It might be that the sequence was not so good. You might try setting the 
prestim to 0 (to match your optseq cmd line).

doug

Yuko Yotsumoto wrote:
> Hi all,
>
> (-------- freesurfer-Darwin-leopard-i686-stable-pub-v4.5.0 --------)
>
> I created sequences for event-related design, using optseq2.
> optseq2 --ntp 150 --tr 2 --psdwin 0 20 1 --ev TG1 2 22 --ev IG1 2 22 --ev CNT 
> 2 22 --ev TGIG 2 22 --ev TGCN 2 22 --nsearch 2000 --focb nCB10pt --nkeep 15 
> --o MO
>
> Then, I did:
> preproc-sess -df sessdirfile -s MO01B -fwhm 5 -fsd bold
> mkanalysis-sess -analysis fmcsm5TER1 -TR 2 -paradigm para.para -designtype 
> event-related -funcstem fmcsm5 -motioncor -runlistfile runfile6 -inorm 
> -polyfit 2 -mcextreg -nconditions 5 -timewindow 20 -prestim 4 -TER 1 
> -autostimdur -force
> mkcontrast-sess -analysis fmcsm5TER1 -contrast AllNull -a 1 -a 2 -a 3 -a 4 -a 
> 5 -c 0
> selxavg3-sess -s MO01B -df sessdirfile -analysis fmcsm5TER1 -overwrite
>
>
> -TER in mkanalysis-sess doesn't seem to be working correct (see the right 
> picture in the link). 
> when I set -TER for mkanalysis-sess to be 2, the plot looks fine (see the 
> left picture in the link).
> http://www.nmr.mgh.harvard.edu/~yuko/images/HDR_TER2_TER1.jpg
>
> Does this mean the sequence I used wasn't good for -TER=1? Or is there a way 
> to make the plot right?
>
> Yuko
>
>
>
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>
>
>   

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

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