Thank you,

The problem was that the computer I was using before had an older version of 
workbench. It works on my current computer.


As far as using

-cifti-label-to-roi

How would that work with files like Human.Brodmann09.32k_fs_LR.dlabel.nii where 
the ROIs in both hemispheres are under the same key? If I want to look at BA44 
in the right hemisphere only, for example, how can I separate it from BA44 in 
the left hemisphere to look at them separately?

Thank you,
Michael


________________________________
From: Timothy Coalson <tsc...@mst.edu>
Sent: Tuesday, September 27, 2016 4:10:15 PM
To: Michael F.W. Dreyfuss
Cc: Burgess, Gregory; hcp-users@humanconnectome.org
Subject: Re: [HCP-Users] ROIs and Betas from Cifti Data

The surface structures in -cifti-separate are much coarser, they represent the 
cifti file organization, not the parcellation areas.  You want CORTEX_LEFT and 
CORTEX_RIGHT for that command to work.  However, the outputs are gifti files, 
not cifti files - it is a format conversion command, and probably not what you 
want to do.

Instead of separating to gifti files, you should use -cifti-label-to-roi on the 
dlabel file to get the areas by name as separate ROIs (as dscalar files), and 
then use -cifti-merge and -cifti-reduce to combine them back into one larger 
ROI.

Tim


On Tue, Sep 27, 2016 at 10:36 AM, Michael F.W. Dreyfuss 
<mid2...@med.cornell.edu<mailto:mid2...@med.cornell.edu>> wrote:
I can get separate the volumetric part of cifti files with a command like:

wb_command -cifti-separate 
ToyNogo_fdr_palm/ToyNogo_results_merged_tstat.dscalar.nii COLUMN -volume 
ACCUMBENS_RIGHT R_Acc_Beta.nii.gz -roi R_NAcc_ROI.nii.gz

But when I try that on surface data I get the error:
wb_command -cifti-separate 
ToyNogo_GlasserParcellation_FLOBS1_fdr_palm/ToyNogo_results_dat_tstat.pscalar.nii
 COLUMN -label R_IFSp_ROI ToyNogo_R_IFSp_Beta.pscalar.nii -roi 
R_IFSp_ROI.plabel.nii

ERROR: unrecognized structure type

The problem seems to be in recognizing the structures name (i.e. R_IFSp_ROI). 
Do you know how I can reference a specific structure or structures with a 
command from a label file, or is there another comparable command you would 
suggest for isolating structures from a label file?

Thank you,
Michael

On Sep 27, 2016, at 10:41 AM, Burgess, Gregory 
<gburg...@wustl.edu<mailto:gburg...@wustl.edu>> wrote:

HCP did not have a task that was geared toward response inhibition. 
Furthermore, although it’s alluring to believe that a single parcel will 
encapsulate all of response inhibition, it’s doubtful.

Why not select a set of parcels in and near IFG, and correct for multiple 
comparisons? Use a meta-analysis as your guide 
(https://urldefense.proofpoint.com/v2/url?u=http-3A__neurosynth.org_analyses_terms_response-2520inhibition_&d=DQIGaQ&c=lb62iw4YL4RFalcE2hQUQealT9-RXrryqt9KZX2qu2s&r=rPclmYysc_z1plf99IoNsmxWf1JolkKMmL6bXnYFSwg&m=Pb-c1m96L6xixMU-j16J-GkC6tGV5lAdGNKy-Tj1ht8&s=DxHCajoqQSf0nIWSDbUHyB6J7F2eax1NswvaNpprHaU&e=
 ). Your statistical power should still benefit from the parcellated analysis 
and reduced number of multiple comparisons, relative to a whole-brain analysis.

--Greg

____________________________________________________________________
Greg Burgess, Ph.D.
Staff Scientist, Human Connectome Project
Washington University School of Medicine
Department of Psychiatry
Phone: 314-362-7864<tel:314-362-7864>
Email: gburg...@wustl.edu<mailto:gburg...@wustl.edu>

On Sep 27, 2016, at 9:26 AM, Michael F.W. Dreyfuss 
<mid2...@med.cornell.edu<mailto:mid2...@med.cornell.edu>> wrote:

I agree, that’s why I was checking in to see if there was a sub parcel you had 
identified as being involved in response inhibition from your tasks, such as 
flanker. There is a lot of background of IFG being involved in response 
inhibition, particularly on go/nogo tasks,, so I was wondering if you had any 
information on specifically where within your parcellation that may be most 
relevant.

On Sep 27, 2016, at 9:57 AM, Harms, Michael 
<mha...@wustl.edu<mailto:mha...@wustl.edu>> wrote:

Just a reminder to be careful here to avoid issues of 
circularity/double-dipping.  You indicated that you had a priori hypotheses 
about IFG involvement, but that doesn’t allow you to then select a particular 
IFG parcel based on your task activation map.  Ideally, you would have selected 
your parcel(s) for analysis prior to ever computing/viewing your activation map 
(unless what you showed was a map from an independent, unrelated set of 
subjects).


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--Greg

____________________________________________________________________
Greg Burgess, Ph.D.
Staff Scientist, Human Connectome Project
Washington University School of Medicine
Department of Psychiatry
Phone: 314-362-7864<tel:314-362-7864>
Email: gburg...@wustl.edu<mailto:gburg...@wustl.edu>


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