Abstract

It is challenging to identify meaningful gene networks because biological interactions are often condition-specific and confounded with external factors. It is necessary to integrate multiple sources of genomic data to facilitate network inference. For example, one can jointly model expression datasets measured from multiple tissues with molecular marker data in so-called genetical genomic studies. In this paper, we propose a joint conditional Gaussian graphical model (JCGGM) that aims for modeling biological processes based on multiple sources of data. This approach is able to integrate multiple sources of information by adopting conditional models combined with joint sparsity regularization. We apply our approach to a real dataset measuring gene expression in four tissues (kidney, liver, heart, and fat) from recombinant inbred rats. Our approach reveals that the liver tissue has the highest level of tissue-specific gene regulations among genes involved in insulin responsive facilitative sugar transporter mediated glucose transport pathway, followed by heart and fat tissues, and this finding can only be attained from our JCGGM approach.

Highlights

  • Inference of gene networks plays an important role in revealing the interactions among genes that may lead to a better understanding of molecular mechanisms in organisms

  • We show that the joint conditional Gaussian graphical model (JCGGM) approach is able to find tissue-specific gene networks

  • This strain was derived from a cross between the spontaneously hypertensive rat (SHR) and the brown norway (BN) strains (Hubner et al, 2005)

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Summary

Introduction

Inference of gene networks plays an important role in revealing the interactions among genes that may lead to a better understanding of molecular mechanisms in organisms. We can define edges through conditional dependence, that is, any two genes connected with an edge in such graphical models are conditionally dependent of each other when the effects from all other genes are explained away. When the expression profiles of two genes are correlated because they are both regulated by some other genes, the graphical model does not put an edge between these two genes because they are conditionally independent given the expressions of the common regulatory genes. In this way, the graphical model produces a more parsimonious graph than a relevance network

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