Evidence map›Paper›PMID 37873366›Full record

ArticlebioRxiv : the preprint server for biology2025

Self-supervised segmentation and characterization of fiber bundles in anatomic tracing data.

Vaanathi Sundaresan, Julia F Lehman, Chiara Maffei, Suzanne N Haber, Anastasia Yendiki

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In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Vaanathi SundaresanDepartment of Computational and Data Sciences, Indian Institute of Science, Bengaluru, Karnataka 560012, India.ORCID 0000-0002-9451-4779
Julia F LehmanDepartment of Pharmacology and Physiology, University of Rochester School of Medicine, Rochester, NY, United States.
Chiara MaffeiAthinoula A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital and Harvard Medical School, Charlestown, MA, United States.
Suzanne N HaberDepartment of Pharmacology and Physiology, University of Rochester School of Medicine, Rochester, NY, United States.
Anastasia YendikiAthinoula A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital and Harvard Medical School, Charlestown, MA, United States.

Funding

The neural network of OCD, linking NHP and human studiesP50MH106435 · NIMH · UNIVERSITY OF ROCHESTER · PI STEVEN A RASMUSSEN · 2015 to 2026
$28.9M
BRAIN CONNECTS: The center for Large-scale Imaging of Neural Circuits (LINC)UM1NS132358 · NINDS · MASSACHUSETTS GENERAL HOSPITAL · PI Suzanne N Haber, Elizabeth M. C. Hillman · 2023 to 2026
$17.5M
Continuity of the Limbic Circuit Through the Basal GangliaR01MH045573 · NIMH · UNIVERSITY OF ROCHESTER · PI HABER, SUZANNE N · 1989 to 2024
$10.1M
Bridging Diffusion MRI and Chemical Tracing for Validation and Inference of Fiber ArchitecturesR01NS119911 · NINDS · MASSACHUSETTS GENERAL HOSPITAL · PI YENDIKI, ANASTASIA · 2021 to 2024
$2.6M
Multimodal mapping of the neurocircuitry of the human prefrontal cortexR01EB021265 · NIBIB · MASSACHUSETTS GENERAL HOSPITAL · PI YENDIKI, ANASTASIA · 2016 to 2019
$2.0M
Mapping Human Neurocircuitry Across Scales with Diffusion MRI and Optical ImagingR01NS127353 · NINDS · MASSACHUSETTS GENERAL HOSPITAL · PI Anastasia Yendiki · 2024 to 2026
$1.9M
NIBIB NIH HHS R01 EB021265NIMH NIH HHS P50 MH106435NIMH NIH HHS R01 MH045573NINDS NIH HHS R01 NS119911NINDS NIH HHS R01 NS127353NINDS NIH HHS UM1 NS132358Wellcome Trust
6 · The paper itself

Abstract

Anatomic tracing is the gold standard tool for delineating brain connections and for validating more recently developed imaging approaches such as diffusion MRI tractography. A key step in the analysis of data from tracer experiments is the careful, manual charting of fiber trajectories on histological sections. This is a very time-consuming process, which limits the amount of annotated tracer data that are available for validation studies. Thus, there is a need to accelerate this process by developing a method for computer-assisted segmentation. Such a method must be robust to the common artifacts in tracer data, including variations in the intensity of stained axons and background, as well as spatial distortions introduced by sectioning and mounting the tissue. The method should also achieve satisfactory performance using limited manually charted data for training. Here we propose the first deep-learning method, with a self-supervised loss function, for segmentation of fiber bundles on histological sections from macaque brains that have received tracer injections. We address the limited availability of manual labels with a semi-supervised training technique that takes advantage of unlabeled data to improve performance. We also introduce anatomic and across-section continuity constraints to improve accuracy. We show that our method can be trained on manually charted sections from a single case and segment unseen sections from different cases, with a true positive rate of ~0.80. We further demonstrate the utility of our method by quantifying the density of fiber bundles as they travel through different white-matter pathways. We show that fiber bundles originating in the same injection site have different levels of density when they travel through different pathways, a finding that can have implications for microstructure-informed tractography methods. The code for our method is available at https://github.com/v-sundaresan/fiberbundle_seg_tracing.

Indexed as

Anatomic tracingcontrastive lossfiber bundle detectionfiber densityself-supervisedtemporal ensembling

Identifiers

PMID37873366
PMCPMC10592842

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.