You wouldn’t need matrix2 (or any of the other matrices), just the normal output seeds to targets would be fine.  

You don’t need to do any registration, as I said below, that’s already taken care of for you by the HCP Pipelines.  

If you are using the FDT GUI, I don’t know how to use that (I’ve only used the command line) so you might need to ask on the FSL list about how to use the FDT GUI (though I’d recommend using the command line).  

Peace,

Matt.

From: Linden Parkes <[email protected]>
Date: Tuesday, July 8, 2014 at 6:34 PM
To: Timothy Coalson <[email protected]>
Cc: Matt Glasser <[email protected]>, "[email protected]" <[email protected]>
Subject: Re: [HCP-Users] Probtrackx surface analysis

Hey - Thanks for the crash course on CIFTI. That cleared a few things up for me, but I'm still not sure how to perform the tractography.

Cheers,
Linden


On 9 July 2014 07:14, Timothy Coalson <[email protected]> wrote:
The extension for CIFTI files is .[type].nii, where type is dconn, dtseries, dscalar, dlabel, pconn, or another such specifier.  It ends in .nii because CIFTI uses the NIFTI-2 format, which specifies that the extension must be .nii, but includes a specialized XML header extension instead of using the NIFTI header for spacing info, etc.  Also, we usually gzip our volume files (CIFTI must not be gzipped when used, as we need on-disk random access due to large file sizes), so volume files we distribute will generally end in .nii.gz.

The standard extensions are listed in the specification, see Appendix A in http://www.nitrc.org/forum/attachment.php?attachid=342&group_id=454&forum_id=1955 for the list, but refer to the main specification in http://www.nitrc.org/forum/forum.php?thread_id=4380&forum_id=1955 for how "unknown" works (it still must end in .nii).

Tim



On Mon, Jul 7, 2014 at 11:17 PM, Linden Parkes <[email protected]> wrote:
Ah okay, what is the file extension for CIFTI? I can only see .nii and .gii files.

I tried following those instructions but came unstuck at the “FreeSurfer Registration” step because I could not find the struct.nii.gz file in the HCP datasets.

I’d like to perform striatal segmentation with tractography. Specifically, using subcortical regions such as the accumbens, caudate and putamen. To this end, I figured that using the aparc cortical regions as “Classification targets”  and choosing Matrix2 was most appropriate. One method I thought of trying was just to get binary volume masks for all the cortical regions in aparc and submitting them. But from my reading of the FSL mailing list, it appears that using surfaces as opposed to volumes is preferable. However, as mentioned above, I came unstuck following the FSL user guide.

Hope this makes sense

Cheers,
Linden

——————————————————————

Linden Parkes

PhD Candidate
Monash Clinical & Imaging Neuroscience (MCIN)
School of Psychological Sciences
Monash Biomedical Imaging
Monash University

A: 770 Blackburn Rd, Clayton, 3168, Vic, Australia
T: +61 3 9902 9435  |  0402 516 574

B7AE8BF0-4F0C-4F0B-9BDE-B582B9331FA1

From: Glasser, Matthew [email protected]
Reply: Glasser, Matthew [email protected]
Date: 8 July 2014 at 2:05:55 pm
To: Linden Parkes [email protected]

Cc: [email protected][email protected]
Subject:  Re: [HCP-Users] Probtrackx surface analysis

HCP data is NIFTI/GIFTI/CIFTI, so the particular files you have there are NIFTI volumes.  The GIFTI surface aparc data are in 

${StudyFolder}/${Subject}/MNINonLinear/fsaverage_LR32k/100307.${Hemisphere}.aparc.32k_fs_LR.label.gii


To use them with probtrackx2, you’ll need to follow the instructions here (unfortunately probtrackx2 currently doesn’t support standard GIFTI surfaces and label files):


To know what matrix you should use, I’d need to know a little bit more about the question you are asking.  matrix2 with nodif_brain_mask as the tract space mask will produce an enormous file.

Peace,

Matt.

From: Linden Parkes <[email protected]>
Date: Monday, July 7, 2014 at 5:21 PM
To: Matt Glasser <[email protected]>
Cc: "[email protected]" <[email protected]>
Subject: Re: [HCP-Users] Probtrackx surface analysis

Oh, I thought the HCP data was distributed in cifti and gifti?
As a first pass I wanted to use all surfaces in aparc as classification targets for a few subcortical volumes rois and am a bit unsure on how to do that.
I'd like to pull out matrix2 for this (seems most appropriate). Can I submit the nodif_brain_mask as the "tract space mask" for this?

Cheers
Linden

On 08/07/2014 2:08 am, "Glasser, Matthew" <[email protected]> wrote:
You would use the white matter surfaces in ${StudyFolder}/${Subject}/T1w/fsaverage_LR32k.  The distributed diffusion data are already in T1w space, so you don’t need to provide transformation matrices.  The surface reference image can be any of the files in ${StudyFolder}/${Subject}/T1w or ${StudyFolder}/${Subject}/T1w/Diffusion.  

Neither of the files you mention are CIFTI files.  What cortical regions are you wanting to track from?

Peace,

Matt.

From: Linden Parkes <[email protected]>
Date: Monday, July 7, 2014 at 3:49 AM
To: "[email protected]" <[email protected]>
Subject: [HCP-Users] Probtrackx surface analysis

Hi HCP users,

I’m trying to run probtrackX on some HCP data, can someone provide some guidance on how to run this using surfaces? I’m following the FSL user guide but they often refer to files which are absent from the HCP data as far I can tell. (e.g., "and also that you have a file called struct.nii.gz that you have used as an input to FreeSurfer recon_all program."

Basically, I’d like to define subcortical seeds and track to cortical surfaces.

For the subcortical seed regions I can easily create binary masks to use as seeds using fslmaths based on intensity values from the freesurfer LUTs. I could do the same with the cortical regions but I have read that tracking to cortical regions is best done with surfaces instead of volumes.

So, when selecting “classification targets” can I simply add in a cifti file? (e.g., 100307/T1w/aparc+aseg.nii.gz OR 100307/T1w/aparc.a2009s+aseg.nii.gz)** and then tell probtrackX to output the matrices I want?

**I assume using the files in the T1w dir is best because these are in the same space as the diffusion data and therefore don’t require transformation.

On a different note, if I select a surface file as a seed instead, it asks for a “surface reference image” for Freesurfer. Which file is best used for this purpose?

Cheers,
Linden

——————————————————————

Linden Parkes

PhD Candidate
Monash Clinical & Imaging Neuroscience (MCIN)
School of Psychological Sciences
Monash Biomedical Imaging
Monash University

A: 770 Blackburn Rd, Clayton, 3168, Vic, Australia
T: +61 3 9902 9435  |  0402 516 574

B7AE8BF0-4F0C-4F0B-9BDE-B582B9331FA1

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