Abstract
Clustering RNA-seq data is used to characterize environment-induced (e.g., treatment) differences in gene expression profiles by separating genes into clusters based on their expression patterns. Wang et al. [2013] recently adopted the bi-Poisson distribution, obtained via the trivariate reduction method, as a model for clustering bivariate RNA-seq data. We discuss the inadequacy of the bi-Poisson distribution in modelling the correlation between dependent Poisson counts, and its impact on clustering such data. We introduce an alternative Gaussian copula model that incorporates a flexible dependence structure for the counts, report simulation results to compare the performance of the Gaussian copula and bi-Poisson models, and investigate the impact on clustering of Poisson counts of misspecified dependence structures. We illustrate our methodology on a lung cancer RNA-seq data.
