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| == Overlaying FSL Feat statistical maps and Higher-Level Analysis == | |
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== Overlaying FSL Feat statistical maps == |
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| Use the following command to display the zmap (zstat1.img) overlaid onto the bert's orig volume. It will display the automatic segmentation, and will also set the threshold at z = 1.3: | Use the following command to display the zmap (zstat1.nii.gz) from the first run overlaid onto the bert's orig volume. It will display the automatic segmentation, and will also set the threshold at z = 2.3: |
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| tkmedit bert orig -aux brain -overlay ./fbert.feat/stats/zstat1.nii.gz \ -overlay-reg ./fbert.feat/reg/freesurfer/anat2exf.register.dat \ -fthresh 1.3 -fmid 2.3 -fslope 1 \ -segmentation ${SUBJECTS_DIR}/bert/mri/aseg ${FREESURFER_HOME}/FreeSurferColorLUT.txt |
tkmedit bert orig.mgz lh.white -aux brain.mgz \ -overlay ./fbert1.feat/stats/zstat1.nii.gz \ -overlay-reg ./fbert1.feat/reg/freesurfer/anat2exf.register.dat \ -segmentation aparc+aseg.mgz -fthresh 2.3 -fmax 4.3 |
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| attachment:tkm-zstat1-cor-128-small.jpg | attachment:tkm-zstat1-cor-128.th23.small.jpg[[BR]] When you click or mouse over a voxel, the cortical or subcortical structure that that voxel belongs to will be displayed in the control panel. You can view any of the volumes in the stats dir in this way as well as the clustered maps in the feat directory. |
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| === 2.0 Sampling statistical maps onto bert's surface === | === 2.0 View statistical maps on bert's surface === To view any of the statistical maps on bert's surface, close the tkmedit GUI (or open a new terminal window) and run: {{{ tksurfer bert lh inflated \ -overlay ./fbert1.feat/stats/zstat1.nii.gz \ -overlay-reg ./fbert1.feat/reg/freesurfer/anat2exf.register.dat \ -fthresh 2.3 -fmid 3.3 -fslope 1 -annot aparc.annot }}} |
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| In order to display the statistical map overlaid onto the surface, the data in fbert.feat must be resampled. This is done with feat2surf. Documentation for what it does and how it does it can be obtained with: | Change the cortical parcellation to outline mode with View->LabelStyle->Outline. You should see the image below:[[BR]] attachment:tks-zstat1-rh-lat.th23.small.jpg [[BR]] When you click or mouse over a vertex, the control panel will display the name of the cortical structure. You can view any of the volumes in the stats dir in this way as well as the clustered maps in the feat directory. You can also run the tkmedit and tksurfer commands above in separate shells and use the Save-Point/Goto-Point functionality to navigate through the volume and surface. === 3.0 Displaying Same-Subject, Cross-Run GFEAT Results === Typically, one collects more than one run/series of functtional data for each subject. The individual runs are analyzed separately, then combined in standard space with GFEAT using a fixed-effects model. Since the data are no longer in the subject's native functional space, a different registration matrix is needed to map the GFEAT results to the individual. Each run of reg-feat2anat will create a reg/freesurfer/anat2std.register.dat. Any one of these can be used to map the GFEAT data to the subject's anatomy. First, verify that the registration is good with: |
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| feat2surf --help | tkregister2 --mov fbert.gfeat/mean_func.nii.gz --surf \ --reg fbert1.feat/reg/freesurfer/anat2std.register.dat |
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| To run it on this data set, run: | mean_func.nii.gz is the mean of the example_func's in standard space. Now show gfeat results on anatomical volume: |
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| feat2surf --feat fbert.feat | tkmedit bert orig.mgz -seg aparc+aseg.mgz \ -ov fbert.gfeat/cope1.feat/stats/zstat1.nii.gz \ -ovreg fbert1.feat/reg/freesurfer/anat2std.register.dat \ -fthresh 2.3 -fmax 4.3 |
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| Verify that this has created four directories under fbert.feat: reg_surf-lh, reg_surf-rh, reg_surf-lh-fsaverage, and reg_surf-rh-fsaverage. Each one of these directories will have a stats directory in which all the statistics from fbert.feat/stats have been resampled onto the surface. The fsaverage directories are resampled onto the common surface spaced (defined by fsaverage). | Here we've used the anat2std.register.dat from the first run. |
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| === 3.0 Viewing statistical maps on bert's surface === | Now show gfeat results on the surface: {{{ tksurfer bert lh inflated -annot aparc.annot \ -ov fbert.gfeat/cope1.feat/stats/zstat1.nii.gz \ -ovreg fbert1.feat/reg/freesurfer/anat2std.register.dat \ -fthresh 2.3 -fmid 3.3 -fslope 1 }}} |
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| To view the statistical maps on the right hemisphere, run tksurfer: | === 3.0 Resampling COPEs to common surface and Higher-Level Analysis === When performing surface-based group analysis of functional data, the COPEs must be sampled to the common surface space (similar to how you must reslice the COPEs from the native functional space into standard space prior to group analysis). The surface sampling can be done in two ways. First, you can use feat2surf as in: |
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| tksurfer bert rh inflated \ -o ./fbert.feat/reg_surf-rh/stats/zstat1.mgh \ -fthresh 1.3 -fmid 2.3 -fslope 1 |
feat2surf --feat fbert1.feat --cope-only |
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| Note that you can run the above tkmedit command (from a different window) simultaneously with the tksurfer command to visualize the same data on the volume and in the surface. You can then use the Save/Goto Point buttons to navigate between the surface and volume. |
This will create fbert.feat/reg_surf-lh-fsaverage/stats for the left hemi (and another for the right). There will be cope1.nii.gz. This looks like a volume because it is in nifti format, but it is really a surface stored in a volume format (note it's dimensions are 1974 x 1 x 83 = 163842 = number of vertices in fsaverage's surface). You can then concatenate these files from different subjects to perform group analysis with FreeSurfer's mri_glmfit or FSL's randomise or flame. |
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| You should see the image below:[[BR]] attachment:tks-zstat1-rh-lat-small.jpg |
Alternatively, when you have multiple runs/subjects, you can use mris_preproc, something like: {{{ mris_preproc --target fsaverage --hemi lh --out xrun/lh.cope1.nii.gz \ --iv fbert1.feat/stats/cope1.nii.gz fbert1.feat/reg/freesurfer/anat2exf.register.dat \ --iv fbert2.feat/stats/cope1.nii.gz fbert2.feat/reg/freesurfer/anat2exf.register.dat }}} This will create the output directory (xrun) and lh.cope1.nii.gz, the copes from each run sampled onto the left hemi of the common surface. In this case it will have only two frames for the two runs. This can then be used as input mri_glmfit, randomise, or flame. You can also resample the variances of the copes with: {{{ mris_preproc --target fsaverage --hemi lh --out xrun/lh.varcope1.nii.gz \ --iv fbert1.feat/stats/varcope1.nii.gz fbert1.feat/reg/freesurfer/anat2exf.register.dat \ --iv fbert2.feat/stats/varcope1.nii.gz fbert2.feat/reg/freesurfer/anat2exf.register.dat }}} |
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| === 4.0 Overlaying zmap onto the FSL's standard volume === | The command below can be used to run a fixed-effects analysis across both runs. Normally, you would probably run a random effects or weight random effects analysis, but since we only have two runs here, we'll use a fixed-effects. The dof=163 is the sum of the dofs from fbert?.feat/stats/dof. The model here is a simple one-sample group mean (OSGM) in which the desgin matrix is simply a column of 1s. For more elaborate designs, use an FSGD file instead of --osgm. |
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| You can also use tkmedit to view your results on the FSL standard volume instead of the individual's anatomical with the following command: |
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| tkmedit -f $FSLDIR/etc/standard/avg152T1_brain.img \ -overlay ./fbert.feat/stats/zstat1.nii.gz \ -overlay-reg ./fbert.feat/reg/freesurfer/std2exf.register.dat \ -fthresh 1.3 -fmid 2.3 -fslope 1 |
mri_glmfit --y xrun/lh.cope1.nii.gz --yffxvar xrun/lh.varcope1.nii.gz --ffxdof 163 \ --osgm --glmdir xrun/lh.osgm.ffx --surf fsaverage lh --label lh.cortex.label |
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| To view the higher-level results, run: {{{ tksurfer fsaverage lh inflated -overlay xrun/lh.osgm.ffx/osgm/sig.mgh \ -fthresh 4 -fmid 5 -fslope 1 -annot aparc.annot }}} There are several differences between this invokation of tksurfer and the one further above. * The subject is fsaverage, not bert * The input is a sig map, which is -log10(p) * The thresholds are significance thresholds, not z. So, 4 means p < .0001. |
[wiki:FsTutorial top] | [wiki:FsTutorial/FslFeatFreeSurfer previous]
Overlaying FSL Feat statistical maps and Higher-Level Analysis
To follow this exercise exactly be sure you've downloaded the [wiki:FsTutorial/Data tutorial data set] before you begin. If you choose not to download the data set you can follow these instructions on your own data, but you will have to substitute your own specific paths and subject names.
In this exercise, the data set of subject bert is used for demonstration. To begin the exercises, first enter the following directory, and then set the current directory to be the default subjects directory using this command:
cd $FREESURFER_HOME/subjects/buckner_data/tutorial_subjs
setenv SUBJECTS_DIR ${PWD}
1.0 Overlaying the statistical map onto the bert's orig volume
Use the following command to display the zmap (zstat1.nii.gz) from the first run overlaid onto the bert's orig volume. It will display the automatic segmentation, and will also set the threshold at z = 2.3:
tkmedit bert orig.mgz lh.white -aux brain.mgz \ -overlay ./fbert1.feat/stats/zstat1.nii.gz \ -overlay-reg ./fbert1.feat/reg/freesurfer/anat2exf.register.dat \ -segmentation aparc+aseg.mgz -fthresh 2.3 -fmax 4.3
You should see the image below:BR attachment:tkm-zstat1-cor-128.th23.small.jpgBR When you click or mouse over a voxel, the cortical or subcortical structure that that voxel belongs to will be displayed in the control panel. You can view any of the volumes in the stats dir in this way as well as the clustered maps in the feat directory.
2.0 View statistical maps on bert's surface
To view any of the statistical maps on bert's surface, close the tkmedit GUI (or open a new terminal window) and run:
tksurfer bert lh inflated \ -overlay ./fbert1.feat/stats/zstat1.nii.gz \ -overlay-reg ./fbert1.feat/reg/freesurfer/anat2exf.register.dat \ -fthresh 2.3 -fmid 3.3 -fslope 1 -annot aparc.annot
Change the cortical parcellation to outline mode with View->LabelStyle->Outline. You should see the image below:BR attachment:tks-zstat1-rh-lat.th23.small.jpg BR When you click or mouse over a vertex, the control panel will display the name of the cortical structure. You can view any of the volumes in the stats dir in this way as well as the clustered maps in the feat directory. You can also run the tkmedit and tksurfer commands above in separate shells and use the Save-Point/Goto-Point functionality to navigate through the volume and surface.
3.0 Displaying Same-Subject, Cross-Run GFEAT Results
Typically, one collects more than one run/series of functtional data for each subject. The individual runs are analyzed separately, then combined in standard space with GFEAT using a fixed-effects model. Since the data are no longer in the subject's native functional space, a different registration matrix is needed to map the GFEAT results to the individual. Each run of reg-feat2anat will create a reg/freesurfer/anat2std.register.dat. Any one of these can be used to map the GFEAT data to the subject's anatomy.
First, verify that the registration is good with:
tkregister2 --mov fbert.gfeat/mean_func.nii.gz --surf \ --reg fbert1.feat/reg/freesurfer/anat2std.register.dat
mean_func.nii.gz is the mean of the example_func's in standard space.
Now show gfeat results on anatomical volume:
tkmedit bert orig.mgz -seg aparc+aseg.mgz \ -ov fbert.gfeat/cope1.feat/stats/zstat1.nii.gz \ -ovreg fbert1.feat/reg/freesurfer/anat2std.register.dat \ -fthresh 2.3 -fmax 4.3
Here we've used the anat2std.register.dat from the first run.
Now show gfeat results on the surface:
tksurfer bert lh inflated -annot aparc.annot \ -ov fbert.gfeat/cope1.feat/stats/zstat1.nii.gz \ -ovreg fbert1.feat/reg/freesurfer/anat2std.register.dat \ -fthresh 2.3 -fmid 3.3 -fslope 1
3.0 Resampling COPEs to common surface and Higher-Level Analysis
When performing surface-based group analysis of functional data, the COPEs must be sampled to the common surface space (similar to how you must reslice the COPEs from the native functional space into standard space prior to group analysis). The surface sampling can be done in two ways.
First, you can use feat2surf as in:
feat2surf --feat fbert1.feat --cope-only
This will create fbert.feat/reg_surf-lh-fsaverage/stats for the left hemi (and another for the right). There will be cope1.nii.gz. This looks like a volume because it is in nifti format, but it is really a surface stored in a volume format (note it's dimensions are 1974 x 1 x 83 = 163842 = number of vertices in fsaverage's surface). You can then concatenate these files from different subjects to perform group analysis with FreeSurfer's mri_glmfit or FSL's randomise or flame.
Alternatively, when you have multiple runs/subjects, you can use mris_preproc, something like:
mris_preproc --target fsaverage --hemi lh --out xrun/lh.cope1.nii.gz \ --iv fbert1.feat/stats/cope1.nii.gz fbert1.feat/reg/freesurfer/anat2exf.register.dat \ --iv fbert2.feat/stats/cope1.nii.gz fbert2.feat/reg/freesurfer/anat2exf.register.dat
This will create the output directory (xrun) and lh.cope1.nii.gz, the copes from each run sampled onto the left hemi of the common surface. In this case it will have only two frames for the two runs. This can then be used as input mri_glmfit, randomise, or flame. You can also resample the variances of the copes with:
mris_preproc --target fsaverage --hemi lh --out xrun/lh.varcope1.nii.gz \ --iv fbert1.feat/stats/varcope1.nii.gz fbert1.feat/reg/freesurfer/anat2exf.register.dat \ --iv fbert2.feat/stats/varcope1.nii.gz fbert2.feat/reg/freesurfer/anat2exf.register.dat
The command below can be used to run a fixed-effects analysis across both runs. Normally, you would probably run a random effects or weight random effects analysis, but since we only have two runs here, we'll use a fixed-effects. The dof=163 is the sum of the dofs from fbert?.feat/stats/dof. The model here is a simple one-sample group mean (OSGM) in which the desgin matrix is simply a column of 1s. For more elaborate designs, use an FSGD file instead of --osgm.
mri_glmfit --y xrun/lh.cope1.nii.gz --yffxvar xrun/lh.varcope1.nii.gz --ffxdof 163 \
--osgm --glmdir xrun/lh.osgm.ffx --surf fsaverage lh --label lh.cortex.labelTo view the higher-level results, run:
tksurfer fsaverage lh inflated -overlay xrun/lh.osgm.ffx/osgm/sig.mgh \ -fthresh 4 -fmid 5 -fslope 1 -annot aparc.annot
There are several differences between this invokation of tksurfer and the one further above.
- The subject is fsaverage, not bert
- The input is a sig map, which is -log10(p)
The thresholds are significance thresholds, not z. So, 4 means p < .0001.
