scSCCNIA: similarity matrix based contrastive clustering with neighbor information aggregation for single-cell RNA sequencing data

The development of single-cell RNA sequencing (scRNA-seq) technology provides unprecedented opportunities for elucidating cell heterogeneity and gene expression. Identifying and discovering cell types through cell clustering is a crucial step in analyzing scRNA-seq data. However, the high-dimensionality nature and frequent dropout events of the data raise great challenges for cell clustering. Here, we propose a novel contrastive clustering framework called scSCCNIA (Similarity-matrix-based Contrastive Clustering with Neighbor Information Aggregation), for the accurate identification of cell clusters from scRNA-seq data. scSCCNIA adopts a Laplacian filter to conduct neighbor information aggregation, constructs different graph views by using special un-shared parameters Siamese encoders for data augmentation, and learns the latent low-dimensional embedding representations via similarity-matrix-based contrastive learning. Comparative analyses of multiple scRNA-seq datasets from different platforms and with varying cell numbers demonstrate that scSCCNIA outperforms existing methods in terms of cell clustering and marker gene identification. Furthermore, scSCCNIA reveals the heterogeneity and functional specificity of various cell types through Gene Ontology terms and Kyoto Encyclopedia of Genes and Genomes enrichment analyses. Overall, scSCCNIA is an effective algorithm for learning latent features from scRNA-seq data, enhancing cell type identification accuracy and facilitating downstream analyses of scRNA-seq data.

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Publication Details

Journal
Briefings in Bioinformatics
Published
2026-02-23
DOI
https://doi.org/10.1093/bib/bbag094
Primary Topic
Single-cell and spatial transcriptomics
Type
article
Field-Weighted Citation Impact
0.00

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article

scSCCNIA: similarity matrix based contrastive clustering with neighbor information aggregation for single-cell RNA sequencing data

Yi-Xiang Wang, Yansen Su, Junfeng Xia, Chun-Hou Zheng
Briefings in Bioinformatics
Single-cell and spatial transcriptomics
article

scSCCNIA: similarity matrix based contrastive clustering with neighbor information aggregation for single-cell RNA sequencing data

Yi-Xiang Wang, Yansen Su, Junfeng Xia, Chun-Hou Zheng
article en

Abstract

The development of single-cell RNA sequencing (scRNA-seq) technology provides unprecedented opportunities for elucidating cell heterogeneity and gene expression. Identifying and discovering cell types through cell clustering is a crucial step in analyzing scRNA-seq data. However, the high-dimensionality nature and frequent dropout events of the data raise great challenges for cell clustering. Here, we propose a novel contrastive clustering framework called scSCCNIA (Similarity-matrix-based Contrastive Clustering with Neighbor Information Aggregation), for the accurate identification of cell clusters from scRNA-seq data. scSCCNIA adopts a Laplacian filter to conduct neighbor information aggregation, constructs different graph views by using special un-shared parameters Siamese encoders for data augmentation, and learns the latent low-dimensional embedding representations via similarity-matrix-based contrastive learning. Comparative analyses of multiple scRNA-seq datasets from different platforms and with varying cell numbers demonstrate that scSCCNIA outperforms existing methods in terms of cell clustering and marker gene identification. Furthermore, scSCCNIA reveals the heterogeneity and functional specificity of various cell types through Gene Ontology terms and Kyoto Encyclopedia of Genes and Genomes enrichment analyses. Overall, scSCCNIA is an effective algorithm for learning latent features from scRNA-seq data, enhancing cell type identification accuracy and facilitating downstream analyses of scRNA-seq data.

Briefings in BioinformaticsVol. 27(2)
Anhui University (CN), Anhui Medical University (CN)
National Natural Science Foundation of China, Anhui University
Openalex Percentile: Top 33%
Single-cell and spatial transcriptomics
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