Mixed-effects modeling identifies dynamic gene interactions in single-cell RNA-seq data, suggesting new analytical methods for gene expression research.
Advancements in single-cell RNA-sequencing (scRNA-seq) technologies generate a wealth of gene expression data that provide exciting opportunities for studying gene-gene interactions systematically at individual cell resolution. Genetic interactions within a cell are tightly regulated and often highly dynamic in response to internal cellular signals and external stimuli. Evidence of these dynamic interactions can often be observed in scRNA-seq data by examining conditional co-expression changes. Existing approaches for studying these dynamic interaction changes in scRNA-seq data do not address the multi-subject hierarchical design commonly considered in single-cell experiments. In this paper, we propose a Mixed-effects framework for differential Coexpression and transcriptional interaction modeling in Single-Cell RNA-seq (scCOSMiX) to account for the cell-cell correlation from the same individual. The proposed copula-based approach allows the zero-inflation, marginal, and association parameters to be modeled as functions of covariates with subject-level random effects, to enable analyses to be tailored to the data under consideration. A series of simulation analyses were conducted to evaluate and compare the performance of scCOSMiX to other existing approaches. We applied the proposed method to both droplet and plate-based scRNA-seq data sets GSE266919 and GSE108989 to illustrate its applicability across distinct scRNA-seq experimental protocols.
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Bussing et al. (2025) studied this question.
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