You can run selxavg3-sess with -per-run and it will give you a different 
output for each run. These results can then be combined in a fixed 
effects analysis using mri_glmfit.
doug

On 05/09/2012 03:09 PM, Caspar M. Schwiedrzik wrote:
> Hi Doug,
> I have done some more debugging of my analysis and tried different 
> filters. If I understand slxavg-sess correctly, the runs are 
> concatenated, and the pcc is computed over all runs.
> Is it possible to run a single subject FFX instead (e.g., by 
> uncommenting lines 205-217, 305-310)?
> Thanks, Caspar
>
> 2012/5/7 Caspar M. Schwiedrzik <cschwie...@rockefeller.edu 
> <mailto:cschwie...@rockefeller.edu>>
>
>     Hi,
>     is it possible that it is a data format problem? I tried forcing
>     fslmaths to give float output using -odt float. This changed
>     mostly the autocorrelations computed during selxavg, but not the pcc.
>     Caspar
>
>
>     2012/5/7 Caspar M. Schwiedrzik <cschwie...@rockefeller.edu
>     <mailto:cschwie...@rockefeller.edu>>
>
>         the cutoff frequencies are 0.0025 Hz and 0.25 Hz.
>         Caspar
>
>         2012/5/7 Douglas N Greve <gr...@nmr.mgh.harvard.edu
>         <mailto:gr...@nmr.mgh.harvard.edu>>
>
>             The mkanalysis command looks ok. I don't know how to
>             interpret those numbers for fslmaths. What are the cutoff
>             frequencies?
>             doug
>
>
>             On 05/07/2012 03:25 PM, Caspar M. Schwiedrzik wrote:
>
>                 Hi Doug,
>                 I use the following command for fslmaths
>                 fslmaths fmc.nii -bptf 200 2 fmcfilt.nii
>
>                 where 200*(TR+2) is 400s, and 2*(TR=2)=4s.
>
>                 and for mkanalysis-sess
>                 -force
>                 -fsd bold
>                 -funcstem fmcfilt
>                 -analysis name
>                 -notask
>                 -tr 2
>                 -runlistfile name
>                 -native
>                 -nskip 5
>                 -mask brain
>                 -tpef name
>                 -taskreg name
>
>                 for debugging, I did not include nuisance regressors.
>                 Caspar
>
>
>                 2012/5/7 Douglas N Greve <gr...@nmr.mgh.harvard.edu
>                 <mailto:gr...@nmr.mgh.harvard.edu>
>                 <mailto:gr...@nmr.mgh.harvard. edu
>                 <mailto:gr...@nmr.mgh.harvard.edu>>>
>
>
>                    What frequencies did you chose for the FSL bandpass
>                 filter? What
>                    is you mkanalysis-sess command?
>
>
>                    On 05/07/2012 02:58 PM, Caspar M. Schwiedrzik wrote:
>
>                        yes
>
>                        2012/5/7 Douglas N Greve
>                 <gr...@nmr.mgh.harvard.edu
>                 <mailto:gr...@nmr.mgh.harvard.edu>
>                 <mailto:gr...@nmr.mgh.harvard. edu
>                 <mailto:gr...@nmr.mgh.harvard.edu>>
>                 <mailto:gr...@nmr.mgh.harvard
>                 <mailto:gr...@nmr.mgh.harvard>. edu
>                 <mailto:gr...@nmr.mgh.harvard. edu
>                 <mailto:gr...@nmr.mgh.harvard.edu>>>>
>
>
>                           Did you regenerate the seeds after filtering?
>
>
>                           On 05/07/2012 02:50 PM, Caspar M.
>                 Schwiedrzik wrote:
>
>                               I have tried analyses with only one seed
>                 time course
>                        (either 1
>                               voxel, mean of a sphere of 1 voxel
>                 radius, or mean of a
>                               functionally defined roi), as well as
>                 several seeds
>                        within the
>                               same design matrix, with the same problem.
>                               All of these analyses did yield higher
>                 pcc when done
>                        without
>                               filtering.
>                               Caspar
>
>                               2012/5/7 Douglas N Greve
>                 <gr...@nmr.mgh.harvard.edu
>                 <mailto:gr...@nmr.mgh.harvard.edu>
>                 <mailto:gr...@nmr.mgh.harvard. edu
>                 <mailto:gr...@nmr.mgh.harvard.edu>>
>                 <mailto:gr...@nmr.mgh.harvard
>                 <mailto:gr...@nmr.mgh.harvard>. edu
>                 <mailto:gr...@nmr.mgh.harvard. edu
>                 <mailto:gr...@nmr.mgh.harvard.edu>>>
>                 <mailto:gr...@nmr.mgh.harvard
>                 <mailto:gr...@nmr.mgh.harvard>
>                 <mailto:gr...@nmr.mgh.harvard
>                 <mailto:gr...@nmr.mgh.harvard>> . edu
>
>
>                 <mailto:gr...@nmr.mgh.harvard
>                 <mailto:gr...@nmr.mgh.harvard>. edu
>                 <mailto:gr...@nmr.mgh.harvard. edu
>                 <mailto:gr...@nmr.mgh.harvard.edu>>>>>
>
>
>                                  Is this doing all of those seeds
>                 simultaneously or
>                        one seed
>                               at a time?
>
>                                  On 05/07/2012 02:25 PM, Caspar M.
>                 Schwiedrzik wrote:
>                 > Hi,
>                 > I am trying to use fslmaths to filter my data before
>                 I plug it
>                                  into a
>                 > resting state analysis. However, once I obtain a pcc
>                 map, all
>                 > correlation coefficients are <0.1, even the
>                 autocorrelation
>                               with the
>                 > seed voxel.
>                 > The data look fine when I open them in Matlab using
>                 MRIread; the
>                 > correlations between individual voxel time courses
>                 obtained in
>                                  Matlab
>                 > is about 0.6.
>                 >
>                 > My analysis stream is as follows:
>                 > a) I filter the data using "fslmaths input -bptf
>                 highpass
>                               lowpass
>                 > output"; from this I obtain a filtered nii.gz file
>                 > b) I extract a seed timecourse from the filtered
>                 data in Matlab
>                 > c) I run mkanalysis-sess with -notask
>                 > d) I run selxavg3-sess
>                 > e) I overlay the pcc.nii
>                 >
>                 > I have tried this with smoothed and unsmoothed data,
>                 with and
>                                  without
>                 > nuisance regressors, with different seeds, with
>                 mri_convert
>                                  after step
>                 > a. It is not a problem with the overlay since the
>                 max values
>                               in pcc
>                 > are all <0.1.
>                 > I noticed that there are some differences in the
>                 nifti header
>                                  (as read
>                 > with MRIread) before and after filtering, but it
>                 seemed to
>                               me that
>                 > they are gone after I used mri_convert.
>                 > I do find much higher correlations with unfiltered data.
>                 > Any advice what could be going wrong here? I am using
>                               Freesurfer 5.1
>                 > and FSL 4.1.9 on Linux.
>                 > Thanks, Caspar
>                 >
>                 >
>                 >
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>                    MGH-NMR Center
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-- 
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MGH-NMR Center
gr...@nmr.mgh.harvard.edu
Phone Number: 617-724-2358
Fax: 617-726-7422

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