I would have a look at PALM’s documentation.  I am not sure.

Peace,

Matt.

From: Lisa Kramarenko 
<lisa.kramare...@gmail.com<mailto:lisa.kramare...@gmail.com>>
Date: Monday, April 10, 2017 at 6:24 AM
To: Matt Glasser <glass...@wustl.edu<mailto:glass...@wustl.edu>>
Cc: "hcp-users@humanconnectome.org<mailto:hcp-users@humanconnectome.org>" 
<hcp-users@humanconnectome.org<mailto:hcp-users@humanconnectome.org>>
Subject: Re: [HCP-Users] Fwd: Help with the group comparison of seed-based FC

Dear Matthew,

thanks again for your answer. Just to clarify, after I run 
-cifti-average-roi–correlation on each participant, do I then merge all the 
.dscalar.nii files for the members of the respective group before comparing the 
groups with PALM? Do I do it with -cifti -concatenate?

thanks for all your help.
best,
Lisa

On 7 April 2017 at 22:07, Glasser, Matthew 
<glass...@wustl.edu<mailto:glass...@wustl.edu>> wrote:

  1.  The order of the pipelines is PreFreeSurfer —> FreeSurfer —> 
PostFreeSurfer —> fMRIVolume —> fMRISurface —> ICA+FIX —> MSMAll —> Analysis.  
MSMAll is not yet officially released, but we have had a few people beta 
testing it.
  2.  The output of -cifti-average-roi–correlation would be a .dscalar.nii 
file.  I would run the command for each participant, as you said you wanted to 
do group level stats (which will be based essentially on the means and 
variances of your group).

Matt.

From: 
<hcp-users-boun...@humanconnectome.org<mailto:hcp-users-boun...@humanconnectome.org>>
 on behalf of Lisa Kramarenko 
<lisa.kramare...@gmail.com<mailto:lisa.kramare...@gmail.com>>
Date: Friday, April 7, 2017 at 9:06 AM
To: "hcp-users@humanconnectome.org<mailto:hcp-users@humanconnectome.org>" 
<hcp-users@humanconnectome.org<mailto:hcp-users@humanconnectome.org>>
Subject: [HCP-Users] Fwd: Help with the group comparison of seed-based FC

Dear Matthew,

thanks for your reply and tips! Naturally, I have a couple more questions.

1. What exactly the order of the pipelines would be? (I am still stuck at the 
functional preprocessing right now, so I'm not that far yet). Would it be both 
functional ones (volume and surface), then ICA+FIX and then MSMAll?

2. I'm sorry but I also didn't quite get the procedure for the 
-cifti-average-roi-correlation. I only have one run per subject so I don't need 
to average the runs.
So when I have the individual outputs after all the above mentioned pipelines 
(.dtseries.nii, right?) do I just use all of them (for one group) with a -cifti 
flag for each as input files in one command or do I run the command for every 
single participant of a group and afterwards merge the outputs? I want to do 
group-level comparison so at some step I need to create group maps. Or am I 
misunderstanding something?

Sorry for such basic confused questions and thanks a lot!

Lisa

On 5 April 2017 at 21:05, Glasser, Matthew 
<glass...@wustl.edu<mailto:glass...@wustl.edu>> wrote:
I recommend you use the MSMAll aligned, ICA+FIX denoised data and use 
wb_command -cifti-average-roi-correlation.  You may or may not chose to do 
something like global signal regression to clean up residual global artifact in 
the data (which ICA+FIX is not designed to remove) depending on if you think 
leaving in global signals will create a bigger positive bias than removing the 
mean of the RSNs will create a negative bias (or just analyze things both 
ways).  We are working on a better solution for this issue that does not 
require removing the mean of the RSNs when cleaning up global artifact (i.e. 
remove the positive bias in connectivity without adding in a negative bias).

You can make a -vol-roi of the hippocampus by extracting it from this file 
${StudyFolder}/${Subject}/MNINonLinear/Results/Atlas_ROIs.2.nii.gz.  I would 
use a -cifti flag for each run of a given subject, but run separate commands 
per subject to generate one dense scalar correlation map per subject.  You can 
then do statistics on these maps (e.g. with the FSL PALM software tool).  You 
may wish to do the Fisher transform on the correlation maps first with 
wb_command -cifti-math “atanh(x)” <output> -var x <input>

Peace,

Matt.

From: 
<hcp-users-boun...@humanconnectome.org<mailto:hcp-users-boun...@humanconnectome.org>>
 on behalf of Lisa Kramarenko 
<lisa.kramare...@gmail.com<mailto:lisa.kramare...@gmail.com>>
Date: Wednesday, April 5, 2017 at 4:40 AM
To: "hcp-users@humanconnectome.org<mailto:hcp-users@humanconnectome.org>" 
<hcp-users@humanconnectome.org<mailto:hcp-users@humanconnectome.org>>
Subject: [HCP-Users] Help with the group comparison of seed-based FC

Hello dear experts,

I am very new to HCP so I am struggling with a lot of confusion and hope you 
can help. I would like to calculate seed-based FC of hippocampus of two groups 
(patients/controls) and to perform a group comparison between them. Now I am 
not sure about how to proceed. I see two possible ways:

1. I could merge .dtseries.nii files for all the subjects in a group with 
cifti-merge to create a group-average dense connectome. However, how do I 
extract the connectivity of the seed of interest and how do I I perform 
statistical analysis on it?
2. Or, if I understand correctly, I can use -cifti-average-roi-correlation. 
However, I am not sure about the inputs. Should I first merge .dtseries.nii 
files for all subjects in a group, take this as <cifti-in> and then extract 
hippocampus from Atlas_ROIs.2.nii.gz with cifti-separate and use it as 
<roi-vol>? Second question is when I managed to run it, what would the output 
be and how do I perform statistical analysis on it?

I would be super grateful if you could clarify what the right way is and give 
me a short step-by-step of how to do a seed-based group-level analysis.

Thanks a lot!
Lisa

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Information or other information of a sensitive nature. If you are not the 
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or the taking of any action in reliance on the contents of this information is 
strictly prohibited. If you have received this email in error, please 
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