scZGA: a novel model based on ZINB distribution and graph attention for scRNA-seq data clustering

BACKGROUND: Identifying different cell types is a prerequisite step in the analysis of single-cell RNA sequencing (scRNA-seq) data, with clustering being a common technique utilized for this purpose. However, high dropout rates inherent in scRNA-seq data and complex intercellular relationships become main challenges in scRNA-seq data analysis. RESULTS: To address these issues, we proposed a novel model based on zero-inflated negative binomial (ZINB) distribution and graph attention network for scRNA-seq data clustering (scZGA). scZGA consists of three key modules. The first module captures the global probabilistic structure using a ZINB model. The second module constructs the graph with Pearson's correlation coefficient, and employs a graph autoencoder with residual connection to learn important neighbor relationships while preserving topological structure information simultaneously. The final module conducts deep clustering through a self-optimizing embedding algorithm. CONCLUSIONS: With these improvements, clustering results show that scZGA consistently achieves higher scores across six scRNA-seq datasets by using evaluation metrics such as normalized mutual information and adjusted rand index.

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Publication Details

Journal
BMC Bioinformatics
Published
2026-05-29
DOI
https://doi.org/10.1186/s12859-026-06503-2
Primary Topic
Single-cell and spatial transcriptomics
Type
article
Field-Weighted Citation Impact
0.00

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article

scZGA: a novel model based on ZINB distribution and graph attention for scRNA-seq data clustering

Zhen Zhou, Ruochen Wang, Ying Liu, Jiacheng Pan et al.
BMC Bioinformatics
Single-cell and spatial transcriptomics
article

scZGA: a novel model based on ZINB distribution and graph attention for scRNA-seq data clustering

Zhen Zhou, Ruochen Wang, Ying Liu, Jiacheng Pan, Yansheng Kan, Chen-Yu Zhang
article en

Abstract

BACKGROUND: Identifying different cell types is a prerequisite step in the analysis of single-cell RNA sequencing (scRNA-seq) data, with clustering being a common technique utilized for this purpose. However, high dropout rates inherent in scRNA-seq data and complex intercellular relationships become main challenges in scRNA-seq data analysis. RESULTS: To address these issues, we proposed a novel model based on zero-inflated negative binomial (ZINB) distribution and graph attention network for scRNA-seq data clustering (scZGA). scZGA consists of three key modules. The first module captures the global probabilistic structure using a ZINB model. The second module constructs the graph with Pearson's correlation coefficient, and employs a graph autoencoder with residual connection to learn important neighbor relationships while preserving topological structure information simultaneously. The final module conducts deep clustering through a self-optimizing embedding algorithm. CONCLUSIONS: With these improvements, clustering results show that scZGA consistently achieves higher scores across six scRNA-seq datasets by using evaluation metrics such as normalized mutual information and adjusted rand index.

BMC Bioinformatics
Chinese Academy of Medical Sciences & Peking Union Medical College (CN), Nanjing Drum Tower Hospital (CN), Chinese Academy of Medical Sciences Dermatology Hospital (CN), China National Chemical Engineering (China) (CN), Tianma Microelectronics (China) (CN), Zhejiang University (CN), Nanjing University (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 9%
Single-cell and spatial transcriptomics
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