Evidence map›Paper›PMID 42079087›Full record

ArticlebioRxiv : the preprint server for biology2026

TomoSwin3D: a Swin3D Transformer for the Identification and Classification of Macromolecules in 3D Cryo-ET Tomograms.

Ashwin Dhakal, Rajan Gyawali, Jianlin Cheng

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2026. 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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0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Ashwin DhakalDepartment of Electrical Engineering and Computer Science, University of Missouri, Columbia, MO 65211, USA.ORCID 0000-0002-4047-9947
Rajan GyawaliDepartment of Electrical Engineering and Computer Science, University of Missouri, Columbia, MO 65211, USA.ORCID 0000-0002-7052-4964
Jianlin ChengDepartment of Electrical Engineering and Computer Science, University of Missouri, Columbia, MO 65211, USA.ORCID 0000-0003-0305-2853

Funding

Deep learning methods for automated and accurate reconstruction of protein structures from cryo-EM image dataR01GM146340 · NIGMS · UNIVERSITY OF MISSOURI-COLUMBIA · PI CHENG, JIANLIN · 2022 to 2025
$1.4M
NIGMS NIH HHS R01 GM146340
6 · The paper itself

Abstract

Cryo-electron tomography (cryo-ET) enables in situ three-dimensional visualization of many protein complexes and other macromolecular assemblies such as ribosomes in cells, yet automated macromolecule particle identification in 3D cryo-ET tomograms remains a major bottleneck due to dose-limited low signal-to-noise ratios, missing-wedge artifacts, and densely crowded cellular backgrounds. We present TomoSwin3D, an end-to-end three-dimensional (3D) macromolecule particle identification and classification pipeline centered on a Swin Transformer-based U-Net that performs particle identification and classification and outputs particle centroid coordinates. TomoSwin3D leverages a multi-channel input representation that augments raw tomogram densities with complementary 3D feature maps capturing edge strength (Sobel gradients), local contrast enhancement (morphological top-hat), and multiscale blob responses (Difference-of-Gaussians), improving detectability of small and low-contrast targets. To better preserve particle geometry and avoid hand-crafted shape assumptions, it adopts occupancy-preserving supervision that directly uses available 3D instance masks rather than heuristic Gaussian/spherical labels and applies scalable patch-wise inference followed by lightweight post-processing (connected-component analysis, size filtering, centroid extraction) for robust centroid coordinate extraction. Across diverse simulated and experimental cryo-ET tomogram benchmarks including SHREC 2021 and 2020 test datasets, EMPIAR dataset, and Cryo-ET data portal dataset, TomoSwin3D achieves strong and consistent performance in detecting proteins and other particles, outperforming existing methods, with a pronounced advantage in picking hard, small protein particles. These results establish TomoSwin3D as a scalable and accurate solution for high-throughput cryo-ET macromolecule particle picking and downstream subtomogram averaging.

Identifiers

PMID42079087
PMCPMC13131780

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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.