Evidence map›Paper›PMID 42157914›Full record

ArticleCurrent genomics2025

Two-Stage Multi-View Graph Spectral Clustering for Single-Cell RNA-Seq Data.

Lianlian Zhang, Junliang Shang, Xiangzhen Kong, Feng Li, Jin-Xing Liu

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In one paragraph

Article in Current genomics, 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

Who cites it

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Lianlian ZhangSchool of Computer Science, Qufu Normal University, Rizhao, 276826, China.
Junliang ShangSchool of Computer Science, Qufu Normal University, Rizhao, 276826, China.
Xiangzhen KongSchool of Computer Science, Qufu Normal University, Rizhao, 276826, China.
Feng LiSchool of Computer Science, Qufu Normal University, Rizhao, 276826, China.
Jin-Xing LiuSchool of Health and Life Sciences, University of Health and Rehabilitation Science, Qingdao, 266113, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: The appearance of single-cell RNA sequencing (scRNA-seq) data has brought a distinctive perspective to studying gene expression at the cell level. However, it faces challenges such as large data volume, sparsity, heterogeneity, and the curse of dimensionality. Current clustering methods still face many challenges in studying cell type distribution and have not utilized the structural relationship information between cells. Methods: To avoid the insufficiency of the single characteristic space of scRNA-seq data in characterizing cell function, this paper constructs multiple view characteristic spaces and utilizes multi-view learning to characterize scRNA-seq information from distinctive perspectives comprehensively. In multi-view learning, the similarity graph is divided into weighted learning and structural learning stages. Through weighting the multi-view similarity graphs, the significance of diverse views and features is underscored. During the structural stage, the emphasis is placed on uncovering potential relationships among different views by preserving common edges in the multi-view similarity graphs. The optimization of the attribute and structure graphs was conducted separately by the alternating direction multiplier method. Results: The performance of the MVGSC was validated using eight different scales of real scRNA-seq datasets, and the experimental results showed that the proposed multi-view clustering method significantly surpasses other single-view clustering methods and multi-view clustering methods. Discussion: When the features of scRNA-seq data are complex and there are significant differences between views, the two-stage multi-view graph method can better capture the complex relationships in the data, demonstrating superior performance compared to a single framework. Conclusion: Two-stage multi-view learning can more accurately capture complex relationships in the data, thereby improving the accuracy of the model. It can also better capture consistency and complementary information in multi-view data, thereby enhancing the generalization ability of the model.

Indexed as

clustering algorithmclustering analysismulti-view feature and structure networkmulti-view graphscRNA-seqspectral clustering

Identifiers

PMID42157914
PMCPMC13154248

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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.