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| It is not the purpose of Brainstorm tutorials to teach you how to use !BrainSuite. But most Brainstorm users are lost when it reaches to the segmentation of the MRI. So here is a short introduction of the !BrainSuite software. | ''Authors: Andrew Krause, Francois Tadel, Anand Joshi, David Shattuck'' |
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| To extract head and cortex meshes from a T1 MRI, you can also try to use: [[Tutorials/SegBrainVisa|BrainVISA]] or [[Tutorials/FreeSurfer]]. | You can use the free BrainSuite and SVReg software package to extract segmented brain surfaces from a T1-weighted MRI image. Surface extraction and segmentation can either be automatic or manual--this tutorial will step you through the automated process (more information on manual tweaks can be found in [[http://brainsuite.org/processing/|BrainSuite's documentation]]). For this tutorial, we will use the auditory_tutorial_T1.nii file: [[http://neuroimage.usc.edu/bst/download.php?file=auditory_tutorial_T1.zip|download]]. After extracting the zip file, you can rename the MRI image as T1.nii for convenience. We will use this filename in the tutorial for convenience. Unlike Brainstorm, Freesurfer and BrainVisa, BrainSuite does not use a database structure for storing subject information and scans. Instead, by default it stores its output in the same folder as the input MRI scan. Thus, it is often best to have each subject's structural scan in its own folder. <<TableOfContents(2,2)>> == Installation == 1. Download the latest version of BrainSuite from http://www.brainsuite.org/download. 1. Install it on your computer by following the instructions in [[http://brainsuite.bmap.ucla.edu/quickstart/installation/|BrainSuite's quick start installation guide]]. 1. Note that you will be using Surface/Volume Registration (SVReg) to do the surface segmentation, so you need to install a compatible [[http://www.mathworks.com/products/compiler/mcr|MATLAB Compiler Runtime]](2015b for BrainSuite 18a). You may ignore any instructions about "Setting up BDP" if you are not planning on using BrainSuite for diffusion imaging. 1. Start BrainSuite (if it is not already open following installation). == Running BrainSuite == 1. Open the T1-weighted scan in BrainSuite by going to '''File > Open Volume'''... and navigating to the auditory tutorial's T1.nii scan.<<BR>><<BR>> {{attachment:brainsuite1small.png}} 1. Check that the scan is in the correct orientation. Some of the modules BrainSuite and SVReg run while processing a scan assume that the scan is in LPI coordinates. Practically, this means the screen should look like below when you open it.<<BR>><<BR>> {{attachment:brainsuite2small.png}} 1. Clicking on menu '''Cortex > Cortical Surface Extraction Sequence'''. <<BR>><<BR>> 1. Check the box next to "'''Register and label brain'''".<<BR>><<BR>> {{attachment:brainsuite14small.png}} 1. BrainSuite has two atlases, '''BrainSuiteAtlas1''' and '''BCI-DNI_brain_atlas'''. If you are using '''BrainSuiteAtlas1 '''here, then you should use '''Colin27_BrainSuite_2016 '''or '''ICBM152_BrainSuite_2016''' as the default anatomy.''' '''If you are using the '''BCI-DNI_brain_atlas '''here, then you should use '''BCI-DNI_BrainSuite_2016 '''as the default anatomy in BrainStorm. 1. At the bottom of the dialog window, check that the filename prefix is "T1" and that the working directory is the Anatomy folder of the CTF tutorial files (or, if you moved the scan to its own folder, that folder). 1. Click "Run All". The full surface creation and segmentation process should take about 0.5 - 1.5 hours, depending on your machine.<<BR>><<BR>> {{attachment:brainsuite13small_v2.png}} == Importing the results in Brainstorm == 1. Switch to the anatomy side of the database explorer 1. Create a new subject, set the default anatomy option to "No, use individual anatomy" 1. Right-click on the subject > Import anatomy folder.<<BR>><<BR>> {{attachment:importMenu.gif}} * '''Import anatomy folder''': Interactive import: asks for the number of vertices expected in the final cortex surfaces and for the location of the fiducials NAS/LPA/RPA. Select this option in the case of an MEG study, when you know exactly where the fiducials were digitized during the MEG acquisition. See tutorial [[https://neuroimage.usc.edu/brainstorm/Tutorials/ChannelFile#Automatic_registration|MRI registration]]. * '''Import anatomy folder (auto)''': Automatic import: Computes the [[https://neuroimage.usc.edu/brainstorm/CoordinateSystems#MNI_coordinates|linear MNI normalization]], uses default positions from the MNI atlas for the NAS/LPA/RPA fiducials, and uses 15000 vertices for the cortex downsampled surfaces. 1. Select one of the BrainSuite import options and select the processing folder: * '''BrainSuite''': Import the T1 MRI, pial and white cortex surfaces, scalp and skull surfaces, registration squares, surface and volume parcellations. * BrainSuite '''+ Volume atlas''': Same as above, with the following addition: Import the volume parcellations available in the subject folder. 1. Manual import: You're prompted for the number of vertices you want in the final cortex surface. This will by extension define the number of dipoles to estimate during the source estimation process. By default we set this value to 15000 for the entire brain (it means 7500 for each hemisphere). <<BR>><<BR>> {{attachment:nvertices.png}} 1. Manual import: The MRI Viewer appears for you to define the anatomical fiducials. See tutorial [[https://neuroimage.usc.edu/brainstorm/Tutorials/ImportAnatomy#Fiducial_points|Import anatomy]]. Click on Save to keep your modifications, and the import will continue. <<BR>><<BR>> {{attachment:fiducialssmall.png||width="415",height="400"}} 1. A figure is automatically shown at the end of the process, to check visually that the low-resolution cortex and head surfaces were properly imported. If it doesn't look like the following picture, do not go any further in your source analysis, fix the anatomy first.<<BR>><<BR>> {{attachment:importresultssmall.png||width="227",height="179"}} == Files imported == The files that are imported from the BrainSuite folder are the following: * '''T1.nii''' (original T1 MRI volume) * '''T1.scalp.dfs''' (head surface) * '''T1.inner_skull.dfs''' (inner skull surface) * '''T1.outer_skull.dfs''' (outer skull surface) * '''T1.left.pial.cortex.svreg.dfs''' (gray/csf interface, left hemisphere) * '''T1.right.pial.cortex.svreg.dfs''' (gray/csf interface, right hemisphere) * '''T1.left.inner.cortex.svreg.dfs''' (white matter, left hemisphere) * '''T1.right.inner.cortex.svreg.dfs''' (white matter, right hemisphere) * '''T1.left.mid.cortex.svreg.dfs''' (registered squares, left hemisphere) * '''T1.right.mid.cortex.svreg.dfs''' (registered squares, right hemisphere) * '''atlas.left.mid.cortex.svreg.dfs''' (registered squares from the atlas, left hemisphere) * '''atlas.right.mid.cortex.svreg.dfs''' (registered squares from the atlas, left hemisphere) * '''brainsuite_labeldescription.xml''' (not imported, but required for properly labelling scouts) * '''T1.svreg.label.nii.gz''' (anatomical BCI-DNI atlas in volume) The successive steps that are automatically performed by Brainstorm: * Import all the surfaces (head, skull, left/right, white/pial) * Read the anatomical label information and SVReg atlases from pial and white matter surfaces * Downsample each hemisphere to the number specified in the options (by default 7500, half of the total default number 15000) * Merge left and right hemispheres for the two cortical surface types: white matter and cortex envelope * Downsample the head and skull surfaces * Delete all the unnecessary surfaces * Import additional volume parcellations The files you can see in the database explorer at the end: * '''MRI''': The T1 MRI of the subject * '''svreg''': Volume SVReg parcellation. * '''01.scalp_1082V''': The head surface (downsampled to 1082 vertices) * '''01.outer_skull_642V''': The skull surface (downsampled to 642 vertices) * '''01.inner_skull_642'''V: The inner skull surface (downsampled to 642 vertices) * '''cortex_270604V''': High-resolution cortical surface that was generated by BrainSuite. * '''cortex_15000V''': Low-resolution cortical surface, downsampled using the '''reducepatch''' function from Matlab (it keeps a meaningful subset of vertices from the original surface). This one appears in green, meaning that it is going to be used as the default by the processes that require a cortex surface) * '''white_270604V''': High-resolution white matter envelope from BrainSuite. * '''white_15000V''': Low-resolution white matter envelope from BrainSuite. * '''subcortical''': Atlas of subcortical regions imported from SVReg volume as labelled surfaces <<BR>><<BR>> {{attachment:files.gif}} == Handling Errors == ==== How to check the quality of the result ==== It's hard to estimate what would be a good cortical reconstruction. Try to spot the most obvious errors, e.g. when the early stages of the brain extraction didn't perform well. Play with the ''Smooth'' slider in the ''Surface ''tab. If it looks like a brain (two separate hemispheres) in both smooth and original views, it is probably OK. Display the cortex surface on top of the MRI slices, to make sure they are well aligned, that the surface follows the folds well, and that the left and right were not flipped: right-click on the low-resolution cortex > MRI registration > Check MRI/surface registration... . {{attachment:alignmrisurfacesmall.png||width="226",height="273"}} ==== The cortex looks bad ==== It is critical to get a good cortex surface for source estimation. If the final cortex surface looks bad, it means that something didn't work well somewhere along the BrainSuite cortical surface extraction sequence. This tutorial is not meant to guide you though troubleshooting BrainSuite results, but most errors in surface generation and segmentation occur at the first step, skull-stripping. If you are ending up with surfaces that include non-brain regions, or are missing large chunks of cortex, this step is where the error occurred. To fix skull-stripping issues, re-open the original T1 scan in BrainSuite. Open the Cortical Surface Extraction Sequence and check the box next to "Register and label brain" as you did above, but this time uncheck "Skull stripping". Next click on Cortex > Skull Stripping (BSE) to open the skull stripping dialog box, as this will let you step back and forth until you get a result that works. First try increasing 'Automated Iterations' from 5 to 10 or 15, and press 'Apply'. If the results do not look satisfactory, then press 'Back' and try again. You can also try entering parameters manually by unchecking 'automated parameter selection'. Common parameter settings that work are: * Diffusion Constant: between 20 and 30 (inclusive) * Edge Constant: 0.6, 0.75, 0.8 * Erosion Size: 1, 2 In general, increasing the edge constant will exclude more areas of the brain (decreasing will include more areas), while increasing the diffusion constant will include more areas. Set the parameters as you want, then click "Step >" until it says "finished skullstripping" above the progress bar. If the results look good, then click "Run All" on the Cortical Surface Extraction Sequence dialog box to run the rest of the segmentation process; if the results do not look good, click "< Back" on the Skull Stripping Tool dialog box until the progress bar returns to 0% and try a different set of parameters. More information can be found in [[http://brainsuite.bmap.ucla.edu/processing/surfaceextraction/bse/tuning-the-bse-parameters/|BrainSuite's documentation]]. If after following these instructions you still don't manage to get good surfaces, you can try to run the automatic MRI segmentation from [[Tutorials/SegBrainVisa|BrainVISA]] or [[Tutorials/LabelFreeSurfer|FreeSurfer]]. ==== The head surface looks bad ==== See the instructions to generate a new head surface file in the [[https://neuroimage.usc.edu/brainstorm/Tutorials/LabelFreeSurfer#Handling_errors|FreeSurfer tutorial]]. == Cortical Parcellations == Checking the box next to "Register and label brain" when running BrainSuite's Cortical Surface Extraction sequence causes BrainSuite to run a companion program called SVReg that implements an automatic parcellation of the cortical surface into anatomical regions. More information on this program can be found here:http://brainsuite.bmap.ucla.edu/processing/svreg/ SVReg's labels are imported into BrainStorm as scouts (cortical regions of interest), and saved directly in the surface files. To check where they are saved: right-click on the low-resolution cortex file > File > View file contents. You can see that there are two "Atlas" structures available, one that has Name='User scouts' and the other with Name='SVReg'. To access them from the interface: 1. Double-click on the low-resolution cortex (works with the original, high-resolution cortex too, it's just longer to display) 2. Go to the ''Scout'' tab, and click on the drop-down list to select "SVReg" {{attachment:svregscoutssmall.png||width="621",height="252"}} ==== Troubleshooting: You do not see the atlas SVReg ==== If you get some error messages in the Matlab command window during the segmention ("Could not find XML label description file brainsuite_labeldescription.xml"), you are using a version of BrainSuite that does not save the file brainsuite_labeldescription.xml in the segmentation folder. Workaround: Copy manually the file brainsuite_labeldescription.xml to the segmentation folder. == Volume parcellations == The SVReg atlas is available as a volume, with the same dimensions as the original T1 MRI. ''[TODO]'' == Subcortical structures: svreg labels == The file T1.svreg.label.nii.gz contains a volume the subcortical regions. Brainstorm reads these volume labels and tesselates some of these regions, groups all the meshes in a large surface file where the regions are identified in an atlas called "Structures". It identifies: 8 bialateral structures (accumbens, amygdala, caudate, hippocampus, pallidum, putamen, thalamus, cerebellum) and 1 central structure (brainstem). You can easily extract one structure (for example the brainstem or the cerebellum) by selecting the corresponding entries in the scouts list and selecting the menu Scout > Edit surface > Keep only selected scouts. It creates a new surface with only the selected regions. If you want to remove one or several structures, use the menu "Remove selected scouts" instead. Read more about the segmentation and labeling process in BrainSuite here: http://brainsuite.org/processing/svreg/ . {{attachment:brainsuite_subcortical_brainstorm.png||width="554",height="331"}} == Template registration for group analysis == BrainSuite provides an accurate registration method to the Brainstorm anatomy templates (Colin27, ICBM152). The registration procedure works in the same way as the FreeSurfer-based registration illustrated in this tutorial: [[Tutorials/CoregisterSubjects|Group studies: Subject coregistration]]. To use this registration, you need to use a template anatomy processed with BrainSuite. <<BR>>Right-click on ''Default anatomy'' > Use template > '''Colin27_BrainSuite_2016''' or '''ICBM152_BrainSuite_2016'''. . {{attachment:coreg.gif||width="554",height="331"}} . <<EmbedContent(http://neuroimage.usc.edu/bst/get_feedback.php?Tutorials/SegBrainSuite)>> |
T1-MRI Segmentation with BrainSuite
Authors: Andrew Krause, Francois Tadel, Anand Joshi, David Shattuck
You can use the free BrainSuite and SVReg software package to extract segmented brain surfaces from a T1-weighted MRI image. Surface extraction and segmentation can either be automatic or manual--this tutorial will step you through the automated process (more information on manual tweaks can be found in BrainSuite's documentation).
For this tutorial, we will use the auditory_tutorial_T1.nii file: download. After extracting the zip file, you can rename the MRI image as T1.nii for convenience. We will use this filename in the tutorial for convenience.
Unlike Brainstorm, Freesurfer and BrainVisa, BrainSuite does not use a database structure for storing subject information and scans. Instead, by default it stores its output in the same folder as the input MRI scan. Thus, it is often best to have each subject's structural scan in its own folder.
Contents
Installation
Download the latest version of BrainSuite from http://www.brainsuite.org/download.
Install it on your computer by following the instructions in BrainSuite's quick start installation guide.
Note that you will be using Surface/Volume Registration (SVReg) to do the surface segmentation, so you need to install a compatible MATLAB Compiler Runtime(2015b for BrainSuite 18a). You may ignore any instructions about "Setting up BDP" if you are not planning on using BrainSuite for diffusion imaging.
Start BrainSuite (if it is not already open following installation).
Running BrainSuite
Open the T1-weighted scan in BrainSuite by going to File > Open Volume... and navigating to the auditory tutorial's T1.nii scan.
Check that the scan is in the correct orientation. Some of the modules BrainSuite and SVReg run while processing a scan assume that the scan is in LPI coordinates. Practically, this means the screen should look like below when you open it.
Clicking on menu Cortex > Cortical Surface Extraction Sequence.
Check the box next to "Register and label brain".
BrainSuite has two atlases, BrainSuiteAtlas1 and BCI-DNI_brain_atlas. If you are using BrainSuiteAtlas1 here, then you should use Colin27_BrainSuite_2016 or ICBM152_BrainSuite_2016 as the default anatomy. If you are using the BCI-DNI_brain_atlas here, then you should use BCI-DNI_BrainSuite_2016 as the default anatomy in BrainStorm.
- At the bottom of the dialog window, check that the filename prefix is "T1" and that the working directory is the Anatomy folder of the CTF tutorial files (or, if you moved the scan to its own folder, that folder).
Click "Run All". The full surface creation and segmentation process should take about 0.5 - 1.5 hours, depending on your machine.
Importing the results in Brainstorm
- Switch to the anatomy side of the database explorer
- Create a new subject, set the default anatomy option to "No, use individual anatomy"
Right-click on the subject > Import anatomy folder.
Import anatomy folder: Interactive import: asks for the number of vertices expected in the final cortex surfaces and for the location of the fiducials NAS/LPA/RPA. Select this option in the case of an MEG study, when you know exactly where the fiducials were digitized during the MEG acquisition. See tutorial MRI registration.
Import anatomy folder (auto): Automatic import: Computes the linear MNI normalization, uses default positions from the MNI atlas for the NAS/LPA/RPA fiducials, and uses 15000 vertices for the cortex downsampled surfaces.
Select one of the BrainSuite import options and select the processing folder:
BrainSuite: Import the T1 MRI, pial and white cortex surfaces, scalp and skull surfaces, registration squares, surface and volume parcellations.
BrainSuite + Volume atlas: Same as above, with the following addition: Import the volume parcellations available in the subject folder.
Manual import: You're prompted for the number of vertices you want in the final cortex surface. This will by extension define the number of dipoles to estimate during the source estimation process. By default we set this value to 15000 for the entire brain (it means 7500 for each hemisphere).
Manual import: The MRI Viewer appears for you to define the anatomical fiducials. See tutorial Import anatomy. Click on Save to keep your modifications, and the import will continue.
A figure is automatically shown at the end of the process, to check visually that the low-resolution cortex and head surfaces were properly imported. If it doesn't look like the following picture, do not go any further in your source analysis, fix the anatomy first.
Files imported
The files that are imported from the BrainSuite folder are the following:
T1.nii (original T1 MRI volume)
T1.scalp.dfs (head surface)
T1.inner_skull.dfs (inner skull surface)
T1.outer_skull.dfs (outer skull surface)
T1.left.pial.cortex.svreg.dfs (gray/csf interface, left hemisphere)
T1.right.pial.cortex.svreg.dfs (gray/csf interface, right hemisphere)
T1.left.inner.cortex.svreg.dfs (white matter, left hemisphere)
T1.right.inner.cortex.svreg.dfs (white matter, right hemisphere)
T1.left.mid.cortex.svreg.dfs (registered squares, left hemisphere)
T1.right.mid.cortex.svreg.dfs (registered squares, right hemisphere)
atlas.left.mid.cortex.svreg.dfs (registered squares from the atlas, left hemisphere)
atlas.right.mid.cortex.svreg.dfs (registered squares from the atlas, left hemisphere)
brainsuite_labeldescription.xml (not imported, but required for properly labelling scouts)
T1.svreg.label.nii.gz (anatomical BCI-DNI atlas in volume)
The successive steps that are automatically performed by Brainstorm:
- Import all the surfaces (head, skull, left/right, white/pial)
- Read the anatomical label information and SVReg atlases from pial and white matter surfaces
- Downsample each hemisphere to the number specified in the options (by default 7500, half of the total default number 15000)
- Merge left and right hemispheres for the two cortical surface types: white matter and cortex envelope
- Downsample the head and skull surfaces
- Delete all the unnecessary surfaces
- Import additional volume parcellations
The files you can see in the database explorer at the end:
MRI: The T1 MRI of the subject
svreg: Volume SVReg parcellation.
01.scalp_1082V: The head surface (downsampled to 1082 vertices)
01.outer_skull_642V: The skull surface (downsampled to 642 vertices)
01.inner_skull_642V: The inner skull surface (downsampled to 642 vertices)
cortex_270604V: High-resolution cortical surface that was generated by BrainSuite.
cortex_15000V: Low-resolution cortical surface, downsampled using the reducepatch function from Matlab (it keeps a meaningful subset of vertices from the original surface). This one appears in green, meaning that it is going to be used as the default by the processes that require a cortex surface)
white_270604V: High-resolution white matter envelope from BrainSuite.
white_15000V: Low-resolution white matter envelope from BrainSuite.
subcortical: Atlas of subcortical regions imported from SVReg volume as labelled surfaces
Handling Errors
How to check the quality of the result
It's hard to estimate what would be a good cortical reconstruction. Try to spot the most obvious errors, e.g. when the early stages of the brain extraction didn't perform well. Play with the Smooth slider in the Surface tab. If it looks like a brain (two separate hemispheres) in both smooth and original views, it is probably OK.
Display the cortex surface on top of the MRI slices, to make sure they are well aligned, that the surface follows the folds well, and that the left and right were not flipped: right-click on the low-resolution cortex > MRI registration > Check MRI/surface registration...
The cortex looks bad
It is critical to get a good cortex surface for source estimation. If the final cortex surface looks bad, it means that something didn't work well somewhere along the BrainSuite cortical surface extraction sequence. This tutorial is not meant to guide you though troubleshooting BrainSuite results, but most errors in surface generation and segmentation occur at the first step, skull-stripping. If you are ending up with surfaces that include non-brain regions, or are missing large chunks of cortex, this step is where the error occurred.
To fix skull-stripping issues, re-open the original T1 scan in BrainSuite. Open the Cortical Surface Extraction Sequence and check the box next to "Register and label brain" as you did above, but this time uncheck "Skull stripping". Next click on Cortex > Skull Stripping (BSE) to open the skull stripping dialog box, as this will let you step back and forth until you get a result that works. First try increasing 'Automated Iterations' from 5 to 10 or 15, and press 'Apply'. If the results do not look satisfactory, then press 'Back' and try again. You can also try entering parameters manually by unchecking 'automated parameter selection'. Common parameter settings that work are:
- Diffusion Constant: between 20 and 30 (inclusive)
- Edge Constant: 0.6, 0.75, 0.8
- Erosion Size: 1, 2
In general, increasing the edge constant will exclude more areas of the brain (decreasing will include more areas), while increasing the diffusion constant will include more areas. Set the parameters as you want, then click "Step >" until it says "finished skullstripping" above the progress bar. If the results look good, then click "Run All" on the Cortical Surface Extraction Sequence dialog box to run the rest of the segmentation process; if the results do not look good, click "< Back" on the Skull Stripping Tool dialog box until the progress bar returns to 0% and try a different set of parameters. More information can be found in BrainSuite's documentation.
If after following these instructions you still don't manage to get good surfaces, you can try to run the automatic MRI segmentation from BrainVISA or FreeSurfer.
The head surface looks bad
See the instructions to generate a new head surface file in the FreeSurfer tutorial.
Cortical Parcellations
Checking the box next to "Register and label brain" when running BrainSuite's Cortical Surface Extraction sequence causes BrainSuite to run a companion program called SVReg that implements an automatic parcellation of the cortical surface into anatomical regions. More information on this program can be found here:http://brainsuite.bmap.ucla.edu/processing/svreg/
SVReg's labels are imported into BrainStorm as scouts (cortical regions of interest), and saved directly in the surface files. To check where they are saved: right-click on the low-resolution cortex file > File > View file contents. You can see that there are two "Atlas" structures available, one that has Name='User scouts' and the other with Name='SVReg'.
To access them from the interface: 1. Double-click on the low-resolution cortex (works with the original, high-resolution cortex too, it's just longer to display) 2. Go to the Scout tab, and click on the drop-down list to select "SVReg"
Troubleshooting: You do not see the atlas SVReg
If you get some error messages in the Matlab command window during the segmention ("Could not find XML label description file brainsuite_labeldescription.xml"), you are using a version of BrainSuite that does not save the file brainsuite_labeldescription.xml in the segmentation folder.
Workaround: Copy manually the file brainsuite_labeldescription.xml to the segmentation folder.
Volume parcellations
The SVReg atlas is available as a volume, with the same dimensions as the original T1 MRI.
[TODO]
Subcortical structures: svreg labels
The file T1.svreg.label.nii.gz contains a volume the subcortical regions. Brainstorm reads these volume labels and tesselates some of these regions, groups all the meshes in a large surface file where the regions are identified in an atlas called "Structures". It identifies: 8 bialateral structures (accumbens, amygdala, caudate, hippocampus, pallidum, putamen, thalamus, cerebellum) and 1 central structure (brainstem). You can easily extract one structure (for example the brainstem or the cerebellum) by selecting the corresponding entries in the scouts list and selecting the menu Scout > Edit surface > Keep only selected scouts. It creates a new surface with only the selected regions. If you want to remove one or several structures, use the menu "Remove selected scouts" instead. Read more about the segmentation and labeling process in BrainSuite here: http://brainsuite.org/processing/svreg/
Template registration for group analysis
BrainSuite provides an accurate registration method to the Brainstorm anatomy templates (Colin27, ICBM152). The registration procedure works in the same way as the FreeSurfer-based registration illustrated in this tutorial: Group studies: Subject coregistration.
To use this registration, you need to use a template anatomy processed with BrainSuite.
Right-click on Default anatomy > Use template > Colin27_BrainSuite_2016 or ICBM152_BrainSuite_2016.
