Dear Matthew,
Thank you very much for your detailed explanation! 1. The current situation of our study is that, we used the HCP MMP1.0 atlas to sample the tfMRI data in order to localize specific functional areas. Since the HCP MMP1.0 is in the MNI space, we used "$SUBJECT/MNINonLinear/fsaverage_LR32k/$SUBJECT.L.midthickness._MSMAll.32k_fs_LR.surf.gii" to do the multiplication. Then I suppose the surface ROI to be acquired in the MNI standard space, and therefore need to use the --xfm and --invxfm in probtrackx2. Is my understanding correct? 2. In this way, do the HCP data contain files that can be used in --xfm, --invxfm and --seedref in surface prob-tracking? 3. In the FSL "surf2surf" format conversion from .func.gii to ASCII type (.asc), is it correct to use "$Subject/MNINonLinear/fsaverage_LR32k/${Subject}.R.white.32k_fs_LR.surf.gii" as the input (-i) and the acquired "ROI.func.gii" as --value? Look forward to your kind guidance. Thanks a lot! Best regards, Xinyang At 2018-04-04 18:44:25, "Glasser, Matthew" <glass...@wustl.edu> wrote: 1. Files in ${StudyFolder}/${Subject}/T1w are in subject’s physical space and files in ${StudyFolder}/${Subject}/MNINonLinear are in MNI standard space. Surfaces without MSMAll are registered with MSMSulc and surfaces with MSMAll are registered with MSMAll. In general MSMAll will have better alignment of cortical areas across subjects. 2. There is no native diffusion space, as this is unnecessary. Tracking occurs subject’s physical space and you can use the surfaces in ${StudyFolder}/${Subject}/T1w/fsaverage_LR32k with MSMAll if you don’t use --xfm and --invxfm or those in ${StudyFolder}/${Subject}/MNINonLinear/fsaverage_LR32k if you do. Peace, Matt. From: Xinyang Liu <xinyang_ie...@163.com> Date: Wednesday, April 4, 2018 at 2:36 AM To: Matt Glasser <glass...@wustl.edu> Cc: HCP 讨论组 <hcp-users@humanconnectome.org> Subject: Re: [HCP-Users] questions about using HCP surface ROIs in prob-tracking Dear Matthew, Thank you very much for your kind reply! Could I continue asking two more new questions? 1. In the preprocessed structural data, both the /${Subject}/T1w/fsaverage_LR32k and /${Subject}/MNINonLinear/fsaverage_LR32k contain white surface files with the same names, such as "${Subject}.L.white.32k_fs_LR.surf.gii" and "${Subject}.L.white.MSMAll.32k_fs_LR.surf.gii". Is there any difference between these files of the same name but under different routes? 2. I am kind of confusing about the space transformation in surface ROI fibre tracking. In the volume-based analysis, there is native diffusion space and standard space, and tractograhpy is done in native diffusion space. For surface data, I suppose the files like "${Subject}.L.white.32k_fs_LR.surf.gii" have already been registered to a 32k standard mesh. Then should the surface ROI fibre tracking go back to native space and how if needed? Best regards, Xinyang At 2018-04-04 00:49:09, "Glasser, Matthew" <glass...@wustl.edu> wrote: 1. Yes, though they can come from a certain (configurable) radius around the vertex, rather than all from the point location with --sampvox. 2. I think probtrackx2 looks for greater than zero, but you could of course binarize them. 3. I believe you can display the surface counts in GIFTI format with --fopd, you might ask more on the FSL list as I haven’t done much tractorgraphy in a while. Peace, Matt. From: <hcp-users-boun...@humanconnectome.org> on behalf of Xinyang Liu <xinyang_ie...@163.com> Date: Tuesday, April 3, 2018 at 1:52 AM To: HCP 讨论组 <hcp-users@humanconnectome.org> Subject: [HCP-Users] questions about using HCP surface ROIs in prob-tracking Dear HCP experts, Hi. As a new learner of the HCP tfMRI surface data, I have some questions when using them as ROIs to do probabilistic tractography. I would be very thankful to receive any of your kind guidance. My questions are as below. 1. I know that in FSL probtrackx2 voxel-based fibre tracking, 5000 streamlines (default) come out from each voxel. How about the case in the surface vertices of the HCP grayordinate space? Is it similar with the voxel-based tracking, like 5000 streamlines coming out from each vertex? 2.The tfMRI surface ROIs usually contain information of signal intensities, would this influence the diffusion tracking results if using them as masks? 3. How to display the surface ROIs (.func.gii or .asc) and output tracking paths (.nii.gz in FSL results) in the same figure? Look forward to your feedbacks. Thank you very much! Best regards, Xinyang Liu _______________________________________________ HCP-Users mailing list HCP-Users@humanconnectome.org http://lists.humanconnectome.org/mailman/listinfo/hcp-users _______________________________________________ HCP-Users mailing list HCP-Users@humanconnectome.org http://lists.humanconnectome.org/mailman/listinfo/hcp-users