Evidence map›Paper›PMID 42139163›Full record

ArticleBriefings in bioinformatics2026

scMarkerGene: an interpretable neural network framework for cell-type-specific marker gene discovery.

Jingkai Zhang, Si Hoi Kou, Jiulu Zhao, Xiaomin Li, Yongbing Zhao

Abstract read
In one paragraph

Article in Briefings in bioinformatics, 2026. 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

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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

5 authors.

Jingkai ZhangCenter for Biomedical Digital Science, Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences, No. 190, Kaiyuan Avenue, Huangpu District, Guangzhou 510530, China.
Si Hoi KouCenter for Biomedical Digital Science, Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences, No. 190, Kaiyuan Avenue, Huangpu District, Guangzhou 510530, China.
Jiulu ZhaoCenter for Biomedical Digital Science, Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences, No. 190, Kaiyuan Avenue, Huangpu District, Guangzhou 510530, China.
Xiaomin LiCenter for Biomedical Digital Science, Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences, No. 190, Kaiyuan Avenue, Huangpu District, Guangzhou 510530, China.
Yongbing ZhaoCenter for Biomedical Digital Science, Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences, No. 190, Kaiyuan Avenue, Huangpu District, Guangzhou 510530, China.ORCID 0000-0002-9917-7425

Funding

National Key Research and Development Program of China 2024YFA1802300Science and Technology Planning Project of Guangdong Province 2023B1212060050Science and Technology Planning Project of Guangdong Province 2023B1212120009Science and Technology Planning Project of Guangdong Province 2023QN10X323Science and Technology Planning Project of Guangdong Province 2023ZT10Y154
6 · The paper itself

Abstract

In single-cell transcriptomics, the accurate identification of cell-type-specific marker genes is fundamental for understanding cellular heterogeneity. However, existing approaches often rely on arbitrary thresholds and clustering heuristics, making them sensitive to noise, annotation bias, and prone to capturing highly expressed rather than truly specific genes. Here, we present scMarkerGene, an interpretable neural network framework for marker gene discovery. scMarkerGene constructs a Contribution Score (CS) matrix that quantitatively measures each gene's influence on cell-type discrimination, transforming neural network predictions into gene-level importance signals. Through a downstream specificity filtering process, scMarkerGene robustly captures cell-type-distinguishing features and demonstrates strong robustness to dropout noise, diverse cell population sizes, varying annotation resolutions, and heterogeneous sequencing technologies. We comprehensively validated scMarkerGene across scRNA-seq datasets from multiple species, as well as on spatial transcriptomics and discretized pseudotime data, where it effectively identified dynamic and spatially resolved marker genes. Collectively, scMarkerGene provides an efficient, accurate, and interpretable framework for single-cell transcriptomic analysis, with broad potential for extension to multi-omics data integration and interpretation. The source code is available at https://scmarkergene.zhaopage.com/.

Indexed as

Neural Networks, ComputerSingle-Cell AnalysisSoftwareAnimalsGene Expression ProfilingGenetic MarkersHumansSingle-Cell Gene Expression AnalysisGenetic Markersartificial intelligencecell identitymarker gene discoverysingle cell data analysis

Identifiers

PMID42139163
PMCPMC13178462

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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.