Yes, but none of these regions is exactly what's typically called IFG, so to 
limit comparisons I was wondering if you knew of a reason that one of them 
should be considered a locus of response inhibition based on your data that 
would warrant using that region as an a priori ROI to look for neural 
correlates of differences in response inhibition.

________________________________
From: Glasser, Matthew <glass...@wustl.edu>
Sent: Monday, September 26, 2016 6:22:50 PM
To: Michael F.W. Dreyfuss; hcp-users@humanconnectome.org; NEUROSCIENCE tim
Subject: Re: [HCP-Users] ROIs and Betas from Cifti Data

Can’t you just click which area is under that cluster?  I didn’t realize you 
already had the data registered.

Peace,

Matt.

From: "Michael F.W. Dreyfuss" 
<mid2...@med.cornell.edu<mailto:mid2...@med.cornell.edu>>
Date: Monday, September 26, 2016 at 4:09 PM
To: Matt Glasser <glass...@wustl.edu<mailto:glass...@wustl.edu>>, 
"hcp-users@humanconnectome.org<mailto:hcp-users@humanconnectome.org>" 
<hcp-users@humanconnectome.org<mailto:hcp-users@humanconnectome.org>>, Timothy 
Coalson <tsc...@mst.edu<mailto:tsc...@mst.edu>>
Subject: Re: [HCP-Users] ROIs and Betas from Cifti Data


Thank you,


I've attached an image with a dot on the cluster I'm interested in. I could 
send you the dscalar file too, but prefer not to distribute to the whole 
listserv.


Since we have a priori hypotheses about the IFG being involved in this task (it 
is a go/nogo task), I want test for an effect specifically in that region 
similar to the one shown that I am seeing. In volumetric analysis I would use 
an anatomically or functionally defined mask and either A) look for a region 
within that mask that survives cluster thresholding to localize where in that 
region is involved or B) test if average betas are different within that region 
between conditions. I was wondering if one of the parcels from your 
parcellation was something you know to be where response inhibition on tasks 
like go/nogo may be localized as a reason for using that parcellation or set of 
parcellations. Otherwise I would be interested in something like a combined 
mask of BA44 and BA45 as representing IFG.


Also, is it possible to do something like TFCE or fdr correction within a 
region like this within palm as that would reduce the area I am looking over 
for an effect and reduce the cluster size needed compared to a whole brain 
analysis?


Thank you,

Michael

________________________________
From: Glasser, Matthew <glass...@wustl.edu<mailto:glass...@wustl.edu>>
Sent: Monday, September 26, 2016 2:18:26 PM
To: Michael F.W. Dreyfuss; NEUROSCIENCE tim
Cc: hcp-users@humanconnectome.org<mailto:hcp-users@humanconnectome.org>
Subject: Re: [HCP-Users] ROIs and Betas from Cifti Data

Is there a surface-based map of this task contrast somewhere that I could look 
at?  Without that I would just be guessing…

Peace,

Matt.

From: "Michael F.W. Dreyfuss" 
<mid2...@med.cornell.edu<mailto:mid2...@med.cornell.edu>>
Date: Monday, September 26, 2016 at 1:13 PM
To: Matt Glasser <glass...@wustl.edu<mailto:glass...@wustl.edu>>, Timothy 
Coalson <tsc...@mst.edu<mailto:tsc...@mst.edu>>
Cc: "hcp-users@humanconnectome.org<mailto:hcp-users@humanconnectome.org>" 
<hcp-users@humanconnectome.org<mailto:hcp-users@humanconnectome.org>>
Subject: Re: [HCP-Users] ROIs and Betas from Cifti Data


Hi Matt, I'm interested in using part of your parcellation to look at response 
inhibition on a go/nogo task. Do you have a sense of which region in your 
parcellation corresponds best to the part of inferior frontal gyrus typically 
implemented in successful nogo response inhibition, and how I could isolate 
that parcel to do an anlysis?


Thank you,

Michael

________________________________
From: Glasser, Matthew <glass...@wustl.edu<mailto:glass...@wustl.edu>>
Sent: Tuesday, September 20, 2016 11:06:10 AM
To: Michael F.W. Dreyfuss; NEUROSCIENCE tim
Cc: hcp-users@humanconnectome.org<mailto:hcp-users@humanconnectome.org>
Subject: Re: [HCP-Users] ROIs and Betas from Cifti Data

As Tim mentions, it sounds like you might want to use a parcellated analysis, 
as this will be more sensitive/powerful and you’ll know exactly what areas you 
are finding.  The HCP’s multi-modal parcellation is available here:

https://balsa.wustl.edu/study/show/RVVG<https://urldefense.proofpoint.com/v2/url?u=https-3A__balsa.wustl.edu_study_show_RVVG&d=DQMF-g&c=lb62iw4YL4RFalcE2hQUQealT9-RXrryqt9KZX2qu2s&r=rPclmYysc_z1plf99IoNsmxWf1JolkKMmL6bXnYFSwg&m=41tIMVdkyw4FbaKBCuAemq30kaX7FtpSn1fT4mnNgb4&s=LSobQp1e_k82tOjzxrgaFuayanqOIOB0FPCI128My64&e=>

Also, the HCP’s task analysis pipeline will allow you to parcellate before 
fitting the GLM, rather than afterwards to get the addition SNR benefits from 
averaging across a parcel.

Peace,

Matt.

From: 
<hcp-users-boun...@humanconnectome.org<mailto:hcp-users-boun...@humanconnectome.org>>
 on behalf of "Michael F.W. Dreyfuss" 
<mid2...@med.cornell.edu<mailto:mid2...@med.cornell.edu>>
Date: Monday, September 19, 2016 at 9:40 PM
To: Timothy Coalson <tsc...@mst.edu<mailto:tsc...@mst.edu>>
Cc: "Michael F.W. Dreyfuss" 
<mid2...@med.cornell.edu<mailto:mid2...@med.cornell.edu>>, 
"hcp-users@humanconnectome.org<mailto:hcp-users@humanconnectome.org>" 
<hcp-users@humanconnectome.org<mailto:hcp-users@humanconnectome.org>>
Subject: Re: [HCP-Users] ROIs and Betas from Cifti Data

Thank you,

Are there any examples available for how to use this, possibly? I have been 
trying to figure these out, but there are a lot of options and  I am just not 
able to decipher how to use these from the help page alone. The errors I am 
getting also do not clarify what I need to do to get the output I am looking 
for.

Before using this kind of multi-band data I had been using afni. To give an 
example of what I would want to do in terms of afni commands (if that’s any 
help), I would have saved all ROIs and then used 3dmaskave to extract mean beta 
weights for a given GLM beta for each subject and then I would relate those 
beta weights so subject’s behavior in R or another stats package.

Definitely agree that there’s not much meaning to a peak coordinate per se. I’m 
just trying to figure out how to report the clusters I am finding. In previous 
reports we would typically focus on broadmann areas or more general regional 
nomenclature (i.e. vmPFC, mid temporal lobe, etc.). Some of the clusters I’m 
finding also cover large areas from motor to visual cortex, so I am trying to 
consider good ways to report that.

At this point I would prefer to use TFCE or some other thresholding method to 
identify contiguous swaths of volumetric and surface activation.

Thank you very much again,
Michael

On Sep 19, 2016, at 6:41 PM, Timothy Coalson 
<tsc...@mst.edu<mailto:tsc...@mst.edu>> wrote:


On Mon, Sep 19, 2016 at 4:51 PM, Michael F.W. Dreyfuss 
<mid2...@med.cornell.edu<mailto:mid2...@med.cornell.edu>> wrote:

Thank you,


How can I turn the ROIs into a label file?

You can use -cifti-find-clusters if you just want spatial contiguity to define 
where ROIs should be considered separate, then use -cifti-label-import to make 
them into a dlabel file.

Also, how can I simply get a list of the ROIs with some information like 
cluster extent and peak voxel to be able to identify what part(s) of the brain 
each ROI is covering?

A single coordinate isn't a faithful representation of the cluster.  You can 
make a figure showing the clusters displayed on the brain (for instance, choose 
two of: beta maps, significance outlines, area outlines), and hopefully also 
provide the unthresholded beta and z maps for others to use.

You can get cluster extent info with -cifti-weighted-stats.

If the question you want to ask is "which areas are involved", you could do a 
parcellated analysis instead of a cluster analysis.

Thank you,

Michael

________________________________
From: Timothy Coalson <tsc...@mst.edu<mailto:tsc...@mst.edu>>
Sent: Monday, September 19, 2016 4:48:28 PM
To: Michael F.W. Dreyfuss
Cc: hcp-users@humanconnectome.org<mailto:hcp-users@humanconnectome.org>
Subject: Re: [HCP-Users] ROIs and Betas from Cifti Data

The wb_command -cifti-weighted-stats command with -mean is probably what you 
want (outputs a number to the command line), though you'll need to have each 
ROI as a separate file and run it separately for each of them.  Alternatively, 
if you turned the ROIs into a label file, you could get -cifti-parcellate to 
make a file where each parcel contains the answer for an ROI.

Tim


On Mon, Sep 19, 2016 at 3:26 PM, Michael F.W. Dreyfuss 
<mid2...@med.cornell.edu<mailto:mid2...@med.cornell.edu>> wrote:

Hello, I have run palm with TFCE on my group level data successfully for a task 
based fMRI study (yay!), and I would like to be able to identify ROIs from my 
cifti data (both surface and volume). I then want to extract subject level beta 
weights for a given condition from those ROIs to relate those betas to behavior 
(offline). Are there simple ways to: 1) identify regions implicated on the 
group level and 2) extract subject-level beta weights from them, such as with 
wb_command?


Thank you,

Michael

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