Evidence map›Paper›PMID 41652996›Full record

ArticleBioinformatics (Oxford, England)2026

CeLLTra: aligning cell names with gene expression via a pathway-informed transformer.

Zhao Li, Zaiyi Zheng, Rongbin Li, Wenbo Chen, Yuntao Yang, Meer A Ali, Jundong Li, W Jim Zheng

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 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
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1 · What the graph read from it

What it found

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2 · The registry

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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

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

8 authors.

Zhao LiDepartment of Bioinformatics & Systems Medicine, McWilliams School of Biomedical Informatics, University of Texas Health Science Center at Houston, Houston, TX 77030, United States.
Zaiyi ZhengDepartment of Electrical and Computer Engineering, University of Virginia, Charlottesville, VA 22903, United States.ORCID 0009-0003-0685-0057
Rongbin LiDepartment of Bioinformatics & Systems Medicine, McWilliams School of Biomedical Informatics, University of Texas Health Science Center at Houston, Houston, TX 77030, United States.
Wenbo ChenDepartment of Bioinformatics & Systems Medicine, McWilliams School of Biomedical Informatics, University of Texas Health Science Center at Houston, Houston, TX 77030, United States.
Yuntao YangDepartment of Genomic Medicine, University of Texas MD Anderson Cancer Center, Houston, TX 77030, United States.
Meer A AliDepartment of Bioinformatics & Systems Medicine, McWilliams School of Biomedical Informatics, University of Texas Health Science Center at Houston, Houston, TX 77030, United States.
Jundong LiDepartment of Electrical and Computer Engineering, University of Virginia, Charlottesville, VA 22903, United States.
W Jim ZhengDepartment of Bioinformatics & Systems Medicine, McWilliams School of Biomedical Informatics, University of Texas Health Science Center at Houston, Houston, TX 77030, United States.ORCID 0000-0001-7411-6047

Funding

Convalescent Plasma to Limit Coronavirus Associated ComplicationsUL1TR003167 · NCATS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI KARP, DANIEL D, MCPHERSON, DAVID D · 2019 to 2023
$45.3M
TRAINING PROGRAM IN COMPUTATIONAL BIOLOGY AND MEDICINET15LM007093 · NLM · RICE UNIVERSITY · PI Lydia E. Kavraki · 1992 to 2026
$20.8M
Center for Clinical and Translational SciencesUM1TR004906 · NCATS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI Maria Eulalia Fernandez, LORNA H. MCNEILL · 2024 to 2026
$16.7M
Engagement and outreach to achieve a FAIR data ecosystem for the BICANU24MH130988 · NIMH · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI HUA XU, Guo-Qiang ZHANG · 2022 to 2026
$4.6M
Finding Combinatorial Drug Repositioning Therapy For Alzheimer'S Disease And Related DementiasR01AG066749 · NIA · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI JIANG, XIAOQIAN, ZHENG, WENJIN JIM · 2020 to 2024
$4.4M
Advancing Drug Repositioning for Alzheimer’s Disease using Real-world DataR56AG069880 · NIA · UNIVERSITY OF FLORIDA · PI BIAN, JIANG, CHEN, YONG · 2021 to 2022
$1.6M
Cancer Prevention and Research Institute of Texas RP170668Department of Defense W81XWH-22-1-0164Gulf Coast Consortia 5T15LM007093-31National Institutes of Health (NIH) 1R01AG066749National Institutes of Health (NIH) 1U24MH130988-01National Institutes of Health (NIH) 1UL1TR003167National Institutes of Health (NIH) 1UM1TR004906-01National Institutes of Health (NIH) 5R56AG069880-02NCATS NIH HHS UL1 TR003167NCATS NIH HHS UM1 TR004906NIA NIH HHS R01 AG066749NIA NIH HHS R56 AG069880NIMH NIH HHS U24 MH130988NLM NIH HHS T15 LM007093
6 · The paper itself

Abstract

motivationSingle-cell RNA sequencing (scRNA-Seq) technology enables detailed exploration of gene expression at the individual cell level, crucial for annotating cell types and understanding cellular diversity. Traditional methods for cell type annotation often rely on marker genes and manual labeling, posing challenges due to low data quality and incomplete reference datasets.

resultsWe developed CeLLTra, a novel contrastive learning framework that leverages a Transformer-based model integrating biological pathway information to group genes into super tokens, effectively capturing comprehensive gene expression from scRNA-Seq data. By combining this pathway-informed Transformer with a pretrained domain-specific language model, CeLLTra accurately aligns cell-type annotations with gene expression profiles. Evaluations on a large-scale human scRNA-Seq dataset showed that CeLLTra significantly outperformed state-of-the-art methods in supervised and zero-shot cell-type prediction. Additionally, CeLLTra generalized well to external datasets, improving clustering performance and enabling better characterization of cancerous cell states in tumor-infiltrating myeloid cells from non-small cell lung cancer patients. AVAILABILITY AND IMPLEMENTATION: CeLLTra is freely available on GitHub (https://github.com/WJZheng-group/CeLLTra) and Zenodo (https://doi.org/10.5281/zenodo.17666735). The datasets underlying this article are the following: GSE201333 and GSE127465. All these datasets are publicly available and can be freely accessed on the Gene Expression Omnibus repository.

Indexed as

Computational BiologyRNA-SeqSoftwareGene Expression ProfilingHumansSingle-Cell Gene Expression AnalysisArtificial IntelligenceCell type annotationDeep learningPathway informed transformerscRNA-Seq

Identifiers

PMID41652996
PMCPMC12881829

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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.