» Articles » PMID: 34604701

Semantic Segmentation of Microscopic Neuroanatomical Data by Combining Topological Priors with Encoder-decoder Deep Networks

Overview
Journal Nat Mach Intell
Publisher Springer Nature
Date 2021 Oct 4
PMID 34604701
Citations 7
Authors
Affiliations
Soon will be listed here.
Abstract

Understanding of neuronal circuitry at cellular resolution within the brain has relied on neuron tracing methods which involve careful observation and interpretation by experienced neuroscientists. With recent developments in imaging and digitization, this approach is no longer feasible with the large scale (terabyte to petabyte range) images. Machine learning based techniques, using deep networks, provide an efficient alternative to the problem. However, these methods rely on very large volumes of annotated images for training and have error rates that are too high for scientific data analysis, and thus requires a significant volume of human-in-the-loop proofreading. Here we introduce a hybrid architecture combining prior structure in the form of topological data analysis methods, based on discrete Morse theory, with the best-in-class deep-net architectures for the neuronal connectivity analysis. We show significant performance gains using our hybrid architecture on detection of topological structure (e.g. connectivity of neuronal processes and local intensity maxima on axons corresponding to synaptic swellings) with precision/recall close to 90% compared with human observers. We have adapted our architecture to a high performance pipeline capable of semantic segmentation of light microscopic whole-brain image data into a hierarchy of neuronal compartments. We expect that the hybrid architecture incorporating discrete Morse techniques into deep nets will generalize to other data domains.

Citing Articles

A semi-supervised fracture-attention model for segmenting tubular objects with improved topological connectivity.

Zhou Y, Zhong L, Wang Z, Ge Y Bioinformatics. 2025; 41(1).

PMID: 39799504 PMC: 11783301. DOI: 10.1093/bioinformatics/btaf013.


Topology-Aware Uncertainty for Image Segmentation.

Gupta S, Zhang Y, Hu X, Prasanna P, Chen C Adv Neural Inf Process Syst. 2024; 36:8186-8207.

PMID: 39484069 PMC: 11526043.


Collaborative augmented reconstruction of 3D neuron morphology in mouse and human brains.

Zhang L, Huang L, Yuan Z, Hang Y, Zeng Y, Li K Nat Methods. 2024; 21(10):1936-1946.

PMID: 39232199 PMC: 11468770. DOI: 10.1038/s41592-024-02401-8.


Adaptive Segmentation of DAPI-stained, C-banded, Aggregated and Overlapping Chromosomes.

Platkov M, Gardos Z, Gurevich L, Levitsky I, Burg A, Amar S Cell Biochem Biophys. 2024; 82(4):3645-3656.

PMID: 39097855 DOI: 10.1007/s12013-024-01453-z.


Integrated platform for multiscale molecular imaging and phenotyping of the human brain.

Park J, Wang J, Guan W, Gjesteby L, Pollack D, Kamentsky L Science. 2024; 384(6701):eadh9979.

PMID: 38870291 PMC: 11830150. DOI: 10.1126/science.adh9979.


References
1.
Khoo V, Dearnaley D, Finnigan D, Padhani A, Tanner S, Leach M . Magnetic resonance imaging (MRI): considerations and applications in radiotherapy treatment planning. Radiother Oncol. 1997; 42(1):1-15. DOI: 10.1016/s0167-8140(96)01866-x. View

2.
LeCun Y, Bengio Y, Hinton G . Deep learning. Nature. 2015; 521(7553):436-44. DOI: 10.1038/nature14539. View

3.
Helmstaedter M, Mitra P . Computational methods and challenges for large-scale circuit mapping. Curr Opin Neurobiol. 2012; 22(1):162-9. PMC: 3406305. DOI: 10.1016/j.conb.2011.11.010. View

4.
Dodt H, Leischner U, Schierloh A, Jahrling N, Mauch C, Deininger K . Ultramicroscopy: three-dimensional visualization of neuronal networks in the whole mouse brain. Nat Methods. 2007; 4(4):331-6. DOI: 10.1038/nmeth1036. View

5.
Lin M, Takahashi Y, Huo B, Hanada M, Nagashima J, Hata J . A high-throughput neurohistological pipeline for brain-wide mesoscale connectivity mapping of the common marmoset. Elife. 2019; 8. PMC: 6384052. DOI: 10.7554/eLife.40042. View