Oh, yes, I was thinking you were starting at 1 not 0. Sorry about that.
doug

On 03/21/2013 12:45 PM, preci...@nmr.mgh.harvard.edu wrote:
> So, to clarify I got the number of the acquisitions that I want to exclude
> from an fs-fast output file: fmcpr.dat in .../project/session/bold/008/
>
> This file starts with scan number 0. So if
> Scan 0 is seconds 0, 1, 2
> Scan 1 is seconds 3, 4, 5
> .....
> Shouldn't then;
> Scan 134 be 402, 403, 404
>
>
> -Ronny
>
>
>> 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
>>> _______________________________________________
>>> Freesurfer mailing list
>>> 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
>> FileDrop: www.nmr.mgh.harvard.edu/facility/filedrop/index.html
>> Outgoing: ftp://surfer.nmr.mgh.harvard.edu/transfer/outgoing/flat/greve/
>>
>> _______________________________________________
>> Freesurfer mailing list
>> 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
FileDrop: www.nmr.mgh.harvard.edu/facility/filedrop/index.html
Outgoing: ftp://surfer.nmr.mgh.harvard.edu/transfer/outgoing/flat/greve/

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