try using mri_convert on the big file, something like
mri_convert f.nii --fsubsample 0 99 1 f.100.nii
This will extract the first 100 time points
doug

On 05/17/2012 04:48 PM, Guthormsen, Amy M wrote:
> Hello,
>
> I would like to use fsfast to analyze retinotopic data that I 
> collected.  I used the traditional 4 stimulus types (clockwise, 
> counterclockwise, expanding, and contracting), but rather than collect 
> each one in its own run, I took data from one long run that contained 
> all the stimuli.  Based on the logs, I can associate the pulse 
> number/dicom file number with a stimulus type.  However, when I tried 
> to just move the sets of dicom files into sub-directories, which I set 
> up as run directories, freesurfer still saw them as belonging to one 
> run (which I assume is taken from meta-data).  My question is, how can 
> I best split up these files so that I can subject them to the 
> FsFastIndividualRetinotopyAnalysis 
> <http://surfer.nmr.mgh.harvard.edu/fswiki/FsFastIndividualRetinotopyAnalysis?action=fullsearch&context=180&value=linkto%3A%22FsFastIndividualRetinotopyAnalysis%22>
>  process?
>
> Thank you,
>
> Amy Guthormsen
>
>
> _______________________________________________
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> Freesurfer@nmr.mgh.harvard.edu
> https://mail.nmr.mgh.harvard.edu/mailman/listinfo/freesurfer

-- 
Douglas N. Greve, Ph.D.
MGH-NMR Center
gr...@nmr.mgh.harvard.edu
Phone Number: 617-724-2358
Fax: 617-726-7422

Bugs: surfer.nmr.mgh.harvard.edu/fswiki/BugReporting
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