Hi Ronny,

On 03/20/2013 05:57 PM, preci...@nmr.mgh.harvard.edu wrote:
> Hello all,
> I am starting to run some analysis using fs-fast and I had a few basic
> questions that I couldn't find answers on the wiki/tutorial.
>
> 1) Format of files for mkanalysis-sess -tpexclude tpexclude.dat
> What is the format of the input file for -tpexclude? Is it simply a single
> column of integers representing the seconds that need to be excluded? My
> example, my TR is 3 and I know I want to remove acquisitions 134 and 140
> because of motion. Do I simply need to have a file that has the following
> content?
> 402
> 403
> 404
> 420
> 421
> 422
This is correct, except that time starts at 0. So time point 1 = 0, tp2 
= 3sec, etc. So tp134 = (134-1)*3 = 399, not 402
>
>
> 2) bold data - Resampling to "common space"
> In the preprocessing step, the bold data is resampled to 76x76x93. My data
> is 96x96x50. Does starting with data that is larger than the "common
> space" cause a problem in the analysis?
No
>
> 3) Viewing analysis for individual bold data runs
> When the First level analysis is completed, the resulting files are a
> combination of all of the bold data runs of the session. Is there a way to
> make it so that I can also see the different activity for individual runs
> within the session or does the analysis only do it by combining data for
> all runs within a session?
By default it combines all the runs. If you want to see what it looks 
like in each run, there are two things you can do. First, you can run 
selxavg3-sess with the -run-wise option. This causes it analyze each run 
separately. This the easy way. Second, you could recode your stimulus 
numbers to be run specific. This means you have to create a new analysis 
and specify new contrasts.
doug
>
> Thanks in advance!
> -Ronny
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>
>

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MGH-NMR Center
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