Evidence map›Paper›PMID 40689508›Full record

ArticleBioinformatics (Oxford, England)2025

IGCLAPS: an interpretable graph contrastive learning method with adaptive positive sampling for scRNA-seq data analysis.

Weihua Zheng, Wenwen Min, Shunfang Wang

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 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

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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

3 authors.

Weihua ZhengDepartment of Computer Science and Engineering, School of Information Science and Engineering, Yunnan University, Kunming 650500, China.
Wenwen MinDepartment of Computer Science and Engineering, School of Information Science and Engineering, Yunnan University, Kunming 650500, China.ORCID 0000-0002-2558-2911
Shunfang WangDepartment of Computer Science and Engineering, School of Information Science and Engineering, Yunnan University, Kunming 650500, China.ORCID 0000-0002-1927-8753

Funding

National Natural Science Foundation of China 62062067National Natural Science Foundation of China 62262069National Natural Science Foundation of China 62462068
6 · The paper itself

Abstract

motivationSingle-cell RNA sequencing (scRNA-seq) technology enables biological research at single-cell resolution. Cell clustering is a crucial task in scRNA-seq data analysis since it provides insights into cell heterogeneity. Although existing methods have made significant progress in this task, it remains challenging to fully utilize the relationship among cells.

resultsWe propose Interpretable Graph Contrastive Learning method with Adaptive Positive Sampling (IGCLAPS), a novel end-to-end graph contrastive clustering method for scRNA-seq data analysis. Specifically, IGCLAPS learns low-dimensional embeddings with a graph transformer, based on which a dual-head graph contrastive learning module is used to perform dimension reduction and cell clustering simultaneously. Besides, an accurate definition of positive sample pairs is crucial in contrastive learning, we devise an adaptive positive sampling module, which dynamically identifies true positive sample pairs based on both expression similarity and soft cluster labels generated by the contrastive learning module. Extensive experiments on a series of real datasets including cell clustering, visualization, and differential expression analysis demonstrate that IGCLAPS can effectively enhance clustering performance and generate interpretable gene expression patterns of scRNA-seq data. AVAILABILITY AND IMPLEMENTATION: The source codes of IGCLAPS are available at https://github.com/ZhengWeihuaYNU/IGCLAPS.

Indexed as

Machine LearningRNA-SeqSequence Analysis, RNASingle-Cell AnalysisSoftwareAlgorithmsCluster AnalysisGene Expression ProfilingHumansSingle-Cell Gene Expression Analysis

Identifiers

PMID40689508
PMCPMC12342183

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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.