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 * Gazula, H., Tregidgo, H.F., Billot, B., Balbastre, Y., Williams Ramirez, J., Herisse, R., Deden-Binder, L.J., Casamitjana, A., Melief, E.J., Latimer, C.S. and Kilgore, M.D., 2024. Machine learning of dissection photographs and surface scanning for quantitative 3D neuropathology. Elife, 12, p.RP91398. [[https://doi.org/10.7554/eLife.91398.4 | doi]]
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Automatic segmentation model uses nnUNet. If you use the automatic segmentation, also cite:
 * Williams Ramirez, J., Zemlyanker, D., Deden-Binder, L., Herisse, R., Garcia Pallares, E., Gopinath, K., Gazula, H., Mount, C., Kozanno, L.N., Marshall, M.S., Connors, T.R., Frosch, M.P., Montine, M., Oakley, D.H., Mac Donald, C.L., Keene, C.D., Hyman, B.T., Fischl, B. and Iglesias, J.E., 2026. A public generalizable AI tool for automated segmentation of coronal brain tissue slabs for 3D neuropathology. PLOS One, 21(8), p.e0355740. [[https://doi.org/10.1371/journal.pone.0355740 | doi]]
 * Gazula, H., Tregidgo, H.F., Billot, B., Balbastre, Y., Williams Ramirez, J., Herisse, R., Deden-Binder, L.J., Casamitjana, A., Melief, E.J., Latimer, C.S. and Kilgore, M.D., 2024. Machine learning of dissection photographs and surface scanning for quantitative 3D neuropathology. Elife, 12, p.RP91398. [[https://doi.org/10.7554/eLife.91398.4|doi]]

The machine learning slice imputation in the reconstruction is described in:

 * Crespo-Aguirre, M., Williams-Ramirez, J., Zemlyanker, D., Hu, X., Deden-Binder, L.J., Herisse, R., Montine, M., Connors, T.R., Mount, C., !MacDonald, C.L., Keene, C.D., Latimer, C.S., Oakley, D.H., Hyman, B.T., Lawry-Aguila, A. and Iglesias, J.E., 2026. Improving neuropathological reconstruction fidelity via AI slice imputation. Acta Neuropathologica Communications. [[https://doi.org/10.1186/s40478-026-02451-3|doi]]

Automatic segmentation model trained using
nnUNet:

 * Williams Ramirez, J., Zemlyanker, D., Deden-Binder, L., Herisse, R., Garcia Pallares, E., Gopinath, K., Gazula, H., Mount, C., Kozanno, L.N., Marshall, M.S., Connors, T.R., Frosch, M.P., Montine, M., Oakley, D.H., Mac Donald, C.L., Keene, C.D., Hyman, B.T., Fischl, B. and Iglesias, J.E., 2026. A public generalizable AI tool for automated segmentation of coronal brain tissue slabs for 3D neuropathology. PLOS One, 21(8), p.e0355740. [[https://doi.org/10.1371/journal.pone.0355740|doi]]
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The machine learning slice imputation in the reconstruction is described in:
 * Crespo-Aguirre, M., Williams-Ramirez, J., Zemlyanker, D., Hu, X., Deden-Binder, L.J., Herisse, R., Montine, M., Connors, T.R., Mount, C., !MacDonald, C.L., Keene, C.D., Latimer, C.S., Oakley, D.H., Hyman, B.T., Lawry-Aguila, A. and Iglesias, J.E., 2026. Improving neuropathological reconstruction fidelity via AI slice imputation. Acta Neuropathologica Communications. [[https://doi.org/10.1186/s40478-026-02451-3 | doi]]


[[https://www.youtube.com/watch?v=wo5meYRaGUY|Click here for a video with an overview of the method]]<<BR>>
{{attachment:video_screenshot.png||width="666",}}
<<BR>><<BR>>
[[https://www.youtube.com/watch?v=wo5meYRaGUY|Click here for a video with an overview of the method]]<<BR>> {{attachment:video_screenshot.png||width="666"}} <<BR>><<BR>>
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'''--photos_of_posterior_side''' must be used for the final reconstruction. '''--photos_of_posterior_side''' must be used for the final reconstruction command.
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{{attachment:19_slab_placement.png||width="667",height="483"}} <<BR>>''Tissue slab placement a) Properly placed tissue b) Tissue placed in a non-anatomical manner.''<<BR>> {{attachment:19_slab_placement.png||height="483",width="667"}} <<BR>>''Tissue slab placement a) Properly placed tissue b) Tissue placed in a non-anatomical manner.''<<BR>>
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{{attachment:20_incorrect_tissue_placement.png||width="659",height="333"}} <<BR>> <<BR>> {{attachment:20_incorrect_tissue_placement.png||height="333",width="659"}} <<BR>> <<BR>>
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{{attachment:21_twoPoint.jpeg||width="664",height="382"}} <<BR>> {{attachment:21_twoPoint.jpeg||height="382",width="664"}} <<BR>>
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'''''Tip''''': It is better to use landmarks that are as far apart as possible, as the relative error when manually setting the reference in pixels per millimeter decreases with greater distances.  '''''Tip''''': It is better to use landmarks that are as far apart as possible, as the relative error when manually setting the reference in pixels per millimeter decreases with greater distances.
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{{attachment:22_fourPoint.png||width="659",height="561"}} <<BR>> {{attachment:22_fourPoint.png||height="561",width="659"}} <<BR>>
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{{attachment:23_fiducials.png||width="416",height="439"}} <<BR>> {{attachment:23_fiducials.png||height="439",width="416"}} <<BR>>
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{{attachment:24_fiducialTissue.png||width="674",height="460"}} <<BR>> {{attachment:24_fiducialTissue.png||height="460",width="674"}} <<BR>>
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{{attachment:25_tissueSpace.png||width="685",height="404"}} <<BR>> {{attachment:25_tissueSpace.png||height="404",width="685"}} <<BR>>
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{{attachment:26_tissueBox.png||width="683",height="403"}} <<BR>> {{attachment:26_tissueBox.png||height="403",width="683"}} <<BR>>
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{{attachment:27_goodContrast.png||width="676",height="478"}} <<BR>> {{attachment:27_goodContrast.png||height="478",width="676"}} <<BR>>
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= Recommended Directory Structure =

We recommend the following directory structure for data and case organization. Each case should have its own directory, and within each case directory, create the following seven subdirectories to store the respective outputs:

 1. photos – Brain slab images (.JPG, .PNG).
 1. deformed - Pixel-corrected images.
 1. point_clouds – Files from the project collected from the surface scanner.
 1. mesh – Watertight mesh processed from point clouds on the scanner (.stl).
 1. masked – Binarized masks created from pixel-corrected photos.
 1. connected_components - .npz files showing the connected components for each image.
 1. recon - Final reconstructed volumes, and segmentations.

Note that during the image preprocessing GUI files under deformed, masked, and connected_components will be automatically generated. After each step, ensure that your data is saved to the appropriate subdirectory. Below is an example of how files should be organized in the recommended structure: <<BR>>
|| {{attachment:28_demoDirectory.png||height="555"}} || {{attachment:29_demoDirectory.png||height="180"}} <<BR>> {{attachment:29.2_demoDirectory.png||height="203"}} ||
<<BR>><<BR>>

= Photo Preprocessing =
The following guide will walk through the steps to preprocessing the brain slab images. This includes pixel correction, binarizing images, and selecting connected components. Make sure Freesurfer is properly sourced, and you have downloaded the model weights before continuing with the tutorial. <<BR>>
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== Pixel Correction Using Fiducials ==
Using the provided fiducial markers, we can correct for non-uniformities in pixel size across the images. If not available this step can be skipped retrospective correction modes can be used in the '''dissection_photo_gui''' covered in the next section. For images with fiducials, a calibration is required for pixel correction. For best results, use an image of the setup without tissue.<<BR>>
= Part 2: Prerprocessing Photographs with the Dissection Photo App =
The dissection photo app has five principal windows for each subject: '''Add photos''', '''Correction''', '''Segmentation''', '''Connected components''' and '''Reconstruction'''. The step bar at the top of the window shows which step is being done, users can click any backtrack by clicking any of the previous steps at any time, alternatively the house icon to return to the Projects screen with a summary of all reconstructions done or in process. For each project work is saved as you go, so the can can be closed at any time to later pick up where you left off.
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To start the fiducial calibration use command '''fiducials_calibration''' Before continuing, make sure the development version of Freesurfer is properly sourced, you have downloaded the model weights, and have set the NNUNET_MODEL_DIR as an environment variable pointing to the segmentation model before continuing with the tutorial. To start the application use command *dissection_photo_2* <<BR>>
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{{attachment:30_fiducialCalibIntro.png||width="550",height="275"}} <<BR>> == Projects Page ==
Each specimen corresponds to a '''project''': a folder which will be populated with the outputs from all steps. The project home contains a summary of all projects and their progress.
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After loading the image, start the calibration process. {{attachment:ds2_00_projects.png||width="600"}} <<BR>> ''Projects Home screen'''
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{{attachment:31_fiducialCalibWindow.png||width="548",height="440"}} <<BR>> * To start processing a new batch of dissection photographs click on '''New Project'''.
* Open a project to continue where you left off or backtrack to any completed steps.
''' Tip ''' For advaced users, the gear icon can be used to change which resources are used by the automatic segmentation model, covered in [[#Automatic segmentation settings|automatic segmentation settings]].
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Pan and zoom can be used to have a precise selection in these GUIs. First, select the center of one of the fiducials, followed by selecting the outer ring.
|| {{attachment:32_fiducialCenter.png||height="237"}} || {{attachment:33_fiducialDiameter.png||height="237"}} ||
||The first selection at the fiducial center. ||The second selection at the outer circle of the fiducial. ||
After naming a project you will be prompted to save a folder of the same name. It is in this folder that the outputs of all steps will be stored.
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After selecting all the points, set the width and height between the fiducial markers. Next, click “Perform calibration,” to save a calibration '.npz' file. This calibration file will be used for automating pixel correction in subsequent steps, as long as the fiducial markers are not moved. <<BR>> == Directory Structure ==
For each project the following directory structure will be populated with all outputs.
||'''Folder / file'''||'''Contents'''||
||`photos/`|| Copy of the original photographs||
||`deformed/`||Pixel-corrected photos||
||`mask/`||Binary tissue masks||
||`connected_components/`||Label maps per slab||
||`recon/`||The 3D-photo reconstruction||
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== Dissection Photo GUI ==
The dissection photo GUI performs all preprocessing tasks, including pixel correction, binarizing images, and selecting connected components.
To run the GUI, source Freesurfer and use command '''dissection_photo_gui'''. The first time the GUI is run it will display instructions on setup of model weights for the segmentation step.<<BR>>
== Step 1. Add photographs ==
1. Drag and drop a folder containing dissection photographs, or click '''Upload Images'''.
1. Select the photographs that should be used for the reconstruction. This can be used to omit repeat photographs, dissection photographs of cerebellar tissue, or pre-slabbing gross photographs. Double click on any image in the grid for a larger preview.
1. If you have or would like to create a calibration file to automate pixel correction, click on '''+ Add a calibration file (optional)''' and follow steps in [[#Making a calibration file|making a calibration file]] and then [[#Prospective Correction (Using fiducial markers and calibration file) | Prospective Correction]]
1. Click '''Get Started'''
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== Pixel Correction ==
In the first menu of the '''dissection_photo_gui''' select the input directory with the unprocessed gross photographs. Photographs should be set in the order such that tissue slabs are seen in the order they were cut. Additionally select the output directory where the pixel-corrected images will be saved. Here we have the option to load an optimal calibration file if available to automate pixel correction. Select '''Go!''' when you have defined the required directories. <<BR>>
=== Optional: Making a calibration file ===
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{{attachment:35_dissection_photo_gui_screen_1.png||width="600",height="400"}} <<BR>> == Step 2: Pixel Correction ==
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If a calibration file was used the next widow will display the pixel-corrected images for quality assurance purposes. Click '''Next''' to proceed assuring the images were corrected.<<BR>><<BR>>
If no calibration file is provided the next window will be for the '''Retrospective Correction''' mode. Select the type of calibration, 2-point, 3-point, or 4-point, and its relevant dimensions in millimeters. The 2-point calibration is used when there is a single axis of ground truth measurement, which enables rough pixel size correction (e.g., one ruler in the image). The 3-point calibration is used when there are three points on the corners of a rectangle – but the fourth point is not available (e.g., there are two orthogonal rulers). The 4-point version should be chosen if the four corners of a rectangle can be identified; this is the default model when the automatic mode with calibration file is used. The 3- and 4-point versions enable perspective correction (approximate with 3 points; exact with 4). We can pan and zoom to make precise selections on the image.<<BR>>
|| {{attachment:36_dissection_photo_gui_screen_2.png||width="400",height="266"}} || {{attachment:37_dissection_photo_gui_screen_2_zoomed.png||width="400",height="266"}} ||
<<BR>>
=== Prospective Correction (Using fiducial markers and calibration file) ===
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After pixel correcting all images, click '''Proceed to Segmentation''' to continue to the next step.<<BR>> === Retrospective Correction (Using a spatial reference within the photographs) ===
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== Tissue Segmentation ==
After selecting an output directory for the masked images, our automatic segmentation tool will immediately start predicting a binary mask per each photograph. If a GPU is available all five folds of the model will be run which will slightly increase segmentation accuracy. After the first photograph is segmented by the model, the user can start cleaning the predicted binary masks. Here the user can pan and zoom like before, but can additionally use a brush tool to remove or add any pixels. Remove any non-slice tissue and the background. The opacity of the predicted mask can also be changed using the provided slider, or toggled using Ctrl+Z. <<BR>>
|| {{attachment:38_dissection_photo_gui_screen_3_noseg.png||width="400",height="266"}} || {{attachment:39_dissection_photo_gui_screen_3_seg.png||width="400",height="266"}} ||
<<BR>>
== Step 3: Binary Segmentation ==
=== Automatic Segmentation Settings ===
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'''IMPORTANT''': The cortical surface should not be part of the masks, so the first (if photographed from the anterior side) or last slice (if photographed from the posterior side) should '''NOT''' be considered. You can either leave it out of the mask or ignore it when processing with the GUI. <<BR>> == Step 4: Slab Connected Components ==
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Once we are satisfied with the mask, click '''Next''' to proceed to the next image. After all images have been segmented and cleaned, click '''Proceed to CC''' to continue to the connected components step. <<BR>>

== Connected Components ==
Like previous steps, select an output directory for the connected components masks. The connected components section of the GUI will display the masked and pixel-corrected photographs. Here the user will draw boxes around the tissue slabs in each photograph. The GUI will then save the connected components as .npy files. <<BR>>

{{attachment:40_dissection_photo_gui_screen_4_tissue.png||width="600",height="400"}} <<BR>>

For each image select slices in order, either anterior-posterior or posterior-anterior. Remain consistent of slice order on all photographs. Connected components are selected by clicking and dragging to draw a box in a region of each individual slab in the photograph. After a box has been drawn in each individual slab, click '''Next ''' to save the output .npy file and move to the next image.

'''Tip''': Make sure no boxes are overlapping.

Once a box is drawn over the tissue, the slab will be colored to show what is being included as one slice.<<BR>>

{{attachment:41_dissection_photo_gui_screen_4_color.png||width="600",height="400"}} <<BR>>

Above is an example of how to correctly draw the boxes within the brain slabs themselves. These boxes inform the GUI that the pixels connected to these slabs are all part of the same tissue slice. Note the box covers tissue from the temporal lobe as it can sometimes be disjoint from the rest of the slab. <<BR>>

Below is an example of how '''__NOT__''' to draw boxes for this GUI. Notice the occurrence of overlap between boxes and the inclusion of an abundance of black space. Try to keep the boxes drawn to small regions within the brain slabs themselves as to not include any background pixels. <<BR>>
{{attachment:42_dissection_photo_gui_screen_4_bad.png||width="600",height="400"}} <<BR>><<BR>>

= Photo Reconstruction =
== Step 5: Photo Reconstruction ==
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= Photo-Synthseg Segmentation = = Part 3: Downstream Tasks =
=
= Photo-Synthseg Segmentation ==
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'''Example for running SynthSeg on a Left Hemisphere''' <<BR>> 
'''Example for running SynthSeg on a Left Hemisphere''' <<BR>>
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 . --parc   . --parc

Photo Reconstruction Documentation



Citation

If you use these tools in your analysis, please cite:

  • Gazula, H., Tregidgo, H.F., Billot, B., Balbastre, Y., Williams Ramirez, J., Herisse, R., Deden-Binder, L.J., Casamitjana, A., Melief, E.J., Latimer, C.S. and Kilgore, M.D., 2024. Machine learning of dissection photographs and surface scanning for quantitative 3D neuropathology. Elife, 12, p.RP91398. doi

The machine learning slice imputation in the reconstruction is described in:

  • Crespo-Aguirre, M., Williams-Ramirez, J., Zemlyanker, D., Hu, X., Deden-Binder, L.J., Herisse, R., Montine, M., Connors, T.R., Mount, C., MacDonald, C.L., Keene, C.D., Latimer, C.S., Oakley, D.H., Hyman, B.T., Lawry-Aguila, A. and Iglesias, J.E., 2026. Improving neuropathological reconstruction fidelity via AI slice imputation. Acta Neuropathologica Communications. doi

Automatic segmentation model trained using nnUNet:

  • Williams Ramirez, J., Zemlyanker, D., Deden-Binder, L., Herisse, R., Garcia Pallares, E., Gopinath, K., Gazula, H., Mount, C., Kozanno, L.N., Marshall, M.S., Connors, T.R., Frosch, M.P., Montine, M., Oakley, D.H., Mac Donald, C.L., Keene, C.D., Hyman, B.T., Fischl, B. and Iglesias, J.E., 2026. A public generalizable AI tool for automated segmentation of coronal brain tissue slabs for 3D neuropathology. PLOS One, 21(8), p.e0355740. doi

  • Isensee, F., Jaeger, P.F., Kohl, S.A., Petersen, J. and Maier-Hein, K.H., 2021. nnU-Net: a self-configuring method for deep learning-based biomedical image segmentation. Nature methods, 18(2), pp.203-211.

Click here for a video with an overview of the method
video_screenshot.png

Purpose

This manual provides an end-to-end guide for using the tools available on FreeSurfer to reconstruct dissection photographs of brain slabs into a 3D-reconstruction for quantitative analysis. Reconstructions are done by registering photographs to a 3D reference like an MRI, a post-mortem surface scan, or an atlas. The guide touches on acquisition of surface scans prior to slabbing, preparing tissue slabs for gross photography, and how to preprocess photographs using the dissection_photo graphical user interface.

Requirements

  • The latest FreeSurfer development version sourced in your terminal.

  • Model files (downloaded once):
  • A CUDA enabled graphics card is optional: segmentation and reconstruction are much faster with one.

Overview

  1. Acquire a 3D reference either a surface scan or an MRI. Without one, slabs are registered to an atlas.

  2. Photograph the tissue slabs

  3. Preprocess the photos on the dissection photo GUI

  4. Reconstruct the 3D volume

  5. Downstream analysis of photographs

Part 1: Acquisition

Surface scanning

A surface scan of the specimen, taken before it is slabbed after the cerebellum is sectioned. The full scanning protocol is available on its own page: Surface Scanning Protocol.

Summary on key requirements of a reference mesh:

  • The cerebellum removed: it is not on the slabs, so including it in the scan leads to an incorrect reconstruction.
  • The sides of the specimen captured.
  • A watertight mesh, saved as .stl. Small holes in the initial point-cloud due to deep sulci are fine - these will be covered by the meshing process.


Preparing Slabs

The following guidelines should be followed when preparing slab images for optimal results.

Guidelines for Brain Slab Image Acquisition

There are some important requirements for the photographic setup of the brain slabs to ensure the best results.

Use a high-contrast background that stands out in uniform contrast to the brain slabs, such as a solid black background. This will make slabs are easier to segment downstream. Using a complex background with color similar to your brain slabs, will lead to a more manual intervention such as having to manually trace contours, which is not only time-consuming but also non-reproducible.

17_low_constrast.png

18_high_contrast.png

Difficult to segment low contrast background.

Easy to segment high contrast background.

Additionally, all tissue block faces must be facing the same direction. All slices should be either from an anterior or a posterior view. Note if slabs are from the posterior view, an extra flag,

--photos_of_posterior_side must be used for the final reconstruction command.

When a single slice produces multiple tissue blocks, they should be placed as similar to the original anatomy as possible. For example, after acquiring slices from the frontal pole, the initial blocks corresponding to the temporal lobe will often be detached from the main block. The following figure shows a) Proper anatomical placement of tissue and, b) Tissue placed too far apart, which is not anatomically accurate.

19_slab_placement.png
Tissue slab placement a) Properly placed tissue b) Tissue placed in a non-anatomical manner.

Another example of difficult tissue placement can be the corpus callosum. In the following figure, we see a good example setup with high contrast for the background and good lighting. However, the placement of the corpus callosum on the rightmost slab is incorrect, which will negatively affect volumetric estimates of the third ventricle.

20_incorrect_tissue_placement.png

Markers for pixel and perspective corrections

To calibrate pixel size, we will need landmarks with known distances in between them to be provided by the user. The minimum requirement is a ruler, which provides us with two discrete landmarks. This enables rough This method is preferable for legacy images that only have a ruler for reference.

21_twoPoint.jpeg

Tip: It is better to use landmarks that are as far apart as possible, as the relative error when manually setting the reference in pixels per millimeter decreases with greater distances.

A more effective setup involves four landmarks placed the corners of a rectangle of known dimensions. This enables us to correct for both pixel size and perspective. In the example below, we can easily tell that the 4 points marked on the grid define a rectangle of dimensions 170x200 mm.

22_fourPoint.png

The optimal scenario is to have 4 points defined by fiducial markers with highly salient features. This enables our software to automatically recognize the fiducials, which minimizes human interaction, reducing time and maximizing reproducibility. We strongly recommend that you print these set fiducials and place them on the corners of the board.

23_fiducials.png

Tip: For best results, affix these fiducials to a small piece of rubber/wood/plastic that lifts them X mm above the board, where X is the thickness of your typical brain slice. Lifting the fiducial minimizes error due to the surface of the brain slice not being at the same distance as the plane of the board surface, but rather a few millimeters above it.

24_fiducialTissue.png

The fiducial form the four corners of our corrected image; hence all tissue should be within the rectangle created from the four fiducial corners. The following image shows slab photos where the fiducials were not placed sufficiently apart.

25_tissueSpace.png

By drawing a rectangle with all fiducial markers, it is clear that much of the tissue lies outside of the pixel-corrected region.

26_tissueBox.png

In summary, here is an example of what an optimal photographic setup would look like, including the uniform, high-contrast background and provided fiducials located at known distances, and consistent lighting on all slabs.

27_goodContrast.png

Tip: It does not matter if slabs are not presented on a grid, as long as the distance between the fiducials is known. The software will draw digital rulers for your images later pixel-correction.

Part 2: Prerprocessing Photographs with the Dissection Photo App

The dissection photo app has five principal windows for each subject: Add photos, Correction, Segmentation, Connected components and Reconstruction. The step bar at the top of the window shows which step is being done, users can click any backtrack by clicking any of the previous steps at any time, alternatively the house icon to return to the Projects screen with a summary of all reconstructions done or in process. For each project work is saved as you go, so the can can be closed at any time to later pick up where you left off.

Before continuing, make sure the development version of Freesurfer is properly sourced, you have downloaded the model weights, and have set the NNUNET_MODEL_DIR as an environment variable pointing to the segmentation model before continuing with the tutorial. To start the application use command *dissection_photo_2*

Projects Page

Each specimen corresponds to a project: a folder which will be populated with the outputs from all steps. The project home contains a summary of all projects and their progress.

ds2_00_projects.png
Projects Home screen

* To start processing a new batch of dissection photographs click on New Project. * Open a project to continue where you left off or backtrack to any completed steps. Tip For advaced users, the gear icon can be used to change which resources are used by the automatic segmentation model, covered in automatic segmentation settings.

After naming a project you will be prompted to save a folder of the same name. It is in this folder that the outputs of all steps will be stored.

Directory Structure

For each project the following directory structure will be populated with all outputs.

Folder / file

Contents

photos/

Copy of the original photographs

deformed/

Pixel-corrected photos

mask/

Binary tissue masks

connected_components/

Label maps per slab

recon/

The 3D-photo reconstruction

Step 1. Add photographs

1. Drag and drop a folder containing dissection photographs, or click Upload Images. 1. Select the photographs that should be used for the reconstruction. This can be used to omit repeat photographs, dissection photographs of cerebellar tissue, or pre-slabbing gross photographs. Double click on any image in the grid for a larger preview. 1. If you have or would like to create a calibration file to automate pixel correction, click on + Add a calibration file (optional) and follow steps in making a calibration file and then Prospective Correction 1. Click Get Started

Optional: Making a calibration file

Step 2: Pixel Correction

Prospective Correction (Using fiducial markers and calibration file)

Retrospective Correction (Using a spatial reference within the photographs)

Step 3: Binary Segmentation

Automatic Segmentation Settings

Step 4: Slab Connected Components

Step 5: Photo Reconstruction

Please see our separate page on the command mri_3d_photo_recon


Part 3: Downstream Tasks

Photo-Synthseg Segmentation

The 3D reconstructed stacks can be segmented with SynthSeg using the flag --photo. Please see the wiki page for SynthSeg for further information.

43_synthseg_photo.jpg

44_synthseg_parc.jpg

Example for running SynthSeg on a Left Hemisphere

  • mri_synthseg \
  • --i ./recon/photo_recon.mgz \
  • --o ./recon/photo_recon_synthseg.mgz \
  • --photo left \
  • --parc

PhotoTools (last edited 2026-10-28 18:50:43 by JonWilliamsRamirez)