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

IF 4 4区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Current Genomics Pub Date : 2025-01-01 Epub Date: 2025-10-10 DOI:10.2174/0113892029387405250921211549
Lianlian Zhang, Junliang Shang, Xiangzhen Kong, Feng Li, Jin-Xing Liu
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引用次数: 0

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.

单细胞RNA-Seq数据的两阶段多视图图光谱聚类。
单细胞RNA测序(scRNA-seq)数据的出现为在细胞水平上研究基因表达带来了独特的视角。然而,它面临着诸如大数据量、稀疏性、异构性和维度诅咒等挑战。目前的聚类方法在研究细胞类型分布方面仍然面临许多挑战,并且没有利用细胞之间的结构关系信息。方法:为避免scRNA-seq数据单一特征空间在表征细胞功能方面的不足,构建多视角特征空间,利用多视角学习,从不同视角对scRNA-seq信息进行综合表征。在多视图学习中,相似图分为加权学习和结构学习两个阶段。通过对多视图相似图进行加权,强调了不同视图和特征的重要性。在结构阶段,重点是通过保留多视图相似图中的公共边来揭示不同视图之间的潜在关系。采用交替方向乘数法分别对属性图和结构图进行优化。结果:使用8个不同尺度的真实scRNA-seq数据集验证了MVGSC的性能,实验结果表明,所提出的多视图聚类方法显著优于其他单视图聚类方法和多视图聚类方法。讨论:当scRNA-seq数据特征复杂且视图之间存在显著差异时,两阶段多视图图方法可以更好地捕捉数据中的复杂关系,表现出优于单一框架的性能。结论:两阶段多视图学习可以更准确地捕捉数据中的复杂关系,从而提高模型的准确性。它还可以更好地捕获多视图数据中的一致性和互补性信息,从而增强模型的泛化能力。
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来源期刊
Current Genomics
Current Genomics 生物-生化与分子生物学
CiteScore
5.20
自引率
0.00%
发文量
29
审稿时长
>0 weeks
期刊介绍: Current Genomics is a peer-reviewed journal that provides essential reading about the latest and most important developments in genome science and related fields of research. Systems biology, systems modeling, machine learning, network inference, bioinformatics, computational biology, epigenetics, single cell genomics, extracellular vesicles, quantitative biology, and synthetic biology for the study of evolution, development, maintenance, aging and that of human health, human diseases, clinical genomics and precision medicine are topics of particular interest. The journal covers plant genomics. The journal will not consider articles dealing with breeding and livestock. Current Genomics publishes three types of articles including: i) Research papers from internationally-recognized experts reporting on new and original data generated at the genome scale level. Position papers dealing with new or challenging methodological approaches, whether experimental or mathematical, are greatly welcome in this section. ii) Authoritative and comprehensive full-length or mini reviews from widely recognized experts, covering the latest developments in genome science and related fields of research such as systems biology, statistics and machine learning, quantitative biology, and precision medicine. Proposals for mini-hot topics (2-3 review papers) and full hot topics (6-8 review papers) guest edited by internationally-recognized experts are welcome in this section. Hot topic proposals should not contain original data and they should contain articles originating from at least 2 different countries. iii) Opinion papers from internationally recognized experts addressing contemporary questions and issues in the field of genome science and systems biology and basic and clinical research practices.
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