CGMFinder Identifies Correlated Gene Modules from 3H scRNA-seq Data

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Abstract

Correlated gene modules (CGMs) contain genes whose expression fluctuates together. Genes in CGMs are often functionally related and regulated by shared transcription factors. CGMs can be identified under steady-state conditions in populations of cells using single-cell RNA sequencing (scRNA-seq). Here, we introduce CGMFinder, a tool for CGM identification using “3H” scRNA-seq data (High mRNA capture efficiency, High cell numbers, and High sequencing depth). CGMFinder employs a graph-based filtering approach, first identifying CGM cores from highly-expressed genes and then linking noisy low-abundance genes to these cores. In lymphoblastoid cell line 3H datasets generated by in-lab and commercial protocols, CGMFinder accurately identifies CGMs enriched for gene ontologies or pathways. In cells grown under hypoxic conditions, CGMFinder successfully identified hypoxia-specific “glycolysis” and “response to oxygen levels” modules. Evaluations using ground truth correlation modules demonstrate that CGMFinder outperforms other CGM identification methods such as WGCNA and FastICA in scRNA-seq data.

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