Clustering scRNA-seq data with the cross-view collaborative information fusion strategy

Single-cell RNA sequencing (scRNA-seq) technology has revolutionized biological research by enabling high-throughput, cellular-resolution gene expression profiling. A critical step in scRNA-seq data analysis is cell clustering, which supports downstream analyses. However, the high-dimensional and sparse nature of scRNA-seq data poses significant challenges to existing clustering methods. Furthermore, integrating gene expression information with potential cell structure data remains largely unexplored. Here, we present scCFIB, a novel information bottleneck (IB)-based clustering algorithm that leverages the power of IB for efficient processing of high-dimensional sparse data and incorporates a cross-view fusion strategy to achieve robust cell clustering. scCFIB constructs a multi-feature space by establishing two distinct views from the original features. We then formulate the cell clustering problem as a target loss function within the IB framework, employing a collaborative information fusion strategy. To further optimize scCFIB's performance, we introduce a novel sequential optimization approach through an iterative process. Benchmarking against established methods on diverse scRNA-seq datasets demonstrates that scCFIB achieves superior performance in scRNA-seq data clustering tasks. Availability: the source code is publicly available on GitHub: https://github.com/weixiaojiao/scCFIB.

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Publication Details

Journal
Briefings in Bioinformatics
Published
2024-09-23
DOI
https://doi.org/10.1093/bib/bbae511
Citations
4
Primary Topic
Single-cell and spatial transcriptomics
Type
article
Field-Weighted Citation Impact
0.94

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article

Clustering scRNA-seq data with the cross-view collaborative information fusion strategy

Zhen Tian, Zhengzheng Lou, Yuanhao Hu, Xiaojiao Wei et al.
4 citations
Briefings in Bioinformatics
Single-cell and spatial transcriptomics
0.94
article

Clustering scRNA-seq data with the cross-view collaborative information fusion strategy

Zhen Tian, Zhengzheng Lou, Yuanhao Hu, Xiaojiao Wei, Yucong Wu, Shizhe Hu
article en
4 citations

Abstract

Single-cell RNA sequencing (scRNA-seq) technology has revolutionized biological research by enabling high-throughput, cellular-resolution gene expression profiling. A critical step in scRNA-seq data analysis is cell clustering, which supports downstream analyses. However, the high-dimensional and sparse nature of scRNA-seq data poses significant challenges to existing clustering methods. Furthermore, integrating gene expression information with potential cell structure data remains largely unexplored. Here, we present scCFIB, a novel information bottleneck (IB)-based clustering algorithm that leverages the power of IB for efficient processing of high-dimensional sparse data and incorporates a cross-view fusion strategy to achieve robust cell clustering. scCFIB constructs a multi-feature space by establishing two distinct views from the original features. We then formulate the cell clustering problem as a target loss function within the IB framework, employing a collaborative information fusion strategy. To further optimize scCFIB's performance, we introduce a novel sequential optimization approach through an iterative process. Benchmarking against established methods on diverse scRNA-seq datasets demonstrates that scCFIB achieves superior performance in scRNA-seq data clustering tasks. Availability: the source code is publicly available on GitHub: https://github.com/weixiaojiao/scCFIB.

Briefings in BioinformaticsVol. 25(6)
University of Electronic Science and Technology of China (CN), Zhengzhou University (CN), Quzhou University (CN)
National Science Foundation, National Natural Science Foundation of China
Partnerships for the goals
Openalex Percentile: Top 25%
Single-cell and spatial transcriptomics
0.94
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Clustering scRNA-seq data with the cross-view collaborative information fusion strategy — Zhen Tian, Zhengzheng Lou, et al. · Briefings in Bioinformatics (2024) | TGRS Research Map | TGRS