Discovery of gene network variability across samples representing multiple classes

摘要

Gene networks have been predicted using the expression profiles from microarray experiments that include multiple samples representing each of several classes or states (e.g., treatments, developmental stages, health status). A framework that integrates Bayesian networks, mixture of gene co-expression models and clustering is proposed to further mine information from the variation of samples within and across classes and enhance the understanding of gene networks. The approach was evaluated on two independent pathways using data from two microarray experiments. Our algorithm succeeded on reconstructing the topology of the gene pathways when benchmarked against empirical reports and randomised data sets. The majority or all the samples within a class shared the same co-expression model and were classified within the corresponding class. Our approach uncovered both gene relationships and profiles that are unique to a particular class or shared across classes.