NEURD offers automated proofreading and feature extraction for connectomics.

TitleNEURD offers automated proofreading and feature extraction for connectomics.
Publication TypeJournal Article
Year of Publication2025
AuthorsCelii B, Papadopoulos S, Ding Z, Fahey PG, Wang E, Papadopoulos C, Kunin AB, Patel S, J Bae A, Bodor AL, Brittain D, Buchanan JA, Bumbarger DJ, Castro MA, Cobos E, Dorkenwald S, Elabbady L, Halageri A, Jia Z, Jordan C, Kapner D, Kemnitz N, Kinn S, Lee K, Li K, Lu R, Macrina T, Mahalingam G, Mitchell E, Mondal SSubhra, Mu S, Nehoran B, Popovych S, Schneider-Mizell CM, Silversmith W, Takeno M, Torres R, Turner NL, Wong W, Wu J, Yu S-C, Yin W, Xenes D, Kitchell LM, Rivlin PK, Rose VA, Bishop CA, Wester B, Froudarakis E, Walker EY, Sinz F, H Seung S, Collman F, da Costa NMaçarico, R Reid C, Pitkow X, Tolias AS, Reimer J
JournalNature
Volume640
Issue8058
Pagination487-496
Date Published2025 Apr
ISSN1476-4687
KeywordsAnimals, Automation, Axons, Connectome, Dendrites, Dendritic Spines, Humans, Imaging, Three-Dimensional, Mice, Microscopy, Electron, Neurons, Software
Abstract

We are in the era of millimetre-scale electron microscopy volumes collected at nanometre resolution1,2. Dense reconstruction of cellular compartments in these electron microscopy volumes has been enabled by recent advances in machine learning3-6. Automated segmentation methods produce exceptionally accurate reconstructions of cells, but post hoc proofreading is still required to generate large connectomes that are free of merge and split errors. The elaborate 3D meshes of neurons in these volumes contain detailed morphological information at multiple scales, from the diameter, shape and branching patterns of axons and dendrites, down to the fine-scale structure of dendritic spines. However, extracting these features can require substantial effort to piece together existing tools into custom workflows. Here, building on existing open source software for mesh manipulation, we present Neural Decomposition (NEURD), a software package that decomposes meshed neurons into compact and extensively annotated graph representations. With these feature-rich graphs, we automate a variety of tasks such as state-of-the-art automated proofreading of merge errors, cell classification, spine detection, axonal-dendritic proximities and other annotations. These features enable many downstream analyses of neural morphology and connectivity, making these massive and complex datasets more accessible to neuroscience researchers.

DOI10.1038/s41586-025-08660-5
Alternate JournalNature
PubMed ID40205208
PubMed Central IDPMC11981913
Grant ListRF1 MH130416 / MH / NIMH NIH HHS / United States
P30 EY002520 / EY / NEI NIH HHS / United States
T15 LM007093 / LM / NLM NIH HHS / United States
U19 MH114830 / MH / NIMH NIH HHS / United States
R01 EY026927 / EY / NEI NIH HHS / United States