Evidence map›Paper›PMID 40343344›Full record

ArticleResearch square2025

TomoScore: A Neural Network Approach for Quality Assessment of Cellular cryo-ET.

Xuqian Tan, Ethan Boniuk, Anisha Abraham, Xueting Zhou, Zhili Yu, Steven J Ludtke, Zhao Wang

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In one paragraph

Article in Research square, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Xuqian TanVerna and Marrs McLean Department of Biochemistry and Molecular Pharmacology, Baylor College of Medicine, Houston, TX 77030, USA.ORCID 0000-0001-6044-8876
Ethan BoniukVerna and Marrs McLean Department of Biochemistry and Molecular Pharmacology, Baylor College of Medicine, Houston, TX 77030, USA.
Anisha AbrahamVerna and Marrs McLean Department of Biochemistry and Molecular Pharmacology, Baylor College of Medicine, Houston, TX 77030, USA.ORCID 0009-0000-0107-6400
Xueting ZhouVerna and Marrs McLean Department of Biochemistry and Molecular Pharmacology, Baylor College of Medicine, Houston, TX 77030, USA.
Zhili YuVerna and Marrs McLean Department of Biochemistry and Molecular Pharmacology, Baylor College of Medicine, Houston, TX 77030, USA.
Steven J LudtkeVerna and Marrs McLean Department of Biochemistry and Molecular Pharmacology, Baylor College of Medicine, Houston, TX 77030, USA.ORCID 0000-0002-1903-1574
Zhao WangVerna and Marrs McLean Department of Biochemistry and Molecular Pharmacology, Baylor College of Medicine, Houston, TX 77030, USA.ORCID 0000-0003-4897-9986

Funding

Investigation of the Cellular and Molecular Mechanisms of Thrombocyte Integrin SignalingR01HL162842 · NHLBI · BAYLOR COLLEGE OF MEDICINE · PI WANG, ZHAO · 2022 to 2025
$1.6M
Support for CryoEM and CryoET Development in the Ludtke LabR35GM151999 · NIGMS · BAYLOR COLLEGE OF MEDICINE · PI STEVEN J LUDTKE · 2024 to 2026
$1.2M
NHLBI NIH HHS R01 HL162842NIGMS NIH HHS R35 GM151999
6 · The paper itself

Abstract

Electron cryo-tomography (cryo-ET) is a powerful imaging tool that allows three-dimensional visualization of subcellular and molecular architecture without chemical fixation. Tomogram quality varies widely, particularly during large high-throughput data collections, and the most common strategy for initial quality assessment is empirical judgment by an expert. Tomograms may be collected for two distinct purposes: annotation of subcellular features and cellular morphology, typically performed at lower magnifications and higher defocus, and subtomogram averaging, at high magnifications, closer to focus. For the first purpose, contrast and the ability to distinguish cellular features of interest are key, whereas for subtomogram averaging, recoverable signal at high resolution is the key factor. We have developed "TomoScore" a deep-learning based tomogram screening tool targeting cellular annotation. This tool provides a single quantitative measure of the suitability of a tomogram for annotation of subcellular features, in terms of the scale of features that can be readily distinguished. We further explore the relationship between accumulated electron dose and resulting quality, suggesting an optimum dose range for cryo-ET data collection. Overall, our study streamlines data processing and reduces the need for human involvement during pre-selection for tomogram segmentation.

Identifiers

PMID40343344
PMCPMC12060984

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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.