Evidence map›Paper›PMID 40671174›Full record

ArticleBriefings in bioinformatics2025

scRECL: representative ensembles with contrastive learning for scRNA-seq data clustering analysis.

Yixiang Huang, Hao Jiang, Wai-Ki Ching, Dong Shen

Abstract read
In one paragraph

Article in Briefings in bioinformatics, 2025. 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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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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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

4 authors.

Yixiang HuangDepartment of Information and Computing Sciences, School of Mathematics, Renmin University of China, No. 59 Zhongguancun Street, Haidian District, Beijing 100872, China.
Hao JiangDepartment of Information and Computing Sciences, School of Mathematics, Renmin University of China, No. 59 Zhongguancun Street, Haidian District, Beijing 100872, China.ORCID 0000-0001-5891-6044
Wai-Ki ChingDepartment of Mathematics, The University of Hong Kong, Pokfulam Road, Hong Kong.
Dong ShenDepartment of Information and Computing Sciences, School of Mathematics, Renmin University of China, No. 59 Zhongguancun Street, Haidian District, Beijing 100872, China.

Funding

National Natural Science Foundation of China 12271522National Natural Science Foundation of China 62173333
6 · The paper itself

Abstract

Single-cell transcriptomics characterizes gene expression profiles at the single-cell level, offering an unprecedented opportunity to understand cellular systems. As a fundamental task in single-cell data analysis, cell clustering significantly contributes to identifying cellular heterogeneity, thereby affecting downstream analyses. A number of deep learning methods have been proposed for clustering single-cell RNA sequencing (scRNA-seq) data. However, the large parameter space makes these methods sensitive to parameter settings. To leverage the strong capabilities of deep learning in capturing complex structures in single-cell data while ensuring algorithmic robustness, we propose a contrastive ensemble learning method named scRECL for scRNA-seq data clustering. In our approach, Siamese neural networks are trained under various $k$-nearest neighbors partitions to obtain low-dimensional embeddings of the scRNA-seq data. Multiplex graphs in representative element selection help filter out noisy and redundant cells. Consequently, contrastive ensemble learning is performed for efficient and effective latent embedding, as well as robust analysis of cellular heterogeneity in scRNA-seq data.

Indexed as

Deep LearningRNA-SeqSequence Analysis, RNASingle-Cell AnalysisAlgorithmsCluster AnalysisComputational BiologyGene Expression ProfilingHumansNeural Networks, ComputerSingle-Cell Gene Expression Analysiscontrastive learningensemble clusteringmultiplex graphscRNA-seq dataSiamese neural network

Identifiers

PMID40671174
PMCPMC12266960

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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.