feb 2011 03:03:28 -0800 Reply-To: Vladimir Bogdanov <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Vladimir Bogdanov <[log in to unmask]> Subject: Re: Check Reg Figures SPM8 - size and arrangement Comments: To: Guillaume Flandin <[log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/mixed; boundary="0-1398234352-1298459008=:63850" Message-ID: <[log in to unmask]> --0-1398234352-1298459008=:63850 Content-Type: text/plain; charset=iso-8859-1 Content-Transfer-Encoding: quoted-printable Thank you, Guillaume! This was very helpful. But I faced other difficulty. The position parameters are in relative units and if we change the proportions of the figure, the images are stretched. I suppose, I need to get the real size of the figure and to incorporate this in the script to keep correct proportions of the images, but I do not know, how to do it. Thank you in advance for your help and sorry for my primitive questions. Sincerely yours, Vladimir --- On Tue, 2/22/11, Guillaume Flandin <[log in to unmask]> wrote: > From: Guillaume Flandin <[log in to unmask]> > Subject: Re: [SPM] Check Reg Figures SPM8 - size and arrangement > To: "Vladimir Bogdanov" <[log in to unmask]> > Date: Tuesday, February 22, 2011, 4:49 PM > Dear Vladimir, > > the following code should get you started (to be executed > when images > are displayed with checkreg): > > global st > h = 1; > for i=1:nnz(~cellfun('isempty',st.vols)) > p1 = get(st.vols{i}.ax{1}.ax,'Position'); > p2 = get(st.vols{i}.ax{2}.ax,'Position'); > p3 = get(st.vols{i}.ax{3}.ax,'Position'); > l = p1(3) + p2(3) + p3(3); sc = > (1-0.01)/l; > p1 = p1*sc; p2 = p2 * sc; p3 = p3 * sc; > set(st.vols{i}.ax{1}.ax,'Position',... > [0 h-p1(4) p1(3) p1(4)]); > set(st.vols{i}.ax{2}.ax,'Position',... > [p1(3)+0.005 h-p2(4) p2(3) > p2(4)]); > set(st.vols{i}.ax{3}.ax,'Position',.... > [p1(3)+p2(3)+0.01 h-p3(4) p3(3) > p3(4)]); > h = h - p1(4)-0.005; > end > > Best, > Guillaume. > > On 22/02/11 14:58, Vladimir Bogdanov wrote: > > Dear John, > > > > Thank you for your response! Where is the part of the > code responsible for this located? 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g/Kiir6EhsHoPyo2D0H5UUVEPhBBsHoPyo2D0H5UUVa6AGweg/KmyqAh4HQ/ yNFFIbP/2Q= --0-1398234352-1298459008=:63850-- ========================================================================Date: Wed, 23 Feb 2011 11:56:05 -0000 Reply-To: Lorelei Howard <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Lorelei Howard <[log in to unmask]> Subject: contrasting/masking parametric variables MIME-Version: 1.0 Content-Type: text/plain;charset=iso-8859-1 Content-Transfer-Encoding: 8bit Message-ID: <[log in to unmask]> Hi everyone, I am running a study which has two types of blocks (1 experimental and 1 control). For each of these blocks I have second-by-second measurements of the same parametric variable. I was wondering whether it would be valid to run a standard t-contrast [1 -1] to identify regions associated with the parametric variable that are more active in the experimental blocks than in the control blocks. Is it OK to do this with parametric regressors? Or, alternatively, could I use some sort of masking procedure to remove brain regions associated with the parametric variable in the control blocks when I examine the effects of the same parametric variable in the experimental blocks? Many Thanks, Lorelei -- Lorelei Howard Ph.D. Student Institute of Behavioural Neuroscience Cognitive, Perceptual and Brain Sciences Department University College London 26 Bedford Way WC1H 0AP +44 (0)20 7679 8553 ========================================================================Date: Wed, 23 Feb 2011 03:57:39 -0800 Reply-To: Vladimir Bogdanov <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Vladimir Bogdanov <[log in to unmask]> Subject: Re: Check Reg Figures SPM8 - size and arrangement: solved! Comments: To: Guillaume Flandin <[log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/mixed; boundary="0-2071618827-1298462259=:64948" Message-ID: <[log in to unmask]> --0-2071618827-1298462259=:64948 Content-Type: text/plain; charset=iso-8859-1 Content-Transfer-Encoding: quoted-printable Dear Guillaume and SPM community, The problem is solved pretty easily. I had to set new figure position parameters and calculate the value of ratio new/old figure proportions (1.7 in my case) which can included in the script, what gives the necessary result (attached) . set(1, 'Position', [600 40 1000 800]) global st h = 1; for i=1:nnz(~cellfun('isempty',st.vols)) p1 = get(st.vols{i}.ax{1}.ax,'Position'); p2 = get(st.vols{i}.ax{2}.ax,'Position'); p3 = get(st.vols{i}.ax{3}.ax,'Position'); l = p1(3) + p2(3) + p3(3); sc = (1-0.01)/l; p1 = p1*sc; p2 = p2 * sc; p3 = p3 * sc; p1(4)=p1(4)*1.7; p1(2)= p1(2)-p1(4); p2(4)=p2(4)*1.7; p2(2)= p2(2)-p1(4); p3(4)=p3(4)*1.7; p3(2)= p3(2)-p1(4); set(st.vols{i}.ax{1}.ax,'Position',... [0 h-p1(4) p1(3) p1(4)]); set(st.vols{i}.ax{2}.ax,'Position',... [p1(3)+0.005 h-p2(4) p2(3) p2(4)]); set(st.vols{i}.ax{3}.ax,'Position',.... [p1(3)+p2(3)+0.01 h-p3(4) p3(3) p3(4)]); h = h - p1(4)-0.005; end Thanks a lot for your advices! Vladimir --- On Tue, 2/22/11, Guillaume Flandin <[log in to unmask]> wrote: > From: Guillaume Flandin <[log in to unmask]> > Subject: Re: [SPM] Check Reg Figures SPM8 - size and arrangement > To: "Vladimir Bogdanov" <[log in to unmask]> > Date: Tuesday, February 22, 2011, 4:49 PM > Dear Vladimir, > > the following code should get you started (to be executed > when images > are displayed with checkreg): > > global st > h = 1; > for i=1:nnz(~cellfun('isempty',st.vols)) > p1 = get(st.vols{i}.ax{1}.ax,'Position'); > p2 = get(st.vols{i}.ax{2}.ax,'Position'); > p3 = get(st.vols{i}.ax{3}.ax,'Position'); > l = p1(3) + p2(3) + p3(3); sc = > (1-0.01)/l; > p1 = p1*sc; p2 = p2 * sc; p3 = p3 * sc; > set(st.vols{i}.ax{1}.ax,'Position',... > [0 h-p1(4) p1(3) p1(4)]); > set(st.vols{i}.ax{2}.ax,'Position',... > [p1(3)+0.005 h-p2(4) p2(3) > p2(4)]); > set(st.vols{i}.ax{3}.ax,'Position',.... > [p1(3)+p2(3)+0.01 h-p3(4) p3(3) > p3(4)]); > h = h - p1(4)-0.005; > end > > Best, > Guillaume. > > On 22/02/11 14:58, Vladimir Bogdanov wrote: > > Dear John, > > > > Thank you for your response! Where is the part of the > code responsible for this located? The SPM script is huge > and I am only a beginner. :) > > > > Sincerely yours, > > Vladimir > > > > > > --- On Tue, 2/22/11, John Ashburner <[log in to unmask]> > wrote: > > > >> From: John Ashburner <[log in to unmask]> > >> Subject: Re: [SPM] Check Reg Figures SPM8 - size > and arrangement > >> To: [log in to unmask] > >> Date: Tuesday, February 22, 2011, 3:39 PM > >> There are no default settings that > >> could be changed to make SPM do > >> what you would like it to do. However, the > beauty of > >> having SPM in > >> MATLAB is that it is relatively easy to tweak the > code to > >> make it do > >> exactly what you want. > >> > >> Best regards, > >> -John > >> > >> On 20 February 2011 22:20, Vladimir Bogdanov > <[log in to unmask]> > >> wrote: > >>> Dear SPM experts, > >>> > >>> By default the size of the images in Check Reg > figure > >> does not allow to see well anatomical details (see > screen1 > >> in attachment). This can be changed manually > (screen2), but > >> those changes take time. > >>> > >>> Is there a simple way do it fast? Is it > possible to > >> change SPM settings somewhere to make the figure > in the same > >> way (different from default) every time we call > Check Reg? > >>> > >>> Thank you in advance for your help, > >>> Vladimir > >>> > >>> Volodymyr Bogdanov, PhD > >>> > >>> Headache Research Unit > >>> GIGA - Neurosciences > >>> University of Liege > >>> CHU T4 +1, Sart Tilman > >>> Av de l'Hpital 1 > >>> 4000 Liege, Belgium > >>> > >>> > >>> > >> > > > > > > > > > > > > > -- > Guillaume Flandin, PhD > Wellcome Trust Centre for Neuroimaging > University College London > 12 Queen Square > London WC1N 3BG > --0-2071618827-1298462259=:64948 Content-Type: image/jpeg; name="scr4.jpg" Content-Transfer-Encoding: base64 Content-Disposition: attachment; filename="scr4.jpg" /9j/4AAQSkZJRgABAQEAeAB4AAD/2wBDAAIBAQIBAQICAgICAgICAwUDAwMD AwYEBAMFBwYHBwcGBwcICQsJCAgKCAcHCg0KCgsMDAwMBwkODw0MDgsMDAz/ 2wBDAQICAgMDAwYDAwYMCAcIDAwMDAwMDAwMDAwMDAwMDAwMDAwMDAwMDAwM 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D0H5UbB6D8qKKiHwgg2D0H5UbB6D8qKKtjYbB6D8qbKoCHgdD/I0UUgZ/9k --0-2071618827-1298462259=:64948-- ========================================================================Date: Wed, 23 Feb 2011 12:54:14 +0000 Reply-To: Ciara Greene <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Ciara Greene <[log in to unmask]> Subject: Multivariate Bayes Mime-Version: 1.0 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain; charset="UTF-8" Message-ID: <[log in to unmask]> Hi all, I'm trying to use the multivariate bayes analysis implemented in SPM8 to compare neural coding models in my data. I have two questions I hope you can help me with: 1. I'm a bit confused by the terminology for the model priors. In the Friston et al. NeuroImage paper where this method is described, the various priors were listed as spatial, smooth, singular and support, while in the SPM GUI the options are compact, sparse, smooth and support. I can't find a description of these new labels anywhere, so I'm not sure if the priors have simply been renamed or if these represent new models that weren't in the old version. What, for example, does a 'compact' model reflect? 2. Is it possible to compare models across subjects using random effects? I know that the Bayesian model selection facility in DCM allows for this, but I don't know how to do it in Multivariate Bayes analysis. The BMS button in the GUI allows comparison of different models, but presumably that uses fixed effects, and isn't suitable for group analysis. I haven't been able to find any options to change the inference method. Thanks for your help, Ciara ========================================================================Date: Wed, 23 Feb 2011 14:25:03 +0100 Reply-To: Torben Ellegaard Lund <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Torben Ellegaard Lund <[log in to unmask]> Subject: Re: SPM Digest - 21 Feb 2011 to 22 Feb 2011 (#2011-56) Comments: To: [log in to unmask] In-Reply-To: <[log in to unmask]> MIME-version: 1.0 Content-type: multipart/alternative; boundary="Boundary_(ID_NJMB/RhTT/0+yoWGjAWH2A)" Message-ID: <[log in to unmask]> --Boundary_(ID_NJMB/RhTT/0+yoWGjAWH2A) Content-type: text/plain; CHARSET=US-ASCII Content-transfer-encoding: quoted-printable Dear Richard If you scan a gel phantom you will be convinced that there is low frequency drift coming from the scanner it self. This is due to a lot of things but probably mainly due to heating induced by mechanical vibrations. I would pick the cut-off frequency based on your particular scanner, (most recent scanners that I have seen have little non-white noise faster than the default 128s period used in SPM). Regarding aliasing of cardiac and respiratory noise it is in no way guaranteed to end up at low frequencies. In fact for typical heart and respiration rates and TR values around 2s the variation i e.g. heart rate is so large that there will be cardiac noise at all frequencies, not just the low ones. you can read more here: Foerster BU, Tomasi D, Caparelli EC. Magnetic field shift due to mechanical vibration in functional magnetic resonance imaging. Magn Reson Med. 2005 Nov;54(5):1261-7. PubMed PMID: 16215962; PubMed Central PMCID: PMC2408718. Lund TE, Madsen KH, Sidaros K, Luo WL, Nichols TE. Non-white noise in fMRI: does modelling have an impact? Neuroimage. 2006 Jan 1;29(1):54-66. Epub 2005 Aug 11. PubMed PMID: 16099175. Smith AM, Lewis BK, Ruttimann UE, Ye FQ, Sinnwell TM, Yang Y, Duyn JH, Frank JA. Investigation of low frequency drift in fMRI signal. Neuroimage. 1999 May;9(5):526-33. PubMed PMID: 10329292. https://www.jiscmail.ac.uk/cgi-bin/wa.exe?A2=SPM;651c37f7.00 Best Torben Torben Ellegaard Lund Associate Professor, PhD The Danish National Research Foundation's Center of Functionally Integrative Neuroscience (CFIN) Aarhus University Aarhus University Hospital Building 10G, 5th floor, room 31 Noerrebrogade 44 8000 Aarhus C Denmark Phone: +4589494380 Fax: +4589494400 http://www.cfin.au.dk [log in to unmask] Den Uge:8 23/02/2011 kl. 01.00 skrev SPM automatic digest system: > Fra: Richard Binney <[log in to unmask]> > Dato: Uge:8 22. feb 2011 12.48.38 CET > Emne: acceptable high pass filtering > > > Dear all, > > Something has recently been said to me that has made me think, and I want to get my head around this a bit more..... > > At what point does high pass filtering becomes ineffective? It has not been a concern for me in the past, but recently it has been suggested to me that a rule of thumb is to set the high pass filter at a minimum of 1.5 x your longest SOA. That seems reasonable if this is equal to or less than 128secs. I say that because I beleive that this is the optimum filter setting to remove low-freq noise associated with cardiac/respiratory noise, etc. But what if you use a filter at a lower frequency (e.g., 260secs)? It has been said to me that this would be OK. But aren't you running a risk of alliasing signal of interest at frequencies lower than 0.01Hz with cardiac/respiratory noise etc? IF this is an acceptable risk with a filter of say 260secs, at what point does it becomes unacceptable and the filter becomes ineffective? Eg., Say you had an enomrous longest SOA of 800 secs, you might want to use a filter set at 1000secs (0.001Hz) just to be sure. would this filter be effectively redundant? > > What other factors might speak to this? Jittered SOAs for example? Using a range of SOAs would of course spread the signal of interest across frequencies increasing sensitivity. Does this have an effect of reducing the risk of alliasing with low-freq noise or are you still losing a significant proprotion of your signal in the <0.1Hz frequencies (either due to noise or a 128 sec filter)? In what manner should this inform your high-pass filter? Should you be concerned with the longest SOA or the mean SOA (fundamental frequency) of your signal? > > Thanks in advance for your help, > > Richard --Boundary_(ID_NJMB/RhTT/0+yoWGjAWH2A) Content-type: text/html; CHARSET=US-ASCII Content-transfer-encoding: quoted-printable Dear Richard

If you scan a gel phantom you will be convinced that there is low frequency drift coming from the  scanner it self. This is due to a lot of things but probably mainly due to heating induced by mechanical vibrations. I would pick the cut-off frequency based on your particular scanner, (most recent scanners that I have seen have little non-white noise faster than the default 128s period used in SPM). Regarding aliasing of cardiac and respiratory noise it is in no way guaranteed to end up at low frequencies. In fact for typical heart and respiration rates and TR values around 2s the variation i e.g. heart rate is so large that there will be cardiac noise at all frequencies, not just the low ones.

you can read more here:

Foerster BU, Tomasi D, Caparelli EC. Magnetic field shift due to mechanical
vibration in functional magnetic resonance imaging. Magn Reson Med. 2005
Nov;54(5):1261-7. PubMed PMID: 16215962; PubMed Central PMCID: PMC2408718.

Lund TE, Madsen KH, Sidaros K, Luo WL, Nichols TE. Non-white noise in fMRI:
does modelling have an impact? Neuroimage. 2006 Jan 1;29(1):54-66. Epub 2005 Aug 
11. PubMed PMID: 16099175.

Smith AM, Lewis BK, Ruttimann UE, Ye FQ, Sinnwell TM, Yang Y, Duyn JH, Frank
JA. Investigation of low frequency drift in fMRI signal. Neuroimage. 1999
May;9(5):526-33. PubMed PMID: 10329292.

https://www.jiscmail.ac.uk/cgi-bin/wa.exe?A2=SPM;651c37f7.00



Best
Torben


Torben Ellegaard Lund
Associate Professor, PhD
The Danish National Research Foundation's Center of Functionally Integrative Neuroscience (CFIN)
Aarhus University
Aarhus University Hospital
Building 10G, 5th floor, room 31
Noerrebrogade 44
8000 Aarhus C
Denmark
Phone: +4589494380
Fax: +4589494400
http://www.cfin.au.dk
[log in to unmask]







Den Uge:8 23/02/2011 kl. 01.00 skrev SPM automatic digest system:

Fra: Richard Binney <[log in to unmask]>
Dato: Uge:8 22. feb 2011 12.48.38 CET
Emne: acceptable high pass filtering


Dear all,
 
Something has recently been said to me that has made me think, and I want to get my head around this a bit more.....
 
At what point does high pass filtering becomes ineffective? It has not been a concern for me in the past, but recently it has been suggested to me that a rule of thumb is to set the high pass filter at a minimum of 1.5 x your longest SOA. That seems reasonable if this is equal to or less than 128secs. I say that because I beleive that this is the optimum filter setting to remove low-freq noise associated with cardiac/respiratory noise, etc. But what if you use a filter at a lower frequency (e.g., 260secs)? It has been said to me that this would be OK. But aren't you running a risk of alliasing signal of interest at frequencies lower than 0.01Hz with cardiac/respiratory noise etc? IF this is an acceptable risk with a filter of say 260secs, at what point does it becomes unacceptable and the filter becomes ineffective? Eg., Say you had an enomrous longest  SOA of 800 secs, you might want to use a filter set at 1000secs (0.001Hz) just to be sure. would this filter be effectively redundant?
 
What other factors might speak to this? Jittered SOAs for example? Using a range of SOAs would of course spread the signal of interest across frequencies increasing sensitivity. Does this have an effect of reducing the risk of alliasing with low-freq noise or are you still losing a significant proprotion of your signal in the <0.1Hz frequencies (either due to noise or a 128 sec filter)? In what manner should this inform your high-pass filter? Should you be concerned with the longest SOA or the mean SOA (fundamental frequency) of your signal? 
 
Thanks in advance for your help,
 
Richard 



--Boundary_(ID_NJMB/RhTT/0+yoWGjAWH2A)-- ========================================================================Date: Wed, 23 Feb 2011 13:25:54 +0000 Reply-To: John Ashburner <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: John Ashburner <[log in to unmask]> Subject: Re: Batch issue Comments: To: Marine Lazouret <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> I'd guess that you have a batch that was created with one version of SPM8 (which is in /Applications/MATLAB_R2008a/spm8 ), and you are trying to run it on a different computer where /Applications/MATLAB_R2008a/spm8/tpm/grey.nii does not exist. Best regards, -John On 23 February 2011 09:10, Marine Lazouret <[log in to unmask]> wrote: > Hello, > I made a batch for spatial pre processing and it stops every time during > segmentation with this message: > Running 'Segment' > Failed 'Segment' > Error using ==> spm_vol>subfunc at 111 > File "/Applications/MATLAB_R2008a/spm8/tpm/grey.nii" does not exist. > In file "/Applications/spm8/spm_vol.m" (v2237), function "subfunc" at line > 111. > In file "/Applications/spm8/spm_vol.m" (v2237), function "subfunc1" at line > 84. > In file "/Applications/spm8/spm_vol.m" (v2237), function "subfunc2" at line > 70. > In file "/Applications/spm8/spm_vol.m" (v2237), function "spm_vol" at line > 54. > In file "/Applications/spm8/spm_preproc.m" (v1143), function "spm_preproc" > at line 66. > In file "/Applications/spm8/config/spm_run_preproc.m" (v2312), function > "spm_run_preproc" at line 19. > No executable modules, but still unresolved dependencies or incomplete > module inputs. > The following modules did not run: > Failed: Segment > Skipped: Normalise: Write > Skipped: Smooth > If i treat my images step by step, nothing goes wrong and I can get to the > end of it. Does any one have an idea where this problem could be coming > from? > -- > Marine > ========================================================================Date: Wed, 23 Feb 2011 09:55:14 -0500 Reply-To: justine dupont <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: justine dupont <[log in to unmask]> Subject: Segmentation anomalies Content-Type: multipart/mixed; boundary="_5f5f7fd2-b3cc-4461-9fb1-7f8576aaf374_" MIME-Version: 1.0 Message-ID: <[log in to unmask]> --_5f5f7fd2-b3cc-4461-9fb1-7f8576aaf374_ Content-Type: multipart/alternative; boundary="_5b2db070-3df8-4055-97e2-8684dd3b694f_" --_5b2db070-3df8-4055-97e2-8684dd3b694f_ Content-Type: text/plain; charset="iso-8859-1" Content-Transfer-Encoding: quoted-printable Dear experts I recently saw something very puzzling with a VBM analysis. I have 40 T1 scans. They all have the same dimensions and voxel size and the raw images all look consistent and normal. Segmentation (with normalisation and modulation) works fine for 38 but for one the GM result is an empty brain (top row of attached image) and for the second the result is a kind of 'half brain' (bottom row of attached image). What causes this and can it be fixed? Many thanks Justine --_5b2db070-3df8-4055-97e2-8684dd3b694f_ Content-Type: text/html; charset="iso-8859-1" Content-Transfer-Encoding: quoted-printable Dear experts

I recently saw something very puzzling with a VBM analysis.  I have 40 T1 scans.  They all have the same dimensions and voxel size and the raw images all look consistent and normal.  Segmentation (with normalisation and modulation) works fine for 38 but for one the GM result is an empty brain (top row of attached image) and for the second the result is a kind of 'half brain' (bottom row of attached image).  

What causes this and can it be fixed?

Many thanks

Justine

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unmask]> Subject: paired t-test issues Mime-Version: 1.0 Content-Type: multipart/mixed; boundary="part-gwZJ1dAgGbAA3cEDw04oc1CAA3yAQAnX3Uu27qORZYmBd" Message-ID: <[log in to unmask]> --part-gwZJ1dAgGbAA3cEDw04oc1CAA3yAQAnX3Uu27qORZYmBd Content-Type: multipart/mixed; boundary="part-vAWAFKNRvVgo4ABWzQAFS9A83UFwC9AbFBM1AiyhuhNcI" This is a multi-part message in MIME format. --part-vAWAFKNRvVgo4ABWzQAFS9A83UFwC9AbFBM1AiyhuhNcI Content-Transfer-Encoding: quoted-printable Content-Type: text/plain; charset="UTF-8" Hello All, After specifying my second level analysis using a paired t-test design, I noticed in the parameter estimability my “betas are not uniquely specified”. I am not sure what this means and wanted to know if I have made a mistake. At the first level analysis from individual subject models, I created two contrasts images for each subject. Each subject underwent two sessions (after different treatments for each scan, at different times points, with identical paradigms) and I wanted to test whether condition A > condition B between the two sessions. I am using spm8 and entered each pair of subject contrasts (17 total using fMRI data) into the second level and used all the defaults for a paired t-test. I have also attached the design matrix. Also, I am not sure what the contrast weights should look like to for the paired t-test design. Any help would be appreciated, also please let me know if you need more information. Thanks in advance. 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========================================================================Date: Wed, 23 Feb 2011 16:17:06 +0100 Reply-To: Marko Wilke <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Marko Wilke <[log in to unmask]> Subject: Re: Segmentation anomalies Comments: To: justine dupont <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1; format=flowed Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> Hello Justine, this looks like the initial affine registration did not work, perhaps due to image inhomogeneity. Aligning the images nicely, for example by coregistering to a template prior to segmentation, may help, as may fiddling with the inhomogeneity parameters (bias FHWM etc.). Good luck, Marko justine dupont wrote: > Dear experts > > I recently saw something very puzzling with a VBM analysis. I have 40 T1 > scans. They all have the same dimensions and voxel size and the raw > images all look consistent and normal. Segmentation (with normalisation > and modulation) works fine for 38 but for one the GM result is an empty > brain (top row of attached image) and for the second the result is a > kind of 'half brain' (bottom row of attached image). > > What causes this and can it be fixed? > > Many thanks > > Justine > -- ____________________________________________________ PD Dr. med. Marko Wilke Facharzt fr Kinder- und Jugendmedizin Leiter, Experimentelle Pdiatrische Neurobildgebung Universitts-Kinderklinik Abt. III (Neuropdiatrie) Marko Wilke, MD, PhD Pediatrician Head, Experimental Pediatric Neuroimaging University Children's Hospital Dept. III (Pediatric Neurology) Hoppe-Seyler-Str. 1 D - 72076 Tbingen, Germany Tel. +49 7071 29-83416 Fax +49 7071 29-5473 [log in to unmask] http://www.medizin.uni-tuebingen.de/kinder/epn ____________________________________________________ ========================================================================Date: Wed, 23 Feb 2011 16:29:39 +0100 Reply-To: Martin Jensen Dietz <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Martin Jensen Dietz <[log in to unmask]> Subject: Re: paired t-test issues Comments: To: Nero Evero <[log in to unmask]> In-Reply-To: <[log in to unmask]> Content-Type: text/plain; charset="Windows-1252" Content-Transfer-Encoding: quoted-printable MIME-Version: 1.0 Message-ID: <[log in to unmask]> Hi Nero, The betas are not unique because subject columns introduce non-orthogonality in the design matrix. This is completely normal however and the default for a paired t-test design matrix. Your contrast weights are zeros(1,17) 1 -1 zeros(1,17) -1 1 Best wishes, Martin On Feb 23, 2011, at 3:59 PM, Nero Evero wrote: > Hello All, > > After specifying my second level analysis using a paired t-test design, I noticed in the parameter estimability my betas are not uniquely specified. I am not sure what this means and wanted to know if I have made a mistake. At the first level analysis from individual subject models, I created two contrasts images for each subject. Each subject underwent two sessions (after different treatments for each scan, at different times points, with identical paradigms) and I wanted to test whether condition A > condition B between the two sessions. I am using spm8 and entered each pair of subject contrasts (17 total using fMRI data) into the second level and used all the defaults for a paired t-test. I have also attached the design matrix. Also, I am not sure what the contrast weights should look like to for the paired t-test design. Any help would be appreciated, also please let me know if you need more information. Thanks in advance. > > Nero > > ========================================================================Date: Wed, 23 Feb 2011 15:39:06 +0000 Reply-To: Chris Filo Gorgolewski <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Chris Filo Gorgolewski <[log in to unmask]> Subject: Re: Neuroimaging Data Processing Workshop 23-24 March 2011, Edinburgh, UK Comments: To: nipy-devel <[log in to unmask]>, [log in to unmask], [log in to unmask], [log in to unmask], freesurfer <[log in to unmask]>, FSL - FMRIB's Software Library <[log in to unmask]> Comments: cc: dtc-edinburgh <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=UTF-8 Message-ID: <[log in to unmask]> Registration is now open. https://www.epay.ed.ac.uk/browse/extra_info.asp?compid=1&catidB&modid=2&prodidE3&deptid$&prodvarid=0 Best regards, Chris Gorgolewski On 18 February 2011 17:58, Chris Filo Gorgolewski <[log in to unmask]> wrote: > Dear all, > > I am delighted to invite you to a Neuroimaging Data Processing > Workshop which will be held on 23-24th of March 2011 at University of > Edinburgh, UK. During the workshop we will cover neuroimaging data > analysis and management with reusable, scalable and reproducible > processing workflows that combine different software packages (such as > SPM, FSL, and FreeSurfer) using NiPyPE framework. The workshop will > also feature talks and demos covering data management, encapsulation > and visualization using PyXNAT and the Connectome Library and Viewer. > More details can be found at the workshop website: > http://nipype.blogspot.com > > Best regards, > Chris Gorgolewski > ========================================================================Date: Wed, 23 Feb 2011 11:51:53 -0500 Reply-To: justine dupont <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: justine dupont <[log in to unmask]> Subject: segmentation anomalies Content-Type: multipart/alternative; boundary="_0dea0aa1-ab97-4673-840d-8dde58316bbb_" MIME-Version: 1.0 Message-ID: <[log in to unmask]> --_0dea0aa1-ab97-4673-840d-8dde58316bbb_ Content-Type: text/plain; charset="iso-8859-1" Content-Transfer-Encoding: quoted-printable Dear Abela, Marko, Shail, Donald and others surprisingly, given the consensus, the images were perfectly aligned. So the mystery remains...? Justine --_0dea0aa1-ab97-4673-840d-8dde58316bbb_ Content-Type: text/html; charset="iso-8859-1" Content-Transfer-Encoding: quoted-printable Dear Abela, Marko, Shail, Donald and others

surprisingly, given the consensus, the images were perfectly aligned. So the mystery remains...? 

Justine



--_0dea0aa1-ab97-4673-840d-8dde58316bbb_-- ========================================================================Date: Wed, 23 Feb 2011 12:27:44 -0500 Reply-To: Jonathan Peelle <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Jonathan Peelle <[log in to unmask]> Subject: Re: Segmentation anomalies In-Reply-To: <[log in to unmask]> Content-Type: text/plain; charset=iso-8859-1 Mime-Version: 1.0 (Apple Message framework v1082) Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> Hi Justine, I think that Marko is correct in that it is worth investigating the image inhomogeneity and bias correction parameters. If the original alignment is ok, as you say, you may be able to try different bias correction settings. Alternatively, you can do a two-pass bias correction procedure, which is probably less elegant but often seems to work. To do this, run segmentation once and output the bias-corrected image, but no segmentations. Then run segmentation again on this bias-corrected image. For images with significant inhomogeneity this often works wonders. Best regards, Jonathan On Feb 23, 2011, at 10:17 AM, Marko Wilke wrote: > Hello Justine, > > this looks like the initial affine registration did not work, perhaps due to image inhomogeneity. Aligning the images nicely, for example by coregistering to a template prior to segmentation, may help, as may fiddling with the inhomogeneity parameters (bias FHWM etc.). > > Good luck, > Marko > > justine dupont wrote: >> Dear experts >> >> I recently saw something very puzzling with a VBM analysis. I have 40 T1 >> scans. They all have the same dimensions and voxel size and the raw >> images all look consistent and normal. Segmentation (with normalisation >> and modulation) works fine for 38 but for one the GM result is an empty >> brain (top row of attached image) and for the second the result is a >> kind of 'half brain' (bottom row of attached image). >> >> What causes this and can it be fixed? >> >> Many thanks >> >> Justine >> > > -- > ____________________________________________________ > PD Dr. med. Marko Wilke > Facharzt fr Kinder- und Jugendmedizin > Leiter, Experimentelle Pdiatrische Neurobildgebung > Universitts-Kinderklinik > Abt. III (Neuropdiatrie) > > > Marko Wilke, MD, PhD > Pediatrician > Head, Experimental Pediatric Neuroimaging > University Children's Hospital > Dept. III (Pediatric Neurology) > > > Hoppe-Seyler-Str. 1 > D - 72076 Tbingen, Germany > Tel. +49 7071 29-83416 > Fax +49 7071 29-5473 > [log in to unmask] > > http://www.medizin.uni-tuebingen.de/kinder/epn > ____________________________________________________ ========================================================================Date: Wed, 23 Feb 2011 20:20:38 +0000 Reply-To: Nero Evero <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Nero Evero <[log in to unmask]> Subject: Re: paired t-test issues Mime-Version: 1.0 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain; charset="UTF-8" Message-ID: <[log in to unmask]> Thank you Martin for your quick responses. I have another question, if anyone could help. After completing the 2nd level analysis and creating my contrast, I noticed I had no significantly activated clusters compared to the series of within-subjects contrasts I created earlier. I was curious why that may be; possibly a lack of power (i.e. only 17 subjects) to detect any significant difference between the two treatments? Again, here is a review of my design for my crossover study: Session 1 --> Treatment 1 --> Scan (Visual paradigm: Active vs. Control) Session 2 --> Treatment 2 --> Scan (Visual paradigm: Active vs. Control) Also, would it be reasonable to run a one-way ANOVA for each session (as opposed to a paired t-test) and compare which regions are significantly activated. With this approach I was concerned I would not be able to infer one treatment was signifcantly different than another, would I be correct? Thanks for any comments in advance. Nero ========================================================================Date: Thu, 24 Feb 2011 03:47:59 +0000 Reply-To: Dashjamts Jargal <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Dashjamts Jargal <[log in to unmask]> Subject: Umodulated image analysis better in discrimination: possible explanation? Mime-Version: 1.0 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain; charset="UTF-8" Message-ID: <[log in to unmask]> Dear all, I am novice in the SPM. There are many questions regarding the interpretation of SPM analysis results modulated versus unmodulated structural images. I am studying Alzheimer subjects compared to healthy aged controls. I have used T1 WI images of same size, orientation and scanner, applied DARTEL tool as implemented in SPM8. Proportional global normalization eliminated multiple scattered areas of interest in the unmodulated date and produced better localization of the findings into MTL structures in modulated data. But still even after proportional global normalization, my globally normalized unmodulated data show larger relevant difference areas and have higher diagnostic accuracy than the globally normalized modulated. What could explain such result? Why the unmodulated demonstrated much more affected areas than the modulated? Is the following correct according to the definition of how modulation works: "perfectly registered unmodulated data should show no difference between the groups"?Does it mean that unmodulated data have some compound of registration failures? When I am adding covariates such as TIV, age and sex to both modulated and unmodulated ANCOVA with normalization, there is only slight improvement.( I think it is improvement because after that I am loosing those few voxels which were in the deep subcortical white matter.) I am looking forward to receiving your comments and thank you for your time. Jargal Dashjamts, PhD-student Kyushu University, Japan/ HSUM, Mongolia ========================================================================Date: Wed, 23 Feb 2011 16:36:13 -0800 Reply-To: Meghan Meyer <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Meghan Meyer <[log in to unmask]> Subject: Re: Contrast Manager Error in SPM8 In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/alternative; boundaryMessage-ID: <[log in to unmask]> --0023547c90239ad82a049cfc6633 Content-Type: text/plain; charset=ISO-8859-1 more info on this error: the model was not estimated bc of a problem using 'svd'.... Running 'Model estimation' SPM8: spm_spm (v3960) 16:29:05 - 23/02/2011 ======================================================================Initialising parameters : ...computingFailed 'Model estimation' Error using ==> svd Input to SVD must not contain NaN or Inf. In file "/space/raid/fmri/spm8/spm_sp.m" (v1143), function "sf_set" at line 1126. In file "/space/raid/fmri/spm8/spm_sp.m" (v1143), function "spm_sp" at line 225. In file "/space/raid/fmri/spm8/spm_spm.m" (v3960), function "spm_spm" at line 439. In file "/space/raid/fmri/spm8/config/spm_run_fmri_est.m" (v3691), function "spm_run_fmri_est" at line 33. Running 'Contrast Manager' Changing directory to: /space/raid8/data/lieber/SWM/SWM08/analysis/swm_ppi_delay6s Failed 'Contrast Manager' Error using ==> spm_run_con at 37 This model has not been estimated. On Wed, Feb 23, 2011 at 4:11 PM, Meghan Meyer <[log in to unmask]> wrote: > Hello, > I'm running 1st level analyses in spm8, but for some of my subjects, i'm > getting the following error below, but i'm not sure why the model would not > have been estimated. the error appears for 9 of my 18 subjects. the other 9 > ran fine. Thanks! > > Running 'Contrast Manager' > Changing directory to: > /space/raid8/data/lieber/SWM/SWM08/analysis/swm_ppi_delay6s > Failed 'Contrast Manager' > Error using ==> spm_run_con at 37 > This model has not been estimated. > In file "/space/raid/fmri/spm8/config/spm_run_con.m" (v3993), function > "spm_run_con" at line 37. > > The following modules did not run: > Failed: fMRI model specification > Failed: Model estimation > Failed: Contrast Manager > > -- > Meghan Meyer, M.A. > Graduate Student > Social Cognitive Neuroscience Lab > UCLA, Psychology > -- Meghan Meyer, M.A. Graduate Student Social Cognitive Neuroscience Lab UCLA, Psychology --0023547c90239ad82a049cfc6633 Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable more info on this error: the model was not estimated bc of a problem using 'svd'....
Running 'Model estimation'

SPM8: spm_spm (v3960) 16:29:05 - 23/02/2011
========================================================================
Initialising parameters : ...computingFailed 'Model estimation'
Error using ==> svd
Input to SVD must not contain NaN or Inf.
In file "/space/raid/fmri/spm8/spm_sp.m" (v1143), function "sf_set" at line 1126.
In file "/space/raid/fmri/spm8/spm_sp.m" (v1143), function "spm_sp" at line 225.
In file "/space/raid/fmri/spm8/spm_spm.m" (v3960), function "spm_spm" at line 439.
In file "/space/raid/fmri/spm8/config/spm_run_fmri_est.m" (v3691), function "spm_run_fmri_est" at line 33.

Running 'Contrast Manager'
Changing directory to: /space/raid8/data/lieber/SWM/SWM08/analysis/swm_ppi_delay6s
Failed 'Contrast Manager'
Error using ==> spm_run_con at 37
This model has not been estimated.

On Wed, Feb 23, 2011 at 4:11 PM, Meghan Meyer <[log in to unmask]> wrote:
Hello,
I'm running 1st level analyses in spm8, but for some of my subjects, i'm getting the following error below, but i'm not sure why the model would not have been estimated. the error appears for 9 of my 18 subjects. the other 9 ran fine. Thanks!

Running 'Contrast Manager'
Changing directory to: /space/raid8/data/lieber/SWM/SWM08/analysis/swm_ppi_delay6s
Failed 'Contrast Manager'
Error using ==> spm_run_con at 37
This model has not been estimated.
In file "/space/raid/fmri/spm8/config/spm_run_con.m" (v3993), function "spm_run_con" at line 37.

The following modules did not run:
Failed: fMRI model specification
Failed: Model estimation
Failed: Contrast Manager

--
Meghan Meyer, M.A.
Graduate Student
Social Cognitive Neuroscience Lab
UCLA, Psychology



--
Meghan Meyer, M.A.
Graduate Student
Social Cognitive Neuroscience Lab
UCLA, Psychology
--0023547c90239ad82a049cfc6633-- ========================================================================Date: Thu, 24 Feb 2011 02:12:23 +0000 Reply-To: Israr Ul Haq <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Israr Ul Haq <[log in to unmask]> Subject: fixed effects analysis across two sessions Mime-Version: 1.0 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain; charset="UTF-8" Message-ID: <[log in to unmask]> Dear Spm users, I am trying to see treatment effects on a patient, by putting his pre and post treatment sessions (all the runs separately) in one fixed effects analysis, and defining post – pre contrast (t) by giving positive one to the experimental condition in the post treatment runs and negative one in the pretreatment runs. This is all being done at the ‘specify first level’ option in spm8. It made sense and the few people I did ask seem to think this was okay too. However I came across something that has me confused and it would be great to hear an explanation. I had been including the control condition in the contrast too, so for the post treatment runs it was included as a negative one and for the pretreatment runs a positive one (just how it’s supposed to be contrasted out of the experiment condition at each session level, by giving it a weightage equal and opposite to the experiment condition). I thought I was getting a reasonable result from the contrast till I fortunately or unfortunately tried a contrast without the control condition, which is positive and negative ones only for the experimental condition, post and pretreatment respectively. This now is giving me FAR less activation then the contrast with the control condition, which is opposite to what i was expecting, since I though the whole point of including the control condition was to subtract activations unrelated to the process of interest, making the result purer so to speak. Since I have a medicine background and limited statistical knowledge, it would be great if you can point out whether this is possible and adding the control condition into each run somehow increases the t statistic when the analysis is done across sessions, or if I am doing something wrong. My t contrast for the fixed effects is: -1 1 -1 1 1 -1 1 -1 . where the sequence of runs put into the model specification part is pre tx run1, pre tx run2, post tx run1 and post tx run2, and each run has an experimental and a control condition. Will extremely appreciate help in this matter. Regards Israr ========================================================================Date: Thu, 24 Feb 2011 09:35:18 +0100 Reply-To: "Kay H. Brodersen" <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: "Kay H. Brodersen" <[log in to unmask]> Subject: Re: multivariate bayes analysis Comments: To: Ciara Greene <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; format=flowed; charset="UTF-8"; reply-type=original Content-Transfer-Encoding: 7bit Message-ID: <9C3287B48E0C415E9A5E53EF766836C4@KHB> Dear Ciara, Great to hear you found the SPM course useful. With regard to your first question: the priors in Multivariate Bayes have not been renamed. Instead, the code actually contains more priors than the GUI offers. You can see this by comparing the priors listed in spm_mvb_estimate (line 78) to those actually supported in spm_mvb_U (starting in line 40). I would suggest starting off by comparing those models that are directly listed in the GUI. Your second question relates to fixed-effects versus random-effects model comparison. SPM currently does not provide a fully automated pipeline for comparing different MVB coding hypotheses (i.e., spatial priors). However, this is easy to do with just a few Matlab commands. You would begin by running MVB separately for all subjects and coding hypotheses. Given n subjects and m models, this results in n*m different MVB.mat files. You then extract the log model evidences from these files (F) and arrange them in an n*m matrix M. (i) For fixed-effects model comparison, you would then compute group Bayes factors as sum(M,1) and select the model with the highest group Bayes factor. This analysis relies on the assumption that the same model is best in all subjects. (ii) For a random-effects model comparison, you can use spm_BMS(M, ...). This approach relaxes the assumption above and explicitly accounts for between-subjects variability. Let me know if this works. I'm copying this to the SPM mailing list so that other users of MVB may benefit from our discussion. Very best wishes Kay -- Kay Henning Brodersen Department of Computer Science Pattern Analysis and Machine Learning Group ETH Zurich Switzerland [log in to unmask] http://people.inf.ethz.ch/bkay/ From: Ciara Greene Sent: Monday, February 21, 2011 3:34 PM To: [log in to unmask] Subject: multivariate bayes analysis Hi Kay, Thanks for the interesting practical session on multivariate analysis at the SPM course last week, I really enjoyed it and I'm hoping to put it to good use. I'm trying out the multivariate bayes method with a view to comparing coding models in my data, and I had a couple of questions; I hope you don't mind answering them! Firstly, I'm a bit confused by the terminology for the model priors. In the Friston et al. NeuroImage paper, the various priors were listed as spatial, smooth, singular and support, while in the SPM GUI the options are compact, sparse, smooth and support. I can't find a description of these new labels anywhere, so I'm not sure if the priors have simply been renamed (e.g. singular becoming compact???) or if these represent new models that weren't in the old version. My second question related to comparing models across subjects. For obvious reasons, I'm not really interested in model comparison within a single subject, I want to see which model seems best in my whole sample (and by extension, in the population). I've read a bit about the new Bayesian model selection method for DCM implemented in SPM8 which allows a random effects comparsion of models across subjects, but I can't get that to work with the multivariate bayes. The BMS button in the GUI allows models to be compared to one another, but presumably that uses fixed effects, and isn't suitable for group analysis. As far as I understand, it also doesn't allow the results of the analyses to be saved out and carried forward to a second level. Do you know if it's possible to use the DCM model selection method outside DCM, or alternatively if there's another way of running a group level analysis here? Thanks in advance for any help you can provide! Ciara ========================================================================Date: Wed, 23 Feb 2011 16:11:21 -0800 Reply-To: Meghan Meyer <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Meghan Meyer <[log in to unmask]> Subject: Contrast Manager Error in SPM8 MIME-Version: 1.0 Content-Type: multipart/alternative; boundaryMessage-ID: <[log in to unmask]> --0023547c8b43a1e6d7049cfc0d30 Content-Type: text/plain; charset=ISO-8859-1 Hello, I'm running 1st level analyses in spm8, but for some of my subjects, i'm getting the following error below, but i'm not sure why the model would not have been estimated. the error appears for 9 of my 18 subjects. the other 9 ran fine. Thanks! Running 'Contrast Manager' Changing directory to: /space/raid8/data/lieber/SWM/SWM08/analysis/swm_ppi_delay6s Failed 'Contrast Manager' Error using ==> spm_run_con at 37 This model has not been estimated. In file "/space/raid/fmri/spm8/config/spm_run_con.m" (v3993), function "spm_run_con" at line 37. The following modules did not run: Failed: fMRI model specification Failed: Model estimation Failed: Contrast Manager -- Meghan Meyer, M.A. Graduate Student Social Cognitive Neuroscience Lab UCLA, Psychology --0023547c8b43a1e6d7049cfc0d30 Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Hello,
I'm running 1st level analyses in spm8, but for some of my subjects, i'm getting the following error below, but i'm not sure why the model would not have been estimated. the error appears for 9 of my 18 subjects. the other 9 ran fine. Thanks!

Running 'Contrast Manager'
Changing directory to: /space/raid8/data/lieber/SWM/SWM08/analysis/swm_ppi_delay6s
Failed 'Contrast Manager'
Error using ==> spm_run_con at 37
This model has not been estimated.
In file "/space/raid/fmri/spm8/config/spm_run_con.m" (v3993), function "spm_run_con" at line 37.

The following modules did not run:
Failed: fMRI model specification
Failed: Model estimation
Failed: Contrast Manager

--
Meghan Meyer, M.A.
Graduate Student
Social Cognitive Neuroscience Lab
UCLA, Psychology
--0023547c8b43a1e6d7049cfc0d30-- ========================================================================Date: Thu, 24 Feb 2011 10:25:46 +0100 Reply-To: Martin Jensen Dietz <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Martin Jensen Dietz <[log in to unmask]> Subject: Re: paired t-test issues Comments: To: Nero Evero <[log in to unmask]> In-Reply-To: <[log in to unmask]> Content-Type: text/plain; charset="us-ascii" Content-Transfer-Encoding: quoted-printable MIME-Version: 1.0 Message-ID: <[log in to unmask]> Hi Nero, ANOVA is used in the case where you wish to test hypothesis concerning >2 beta or contrast images. Using a paired t-test on 2 contrast images, as in your case, is more straight forward. Alternatively, you could subtract your contrast images in ImCalc and perform a one-sample t-test. Best wishes, Martin On Feb 23, 2011, at 9:20 PM, Nero Evero wrote: > Thank you Martin for your quick responses. I have another question, if anyone could help. After completing the 2nd level analysis and creating my contrast, I noticed I had no significantly activated clusters compared to the series of within-subjects contrasts I created earlier. I was curious why that may be; possibly a lack of power (i.e. only 17 subjects) to detect any significant difference between the two treatments? Again, here is a review of my design for my crossover study: > > Session 1 --> Treatment 1 --> Scan (Visual paradigm: Active vs. Control) > > Session 2 --> Treatment 2 --> Scan (Visual paradigm: Active vs. Control) > > Also, would it be reasonable to run a one-way ANOVA for each session (as opposed to a paired t-test) and compare which regions are significantly activated. With this approach I was concerned I would not be able to infer one treatment was signifcantly different than another, would I be correct? Thanks for any comments in advance. > > Nero ========================================================================Date: Thu, 24 Feb 2011 12:03:13 +0100 Reply-To: guillaume auzias <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: guillaume auzias <[log in to unmask]> Subject: DARTEL create template: minimum number of subjects? MIME-Version: 1.0 Content-Type: multipart/alternative; boundaryMessage-ID: [log in to unmask]> --0016364ee4e2e918b9049d0528d9 Content-Type: text/plain; charset=ISO-8859-1 Hello, I've not been able to find in the SPM list archives a clear answer to the following questions: Is there a minimum number of subjects required for the template creation using DARTEL? Does the registration of a pair of brains through a specifically created 2-brains template makes any sense? Thanks for any input, Guillaume --0016364ee4e2e918b9049d0528d9 Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Hello,

I've not been able to find in the SPM list archives a clear answer to the following questions:

Is there a minimum number of subjects required for the template creation using DARTEL?
Does the registration of a pair of brains through a specifically created 2-brains template makes any sense?

Thanks for any input,

Guillaume
--0016364ee4e2e918b9049d0528d9-- ========================================================================Date: Thu, 24 Feb 2011 19:16:50 +0800 Reply-To: li jian <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: li jian <[log in to unmask]> Subject: Re: MATLAB Out of Memory error Comments: To: Dennis Thompson <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/alternative; boundaryMessage-ID: <[log in to unmask]> --0016e64bbe8ea02358049d055915 Content-Type: text/plain; charset=GB2312 Content-Transfer-Encoding: quoted-printable maybe you can add the virtual memory in window system. http://www.delete-computer-history.com/increase-virtual-memory.html Addtionally, you could used "free" command in matlab. 2011/2/19 Dennis Thompson <[log in to unmask]> > Window 32 bit limits you to 2 GB of memory by default . There are some > tricks to boost that to 3GB as outlined by Matlab in this link > > > http://www.mathworks.com/help/techdoc/matlab_prog/brh72ex-49.html#brh72ex-67 > > > Here at the IRC we do all our processing on 64 bit linux computers. Have > not had a "Out of memory error" in years. > > > > On Thu, Feb 17, 2011 at 7:32 PM, Nero Evero <[log in to unmask]> wrote: > >> Hello All, >> >> We are trying to run a fixed effects analysis using SPM8 on a Windows 7 >> 32-bit OS with 4GM of RAM. We have 120 subjects/sessions with a total of >> 6600 scans (55/session). The analysis stops during the parameter estimation >> and gives the following erroe message: >> >> Initialising parameters : ...done >> Output images : ...initialised >> Plane 1/46 , block 1/3 : >> ...estimation??? Out of memory. Type HELP MEMORY for your options. >> >> Error in ==> spm_spm at 715 >> CY = CY + Y*Y'; >> >> Error in ==> spm_getSPM at 233 >> SPM = spm_spm(SPM); >> >> Error in ==> spm_results_ui at 277 >> [SPM,xSPM] = spm_getSPM; >> >> ??? Error while evaluating uicontrol Callback >> >> I tried adding more memory to SPM (i.e. by changing defaults.stats.maxmem >> to about 2GB), but I still received the error. Looking through the archives >> it seems like the common solution is to change to a 64-bit OS, but I wanted >> to know if there was any other possible solutions? Thanks in adavance. >> >> Nero >> > > --  Jian Li, Institute of neuroinformatics, Dalian University of Technology, NO.2 Linggong Rd, Dalian, P.R.China 116024 --0016e64bbe8ea02358049d055915 Content-Type: text/html; charset=GB2312 Content-Transfer-Encoding: quoted-printable
maybe you can add the virtual memory in window system.
Addtionally, you could used "free" command in matlab.
 


 
2011/2/19 Dennis Thompson <[log in to unmask]>
Window 32 bit limits you to 2 GB of memory by default .  There are some tricks to boost that to 3GB as outlined by Matlab in this link

http://www.mathworks.com/help/techdoc/matlab_prog/brh72ex-49.html#brh72ex-67


Here at the IRC we do all our processing on 64 bit linux computers.  Have not had a "Out of memory error" in years.



On Thu, Feb 17, 2011 at 7:32 PM, Nero Evero <[log in to unmask]> wrote:
Hello All,

We are trying to run a fixed effects analysis using SPM8 on a Windows 7 32-bit OS with 4GM of RAM.  We have 120 subjects/sessions with a total of 6600 scans (55/session).  The analysis stops during the parameter estimation and gives the following erroe message:

Initialising parameters                 :                        ...done
Output images                           :                 ...initialised
Plane   1/46 , block   1/3              :                  ...estimation??? Out of memory. Type HELP MEMORY for your options.

Error in ==> spm_spm at 715
               CY         = CY + Y*Y';

Error in ==> spm_getSPM at 233
        SPM = spm_spm(SPM);

Error in ==> spm_results_ui at 277
       [SPM,xSPM] = spm_getSPM;

??? Error while evaluating uicontrol Callback

I tried adding more memory to SPM (i.e. by changing defaults.stats.maxmem to about 2GB), but I still received the error.  Looking through the archives it seems like the common solution is to change to a 64-bit OS, but I wanted to know if there was any other possible solutions?  Thanks in adavance.

Nero




--

Jian Li,
Institute of neuroinformatics,
Dalian University of Technology,
NO.2 Linggong Rd,
Dalian, P.R.China
116024
--0016e64bbe8ea02358049d055915-- ========================================================================Date: Thu, 24 Feb 2011 12:41:49 +0100 Reply-To: "Kay H. Brodersen" <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: "Kay H. Brodersen" <[log in to unmask]> Subject: Re: multivariate bayes analysis Comments: To: MS Al-Rawi <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; format=flowed; charset="iso-8859-1"; reply-type=original Content-Transfer-Encoding: 7bit Message-ID: Dear Rawi, Multivariate Bayes becomes accessible once you have loaded the results from a first-level GLM analysis. Use the 'Results' button to do that, which will make the three MVB-related buttons appear: multivariate Bayes, BMS, and p-value. For details, see slide 38 in: http://www.fil.ion.ucl.ac.uk/spm/course/slides11-zurich/Kay_Multivariate.pdf Best wishes Kay -----Original Message----- From: MS Al-Rawi Sent: Thursday, February 24, 2011 12:33 PM To: Kay H. Brodersen Cc: [log in to unmask] Subject: Re: [SPM] multivariate bayes analysis Hello Kay.... I want to give MVB a try, however, I don't see anything in the SPM_GUI->MVB. But, yet, there are mvb related functions, e.g. spm_mvb.m, etc. (SPM was updated using r4010). All the best, -Rawi ----- Original Message ---- > From: Kay H. Brodersen <[log in to unmask]> > To: [log in to unmask] > Sent: Thu, February 24, 2011 8:35:18 AM > Subject: Re: [SPM] multivariate bayes analysis > > Dear Ciara, > > Great to hear you found the SPM course useful. With regard to your first > question: the priors in Multivariate Bayes have not been renamed. > Instead, > the code actually contains more priors than the GUI offers. You can see > this > by comparing the priors listed in spm_mvb_estimate (line 78) to those > actually supported in spm_mvb_U (starting in line 40). I would suggest > starting off by comparing those models that are directly listed in the > GUI. > > Your second question relates to fixed-effects versus random-effects model > comparison. SPM currently does not provide a fully automated pipeline for > comparing different MVB coding hypotheses (i.e., spatial priors). > However, > this is easy to do with just a few Matlab commands. You would begin by > running MVB separately for all subjects and coding hypotheses. Given n > subjects and m models, this results in n*m different MVB.mat files. You > then > extract the log model evidences from these files (F) and arrange them in > an > n*m matrix M. > > (i) For fixed-effects model comparison, you would then compute group > Bayes > factors as sum(M,1) and select the model with the highest group Bayes > factor. This analysis relies on the assumption that the same model is > best > in all subjects. > > (ii) For a random-effects model comparison, you can use spm_BMS(M, ...). > This approach relaxes the assumption above and explicitly accounts for > between-subjects variability. > > Let me know if this works. I'm copying this to the SPM mailing list so > that > other users of MVB may benefit from our discussion. > > Very best wishes > Kay > > -- > Kay Henning Brodersen > > Department of Computer Science > Pattern Analysis and Machine Learning Group > ETH Zurich > Switzerland > > [log in to unmask] > http://people.inf.ethz.ch/bkay/ > > > > > From: Ciara Greene > Sent: Monday, February 21, 2011 3:34 PM > To: [log in to unmask] > Subject: multivariate bayes analysis > > Hi Kay, > > Thanks for the interesting practical session on multivariate analysis at > the > SPM course last week, I really enjoyed it and I'm hoping to put it to > good > use. I'm trying out the multivariate bayes method with a view to > comparing > coding models in my data, and I had a couple of questions; I hope you > don't > mind answering them! > > Firstly, I'm a bit confused by the terminology for the model priors. In > the > Friston et al. NeuroImage paper, the various priors were listed as > spatial, > smooth, singular and support, while in the SPM GUI the options are > compact, > sparse, smooth and support. I can't find a description of these new > labels > anywhere, so I'm not sure if the priors have simply been renamed (e.g. > singular becoming compact???) or if these represent new models that > weren't > in the old version. > > My second question related to comparing models across subjects. For > obvious > reasons, I'm not really interested in model comparison within a single > subject, I want to see which model seems best in my whole sample (and by > extension, in the population). I've read a bit about the new Bayesian > model > selection method for DCM implemented in SPM8 which allows a random > effects > comparsion of models across subjects, but I can't get that to work with > the > multivariate bayes. The BMS button in the GUI allows models to be > compared > to one another, but presumably that uses fixed effects, and isn't > suitable > for group analysis. As far as I understand, it also doesn't allow the > results of the analyses to be saved out and carried forward to a second > level. Do you know if it's possible to use the DCM model selection method > outside DCM, or alternatively if there's another way of running a group > level analysis here? > > Thanks in advance for any help you can provide! > > Ciara ========================================================================Date: Thu, 24 Feb 2011 11:49:25 +0000 Reply-To: Paula Banca <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Paula Banca <[log in to unmask]> Subject: Question regarding DCM MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Message-ID: <[log in to unmask]> Hello! From what I read, the best method to study connectivity (when we are dealing with fMRI data) is the DCM (dynamic causal model) which runs in SPM. However, this has been a problem for me because I have all my functional data analysed by BrainVoyager and I can't use the files from BV in SPM. Does any of you know if there is any possiblity to export data from BrainVoyager into SPM, namely the design matrix and the time series, which are the two ingredients that DCM requires? Thanks! Best regards, Paula Banca ========================================================================Date: Thu, 24 Feb 2011 12:14:22 +0000 Reply-To: John Ashburner <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: John Ashburner <[log in to unmask]> Subject: Re: Umodulated image analysis better in discrimination: possible explanation? Comments: To: Dashjamts Jargal <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> > I am novice in the SPM. There are many questions regarding the interpretation of SPM analysis results modulated versus unmodulated structural images. I am studying Alzheimer subjects compared to healthy aged controls. I have used T1 WI images of same size, orientation and scanner, applied DARTEL tool as implemented in SPM8. Proportional global normalization eliminated multiple scattered areas of interest in the unmodulated date and produced better localization of the findings into MTL structures in modulated data. But still even after proportional global normalization, my globally normalized unmodulated data show larger relevant difference areas and have higher diagnostic accuracy than the globally normalized modulated. What could explain such result? I don't know, but there are a variety of possible explanations.: 1) In those areas, maybe Jacobian scaling is capturing more of the within group variability, relative to the difference between the populations. The t stat is proportional to the difference between the groups, divided by the square root of the within-group variance. 2) Enlarged ventricles etc may result in systematic displacements of structures, making fully accurate alignment of some regions more difficult. Even a tiny systematic shift can result in pretty significant t statistics. 3) The frequencies encoded by the deformation are slightly lower than those encoded by the segmentation,so more detailed volumes are being normalised (ie divided by) some volume measure that extends over a larger region. With Dartel, information is lower frequency along the direction in which the brain deforms (See eg Ashburner & Friston, NeuroImage, in press). 4) Random statistical fluke. 5) Something else. Differences between anatomies can be described using features other than local volumetric changes. For example, local shearing may result in the same volume, but relatively different lengths or areas. > Why the unmodulated demonstrated much more affected areas than the modulated? I'm not sure, but it is not clear to me what "unmodulated" features actually represent quantitatively. Jacobian scaled features have a quantitative interpretation. > Is the following correct according to the definition of how modulation works: "perfectly registered unmodulated data should show no difference between the groups"? If grey matter tissue classes were all exactly aligned with each other, then they would be identical with each other. In practice though, such perfect registration is impossible to achieve because image registration has to be regularised. If images are aligned using a particular form of registration approach (LDDMM or Geodesic Shooting), the residual difference between a warped scan and the template, scaled by the Jacobian determinant of the transform, can have a mechanistic interpretation. It's a bit hard to explain without resorting to the underlying maths, but the following is an example of where it has been used: http://www.ncbi.nlm.nih.gov/pubmed/20879441?dopt=Abstract http://www.rrmind.research.va.gov/RRMINDRESEARCH/docs/Joshi_Workshop_2010.pdf > Does it mean that unmodulated data have some compound of registration failures? Not necessarily. Image registration simply can not be 100% exact. > When I am adding covariates such as TIV, age and sex to both modulated and unmodulated ANCOVA with normalization, there is only slight improvement.( I think it is improvement because after that I am loosing those few voxels which were in the deep subcortical white matter.) I am looking forward to receiving your comments and thank you for your time. I don't have a good answer here. Maybe someone else out there could comment. Best regards, -John ========================================================================Date: Thu, 24 Feb 2011 12:18:14 +0000 Reply-To: John Ashburner <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: John Ashburner <[log in to unmask]> Subject: Re: DARTEL create template: minimum number of subjects? Comments: To: guillaume auzias <[log in to unmask]> In-Reply-To: [log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Message-ID: <[log in to unmask]> Pairwise registration of brains this way makes perfect sense. This is what was done for the evaluations of various registration algorithms by Klein et al (as some collaborators objected to group-wise registration). Best regards, -John On 24 February 2011 11:03, guillaume auzias <[log in to unmask]> wrote: > Hello, > > I've not been able to find in the SPM list archives a clear answer to the > following questions: > > Is there a minimum number of subjects required for the template creation > using DARTEL? > Does the registration of a pair of brains through a specifically created > 2-brains template makes any sense? > > Thanks for any input, > > Guillaume > ========================================================================Date: Thu, 24 Feb 2011 09:05:43 -0500 Reply-To: "MCLAREN, Donald" <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: "MCLAREN, Donald" <[log in to unmask]> Subject: Re: fixed effects analysis across two sessions Comments: To: Israr Ul Haq <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=windows-1252 Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> The control condition helps for a number of reasons: (1) it allows you to ignore baseline shifts due to the drug (e.g. Drug increases or decreases general neural activity; (2) it makes it a within-subject comparison which almost always has more power than between subjects(e.g. If A increases by 5 in one subject and 2 in another, then you will have large variability; however if B increases by 4 and 1, respectively, there is low variability for A-B; (3) without knowing your design, it's hard to interpret the implicit baseline and whether it is tied to any cognitive state or tied to statistics. The latter occurs when you have all your data occurring in your two conditions. If this is the case, then the baseline is completely arbitrary and would easily explain your results. On Wednesday, February 23, 2011, Israr Ul Haq <[log in to unmask]> wrote: > Dear Spm users, > > I am trying to see treatment effects on a patient, by putting his pre and post treatment sessions (all the runs separately) in one fixed effects analysis, and defining post pre contrast (t) by giving positive one to the experimental condition in the post treatment runs and negative one in the pretreatment runs. This is all being done at the specify first level option in spm8. It made sense and the few people I did ask seem to think this was okay too. However I came across something that has me confused and it would be great to hear an explanation. I had been including the control condition in the contrast too, so for the post treatment runs it was included as a negative one and for the pretreatment runs a positive one (just how its supposed to be contrasted out of the experiment condition at each session level, by giving it a weightage equal and opposite to the experiment condition). > I thought I was getting a reasonable result from the contrast till I fortunately or unfortunately tried a contrast without the control condition, which is positive and negative ones only for the experimental condition, post and pretreatment respectively. This now is giving me FAR less activation then the contrast with the control condition, which is opposite to what i was expecting, since I though the whole point of including the control condition was to subtract activations unrelated to the process of interest, making the result purer so to speak. Since I have a medicine background and limited statistical knowledge, it would be great if you can point out whether this is possible and adding the control condition into each run somehow increases the t statistic when the analysis is done across sessions, or if I am doing something wrong. My t contrast for the fixed effects is: > -1 1 -1 1 1 -1 1 -1 . where the sequence of runs put into the model specification part is pre tx run1, pre tx run2, post tx run1 and post tx run2, and each run has an experimental and a control condition. Will extremely appreciate help in this matter. > > Regards > Israr > -- Best Regards, Donald McLaren ================= D.G. McLaren, Ph.D. Postdoctoral Research Fellow, GRECC, Bedford VA Research Fellow, Department of Neurology, Massachusetts General Hospital and Harvard Medical School Office: (773) 406-2464 ===================== This e-mail contains CONFIDENTIAL INFORMATION which may contain PROTECTED HEALTHCARE INFORMATION and may also be LEGALLY PRIVILEGED and which is intended only for the use of the individual or entity named above. If the reader of the e-mail is not the intended recipient or the employee or agent responsible for delivering it to the intended recipient, you are hereby notified that you are in possession of confidential and privileged information. Any unauthorized use, disclosure, copying or the taking of any action in reliance on the contents of this information is strictly prohibited and may be unlawful. If you have received this e-mail unintentionally, please immediately notify the sender via telephone at (773) 406-2464 or email. ========================================================================Date: Thu, 24 Feb 2011 15:03:56 +0000 Reply-To: Simon Vandekar <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Simon Vandekar <[log in to unmask]> Subject: DARTEL Flow fields problem? Mime-Version: 1.0 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain; charset="UTF-8" Message-ID: <[log in to unmask]> Hi John and SPMers, I am attempting to normalise my fMRI data using the steps described in pages 440 and 441 of the spm8 manual: 1. Slice timing 2. Realign: Estimate and Reslice 3. Coregister the structural to functional images 4. Registration looks good. 5. Segment the anatomicals the SPM5 routine 6. Initial Import- use the *seg_sn files 7. Run Dartel with dependency on the gray and white matter images output by import step 8. Normalise to MNI, select the template6 from dartel output, the subject's flow field, and normalise the ra* files (slice timing, resliced). The output I get is sdra* files. When I compare the output to the mni template it looks as if the subject's image has not been normalised. I am suspicious of the flow field because if I look at the individual subjects' uc1* image it is an empty black box. What am I doing incorrectly here? Thanks in advance, Simon ========================================================================Date: Thu, 24 Feb 2011 15:43:34 +0000 Reply-To: Alexa Morcom <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Alexa Morcom <[log in to unmask]> Subject: PhD studentships in Neuroinformatics and Computational Neuroscience, Edinburgh MIME-Version: 1.0 Content-Type: multipart/mixed; boundary="----------=_1298562215-12437-60" Content-Transfer-Encoding: binary Message-ID: <[log in to unmask]> This is a multi-part message in MIME format... ------------=_1298562215-12437-60 Received: from mail-qy0-f181.google.com (mail-qy0-f181.google.com [209.85.216.181]) (authenticated user=malexa mech=PLAIN bits=0) by lmtp1.ucs.ed.ac.uk (8.13.8/8.13.7) with ESMTP id p1OFhYEx008082 (version=TLSv1/SSLv3 cipher=RC4-SHA bits8 verify=NOT) for <[log in to unmask]>; Thu, 24 Feb 2011 15:43:35 GMT Received: by qyg14 with SMTP id 14so573273qyg.12 for <[log in to unmask]>; Thu, 24 Feb 2011 07:43:34 -0800 (PST) MIME-Version: 1.0 Received: by 10.229.87.13 with SMTP id u13mr827545qcl.55.1298562214194; Thu, 24 Feb 2011 07:43:34 -0800 (PST) Received: by 10.229.241.147 with HTTP; Thu, 24 Feb 2011 07:43:34 -0800 (PST) Date: Thu, 24 Feb 2011 15:43:34 +0000 Message-ID: <[log in to unmask]> Subject: PhD studentships in Neuroinformatics and Computational Neuroscience, Edinburgh From: Alexa Morcom <[log in to unmask]> To: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> Content-Type: multipart/alternative; boundaryX-Edinburgh-Scanned: at lmtp1.ucs.ed.ac.uk with MIMEDefang 2.52, Sophie, Sophos Anti-Virus X-Scanned-By: MIMEDefang 2.52 on 129.215.149.64 --0016364ee0347ef4ab049d091383 Content-Type: text/plain; charset=ISO-8859-1 Content-Disposition: inline Dear all - please see below for full particulars and contact information. Alexa _________________________________________________ PhD studentships in Neuroinformatics and Computational Neuroscience, Edinburgh 2011-2012 applications for fully-funded PhD studentships at the University of Edinburgh Doctoral Training Centre (DTC) in Neuroinformatics and Computational Neuroscience are now being considered. The DTC is a world-class centre for research at the interface between neuroscience and the engineering, computational, and physical sciences. Our four-year programme is ideal for students with strong computational and analytical skills who want to employ cutting-edge methodology to advance research in neuroscience and related fields, or to apply ideas from neuroscience to computational problems. The first year consists of courses in neuroscience and informatics, as well as lab projects. This is followed by a three-year PhD project done in collaboration with one of the many departments and institutes affiliated with the DTC. Current DTC PhD topics fall into five main areas: * Computational neuroscience: Using analytical and computational models, potentially supplemented with experiments, to gain quantitative understanding of the nervous system. Many projects focus on the development and function of sensory and motor systems in animals, including neural coding, learning, and memory. * Biomedical imaging algorithms and tools: Using advanced data analysis techniques, such as machine learning and Bayesian approaches, for imaging-based diagnosis and research. * Cognitive science: Studying human cognitive processes and analysing them in computational terms. * Neuromorphic engineering: Using insights from neuroscience to help build better hardware, such as neuromorphic VLSI circuits and robots that perform robustly under natural conditions. * Software systems and applications: Using discoveries from neuroscience to develop software that can handle real-world data, such as video, audio, or speech. Other related areas of research may also be considered. Edinburgh has a large, world-class research community in these areas and leads the UK in creating a coherent programme in neuroinformatics and computational neuroscience. Edinburgh has often been voted 'best place to live in Britain', and has many exciting cultural and student activities. Students with a strong background in computer science, mathematics, physics, or engineering are particularly encouraged to apply. Highly motivated students with other backgrounds will also be considered. 15 full studentships (including stipend of 14,082-16,870 UK pounds/year) are available to permanent UK residents or other EU citizens who have been residing in the UK for the past three years (e.g. for education); see the web site (below) for full details. Other applicants can be accepted if they provide their own funding, typically via a scholarship from their country of origin. Further information and application forms can be obtained from: http://www.anc.ed.ac.uk/dtc For full consideration for entry in September 2011, the deadline for complete applications is March 31st, 2011. -- Dr. Alexa Morcom RCUK Academic Fellow Centre for Cognitive & Neural Systems/ Centre for Cognitive Ageing & Cognitive Epidemiology Psychology, University of Edinburgh http://www.ccns.sbms.mvm.ed.ac.uk/people/academic/morcom.html The University of Edinburgh is a charitable body, registered in Scotland, with registration number SC005336 --0016364ee0347ef4ab049d091383 Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Content-Disposition: inline Dear all - please see below for full particulars and contact information.

Alexa
_________________________________________________

PhD studentships in Neuroinformatics and Computational Neuroscience, Edinburgh

2011-2012 applications for fully-funded PhD studentships at the
University of Edinburgh Doctoral Training Centre (DTC) in
Neuroinformatics and Computational Neuroscience are now being
considered. The DTC is a world-class centre for research at the
interface between neuroscience and the engineering, computational, and
physical sciences.

Our four-year programme is ideal for students with strong
computational and analytical skills who want to employ cutting-edge
methodology to advance research in neuroscience and related fields, or
to apply ideas from neuroscience to computational problems. The first
year consists of courses in neuroscience and informatics, as well as
lab projects. This is followed by a three-year PhD project done in
collaboration with one of the many departments and institutes
affiliated with the DTC.

Current DTC PhD topics fall into five main areas:

* Computational neuroscience: Using analytical and computational
models, potentially supplemented with experiments, to gain
quantitative understanding of the nervous system. Many projects
focus on the development and function of sensory and motor systems
in animals, including neural coding, learning, and memory.

* Biomedical imaging algorithms and tools: Using advanced data
analysis techniques, such as machine learning and Bayesian
approaches, for imaging-based diagnosis and research.

* Cognitive science: Studying human cognitive processes and analysing
them in computational terms.

* Neuromorphic engineering: Using insights from neuroscience to help
build better hardware, such as neuromorphic VLSI circuits and robots
that perform robustly under natural conditions.

* Software systems and applications: Using discoveries from
neuroscience to develop software that can handle real-world data,
such as video, audio, or speech.


Other related areas of research may also be considered. Edinburgh has
a large, world-class research community in these areas and leads the
UK in creating a coherent programme in neuroinformatics and
computational neuroscience. Edinburgh has often been voted 'best place
to live in Britain', and has many exciting cultural and student
activities.

Students with a strong background in computer science, mathematics,
physics, or engineering are particularly encouraged to apply. Highly
motivated students with other backgrounds will also be considered.

15 full studentships (including stipend of 14,082-16,870 UK
pounds/year) are available to permanent UK residents or other EU
citizens who have been residing in the UK for the past three years
(e.g. for education); see the web site (below) for full details.
Other applicants can be accepted if they provide their own funding,
typically via a scholarship from their country of origin.

Further information and application forms can be obtained from:
http://www.anc.ed.ac.uk/dtc

For full consideration for entry in September 2011, the deadline for
complete applications is March 31st, 2011.


--
Dr. Alexa Morcom
RCUK Academic Fellow
Centre for Cognitive & Neural Systems/ Centre for Cognitive Ageing & Cognitive Epidemiology
Psychology, University of Edinburgh
http://www.ccns.sbms.mvm.ed.ac.uk/people/academic/morcom.html

The University of Edinburgh is a charitable body, registered in Scotland, with registration number SC005336


--0016364ee0347ef4ab049d091383-- ------------=_1298562215-12437-60 Content-Type: text/plain Content-Disposition: inline Content-Transfer-Encoding: 7bit MIME-Version: 1.0 X-Mailer: MIME-tools 5.420 (Entity 5.420) Content-Description: Edinburgh University charitable status The University of Edinburgh is a charitable body, registered in Scotland, with registration number SC005336. ------------=_1298562215-12437-60-- ========================================================================Date: Thu, 24 Feb 2011 15:47:10 +0000 Reply-To: John Ashburner <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: John Ashburner <[log in to unmask]> Subject: Re: DARTEL Flow fields problem? Comments: To: Simon Vandekar <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> It is a bit suspicious if all the u_*.nii are just zero. I'm not sure why this would be the case. Do the template*.nii files seem to be OK? Best regards, John On 24 February 2011 15:03, Simon Vandekar <[log in to unmask]> wrote: > Hi John and SPMers, > > I am attempting to normalise my fMRI data using the steps described in pages 440 and 441 of the spm8 manual: > > 1. Slice timing > 2. Realign: Estimate and Reslice > 3. Coregister the structural to functional images > 4. Registration looks good. > 5. Segment the anatomicals the SPM5 routine > 6. Initial Import- use the *seg_sn files > 7. Run Dartel with dependency on the gray and white matter images output by import step > 8. Normalise to MNI, select the template6 from dartel output, the subject's flow field, and normalise the ra* files (slice timing, resliced). > > The output I get is sdra* files. When I compare the output to the mni template it looks as if the subject's image has not been normalised. I am suspicious of the flow field because if I look at the individual subjects' uc1* image it is an empty black box. > > What am I doing incorrectly here? > > Thanks in advance, > Simon > ========================================================================Date: Thu, 24 Feb 2011 17:14:25 +0100 Reply-To: =?ISO-8859-1?Q?Rainer_Bgle?= <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: =?ISO-8859-1?Q?Rainer_Bgle?= <[log in to unmask]> Subject: Re: Negative values in DCM.A Comments: To: Maria Dauvermann <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/alternative; boundary cf3054a719d2a53a049d0981e7 Message-ID: <[log in to unmask]> --20cf3054a719d2a53a049d0981e7 Content-Type: text/plain; charset=ISO-8859-1 Hello Maria, as far as I understand this, connection parameters in DCM are change rates, i.e. area 1 reduces the activity in area 2 (if a21 < 0). As stated in Friston 2003, connection parameters are always relative to parameters of self connections (which have to be negative to ensure a stable system). Regards, Rainer On Thu, Feb 24, 2011 at 8:58 AM, Maria Dauvermann < [log in to unmask]> wrote: > Hello, > > I had a look at the values in DCM.A after I have estimated the DCMs. > > What does a negative value in the intrinsic connection mean? How do I > interprete this result? > > Thanks for your help. > > BW, Maria > --20cf3054a719d2a53a049d0981e7 Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Hello Maria,

as far as I understand this, connection parameters in DCM are change rates, i.e. area 1 reduces the activity in area 2 (if a21 < 0).

As stated in Friston 2003, connection parameters are always relative to parameters of self connections (which have to be negative to ensure a stable system).

Regards,
Rainer



On Thu, Feb 24, 2011 at 8:58 AM, Maria Dauvermann <[log in to unmask]> wrote:
Hello,

I had a look at the values in DCM.A after I have estimated the DCMs.

What does a negative value in the intrinsic connection mean? How do I interprete this result?

Thanks for your help.

BW, Maria

--20cf3054a719d2a53a049d0981e7-- ========================================================================Date: Thu, 24 Feb 2011 11:27:25 -0500 Reply-To: simon vandekar <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: simon vandekar <[log in to unmask]> Subject: Re: DARTEL Flow fields problem? Comments: To: John Ashburner <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/mixed; boundarye6ba4fc3661fad66049d09bbb3 Message-ID: <[log in to unmask]> --90e6ba4fc3661fad66049d09bbb3 Content-Type: multipart/alternative; boundarye6ba4fc3661fad59049d09bbb1 --90e6ba4fc3661fad59049d09bbb1 Content-Type: text/plain; charset=ISO-8859-1 Thanks for the reply John, As far as I can tell the template*.nii files look good, they are gray matter images. There is also a u_rc1*_Template.nii in the same folder as my template*.nii files, I've attached the image for that. Is that what my flow fields are suppose to look like? Thank you, Simon On Thu, Feb 24, 2011 at 10:47 AM, John Ashburner <[log in to unmask]>wrote: > It is a bit suspicious if all the u_*.nii are just zero. I'm not sure > why this would be the case. Do the template*.nii files seem to be OK? > > Best regards, > John > > On 24 February 2011 15:03, Simon Vandekar <[log in to unmask]> wrote: > > Hi John and SPMers, > > > > I am attempting to normalise my fMRI data using the steps described in > pages 440 and 441 of the spm8 manual: > > > > 1. Slice timing > > 2. Realign: Estimate and Reslice > > 3. Coregister the structural to functional images > > 4. Registration looks good. > > 5. Segment the anatomicals the SPM5 routine > > 6. Initial Import- use the *seg_sn files > > 7. Run Dartel with dependency on the gray and white matter images output > by import step > > 8. Normalise to MNI, select the template6 from dartel output, the > subject's flow field, and normalise the ra* files (slice timing, resliced). > > > > The output I get is sdra* files. When I compare the output to the mni > template it looks as if the subject's image has not been normalised. I am > suspicious of the flow field because if I look at the individual subjects' > uc1* image it is an empty black box. > > > > What am I doing incorrectly here? > > > > Thanks in advance, > > Simon > > > --90e6ba4fc3661fad59049d09bbb1 Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Thanks for the reply John,

As far as I can tell the template*.nii files look good, they are gray matter images. There is also a u_rc1*_Template.nii in the same folder as my template*.nii files, I've attached the image for that. Is that what my flow fields are suppose to look like?

Thank you,
Simon

On Thu, Feb 24, 2011 at 10:47 AM, John Ashburner <[log in to unmask]> wrote:
It is a bit suspicious if all the u_*.nii are just zero. I'm not sure
why this would be the case. Do the template*.nii files seem to be OK?

Best regards,
John

On 24 February 2011 15:03, Simon Vandekar <[log in to unmask]> wrote:
> Hi John and SPMers,
>
> I am attempting to normalise my fMRI data using the steps described in pages 440 and 441 of the spm8 manual:
>
> 1. Slice timing
> 2. Realign: Estimate and Reslice
> 3. Coregister the structural to functional images
> 4. Registration looks good.
> 5. Segment the anatomicals the SPM5 routine
> 6. Initial Import- use the *seg_sn files
> 7. Run Dartel with dependency on the gray and white matter images output by import step
> 8. Normalise to MNI, select the template6 from dartel output, the subject's flow field, and normalise the ra* files (slice timing, resliced).
>
> The output I get is sdra* files. When I compare the output to the mni template it looks as if the subject's image has not been normalised. I am suspicious of the flow field because if I look at the individual subjects' uc1* image it is an empty black box.
>
> What am I doing incorrectly here?
>
> Thanks in advance,
> Simon
>

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========================================================================Date: Thu, 24 Feb 2011 11:35:22 -0500 Reply-To: Ghazi Saidi Ladan <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Ghazi Saidi Ladan <[log in to unmask]> Subject: deactivation MIME-Version: 1.0 Content-Type: text/plain; charset="iso-8859-1" Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> Dear All, could you please explain to me what it means to have a deactivation and what it means to have more deactivation in the second phase of learning than in the first? I would also appreciate some relevant references, thank you, Ladan Ladan Ghazisaidi tudiante au Doctorat en Sciences Biomdicales Universit de Montral, Centre de recherche Institut universitaire de griatrie de Montral 4545 Ch. Queen Mary Montral, Qubec H3W 1W5 tl. 514 340-3540 poste 4700 e-mail: [log in to unmask] ========================================================================Date: Thu, 24 Feb 2011 12:08:38 -0500 Reply-To: "MCLAREN, Donald" <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: "MCLAREN, Donald" <[log in to unmask]> Subject: Re: deactivation Comments: To: Ghazi Saidi Ladan <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> Deactivation means that you have less activity than baseline. I am not sure that I have seen studies where deactivation increases with learning. In repetition paradigms, the deactivation is less with each repetition. Best Regards, Donald McLaren ================= D.G. McLaren, Ph.D. Postdoctoral Research Fellow, GRECC, Bedford VA Research Fellow, Department of Neurology, Massachusetts General Hospital and Harvard Medical School Office: (773) 406-2464 ===================== This e-mail contains CONFIDENTIAL INFORMATION which may contain PROTECTED HEALTHCARE INFORMATION and may also be LEGALLY PRIVILEGED and which is intended only for the use of the individual or entity named above. If the reader of the e-mail is not the intended recipient or the employee or agent responsible for delivering it to the intended recipient, you are hereby notified that you are in possession of confidential and privileged information. Any unauthorized use, disclosure, copying or the taking of any action in reliance on the contents of this information is strictly prohibited and may be unlawful. If you have received this e-mail unintentionally, please immediately notify the sender via telephone at (773) 406-2464 or email. On Thu, Feb 24, 2011 at 11:35 AM, Ghazi Saidi Ladan <[log in to unmask]> wrote: > Dear All, > could you please explain to me what it means to have a deactivation and what it means to have more deactivation in the second phase of learning than in the first? > I would also appreciate some relevant references, > thank you, > Ladan > > > Ladan Ghazisaidi > tudiante au Doctorat en Sciences Biomdicales > Universit de Montral, > Centre de recherche Institut universitaire de griatrie de Montral > 4545 Ch. Queen Mary Montral, Qubec H3W 1W5 > tl. 514 340-3540 poste 4700 > e-mail: [log in to unmask] > ========================================================================Date: Thu, 24 Feb 2011 17:28:27 +0000 Reply-To: John Ashburner <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: John Ashburner <[log in to unmask]> Subject: Re: DARTEL Flow fields problem? Comments: To: simon vandekar <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> The flow field looks pretty OK to me. I thought that you were referring to something that was uniformly grey. This is the x component. The other components can be viewed by looking at u_rc1*_Template.nii,2 and u_rc1*_Template.nii,3 (by changing the 1 in the file selector to 1:3). Also note that the main objective of Dartel is to align all the scans in the study together. When you normalise to MNI space, the images that are closely aligned within study are all affine transformed to MNI space. The version of MNI space is only really defined for affine aligned brain images (ie the rather blurred averages). You should note that the single subject brain that people often overlay their results on does not define MNI space. It is just the scan of a single individual that has been affine registered to MNI space. Best regards, -John On 24 February 2011 16:27, simon vandekar <[log in to unmask]> wrote: > Thanks for the reply John, > > As far as I can tell the template*.nii files look good, they are gray matter > images. There is also a u_rc1*_Template.nii in the same folder as my > template*.nii files, I've attached the image for that. Is that what my flow > fields are suppose to look like? > > Thank you, > Simon > > On Thu, Feb 24, 2011 at 10:47 AM, John Ashburner <[log in to unmask]> > wrote: >> >> It is a bit suspicious if all the u_*.nii are just zero. I'm not sure >> why this would be the case. Do the template*.nii files seem to be OK? >> >> Best regards, >> John >> >> On 24 February 2011 15:03, Simon Vandekar <[log in to unmask]> wrote: >> > Hi John and SPMers, >> > >> > I am attempting to normalise my fMRI data using the steps described in >> > pages 440 and 441 of the spm8 manual: >> > >> > 1. Slice timing >> > 2. Realign: Estimate and Reslice >> > 3. Coregister the structural to functional images >> > 4. Registration looks good. >> > 5. Segment the anatomicals the SPM5 routine >> > 6. Initial Import- use the *seg_sn files >> > 7. Run Dartel with dependency on the gray and white matter images output >> > by import step >> > 8. Normalise to MNI, select the template6 from dartel output, the >> > subject's flow field, and normalise the ra* files (slice timing, resliced). >> > >> > The output I get is sdra* files. When I compare the output to the mni >> > template it looks as if the subject's image has not been normalised. I am >> > suspicious of the flow field because if I look at the individual subjects' >> > uc1* image it is an empty black box. >> > >> > What am I doing incorrectly here? >> > >> > Thanks in advance, >> > Simon >> > > > ========================================================================Date: Thu, 24 Feb 2011 17:35:45 +0000 Reply-To: Chien-Ho Lin <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Chien-Ho Lin <[log in to unmask]> Subject: script to flip MR images left to right (or vice versa) Mime-Version: 1.0 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain; charset="UTF-8" Message-ID: <[log in to unmask]> Hi, I stuides patients with stroke doing some behavior paradigm in fMRI. Patients always used their affected limb for the task so some patients used left hand some used right hand. Now I would like to flip the left and right of the images so patients' lesional hemisphere are on the same side. Is there any script in spm 5 or 8 can help to accomplish this goal? I found a m file called spm_flip.m but it seems support only spm2. Your assistance are well appreciated. Thank you so much. Janice ========================================================================Date: Thu, 24 Feb 2011 18:03:09 +0000 Reply-To: Vy Dinh <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Vy Dinh <[log in to unmask]> Subject: Re: Contrast Manager Error in SPM8 Comments: To: Meghan Meyer <[log in to unmask]> In-Reply-To: <[log in to unmask]> Content-Type: multipart/alternative; boundary="_000_242AD0D3D1EDCE48AA6268ABC41C044D434FEDEBRUKWEXMAIL001ru_" MIME-Version: 1.0 Message-ID: <[log in to unmask]> --_000_242AD0D3D1EDCE48AA6268ABC41C044D434FEDEBRUKWEXMAIL001ru_ Content-Type: text/plain; charset="iso-8859-1" Content-Transfer-Encoding: quoted-printable Hi Meghan, I also came across the error message "Input to SVD..." yesterday. After some debugging, we learned that our BETA values had NaNs for some voxels. If you do a search in the forum for betas and NaNs, you will come across a post that discusses how extra brain voxels in a ROI can result in NaNs. Although I encountered my error during VOI extraction (and not model estimation), I think that this may also be your problem. Did you specify an explicit mask for the model estimation? If so, it may mean that your mask may too big. I also had this issue in the past where my model estimation failed and I resolved it by using a smaller explicity mask AND downloading the 4010 version of SPM8. Hope that helps. Best, Vy T.U. Dinh Research Assistant, Neurological Sciences Rush University Medical Center Phone: (312) 563-3853 Fax: (312) 563-4660 Email: [log in to unmask] ________________________________ From: SPM (Statistical Parametric Mapping) [[log in to unmask]] on behalf of Meghan Meyer [[log in to unmask]] Sent: Wednesday, February 23, 2011 6:36 PM To: [log in to unmask] Subject: Re: [SPM] Contrast Manager Error in SPM8 more info on this error: the model was not estimated bc of a problem using 'svd'.... Running 'Model estimation' SPM8: spm_spm (v3960) 16:29:05 - 23/02/2011 ======================================================================== Initialising parameters : ...computingFailed 'Model estimation' Error using ==> svd Input to SVD must not contain NaN or Inf. In file "/space/raid/fmri/spm8/spm_sp.m" (v1143), function "sf_set" at line 1126. In file "/space/raid/fmri/spm8/spm_sp.m" (v1143), function "spm_sp" at line 225. In file "/space/raid/fmri/spm8/spm_spm.m" (v3960), function "spm_spm" at line 439. In file "/space/raid/fmri/spm8/config/spm_run_fmri_est.m" (v3691), function "spm_run_fmri_est" at line 33. Running 'Contrast Manager' Changing directory to: /space/raid8/data/lieber/SWM/SWM08/analysis/swm_ppi_delay6s Failed 'Contrast Manager' Error using ==> spm_run_con at 37 This model has not been estimated. On Wed, Feb 23, 2011 at 4:11 PM, Meghan Meyer <[log in to unmask]> wrote: Hello, I'm running 1st level analyses in spm8, but for some of my subjects, i'm getting the following error below, but i'm not sure why the model would not have been estimated. the error appears for 9 of my 18 subjects. the other 9 ran fine. Thanks! Running 'Contrast Manager' Changing directory to: /space/raid8/data/lieber/SWM/SWM08/analysis/swm_ppi_delay6s Failed 'Contrast Manager' Error using ==> spm_run_con at 37 This model has not been estimated. In file "/space/raid/fmri/spm8/config/spm_run_con.m" (v3993), function "spm_run_con" at line 37. The following modules did not run: Failed: fMRI model specification Failed: Model estimation Failed: Contrast Manager -- Meghan Meyer, M.A. Graduate Student Social Cognitive Neuroscience Lab UCLA, Psychology -- Meghan Meyer, M.A. Graduate Student Social Cognitive Neuroscience Lab UCLA, Psychology --_000_242AD0D3D1EDCE48AA6268ABC41C044D434FEDEBRUKWEXMAIL001ru_ Content-Type: text/html; charset="iso-8859-1" Content-Transfer-Encoding: quoted-printable
Hi Meghan,

I also came across the error message "Input to SVD..." yesterday. After some debugging, we learned that our BETA values had NaNs for some voxels. If you do a search in the forum for betas and NaNs, you will come across a post that discusses how extra brain voxels in a ROI can result in NaNs. Although I encountered my error during VOI extraction (and not model estimation), I think that this may also be your problem. Did you specify an explicit mask for the model estimation? If so, it may mean that your mask may too big. I also had this issue in the past where my model estimation failed and I resolved it by using a smaller explicity mask AND downloading the 4010 version of SPM8. Hope that helps.

Best,

Vy T.U. Dinh
Research Assistant, Neurological Sciences
Rush University Medical Center
Phone: (312) 563-3853
Fax: (312) 563-4660
Email: [log in to unmask]

From: SPM (Statistical Parametric Mapping) [[log in to unmask]] on behalf of Meghan Meyer [[log in to unmask]]
Sent: Wednesday, February 23, 2011 6:36 PM
To: [log in to unmask]
Subject: Re: [SPM] Contrast Manager Error in SPM8

more info on this error: the model was not estimated bc of a problem using 'svd'....
Running 'Model estimation'

SPM8: spm_spm (v3960)                              16:29:05 - 23/02/2011
========================================================================
Initialising parameters                 :                   ...computingFailed  'Model estimation'
Error using ==> svd
Input to SVD must not contain NaN or Inf.
In file "/space/raid/fmri/spm8/spm_sp.m" (v1143), function "sf_set" at line 1126.
In file "/space/raid/fmri/spm8/spm_sp.m" (v1143), function "spm_sp" at line 225.
In file "/space/raid/fmri/spm8/spm_spm.m" (v3960), function "spm_spm" at line 439.
In file "/space/raid/fmri/spm8/config/spm_run_fmri_est.m" (v3691), function "spm_run_fmri_est" at line 33.

Running 'Contrast Manager'
   Changing directory to: /space/raid8/data/lieber/SWM/SWM08/analysis/swm_ppi_delay6s
Failed  'Contrast Manager'
Error using ==> spm_run_con at 37
This model has not been estimated.

On Wed, Feb 23, 2011 at 4:11 PM, Meghan Meyer <[log in to unmask]> wrote:
Hello,
I'm running 1st level analyses in spm8, but for some of my subjects, i'm getting the following error below, but i'm not sure why the model would not have been estimated. the error appears for 9 of my 18 subjects. the other 9 ran fine. Thanks!

Running 'Contrast Manager'
   Changing directory to: /space/raid8/data/lieber/SWM/SWM08/analysis/swm_ppi_delay6s
Failed  'Contrast Manager'
Error using ==> spm_run_con at 37
This model has not been estimated.
In file "/space/raid/fmri/spm8/config/spm_run_con.m" (v3993), function "spm_run_con" at line 37.

The following modules did not run:
Failed: fMRI model specification
Failed: Model estimation
Failed: Contrast Manager

--
Meghan Meyer, M.A.
Graduate Student
Social Cognitive Neuroscience Lab
UCLA, Psychology



--
Meghan Meyer, M.A.
Graduate Student
Social Cognitive Neuroscience Lab
UCLA, Psychology
--_000_242AD0D3D1EDCE48AA6268ABC41C044D434FEDEBRUKWEXMAIL001ru_-- ========================================================================Date: Thu, 24 Feb 2011 18:26:08 +0000 Reply-To: Meng-Chuan Lai <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Meng-Chuan Lai <[log in to unmask]> Subject: "proportional scaling" in model specification - questions for the batch itself Mime-Version: 1.0 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain; charset="UTF-8" Message-ID: <[log in to unmask]> Dear John and SPM designers/users, I have 2 questions regarding how the batch for 2nd level analysis actually works: 1. I've run a VBM analysis using factorial design. I selected at the end of batch "Global normalisation - Normalisation - proportional" since I would like to model GLM on GM regional volume relative to total GM volume (my inputs are modulated GM images). I learned that this setting will adjust individual map voxel values by dividing them by the sum (or mean?) of the individual image, is this the case? Could you please clarify how the individual-level re-scaling is actually done, in terms of what are the scaling factors (sum or mean or others) etc? 2. In the batch I also select absolute threshold masking. Could you please clarify if the individual scaling factor (mean or sum or others of the individual map) is from the original input image, or the image thresholded by this absolute threshold masking? I asked these because I would need to get the rescaled voxel values and do some post-hoc analysis, but this cannot be done directly since the rescaling is run inside the batch and no extra rescaled maps are generated. I would need to calculate it outside SPM so the clarifications will be very helpful. Thank you very much!! regards, Meng-chuan ========================================================================Date: Thu, 24 Feb 2011 19:54:52 +0000 Reply-To: Israr Ul Haq <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Israr Ul Haq <[log in to unmask]> Subject: Re: fixed effects analysis across two sessions Comments: To: Donald McLaren <[log in to unmask]> Mime-Version: 1.0 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain Message-ID: <[log in to unmask]> Thanks a lot, This makes sense, particularly the second explanation. although the runs1 and 2 I specified were from the same subject and the whole analysis is being done for each subject separately but I suppose in a way its the same thing and is taking into account the variability across runs. My model is actually an overt naming task, the experimental condition includes a semantic process of interest whereas the control condition has all but that. Thinking about this though, how is the direction of the change from pre to post treatment (in a voxel) taken into account? I computed a pre - post treatment contrast to check whether it will give me the same voxels (worried that the areas included both positive and negative change over the two sessions in my first contrast) and was relieved to see different voxels. However, if its not too cumbersome, can you please explain how the eventual t statistic is being computed in such a multi session analysis with two independent conditions? Heres what I understand; for each voxel, a correlation coefficient (r) is calculated for each stimulus of a specified condition, and all the r values in a run give a distribution for that condition, with a mean and standard deviation. These are then utilized in the t tests of no significant difference, where the linear t contrasts between two conditions are setup such that whether for that particular voxel, one condition had significantly different signal than the other, using the mean and sd of the r values. What i am trying to wrap my head around is how based on the weightings that we specificy (i.e +1 or -1), the t statistic is calculated for exp > control vs control > exp, since in both cases, what we are essentially inputting is the difference between the means. Intuitively it would seem that it would give a voxel as significant only if the condition weighted +1 also has the higher mean of the two conditions being contrasted. But if so, how would this apply to multiple runs and sessions, or more specifically what would be the sequence of computations in my design? Theres a plus one weighting in both pre and post treatment runs, albeit for different conditions. Thanks Israr ========================================================================Date: Thu, 24 Feb 2011 15:27:00 -0500 Reply-To: simon vandekar <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: simon vandekar <[log in to unmask]> Subject: Re: DARTEL Flow fields problem? Comments: To: John Ashburner <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/mixed; boundaryaec53f398fec3f19049d0d0af8 Message-ID: <[log in to unmask]> --bcaec53f398fec3f19049d0d0af8 Content-Type: multipart/alternative; boundaryaec53f398fec3f06049d0d0af6 --bcaec53f398fec3f06049d0d0af6 Content-Type: text/plain; charset=ISO-8859-1 Hi John, Thanks again for your help and sorry for all the emails. The flow fields that 'Normalise to MNI' asks for are the individual subjects' flow fields 'u_c1*.nii which look like the 3rd image selected in the attached picture. Also included in this picture are a template, and subject's functional scan after the 'normalise to MNI' step. Thank you, Simon On Thu, Feb 24, 2011 at 12:28 PM, John Ashburner <[log in to unmask]>wrote: > The flow field looks pretty OK to me. I thought that you were > referring to something that was uniformly grey. This is the x > component. The other components can be viewed by looking at > u_rc1*_Template.nii,2 and u_rc1*_Template.nii,3 (by changing the 1 in > the file selector to 1:3). > > Also note that the main objective of Dartel is to align all the scans > in the study together. When you normalise to MNI space, the images > that are closely aligned within study are all affine transformed to > MNI space. The version of MNI space is only really defined for affine > aligned brain images (ie the rather blurred averages). You should > note that the single subject brain that people often overlay their > results on does not define MNI space. It is just the scan of a single > individual that has been affine registered to MNI space. > > Best regards, > -John > > On 24 February 2011 16:27, simon vandekar <[log in to unmask]> wrote: > > Thanks for the reply John, > > > > As far as I can tell the template*.nii files look good, they are gray > matter > > images. There is also a u_rc1*_Template.nii in the same folder as my > > template*.nii files, I've attached the image for that. Is that what my > flow > > fields are suppose to look like? > > > > Thank you, > > Simon > > > > On Thu, Feb 24, 2011 at 10:47 AM, John Ashburner <[log in to unmask]> > > wrote: > >> > >> It is a bit suspicious if all the u_*.nii are just zero. I'm not sure > >> why this would be the case. Do the template*.nii files seem to be OK? > >> > >> Best regards, > >> John > >> > >> On 24 February 2011 15:03, Simon Vandekar <[log in to unmask]> wrote: > >> > Hi John and SPMers, > >> > > >> > I am attempting to normalise my fMRI data using the steps described in > >> > pages 440 and 441 of the spm8 manual: > >> > > >> > 1. Slice timing > >> > 2. Realign: Estimate and Reslice > >> > 3. Coregister the structural to functional images > >> > 4. Registration looks good. > >> > 5. Segment the anatomicals the SPM5 routine > >> > 6. Initial Import- use the *seg_sn files > >> > 7. Run Dartel with dependency on the gray and white matter images > output > >> > by import step > >> > 8. Normalise to MNI, select the template6 from dartel output, the > >> > subject's flow field, and normalise the ra* files (slice timing, > resliced). > >> > > >> > The output I get is sdra* files. When I compare the output to the mni > >> > template it looks as if the subject's image has not been normalised. I > am > >> > suspicious of the flow field because if I look at the individual > subjects' > >> > uc1* image it is an empty black box. > >> > > >> > What am I doing incorrectly here? > >> > > >> > Thanks in advance, > >> > Simon > >> > > > > > > --bcaec53f398fec3f06049d0d0af6 Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Hi John,

Thanks again for your help and sorry for all the emails. The flow fields that 'Normalise to MNI' asks for are the individual subjects' flow fields 'u_c1*.nii which look like the 3rd image selected in the attached picture. Also included in this picture are a template, and subject's functional scan after the 'normalise to MNI' step.

Thank you,
Simon


On Thu, Feb 24, 2011 at 12:28 PM, John Ashburner <[log in to unmask]> wrote:
The flow field looks pretty OK to me. I thought that you were
referring to something that was uniformly grey. This is the x
component. The other components can be viewed by looking at
u_rc1*_Template.nii,2 and u_rc1*_Template.nii,3 (by changing the 1 in
the file selector to 1:3).

Also note that the main objective of Dartel is to align all the scans
in the study together. When you normalise to MNI space, the images
that are closely aligned within study are all affine transformed to
MNI space. The version of MNI space is only really defined for affine
aligned brain images (ie the rather blurred averages). You should
note that the single subject brain that people often overlay their
results on does not define MNI space. It is just the scan of a single
individual that has been affine registered to MNI space.

Best regards,
-John

On 24 February 2011 16:27, simon vandekar <[log in to unmask]> wrote:
> Thanks for the reply John,
>
> As far as I can tell the template*.nii files look good, they are gray matter
> images. There is also a u_rc1*_Template.nii in the same folder as my
> template*.nii files, I've attached the image for that. Is that what my flow
> fields are suppose to look like?
>
> Thank you,
> Simon
>
> On Thu, Feb 24, 2011 at 10:47 AM, John Ashburner <[log in to unmask]>
> wrote:
>>
>> It is a bit suspicious if all the u_*.nii are just zero. I'm not sure
>> why this would be the case. Do the template*.nii files seem to be OK?
>>
>> Best regards,
>> John
>>
>> On 24 February 2011 15:03, Simon Vandekar <[log in to unmask]> wrote:
>> > Hi John and SPMers,
>> >
>> > I am attempting to normalise my fMRI data using the steps described in
>> > pages 440 and 441 of the spm8 manual:
>> >
>> > 1. Slice timing
>> > 2. Realign: Estimate and Reslice
>> > 3. Coregister the structural to functional images
>> > 4. Registration looks good.
>> > 5. Segment the anatomicals the SPM5 routine
>> > 6. Initial Import- use the *seg_sn files
>> > 7. Run Dartel with dependency on the gray and white matter images output
>> > by import step
>> > 8. Normalise to MNI, select the template6 from dartel output, the
>> > subject's flow field, and normalise the ra* files (slice timing, resliced).
>> >
>> > The output I get is sdra* files. When I compare the output to the mni
>> > template it looks as if the subject's image has not been normalised. I am
>> > suspicious of the flow field because if I look at the individual subjects'
>> > uc1* image it is an empty black box.
>> >
>> > What am I doing incorrectly here?
>> >
>> > Thanks in advance,
>> > Simon
>> >
>
>

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BgQDgntmUN4bBaJAFIgCUeDCCgQEA4IBwQtP4Fx6FIgCUSAKRIE9CgQEA4IBwT0zKO+NAlEgCkSB KHBhBQKCAcGA4IUncC49CkSBKBAFosAeBQKCAcGA4J4ZlPdGgSgQBaJAFLiwAgHBgGBA8MITOJce BaJAFIgCUWCPAgHBgGBAcM8MynujQBSIAlEgClxYgYBgQDAgeOEJnEuPAlEgCkSBKLBHgYBgQDAg uGcG5b1RIApEgSgQBS6sQEAwIBgQvPAEzqVHgSgQBaJAFNijQEAwIBgQ3DOD8t4oEAWiQBSIAhdW ICAYEAwIXngC59KjQBSIAlEgCuxRICAYEAwI7plBeW8UiAJRIApEgQsrEBAMCAYELzyBc+lRIApE gSgQBfYoEBAMCAYE98ygvDcKRIEoEAWiwIUVCAgGBAOCF57AufQoEAWiQBSIAnsUCAgGBAOCe2ZQ 3hsFokAUiAJR4MIKBAQDggHBC0/gXHoUiAJRIApEgT0KBAQDggHBPTMo740CUSAKRIEocGEFAoIB wYDghSdwLj0KRIEoEAWiwB4FAoIBwYDgnhmU90aBKBAFokAUuLACAcGAYEDwwhM4lx4FokAUiAJR YI8CAcGAYEBwzwzKe6NAFIgCUSAKXFiBgODpIPiDTSD2g5Ov+8JjPpceBaJAFIgCUSAK/D8FvgPB KBIFokAUiAJRIApEgSjwLAUCgs963rnbKBAFokAUiAJRIAp8p0BAMIMhCkSBKBAFokAUiAIPVeD/ B+eqrtuYzECGAAAAAElFTkSuQmCC --bcaec53f398fec3f19049d0d0af8-- ========================================================================Date: Thu, 24 Feb 2011 15:42:24 -0500 Reply-To: "MCLAREN, Donald" <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: "MCLAREN, Donald" <[log in to unmask]> Subject: Re: fixed effects analysis across two sessions Comments: To: Israr Ul Haq <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> Israr, Let me start of on the issue of means, sd, r, and t-statistics (basic ideas). (1) beta ~ weight of a particular IV (e.g. column) (2) sd ~ weight of overall variance based on covariance of betas (3) beta=sd(XY)/var(X); r=beta*sd(x)/sd(y) {for linear regression, for multiple linear regression and general linear models, you compute partial correlations} (4) r=sqrt(t^2/(t^2+df) OR t=beta-0/sd The beta and residual of the model form the basis of the r, not the other way around. Everything is test against a mean of 0. Since fMRI values are non-zero, a constant is included to account for the non-zero mean of the data. It is the betas (not r) that are compared statistically. Contrasts: Run1-C1 Run1-C2 Run2-C1 Run2-C2 Run3-C1 Run3-C2 Run4-C1 Run4-C2 1 -1 1 -1 0 0 0 0 tests C1>C2 for pretreatment 0 0 0 0 1 -1 1 -1 tests C1>C2 for postreatment 1 -1 1 -1 -1 1 -1 1 tests (C1>C2 for pretreatment) > (C1>C2 for postreatment) 1 means you add the beta, -1 means you subtract the beta, AND it is the sum of the added and subtracted betas that give you the value to compare against 0. T-statistic (matrix notation not included): T=Contrast*beta/(ResMS*Contrasts*covbeta*Contrasts) which can be thought of as effect-mean (effect-0) divided by the variance. Now, if you have multiple subjects, you take the Contrast*beta part of the T-statistic(con_* images) to the second level modelling. Let me know if that clarified the issue. Best Regards, Donald McLaren ================= D.G. McLaren, Ph.D. Postdoctoral Research Fellow, GRECC, Bedford VA Research Fellow, Department of Neurology, Massachusetts General Hospital and Harvard Medical School Office: (773) 406-2464 ===================== This e-mail contains CONFIDENTIAL INFORMATION which may contain PROTECTED HEALTHCARE INFORMATION and may also be LEGALLY PRIVILEGED and which is intended only for the use of the individual or entity named above. If the reader of the e-mail is not the intended recipient or the employee or agent responsible for delivering it to the intended recipient, you are hereby notified that you are in possession of confidential and privileged information. Any unauthorized use, disclosure, copying or the taking of any action in reliance on the contents of this information is strictly prohibited and may be unlawful. If you have received this e-mail unintentionally, please immediately notify the sender via telephone at (773) 406-2464 or email. On Thu, Feb 24, 2011 at 2:54 PM, Israr Ul Haq <[log in to unmask]> wrote: > Thanks a lot, This makes sense, particularly the second explanation. although the runs1 and 2 I specified were from the same subject and the whole analysis is being done for each subject separately but I suppose in a way its the same thing and is taking into account the variability across runs. My model is actually an overt naming task, the experimental condition includes a semantic process of interest whereas the control condition has all but that. > > Thinking about this though, how is the direction of the change from pre to post treatment (in a voxel) taken into account? I computed a pre - post treatment contrast to check whether it will give me the same voxels (worried that the areas included both positive and negative change over the two sessions in my first contrast) and was relieved to see different voxels. However, if its not too cumbersome, can you please explain how the eventual t statistic is being computed in such a multi session analysis with two independent conditions? Heres what I understand; for each voxel, a correlation coefficient (r) is calculated for each stimulus of a specified condition, and all the r values in a run give a distribution for that condition, with a mean and standard deviation. These are then utilized in the t tests of no significant difference, where the linear t contrasts between two conditions are setup such that whether for that particular voxel, one condition had significantly different signal than the other, using the mean and sd of the r values. What i am trying to wrap my head around is how based on the weightings that we specificy (i.e +1 or -1), the t statistic is calculated for exp > control vs control > exp, since in both cases, what we are essentially inputting is the difference between the means. Intuitively it would seem that it would give a voxel as significant only if the condition weighted +1 also has the higher mean of the two conditions being contrasted. But if so, how would this apply to multiple runs and sessions, or more specifically what would be the sequence of computations in my design? Theres a plus one weighting in both pre and post treatment runs, albeit for different conditions. > > Thanks > Israr > > > > ========================================================================Date: Thu, 24 Feb 2011 20:51:15 +0000 Reply-To: John Ashburner <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: John Ashburner <[log in to unmask]> Subject: Re: DARTEL Flow fields problem? Comments: To: simon vandekar <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> Something has certainly gone wrong here. One possibility (which was my fault - sorry) is that you are using an early version of SPM5, which had a bug in the normalise to MNI option. This was fixed in a later set of SPM8 updates. The sequence of procedures that you described in your earlier email all look perfectly correct. You could narrow down the possible causes of the problem by using the normalise option of Dartel (not the normalise to MNI option), which should bring your fMRI and anatomical scans into alignment with the Template_6.nii. Bye for now, -John On 24 February 2011 20:27, simon vandekar <[log in to unmask]> wrote: > Hi John, > > Thanks again for your help and sorry for all the emails. The flow fields > that 'Normalise to MNI' asks for are the individual subjects' flow fields > 'u_c1*.nii which look like the 3rd image selected in the attached picture. > Also included in this picture are a template, and subject's functional scan > after the 'normalise to MNI' step. > > Thank you, > Simon > > > On Thu, Feb 24, 2011 at 12:28 PM, John Ashburner <[log in to unmask]> > wrote: >> >> The flow field looks pretty OK to me. I thought that you were >> referring to something that was uniformly grey. This is the x >> component. The other components can be viewed by looking at >> u_rc1*_Template.nii,2 and u_rc1*_Template.nii,3 (by changing the 1 in >> the file selector to 1:3). >> >> Also note that the main objective of Dartel is to align all the scans >> in the study together. When you normalise to MNI space, the images >> that are closely aligned within study are all affine transformed to >> MNI space. The version of MNI space is only really defined for affine >> aligned brain images (ie the rather blurred averages). You should >> note that the single subject brain that people often overlay their >> results on does not define MNI space. It is just the scan of a single >> individual that has been affine registered to MNI space. >> >> Best regards, >> -John >> >> On 24 February 2011 16:27, simon vandekar <[log in to unmask]> wrote: >> > Thanks for the reply John, >> > >> > As far as I can tell the template*.nii files look good, they are gray >> > matter >> > images. There is also a u_rc1*_Template.nii in the same folder as my >> > template*.nii files, I've attached the image for that. Is that what my >> > flow >> > fields are suppose to look like? >> > >> > Thank you, >> > Simon >> > >> > On Thu, Feb 24, 2011 at 10:47 AM, John Ashburner <[log in to unmask]> >> > wrote: >> >> >> >> It is a bit suspicious if all the u_*.nii are just zero. I'm not sure >> >> why this would be the case. Do the template*.nii files seem to be OK? >> >> >> >> Best regards, >> >> John >> >> >> >> On 24 February 2011 15:03, Simon Vandekar <[log in to unmask]> wrote: >> >> > Hi John and SPMers, >> >> > >> >> > I am attempting to normalise my fMRI data using the steps described >> >> > in >> >> > pages 440 and 441 of the spm8 manual: >> >> > >> >> > 1. Slice timing >> >> > 2. Realign: Estimate and Reslice >> >> > 3. Coregister the structural to functional images >> >> > 4. Registration looks good. >> >> > 5. Segment the anatomicals the SPM5 routine >> >> > 6. Initial Import- use the *seg_sn files >> >> > 7. Run Dartel with dependency on the gray and white matter images >> >> > output >> >> > by import step >> >> > 8. Normalise to MNI, select the template6 from dartel output, the >> >> > subject's flow field, and normalise the ra* files (slice timing, >> >> > resliced). >> >> > >> >> > The output I get is sdra* files. When I compare the output to the mni >> >> > template it looks as if the subject's image has not been normalised. >> >> > I am >> >> > suspicious of the flow field because if I look at the individual >> >> > subjects' >> >> > uc1* image it is an empty black box. >> >> > >> >> > What am I doing incorrectly here? >> >> > >> >> > Thanks in advance, >> >> > Simon >> >> > >> > >> > > > ========================================================================Date: Thu, 24 Feb 2011 15:16:32 -0800 Reply-To: Michael T Rubens <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Michael T Rubens <[log in to unmask]> Subject: Re: script to flip MR images left to right (or vice versa) Comments: To: Chien-Ho Lin <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/alternative; boundaryMessage-ID: <[log in to unmask]> --0023547c93373a30ff049d0f6945 Content-Type: text/plain; charset=UTF-8 how about this: %%% v = spm_vol('/image_path/brain.img'); x = spm_read_vols(v); x = x(size(x,1):-1:1,:,:); [path file] = fileparts(v.fname); v.fname = fullfile(path,['flipped_' file'); spm_write_vol(v,x) %%% cheers, michael On Thu, Feb 24, 2011 at 9:35 AM, Chien-Ho Lin <[log in to unmask]> wrote: > Hi, > > I stuides patients with stroke doing some behavior paradigm in fMRI. > Patients always used their affected limb for the task so some patients used > left hand some used right hand. > Now I would like to flip the left and right of the images so patients' > lesional hemisphere are on the same side. > > Is there any script in spm 5 or 8 can help to accomplish this goal? > > I found a m file called spm_flip.m but it seems support only spm2. > > Your assistance are well appreciated. > > Thank you so much. > > Janice > -- Research Associate Gazzaley Lab Department of Neurology University of California, San Francisco --0023547c93373a30ff049d0f6945 Content-Type: text/html; charset=UTF-8 Content-Transfer-Encoding: quoted-printable how about this:
%%%

v = spm_vol('/image_path/brain.img');
x = spm_read_vols(v);

x = x(size(x,1):-1:1,:,:);

[path file] = fileparts(v.fname);
v.fname = fullfile(path,['flipped_' file');

spm_write_vol(v,x)

%%%


cheers,
michael

On Thu, Feb 24, 2011 at 9:35 AM, Chien-Ho Lin <[log in to unmask]> wrote:
Hi,

I stuides patients with stroke doing some behavior paradigm in fMRI.
Patients always used their affected limb for the task so some patients used left hand some used right hand.
Now I would like to flip the left and right of the images so patients' lesional hemisphere are on the same side.

Is there any script in spm 5 or 8 can help to accomplish this goal?

I found a m file called spm_flip.m but it seems support only spm2.

Your assistance are well appreciated.

Thank you so much.

Janice



--
Research Associate
Gazzaley Lab
Department of Neurology
University of California, San Francisco
--0023547c93373a30ff049d0f6945-- ========================================================================Date: Thu, 24 Feb 2011 17:28:03 -0600 Reply-To: Pilar Archila-Suerte <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Pilar Archila-Suerte <[log in to unmask]> Subject: Order of subject files in ANOVA batch MIME-Version: 1.0 Content-Type: multipart/alternative; boundaryMessage-ID: <[log in to unmask]> --0016e64c1cf0cd62ce049d0f91a3 Content-Type: text/plain; charset=UTF-8 Dear SPM list, In setting ANOVAs in SPM, do the subject files need to be in the same order under each cell? I just ran two trial trial batches, one with the same order of subjects and one with a different order. The areas of activity are very similar but the order in which the areas show up as more or less intensive did vary. Any insight as to how SPM does this? should I stick to the same order of subjects for clarity? Thanks, Pilar A . --0016e64c1cf0cd62ce049d0f91a3 Content-Type: text/html; charset=UTF-8 Content-Transfer-Encoding: quoted-printable Dear SPM list, 
In setting ANOVAs in SPM, do the subject files need to be in the same order under each cell?

I just ran two trial trial batches, one with the same order of subjects and one with a different order. The areas of activity are very similar but the order in which the areas show up as more or less intensive did vary.

Any insight as to how SPM does this? should I stick to the same order of subjects for clarity?

Thanks,
Pilar A .
--0016e64c1cf0cd62ce049d0f91a3-- ========================================================================Date: Thu, 24 Feb 2011 18:38:16 -0500 Reply-To: "MCLAREN, Donald" <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: "MCLAREN, Donald" <[log in to unmask]> Subject: Re: Order of subject files in ANOVA batch Comments: To: Pilar Archila-Suerte <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Message-ID: <[log in to unmask]> You should use the flexible factorial for repeated measure designs with factors for subject and condition in your design. Best Regards, Donald McLaren ================D.G. McLaren, Ph.D. Postdoctoral Research Fellow, GRECC, Bedford VA Research Fellow, Department of Neurology, Massachusetts General Hospital and Harvard Medical School Office: (773) 406-2464 ====================This e-mail contains CONFIDENTIAL INFORMATION which may contain PROTECTED HEALTHCARE INFORMATION and may also be LEGALLY PRIVILEGED and which is intended only for the use of the individual or entity named above. If the reader of the e-mail is not the intended recipient or the employee or agent responsible for delivering it to the intended recipient, you are hereby notified that you are in possession of confidential and privileged information. Any unauthorized use, disclosure, copying or the taking of any action in reliance on the contents of this information is strictly prohibited and may be unlawful. If you have received this e-mail unintentionally, please immediately notify the sender via telephone at (773) 406-2464 or email. On Thu, Feb 24, 2011 at 6:28 PM, Pilar Archila-Suerte <[log in to unmask]> wrote: > Dear SPM list, > In setting ANOVAs in SPM, do the subject files need to be in the same order > under each cell? > I just ran two trial trial batches, one with the same order of subjects and > one with a different order. The areas of activity are very similar but the > order in which the areas show up as more or less intensive did vary. > Any insight as to how SPM does this? should I stick to the same order of > subjects for clarity? > Thanks, > Pilar A . ========================================================================Date: Thu, 24 Feb 2011 17:44:46 -0600 Reply-To: Pilar Archila-Suerte <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Pilar Archila-Suerte <[log in to unmask]> Subject: Re: Order of subject files in ANOVA batch Comments: To: "MCLAREN, Donald" <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/alternative; boundaryMessage-ID: <[log in to unmask]> --0016367b60fa2fded8049d0fcf11 Content-Type: text/plain; charset=UTF-8 Mine is actually not a repeated measures design. I'm running a full factorial and I just want to compare activity in one group vs. another. Do the con files need to be in the same order in each cell in this case? Pilar On Thu, Feb 24, 2011 at 5:38 PM, MCLAREN, Donald <[log in to unmask]>wrote: > You should use the flexible factorial for repeated measure designs > with factors for subject and condition in your design. > > Best Regards, Donald McLaren > ================> D.G. McLaren, Ph.D. > Postdoctoral Research Fellow, GRECC, Bedford VA > Research Fellow, Department of Neurology, Massachusetts General > Hospital and Harvard Medical School > Office: (773) 406-2464 > ====================> This e-mail contains CONFIDENTIAL INFORMATION which may contain > PROTECTED HEALTHCARE INFORMATION and may also be LEGALLY PRIVILEGED > and which is intended only for the use of the individual or entity > named above. If the reader of the e-mail is not the intended recipient > or the employee or agent responsible for delivering it to the intended > recipient, you are hereby notified that you are in possession of > confidential and privileged information. Any unauthorized use, > disclosure, copying or the taking of any action in reliance on the > contents of this information is strictly prohibited and may be > unlawful. If you have received this e-mail unintentionally, please > immediately notify the sender via telephone at (773) 406-2464 or > email. > > > > On Thu, Feb 24, 2011 at 6:28 PM, Pilar Archila-Suerte > <[log in to unmask]> wrote: > > Dear SPM list, > > In setting ANOVAs in SPM, do the subject files need to be in the same > order > > under each cell? > > I just ran two trial trial batches, one with the same order of subjects > and > > one with a different order. The areas of activity are very similar but > the > > order in which the areas show up as more or less intensive did vary. > > Any insight as to how SPM does this? should I stick to the same order of > > subjects for clarity? > > Thanks, > > Pilar A . > --0016367b60fa2fded8049d0fcf11 Content-Type: text/html; charset=UTF-8 Content-Transfer-Encoding: quoted-printable Mine is actually not a repeated measures design. I'm running a full factorial and I just want to compare activity in one group vs. another. Do the con files need to be in the same order in each cell in this case?

Pilar 

On Thu, Feb 24, 2011 at 5:38 PM, MCLAREN, Donald <[log in to unmask]> wrote:
You should use the flexible factorial for repeated measure designs
with factors for subject and condition in your design.

Best Regards, Donald McLaren
=================
D.G. McLaren, Ph.D.
Postdoctoral Research Fellow, GRECC, Bedford VA
Research Fellow, Department of Neurology, Massachusetts General
Hospital and Harvard Medical School
Office: (773) 406-2464
=====================
This e-mail contains CONFIDENTIAL INFORMATION which may contain
PROTECTED HEALTHCARE INFORMATION and may also be LEGALLY PRIVILEGED
and which is intended only for the use of the individual or entity
named above. If the reader of the e-mail is not the intended recipient
or the employee or agent responsible for delivering it to the intended
recipient, you are hereby notified that you are in possession of
confidential and privileged information. Any unauthorized use,
disclosure, copying or the taking of any action in reliance on the
contents of this information is strictly prohibited and may be
unlawful. If you have received this e-mail unintentionally, please
immediately notify the sender via telephone at (773) 406-2464 or
email.



On Thu, Feb 24, 2011 at 6:28 PM, Pilar Archila-Suerte
<[log in to unmask]> wrote:
> Dear SPM list,
> In setting ANOVAs in SPM, do the subject files need to be in the same order
> under each cell?
> I just ran two trial trial batches, one with the same order of subjects and
> one with a different order. The areas of activity are very similar but the
> order in which the areas show up as more or less intensive did vary.
> Any insight as to how SPM does this? should I stick to the same order of
> subjects for clarity?
> Thanks,
> Pilar A .
--0016367b60fa2fded8049d0fcf11-- ========================================================================Date: Thu, 24 Feb 2011 15:50:51 -0800 Reply-To: J S Lee <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: J S Lee <[log in to unmask]> Subject: Re: Can't find driving effects for PPI analysis Comments: To: [log in to unmask] MIME-Version: 1.0 Content-Type: multipart/mixed; boundary="----=_NextPart_000_98E4_01CBD43A.9CB39E80" Message-ID: <[log in to unmask]> This is a multi-part message in MIME format. ------=_NextPart_000_98E4_01CBD43A.9CB39E80 Content-Type: multipart/alternative; boundary="----=_NextPart_001_98E5_01CBD43A.9CB39E80" ------=_NextPart_001_98E5_01CBD43A.9CB39E80 Content-Type: text/plain; charset="iso-8859-1" Content-Transfer-Encoding: 7bit Hi Donald, Thank you for your reply! I am using SPM8. I looked at the SPM.xX.X values for each subject. The values in the SPM.xX.X *PSY* columns for each of my models line up perfectly across subjects. For the different models within a subject, there also seems to be correspondence for the PSY negative values (although there are slight baseline shifts between different models). The values in the PPI column, however, do not correspond so well. I don't think I would have expected the PPI values to correspond across subjects, however, because the VOI values differ from subject to subject, so the PPI should also differ as it represents an interaction? The PPI values for different models in the same subject also do not show perfect correspondence (png attached: It shows 2 subjects' SPM.xX.X PPI values over the first 80 scans. The All conds - control model and Cond 1 - control PPI values are plotted for each subject. I didn't include the Cond 2 - control, Cond 3 - control, etc. for clarity). All models are coming from the same VOI, so I think the adjustment has to be the same for all models (all extractions were adjusted for an F contrast of the effects of interest at the first-level model). Is this what you meant? The voxels are also identical (again, coming from the same VOI I think they have to be?). Thank you very much for taking the time to consider my question--even looking at the PSY and PPI columns has been useful! Jamie > >Are you using SPM8? The issue of summing was fixed in one of the later >releases of SPM5, so if you have an older version, that could explain >some of the issue. You could check to make sure that negative aspects >of the SPM.xX.X for the PPI term are the same for all subjects. You >could plot them. >Are you using the same adjustment for all models? >Are you using exactly the same voxels for all models? > >On Tue, Feb 22, 2011 at 6:21 PM, J S Lee <[log in to unmask]> wrote: >> Dear list, >> >> I conducted a PPI analysis in an experiment with 6 conditions. To replicate >> a previous study's PPI analysis, I was interested in connectivity >> differences between 5 of the conditions compared to the control (6th) >> condition, so extracted my VOI (using an all effects of interest contrast), >> then created a PPI model with a [1 1 1 1 1 -1] weighting for the >> psychological context regressor. I get a reasonable replication of the same >> PPI effects from the previous study, so the results are sensible. >> >> However, in that previous study, there were not enough trials of each of the >> 5 conditions to realistically analyze them separately, which is why I >> collapsed across them. In this study, there are many more trials, so I was >> hoping to look at which of the 5 conditions were driving the original PPI >> results. I was given hope when the initial PPI replicated in this new study. >> However, when I create separate PPI models for each condition versus control >> (e.g., context regressors using [1 0 0 0 0 -1] for model 1, [0 1 0 0 0 -1] >> for model 2, etc.), NONE of these analyses show the same pattern as the 1 1 >> 1 1 1 -1 model does. Mostly there are no significant (or anywhere near >> significant) results, and those random speckles that do show up at low >> threshold are not in the same places. >> >> Is it theoretically possible that 5 conditions vs 1 other can produce a PPI, >> but that none of those conditions singly vs the 1 other can do that? Or must >> there be an error? I have checked the microtime onset files to make the >> context is specified correctly, and made sure everything matches up in terms >> of specifying the conditions. Everything about the models looks fine to me. >> I know the 5 conditions vs 1 is a bit unbalanced, but it replicates the >> previous study (in which the 5 vs 1 were equal in terms of number of >> trials), and I understand that when creating the context variable one does >> NOT sum the vector to zero the way one would in defining a contrast for a >> regional activation analysis. >> >> Many thanks in advance for any thoughts, >> Jamie Lee

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------=_NextPart_001_98E5_01CBD43A.9CB39E80 Content-Type: text/html Content-Transfer-Encoding: 7bit Hi Donald,
Thank you for your reply!
I am using SPM8.
I looked at the SPM.xX.X values for each subject. The values in the SPM.xX.X *PSY* columns for each of my models line up perfectly across subjects. For the different models within a subject, there also seems to be correspondence for the PSY negative values (although there are slight baseline shifts between different models). The values in the PPI column, however, do not correspond so well. I don't think I would have expected the PPI values to correspond across subjects, however, because the VOI values differ from subject to subject, so the PPI should also differ as it represents an interaction? The PPI values for different models in the same subject also do not show perfect correspondence (png attached: It shows 2 subjects' SPM.xX.X PPI values over the first 80 scans. The All conds - control model and Cond 1 - control PPI values are plotted for each subject. I didn't include the Cond 2 - control, Cond 3 - control, etc. for clarity).

All models are coming from the same VOI, so I think the adjustment has to be the same for all models (all extractions were adjusted for an F contrast of the effects of interest at the first-level model). Is this what you meant?
The voxels are also identical (again, coming from the same VOI I think they have to be?).


Thank you very much for taking the time to consider my question--even looking at the PSY and PPI columns has been useful!

Jamie

>
>Are you using SPM8? The issue of summing was fixed in one of the later
>releases of SPM5, so if you have an older version, that could explain
>some of the issue. You could check to make sure that negative aspects
>of the SPM.xX.X for the PPI term are the same for all subjects. You
>could plot them.
>Are you using the same adjustment for all models?
>Are you using exactly the same voxels for all models?


>
>On Tue, Feb 22, 2011 at 6:21 PM, J S Lee <[log in to unmask]> wrote:
>> Dear list,
>>
>> I conducted a PPI analysis in an experiment with 6 conditions. To replicate
>> a previous study's PPI analysis, I was interested in connectivity
>> differences between 5 of the conditions compared to the control (6th)
>> condition, so extracted my VOI (using an all effects of interest contrast),
>> then created a PPI model with a [1 1 1 1 1 -1] weighting for the
>> psychological context regressor. I get a reasonable replication of the same
>> PPI effects from the previous study, so the results are sensible.
>>
>> However, in that previous study, there were not enough trials of each of the
>> 5 conditions to realistically analyze them separately, which is why I
>> collapsed across them. In this study, there are many more trials, so I was
>> hoping to look at which of the 5 conditions were driving the original PPI
>> results. I was given hope when the initial PPI replicated in this new study.
>> However, when I create separate PPI models for each condition versus control
>> (e.g., context regressors using [1 0 0 0 0 -1] for model 1, [0 1 0 0 0 -1]
>> for model 2, etc.), NONE of these analyses show the same pattern as the 1 1
>> 1 1 1 -1 model does. Mostly there are no significant (or anywhere near
>> significant) results, and those random speckles that do show up at low
>> threshold are not in the same places.
>>
>> Is it theoretically possible that 5 conditions vs 1 other can produce a PPI,
>> but that none of those conditions singly vs the 1 other can do that? Or must
>> there be an error? I have checked the microtime onset files to make the
>> context is specified correctly, and made sure everything matches up in terms
>> of specifying the conditions. Everything about the models looks fine to me.
>> I know the 5 conditions vs 1 is a bit unbalanced, but it replicates the
>> previous study (in which the 5 vs 1 were equal in terms of number of
>> trials), and I understand that when creating the context variable one does
>> NOT sum the vector to zero the way one would in defining a contrast for a
>> regional activation analysis.
>>
>> Many thanks in advance for any thoughts,
>> Jamie Lee

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========================================================================Date: Fri, 25 Feb 2011 05:25:48 +0000 Reply-To: Israr Ul Haq <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Israr Ul Haq <[log in to unmask]> Subject: Re: fixed effects analysis across two sessions Comments: To: Donald McLaren <[log in to unmask]> Mime-Version: 1.0 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain Message-ID: <[log in to unmask]> Dear Donald, I remember reading about beta and the GLM and how its calculated by using the matrix inverse, when I first started out reading about it. For some reason I formed the whole concept of individual correlations for each time point of a voxel and the subsequent distribution with its mean and sd as a way of representing what actually beta is representing, the weights of columns. Perhaps because the visualization came easier. Thankyou very much for taking time to point this out. What I understand from your explanation is that contrast*beta is essentially the output of adding and subtracting the individual values of the betas, based on the 1's and the -1's in the contrast, 1 meaning the beta will be added and -1, it will be subtracted. I guess for my question about the direction of change in terms of betas, how does the t statistic differ between a certain value of contrast*beta and an equal but a negative value of the same. Since the absolute difference between the effect and the mean is the same, does it take into account whether the contrast*beta is a positive or a negative value? Thanks Israr ========================================================================Date: Fri, 25 Feb 2011 10:54:06 +0100 Reply-To: Martin Jensen Dietz <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Martin Jensen Dietz <[log in to unmask]> Subject: Re: Order of subject files in ANOVA batch Comments: To: Pilar Archila-Suerte <[log in to unmask]> In-Reply-To: <[log in to unmask]> Content-Type: text/plain; charset="us-ascii" Content-Transfer-Encoding: quoted-printable MIME-Version: 1.0 Message-ID: <[log in to unmask]> Hi Pilar, When comparing 2 independent groups use a two-sample t-test which is very straight forward Martin -- Martin Dietz [log in to unmask] On Feb 25, 2011, at 12:44 AM, Pilar Archila-Suerte wrote: Mine is actually not a repeated measures design. I'm running a full factorial and I just want to compare activity in one group vs. another. Do the con files need to be in the same order in each cell in this case? Pilar On Thu, Feb 24, 2011 at 5:38 PM, MCLAREN, Donald <[log in to unmask]> wrote: You should use the flexible factorial for repeated measure designs with factors for subject and condition in your design. Best Regards, Donald McLaren ================= D.G. McLaren, Ph.D. Postdoctoral Research Fellow, GRECC, Bedford VA Research Fellow, Department of Neurology, Massachusetts General Hospital and Harvard Medical School Office: (773) 406-2464 ===================== This e-mail contains CONFIDENTIAL INFORMATION which may contain PROTECTED HEALTHCARE INFORMATION and may also be LEGALLY PRIVILEGED and which is intended only for the use of the individual or entity named above. If the reader of the e-mail is not the intended recipient or the employee or agent responsible for delivering it to the intended recipient, you are hereby notified that you are in possession of confidential and privileged information. Any unauthorized use, disclosure, copying or the taking of any action in reliance on the contents of this information is strictly prohibited and may be unlawful. If you have received this e-mail unintentionally, please immediately notify the sender via telephone at (773) 406-2464 or email. On Thu, Feb 24, 2011 at 6:28 PM, Pilar Archila-Suerte <[log in to unmask]> wrote: > Dear SPM list, > In setting ANOVAs in SPM, do the subject files need to be in the same order > under each cell? > I just ran two trial trial batches, one with the same order of subjects and > one with a different order. The areas of activity are very similar but the > order in which the areas show up as more or less intensive did vary. > Any insight as to how SPM does this? should I stick to the same order of > subjects for clarity? > Thanks, > Pilar A . ========================================================================Date: Fri, 25 Feb 2011 11:42:31 +0100 Reply-To: "Maarten A.S. Boksem" <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: "Maarten A.S. Boksem" <[log in to unmask]> Subject: PhD position in Decision Neuroscience MIME-Version: 1.0 Content-Type: multipart/alternative; boundaryMessage-ID: <[log in to unmask]> --0015174c187ee518de049d18fd88 Content-Type: text/plain; charset=ISO-8859-1 *PhD position in Decision Neuroscience at the Erasmus University Rotterdam* *and Donders Institute Nijmegen* The Erasmus Center for Neuroeconomics (ECNE) at the Rotterdam School of Management, Erasmus University and the Donders Institute for Brain, Cognition and Behaviour at Radboud University Nijmegen announce an opening for a PhD researcher to join an active group of researchers in the Center in the field of decision neuroscience/neuroeconomics/neuromarketing. This position will be jointly supervised by Prof. Ale Smidts (Erasmus), Dr. Alan Sanfey (Donders Institute) and Dr. Maarten Boksem (Erasmus and Donders). We currently seek outstanding applicants whose research interests lie at the intersection of decision-making, behavioral economics, and neuroscience and who are interested in studying the brain mechanisms that underlie decision-making. Particular interests of our group are the neural mechanisms that underlie social influences on decisions, emotion regulation and self-control involved in decision-making, and the role of risk and reward in such decisions. We are especially interested in applicants whose research can build bridges between existing strengths in consumer-behavior research at the marketing department of the Rotterdam School of Management and decision neuroscience at the Donders Institute. The Erasmus Center for Neuroeconomics is dedicated to conducting cutting-edge interdisciplinary research in decision neuroscience, and hosts the Erasmus Behavioral Lab which provides an excellent infrastructure for conducting behavioral and EEG/ERP experiments. The Donders Institute is a leading research institute in cognitive neuroscience and provides excellent resources for functional neuroimaging by means of two research-dedicated fMRI scanners, an MEG scanner, and EEG and TMS facilities. Additional facilities are available for the collection and analysis of genetic samples. The collaboration between Erasmus University and the Donders Institute provides an outstanding environment for studying the neural underpinnings of decision-making behavior, and the successful applicant will have full access to the facilities in both institutions. *Requirements for the PhD position * Successful candidates must have a relevant Masters degree, preferably with a background in cognitive neuroscience, cognitive psychology, or biological psychology. Candidates with a background in consumer behavior or economics, with proven evidence or a strong interest in developing cognitive neuroscience and imaging skills, are also invited to apply. A tailored PhD course program will be developed. The PhD position is for four years. PhDs receive a regular employment contract for a doctoral student. See the ERIM Doctoral Program for further information on the facilities of PhD students at Erasmus. Preferred starting date: September 2011. Applications, including CV, a brief summary of current and proposed research, and at least two letters of recommendation, should be submitted through the ERIM application website (http://www.erim.eur.nl). submit your application preferably before April 1, 2011. PhD applicants may be requested to provide GRE/ GMAT scores and TOEFLl /IELTS language scores. For further information on the position, visit our website erim.nl/neuroconomics or contact Prof. Ale Smidts ([log in to unmask]) or Dr. Maarten Boksem ( [log in to unmask]). -- Dr. Maarten A.S. Boksem RSM Erasmus University Burgemeester Oudlaan 50 3062 PA Rotterdam The Netherlands Donders Institute for Brain, Cognition and Behaviour Centre for Cognitive Neuroimaging P.O. Box 9101 6500 HB Nijmegen The Netherlands +31 (0) 24 36 68063 [log in to unmask] www.Boksem.nl --0015174c187ee518de049d18fd88 Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable

PhD position in Decision Neuroscience at the Erasmus University Rotterdam

and Donders Institute Nijmegen

The Erasmus Center for Neuroeconomics (ECNE) at the Rotterdam School of Management, Erasmus University and the Donders Institute for Brain, Cognition and Behaviour at Radboud University Nijmegen announce an opening for a PhD researcher to join an active group of researchers in the Center in the field of decision neuroscience/neuroeconomics/neuromarketing. This position will be jointly supervised by Prof. Ale Smidts (Erasmus), Dr. Alan Sanfey (Donders Institute) and Dr. Maarten Boksem (Erasmus and Donders).

We currently seek outstanding applicants whose research interests lie at the intersection of decision-making, behavioral economics, and neuroscience and who are interested in studying the brain mechanisms that underlie decision-making. Particular interests of our group are the neural mechanisms that underlie social influences on decisions, emotion regulation and self-control involved in decision-making, and the role of risk and reward in such decisions. We are especially interested in applicants whose research can build bridges between existing strengths in consumer-behavior research at the marketing department of the Rotterdam School of Management and decision neuroscience at the Donders Institute.

The Erasmus Center for Neuroeconomics is dedicated to conducting cutting-edge interdisciplinary research in decision neuroscience, and hosts the Erasmus Behavioral Lab which provides an excellent infrastructure for conducting behavioral and EEG/ERP experiments. The Donders Institute is a leading research institute in cognitive neuroscience and provides excellent resources for functional neuroimaging by means of two research-dedicated fMRI scanners, an MEG scanner, and EEG and TMS facilities. Additional facilities are available for the collection and analysis of genetic samples. The collaboration between Erasmus University and the Donders Institute provides an outstanding environment for studying the neural underpinnings of decision-making behavior, and the successful applicant will have full access to the facilities in both institutions.

Requirements for the PhD position

Successful candidates must have a relevant Masters degree, preferably with a background in cognitive neuroscience, cognitive psychology, or biological psychology. Candidates with a background in consumer behavior or economics, with proven evidence or a strong interest in developing cognitive neuroscience and imaging skills, are also invited to apply. A tailored PhD course program will be developed. The PhD position is for four years. PhDs receive a regular employment contract for a doctoral student. See the ERIM Doctoral Program for further information on the facilities of PhD students at Erasmus.

Preferred starting date: September 2011.

Applications, including CV, a brief summary of current and proposed research, and at least two letters of recommendation, should be submitted through the ERIM application website (http://www.erim.eur.nl). submit your application preferably before April 1, 2011. PhD applicants may be requested to provide GRE/ GMAT scores and TOEFLl /IELTS language scores. For further information on the position, visit our website erim.nl/neuroconomics or contact Prof. Ale Smidts ([log in to unmask]) or Dr. Maarten Boksem ([log in to unmask]).


--
Dr. Maarten A.S. Boksem

RSM
Erasmus University
Burgemeester Oudlaan 50
3062 PA Rotterdam
The Netherlands

Donders Institute for Brain, Cognition and Behaviour
Centre for Cognitive Neuroimaging
P.O. Box 9101
6500 HB Nijmegen
The Netherlands


--0015174c187ee518de049d18fd88-- ========================================================================Date: Fri, 25 Feb 2011 22:39:16 +1100 Reply-To: Richard Morris <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Richard Morris <[log in to unmask]> Subject: Re: script to flip MR images left to right (or vice versa) In-Reply-To: <[log in to unmask]> Content-Type: multipart/alternative; boundary="_000_61FCD4EC1B8E4B6FBEE491DCCD0A91DAunsweduau_" MIME-Version: 1.0 Message-ID: <[log in to unmask]> --_000_61FCD4EC1B8E4B6FBEE491DCCD0A91DAunsweduau_ Content-Type: text/plain; charset="us-ascii" Content-Transfer-Encoding: quoted-printable I'm not sure, but I think you can use the image calculator in SPM, with the following function: f = 'Inv(i1)' On 25/02/2011, at 10:16 AM, Michael T Rubens wrote: how about this: %%% v = spm_vol('/image_path/brain.img'); x = spm_read_vols(v); x = x(size(x,1):-1:1,:,:); [path file] = fileparts(v.fname); v.fname = fullfile(path,['flipped_' file'); spm_write_vol(v,x) %%% cheers, michael On Thu, Feb 24, 2011 at 9:35 AM, Chien-Ho Lin <[log in to unmask]> wrote: Hi, I stuides patients with stroke doing some behavior paradigm in fMRI. Patients always used their affected limb for the task so some patients used left hand some used right hand. Now I would like to flip the left and right of the images so patients' lesional hemisphere are on the same side. Is there any script in spm 5 or 8 can help to accomplish this goal? I found a m file called spm_flip.m but it seems support only spm2. Your assistance are well appreciated. Thank you so much. Janice -- Research Associate Gazzaley Lab Department of Neurology University of California, San Francisco --_000_61FCD4EC1B8E4B6FBEE491DCCD0A91DAunsweduau_ Content-Type: text/html; charset="us-ascii" Content-Transfer-Encoding: quoted-printable I'm not sure, but I think you can use the image calculator in SPM, with the following function:

f = 'Inv(i1)'


On 25/02/2011, at 10:16 AM, Michael T Rubens wrote:

how about this:
%%%

v = spm_vol('/image_path/brain.img');
x = spm_read_vols(v);

x = x(size(x,1):-1:1,:,:);

[path file] = fileparts(v.fname);
v.fname = fullfile(path,['flipped_' file');

spm_write_vol(v,x)

%%%


cheers,
michael

On Thu, Feb 24, 2011 at 9:35 AM, Chien-Ho Lin <[log in to unmask]> wrote:
Hi,

I stuides patients with stroke doing some behavior paradigm in fMRI.
Patients always used their affected limb for the task so some patients used left hand some used right hand.
Now I would like to flip the left and right of the images so patients' lesional hemisphere are on the same side.

Is there any script in spm 5 or 8 can help to accomplish this goal?

I found a m file called spm_flip.m but it seems support only spm2.

Your assistance are well appreciated.

Thank you so much.

Janice



--
Research Associate
Gazzaley Lab
Department of Neurology
University of California, San Francisco

--_000_61FCD4EC1B8E4B6FBEE491DCCD0A91DAunsweduau_-- ========================================================================Date: Fri, 25 Feb 2011 11:54:19 +0000 Reply-To: Rosa Sanchez Panchuelo <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Rosa Sanchez Panchuelo <[log in to unmask]> Subject: Re: script to flip MR images left to right (or vice versa) Comments: To: Richard Morris <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/alternative; boundary="------------040105050906060404020507" Message-ID: <[log in to unmask]> This is a multi-part message in MIME format. --------------040105050906060404020507 Content-Type: text/plain; charset=ISO-8859-1; format=flowed Content-Transfer-Encoding: 7bit You can do it easily with fsl: fslswapdim input_image.img -x outpu_image.img -x will flip the image in the RL direction. On 25/02/2011 11:39, Richard Morris wrote: > I'm not sure, but I think you can use the image calculator in SPM, > with the following function: > > f = 'Inv(i1)' > > > On 25/02/2011, at 10:16 AM, Michael T Rubens wrote: > >> how about this: >> %%% >> >> v = spm_vol('/image_path/brain.img'); >> x = spm_read_vols(v); >> >> x = x(size(x,1):-1:1,:,:); >> >> [path file] = fileparts(v.fname); >> v.fname = fullfile(path,['flipped_' file'); >> >> spm_write_vol(v,x) >> >> %%% >> >> >> cheers, >> michael >> >> On Thu, Feb 24, 2011 at 9:35 AM, Chien-Ho Lin <[log in to unmask] >> > wrote: >> >> Hi, >> >> I stuides patients with stroke doing some behavior paradigm in fMRI. >> Patients always used their affected limb for the task so some >> patients used left hand some used right hand. >> Now I would like to flip the left and right of the images so >> patients' lesional hemisphere are on the same side. >> >> Is there any script in spm 5 or 8 can help to accomplish this goal? >> >> I found a m file called spm_flip.m but it seems support only spm2. >> >> Your assistance are well appreciated. >> >> Thank you so much. >> >> Janice >> >> >> >> >> -- >> Research Associate >> Gazzaley Lab >> Department of Neurology >> University of California, San Francisco > -- Rosa Maria Sanchez Panchuelo Post-doctoral Research fellow Sir Peter Mansfield Magnetic Resonance Centre University of Nottingham University Park Nottingham, NG7 2RD United Kingdom +44 115 84 66003 This message and any attachment are intended solely for the addressee and may contain confidential information. If you have received this message in error, please send it back to me, and immediately delete it. Please do not use, copy or disclose the information contained in this message or in any attachment. Any views or opinions expressed by the author of this email do not necessarily reflect the views of the University of Nottingham. This message has been checked for viruses but the contents of an attachment may still contain software viruses which could damage your computer system: you are advised to perform your own checks. Email communications with the University of Nottingham may be monitored as permitted by UK legislation. --------------040105050906060404020507 Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: 7bit You can do it easily with fsl:
fslswapdim input_image.img -x outpu_image.img
-x will flip the image in the RL direction. 

On 25/02/2011 11:39, Richard Morris wrote:
[log in to unmask]" type="cite">I'm not sure, but I think you can use the image calculator in SPM, with the following function:

f = 'Inv(i1)'


On 25/02/2011, at 10:16 AM, Michael T Rubens wrote:

how about this:
%%%

v = spm_vol('/image_path/brain.img');
x = spm_read_vols(v);

x = x(size(x,1):-1:1,:,:);

[path file] = fileparts(v.fname);
v.fname = fullfile(path,['flipped_' file');

spm_write_vol(v,x)

%%%


cheers,
michael

On Thu, Feb 24, 2011 at 9:35 AM, Chien-Ho Lin <[log in to unmask]> wrote:
Hi,

I stuides patients with stroke doing some behavior paradigm in fMRI.
Patients always used their affected limb for the task so some patients used left hand some used right hand.
Now I would like to flip the left and right of the images so patients' lesional hemisphere are on the same side.

Is there any script in spm 5 or 8 can help to accomplish this goal?

I found a m file called spm_flip.m but it seems support only spm2.

Your assistance are well appreciated.

Thank you so much.

Janice



--
Research Associate
Gazzaley Lab
Department of Neurology
University of California, San Francisco



--
Rosa Maria Sanchez Panchuelo
Post-doctoral Research fellow
Sir Peter Mansfield Magnetic Resonance Centre
University of Nottingham
University Park
Nottingham, NG7 2RD
United Kingdom
+44 115 84 66003

 

This message and any attachment are intended solely for the addressee and may contain confidential information. If you have received this message in error, please send it back to me, and immediately delete it. Please do not use, copy or disclose the information contained in this message or in any attachment. Any views or opinions expressed by the author of this email do not necessarily reflect the views of the University of Nottingham.

This message has been checked for viruses but the contents of an attachment may still contain software viruses which could damage your computer system: you are advised to perform your own checks. Email communications with the University of Nottingham may be monitored as permitted by UK legislation.

--------------040105050906060404020507-- ========================================================================Date: Fri, 25 Feb 2011 08:19:45 -0600 Reply-To: Michael Harms <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Michael Harms <[log in to unmask]> Subject: Re: script to flip MR images left to right (or vice versa) Comments: To: Rosa Sanchez Panchuelo <[log in to unmask]> In-Reply-To: <[log in to unmask]> Content-Type: text/plain Mime-Version: 1.0 Content-Transfer-Encoding: 7bit Message-ID: <[log in to unmask]> A note of caution about using fslswapdim in this manner however: If you do that, the data order and the header information stored in the sform/qform will no longer be in sync. So, what the sform/qform defines to be "left" will no longer be the subject's true left (assuming the labels in the original data were correct)! Read the following FSL page if you want all the details: http://www.fmrib.ox.ac.uk/fsl/avwutils/index.html Best, -MH On Fri, 2011-02-25 at 11:54 +0000, Rosa Sanchez Panchuelo wrote: > You can do it easily with fsl: > fslswapdim input_image.img -x outpu_image.img > -x will flip the image in the RL direction. > > On 25/02/2011 11:39, Richard Morris wrote: > > I'm not sure, but I think you can use the image calculator in SPM, > > with the following function: > > > > > > f = 'Inv(i1)' > > > > > > > > On 25/02/2011, at 10:16 AM, Michael T Rubens wrote: > > > > > how about this: > > > %%% > > > > > > > > > v = spm_vol('/image_path/brain.img'); > > > x = spm_read_vols(v); > > > > > > > > > x = x(size(x,1):-1:1,:,:); > > > > > > > > > [path file] = fileparts(v.fname); > > > v.fname = fullfile(path,['flipped_' file'); > > > > > > > > > spm_write_vol(v,x) > > > > > > > > > %%% > > > > > > > > > > > > > > > cheers, > > > michael > > > > > > On Thu, Feb 24, 2011 at 9:35 AM, Chien-Ho Lin > > > <[log in to unmask]> wrote: > > > Hi, > > > > > > I stuides patients with stroke doing some behavior > > > paradigm in fMRI. > > > Patients always used their affected limb for the task so > > > some patients used left hand some used right hand. > > > Now I would like to flip the left and right of the images > > > so patients' lesional hemisphere are on the same side. > > > > > > Is there any script in spm 5 or 8 can help to accomplish > > > this goal? > > > > > > I found a m file called spm_flip.m but it seems support > > > only spm2. > > > > > > Your assistance are well appreciated. > > > > > > Thank you so much. > > > > > > Janice > > > > > > > > > > > > -- > > > Research Associate > > > Gazzaley Lab > > > Department of Neurology > > > University of California, San Francisco > > > > > > > > > > -- > Rosa Maria Sanchez Panchuelo > Post-doctoral Research fellow > Sir Peter Mansfield Magnetic Resonance Centre > University of Nottingham > University Park > Nottingham, NG7 2RD > United Kingdom > +44 115 84 66003 > > > > > > This message and any attachment are intended solely for the addressee > and may contain confidential information. If you have received this > message in error, please send it back to me, and immediately delete > it. Please do not use, copy or disclose the information contained in > this message or in any attachment. Any views or opinions expressed by > the author of this email do not necessarily reflect the views of the > University of Nottingham. > > This message has been checked for viruses but the contents of an > attachment may still contain software viruses which could damage your > computer system: you are advised to perform your own checks. Email > communications with the University of Nottingham may be monitored as > permitted by UK legislation. > ========================================================================Date: Fri, 25 Feb 2011 15:23:11 +0100 Reply-To: =?ISO-8859-1?Q?Rainer_Bgle?= <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: =?ISO-8859-1?Q?Rainer_Bgle?= <[log in to unmask]> Subject: Re: Negative values in DCM.A Comments: To: Maria Dauvermann <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/alternative; boundaryMessage-ID: <[log in to unmask]> --00504502e3d0ea2d57049d1c1166 Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Dear Maria, to clarify a little: -self connections need to be negative or the activation in this region would go to infinity (and with that the whole network would become unstable) -all connections are (defined) relative to self-connections because the self-connections are 'fixed' to mean=-1 with priors for their mean and variance such that the probability of the system becoming unstable being very small. (This leaves a renormalization parameters corresponding to a decay rate, fixed to 1s.) -connections in DCM are change rates, i.e. a12 tells you how much of the current state/activation (on neuronal level) at time t of region 2 is added to the change in region 1 (at time t). There might be influences from other regions on region 2 which have to be considered, but if if a12 is the sole connection, we can say: *** a12=0.1 means 10% of the state in region 2 is added to the state (activity) of region 1 and analog for a12=-0.1, this corresponds to a subtraction by 10% of the state in region 2 from the state in region 1. Regards, Rainer On Fri, Feb 25, 2011 at 8:48 AM, Maria Dauvermann < [log in to unmask]> wrote: > Dear Rainer, > > thank you very much for your reply. Now I understand why there are negative > values in the self connections but I also have positive values in some DCMs. > What does that mean? > > BW, Maria > > > > > On 24 February 2011 16:14, Rainer Bgle <[log in to unmask]>wrote: > >> Hello Maria, >> >> as far as I understand this, connection parameters in DCM are change >> rates, i.e. area 1 reduces the activity in area 2 (if a21 < 0). >> >> As stated in Friston 2003, connection parameters are always relative to >> parameters of self connections (which have to be negative to ensure a stable >> system). >> >> Regards, >> Rainer >> >> >> >> On Thu, Feb 24, 2011 at 8:58 AM, Maria Dauvermann < >> [log in to unmask]> wrote: >> >>> Hello, >>> >>> I had a look at the values in DCM.A after I have estimated the DCMs. >>> >>> What does a negative value in the intrinsic connection mean? How do I >>> interprete this result? >>> >>> Thanks for your help. >>> >>> BW, Maria >>> >> >> > --00504502e3d0ea2d57049d1c1166 Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Dear Maria,

to clarify a little:

-self connections need to be negative or the activation in this region would go to infinity (and with that the whole network would become unstable)
-all connections are (defined) relative to self-connections because the self-connections are 'fixed' to mean=-1 with priors for their mean and variance such that the probability of the system becoming unstable being very small. (This leaves a renormalization parameters corresponding to a decay rate, fixed to 1s.)
-connections in DCM are change rates, i.e. a12 tells you how much of the current state/activation (on neuronal level) at time t of region 2 is added to the change in region 1 (at time t). There might be influences from other regions on region 2 which have to be considered, but if if a12 is the sole connection, we can say:
*** a12=0.1 means 10% of the state in region 2 is added to the state (activity) of region 1
and analog for a12=-0.1, this corresponds to a subtraction by 10% of the state in region 2 from the state in region 1.

Regards,
Rainer

On Fri, Feb 25, 2011 at 8:48 AM, Maria Dauvermann <[log in to unmask]> wrote:
Dear Rainer,

thank you very much for your reply. Now I understand why there are negative values in the self connections but I also have positive values in some DCMs. What does that mean?

BW, Maria




On 24 February 2011 16:14, Rainer Bgle <[log in to unmask]> wrote:
Hello Maria,

as far as I understand this, connection parameters in DCM are change rates, i.e. area 1 reduces the activity in area 2 (if a21 < 0).

As stated in Friston 2003, connection parameters are always relative to parameters of self connections (which have to be negative to ensure a stable system).

Regards,
Rainer



On Thu, Feb 24, 2011 at 8:58 AM, Maria Dauvermann <[log in to unmask]> wrote:
Hello,

I had a look at the values in DCM.A after I have estimated the DCMs.

What does a negative value in the intrinsic connection mean? How do I interprete this result?

Thanks for your help.

BW, Maria



--00504502e3d0ea2d57049d1c1166-- ========================================================================Date: Fri, 25 Feb 2011 10:13:26 -0500 Reply-To: "MCLAREN, Donald" <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: "MCLAREN, Donald" <[log in to unmask]> Subject: Re: Can't find driving effects for PPI analysis Comments: To: J S Lee <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> As you can see the *PSY* negative columns do line up well together, but the positives do not. Samething with the PPI, where you have the control condition, the curves line up. Now, if we think about the concept of the the general linear model (Y=BX)... Trying to fit the all-control vector to the data is much different than fitting the condition1-control vector. I think this reiterates the point I'm making in a paper I'm about to submit on PPI. That is PPI as it is currently implemented fits these vectors above, rather than fitting a vector for condition1, condition2, .., and control. In splitting them up, one is then estimating the relationship of each component, rather than the joint relationship. My hunch is that if you were to separate them conditions, you would either eliminate the average effect OR more likely find out which one is driving the effect. When you only model 2 conditions, there is a chance that you attribute the variance of the data to the wrong factor or it ends up in the error term. Also, when you only model 2 conditions, you are only modelling the activitation effect of those 2 conditions. Modelling has shown that the individual model fit is improved when you separate the conditions. I'm adding some comments to the code for splitting the vectors and have termed the approach "a generalizable form of PPI (gPPI)" and hopefully can provide you with the code later today. Best Regards, Donald McLaren ================= D.G. McLaren, Ph.D. Postdoctoral Research Fellow, GRECC, Bedford VA Research Fellow, Department of Neurology, Massachusetts General Hospital and Harvard Medical School Office: (773) 406-2464 ===================== This e-mail contains CONFIDENTIAL INFORMATION which may contain PROTECTED HEALTHCARE INFORMATION and may also be LEGALLY PRIVILEGED and which is intended only for the use of the individual or entity named above. If the reader of the e-mail is not the intended recipient or the employee or agent responsible for delivering it to the intended recipient, you are hereby notified that you are in possession of confidential and privileged information. Any unauthorized use, disclosure, copying or the taking of any action in reliance on the contents of this information is strictly prohibited and may be unlawful. If you have received this e-mail unintentionally, please immediately notify the sender via telephone at (773) 406-2464 or email. On Thu, Feb 24, 2011 at 6:50 PM, J S Lee <[log in to unmask]> wrote: > Hi Donald, > Thank you for your reply! > I am using SPM8. > I looked at the SPM.xX.X values for each subject. The values in the SPM.xX.X > *PSY* columns for each of my models line up perfectly across subjects. For > the different models within a subject, there also seems to be correspondence > for the PSY negative values (although there are slight baseline shifts > between different models). The values in the PPI column, however, do not > correspond so well. I don't think I would have expected the PPI values to > correspond across subjects, however, because the VOI values differ from > subject to subject, so the PPI should also differ as it represents an > interaction? The PPI values for different models in the same subject also do > not show perfect correspondence (png attached: It shows 2 subjects' SPM.xX.X > PPI values over the first 80 scans. The All conds - control model and Cond 1 > - control PPI values are plotted for each subject. I didn't include the Cond > 2 - control, Cond 3 - control, etc. for clarity). > > All models are coming from the same VOI, so I think the adjustment has to be > the same for all models (all extractions were adjusted for an F contrast of > the effects of interest at the first-level model). Is this what you meant? > The voxels are also identical (again, coming from the same VOI I think they > have to be?). > > > Thank you very much for taking the time to consider my question--even > looking at the PSY and PPI columns has been useful! > > Jamie > >> >>Are you using SPM8? The issue of summing was fixed in one of the later >>releases of SPM5, so if you have an older version, that could explain >>some of the issue. You could check to make sure that negative aspects >>of the SPM.xX.X for the PPI term are the same for all subjects. You >>could plot them. >>Are you using the same adjustment for all models? >>Are you using exactly the same voxels for all models? > > >> >>On Tue, Feb 22, 2011 at 6:21 PM, J S Lee <[log in to unmask]> wrote: >>> Dear list, >>> >>> I conducted a PPI analysis in an experiment with 6 conditions. To >>> replicate >>> a previous study's PPI analysis, I was interested in connectivity >>> differences between 5 of the conditions compared to the control (6th) >>> condition, so extracted my VOI (using an all effects of interest >>> contrast), >>> then created a PPI model with a [1 1 1 1 1 -1] weighting for the >>> psychological context regressor. I get a reasonable replication of the >>> same >>> PPI effects from the previous study, so the results are sensible. >>> >>> However, in that previous study, there were not enough trials of each of >>> the >>> 5 conditions to realistically analyze them separately, which is why I >>> collapsed across them. In this study, there are many more trials, so I >>> was >>> hoping to look at which of the 5 conditions were driving the original PPI >>> results. I was given hope when the initial PPI replicated in this new >>> study. >>> However, when I create separate PPI models for each condition versus >>> control >>> (e.g., context regressors using [1 0 0 0 0 -1] for model 1, [0 1 0 0 0 >>> -1] >>> for model 2, etc.), NONE of these analyses show the same pattern as the 1 >>> 1 >>> 1 1 1 -1 model does. Mostly there are no significant (or anywhere near >>> significant) results, and those random speckles that do show up at low >>> threshold are not in the same places. >>> >>> Is it theoretically possible that 5 conditions vs 1 other can produce a >>> PPI, >>> but that none of those conditions singly vs the 1 other can do that? Or >>> must >>> there be an error? I have checked the microtime onset files to make the >>> context is specified correctly, and made sure everything matches up in >>> terms >>> of specifying the conditions. Everything about the models looks fine to >>> me. >>> I know the 5 conditions vs 1 is a bit unbalanced, but it replicates the >>> previous study (in which the 5 vs 1 were equal in terms of number of >>> trials), and I understand that when creating the context variable one >>> does >>> NOT sum the vector to zero the way one would in defining a contrast for a >>> regional activation analysis. >>> >>> Many thanks in advance for any thoughts, >>> Jamie Lee > > _______________________________________________________________ > Get the Free email that has everyone talking at http://www.mail2world.com > Unlimited Email Storage POP3 Calendar SMS Translator Much More! ========================================================================Date: Fri, 25 Feb 2011 15:26:24 +0000 Reply-To: "Stephen J. Fromm" <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: "Stephen J. Fromm" <[log in to unmask]> Subject: Re: Can't find driving effects for PPI analysis Comments: To: Donald McLaren <[log in to unmask]> Mime-Version: 1.0 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain; charset="UTF-8" Message-ID: <[log in to unmask]> Donald, You wrote, "The issue of summing was fixed in one of the later releases of SPM5,..." Are you saying that it's now OK if the weights used sum to zero, when before they shouldn't? Best, S ========================================================================Date: Fri, 25 Feb 2011 16:23:05 +0000 Reply-To: "Stephen J. Fromm" <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: "Stephen J. Fromm" <[log in to unmask]> Subject: DCM: significance and graph connectivity Mime-Version: 1.0 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain; charset="UTF-8" Message-ID: <[log in to unmask]> I'm working on a DCM project. So far the best fitting model looks like this: DI--->R1 ==> R2 ==> R3 ^ ^ | | MI1 MI2 That is: * there are three regions, with intrinsic connections from R1 to R2 and R2 to R3 * there is one driving input DI acting on R1 * there are two modulatory connections MI1 and MI2 acting on the two between-regions intrinsic connections (The experimental variables for MI1 and MI2 are identical.) At the group level, the second connection (R2 ==> R3) is significant, but the first (R1 ==> R2) isn't. Conceptually, this doesn't make sense, insofar as the only way the system perturbations introduced by the DI can get to (R2 ==> R3) is through (R1 ==> R2). Does this reduce the credibility of the model? Or is it alone not enough to do that because of the possible vagaries of what is significant? TIA, S ========================================================================Date: Fri, 25 Feb 2011 11:38:07 -0500 Reply-To: "MCLAREN, Donald" <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: "MCLAREN, Donald" <[log in to unmask]> Subject: Re: Can't find driving effects for PPI analysis Comments: To: "Stephen J. Fromm" <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Message-ID: <[log in to unmask]> I am saying two things: (1) You are contrasting the positive weight conditions against the negative weighted conditions in such a manner that the connectivity of the positive weights (1s) are assumed to be the same (e.g. if you have 3 conditions and a control AND contrast conditions versus control, you assume that the connectivity during the conditions is the same) and the same is true for the negatives (-1s). They should sum to 0 unless there are 2 conditions OR you think the connectivity is different between the positive and negative conditions, but assumptions like this are bad. (1b) Along those same lines, if you have 2 conditions plus fixation, then you are assuming that connectivity for yoru conditions is less than fixation in one condition and greater than fixation in the other. (2) gPPI -- model each condition as a separate interaction. Now if you have 3 conditions and fixation, you will get three PPI values - one for each condition. Then, you can compare the three conditions to each other as you do in fMRI activation analyses. Additionally, if you were to add the vectors for each condition together with the weights used in step 1, you would recover the same joint vector. The critical difference is the joint vector has imposed a relationship on your data that may or may not be true more complex designs. Hope that clarifies my comment from earlier. Let me know if it didn't. Best Regards, Donald McLaren ================D.G. McLaren, Ph.D. Postdoctoral Research Fellow, GRECC, Bedford VA Research Fellow, Department of Neurology, Massachusetts General Hospital and Harvard Medical School Office: (773) 406-2464 ====================This e-mail contains CONFIDENTIAL INFORMATION which may contain PROTECTED HEALTHCARE INFORMATION and may also be LEGALLY PRIVILEGED and which is intended only for the use of the individual or entity named above. If the reader of the e-mail is not the intended recipient or the employee or agent responsible for delivering it to the intended recipient, you are hereby notified that you are in possession of confidential and privileged information. Any unauthorized use, disclosure, copying or the taking of any action in reliance on the contents of this information is strictly prohibited and may be unlawful. If you have received this e-mail unintentionally, please immediately notify the sender via telephone at (773) 406-2464 or email. On Fri, Feb 25, 2011 at 10:26 AM, Stephen J. Fromm <[log in to unmask]> wrote: > Donald, > > You wrote, > > "The issue of summing was fixed in one of the later releases of SPM5,..." > > Are you saying that it's now OK if the weights used sum to zero, when before they shouldn't? > > Best, > > S > > > ========================================================================Date: Fri, 25 Feb 2011 16:44:41 +0000 Reply-To: Mohamed Seghier <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Mohamed Seghier <[log in to unmask]> Subject: Re: DCM: significance and graph connectivity Comments: To: "Stephen J. Fromm" <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=UTF-8; format=flowed Content-Transfer-Encoding: 7bit Message-ID: <[log in to unmask]> Hi Stephen, Are you using DCM8 or DCM10? If your connection R1==>R2 is not significant at the group level, then it is possible that (1) your modulatory parameter MI1 is significant, which may suggest that the inter-regional interaction between R1 and R2 increased "specifically" during your context MI1; or (2) you have a large inter-subject variability on this connection. For a similar situation, see Figure 24 in Karl's 2003 paper (Friston 2003 p1298: connection V1-to-V5 not significant but motion modulation was significant)... I hope this helps, Mohamed On 25/02/2011 16:23, Stephen J. Fromm wrote: > I'm working on a DCM project. So far the best fitting model looks like this: > > > DI--->R1 ==> R2 ==> R3 > ^ ^ > | | > MI1 MI2 > > That is: > * there are three regions, with intrinsic connections from R1 to R2 and R2 to R3 > * there is one driving input DI acting on R1 > * there are two modulatory connections MI1 and MI2 acting on the two between-regions intrinsic connections > > (The experimental variables for MI1 and MI2 are identical.) > > At the group level, the second connection (R2 ==> R3) is significant, but the first (R1 ==> R2) isn't. Conceptually, this doesn't make sense, insofar as the only way the system perturbations introduced by the DI can get to (R2 ==> R3) is through (R1 ==> R2). > > Does this reduce the credibility of the model? Or is it alone not enough to do that because of the possible vagaries of what is significant? > > TIA, > > S > > ========================================================================Date: Fri, 25 Feb 2011 10:47:46 -0600 Reply-To: Darren Gitelman <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Darren Gitelman <[log in to unmask]> Subject: Re: DCM: significance and graph connectivity Comments: To: Mohamed Seghier <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/alternative; boundary cf30434548f1250a049d1e16a0 Message-ID: [log in to unmask]> --20cf30434548f1250a049d1e16a0 Content-Type: text/plain; charset=ISO-8859-1 Mohamed Would your response below differ depending on whether he was using DCM8 vs. DCM10? Darren On Fri, Feb 25, 2011 at 10:44 AM, Mohamed Seghier < [log in to unmask]> wrote: > Hi Stephen, > > Are you using DCM8 or DCM10? > If your connection R1==>R2 is not significant at the group level, then it > is possible that (1) your modulatory parameter MI1 is significant, which may > suggest that the inter-regional interaction between R1 and R2 increased > "specifically" during your context MI1; or (2) you have a large > inter-subject variability on this connection. For a similar situation, see > Figure 24 in Karl's 2003 paper (Friston 2003 p1298: connection V1-to-V5 not > significant but motion modulation was significant)... > > I hope this helps, > > Mohamed > > > > On 25/02/2011 16:23, Stephen J. Fromm wrote: > >> I'm working on a DCM project. So far the best fitting model looks like >> this: >> >> >> DI--->R1 ==> R2 ==> R3 >> ^ ^ >> | | >> MI1 MI2 >> >> That is: >> * there are three regions, with intrinsic connections from R1 to R2 and R2 >> to R3 >> * there is one driving input DI acting on R1 >> * there are two modulatory connections MI1 and MI2 acting on the two >> between-regions intrinsic connections >> >> (The experimental variables for MI1 and MI2 are identical.) >> >> At the group level, the second connection (R2 ==> R3) is significant, but >> the first (R1 ==> R2) isn't. Conceptually, this doesn't make sense, >> insofar as the only way the system perturbations introduced by the DI can >> get to (R2 ==> R3) is through (R1 ==> R2). >> >> Does this reduce the credibility of the model? Or is it alone not enough >> to do that because of the possible vagaries of what is significant? >> >> TIA, >> >> S >> >> >> -- Darren Gitelman, MD Northwestern University 710 N. Lake Shore Dr., 1122 Chicago, IL 60611 Ph: (312) 908-8614 Fax: (312) 908-5073 --20cf30434548f1250a049d1e16a0 Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Mohamed

Would your response below differ depending on whether he was using DCM8 vs. DCM10?

Darren

On Fri, Feb 25, 2011 at 10:44 AM, Mohamed Seghier <[log in to unmask]> wrote:
Hi Stephen,

Are you using DCM8 or DCM10?
If your connection R1==>R2 is not significant at the group level, then it is possible that (1) your modulatory parameter MI1 is significant, which may suggest that the inter-regional interaction between R1 and R2 increased "specifically" during your context MI1; or (2) you have a large inter-subject variability on this connection. For a similar situation, see Figure 24 in Karl's 2003 paper (Friston 2003 p1298: connection V1-to-V5 not significant but motion modulation was significant)...

I hope this helps,

Mohamed



On 25/02/2011 16:23, Stephen J. Fromm wrote:
I'm working on a DCM project. So far the best fitting model looks like this:


DI--->R1 ==> R2 ==> R3
^ ^
| |
MI1 MI2

That is:
* there are three regions, with intrinsic connections from R1 to R2 and R2 to R3
* there is one driving input DI acting on R1
* there are two modulatory connections MI1 and MI2 acting on the two between-regions intrinsic connections

(The experimental variables for MI1 and MI2 are identical.)

At the group level, the second connection (R2 ==> R3) is significant, but the first (R1 ==> R2) isn't. Conceptually, this doesn't make sense, insofar as the only way the system perturbations introduced by the DI can get to (R2 ==> R3) is through (R1 ==> R2).

Does this reduce the credibility of the model? Or is it alone not enough to do that because of the possible vagaries of what is significant?

TIA,

S





--
Darren Gitelman, MD
Northwestern University
710 N. Lake Shore Dr., 1122
Chicago, IL 60611
Ph: (312) 908-8614
Fax: (312) 908-5073
--20cf30434548f1250a049d1e16a0-- ========================================================================Date: Fri, 25 Feb 2011 11:47:39 -0500 Reply-To: "Fromm, Stephen (NIH/NIMH) [C]" <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: "Fromm, Stephen (NIH/NIMH) [C]" <[log in to unmask]> Subject: Re: DCM: significance and graph connectivity Comments: To: Mohamed Seghier <[log in to unmask]> In-Reply-To: <[log in to unmask]> Content-Type: text/plain; charset="us-ascii" Content-Transfer-Encoding: quoted-printable MIME-Version: 1.0 Message-ID: <[log in to unmask]> Dear Mohamed, Thanks for the quick, informative reply. I'm using DCM8, and probably not the newest version of SPM8 either (ie not 4010). I'll look at the example you cite from the seminal DCM paper. Best, Stephen J. Fromm, PhD Contractor, NIMH/MAP (301) 451--9265 ________________________________________ From: Mohamed Seghier [[log in to unmask]] Sent: Friday, February 25, 2011 11:44 AM To: Fromm, Stephen (NIH/NIMH) [C] Cc: [log in to unmask] Subject: Re: [SPM] DCM: significance and graph connectivity Hi Stephen, Are you using DCM8 or DCM10? If your connection R1==>R2 is not significant at the group level, then it is possible that (1) your modulatory parameter MI1 is significant, which may suggest that the inter-regional interaction between R1 and R2 increased "specifically" during your context MI1; or (2) you have a large inter-subject variability on this connection. For a similar situation, see Figure 24 in Karl's 2003 paper (Friston 2003 p1298: connection V1-to-V5 not significant but motion modulation was significant)... I hope this helps, Mohamed On 25/02/2011 16:23, Stephen J. Fromm wrote: > I'm working on a DCM project. So far the best fitting model looks like this: > > > DI--->R1 ==> R2 ==> R3 > ^ ^ > | | > MI1 MI2 > > That is: > * there are three regions, with intrinsic connections from R1 to R2 and R2 to R3 > * there is one driving input DI acting on R1 > * there are two modulatory connections MI1 and MI2 acting on the two between-regions intrinsic connections > > (The experimental variables for MI1 and MI2 are identical.) > > At the group level, the second connection (R2 ==> R3) is significant, but the first (R1 ==> R2) isn't. Conceptually, this doesn't make sense, insofar as the only way the system perturbations introduced by the DI can get to (R2 ==> R3) is through (R1 ==> R2). > > Does this reduce the credibility of the model? Or is it alone not enough to do that because of the possible vagaries of what is significant? > > TIA, > > S > >========================================================================Date: Fri, 25 Feb 2011 16:55:34 +0000 Reply-To: Artur <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Artur <[log in to unmask]> Subject: Re: deactivation Comments: To: Ladan Ghazi Saidi <[log in to unmask]> Mime-Version: 1.0 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain; charset="UTF-8" Message-ID: <[log in to unmask]> Hi, It depends on the locus of "deactivation" spot and the type of learning. E.g. one may see a decrease in hippocampal BOLD signal accompanied by increase in implicit memory performance. For more details check out Russ Poldrack's and others' papers on hippocampus-caudate interactions. Email me if you want a package of papers on the topic. Best regards, Art ========================================================================Date: Fri, 25 Feb 2011 17:29:44 +0000 Reply-To: Mohamed Seghier <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Mohamed Seghier <[log in to unmask]> Subject: Re: DCM: significance and graph connectivity Comments: To: Darren Gitelman <[log in to unmask]> In-Reply-To: [log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/alternative; boundary="------------080208090307080100090302" Message-ID: <[log in to unmask]> This is a multi-part message in MIME format. --------------080208090307080100090302 Content-Type: text/plain; charset=ISO-8859-1; format=flowed Content-Transfer-Encoding: 7bit Hi Darren, A short response: yes it is also valid for DCM10... But.... My understanding is that, in DCM8, any "posterior" effects in intrinsic connectivity is expressed within the inter-regional connections (the off-diagonal of the A matrix, as all self-connections were fixed to "-1", although used as a scaling factor). In DCM10, the self-connections are allowed to deviate/vary from "-1" and thus inter-regional interactions that were significant in DCM8 may be different in DCM10 (i.e. as these effects can now be expressed in the self-connections). In other words, the generic model is more "flexible" in DCM10 than DCM8... I hope this makes sense... Note also that in DCM10 you have the option to mean-centre your inputs which makes the intrinsic (endogenous) connectivity parameters equal to the "average" connectivity across all conditions of your driving input(s). This is different from the previous interpretation of a "baseline" connectivity that was considered in DCM8... For more details, see Klaas's email of 22/11/2010... I hope this helps, Mohamed On 25/02/2011 16:47, Darren Gitelman wrote: > Mohamed > > Would your response below differ depending on whether he was using > DCM8 vs. DCM10? > > Darren > > On Fri, Feb 25, 2011 at 10:44 AM, Mohamed Seghier > <[log in to unmask] > wrote: > > Hi Stephen, > > Are you using DCM8 or DCM10? > If your connection R1==>R2 is not significant at the group level, > then it is possible that (1) your modulatory parameter MI1 is > significant, which may suggest that the inter-regional interaction > between R1 and R2 increased "specifically" during your context > MI1; or (2) you have a large inter-subject variability on this > connection. For a similar situation, see Figure 24 in Karl's 2003 > paper (Friston 2003 p1298: connection V1-to-V5 not significant but > motion modulation was significant)... > > I hope this helps, > > Mohamed > > > > On 25/02/2011 16:23, Stephen J. Fromm wrote: > > I'm working on a DCM project. So far the best fitting model > looks like this: > > > DI--->R1 ==> R2 ==> R3 > ^ ^ > | | > MI1 MI2 > > That is: > * there are three regions, with intrinsic connections from R1 > to R2 and R2 to R3 > * there is one driving input DI acting on R1 > * there are two modulatory connections MI1 and MI2 acting on > the two between-regions intrinsic connections > > (The experimental variables for MI1 and MI2 are identical.) > > At the group level, the second connection (R2 ==> R3) is > significant, but the first (R1 ==> R2) isn't. Conceptually, > this doesn't make sense, insofar as the only way the system > perturbations introduced by the DI can get to (R2 ==> R3) is > through (R1 ==> R2). > > Does this reduce the credibility of the model? Or is it alone > not enough to do that because of the possible vagaries of what > is significant? > > TIA, > > S > > > > > > -- > Darren Gitelman, MD > Northwestern University > 710 N. Lake Shore Dr., 1122 > Chicago, IL 60611 > Ph: (312) 908-8614 > Fax: (312) 908-5073 --------------080208090307080100090302 Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: 7bit
Hi Darren,

A short response: yes it is also valid for DCM10... But....
My understanding is that, in DCM8, any "posterior" effects in intrinsic connectivity is expressed within the inter-regional connections (the off-diagonal of the A matrix, as all self-connections were fixed to "-1", although used as a scaling factor). In DCM10, the self-connections are allowed to deviate/vary from "-1" and thus inter-regional interactions that were significant in DCM8 may be different in DCM10 (i.e. as these effects can now be expressed in the self-connections). In other words, the generic model is more "flexible" in DCM10 than DCM8...  I hope this makes sense...
Note also that in DCM10 you have the option to mean-centre your inputs which makes the intrinsic (endogenous) connectivity parameters equal to the “average” connectivity across all conditions of your driving input(s). This is different from the previous interpretation of a "baseline" connectivity that was considered in DCM8...
For more details, see Klaas's email of  22/11/2010...

I hope this helps,

Mohamed
  



On 25/02/2011 16:47, Darren Gitelman wrote:
[log in to unmask]" type="cite">Mohamed

Would your response below differ depending on whether he was using DCM8 vs. DCM10?

Darren

On Fri, Feb 25, 2011 at 10:44 AM, Mohamed Seghier <[log in to unmask]> wrote:
Hi Stephen,

Are you using DCM8 or DCM10?
If your connection R1==>R2 is not significant at the group level, then it is possible that (1) your modulatory parameter MI1 is significant, which may suggest that the inter-regional interaction between R1 and R2 increased "specifically" during your context MI1; or (2) you have a large inter-subject variability on this connection. For a similar situation, see Figure 24 in Karl's 2003 paper (Friston 2003 p1298: connection V1-to-V5 not significant but motion modulation was significant)...

I hope this helps,

Mohamed



On 25/02/2011 16:23, Stephen J. Fromm wrote:
I'm working on a DCM project.  So far the best fitting model looks like this:


    DI--->R1 ==>  R2 ==>  R3
                    ^           ^
                    |             |
                   MI1         MI2

That is:
* there are three regions, with intrinsic connections from R1 to R2 and R2 to R3
* there is one driving input DI acting on R1
* there are two modulatory connections MI1 and MI2 acting on the two between-regions intrinsic connections

(The experimental variables for MI1 and MI2 are identical.)

At the group level, the second connection (R2 ==>  R3) is significant, but the first (R1 ==>  R2) isn't.  Conceptually, this doesn't make sense, insofar as the only way the system perturbations introduced by the DI can get to (R2 ==>  R3) is through (R1 ==>  R2).

Does this reduce the credibility of the model?  Or is it alone not enough to do that because of the possible vagaries of what is significant?

TIA,

S





--
Darren Gitelman, MD
Northwestern University
710 N. Lake Shore Dr., 1122
Chicago, IL 60611
Ph: (312) 908-8614
Fax: (312) 908-5073

--------------080208090307080100090302-- ========================================================================Date: Fri, 25 Feb 2011 20:33:16 +0100 Reply-To: SALEM BOUSSIDA <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: SALEM BOUSSIDA <[log in to unmask]> Subject: Mixed effects group analysis questions MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1; format=flowed Content-Transfer-Encoding: 7bit Message-ID: <[log in to unmask]> Dear SPMers, I have a group of 7 subjects (rats) and I would like to perform a group analysis (mixed effects). I have done the 1st level analysis (fixed effects) for each subject and I have two con_001 and con_002 images, wich are respectively the contrast image for a positive effect (activation) and for a negative effect (deactivation) of one condition (current stimulation) . Then, I have done a one-sample-t-test : I feed all the con_001 of each subject into the 2nd level analysis , then I entered a T contrast [1] and SPM displayed the thresholded T-statistic image. But when I entered a F contrast [1], I have got this error: " ??? Inf computed by model function, fitting cannot continue. Try using or tightening upper and lower bounds on coefficients. " Based on the procedure described in SPM8 manuel concerning the "face group data", It is mentionned that I have to enter a F contrast. I am confused by this and I have some questions: (1) which contrast should I enter, F or T contrast? and what is the differenece between them? (2) Is the one-sample-t-test, the appropriate one to run mixed effects analysis? (3) Do I have to run two separate "one-sample-t-test" for positive(activation) and negative-deactivation) effects? Thank you for your help. Best regards, Salem ========================================================================Date: Fri, 25 Feb 2011 17:13:46 -0500 Reply-To: "MCLAREN, Donald" <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: "MCLAREN, Donald" <[log in to unmask]> Subject: Re: Mixed effects group analysis questions Comments: To: SALEM BOUSSIDA <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> Salem, This isn't a mixed effects design as you only have one group and only one condition. What you want to do is to use the con_001 images in a one-sample t-test. DO NOT USE the con_002 images in the model. I suspect that might have been what happened. Your design (SPM.xX.X)hould have a size of [7 1]; load SPM.mat and then use size(SPM.xX.X) to find the answer. A t-contrast of 1 will find the regions that are activated. A t-contrast of -1 will find regions that are deactivated. An F-contrast is simply the square of the 2 t-tests and does not have a direction. Best Regards, Donald McLaren ================= D.G. McLaren, Ph.D. Postdoctoral Research Fellow, GRECC, Bedford VA Research Fellow, Department of Neurology, Massachusetts General Hospital and Harvard Medical School Office: (773) 406-2464 ===================== This e-mail contains CONFIDENTIAL INFORMATION which may contain PROTECTED HEALTHCARE INFORMATION and may also be LEGALLY PRIVILEGED and which is intended only for the use of the individual or entity named above. If the reader of the e-mail is not the intended recipient or the employee or agent responsible for delivering it to the intended recipient, you are hereby notified that you are in possession of confidential and privileged information. Any unauthorized use, disclosure, copying or the taking of any action in reliance on the contents of this information is strictly prohibited and may be unlawful. If you have received this e-mail unintentionally, please immediately notify the sender via telephone at (773) 406-2464 or email. On Fri, Feb 25, 2011 at 2:33 PM, SALEM BOUSSIDA <[log in to unmask]> wrote: > Dear SPMers, > > I have a group of 7 subjects (rats) and I would like to perform a group > analysis (mixed effects). > I have done the 1st level analysis (fixed effects) for each subject and I > have two con_001 and con_002 images, wich are respectively the contrast > image for a positive effect (activation) and for a negative effect > (deactivation) of one condition (current stimulation) . > Then, I have done a one-sample-t-test : I feed all the con_001 of each > subject into the 2nd level analysis , then I entered a T contrast [1] and > SPM displayed the thresholded T-statistic image. But when I entered a F > contrast [1], I have got this error: > " > > ??? Inf computed by model function, fitting cannot continue. > Try using or tightening upper and lower bounds on coefficients. > > " > > Based on the procedure described in SPM8 manuel concerning the "face group > data", It is mentionned that I have to enter a F contrast. > I am confused by this and I have some questions: > (1) which contrast should I enter, F or T contrast? and what is the > differenece between them? > (2) Is the one-sample-t-test, the appropriate one to run mixed effects > analysis? > (3) Do I have to run two separate "one-sample-t-test" for > positive(activation) and negative-deactivation) effects? > > > Thank you for your help. > > Best regards, > > Salem > ========================================================================Date: Fri, 25 Feb 2011 17:25:10 -0500 Reply-To: "MCLAREN, Donald" <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: "MCLAREN, Donald" <[log in to unmask]> Subject: Re: fixed effects analysis across two sessions Comments: To: Israr Ul Haq <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> If contrast*beta>0, then the t-statistic is positive. If contrast*beta<0, then the t-statistic is negative. Best Regards, Donald McLaren ================= D.G. McLaren, Ph.D. Postdoctoral Research Fellow, GRECC, Bedford VA Research Fellow, Department of Neurology, Massachusetts General Hospital and Harvard Medical School Office: (773) 406-2464 ===================== This e-mail contains CONFIDENTIAL INFORMATION which may contain PROTECTED HEALTHCARE INFORMATION and may also be LEGALLY PRIVILEGED and which is intended only for the use of the individual or entity named above. If the reader of the e-mail is not the intended recipient or the employee or agent responsible for delivering it to the intended recipient, you are hereby notified that you are in possession of confidential and privileged information. Any unauthorized use, disclosure, copying or the taking of any action in reliance on the contents of this information is strictly prohibited and may be unlawful. If you have received this e-mail unintentionally, please immediately notify the sender via telephone at (773) 406-2464 or email. On Fri, Feb 25, 2011 at 12:25 AM, Israr Ul Haq <[log in to unmask]> wrote: > Dear Donald, > > I remember reading about beta and the GLM and how its calculated by using the matrix inverse, when I first started out reading about it. For some reason I formed the whole concept of individual correlations for each time point of a voxel and the subsequent distribution with its mean and sd as a way of representing what actually beta is representing, the weights of columns. Perhaps because the visualization came easier. Thankyou very much for taking time to point this out. > > What I understand from your explanation is that contrast*beta is essentially the output of adding and subtracting the individual values of the betas, based on the 1's and the -1's in the contrast, 1 meaning the beta will be added and -1, it will be subtracted. I guess for my question about the direction of change in terms of betas, how does the t statistic differ between a certain value of contrast*beta and an equal but a negative value of the same. Since the absolute difference between the effect and the mean is the same, does it take into account whether the contrast*beta is a positive or a negative value? > > Thanks > Israr > > ========================================================================Date: Fri, 25 Feb 2011 17:47:20 -0500 Reply-To: John Fredy <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: John Fredy <[log in to unmask]> Subject: comparing blocks with different durations MIME-Version: 1.0 Content-Type: multipart/alternative; boundaryMessage-ID: <[log in to unmask]> --0016368e2380d64648049d231c4f Content-Type: text/plain; charset=ISO-8859-1 Hello all, I like to know if is possible compare two conditions with different durations, that is, task with duration of 40 s and control with duration of 20 s. Thanks in advance John Ochoa Universidad de Antioquia --0016368e2380d64648049d231c4f Content-Type: text/html; charset=ISO-8859-1 Hello all, I like to know if is possible compare two conditions with different durations, that is, task with duration of 40 s and control with duration of 20 s.

Thanks in advance

John Ochoa
Universidad de Antioquia
--0016368e2380d64648049d231c4f-- ========================================================================Date: Sat, 26 Feb 2011 01:02:42 +0100 Reply-To: Salem Boussida <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Salem Boussida <[log in to unmask]> Subject: Re: Mixed effects group analysis questions Comments: To: "MCLAREN, Donald" <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=UTF-8; DelSp="Yes"; format="flowed" Content-Disposition: inline Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> Dear Donald, Thank you for your help. I am still confused about some details: "MCLAREN, Donald" <[log in to unmask]> a écrit : > Salem, > > This isn't a mixed effects design as you only have one group and only > one condition. What you want to do is to use the con_001 images in a > one-sample t-test. DO NOT USE the con_002 images in the model. I > suspect that might have been what happened. I am still confused about "mixed effects analysis"and random effects analysis. In prevoius discussions from SPMlist users and the notes from Terry Oakes page (http://psyphz.psych.wisc.edu/~oakes/spm/spm_random_effects.html), it is mentioned that "Random-Effects" analysis is also referred to as a "Mixed Effects" analysis, since it considers both within- and between-subject variance. Also, in SPM manual, the one-sample-t-test is considered as a "random effects analysis". Any comments about this? Which test (in SPM) should I use to consider both fixed and random effects? > > Your design (SPM.xX.X)hould have a size of [7 1]; load SPM.mat and > then use size(SPM.xX.X) to find the answer. The "SPM.xX.X" command gives me : SPM.xX.X = 1 1 1 1 1 1 1 Is it right? > > A t-contrast of 1 will find the regions that are activated. A > t-contrast of -1 will find regions that are deactivated. An F-contrast > is simply the square of the 2 t-tests and does not have a direction. > Thank you again for your help. Best regards, Salem > Best Regards, Donald McLaren > ================= > D.G. McLaren, Ph.D. > Postdoctoral Research Fellow, GRECC, Bedford VA > Research Fellow, Department of Neurology, Massachusetts General > Hospital and Harvard Medical School > Office: (773) 406-2464 > ===================== > This e-mail contains CONFIDENTIAL INFORMATION which may contain > PROTECTED HEALTHCARE INFORMATION and may also be LEGALLY PRIVILEGED > and which is intended only for the use of the individual or entity > named above. If the reader of the e-mail is not the intended recipient > or the employee or agent responsible for delivering it to the intended > recipient, you are hereby notified that you are in possession of > confidential and privileged information. Any unauthorized use, > disclosure, copying or the taking of any action in reliance on the > contents of this information is strictly prohibited and may be > unlawful. If you have received this e-mail unintentionally, please > immediately notify the sender via telephone at (773) 406-2464 or > email. > > > > On Fri, Feb 25, 2011 at 2:33 PM, SALEM BOUSSIDA > <[log in to unmask]> wrote: >> Dear SPMers, >> >> I have a group of 7 subjects (rats) and I would like to perform a group >> analysis (mixed effects). >> I have done the 1st level analysis (fixed effects) for each subject and  I >> have two con_001 and con_002 images, wich are respectively the contrast >> image for a positive effect (activation) and for a negative effect >> (deactivation) of one condition (current stimulation) . >> Then, I have done a one-sample-t-test : I feed all the con_001 of each >> subject into the 2nd level analysis , then I entered a T contrast [1]  and >> SPM displayed the thresholded T-statistic image. But when I entered a F >> contrast [1], I have got this error: >> " >> >> ??? Inf computed by model function, fitting cannot continue. >> Try using or tightening upper and lower bounds on coefficients. >> >> " >> >> Based on the procedure described in SPM8 manuel concerning the "face group >> data", It is mentionned that I have to enter a F contrast. >> I am  confused by this and I have some questions: >> (1) which contrast should I enter, F or T contrast? and what is the >> differenece between them? >> (2) Is the one-sample-t-test, the appropriate one to run mixed effects >> analysis? >> (3) Do I have to run two separate "one-sample-t-test" for >> positive(activation) and negative-deactivation) effects? >> >> >> Thank you for your help. >> >> Best regards, >> >> Salem >> > ========================================================================Date: Fri, 25 Feb 2011 22:04:49 -0500 Reply-To: "MCLAREN, Donald" <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: "MCLAREN, Donald" <[log in to unmask]> Subject: Re: Mixed effects group analysis questions Comments: To: Salem Boussida <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> On Fri, Feb 25, 2011 at 7:02 PM, Salem Boussida <[log in to unmask]> wrote: > Dear Donald, > > Thank you for your help. I am still confused about some details: > > > "MCLAREN, Donald" <[log in to unmask]> a crit: > >> Salem, >> >> This isn't a mixed effects design as you only have one group and only >> one condition. What you want to do is to use the con_001 images in a >> one-sample t-test. DO NOT USE the con_002 images in the model. I >> suspect that might have been what happened. > > I am still confused about "mixed effects analysis"and random effects > analysis. In prevoius discussions from SPMlist users and the notes from > Terry Oakes page > (http://psyphz.psych.wisc.edu/~oakes/spm/spm_random_effects.html), it is > mentioned that "Random-Effects" analysis is also referred to as a "Mixed > Effects" analysis, since it considers both within- and between-subject > variance. Also, in SPM manual, the one-sample-t-test is considered as a > "random effects analysis". > Any comments about this? > Which test (in SPM) should I use to consider both fixed and random effects? The whole discussion of fixed effects and random effects are best left to the field of statistician. If you want the details of why it could be considered either, see Ch.12 in Human Brain Function. It is better to think of the analysis as within-subject factor and within-subject errors OR between-subject factors and between errors. In group comparison or comparing the group against zero, you have between subject errors (1 sample t-test, 2-sample t-test, ANOVA). Paired t-tests and repeated measures ANOVAs have within-subject error terms. And then, you can have models with both within-subject and between-subject errors. > > > >> >> Your design (SPM.xX.X)hould have a size of [7 1]; load SPM.mat and >> then use size(SPM.xX.X) to find the answer. > > The "SPM.xX.X" command gives me : SPM.xX.X = > 1 > 1 > 1 > 1 > 1 > 1 > 1 > Is it right? Yes. > >> >> A t-contrast of 1 will find the regions that are activated. A >> t-contrast of -1 will find regions that are deactivated. An F-contrast >> is simply the square of the 2 t-tests and does not have a direction. >> > Thank you again for your help. > > Best regards, > > Salem > > >> Best Regards, Donald McLaren >> ================= >> D.G. McLaren, Ph.D. >> Postdoctoral Research Fellow, GRECC, Bedford VA >> Research Fellow, Department of Neurology, Massachusetts General >> Hospital and Harvard Medical School >> Office: (773) 406-2464 >> ===================== >> This e-mail contains CONFIDENTIAL INFORMATION which may contain >> PROTECTED HEALTHCARE INFORMATION and may also be LEGALLY PRIVILEGED >> and which is intended only for the use of the individual or entity >> named above. If the reader of the e-mail is not the intended recipient >> or the employee or agent responsible for delivering it to the intended >> recipient, you are hereby notified that you are in possession of >> confidential and privileged information. Any unauthorized use, >> disclosure, copying or the taking of any action in reliance on the >> contents of this information is strictly prohibited and may be >> unlawful. If you have received this e-mail unintentionally, please >> immediately notify the sender via telephone at (773) 406-2464 or >> email. >> >> >> >> On Fri, Feb 25, 2011 at 2:33 PM, SALEM BOUSSIDA >> <[log in to unmask]> wrote: >>> >>> Dear SPMers, >>> >>> I have a group of 7 subjects (rats) and I would like to perform a group >>> analysis (mixed effects). >>> I have done the 1st level analysis (fixed effects) for each subject and >>> I >>> have two con_001 and con_002 images, wich are respectively the contrast >>> image for a positive effect (activation) and for a negative effect >>> (deactivation) of one condition (current stimulation) . >>> Then, I have done a one-sample-t-test : I feed all the con_001 of each >>> subject into the 2nd level analysis , then I entered a T contrast [1] >>> and >>> SPM displayed the thresholded T-statistic image. But when I entered a F >>> contrast [1], I have got this error: >>> " >>> >>> ??? Inf computed by model function, fitting cannot continue. >>> Try using or tightening upper and lower bounds on coefficients. >>> >>> " >>> >>> Based on the procedure described in SPM8 manuel concerning the "face >>> group >>> data", It is mentionned that I have to enter a F contrast. >>> I am confused by this and I have some questions: >>> (1) which contrast should I enter, F or T contrast? and what is the >>> differenece between them? >>> (2) Is the one-sample-t-test, the appropriate one to run mixed effects >>> analysis? >>> (3) Do I have to run two separate "one-sample-t-test" for >>> positive(activation) and negative-deactivation) effects? >>> >>> >>> Thank you for your help. >>> >>> Best regards, >>> >>> Salem >>> >> > > > > > ========================================================================Date: Fri, 25 Feb 2011 23:37:15 -0500 Reply-To: Jonathan Peelle <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Jonathan Peelle <[log in to unmask]> Subject: Re: Mixed effects group analysis questions In-Reply-To: <[log in to unmask]> Content-Type: text/plain; charset=us-ascii Mime-Version: 1.0 (Apple Message framework v1082) Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> Dear Salem, > The whole discussion of fixed effects and random effects are best left > to the field of statistician. If you want the details of why it could > be considered either, see Ch.12 in Human Brain Function. To follow on what Donald said, a couple of further reference that may be of interest regarding mixed effects and group studies: Friston KJ, Stephan KE, Lund TE, Morcom A, Kiebel S (2005) Mixed-effects and fMRI studies. NeuroImage 24:244-252. Mumford JA, Nichols T (2009) Simple group fMRI modeling and inference. NeuroImage 47:1469-1475. Best regards, Jonathan -- Dr. Jonathan Peelle Department of Neurology University of Pennsylvania 3 West Gates 3400 Spruce Street Philadelphia, PA 19104 USA http://jonathanpeelle.net/ ========================================================================Date: Sat, 26 Feb 2011 15:25:26 +1100 Reply-To: =?ISO-8859-1?Q?Kristian_Lwe?= <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: =?ISO-8859-1?Q?Kristian_Lwe?= <[log in to unmask]> Subject: spm_hrf: delay of response and resulting peak MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1; format=flowed Content-Transfer-Encoding: 7bit Message-ID: <[log in to unmask]> Dear SPM'ers, playing around with the function spm_hrf, I noticed the following: The resulting hrf peaks one second earlier than I would expect given the specified delay of response (relative to onset), i.e. p(1). E.g., issueing the following command, shows the above mentioned. figure; hold on; TR = 1; peak = 6; plot(0:32, spm_hrf(TR, [peak 16 1 1 6 0 32])); plot([peak peak],[-1 1],'--r'); grid on; xlim([-1 35]); I was under the impression, that the delay of response effectively is the peak of the hrf. Probably I'm missing something obvious here, I would be thankful for any guidance on this. Cheers, Kristian ========================================================================Date: Sat, 26 Feb 2011 19:35:04 +0100 Reply-To: Stefan =?iso-8859-1?b?S2z2cHBlbA==? <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Stefan =?iso-8859-1?b?S2z2cHBlbA==? <[log in to unmask]> Subject: PhD position in Freiburg: Clinical applications of pattern recognition methods In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1; DelSp="Yes"; format="flowed" Content-Disposition: inline Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> A 3-years doctoral position (50% TV-L 13) is available from April 2011 at the Freiburg Brain Imaging Center (FBI, http://www.uniklinik-freiburg.de/fbi/live/index_en.html) in Germany. The candidate can obtain a PhD in the field of Psychology, Medicine or Biology The candidate will apply pattern recognition methods to multivariate data (e.g. imaging, neuropsychological test results) to improve our understanding of neurodegenerative diseases (http://www.uniklinik-freiburg.de/fbi/live/forschung/AutomatedDiagnosing_en.html). We offer The FBI (http://www.uniklinik-freiburg.de/fbi/live/index_en.html) combins efforts in neuroimaging research of the departments of Psychiatry/Psychotherapie, Neurology, Neuroradiology and Neurosurgery. It is closely collaborating with the Center for Data Analyses and Modelling (http://www.fdm.uni-freiburg.de/projects/dynamic-processes-in-life-sciences) and the Department for Pattern recognition methods (http://lmb.informatik.uni-freiburg.de/index.en.html). Support for MRI sequence development is provided by the Department of MR-Physics, that is also part of the FBI. Starting April 2011, we will begin a continuous education program in the field of neuroimaging. We require Applicants must hold a master degree or equivalent in medicine, psychology or a related field. Previous programming experience (e.g. Matlab) is advantageous but not required. Sound knowledge of statistics as well as good IT skills are essential. Disabled applicants are preferred if qualification is equal. Please send applications to Dr. Stefan Klppel. For informal enquiries call +49 761 270 66400 or email [log in to unmask] . http://www.uniklinik-freiburg.de/fbi/live/members/kloeppel_en.html ========================================================================Date: Sun, 27 Feb 2011 20:16:32 +1100 Reply-To: Bill Budd <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Bill Budd <[log in to unmask]> Organization: University of Newcastle Subject: Re: script to flip MR images left to right (or vice versa) Comments: To: Michael Harms <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-version: 1.0 Content-transfer-encoding: 7BIT Content-type: text/plain; charset=us-ascii Message-ID: <[log in to unmask]> Another note of caution is that brains are not entirely symmetrical, structurally or functionally. So flipping MRI images may not result in a spatially homogenous data set for your analysis even though they are consistent in terms of the lesioned hemisphere. One option to address the lack of anatomical asymmetry is to flip epi images prior to normalisation and then normalise using symmetrical priors. (See Didolet et al, 2010 for an example creating a symmetrical template). Others on this list might have more detailed information but this approach may create additional problems with normalisation routines and anatomical labelling/ROI analyses and doesn't address the issue of functional asymmetries. Cheers -Bill > -----Original Message----- > From: SPM (Statistical Parametric Mapping) [mailto:[log in to unmask]] > On Behalf Of Michael Harms > Sent: Saturday, 26 February 2011 1:20 AM > To: [log in to unmask] > Subject: Re: [SPM] script to flip MR images left to right (or vice > versa) > > A note of caution about using fslswapdim in this manner however: > If you do that, the data order and the header information stored in the > sform/qform will no longer be in sync. So, what the sform/qform defines > to be "left" will no longer be the subject's true left (assuming the > labels in the original data were correct)! > > Read the following FSL page if you want all the details: > http://www.fmrib.ox.ac.uk/fsl/avwutils/index.html > > Best, > -MH > > On Fri, 2011-02-25 at 11:54 +0000, Rosa Sanchez Panchuelo wrote: > > You can do it easily with fsl: > > fslswapdim input_image.img -x outpu_image.img > > -x will flip the image in the RL direction. > > > > On 25/02/2011 11:39, Richard Morris wrote: > > > I'm not sure, but I think you can use the image calculator in SPM, > > > with the following function: > > > > > > > > > f = 'Inv(i1)' > > > > > > > > > > > > On 25/02/2011, at 10:16 AM, Michael T Rubens wrote: > > > > > > > how about this: > > > > %%% > > > > > > > > > > > > v = spm_vol('/image_path/brain.img'); > > > > x = spm_read_vols(v); > > > > > > > > > > > > x = x(size(x,1):-1:1,:,:); > > > > > > > > > > > > [path file] = fileparts(v.fname); > > > > v.fname = fullfile(path,['flipped_' file'); > > > > > > > > > > > > spm_write_vol(v,x) > > > > > > > > > > > > %%% > > > > > > > > > > > > > > > > > > > > cheers, > > > > michael > > > > > > > > On Thu, Feb 24, 2011 at 9:35 AM, Chien-Ho Lin > > > > <[log in to unmask]> wrote: > > > > Hi, > > > > > > > > I stuides patients with stroke doing some behavior > > > > paradigm in fMRI. > > > > Patients always used their affected limb for the task so > > > > some patients used left hand some used right hand. > > > > Now I would like to flip the left and right of the images > > > > so patients' lesional hemisphere are on the same side. > > > > > > > > Is there any script in spm 5 or 8 can help to accomplish > > > > this goal? > > > > > > > > I found a m file called spm_flip.m but it seems support > > > > only spm2. > > > > > > > > Your assistance are well appreciated. > > > > > > > > Thank you so much. > > > > > > > > Janice > > > > > > > > > > > > > > > > -- > > > > Research Associate > > > > Gazzaley Lab > > > > Department of Neurology > > > > University of California, San Francisco > > > > > > > > > > > > > > > > -- > > Rosa Maria Sanchez Panchuelo > > Post-doctoral Research fellow > > Sir Peter Mansfield Magnetic Resonance Centre > > University of Nottingham > > University Park > > Nottingham, NG7 2RD > > United Kingdom > > +44 115 84 66003 > > > > > > > > > > > > This message and any attachment are intended solely for the addressee > > and may contain confidential information. If you have received this > > message in error, please send it back to me, and immediately delete > > it. Please do not use, copy or disclose the information contained in > > this message or in any attachment. Any views or opinions expressed by > > the author of this email do not necessarily reflect the views of the > > University of Nottingham. > > > > This message has been checked for viruses but the contents of an > > attachment may still contain software viruses which could damage your > > computer system: you are advised to perform your own checks. Email > > communications with the University of Nottingham may be monitored as > > permitted by UK legislation. > > ========================================================================Date: Sun, 27 Feb 2011 20:12:49 +0800 Reply-To: =?UTF-8?B?6aOe6bif?= <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: =?UTF-8?B?6aOe6bif?= <[log in to unmask]> Subject: Re: Negative values in DCM.A Comments: To: Maria Dauvermann <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=UTF-8 Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> Dear Maria, Once I have asked a similar question as yours. In the situation of DCM for EEG/MEG, the number in DCM.A means that the coupling strength is exp(number) times the prior coupling. As for the fmri, I'm not very clear either. I Hope this helps. Haoran. At 2011-02-24 15:58:16,"Maria Dauvermann" <[log in to unmask]> wrote: >Hello, > >I had a look at the values in DCM.A after I have estimated the DCMs. > >What does a negative value in the intrinsic connection mean? How do I interprete this result? > >Thanks for your help. > >BW, Maria ========================================================================Date: Sun, 27 Feb 2011 20:27:05 +0800 Reply-To: =?GBK?B?t8nE8Q==?= <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: =?GBK?B?t8nE8Q==?= <[log in to unmask]> Subject: [SPM DCM] how to specify the modulation? MIME-Version: 1.0 Content-Type: multipart/alternative; boundary="----=_Part_52522_731246145.1298809625622" Message-ID: <[log in to unmask]> ------=_Part_52522_731246145.1298809625622 Content-Type: text/plain; charset=GBK Content-Transfer-Encoding: base64 SGVsbG8gYWxsLAqhoaGhV2hlbiB5b3UgYW5hbHlzaXMgeW91ciBkYXRhIHdpdGggdGhlIG1ldGhv ZCBvZiBEQ00sIGhhdmUgeW91IGV2ZXIgbWV0IHRoZSBwcm9ibGVtIGFib3V0IGhvdyB0byBzcGVj aWZ5IHRoZSBtb2R1bGF0aW9uPyBOb3cgSSBjaG9vc2UgNyBiYXNpYyBtb2RlbHMsIGFuZCB0aGVu IGFzc3VtZSBhbGwgdGhlIGNvbm5lY3Rpb25zIGluIGVhY2ggYmFzaWMgbW9kZWwgYXJlIG1vZHVs YXRlZCBieSB0aGUgZXhwZXJpbWVudGFsIG1hbmlwdWxhdGlvbi4gV2hhdCBJIHdhbnQgdG8ga25v dyBpcyB0aGF0IHdoZXRoZXIgb3Igbm90IHRoaXMgaXMgcmVhc29uYWJsZS6hoaGhoaGhoaGhoaGh oaGhoaGhoaGhoaGhoaGhSW4gYWRkaXRpb24sIGlzIGl0IHBvc3NpYmxlIHRoYXQgdGhlIGNvbm5l Y3Rpb25zIGJldHdlZW4gdHdvIHNvdXJjZXMgY291bGQgaW5jbHVkZSBmb3J3YXJkIGNvbm5lY3Rp dml0eSwgYmFja3dhcmQgY29ubmVjdGl2aXR5IGFuZCBsYXRlcmFsIGNvbm5lY3Rpdml0eSBhdCB0 aGUgc2FtZSB0aW1lPwqhoaGhQW55IGhlbHAgd2lsbCBiZSBncmF0ZWZ1bCEKCgotLQoKSGFvcmFu IExJIChNUykKQnJhaW4gSW1hZ2luZyBMYWIsClJlc2VhcmNoIENlbnRlciBmb3IgTGVhcm5pbmcg U2NpZW5jZSwKU291dGhlYXN0IFVuaXZlcnNpdHkKMiBTaSBQYWkgTG91ICwgTmFuamluZywgMjEw MDk2LCBQLlIuQ2hpbmE------=_Part_52522_731246145.1298809625622 Content-Type: text/html; charset=GBK Content-Transfer-Encoding: base64 PERJVj48L0RJVj4KPERJVj5IZWxsbyBhbGwsPC9ESVY+CjxESVY+oaGhoVdoZW4geW91IGFuYWx5 c2lzIHlvdXIgZGF0YSB3aXRoIHRoZSBtZXRob2Qgb2YgRENNLCBoYXZlIHlvdSBldmVyIG1ldCB0 aGUgcHJvYmxlbSZuYnNwO2Fib3V0IGhvdyB0byBzcGVjaWZ5IHRoZSBtb2R1bGF0aW9uPyZuYnNw O05vdyBJIGNob29zZSA3IGJhc2ljIG1vZGVscywgYW5kIHRoZW4gYXNzdW1lIGFsbCB0aGUgY29u bmVjdGlvbnMgaW4gZWFjaCBiYXNpYyBtb2RlbCZuYnNwO2FyZSBtb2R1bGF0ZWQgYnkgdGhlIGV4 cGVyaW1lbnRhbCBtYW5pcHVsYXRpb24uJm5ic3A7V2hhdCZuYnNwO0kgd2FudCB0byBrbm93IGlz IHRoYXQgd2hldGhlciBvciBub3QgdGhpcyBpcyZuYnNwO3JlYXNvbmFibGUuoaGhoaGhoaGhoaGh oaGhoaGhoaGhoaGhoaGhoUluIGFkZGl0aW9uLCBpcyBpdCBwb3NzaWJsZSB0aGF0IHRoZSBjb25u ZWN0aW9ucyBiZXR3ZWVuIHR3byBzb3VyY2VzJm5ic3A7Y291bGQmbmJzcDtpbmNsdWRlJm5ic3A7 Zm9yd2FyZCBjb25uZWN0aXZpdHksIGJhY2t3YXJkIGNvbm5lY3Rpdml0eSBhbmQgbGF0ZXJhbCBj b25uZWN0aXZpdHkgYXQgdGhlIHNhbWUgdGltZT8gPEJSPqGhoaFBbnkgaGVscCB3aWxsIGJlIGdy YXRlZnVsITxCUj48QlI+PC9ESVY+CjxESVY+LS08QlI+CjxESVY+PEZPTlQgY29sb3I9IiMwMDgw MDAiIGZhY2U9IkFyaWFsIj5IYW9yYW4gTEkgKE1TKTxCUj5CcmFpbiBJbWFnaW5nIExhYiw8QlI+ UmVzZWFyY2ggQ2VudGVyIGZvciBMZWFybmluZyBTPEZPTlQgY29sb3I9IiMwMDgwMDAiPmNpPC9G T05UPmVuY2UsPEJSPlNvdXRoZWFzdCBVbml2ZXJzaXR5PEJSPjIgU2kgUGFpIExvdSAsIE5hbmpp bmcsIDIxMDA5NiwgUC5SLkNoaW5hPC9GT05UPjwvRElWPjwvRElWPjxicj48YnI+PHNwYW4gdGl0 bGU9Im5ldGVhc2Vmb290ZXIiPjxzcGFuIGlkPSJuZXRlYXNlX21haWxfZm9vdGVyIj48L3NwYW4+ PC9zcGFuPg=------=_Part_52522_731246145.1298809625622-- ========================================================================Date: Sun, 27 Feb 2011 15:13:43 +0000 Reply-To: Nynke L <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Nynke L <[log in to unmask]> Subject: Second level t-test: test against other value than zero Mime-Version: 1.0 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain; charset="UTF-8" Message-ID: <[log in to unmask]> Hello all, I have a particular group level analysis for which I want to use spm. However, till now I don't manage to so I hope you have suggestions for me. I use fMRI for the prediction of a certain binary outcome. Therefore, I use a different classification software package that computes prediction-accuracies for all voxels. For each subject, I have a .nii file with as values the accuracies (range between 0 and 1). So, this is a brain map just like you usually feed to the second level. What I want to test in the second level analysis is which brain areas have accuracies significantly higher than 0.5. So I want to test against the null-hypothesis that accuracies are 0.5 or lower. Now the problem is that the 1 sample t-test in spm on default tests against the null-hypothesis that the values are zero or higher.... So my first question is whether it is possible to set a custum value for the t-test to test against a manually set value? I already tried a different approach, namely subtracting 0.5 from the values in my input images (to put them in the default spm t-test). However, when I trie to do this with the image calculator of spm (with as expression i1 - 0.5) I do not get correct results: I do not get a map with exactly 0.5 subtracted from each value but a range between 0.4-0.6. It seems that spm-image-calc is also doing something else with the image... So my second question is: how can I make image-calc subtract exactly 0.5 from all values in the image? Thanks in advance! Best regards, Nynke van der Laan ========================================================================Date: Sun, 27 Feb 2011 07:22:05 -0800 Reply-To: Faezeh Vedaei <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Faezeh Vedaei <[log in to unmask]> Subject: display result on template MRI MIME-Version: 1.0 Content-Type: multipart/alternative; boundary="0-614849790-1298820125=:2452" Message-ID: <[log in to unmask]> --0-614849790-1298820125=:2452 Content-Type: text/plain; charset=iso-8859-1 Content-Transfer-Encoding: quoted-printable I am working with some data by SPM8,as a question how can I display my brain glass result on multiple slices of atemplate MRI to view regions of hyperperfusion and hypoperfusion? --0-614849790-1298820125=:2452 Content-Type: text/html; charset=iso-8859-1 Content-Transfer-Encoding: quoted-printable
I am working with some data by SPM8,as a question how can I display my brain glass result on multiple slices of a template MRI to view regions of hyperperfusion and hypoperfusion?

--0-614849790-1298820125=:2452-- ========================================================================Date: Sun, 27 Feb 2011 07:25:39 -0800 Reply-To: Faezeh Vedaei <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Faezeh Vedaei <[log in to unmask]> Subject: display result on template MRI MIME-Version: 1.0 Content-Type: multipart/alternative; boundary="0-2098163962-1298820339=:20497" Message-ID: <[log in to unmask]> --0-2098163962-1298820339=:20497 Content-Type: text/plain; charset=iso-8859-1 Content-Transfer-Encoding: quoted-printable I am working with some data by SPM8,as a question how can I display my brain glass result on multiple slices of atemplate MRI to view regions of hyperperfusion and hypoperfusion? --0-2098163962-1298820339=:20497 Content-Type: text/html; charset=iso-8859-1 Content-Transfer-Encoding: quoted-printable


I am working with some data by SPM8,as a question how can I display my brain glass result on multiple slices of a template MRI to view regions of hyperperfusion and hypoperfusion?


--0-2098163962-1298820339=:20497-- ========================================================================Date: Sun, 27 Feb 2011 20:41:27 +0100 Reply-To: Leonhard Schilbach <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Leonhard Schilbach <[log in to unmask]> Subject: Call for Papers; Frontiers Special Topic: Toward a neuroscience of social interaction Content-Type: text/plain; charset=windows-1252 Content-Transfer-Encoding: quoted-printable Mime-Version: 1.0 (Apple Message framework v1082) Message-ID: <[log in to unmask]> Dear colleagues, this is to draw your attention toward and invite submissions for an upcoming Frontiers in Neuroscience Special Topic entitled: "Toward a neuroscience of social interaction" Please find more details below and on the Frontiers website: http://www.frontiersin.org/Human%20Neuroscience/specialtopics/towards_a_neuroscience_of_soci/211 -Deadline for submission of abstracts: 30 Sept 2011 -Deadline for submission of full manuscripts: 31 Dec 2011 Looking forward to your contributions! Best regards, Leo Schilbach -- Towards a neuroscience of social interaction Hosted By: Ulrich Pfeiffer, University Hospital Cologne, Germany Bert Timmermans, University Hospital Cologne, Germany Kai Vogeley, University Hospital Cologne, Germany Chris Frith, Wellcome Trust Centre for Neuroimaging at University College London, United Kingdom Leonhard Schilbach, Max-Planck-Institute for Neurological Research, Germany The burgeoning field of social neuroscience has begun to illuminate the complex biological bases of human social cognitive abilities. However, in spite of being based on the premise of investigating the neural bases of interacting minds, the majority of studies have focused on studying brains in isolation using paradigms that investigate offline social cognition, i.e. social cognition from a detached observer's point of view, asking study participants to read out the mental states of others without being engaged in interaction with them. Consequently, the neural correlates of real-time social interaction have remained elusive and may paradoxically represent the 'dark matter' of social neuroscience. More recently, a growing number of researchers have begun to study online social cognition, i.e. social cognition from a participant's point of view, based on the assumption that there is something fundamentally different when we are actively engaged with others in real-time social interaction as compared to when we merely observe them. Whereas, for offline social cognition, interaction and feedback are merely a way of gathering data about the other person that feeds into processing algorithms 'inside the agent, it has been proposed that in online social cognition the knowledge of the other at least in part resides in the interaction dynamics between the agents. Furthermore being a participant in an ongoing interaction may entail a commitment toward being responsive created by important differences in the motivational foundations of online and offline social cognition. In order to promote the development of the neuroscientific investigation of online social cognition, this Frontiers Special Topic aims at bringing together contributions from researchers in social neuroscience and related fields, whose work involves the study of at least two individuals and sometimes two brains, rather than single individuals and brains responding to a social context. Specifically, this special issue will adopt an interdisciplinary perspective on what it is that separates online from offline social cognition and the putative differences in the recruitment of underlying processes and mechanisms. Here, an important focal point will be to address the various roles of social interaction in contributing to and at times constituting our awareness of other minds. For this Special Topic, we, therefore, solicit reviews, original research articles, opinion and method papers, which address the investigation of social interaction and go beyond traditional concepts and ways of experimentation in doing so. While focusing on work in the neurosciences, this Special Topic also welcomes contributions in the form of behavioral studies, psychophysiological investigations, methodological innovations, computational approaches, developmental and patient studies. By focusing on cutting-edge research in social neuroscience and related fields, this Frontiers Special Issue will create new insights concerning the neurobiology of social interaction and holds the promise of helping social neuroscience to really go social. -- Leonhard Schilbach, MD Department of Psychiatry and Psychotherapy University of Cologne, Germany [log in to unmask] & Max-Planck-Institute for Neurological Research Cologne, Germany [log in to unmask]: Sun, 27 Feb 2011 17:17:44 -0500 Reply-To: John Fredy <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: John Fredy <[log in to unmask]> Subject: Re: display result on template MRI Comments: To: Faezeh Vedaei <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/alternative; boundaryMessage-ID: <[log in to unmask]> --0016368e2380ab9416049d4aeebc Content-Type: text/plain; charset=ISO-8859-1 Hello Faezeh, I use xjview ( http://www.alivelearn.net/xjview8/ ) Regards On Sun, Feb 27, 2011 at 10:25 AM, Faezeh Vedaei <[log in to unmask]> wrote: > > > I am working with some data by SPM8,as a question how can I display my > brain glass result on multiple slices of a template MRI to view regions of > hyperperfusion and hypoperfusion? > > > --0016368e2380ab9416049d4aeebc Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Hello Faezeh, I use xjview ( http://www.alivelearn.net/xjview8/ )

Regards

On Sun, Feb 27, 2011 at 10:25 AM, Faezeh Vedaei <[log in to unmask]> wrote:


I am working with some data by SPM8,as a question how can I display my brain glass result on multiple slices of atemplate MRI to view regions of hyperperfusion and hypoperfusion?



--0016368e2380ab9416049d4aeebc-- ========================================================================Date: Sun, 27 Feb 2011 17:22:30 -0500 Reply-To: "MCLAREN, Donald" <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: "MCLAREN, Donald" <[log in to unmask]> Subject: Re: display result on template MRI Comments: To: Faezeh Vedaei <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> Click Overlay --> sections OR Overlay --> slices MRIcron is also useful Best Regards, Donald McLaren ================= D.G. McLaren, Ph.D. Postdoctoral Research Fellow, GRECC, Bedford VA Research Fellow, Department of Neurology, Massachusetts General Hospital and Harvard Medical School Office: (773) 406-2464 ===================== This e-mail contains CONFIDENTIAL INFORMATION which may contain PROTECTED HEALTHCARE INFORMATION and may also be LEGALLY PRIVILEGED and which is intended only for the use of the individual or entity named above. If the reader of the e-mail is not the intended recipient or the employee or agent responsible for delivering it to the intended recipient, you are hereby notified that you are in possession of confidential and privileged information. Any unauthorized use, disclosure, copying or the taking of any action in reliance on the contents of this information is strictly prohibited and may be unlawful. If you have received this e-mail unintentionally, please immediately notify the sender via telephone at (773) 406-2464 or email. On Sun, Feb 27, 2011 at 10:22 AM, Faezeh Vedaei <[log in to unmask]> wrote: > I am working with some data by SPM8,as a question how can I display my brain > glass result on multiple slices of atemplate MRI to view regions of > hyperperfusion and hypoperfusion? > ========================================================================Date: Sun, 27 Feb 2011 14:25:32 -0800 Reply-To: Vladimir Bogdanov <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Vladimir Bogdanov <[log in to unmask]> Subject: Re: display result on template MRI Comments: To: Faezeh Vedaei <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/alternative; boundary="0-1112837336-1298845532=:86375" Message-ID: <[log in to unmask]> --0-1112837336-1298845532=:86375 Content-Type: text/plain; charset=iso-8859-1 Content-Transfer-Encoding: quoted-printable When you explore your results, in the window "Results" click on "overlays" in the group "Display". Here you can select "sections". In the menu wich is opened by this action you can select either a normalized individual structural image form the proper folder of your subject or a T1 image from SPM8\canonical. I hope this is helpful. Vladimir --- On Sun, 2/27/11, Faezeh Vedaei <[log in to unmask]> wrote: From: Faezeh Vedaei <[log in to unmask]> Subject: [SPM] display result on template MRI To: [log in to unmask] Date: Sunday, February 27, 2011, 4:25 PM I am working with some data by SPM8,as a question how can I display my brain glass result on multiple slices of atemplate MRI to view regions of hyperperfusion and hypoperfusion? --0-1112837336-1298845532=:86375 Content-Type: text/html; charset=iso-8859-1 Content-Transfer-Encoding: quoted-printable
When you explore your results, in the window "Results" click on "overlays" in the group "Display". Here you can select "sections". In the menu wich is opened by this action you can select either a normalized individual structural image form the proper folder of your subject or a T1 image from SPM8\canonical.

I hope this is helpful.

Vladimir

--- On Sun, 2/27/11, Faezeh Vedaei <[log in to unmask]> wrote:

From: Faezeh Vedaei <[log in to unmask]>
Subject: [SPM] display result on template MRI
To: [log in to unmask]
Date: Sunday, February 27, 2011, 4:25 PM



I am working with some data by SPM8,as a question how can I display my brain glass result on multiple slices of a template MRI to view regions of hyperperfusion and hypoperfusion?



--0-1112837336-1298845532=:86375-- ========================================================================Date: Sun, 27 Feb 2011 19:55:57 -0500 Reply-To: Yune Lee <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Yune Lee <[log in to unmask]> Subject: normalization failure (anterior posterior mismatch) MIME-Version: 1.0 Content-Type: multipart/mixed; boundaryMessage-ID: <[log in to unmask]> --001636283ab280d810049d4d24ad Content-Type: multipart/alternative; boundary --001636283ab280d804049d4d24ab Content-Type: text/plain; charset=ISO-8859-1 Dear SPM experts, I've encountered a normalization failure, such that there is a mismatch of anterior-posterior between a template (EPI.nii) and a source image (meanbold.nii) This is clearly shown in the attached PDF file. Any help wold be greatly appreciated. Thanks in advance, YSL --001636283ab280d804049d4d24ab Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable
Dear SPM experts,
I've encountered a normalization failure, such that there is a mismatch of anterior-posterior between a template (EPI.nii) and a source image (meanbold.nii)
This is clearly shown in the attached PDF file.
Any help wold be greatly appreciated.

Thanks in advance,
YSL



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RkVCMjgwMTcwQjM1Q0M1OTQ5NkE0Qzg1NkRDQz5dCj4+CnN0YXJ0eHJlZgozODUyNwolJUVPRgo--001636283ab280d810049d4d24ad-- ========================================================================Date: Sun, 27 Feb 2011 20:56:27 -0500 Reply-To: Glen Lee <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Glen Lee <[log in to unmask]> Subject: SPM8 error MIME-Version: 1.0 Content-Type: multipart/mixed; boundary cf3071c9bae64ca3049d4dfcd2 Message-ID: <[log in to unmask]> --20cf3071c9bae64ca3049d4dfcd2 Content-Type: multipart/alternative; boundary cf3071c9bae64c93049d4dfcd0 --20cf3071c9bae64c93049d4dfcd0 Content-Type: text/plain; charset=ISO-8859-1 Hello SPMers, Does anybody help me figuring out what this error message (Error using ==> < a href="matlab: opentonline ('cfg_util.m',808,0)"> cfg_util at 808 ) mean and how i can resolve this issue? I get this same error no matter what I try (e.g., realign, normalize, etc) in SPM8 (also see attached) Let me know. Thanks in advance. Glen --20cf3071c9bae64c93049d4dfcd0 Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Hello SPMers,
Does anybody help me figuring out what this error message (Error using ==> < a href="matlab: opentonline ('cfg_util.m',808,0)"> cfg_util at 808 </a>) mean and how i can resolve this issue?
I get this same error no matter what I try (e.g., realign, normalize, etc) in SPM8 (also see attached)
Let me know. Thanks in advance.

Glen


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iwACQF8kKQcCEIAABCAAAQhAAAIQgAAEIDBiAggAI+4cqgYBCEAAAhCAAAQgAAEIQAACEOiLAAJA XyQpBwIQgAAEIAABCEAAAhCAAAQgMGICCAAj7hyqBgEIQAACEIAABCAAAQhAAAIQ6IsAAkBfJCkH AhCAAAQgAAEIQAACEIAABCAwYgIIACPuHKoGAQhAAAIQgAAEIAABCEAAAhDoi8D/D/7vpu3uE6+o AAAAAElFTkSuQmCC --20cf3071c9bae64ca3049d4dfcd2-- ========================================================================Date: Sun, 27 Feb 2011 22:30:29 -0500 Reply-To: "MCLAREN, Donald" <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: "MCLAREN, Donald" <[log in to unmask]> Subject: Re: Second level t-test: test against other value than zero Comments: To: Nynke L <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/alternative; boundary cf3054a2f72ca08e049d4f4d70 Message-ID: [log in to unmask]> --20cf3054a2f72ca08e049d4f4d70 Content-Type: text/plain; charset=ISO-8859-1 Set the interpolation option to nearest neighbor. That should make it exact. Also, you might want to think about other transforms since the data is likely not to be normally distributed. Best Regards, Donald McLaren ================D.G. McLaren, Ph.D. Postdoctoral Research Fellow, GRECC, Bedford VA Research Fellow, Department of Neurology, Massachusetts General Hospital and Harvard Medical School Office: (773) 406-2464 ====================This e-mail contains CONFIDENTIAL INFORMATION which may contain PROTECTED HEALTHCARE INFORMATION and may also be LEGALLY PRIVILEGED and which is intended only for the use of the individual or entity named above. If the reader of the e-mail is not the intended recipient or the employee or agent responsible for delivering it to the intended recipient, you are hereby notified that you are in possession of confidential and privileged information. Any unauthorized use, disclosure, copying or the taking of any action in reliance on the contents of this information is strictly prohibited and may be unlawful. If you have received this e-mail unintentionally, please immediately notify the sender via telephone at (773) 406-2464 or email. On Sun, Feb 27, 2011 at 10:13 AM, Nynke L <[log in to unmask]>wrote: > Hello all, > > I have a particular group level analysis for which I want to use spm. > However, till now I don't manage to so I hope you have suggestions for me. > > I use fMRI for the prediction of a certain binary outcome. Therefore, I use > a different classification software package that computes > prediction-accuracies for all voxels. For each subject, I have a .nii file > with as values the accuracies (range between 0 and 1). So, this is a brain > map just like you usually feed to the second level. > > What I want to test in the second level analysis is which brain areas have > accuracies significantly higher than 0.5. So I want to test against the > null-hypothesis that accuracies are 0.5 or lower. Now the problem is that > the 1 sample t-test in spm on default tests against the null-hypothesis that > the values are zero or higher.... So my first question is whether it is > possible to set a custum value for the t-test to test against a manually set > value? > > I already tried a different approach, namely subtracting 0.5 from the > values in my input images (to put them in the default spm t-test). However, > when I trie to do this with the image calculator of spm (with as expression > i1 - 0.5) I do not get correct results: I do not get a map with exactly 0.5 > subtracted from each value but a range between 0.4-0.6. It seems that > spm-image-calc is also doing something else with the image... So my second > question is: how can I make image-calc subtract exactly 0.5 from all values > in the image? > > Thanks in advance! > > Best regards, > Nynke van der Laan > --20cf3054a2f72ca08e049d4f4d70 Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Set the interpolation option to nearest neighbor. That should make it exact.

Also, you might want to think about other transforms since the data is likely not to be normally distributed.

Best Regards, Donald McLaren
=================
D.G. McLaren, Ph.D.
Postdoctoral Research Fellow, GRECC, Bedford VA
Research Fellow, Department of Neurology, Massachusetts General Hospital and Harvard Medical School
Office: (773) 406-2464
=====================
This e-mail contains CONFIDENTIAL INFORMATION which may contain PROTECTED HEALTHCARE INFORMATION and may also be LEGALLY PRIVILEGED and which is intended only for the use of the individual or entity named above. If the reader of the e-mail is not the intended recipient or the employee or agent responsible for delivering it to the intended recipient, you are hereby notified that you are in possession of confidential and privileged information. Any unauthorized use, disclosure, copying or the taking of any action in reliance on the contents of this information is strictly prohibited and may be unlawful. If you have received this e-mail unintentionally, please immediately notify the sender via telephone at (773) 406-2464 or email.


On Sun, Feb 27, 2011 at 10:13 AM, Nynke L <[log in to unmask]> wrote:
Hello all,

I have a particular group level analysis for which I want to use spm. However, till now I don't manage to so I hope you have suggestions for me.

I use fMRI for the prediction of a certain binary outcome. Therefore, I use a different classification software package that computes prediction-accuracies for all voxels. For each subject, I have a .nii file with as values the accuracies (range between 0 and 1). So, this is a brain map just like you usually feed to the second level.

What I want to test in the second level analysis is which brain areas have accuracies significantly higher than 0.5. So I want to test against the null-hypothesis that accuracies are 0.5 or lower. Now the problem is that the 1 sample t-test in spm on default tests against the null-hypothesis that the values are zero or higher.... So my first question is whether it is possible to set a custum value for the t-test to test against a manually set value?

I already tried a different approach, namely subtracting 0.5 from the values in my input images (to put them in the default spm t-test). However, when I trie to do this with the image calculator of spm (with as expression i1 - 0.5) I do not get correct results: I do not get a map with exactly 0.5 subtracted from each value but a range between 0.4-0.6. It seems that spm-image-calc is also doing something else with the image... So my second question is: how can I make image-calc subtract exactly 0.5 from all values in the image?

Thanks in advance!

Best regards,
Nynke van der Laan

--20cf3054a2f72ca08e049d4f4d70-- ========================================================================Date: Mon, 28 Feb 2011 09:55:35 +0100 Reply-To: Marko Wilke <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Marko Wilke <[log in to unmask]> Subject: Re: SPM8 error Comments: To: Glen Lee <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1; format=flowed Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> Hi Glen, this could be an installation problem, perhaps try using a newly-downloaded SPM, install the latest updates on top of it and install it into a directory without spaces (say, 'C:\Test\SPM8'), and then only add this directory to the Matlab path. Cheers, Marko Glen Lee wrote: > Hello SPMers, > Does anybody help me figuring out what this error message (Error using > ==> < a href="matlab: opentonline ('cfg_util.m',808,0)"> cfg_util at 808 > ) mean and how i can resolve this issue? > I get this same error no matter what I try (e.g., realign, normalize, > etc) in SPM8 (also see attached) > Let me know. Thanks in advance. > > Glen > > -- ____________________________________________________ PD Dr. med. Marko Wilke Facharzt fr Kinder- und Jugendmedizin Leiter, Experimentelle Pdiatrische Neurobildgebung Universitts-Kinderklinik Abt. III (Neuropdiatrie) Marko Wilke, MD, PhD Pediatrician Head, Experimental Pediatric Neuroimaging University Children's Hospital Dept. III (Pediatric Neurology) Hoppe-Seyler-Str. 1 D - 72076 Tbingen, Germany Tel. +49 7071 29-83416 Fax +49 7071 29-5473 [log in to unmask] http://www.medizin.uni-tuebingen.de/kinder/epn ____________________________________________________ ========================================================================Date: Mon, 28 Feb 2011 09:06:14 +0000 Reply-To: John Ashburner <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: John Ashburner <[log in to unmask]> Subject: Re: normalization failure (anterior posterior mismatch) Comments: To: Yune Lee <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> Before running the spatial normalisation, you'll need to ensure that the image is in approximate alignment with the templates (Check Reg button). For these images, it appears that they are either rotated by 180 degrees (about the z axis) or flipped in the anterior posterior direction. Best regards, -John On 28 February 2011 00:55, Yune Lee <[log in to unmask]> wrote: > > Dear SPM experts, > I've encountered a normalization failure, such that there is a mismatch of > anterior-posterior between a template (EPI.nii) and a source image > (meanbold.nii) > This is clearly shown in the attached PDF file. > Any help wold be greatly appreciated. > > Thanks in advance, > YSL > > > > ========================================================================Date: Mon, 28 Feb 2011 14:41:37 +0530 Reply-To: sarika cherodath <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: sarika cherodath <[log in to unmask]> Subject: question on VOI analysis MIME-Version: 1.0 Content-Type: multipart/alternative; boundaryMessage-ID: <[log in to unmask]> --00248c05002ff8481b049d5412cf Content-Type: text/plain; charset=ISO-8859-1 Hi SPMers, I have been trying to perform VOI analysis to obtain signal changes at a particular area for individual subjects in the dataset, so as to make correlations with behavioral scores. When i tried to calculate the values, SPM returns the same value for all subjects! Can anybody explain why this might be? The dataset has been analysed at second level and then moved to another directory (along with first level data). Is it possible that SPM is not able to access the data because of the path change?? Thanks in advance, -- Sarika Cherodath Graduate Student National Brain Research Centre Manesar, Gurgaon -122050 India --00248c05002ff8481b049d5412cf Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable

Hi SPMers,

I have been trying to perform VOI analysis to obtain signal changes at a particular area for individual subjects in the dataset, so as to make correlations with behavioral scores. When i tried to calculate the values, SPM returns the same value for all subjects! Can anybody explain why this might be? The dataset has been analysed at second level and then moved to another directory (along with first level data). Is it possible that SPM is not able to access the data because of the path change??

Thanks in advance,
--
Sarika Cherodath
Graduate Student
National Brain Research Centre
Manesar, Gurgaon -122050
India

--00248c05002ff8481b049d5412cf-- ========================================================================Date: Mon, 28 Feb 2011 10:13:17 +0100 Reply-To: Michels Lars <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Michels Lars <[log in to unmask]> Subject: Postdoctoral Fellowship in multimodal developmental neuroimaging Comments: To: [log in to unmask] MIME-Version: 1.0 Content-Type: multipart/alternative; boundary="----_=_NextPart_001_01CBD727.BC9EDDD6" Message-ID: <[log in to unmask]> This is a multi-part message in MIME format. ------_=_NextPart_001_01CBD727.BC9EDDD6 Content-Type: text/plain; charset="iso-8859-1" Content-Transfer-Encoding: quoted-printable Applications are invited for an 18 month postdoctoral fellowship in the human multimodal neuroimaging project "Linking the major system markers for typical and atypical brain development: a multimodal imaging and spectroscopy study" (http://www.zihp.uzh.ch/1610.php#45) funded by the Zrich Institute of Human Physiology. This study will investigate the major physiological markers of brain development, using a combination of multimodal brain imaging (e.g., simultaneous EEG-fMRI, see Lchinger et al., 2011, NeuroImage, in press) and MR-spectroscopy methods (i.e., GABA, see O'Gorman et al., 2011, J. of Mag. Reson. Img., in press). The initial phase of the study will establish baseline neurotransmitter levels, cerebral blood flow (e.g., perfusion MRI) and EEG frequency and power at rest in children, adolescents, and adults. Examining the interactions between these markers and the changes they demonstrate with age and hormone levels will allow to better understanding the global and regional processes underlying brain maturation. In addition, we will investigate changes in these physiological markers with (a) memory tasks (see Michels et al., 2010, PLoS ONE) and (b) attention deficit hyperactivity disorder (ADHD, see Doehnert et al., Biol Psychiatry, 2010). The starting date of the position is May 2011. Our department is equipped with 64-channel fMRI-compatible EEG equipment and a 3 Tesla GE scanner, which is mainly dedicated for research questions. The successful applicant will have a PhD research background in Cognitive Neuroscience, Neurophysiology, Psychology, Neuropsychology, or related fields. Fluency in English and the ability to work within a multidisciplinary team are essential. Applicants must be experienced at conducting fMRI and/or EEG studies -demonstrated by at least 2 first author publications in international peer-reviewed journals- and be familiar with analysis software such as SPM/Matlab, BrainVoyager and/or FSL. Experience with stimulus presentation software (such as Presentation), UNIX, and programming languages a plus. Salaries are in accordance with the Swiss National Research Foundation. APPLICATION INSTRUCTIONS: To apply, please send a curriculum vitae, a personal statement describing research interests, 3 letters of recommendations, and up to 3 article reprints/preprints (max. 2 MB!!!) to: Dr Lars Michels [log in to unmask] MR-Zentrum University Children's Hospital Steinwiesstrasse 75 Zrich 8032 Switzerland Reviews of applications will begin on the 1st of March and will continue until the position is filled. ------_=_NextPart_001_01CBD727.BC9EDDD6 Content-Type: text/html; charset="iso-8859-1" Content-Transfer-Encoding: quoted-printable

Applications are invited for an 18 month postdoctoral fellowship in the human multimodal neuroimaging project “Linking the major system markers for typical and atypical brain development: a multimodal imaging and spectroscopy study” (http://www.zihp.uzh.ch/1610.php#45) funded by the Zrich Institute of Human Physiology.

This study will investigate the major physiological markers of brain development, using a combination of multimodal brain imaging (e.g., simultaneous EEG-fMRI, see Lchinger et al., 2011, NeuroImage, in press) and MR-spectroscopy methods (i.e., GABA, see O’Gorman et al., 2011, J. of Mag. Reson. Img., in press). The initial phase of the study will establish baseline neurotransmitter levels, cerebral blood flow (e.g., perfusion MRI) and EEG frequency and power at rest in children, adolescents, and adults. Examining the interactions between these markers and the changes they demonstrate with age and hormone levels will allow to better understanding the global and regional processes underlying brain maturation. In addition, we will investigate changes in these physiological markers with (a) memory tasks (see Michels et al., 2010, PLoS ONE) and (b) attention deficit hyperactivity disorder (ADHD, see Doehnert et al., Biol Psychiatry, 2010). The starting date of the position is May 2011. Our department is equipped with 64-channel fMRI-compatible EEG equipment and a 3 Tesla GE scanner, which is mainly dedicated for research questions.

 

The successful applicant will have a PhD research background in Cognitive Neuroscience, Neurophysiology, Psychology, Neuropsychology, or related fields. Fluency in English and the ability to work within a multidisciplinary team are essential. Applicants must be experienced at conducting fMRI and/or EEG studies –demonstrated by at least 2 first author publications in international peer-reviewed journals– and be familiar with analysis software such as SPM/Matlab, BrainVoyager and/or FSL. Experience with stimulus presentation software (such as Presentation), UNIX, and programming languages a plus.

 

Salaries are in accordance with the Swiss National Research Foundation.

 

APPLICATION INSTRUCTIONS: To apply, please send a curriculum vitae, a personal statement describing research interests, 3 letters of recommendations, and up to 3 article reprints/preprints (max. 2 MB!!!) to:

 

Dr Lars Michels

[log in to unmask]

MR-Zentrum

University Children’s Hospital

Steinwiesstrasse 75

Zrich 8032

Switzerland

 

Reviews of applications will begin on the 1st of March and will continue until the position is filled.

 

------_=_NextPart_001_01CBD727.BC9EDDD6-- ========================================================================Date: Mon, 28 Feb 2011 09:48:36 +0000 Reply-To: Vincent Koppelmans <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Vincent Koppelmans <[log in to unmask]> Subject: Adjusting Dartel for ICV: RC volumes or C volumes Mime-Version: 1.0 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain; charset="UTF-8" Message-ID: <[log in to unmask]> Dear SPM experts, If you adjust for intra cranial volume in a dartel analyses on gray matter, would it be best to have your ICV calculated from the RC files or the C files. I have read that C files are a little bit more accurate than the RC files. Then again, the dartel analysis uses RC files, therefore volumes calculated from RC files would match the data best, right? Kind regards, Vincent ========================================================================Date: Mon, 28 Feb 2011 11:43:44 +0100 Reply-To: =?ISO-8859-1?Q?Gemma_Mont?= <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: =?ISO-8859-1?Q?Gemma_Mont?= <[log in to unmask]> Subject: Re: Adjusting Dartel for ICV: RC volumes or C volumes Comments: To: Vincent Koppelmans <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/alternative; boundaryMessage-ID: <[log in to unmask]> --0015175cb1445b46e5049d555ca2 Content-Type: text/plain; charset=ISO-8859-1 Hi Vincent, I suggest you use the c*.nii files. They are the tissue classes in native space. You are right, DARTEL takes information encoded in the rc*.nii files. However, the flow fields u_rc1*.nii files are applied to the c1*.nii to create the warped files. So finally, you obtain files in the form swmc1*.nii, either in the DARTEL space or in the MNI space. You can check that the volumes of the GM Jacobian scaled images (without smoothing) by DARTEL are the same than the volume of the GM segments in native space (c1*.nii files). Hope this helps, Gemma On 28 February 2011 10:48, Vincent Koppelmans <[log in to unmask]>wrote: > Dear SPM experts, > > If you adjust for intra cranial volume in a dartel analyses on gray matter, > would it be best to have your ICV calculated from the RC files or the C > files. I have read that C files are a little bit more accurate than the RC > files. Then again, the dartel analysis uses RC files, therefore volumes > calculated from RC files would match the data best, right? Kind regards, > > Vincent > <[log in to unmask]> --0015175cb1445b46e5049d555ca2 Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Hi Vincent,
I suggest you use the c*.nii files. They are the tissue classes in native space.

You are right, DARTEL takes information encoded in the rc*.nii files. However, the flow fields u_rc1*.nii files are applied to the c1*.nii to create the warped files. So finally, you obtain files in the form swmc1*.nii, either in the DARTEL space or in the MNI space. You can check that the volumes of the GM Jacobian scaled images (without smoothing) by DARTEL are the same than the volume of the GM segments in native space (c1*.nii files).

Hope this helps,
Gemma

On 28 February 2011 10:48, Vincent Koppelmans <[log in to unmask]> wrote:
Dear SPM experts,

If you adjust for intra cranial volume in a dartel analyses on gray matter, would it be best to have your ICV calculated from the RC files or the C files. I have read that C files are a little bit more accurate than the RC files. Then again, the dartel analysis uses RC files, therefore volumes calculated from RC files would match the data best, right? Kind regards,

Vincent

--0015175cb1445b46e5049d555ca2-- ========================================================================Date: Mon, 28 Feb 2011 11:50:23 +0100 Reply-To: michel grothe <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: michel grothe <[log in to unmask]> Subject: Re: Adjusting Dartel for ICV: RC volumes or C volumes Comments: To: [log in to unmask] In-Reply-To: <[log in to unmask]> Content-Type: multipart/alternative; boundary="_90f969e0-6ae7-4793-8d3b-790a0b77c215_" MIME-Version: 1.0 Message-ID: <[log in to unmask]> --_90f969e0-6ae7-4793-8d3b-790a0b77c215_ Content-Type: text/plain; charset="iso-8859-1" Content-Transfer-Encoding: quoted-printable Dear Vincent, the rc*-files are rigid-body (6-P) transformed versions of the c*-files and total tissue calculations should therefore be exactly the same between the two files. Given that modulation aims to preserve the native amount of tissue, totals calculated from mwrc*-files should also be equal to the ones calculated from c*- or rc*-files, although they might differ slightly because of interpolation issues. Do totals calculated from the different image-types differ in your case? Best regards, Michel > Date: Mon, 28 Feb 2011 09:48:36 +0000 > From: [log in to unmask] > Subject: [SPM] Adjusting Dartel for ICV: RC volumes or C volumes > To: [log in to unmask] > > Dear SPM experts, > > If you adjust for intra cranial volume in a dartel analyses on gray matter, would it be best to have your ICV calculated from the RC files or the C files. I have read that C files are a little bit more accurate than the RC files. Then again, the dartel analysis uses RC files, therefore volumes calculated from RC files would match the data best, right? Kind regards, > > Vincent --_90f969e0-6ae7-4793-8d3b-790a0b77c215_ Content-Type: text/html; charset="iso-8859-1" Content-Transfer-Encoding: quoted-printable Dear Vincent,

the rc*-files are rigid-body (6-P) transformed versions of the c*-files and total tissue calculations should therefore be exactly the same between the two files. Given that modulation aims to preserve the native amount of tissue, totals calculated from mwrc*-files should also be equal to the ones calculated from c*- or rc*-files, although they might differ slightly because of interpolation issues. Do totals calculated from the different image-types differ in your case?  

Best regards,
Michel

> Date: Mon, 28 Feb 2011 09:48:36 +0000
> From: [log in to unmask]
> Subject: [SPM] Adjusting Dartel for ICV: RC volumes or C volumes
> To: [log in to unmask]
>
> Dear SPM experts,
>
> If you adjust for intra cranial volume in a dartel analyses on gray matter, would it be best to have your ICV calculated from the RC files or the C files. I have read that C files are a little bit more accurate than the RC files. Then again, the dartel analysis uses RC files, therefore volumes calculated from RC files would match the data best, right? Kind regards,
>
> Vincent
--_90f969e0-6ae7-4793-8d3b-790a0b77c215_-- ========================================================================Date: Mon, 28 Feb 2011 10:59:22 +0000 Reply-To: Vladimir Litvak <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Vladimir Litvak <[log in to unmask]> Subject: Re: [SPM DCM] how to specify the modulation? Comments: To: =?UTF-8?B?6aOe6bif?= <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=UTF-8 Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> Dear Haoran, 2011/2/27 飞鸟 <[log in to unmask]>: > Hello all, >   When you analysis your data with the method of DCM, have you ever met the > problem about how to specify the modulation? Now I choose 7 basic models, > and then assume all the connections in each basic model are modulated by the > experimental manipulation. What I want to know is that whether or not this > is reasonable Usually one would have a hypothesis about which specific connections are affected by the experimental condition. >In addition, is it possible that the connections > between two sources could include forward connectivity, backward > connectivity and lateral connectivity at the same time? No. Every connection can only have one type. Vladimir >   Any help will be grateful! > > -- > Haoran LI (MS) > Brain Imaging Lab, > Research Center for Learning Science, > Southeast University > 2 Si Pai Lou , Nanjing, 210096, P.R.China > > ========================================================================Date: Mon, 28 Feb 2011 12:02:19 +0100 Reply-To: Marko Wilke <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Marko Wilke <[log in to unmask]> Subject: F-values MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1; format=flowed Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> Dear All, at the risk of (once again) exhibiting my statistical ignorance, I wanted to ask for feedback re: an effect I see when doing F-tests. I am comparing sessions with different numbers of covariates and compute an omnibus F-test in SPM (for the covariates only) and sum the resulting F-values. As expected, I see that there seems to be an optimum number of covariates as the sum of F-values first increases, then decreases when adding more covariates. I expected this to be a function of the degrees of freedom but I cannot seem to find the piece of code where these are taken into account. Any input is appreciated. Cheers, Marko -- ____________________________________________________ PD Dr. med. Marko Wilke Facharzt fr Kinder- und Jugendmedizin Leiter, Experimentelle Pdiatrische Neurobildgebung Universitts-Kinderklinik Abt. III (Neuropdiatrie) Marko Wilke, MD, PhD Pediatrician Head, Experimental Pediatric Neuroimaging University Children's Hospital Dept. III (Pediatric Neurology) Hoppe-Seyler-Str. 1 D - 72076 Tbingen, Germany Tel. +49 7071 29-83416 Fax +49 7071 29-5473 [log in to unmask] http://www.medizin.uni-tuebingen.de/kinder/epn ____________________________________________________ ========================================================================Date: Mon, 28 Feb 2011 14:12:21 +0000 Reply-To: SUBSCRIBE FSL Patricia Pires <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: SUBSCRIBE FSL Patricia Pires <[log in to unmask]> Subject: DTI with SPM Mime-Version: 1.0 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain; charset="UTF-8" Message-ID: <[log in to unmask]> Hello, i am new in the SPM forum and i will be glad if somebody could help me. My question is concerning to preocess DTI images with SPM. I have processed DTI images (FA; MD, RD...) with FSL. Could anyone tell me some lecture to find how process (e.g. FA images) with SPM or where to find information concernig SPM and FSL procedures softwares differences? Thank you very much, Patricia. ========================================================================Date: Mon, 28 Feb 2011 15:25:26 +0100 Reply-To: Janani Dhinakaran <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Janani Dhinakaran <[log in to unmask]> Subject: Unsubscribe me please MIME-Version: 1.0 Content-Type: multipart/alternative; boundary cf3079b77ea0b2a8049d5874c7 Message-ID: <[log in to unmask]> --20cf3079b77ea0b2a8049d5874c7 Content-Type: text/plain; charset=UTF-8 Thank you. --20cf3079b77ea0b2a8049d5874c7 Content-Type: text/html; charset=UTF-8 Thank you.
--20cf3079b77ea0b2a8049d5874c7-- ========================================================================Date: Mon, 28 Feb 2011 15:29:46 +0100 Reply-To: Wolfgang Weber-Fahr <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Wolfgang Weber-Fahr <[log in to unmask]> Subject: Job Anouncement ZI-Mannheim, Germany MIME-Version: 1.0 Content-Type: text/plain; charset=UTF-8; format=flowed Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> The Central Institute of Mental Health (State Foundation) is an internationally renowned research institute in the field of psychiatry and neuroscience, home of the Department of Psychiatry of the Medical Faculty Mannheim of the University of Heidelberg as well as psychiatric hospital with 255 inpatient and 52 day-hospital beds. Within several new projects funded by the European Union and the Federal Ministry of Education and Research we offer 2 Positions for PostDocs and PhD-Students in the area of rodent magnetic resonance functional-, perfusion- and diffusion tensor (DTI) imaging at 9.4 Tesla. The Central Institute of Mental Health is equipped with a latest generation 210 mm horizontalbore Bruker BioSpec animal system and additional cryogenic MR coils for 1H and 13C detection in the mouse brain as well as two 3 Tesla human whole body MR-scanners. The positions are for two years initially and located in the research group Translational Imaging. Potential applicants should have a diploma or master in physics, physical chemistry or neuroscience, or an equivalent field. The ideal candidate from the quantitative sciences has a solid background in NMR physics, signal detection and processing theory, and is familiar with the Bruker Paravision environment. Experience in other computer languages, Matlab or IDL, is desirable. We have openings in these primary fields of research: • Establishment of manganese enhanced magnetic resonance imaging (MEMRI) for a the longitudinal assessment of connectivity and neuronal activity in experimental animals. • Development of methods for the acquisition and post processing of functional BOLD imaging data with optogenetics for the identification and investigation of brain networks. • Diffusion Tensor Imaging for the investigation of structural integrity in different psychiatric mouse-models. The candidate would also collaborate on several ongoing animal studies of schizophrenia, depression, substance abuse and other psychiatric disorders in mouse and rat models. The assistance in the general supervision of the animal scanner would also be part of the position. More information can be found at http://www.zi-mannheim.de/transl_imaging.html. We offer an interesting job in a leading research hospital with a strong emphasis on MR-Imaging, salary is according to the German TV-L pay scale, including the social benefits of the public service sector. For further information please contact Dr. Wolfgang Weber-Fahr, Tel. +49 621 1703-2961, E-Mail: [log in to unmask] Homepage: www.zi-mannheim.de/start_en.html ---------------------------------------------------------- Wolfgang Weber-Fahr, Dr.rer.nat. Head RG Translational Imaging Neuroimaging Department Central Institute of Mental Health J5 68072 Mannheim Germany email:[log in to unmask] phone: ++49 621 1703 2961 ========================================================================Date: Mon, 28 Feb 2011 10:36:54 -0500 Reply-To: zao liu <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: zao liu <[log in to unmask]> Subject: regions of brain corresponding to VBM coordinates MIME-Version: 1.0 Content-Type: multipart/alternative; boundaryMessage-ID: <[log in to unmask]> --0015174bf21c068a29049d5973e3 Content-Type: text/plain; charset=ISO-8859-1 *Dear All,* ** *I did VBM analysis on our T1-w images and would like to know if there is a way to get the names of regions of activation in the brain from the coordinates (which comes as a report at the end of VBM, i.e voxelwise, cluster wise and set level reports). One more clarification the coordinates reported are in MNI right and are mm not voxel coordinates right.* --0015174bf21c068a29049d5973e3 Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable
Dear All,
I did VBM analysis on our T1-w images and would like to know if there is a way to get the names ofregions of activation in the brainfrom the coordinates (whichcomes as a report at the end of VBM, i.evoxelwise, cluster wise and set level reports). One more clarificationthe coordinates reported are inMNI rightand aremm not voxel coordinates right.
--0015174bf21c068a29049d5973e3-- ========================================================================Date: Mon, 28 Feb 2011 16:35:44 +0000 Reply-To: Richard Binney <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Richard Binney <[log in to unmask]> Subject: PPI: adjust for effects of interest MIME-Version: 1.0 Content-Type: multipart/alternative; boundarye6ba1efe9a7601f6049d5a45df Message-ID: <[log in to unmask]> --90e6ba1efe9a7601f6049d5a45df Content-Type: text/plain; charset=ISO-8859-1 Hi Darren G/ Karl F/other PPI-ers, I can't find any posts on this and wondered if you can clear it up for me. In extracting the principal eigenvariate from your VOI, you are asked if you want to adjust the extracted timecourse. When should you adjust and when should you not worry? what is the impact of adjusting? My impression was that the raw timecourse would be extracted always. The option to adjust suggests this is not always true. Do you use this option (only?) when you have time or dispersion derivatives and/or motion regressors? I have a parametric design with two conditions (tasks) and two parametric modulations per condition. The design matrix therefore has 6 regressors of interest. Motion regressors are also included. In extracting the timecourse should I adjust using an F-contrast spaning the first 6 columns only ([1 1 1 1 1 1]->right-padded with zeros)?? Is it problematic if I have not done this? What are the consequences? What about if I were only interested in the parametric modulations of the first condition in the PPI analysis? Should I adjust for the first 3 columns only ([1 1 1 0 0 0])? All your comments will be greatly appreciated. Richard --90e6ba1efe9a7601f6049d5a45df Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable
Hi Darren G/ Karl F/other PPI-ers,
I can't find any posts on this and wondered if you can clear it up for me.
In extracting the principal eigenvariate from your VOI, you are asked if you want to adjust the extracted timecourse. When should you adjust and when should you not worry? what is the impact of adjusting?
My impression was that the raw timecourse would be extracted always. The option to adjust suggests this is not always true. Do you use this option (only?)when you have time or dispersion derivatives and/or motion regressors?
I have a parametric design with two conditions (tasks)and two parametric modulations per condition. The design matrix therefore has 6 regressors of interest. Motion regressors are also included. In extracting the timecourse should I adjust using an F-contrast spaning the first 6 columns only ([1 1 1 1 1 1]->right-padded with zeros)?? Is it problematic if I have not done this? What are the consequences?
What about if I were only interested in the parametric modulations of the first condition in the PPI analysis? Should I adjust for the first 3 columns only ([1 1 1 0 0 0])?
All your comments will be greatly appreciated.
Richard
--90e6ba1efe9a7601f6049d5a45df-- ========================================================================Date: Mon, 28 Feb 2011 11:42:00 -0500 Reply-To: "MCLAREN, Donald" <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: "MCLAREN, Donald" <[log in to unmask]> Subject: Re: PPI: adjust for effects of interest Comments: To: Richard Binney <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/alternative; boundary cf3054a4b5dbb06a049d5a5beb Message-ID: <[log in to unmask]> --20cf3054a4b5dbb06a049d5a5beb Content-Type: text/plain; charset=ISO-8859-1 Richard, I'd use an F-contrast that is one row per condition/modulator. In your case: 1 0 0 0 0 0 ... 0 1 0 0 0 0 ... 0 0 1 0 0 0 ... 0 0 0 1 0 0 ... 0 0 0 0 1 0 ... 0 0 0 0 0 1 ... The goal of the adjustment is to extract only the BOLD signal related to neural activity and eliminate the activity due to motion. Best Regards, Donald McLaren ================D.G. McLaren, Ph.D. Postdoctoral Research Fellow, GRECC, Bedford VA Research Fellow, Department of Neurology, Massachusetts General Hospital and Harvard Medical School Office: (773) 406-2464 ====================This e-mail contains CONFIDENTIAL INFORMATION which may contain PROTECTED HEALTHCARE INFORMATION and may also be LEGALLY PRIVILEGED and which is intended only for the use of the individual or entity named above. If the reader of the e-mail is not the intended recipient or the employee or agent responsible for delivering it to the intended recipient, you are hereby notified that you are in possession of confidential and privileged information. Any unauthorized use, disclosure, copying or the taking of any action in reliance on the contents of this information is strictly prohibited and may be unlawful. If you have received this e-mail unintentionally, please immediately notify the sender via telephone at (773) 406-2464 or email. On Mon, Feb 28, 2011 at 11:35 AM, Richard Binney < [log in to unmask]> wrote: > Hi Darren G/ Karl F/other PPI-ers, > > I can't find any posts on this and wondered if you can clear it up for me. > > In extracting the principal eigenvariate from your VOI, you are asked if > you want to adjust the extracted timecourse. When should you adjust and when > should you not worry? what is the impact of adjusting? > > My impression was that the raw timecourse would be extracted always. The > option to adjust suggests this is not always true. Do you use this option > (only?) when you have time or dispersion derivatives and/or motion > regressors? > > I have a parametric design with two conditions (tasks) and two parametric > modulations per condition. The design matrix therefore has 6 regressors of > interest. Motion regressors are also included. In extracting the timecourse > should I adjust using an F-contrast spaning the first 6 columns only ([1 1 1 > 1 1 1]->right-padded with zeros)?? Is it problematic if I have not done > this? What are the consequences? > > What about if I were only interested in the parametric modulations of the > first condition in the PPI analysis? Should I adjust for the first 3 columns > only ([1 1 1 0 0 0])? > > All your comments will be greatly appreciated. > > Richard > --20cf3054a4b5dbb06a049d5a5beb Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable
Richard,

I'd use an F-contrast that is one row per condition/modulator. In your case:
1 0 0 0 0 0 ...
0 1 0 0 0 0 ...
0 0 1 0 0 0 ...
0 0 0 1 0 0 ...
0 0 0 0 1 0 ...
0 0 0 0 0 1 ...

The goal of the adjustment is to extract only the BOLD signal related to neural activity and eliminate the activity due to motion.

Best Regards, Donald McLaren
=================
D.G. McLaren, Ph.D.
Postdoctoral Research Fellow, GRECC, Bedford VA
Research Fellow, Department of Neurology, Massachusetts General Hospital and Harvard Medical School
Office: (773) 406-2464
=====================
This e-mail contains CONFIDENTIAL INFORMATION which may contain PROTECTED HEALTHCARE INFORMATION and may also be LEGALLY PRIVILEGED and which is intended only for the use of the individual or entity named above. If the reader of the e-mail is not the intended recipient or the employee or agent responsible for delivering it to the intended recipient, you are hereby notified that you are in possession of confidential and privileged information. Any unauthorized use, disclosure, copying or the taking of any action in reliance on the contents of this information is strictly prohibited and may be unlawful. If you have received this e-mail unintentionally, please immediately notify the sender via telephone at (773) 406-2464 or email.


On Mon, Feb 28, 2011 at 11:35 AM, Richard Binney <[log in to unmask]> wrote:
Hi Darren G/ Karl F/other PPI-ers,
I can't find any posts on this and wondered if you can clear it up for me.
In extracting the principal eigenvariate from your VOI, you are asked if you want to adjust the extracted timecourse. When should you adjust and when should you not worry? what is the impact of adjusting?
My impression was that the raw timecourse would be extracted always. The option to adjust suggests this is not always true. Do you use this option (only?)when you have time or dispersion derivatives and/or motion regressors?
I have a parametric design with two conditions (tasks)and two parametric modulations per condition. The design matrix therefore has 6 regressors of interest. Motion regressors are also included. In extracting the timecourse should I adjust using an F-contrast spaning the first 6 columns only ([1 1 1 1 1 1]->right-padded with zeros)?? Is it problematic if I have not done this? What are the consequences?
What about if I were only interested in the parametric modulations of the first condition in the PPI analysis? Should I adjust for the first 3 columns only ([1 1 1 0 0 0])?
All your comments will be greatly appreciated.
Richard

--20cf3054a4b5dbb06a049d5a5beb-- ========================================================================Date: Mon, 28 Feb 2011 11:31:33 -0600 Reply-To: Pilar Archila-Suerte <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Pilar Archila-Suerte <[log in to unmask]> Subject: Art repair - mean signal change MIME-Version: 1.0 Content-Type: multipart/alternative; boundaryMessage-ID: <[log in to unmask]> --0015177fcec43a8612049d5b0ea2 Content-Type: text/plain; charset=UTF-8 SPM Users, When using the "scaling to percent signal change" option in ArtRepair, sometimes I get what I want from the files selected and sometimes I don't (depending on which files I select). Why would ArtRepair give this answer: *Direct calls to spm_defauts are deprecated.* *Please use spm('Defaults',modality) or spm_get_defaults instead.* *Automatically estimated peak and contrast scaling.* * Normalizing by beta_0008.img* *Peak value = 4.97* *Contrast sum = 0.996* *Mean value = NaN* *(peak/contrast_sum)*100/bmean = **NaN* * * *ans =* * * * 4.9700 0.9960 ** NaN* All files follow the same path so I don't think that's the problem. Does anybody know why this is happening and how I can fix this? Thank you, Pilar A. --0015177fcec43a8612049d5b0ea2 Content-Type: text/html; charset=UTF-8 Content-Transfer-Encoding: quoted-printable
SPM Users,
When using the "scaling to percent signal change" option in ArtRepair, sometimes I get what I want from the files selected and sometimes I don't (depending on which files I select).

Why would ArtRepair give this answer:

Direct calls to spm_defauts are deprecated.
Please use spm('Defaults',modality) or spm_get_defaults instead.
Automatically estimated peak and contrast scaling.
 Normalizing by beta_0008.img
Peak value    = 4.97
Contrast sum  = 0.996
Mean value    = NaN
(peak/contrast_sum)*100/bmean  = NaN

ans =

    4.9700    0.9960       NaN

 All files follow the same path so I don't think that's the problem. Does anybody know why this is happening and how I can fix this?

Thank you,
Pilar A. 
--0015177fcec43a8612049d5b0ea2-- ========================================================================Date: Mon, 28 Feb 2011 12:36:59 -0500 Reply-To: Chris Watson <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Chris Watson <[log in to unmask]> Subject: Re: Art repair - mean signal change Comments: To: Pilar Archila-Suerte <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset="UTF-8"; format=flowed Content-Transfer-Encoding: 7bit Message-ID: <[log in to unmask]> I think that was a bug in an older version of ArtRepair. Do you have the latest version? Pilar Archila-Suerte wrote: > SPM Users, > When using the "scaling to percent signal change" option in ArtRepair, > sometimes I get what I want from the files selected and sometimes I > don't (depending on which files I select). > > Why would ArtRepair give this answer: > > /Direct calls to spm_defauts are deprecated./ > /Please use spm('Defaults',modality) or spm_get_defaults instead./ > /Automatically estimated peak and contrast scaling./ > / Normalizing by beta_0008.img/ > /Peak value = 4.97/ > /Contrast sum = 0.996/ > /Mean value = NaN/ > /(peak/contrast_sum)*100/bmean = /*/NaN/* > / > / > /ans =/ > / > / > / 4.9700 0.9960 /*/ NaN/* > > All files follow the same path so I don't think that's the > problem. Does anybody know why this is happening and how I can fix this? > > Thank you, > Pilar A. ========================================================================Date: Mon, 28 Feb 2011 11:38:50 -0600 Reply-To: Pilar Archila-Suerte <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Pilar Archila-Suerte <[log in to unmask]> Subject: Re: Art repair - mean signal change Comments: To: Chris Watson <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/alternative; boundaryMessage-ID: <[log in to unmask]> --00163683195045f1c4049d5b2847 Content-Type: text/plain; charset=UTF-8 I have ArtRepair v4. Isn't this the latest version? On Mon, Feb 28, 2011 at 11:36 AM, Chris Watson < [log in to unmask]> wrote: > I think that was a bug in an older version of ArtRepair. Do you have the > latest version? > > > Pilar Archila-Suerte wrote: > >> SPM Users, >> When using the "scaling to percent signal change" option in ArtRepair, >> sometimes I get what I want from the files selected and sometimes I don't >> (depending on which files I select). >> >> Why would ArtRepair give this answer: >> >> /Direct calls to spm_defauts are deprecated./ >> /Please use spm('Defaults',modality) or spm_get_defaults instead./ >> /Automatically estimated peak and contrast scaling./ >> / Normalizing by beta_0008.img/ >> /Peak value = 4.97/ >> /Contrast sum = 0.996/ >> /Mean value = NaN/ >> /(peak/contrast_sum)*100/bmean = /*/NaN/* >> / >> / >> /ans =/ >> / >> / >> / 4.9700 0.9960 /*/ NaN/* >> >> All files follow the same path so I don't think that's the problem. Does >> anybody know why this is happening and how I can fix this? >> >> Thank you, >> Pilar A. >> > --00163683195045f1c4049d5b2847 Content-Type: text/html; charset=UTF-8 Content-Transfer-Encoding: quoted-printable I have ArtRepair v4. Isn't this the latest version?

On Mon, Feb 28, 2011 at 11:36 AM, Chris Watson <[log in to unmask]> wrote:
I think that was a bug in an older version of ArtRepair. Do you have the latest version?


Pilar Archila-Suerte wrote:
SPM Users,
When using the "scaling to percent signal change" option in ArtRepair, sometimes I get what I want from the files selected and sometimes I don't (depending on which files I select).

Why would ArtRepair give this answer:

/Direct calls to spm_defauts are deprecated./
/Please use spm('Defaults',modality) or spm_get_defaults instead./
/Automatically estimated peak and contrast scaling./
/ Normalizing by beta_0008.img/
/Peak value    = 4.97/
/Contrast sum  = 0.996/
/Mean value    = NaN/
/(peak/contrast_sum)*100/bmean  = /*/NaN/*
/
/
/ans =/
/
/
/    4.9700    0.9960    /*/   NaN/*

 All files follow the same path so I don't think that's the problem. Does anybody know why this is happening and how I can fix this?

Thank you,
Pilar A.





--00163683195045f1c4049d5b2847-- ========================================================================Date: Mon, 28 Feb 2011 12:47:00 -0500 Reply-To: Jason Steffener <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Jason Steffener <[log in to unmask]> Subject: matlabbatch "decode dependencies" MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Message-ID: <[log in to unmask]> Dear All, Hello all. I am trying to create some provenance info from an SPM batch file. So I would like to take an SPM job file and read through it to pull out the different steps, the data and the parameters. I have no problem doing this EXCEPT where I have specified some dependencies. I am having trouble decoding what the dependencies refer to. Essentially if I have the following steps: Realign << Input data Reslice >> Output data smooth << Output data from reslice I would like the following: Step1 Realign input data: FILENAME parameters :XX Step2 Reslice input data: output from Step 1 output data: rFILENAME parameters: XX Step3 Smooth input data: rFILENAME output data: srFILENAME parameters: XX And ideas? Or if someone can point me to the code that translates the dependencies in the job file into something I can figure out, that would also be great. Thank you, Jason -- Jason Steffener, Ph.D. Department of Neurology Columbia University http://www.cogneurosci.org/steffener.html ========================================================================Date: Mon, 28 Feb 2011 14:08:11 +0100 Reply-To: Alexander Hammers <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Alexander Hammers <[log in to unmask]> Subject: Re: question on VOI analysis Comments: To: sarika cherodath <[log in to unmask]> In-Reply-To: <[log in to unmask]> Mime-Version: 1.0 (Apple Message framework v1082) Content-Type: multipart/mixed; boundary=Apple-Mail-79-616227633 Message-ID: <[log in to unmask]> --Apple-Mail-79-616227633 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain; charset=us-ascii Dear Sarika, How did you define the VOI(s)? If they are in MNI space as your second level implies, then you're applying one VOI to all the subjects... and this will unsurprisingly have the same volume in all. I don't know what kind of data you have - it sounds like fMRI. An approximation of individual volumetrics would be to backtransform your standard space VOIs into individual space - if you've used Unified Segmentation for your MRI spatial normalisation, then the *inv_seg_sn.mat file can accomplish this. Such a procedure's accuracy will be limited by 1) the quality and provenience of your standard space VOI (see our recent thread on single-subject vs multi-subject atlases) and 2) the low-ish number of degrees of freedom of the transformation for standard normalisation and Unified Segmentation. Point #2 should be improve-able if you use DARTEL. The gold standard for just one particular area would be to devise a protocol, check the reliability of results and ideally their veracity, and then outline those areas by hand in your subjects. Hope this helps, Best wishes, Alexander ----------------------------- Alexander Hammers, MD PhD --Apple-Mail-79-616227633 Content-Disposition: inline; filename=image.png Content-Type: image/png; name="image.png" Content-Transfer-Encoding: base64 iVBORw0KGgoAAAANSUhEUgAAALAAAAA6CAIAAACf/kS3AAAgAElEQVR4Ae2ceZxVxbH4+2x3mXtn hhmG2cFhF8GYKLKoEX9KDD81RiCaRY1LNL9sRhOXmBhjjJo8RNREn8a4JmqIAU2UKCQmGhcERRZZ BEEWYdgZmJm7nv19+zZcBh0igx/+ePymxUOfPtXV1VXVVdXVfdHCMBTdpZsDezig76l0/93NAcmB boXo1oN9ONCtEPuwo/ulWyG6dWAfDhxahbCFcAoxqye8vMgI4YpAhME+FBzQixvupLsn+3p+iwh5 5njuv6RzwuW74wvhMS5Pl2p3+VgOaId2lxHaIvSEowsjLjQiFtvVXV4MEf9YyjoCIEtb5ErcuFSF iJ0JI0lNM3xHGJGOYHvreSFiKF9OBGW+KYzAdXTNEDp/9sJ01zrjwKFlkBdGhZ+wY7pt+oL/dMsS UUNEO6PkP7UZvigJ457li0igeVq5VC6RN/ZrInw5giXcMscUaWySjmaYBhR0l4/jwKFVCE1khWVH 83rUMzJRlrcubCvX9WXqaCG+RpNOwNVN08ll9FBE9u97NE9IyxRtdcOg3E9rXlmEJo/W7vIxHDi0 CqHrJakgKiJWxhJWKMycsKMiHhBadK1E9KxvCMM0867t4zTiCTRED639YfEsW9Ah08PXskKLpU0A 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H8SOlH35yxt56M1FS3n6QZPJfX+ZmcZ6GJyERQrWoVshuszg/20dCCBCg1/ykZPk4r+6HUzqmjxF wYkU3AkHJwT+aExhcoet3+i2EEp58QicZGEhCCzxF/JaM6cZAdu9wiF44MrNKt5EXnw+bHcYkhWH 9eSUrA/kaXgut3zIALF/4MxbbsXlDxC40kFv9IBL8VRwJDI5LBsO29IdVB62oj24iXVbiIPj22Hb q1shDlvRHtzEuhXi4Ph22PbqVojDVrQHN7H/AWFrGkuL8nFSAAAAAElFTkSuQmCC --Apple-Mail-79-616227633 Content-Transfer-Encoding: quoted-printable Content-Type: text/plain; charset=windows-1252 Chair in Functional Neuroimaging Neurodis Foundation http://www.fondation-neurodis.org/ Postal Address: CERMEP Imagerie du Vivant Hpital Neurologique Pierre Wertheimer 59 Boulevard Pinel, 69003 Lyon, France Telephone +33-(0)4-72 68 86 34 Fax +33-(0)4-72 68 86 10 Email [log in to unmask];[log in to unmask] --------------------------------- Other affiliations: Visiting Reader; Honorary Consultant Neurologist Division of Neuroscience and Mental Health, Faculty of Medicine Imperial College London, UK --------------------------------- Honorary Reader in Neurology; Honorary Consultant Neurologist Department of Clinical and Experimental Epilepsy National Hospital for Neurology and Neurosurgery/ Institute of Neurology, University College London, UK On 28 Feb 2011, at 10:11, sarika cherodath wrote: > > Hi SPMers, > > I have been trying to perform VOI analysis to obtain signal changes at a particular area for individual subjects in the dataset, so as to make correlations with behavioral scores. When i tried to calculate the values, SPM returns the same value for all subjects! Can anybody explain why this might be? The dataset has been analysed at second level and then moved to another directory (along with first level data). Is it possible that SPM is not able to access the data because of the path change?? > > Thanks in advance, > -- > Sarika Cherodath > Graduate Student > National Brain Research Centre > Manesar, Gurgaon -122050 > India > --Apple-Mail-79-616227633-- ========================================================================Date: Mon, 28 Feb 2011 15:14:22 -0500 Reply-To: Jeffrey West <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Jeffrey West <[log in to unmask]> Subject: question regarding flexible factorial model Mime-Version: 1.0 Content-Type: multipart/alternative; boundary="=__Part4569690E.0__=" Message-ID: <[log in to unmask]> This is a MIME message. If you are reading this text, you may want to consider changing to a mail reader or gateway that understands how to properly handle MIME multipart messages. --=__Part4569690E.0__Content-Type: text/plain; charset=US-ASCII Content-Transfer-Encoding: quoted-printable Hello. I have question relating to setting up a flexible factorial model with 2 groups, each group has 4 conditions. I have 3 factors: 1 = subject (independent, variance equal), 2 = group (independent, variance not equal), 3 = condition (not independent, variance equal) For the subject level, I entered in 20 subjects, for each subject, I entered in the the 4 scans: con_image 1,2,3,4. For conditions, I entered 1 2 3 4. Once all 20 subjects were completed, I entered 3 main effects, and interaction: main effect: 1, main effect: 2, main effect: 3, interaction: 2 3. The model did not run and I got the following error message: Running job #2 ----------------------------------------------------------------------- Running 'Factorial design specification' Failed 'Factorial design specification' Index exceeds matrix dimensions. In file "C:\Documents and Settings\JWest\Desktop\spm8\config\spm_run_factorial_design.m" (v3067), function "spm_run_factorial_design" at line 482. The following modules did not run: Failed: Factorial design specification I feel like the error is in the subject level: either the scan or the conditions. I do not feel like the conditions step is correct. Can anyone please explain what I did wrong setting up my model. Thank you for any suggestions. Jef Jeffrey West, M.A. Research Analyst Maryland Psychiatric Research Center Baltimore, Maryland 21228-0247 Phone: 410-402-6018 email: [log in to unmask] --=__Part4569690E.0__Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Content-Description: HTML
Hello.
 
I have question relating to setting up a flexible factorial model with 2 groups, each group has 4 conditions.
 
I have 3 factors: 1 = subject (independent, variance equal), 2 = group (independent, variance not equal), 3 = condition (not independent, variance equal)
 
For the subject level, I entered in 20 subjects, for each subject, I entered in the the 4 scans: con_image 1,2,3,4. For conditions, I entered 1 2 3 4. Once all 20 subjects were completed, I entered 3 main effects, and interaction: main effect: 1, main effect: 2, main effect: 3, interaction: 2 3.
 
The model did not run and I got the following error message:
 
Running job #2
-----------------------------------------------------------------------
Running 'Factorial design specification'
Failed  'Factorial design specification'
Index exceeds matrix dimensions.
In file "C:\Documents and Settings\JWest\Desktop\spm8\config\spm_run_factorial_design.m" (v3067), function "spm_run_factorial_design" at line 482.
 
The following modules did not run:
Failed: Factorial design specification
 
I feel like the error is in the subject level: either the scan or the conditions. I do not feel like the conditions step is correct. Can anyone please explain what I did wrong setting up my model.
 
Thank you for any suggestions.
 
Jef
 
 
Jeffrey West, M.A.
Research Analyst
Maryland Psychiatric Research Center
Baltimore, Maryland 21228-0247
Phone: 410-402-6018
email: [log in to unmask]
 
 
--=__Part4569690E.0__=-- ========================================================================Date: Tue, 1 Mar 2011 09:17:07 +1300 Reply-To: Ehsan Negahbani <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Ehsan Negahbani <[log in to unmask]> Subject: Unsubscribe me please MIME-Version: 1.0 Content-Type: multipart/alternative; boundaryMessage-ID: <[log in to unmask]> --0022150475f729946e049d5d5d2c Content-Type: text/plain; charset=ISO-8859-1 -- Ehsan --0022150475f729946e049d5d5d2c Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable

--
Ehsan
--0022150475f729946e049d5d5d2c-- ========================================================================Date: Mon, 28 Feb 2011 22:28:55 +0000 Reply-To: Vladimir Litvak <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Vladimir Litvak <[log in to unmask]> Subject: Re: spm_eeg_convert2scalp Comments: To: Erick Britis Ortiz <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Message-ID: [log in to unmask]> Hi Erick, SPM uses the same algorithm as Fieldtrip to generate a layout from the sensor array so it should be quite similar, just the convention for representing it is slightly different. I don't know what exactly the problem is so it's hard for me to advise you. In principle you can use the GUI functionality in Prepare or your own script to generate any layout you like and then load it as a channel template file via Prepare (this is a mat-file, there is an example for CTF in EEGTemplates). Best, Vladimir On Mon, Feb 28, 2011 at 10:22 PM, Erick Britis Ortiz <[log in to unmask]> wrote: > > Hi Vladimir, > > I have been using spm_eeg_convert2images to transform my MEG frequency > analysis results to image volumes and run statistics. The objective > being to determine lateralization in language (in children) by frequency. > > I assumed that spm_eeg_convert2scalp would use a standard 2D layout ( > la Fieldtrip), and when I checked, this is not true. This makes > lateralization studies, for instance, much more difficult, and I could > think of others. What is the advantage? > > My guess was that setting D.channels.X_plot2D and Y_plot2D to empty > would generate a default arrangement, but this also did not work. Could > you shed some light at the issue? > > Best, > Erick > > ========================================================================Date: Mon, 28 Feb 2011 23:08:58 +0000 Reply-To: Vladimir Litvak <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Vladimir Litvak <[log in to unmask]> Subject: Re: spm_eeg_convert2scalp Comments: To: Erick Britis Ortiz <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: text/plain; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Message-ID: <[log in to unmask]> These 2D locations are created by projecting 3D locations represented in head coordinates so the differences you find are due to different head positions of your subjects in the helmet. This is by design, but you also can load a standard channel template file for all your subjects. Vladimir On Mon, Feb 28, 2011 at 10:55 PM, Erick Britis Ortiz <[log in to unmask]> wrote: > > Thank you as always for the prompt response! > > For you to know at least what I am talking about, a picture is attached > with the projected MEG sensors (colored by region) in my 22 subjects. > Left is greenish, right is reddish. > > The problem is that I see no reason for the MEG sensors not to have > simply a standard position. In the Fieldtrip plots, they have (for > example, in CTF151.lay). I will follow your advice, no matter. But this > is a bit dangerous in the general case, don't you think? As I said, I > just do not know if it is by design, else I could "fix" it. > > Best, > Erick > > On 2011-02-28 23:28, Vladimir Litvak wrote: >> Hi Erick, >> >> SPM uses the same algorithm as Fieldtrip to generate a layout from the >> sensor array so it should be quite similar, just the convention for >> representing it is slightly different. I don't know what exactly the >> problem is so it's hard for me to advise you. In principle you can use >> the GUI functionality in Prepare or your own script to generate any >> layout you like and then load it as a channel template file via >> Prepare (this is a mat-file, there is an example for CTF in >> EEGTemplates). >> >> Best, >> >> Vladimir >> >> >> >> On Mon, Feb 28, 2011 at 10:22 PM, Erick Britis Ortiz >> <[log in to unmask]> wrote: >>> >>> Hi Vladimir, >>> >>> I have been using spm_eeg_convert2images to transform my MEG frequency >>> analysis results to image volumes and run statistics. The objective >>> being to determine lateralization in language (in children) by frequency. >>> >>> I assumed that spm_eeg_convert2scalp would use a standard 2D layout ( >>> la Fieldtrip), and when I checked, this is not true. This makes >>> lateralization studies, for instance, much more difficult, and I could >>> think of others. What is the advantage? >>> >>> My guess was that setting D.channels.X_plot2D and Y_plot2D to empty >>> would generate a default arrangement, but this also did not work. Could >>> you shed some light at the issue? >>> >>> Best, >>> Erick >>> >>> >> > > ========================================================================Date: Mon, 28 Feb 2011 18:34:38 -0500 Reply-To: Pieter van de Vijver <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Pieter van de Vijver <[log in to unmask]> Subject: Re: question regarding flexible factorial model Comments: To: Jeffrey West <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/alternative; boundaryaec51a894a8f7f93049d601f97 Message-ID: <[log in to unmask]> --bcaec51a894a8f7f93049d601f97 Content-Type: text/plain; charset=ISO-8859-1 Hi Jeff, You should enter conditions for subjects in a nscans x factor matrix. The rows are your scans (4 in your case) and the columns indicate the factors (2, one for group and one for condition, subject is automatically modelled). So for a subject in group 2 with scans for all four conditions you would need: [2 1 2 2 2 3 2 4] Make sure your scans are entered in the right order! Also, main effect for subjects doesn't need to be specified, this is done automatically (this is because you chose 'Subjects' at the 'Specify Subjects or all Scans & Factors'). Good luck, Pieter On Mon, Feb 28, 2011 at 3:14 PM, Jeffrey West <[log in to unmask]>wrote: > Hello. > > I have question relating to setting up a flexible factorial model with 2 > groups, each group has 4 conditions. > > I have 3 factors: 1 = subject (independent, variance equal), 2 = group > (independent, variance not equal), 3 = condition (not independent, variance > equal) > > For the subject level, I entered in 20 subjects, for each subject, I > entered in the the 4 scans: con_image 1,2,3,4. For conditions, I entered 1 2 > 3 4. Once all 20 subjects were completed, I entered 3 main effects, and > interaction: main effect: 1, main effect: 2, main effect: 3, interaction: 2 > 3. > > The model did not run and I got the following error message: > > *Running job #2 > ----------------------------------------------------------------------- > Running 'Factorial design specification' > Failed 'Factorial design specification' > Index exceeds matrix dimensions. > In file "C:\Documents and > Settings\JWest\Desktop\spm8\config\spm_run_factorial_design.m" (v3067), > function "spm_run_factorial_design" at line 482.* > > *The following modules did not run: > Failed: Factorial design specification* > ** > I feel like the error is in the subject level: either the scan or the > conditions. I do not feel like the conditions step is correct. Can anyone > please explain what I did wrong setting up my model. > > Thank you for any suggestions. > > Jef > > > Jeffrey West, M.A. > Research Analyst > Maryland Psychiatric Research Center > Baltimore, Maryland 21228-0247 > Phone: 410-402-6018 > email: [log in to unmask] > > > --bcaec51a894a8f7f93049d601f97 Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Hi Jeff,

You should enter conditions for subjects in a nscans x factor matrix. The rows are your scans (4 in your case) and the columns indicate the factors (2, one for group and one for condition, subject is automatically modelled).
So for a subject in group 2 with scans for all four conditions you would need:
[2 1
2 2
2 3
2 4]
Make sure your scans are entered in the right order!

Also, main effect for subjects doesn't need to be specified, this is done automatically (this is because you chose 'Subjects' at the 'Specify Subjects or all Scans & Factors').

Good luck,

Pieter


On Mon, Feb 28, 2011 at 3:14 PM, Jeffrey West <[log in to unmask]> wrote:
Hello.
I have question relating to setting up a flexible factorial model with 2 groups, each group has4 conditions.
I have 3 factors: 1 = subject (independent, variance equal), 2 = group (independent, variance not equal), 3 = condition (not independent, variance equal)
For the subject level, I entered in 20 subjects, for each subject, I entered in the the 4 scans: con_image 1,2,3,4. For conditions, I entered 1 2 3 4. Once all 20 subjects were completed, I entered 3 main effects, and interaction: main effect: 1, main effect: 2, main effect: 3, interaction: 2 3.
The model did not run and I got the following error message:
Running job #2
-----------------------------------------------------------------------
Running 'Factorial design specification'
Failed 'Factorial design specification'
Index exceeds matrix dimensions.
In file "C:\Documents and Settings\JWest\Desktop\spm8\config\spm_run_factorial_design.m" (v3067), function "spm_run_factorial_design" at line 482.
The following modules did not run:
Failed: Factorial design specification
I feel like the error is in the subject level: either the scan or the conditions. I do not feel like the conditions step is correct. Can anyone please explain what I did wrong setting up my model.
Thank you for any suggestions.
Jef
Jeffrey West, M.A.
Research Analyst
Maryland Psychiatric Research Center
Baltimore, Maryland 21228-0247
Phone: 410-402-6018
email: [log in to unmask]

--bcaec51a894a8f7f93049d601f97-- ========================================================================Date: Mon, 28 Feb 2011 18:38:06 -0500 Reply-To: Pieter van de Vijver <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: Pieter van de Vijver <[log in to unmask]> Subject: Re: question regarding flexible factorial model Comments: To: Jeffrey West <[log in to unmask]> In-Reply-To: <[log in to unmask]> MIME-Version: 1.0 Content-Type: multipart/alternative; boundarye6ba6e8996ee354c049d602b47 Message-ID: <[log in to unmask]> --90e6ba6e8996ee354c049d602b47 Content-Type: text/plain; charset=ISO-8859-1 Sorry, small correction. Main effect for subjects DOES need to be specified. Pieter On Mon, Feb 28, 2011 at 6:34 PM, Pieter van de Vijver <[log in to unmask]>wrote: > Hi Jeff, > > You should enter conditions for subjects in a nscans x factor matrix. The > rows are your scans (4 in your case) and the columns indicate the factors > (2, one for group and one for condition, subject is automatically > modelled). > So for a subject in group 2 with scans for all four conditions you would > need: > [2 1 > 2 2 > 2 3 > 2 4] > Make sure your scans are entered in the right order! > > Also, main effect for subjects doesn't need to be specified, this is done > automatically (this is because you chose 'Subjects' at the 'Specify Subjects > or all Scans & Factors'). > > Good luck, > > Pieter > > > On Mon, Feb 28, 2011 at 3:14 PM, Jeffrey West <[log in to unmask]>wrote: > >> Hello. >> >> I have question relating to setting up a flexible factorial model with 2 >> groups, each group has 4 conditions. >> >> I have 3 factors: 1 = subject (independent, variance equal), 2 = group >> (independent, variance not equal), 3 = condition (not independent, variance >> equal) >> >> For the subject level, I entered in 20 subjects, for each subject, I >> entered in the the 4 scans: con_image 1,2,3,4. For conditions, I entered 1 2 >> 3 4. Once all 20 subjects were completed, I entered 3 main effects, and >> interaction: main effect: 1, main effect: 2, main effect: 3, interaction: 2 >> 3. >> >> The model did not run and I got the following error message: >> >> *Running job #2 >> ----------------------------------------------------------------------- >> Running 'Factorial design specification' >> Failed 'Factorial design specification' >> Index exceeds matrix dimensions. >> In file "C:\Documents and >> Settings\JWest\Desktop\spm8\config\spm_run_factorial_design.m" (v3067), >> function "spm_run_factorial_design" at line 482.* >> >> *The following modules did not run: >> Failed: Factorial design specification* >> ** >> I feel like the error is in the subject level: either the scan or the >> conditions. I do not feel like the conditions step is correct. Can anyone >> please explain what I did wrong setting up my model. >> >> Thank you for any suggestions. >> >> Jef >> >> >> Jeffrey West, M.A. >> Research Analyst >> Maryland Psychiatric Research Center >> Baltimore, Maryland 21228-0247 >> Phone: <410-402-6018>410-402-6018 >> email: [log in to unmask] >> >> >> > > --90e6ba6e8996ee354c049d602b47 Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Sorry, small correction. Main effect for subjects DOES need to be specified.

Pieter

On Mon, Feb 28, 2011 at 6:34 PM, Pieter van de Vijver <[log in to unmask]> wrote:
Hi Jeff,

You should enter conditions for subjects in a nscans x factor matrix. The rows are your scans (4 in your case) and the columns indicate the factors (2, one for group and one for condition, subject is automatically modelled).
So for a subject in group 2 with scans for all four conditions you would need:
[2 1
2 2
2 3
2 4]
Make sure your scans are entered in the right order!

Also, main effect for subjects doesn't need to be specified, this is done automatically (this is because you chose 'Subjects' at the 'Specify Subjects or all Scans & Factors').

Good luck,

Pieter


On Mon, Feb 28, 2011 at 3:14 PM, Jeffrey West <[log in to unmask]> wrote:
Hello.
I have question relating to setting up a flexible factorial model with 2 groups, each group has4 conditions.
I have 3 factors: 1 = subject (independent, variance equal), 2 = group (independent, variance not equal), 3 = condition (not independent, variance equal)
For the subject level, I entered in 20 subjects, for each subject, I entered in the the 4 scans: con_image 1,2,3,4. For conditions, I entered 1 2 3 4. Once all 20 subjects were completed, I entered 3 main effects, and interaction: main effect: 1, main effect: 2, main effect: 3, interaction: 2 3.
The model did not run and I got the following error message:
Running job #2
-----------------------------------------------------------------------
Running 'Factorial design specification'
Failed 'Factorial design specification'
Index exceeds matrix dimensions.
In file "C:\Documents and Settings\JWest\Desktop\spm8\config\spm_run_factorial_design.m" (v3067), function "spm_run_factorial_design" at line 482.
The following modules did not run:
Failed: Factorial design specification
I feel like the error is in the subject level: either the scan or the conditions. I do not feel like the conditions step is correct. Can anyone please explain what I did wrong setting up my model.
Thank you for any suggestions.
Jef
Jeffrey West, M.A.
Research Analyst
Maryland Psychiatric Research Center
Baltimore, Maryland 21228-0247
Phone: 410-402-6018
email: [log in to unmask]


--90e6ba6e8996ee354c049d602b47-- ========================================================================Date: Mon, 28 Feb 2011 18:44:34 -0500 Reply-To: John Fredy <[log in to unmask]> Sender: "SPM (Statistical Parametric Mapping)" <[log in to unmask]> From: John Fredy <[log in to unmask]> Subject: sparse data analysis MIME-Version: 1.0 Content-Type: multipart/alternative; boundaryMessage-ID: <[log in to unmask]> --0016364991e7155337049d6043e2 Content-Type: text/plain; charset=ISO-8859-1 Hello all, I have recorded 80 volumes in a block design experiment with a TR of 6 seconds where 3 seconds are silence, the machine is silence, and the other 3 seconds are used for the adquisition. In the 3 seconds of machine silence I present a stimulus, 0.5 seconds later of the begins of the silence, with an aproximated duration of 1.5 seconds What is the best strategy for processing this data? Regards John Ochoa Universidad de Antioquia --0016364991e7155337049d6043e2 Content-Type: text/html; charset=ISO-8859-1 Content-Transfer-Encoding: quoted-printable Hello all, I have recorded 80 volumes in a block design experiment with a TR of 6 seconds where 3 seconds are silence, the machine is silence, and the other 3 seconds are used for the adquisition. In the 3 seconds of machine silence I present a stimulus, 0.5 seconds later of the begins of the silence, with an aproximated duration of 1.5 seconds

What is the best strategy for processing this data?

Regards

John Ochoa
Universidad de Antioquia
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