Evidence map›Paper›PMID 39487083›Full record

ArticleBriefings in bioinformatics2024

Graph contrastive learning as a versatile foundation for advanced scRNA-seq data analysis.

Zhenhao Zhang, Yuxi Liu, Meichen Xiao, Kun Wang, Yu Huang, Jiang Bian, Ruolin Yang, Fuyi Li

Abstract read
In one paragraph

Article in Briefings in bioinformatics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

10 citing papers in PubMed.

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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.

Zhenhao ZhangCollege of Life Sciences, Northwest A&F University, Yangling, 712100 Shaanxi, China.
Yuxi LiuCollege of Medicine, University of Florida, Gainesville, FL 32610, USA.
Meichen XiaoCollege of Life Sciences, Northwest A&F University, Yangling, 712100 Shaanxi, China.
Kun WangCollege of Life Sciences, Northwest A&F University, Yangling, 712100 Shaanxi, China.
Yu HuangCollege of Medicine, University of Florida, Gainesville, FL 32610, USA.
Jiang BianCollege of Medicine, University of Florida, Gainesville, FL 32610, USA.
Ruolin YangCollege of Life Sciences, Northwest A&F University, Yangling, 712100 Shaanxi, China.
Fuyi LiCollege of Information Engineering, Northwest A&F University, Yangling, 712100 Shaanxi, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Single-cell RNA sequencing (scRNA-seq) offers unprecedented insights into transcriptome-wide gene expression at the single-cell level. Cell clustering has been long established in the analysis of scRNA-seq data to identify the groups of cells with similar expression profiles. However, cell clustering is technically challenging, as raw scRNA-seq data have various analytical issues, including high dimensionality and dropout values. Existing research has developed deep learning models, such as graph machine learning models and contrastive learning-based models, for cell clustering using scRNA-seq data and has summarized the unsupervised learning of cell clustering into a human-interpretable format. While advances in cell clustering have been profound, we are no closer to finding a simple yet effective framework for learning high-quality representations necessary for robust clustering. In this study, we propose scSimGCL, a novel framework based on the graph contrastive learning paradigm for self-supervised pretraining of graph neural networks. This framework facilitates the generation of high-quality representations crucial for cell clustering. Our scSimGCL incorporates cell-cell graph structure and contrastive learning to enhance the performance of cell clustering. Extensive experimental results on simulated and real scRNA-seq datasets suggest the superiority of the proposed scSimGCL. Moreover, clustering assignment analysis confirms the general applicability of scSimGCL, including state-of-the-art clustering algorithms. Further, ablation study and hyperparameter analysis suggest the efficacy of our network architecture with the robustness of decisions in the self-supervised learning setting. The proposed scSimGCL can serve as a robust framework for practitioners developing tools for cell clustering. The source code of scSimGCL is publicly available at https://github.com/zhangzh1328/scSimGCL.

Indexed as

Single-Cell AnalysisAlgorithmsCluster AnalysisComputational BiologyGene Expression ProfilingHumansMachine LearningNeural Networks, ComputerRNA-SeqSequence Analysis, RNASingle-Cell Gene Expression AnalysisSoftwareTranscriptomecell-cell graphcell clusteringgraph contrastive learningscRNA-seq dataself-supervised learning

Identifiers

PMID39487083
PMCPMC11530284

What OpenQuestion holds

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LicenceCC BY-NC
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Registered trials

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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.