Evidence map›Paper›PMID 40581778›Full record

ArticleBioinformatics (Oxford, England)2025

scGT:integration algorithm for single-cell RNA-seq and ATAC-seq based on graph transformer.

Yunjing Qi, Yulong Kan, Jing Qi, Shuilin Jin

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Yunjing QiSchool of Mathematics, Harbin Institute of Technology, Harbin 150000, China.
Yulong KanSchool of Mathematics, Harbin Institute of Technology, Harbin 150000, China.ORCID 0000-0002-9200-5161
Jing QiSchool of Mathematics, Harbin Institute of Technology, Harbin 150000, China.
Shuilin JinSchool of Mathematics, Harbin Institute of Technology, Harbin 150000, China.ORCID 0000-0002-2318-432X

Funding

Heilongjiang Postdoctoral Foundation LBH-Z23020Key Research and Development Program of Heilongjiang 2022ZX01A19National Natural Science Foundation of China 12301623National Natural Science Foundation of China 62172122National Natural Science Foundation of China 62271173Natural Science Foundation of Heilongjiang Province JQ2023A003Natural Science Foundation of Heilongjiang Province LH2024A003Postdoctoral Fellowship Program of CPSF GZC20233473
6 · The paper itself

Abstract

motivationMulti-omics analysis of individual cells offers remarkable opportunities for exploring the dynamics and relationships of gene regulatory states across large atlas data. However, the current integration algorithms have limited performance, largely due to ignoring the impact of correlation features within the dataset on the discrepancies between omics.

resultsIn this study, we propose scGT, a model based on Graph Transformer for single-cell RNA-seq and ATAC-seq data, which leverages the robust graph structures strengthened by correlation features present in each raw dataset to harmonize representations of multi-omics data, enabling the integration of multi-omics and effective label transfer. We compare scGT with other state-of-the-art methods on paired and unpaired datasets. The results show that scGT accomplishes more accurate label transfer and is capable of integrating datasets with millions of cells. Meanwhile, scGT achieves better performance for preserving biological variation during integration. AVAILABILITY AND IMPLEMENTATION: The source code and data used in this article can be found at https://github.com/Jinsl-lab/scGT.

Indexed as

AlgorithmsChromatin Immunoprecipitation SequencingRNA-SeqSequence Analysis, RNASingle-Cell AnalysisSoftwareHumansSingle-Cell Gene Expression Analysis

Identifiers

PMID40581778
PMCPMC12233090

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