Demonstrates improved clustering accuracy in scRNA-seq data, indicating enhanced cell type identification.
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. 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. 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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Kan et al. (2026) studied this question.
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