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Dear Flavia, You can use the 'Spectrum' option in the time-frequency module. Then if you use scalp x frequency option when exporting to images you will get 3D images. If you use just 'frequency' you'll get 1D images averaged over channels. Best, Vladimir On Sat, Jul 25, 2015 at 1:02 PM, Flavia Di Pietro < [log in to unmask]> wrote: > Dear Vladimir. > > Thanks to your help I was able to assign channel locations to my EEG data. > Thanks also for the SPM UCL videos online - they are extremely useful for > those of us who are so far away! > > I am hoping you might be able to provide me with a bit of guidance. Our > EEG study is very simple - we are measuring eyes open and eyes closed > conditions only. We are measuring this in chronic pain patients and healthy > controls. The reason it so simple is that we are associating the EEG > measures with MR spectroscopy levels. > > So all we really are looking for in the EEG is differences in power. We > hypothesise that the patients will display lower frequency activity, and > peak activity in lower frequency bands, than in controls. Ideally we will > present power in different frequency bands, and also be able to identify > any channels/locations that are different between the two groups. > > As I understand it, the analysis in SPM can be performed in numerous ways > - depending on what it is that you are trying to find and demonstrate in > the data. > > My question is: how do I (or is it possible to) generate results/graphics > of the power across the frequency range in SPM? That is, can I generate > global power spectra graphs with frequency along the x-axis and power along > the y-axis? > > I hope that makes some sense! > > Thanks very much indeed, I look forward to hearing from you. > > Flavia > > > *Flavia Di Pietro, PhD* > Postdoctoral Research Associate > Neural Imaging Laboratory > Sydney Medical School > University of Sydney > Phone: +61 2 9351 6878 > ------------------------------ > *From:* Flavia Di Pietro > *Sent:* 18 May 2015 11:16 > *To:* Vladimir Litvak > *Subject:* RE: [SPM] SPM for EEG > > Hello Vladimir, > > Thanks very much indeed for your email, and for responding to my query so > quickly. > > I am going to try your solution today and I will let you know how it goes! > > Thanks again. > > Kind regards, > > Flavia > > *Flavia Di Pietro, PhD* > Postdoctoral Research Associate > Neural Imaging Laboratory > Sydney Medical School > University of Sydney > Phone: +61 2 9351 6878 > ------------------------------ > *From:* Vladimir Litvak [[log in to unmask]] > *Sent:* 15 May 2015 18:57 > *To:* Flavia Di Pietro > *Cc:* [log in to unmask] > *Subject:* Re: [SPM] SPM for EEG > > Dear Flavia, > > This indeed indicates that the channel locations were not assigned > automatically. There can be several possible reasons for this, the most > common are: > > 1) Your cap (as identified by your channel labels) is not one of those > that can be automatically recognised (extended 10-20, biosemi, ant). > 2) You do use extended 10-20 but with too few electrodes (I think you need > above 10-15 for it to work). > 3) You have an EGI system where there are different caps for the same > channel number so automatic assignment is not possible. > > > The solution in all cases is to load the locations file manually (see > page 100 in the manual http://www.fil.ion.ucl.ac.uk/spm/doc/manual.pdf). > You can try to find your cap in spm/EEGtemplates directory. That could work > for cases 2 and 3 above. If it's not there, you must prepare your own > locations file and load it. Then you should follow the steps described in > the same chapter to coregister (not necessary if you load from > EEGtemplates), project location to 2D, apply and save. > > Best, > > Vladimir > > > On Fri, May 15, 2015 at 8:36 AM, Flavia Di Pietro < > [log in to unmask]> wrote: > >> Hi there, >> >> >> I recently started using SPM for analysis of some EEG data. >> >> >> I have completed (I think!) all necessary pre-processing steps. >> Throughout the process, however, I have noticed that in my ‘Display’ >> function, I am only able to view my channels accurately in the Standard >> mode, but not in the Scalp mode. Specifically, in the Scalp mode, my >> channels are not plotted in the 2D space as they are in the manual (on >> p.360 Version 8 manual) but just in horizontal lines. >> >> >> This makes me think that I have missed a step (i.e. in informing SPM of >> my channel locations, for example) or that some error has occurred. I >> gather if I do not rectify this then I will not be able to do analysis in >> sensory space etc, later on down the track. >> >> >> I wonder if anyone else has had this issue, or can shed any light? >> >> >> Thanks in anticipation! >> >> >> Flavia >> >> *Flavia Di Pietro, PhD* >> Postdoctoral Research Associate >> Neural Imaging Laboratory >> Sydney Medical School >> University of Sydney >> Phone: +61 2 9351 6878 >> > >