So, there is no problem with the two different kind of dm4 from the tow data? 31 and 62 for running TBSS? Thank you for your patience, Rosalia. 2015-10-06 20:54 GMT+02:00 Daniel Kim <[log in to unmask]>: > Looks good. > dim4 on the concatenated data simply indicates that now there are 62 > volumes instead of 31 - doubled because of the concatenation. > > > On 2015-10-06, at 11:37 AM, Rosalia Dacosta Aguayo wrote: > > Hi Daniel, > > This is the report of the data of one of my patients I had no problems > with DTIFIT > > rosalia@rosalia-PORTEGE-Z930:~$ cd > /home/rosalia/Desktop/ESTUDIO_DTI_BIOMARCADORES/PATIENTS/adp_p3 > rosalia@rosalia-PORTEGE-Z930:~/Desktop/ESTUDIO_DTI_BIOMARCADORES/PATIENTS/adp_p3$ > fslsize data.nii.gz > dim1 122 > dim2 122 > dim3 65 > dim4 31 > pixdim1 1.967213 > pixdim2 1.967213 > pixdim3 2.000000 > pixdim4 1.000000 > rosalia@rosalia-PORTEGE-Z930 > :~/Desktop/ESTUDIO_DTI_BIOMARCADORES/PATIENTS/adp_p3 > > And this is the information after doing the new > approach...concatenation....just the steps you describe: > > rosalia@rosalia-PORTEGE-Z930:~$ cd > /home/rosalia/Desktop/ESTUDIO_DTI_BIOMARCADORES/PATIENTS/jmsb_p3 > rosalia@rosalia-PORTEGE-Z930:~/Desktop/ESTUDIO_DTI_BIOMARCADORES/PATIENTS/jmsb_p3$ > fslsize data.nii.gz > dim1 122 > dim2 122 > dim3 65 > dim4 * 62* > pixdim1 1.967213 > pixdim2 1.967213 > pixdim3 2.000000 > pixdim4 1.000000 > rosalia@rosalia-PORTEGE-Z930:~/Desktop/ESTUDIO_DTI_BIOMARCADORES/PATIENTS/jmsb_p3$ > > > Should I be worried with this difference in dim4? > > Rosalia. > > 2015-10-06 20:30 GMT+02:00 Daniel Kim <[log in to unmask]>: > >> Hmm... that does not sound good. >> Maybe start from the beginning. >> - Convert raw data using dcm2nii and obtain two raw dti nii.gz files: >> name them dti1.nii.gz dti2.nii.gz >> - concatenate nii.gz files to form one nii.gz file: fslmerge -t >> dti_merged.nii.gz dti1.nii.gz dti2.nii.gz >> - check dti_merged.nii.gz dimensions: fslsize dti_merged.nii.gz > this >> should give you same x,y,z dimensions as dti1 and dti2 but a larger t >> dimensions (if that's not the case, check dti1 and dti2 to make sure >> nothing was corrupted during conversion). >> - concatenate bvals and bvecs files (as mentioned before) >> - run eddy_correct on dti_merged.nii.gz: eddy_correct dti_merged.nii.gz >> data 0 >> - get brain mask from eddy corrected data.nii.gz: fslroi data nodif 0 1; >> bet nodif nodif_brain -m >> - run dtifit using concatenated bvals and bvecs on data.nii.gz >> >> hope that helps >> >> Danny Kim >> On 2015-10-06, at 11:22 AM, Rosalia Dacosta Aguayo wrote: >> >> Hi Danny, >> >> Now, doing eddy_correct of my concatenated data I see that I have the >> double of slices...I was used to average my two data sets...and now it >> worries me that my ofther files have less directions that those two ones.... >> >> Rosalia. >> >> 2015-10-06 20:18 GMT+02:00 Daniel Kim <[log in to unmask]>: >> >>> No worries. >>> It's also a good practice to look at the data before running dtifit and >>> remove directions that are heavily corrupted with motion or artifacts. >>> >>> Good luck! >>> >>> Danny Kim >>> >>> >>> On 2015-10-06, at 11:07 AM, Rosalia Dacosta Aguayo wrote: >>> >>> Thanks Daniel, >>> >>> This is more clear for me...when you have never done this before you >>> feel very unsure about how to do it. Now it is perfect clear: paste 1 colum >>> of first bvec with the first column of the second bvec and so on..with >>> second and third columns... >>> >>> Thank you a lot. >>> >>> Now I feel more relieve. >>> >>> Warm regards, >>> >>> Rosalia >>> >>> 2015-10-06 19:58 GMT+02:00 Daniel Kim <[log in to unmask]>: >>> >>>> Hi Rosalia >>>> >>>> Concatenating bvals and bvecs: >>>> >>>> Let's say bvals from DTI1: b11 b12 b13 b14 b15 ... b1n >>>> and bvals from DTI2: b21 b22 b23 b24 b25 .... b2n >>>> >>>> then use a text editor to copy and paste DTI2's bvals to form a new >>>> concatenated bvals: b11 b12 b13 ... b1n b21 b22 b23 ... b2n >>>> >>>> Same with bvecs - bvecs from DTI1: >>>> v111 v112 v113 v114 v115 ... v11n >>>> v121 v122 v123 v124 v125 ... v12n >>>> v131 v132 v133 v134 v135 ... v13n >>>> >>>> And bvecs from DTI2: >>>> v211 v212 v213 v214 v215 ... v21n >>>> v221 v222 v223 v224 v225 ... v22n >>>> v231 v232 v233 v234 v235 ... v23n >>>> >>>> Then use a text editor to concatenate bvecs to look like this: >>>> v111 v112 v113 v114 v115 ... v11n v211 v212 v213 v214 v215 ... v21n >>>> v121 v122 v123 v124 v125 ... v12n v221 v222 v223 v224 v225 ... v22n >>>> v131 v132 v133 v134 v135 ... v13n v231 v232 v233 v234 v235 ... v23n >>>> >>>> Hope that helps. >>>> >>>> Danny Kim >>>> >>>> On 2015-10-06, at 10:41 AM, Rosalia Dacosta Aguayo wrote: >>>> >>>> I have concatenated first...but still with doubts regarding bvals and >>>> bvecs files...please which is the next step? could you help me, please? >>>> >>>> 2015-10-06 19:18 GMT+02:00 Tibor Auer <[log in to unmask]>: >>>> >>>>> I call data the output of the merge (before eddy_correct). >>>>> >>>>> >>>>> >>>>> If you concatenate, then concatenation is the first step! >>>>> >>>>> >>>>> >>>>> Vale, >>>>> >>>>> >>>>> >>>>> Auer, Tibor M.D. Ph.D. >>>>> >>>>> MRC Cognition and Brain Sciences Unit >>>>> 15 Chaucer Road >>>>> Cambridge >>>>> CB2 7EF >>>>> >>>>> United Kingdom >>>>> >>>>> Phone/Work: +44-(0)1223-273613 >>>>> >>>>> Mail: [log in to unmask] >>>>> >>>>> >>>>> >>>>> *From:* FSL - FMRIB's Software Library [mailto:[log in to unmask]] *On >>>>> Behalf Of *Rosalia Dacosta Aguayo >>>>> *Sent:* Tuesday, October 06, 2015 6:16 PM >>>>> >>>>> *To:* [log in to unmask] >>>>> *Subject:* Re: [FSL] Having problems with DTIFIT with only two >>>>> subjects... >>>>> >>>>> >>>>> >>>>> Just to know if we are speaking about the same: >>>>> >>>>> I call data to the results of first apply eddy_correct to dti_1 and >>>>> dti_2 and then averaging the results with fslmaths..... >>>>> >>>>> >>>>> >>>>> 2015-10-06 19:13 GMT+02:00 Tibor Auer <[log in to unmask]>: >>>>> >>>>> fslmerge *–t* data data_1 data_2 >>>>> >>>>> should merge data_1 and data_2, so data will contain volumes of both >>>>> both data_1 and data_2. >>>>> >>>>> fslsize data à dim4 should be fslsize data_1 à dim4 + fslsize data_2 à >>>>> dim4 >>>>> >>>>> Vale, >>>>> >>>>> >>>>> >>>>> Auer, Tibor M.D. Ph.D. >>>>> >>>>> MRC Cognition and Brain Sciences Unit >>>>> 15 Chaucer Road >>>>> Cambridge >>>>> CB2 7EF >>>>> >>>>> United Kingdom >>>>> >>>>> Phone/Work: +44-(0)1223-273613 >>>>> >>>>> Mail: [log in to unmask] >>>>> >>>>> >>>>> >>>>> *From:* FSL - FMRIB's Software Library [mailto:[log in to unmask]] *On >>>>> Behalf Of *Rosalia Dacosta Aguayo >>>>> *Sent:* Tuesday, October 06, 2015 6:03 PM >>>>> >>>>> >>>>> *To:* [log in to unmask] >>>>> *Subject:* Re: [FSL] Having problems with DTIFIT with only two >>>>> subjects... >>>>> >>>>> >>>>> >>>>> data or dti_1 and dti_2?? >>>>> >>>>> >>>>> >>>>> 2015-10-06 18:40 GMT+02:00 Tibor Auer <[log in to unmask]>: >>>>> >>>>> fslmerge *–t* data data_1 data_2 >>>>> >>>>> >>>>> >>>>> Vale, >>>>> >>>>> >>>>> >>>>> Auer, Tibor M.D. Ph.D. >>>>> >>>>> MRC Cognition and Brain Sciences Unit >>>>> 15 Chaucer Road >>>>> Cambridge >>>>> CB2 7EF >>>>> >>>>> United Kingdom >>>>> >>>>> Phone/Work: +44-(0)1223-273613 >>>>> >>>>> Mail: [log in to unmask] >>>>> >>>>> >>>>> >>>>> *From:* FSL - FMRIB's Software Library [mailto:[log in to unmask]] *On >>>>> Behalf Of *Rosalia Dacosta Aguayo >>>>> *Sent:* Tuesday, October 06, 2015 4:58 PM >>>>> *To:* [log in to unmask] >>>>> >>>>> >>>>> *Subject:* Re: [FSL] Having problems with DTIFIT with only two >>>>> subjects... >>>>> >>>>> >>>>> >>>>> Dear FSL experts and Michel, >>>>> >>>>> >>>>> Sorry, when I try fslmerge to concatenate the two datasets acquired >>>>> for the same subject in the same scanner.... I write: >>>>> >>>>> fslmerge data dti_1.nii.gz dti_2.nii.gz and nothing happens >>>>> >>>>> It tells the following I do not understand well: >>>>> >>>>> Usage: fslmerge <-x/y/z/t/a/tr> <output> <file1 file2 .......> [tr >>>>> value in seconds] >>>>> >>>>> -t : concatenate images in time >>>>> -x : concatenate images in the x direction >>>>> -y : concatenate images in the y direction >>>>> -z : concatenate images in the z direction >>>>> -a : auto-choose: single slices -> volume, volumes -> 4D (time >>>>> series) >>>>> -tr : concatenate images in time and set the output image tr to >>>>> the final option value >>>>> >>>>> I guess I should use -t option but I am not sure...any one of you >>>>> could help me with this? >>>>> >>>>> Thanks a lot, >>>>> >>>>> Rosalia. >>>>> >>>>> >>>>> >>>>> >>>>> >>>>> 2015-10-06 16:05 GMT+02:00 Rosalia Dacosta Aguayo <[log in to unmask] >>>>> >: >>>>> >>>>> Hi Michael, >>>>> >>>>> >>>>> >>>>> Thank you very much for your reply. >>>>> >>>>> >>>>> >>>>> I will try this option too. There are remaining two new subjects and I >>>>> would like to run TBSS as soon as possible. >>>>> >>>>> >>>>> >>>>> Yours sincerely, >>>>> >>>>> >>>>> >>>>> Rosalia. >>>>> >>>>> >>>>> >>>>> >>>>> >>>>> >>>>> >>>>> 2015-10-06 15:50 GMT+02:00 Harms, Michael <[log in to unmask]>: >>>>> >>>>> >>>>> >>>>> Instead of coregistering/averaging maps after DTIFIT, the more typical >>>>> approach would be to simply concatenate ('fslmerge') the two original runs, >>>>> concatenate the bvals/bvecs files, and then just run eddy_correct and >>>>> dtifit using those concatenated files (i.e., as if all the data was >>>>> collected in a single run in the first place). >>>>> >>>>> >>>>> >>>>> cheers, >>>>> >>>>> -MH >>>>> >>>>> >>>>> >>>>> -- >>>>> >>>>> Michael Harms, Ph.D. >>>>> >>>>> ----------------------------------------------------------- >>>>> >>>>> Conte Center for the Neuroscience of Mental Disorders >>>>> >>>>> Washington University School of Medicine >>>>> >>>>> Department of Psychiatry, Box 8134 >>>>> >>>>> 660 South Euclid Ave. Tel: 314-747-6173 >>>>> >>>>> St. Louis, MO 63110 Email: [log in to unmask] >>>>> >>>>> >>>>> >>>>> *From: *Tibor Auer <[log in to unmask]> >>>>> *Reply-To: *FSL - FMRIB's Software Library <[log in to unmask]> >>>>> *Date: *Tuesday, October 6, 2015 5:38 AM >>>>> *To: *FSL - FMRIB's Software Library <[log in to unmask]> >>>>> *Subject: *Re: [FSL] Having problems with DTIFIT with only two >>>>> subjects... >>>>> >>>>> >>>>> >>>>> Dear Rosalia, >>>>> >>>>> >>>>> >>>>> How did you actually averaged the imagesin step e)? Are you sure there >>>>> was no dimension reduction? Have you checked whether the output data.nii.gz >>>>> is actually a 4D dataset with same amount of volumes as the number of >>>>> entries in the bvals/bvecs. >>>>> >>>>> >>>>> >>>>> However, there are some more conceptual issues: >>>>> >>>>> 1. In step d), you first registered data_1 to data_2* and* >>>>> data_2 to data_1. So at the end, they are not aligned at all! >>>>> >>>>> 2. Which bvals/bvecs have you used? The set from data_1 or from >>>>> data_2? >>>>> >>>>> >>>>> >>>>> And more importantly: >>>>> >>>>> It is not advised to register raw DTI images, because then you disrupt >>>>> the consistency between the geometry of the images and the geometry of the >>>>> bvecs. One solution is to transform the bvecs, as well; but it is also >>>>> suboptimal. >>>>> >>>>> My recommendation is to analyse the two datasets separately without >>>>> any registration, and coregister+average the metric images (e.g. FA maps) >>>>> after DTIFIT. >>>>> >>>>> >>>>> >>>>> Vale, >>>>> >>>>> >>>>> >>>>> Auer, Tibor M.D. Ph.D. >>>>> >>>>> MRC Cognition and Brain Sciences Unit >>>>> 15 Chaucer Road >>>>> Cambridge >>>>> CB2 7EF >>>>> >>>>> United Kingdom >>>>> >>>>> Phone/Work: +44-(0)1223-273613 >>>>> >>>>> Mail: [log in to unmask] >>>>> >>>>> >>>>> >>>>> *From:* Rosalia Dacosta Aguayo [mailto:[log in to unmask] >>>>> <[log in to unmask]>] >>>>> *Sent:* Tuesday, October 06, 2015 11:05 AM >>>>> *To:* FSL - FMRIB's Software Library <[log in to unmask]> >>>>> *Subject:* Having problems with DTIFIT with only two subjects... >>>>> >>>>> >>>>> >>>>> Dear FSL team, >>>>> >>>>> I must be doing something wrong but I can not guess where is the >>>>> problem. I have two groups of 12 subjects. >>>>> >>>>> 1. I have two DTI acquisitions (dti_1 and dti_2) from the same subject >>>>> in the same scanner (the last two subjects to include in the study). And I >>>>> did the following steps in order to prepare my two subjects. >>>>> >>>>> a) From DICOM to NIFTI (dcm2nii) >>>>> >>>>> b) eddy_correct dti_1 data_1 0 >>>>> >>>>> c) eddy_correct dti_2 data_2 0 >>>>> >>>>> d) Here I thing there is the problem...but I do not know to manage >>>>> with them in order to ensure that both images are well aligned. I did the >>>>> following for co-registration of the two images. >>>>> >>>>> >>>>> - flirt -in data_2.nii.gz -ref data_1.nii.gz -out data_2_registered >>>>> -bins 256 -cost corratio -searchrx 0 0 -searchry 0 0 -searchrz 0 0 -dof 6 >>>>> -interp trilinear >>>>> >>>>> - flirt -in data_1.nii.gz -ref data_2_registered.nii.gz -out >>>>> data_1_registered -bins 256 -cost corratio -searchrx 0 0 -searchry 0 0 >>>>> -searchrz 0 0 -dof 6 -interp trilinear >>>>> >>>>> >>>>> >>>>> >>>>> >>>>> e) Averaging of data_1_registered and data_2_registered -out = data >>>>> >>>>> f) Creation of the nodif.nii.gz with fslroi from data >>>>> >>>>> g)Creation of nodif_brain_mask with BET >>>>> >>>>> h) FSL --> DTIFIT Reconstruct diffusion tensors --> specify files >>>>> manually (data, nodif_brain_mask, bvecs and bvals). >>>>> >>>>> *I get the following error message: Erros: Erro: data and bvals / >>>>> bvecs do not contain the same number of entries * >>>>> >>>>> >>>>> >>>>> *I hope I have explained well all I have done in order to facilitate >>>>> the finding of my error...* >>>>> >>>>> With my best regards, >>>>> >>>>> Rosalia. >>>>> >>>>> >>>>> >>>>> >>>>> >>>>> >>>>> >>>>> >>>>> ------------------------------ >>>>> >>>>> The materials in this message are private and may contain Protected >>>>> Healthcare Information or other information of a sensitive nature. 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