Thank you both for the input.
What I'm interested in is defining regions of interest in individual
subjects from a task run. Hence, the parcellated analysis does not seem the
right fit for this application (unless I had individual parcels defined in
some other fashion, e.g. from an individual resting-state parcellation).
A permutation analysis (PALM) cannot be applied on a single subject's data,
with only one run (unless I run a level 1 analysis many times shuffling
conditions within the run?) - I'll take a look at it though for future
reference.
This leaves me with Matt's suggestion of a gradient-based approach. I
remember this from the HCP course indeed, and I was very eager to try it on
my data after seeing the beautiful results Matt was getting using gradients
on task & myelin maps. When I tried running -cifti-gradient on my own
contrast maps (this is not HCP data), the results were not very clear
visually - lots of noise and clear boundaries difficult to detect. Perhaps
I need a little more guidance on getting the gradient approach to work for
ROI definition. Should I do much smoothing on the surface before detecting
gradients? Is there a way in which you post-process the gradient map to
make boundaries clearer? Maybe I should take a look at the methods
published by the Petersen group for RS based parcellation using gradients?
Matt, please let me know the pipeline you would suggest.
Thanks for your help!
- Julien


On Sat, Oct 10, 2015 at 3:08 AM Anderson M. Winkler <wink...@fmrib.ox.ac.uk>
wrote:

> Hi Julien,
>
> Indeed, as Matt said, you can use PALM, which does then a permutation test
> (it is superior to Monte Carlo tests in that MC don't bypass the usual
> assumptions of parametric tests). Of course, if MC tests were better, PALM
> would surely be using them :-)
>
> Currently there are some difficulties with the CIFTI format, though. It
> can read/write dtseries if the Workbench is installed, but the CIFTI
> functions aren't stable and can crash easily. However, PALM can also work
> with FreeSurfer formats and with GIFTI and NIFTI, so that you can convert
> from CIFTI to one of these formats, run the test, then convert back to
> CIFTI using the Workbench tools.
>
> PALM has the ability to take into account the family structure of the HCP
> data, and one of the reasons why it was developed was precisely so that we
> could use permutation tests with HCP.
>
> All the best,
>
> Anderson
>
>
>
>
>
> On 10 October 2015 at 02:16, Glasser, Matthew <glass...@wustl.edu> wrote:
>
>> If you are after area-wise activation in individual subjects, would you
>> be willing to do a parcellated (i.e. area-wise) analysis where you could
>> use something simple like FDR or Bonferroni (and get substantial SNR/power
>> benefits)?  If what you are actually after is to define regions of
>> activation (instead of assessing the statistical significance of the
>> activation in every grayordinate), I wouldn’t use statistical thresholding
>> but instead would use gradients in the effect size map to identify most
>> probably boundaries.
>>
>> In most cases for multiple comparison correction we are recommending
>> people to use FSL’s PALM, but it is permutation-based.
>>
>> Peace,
>>
>> Matt.
>>
>> From: <hcp-users-boun...@humanconnectome.org> on behalf of Julien Dubois
>> <jcrdub...@gmail.com>
>> Date: Friday, October 9, 2015 at 4:53 PM
>> To: "hcp-users@humanconnectome.org" <hcp-users@humanconnectome.org>
>> Subject: [HCP-Users] Cluster-extent thresholding of CIFTI data
>>
>> Dear HCP developers,
>>
>> I'm wondering if you have come up with a good cluster-extent thresholding
>> procedure and implemented it as part of the workbench yet. I have seen a
>> couple of threads here
>> <https://www.mail-archive.com/hcp-users%40humanconnectome.org/msg00893.html>
>> and here
>> <https://www.mail-archive.com/hcp-users%40humanconnectome.org/msg00993.html>
>> re: this issue.
>>
>> One strategy would be to go the Monte Carlo way, considering the two
>> surfaces and the volume separately (cf. Hagler et al 2006
>> <http://www.sciencedirect.com/science/article/pii/S1053811906007919> for
>> the surface, which seems to be implemented in Freesurfer as mri_mcsim
>> <https://surfer.nmr.mgh.harvard.edu/fswiki/BuildYourOwnMonteCarlo> and
>> mri_glmfit-sim for the surface; and of course the very popular AlphaSim
>> <http://afni.nimh.nih.gov/pub/dist/doc/program_help/AlphaSim.html>,
>> superseded by 3dClustSim
>> <http://afni.nimh.nih.gov/pub/dist/doc/program_help/3dClustSim.html>, in
>> AFNI for the volume).
>>
>> Another way would be to go the Random Field Theory route. It's done in
>> the volume in SPM with spm_uc_clusterFDR.m; I'm sure it has been adapted to
>> surface data in some software suites (looks like the matlab code
>> <http://www.math.mcgill.ca/keith/fmristat/toolbox/stat_threshold.m> in
>> this old thread
>> <https://mail.nmr.mgh.harvard.edu/pipermail/freesurfer/2007-August/005881.html>
>> could work).
>>
>> Finally, FSL's randomize is another option that would play well with both
>> surface & volume at the same time, and it seems to be the route you've
>> taken. However (*correct me if I'm wrong*), this is not applicable to
>> single-subject data with one run only, which is one of my interests.
>>
>> Please advise on the current status of development, and whether I need to
>> "hack" my own cluster extent threshold correction based on MC or RFT for
>> CIFTI data (if anyone knows any other good code resources to perform these
>> analyses on surface/volume data, please share!).
>>
>> Thanks,
>> - Julien
>>
>> --
>> Julien Dubois
>> Postdoctoral Scholar
>> California Institute of Technology, Pasadena, CA
>> http://emotion.caltech.edu/~jdubois
>>
>> _______________________________________________
>> HCP-Users mailing list
>> HCP-Users@humanconnectome.org
>> http://lists.humanconnectome.org/mailman/listinfo/hcp-users
>>
>> _______________________________________________
>> HCP-Users mailing list
>> HCP-Users@humanconnectome.org
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>>
>
> --
Julien Dubois
Postdoctoral Scholar
California Institute of Technology, Pasadena, CA
http://emotion.caltech.edu/~jdubois

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