Abstract

BackgroundRecent advances in high-throughput technology and the emergence of large-scale genomic datasets have enabled detection of genomic features that affect clinical outcomes. Although many previous computational studies have analysed the effect of each single gene or the additive effects of multiple genes on the clinical outcome, less attention has been devoted to the identification of gene-gene interactions of general type that are associated with the clinical outcome. Moreover, the integration of information from multiple molecular profiles adds another challenge to this problem. Recently, network-based approaches have gained huge popularity. However, previous network construction methods have been more concerned with the relationship between features only, rather than the effect of feature interactions on clinical outcome.MethodsWe propose a mutual information-based integrative network analysis framework (MINA) that identifies gene pairs associated with clinical outcome and systematically analyses the resulting networks over multiple genomic profiles. We implement an efficient non-parametric testing scheme that ensures the significance of detected gene interactions. We develop a tool named MINA that automates the proposed analysis scheme of identifying outcome-associated gene interactions and generating various networks from those interacting pairs for downstream analysis.ResultsWe demonstrate the proposed framework using real data from ovarian cancer patients in The Cancer Genome Atlas (TCGA). Statistically significant gene pairs associated with survival were identified from multiple genomic profiles, which include many individual genes that have weak or no effect on survival. Moreover, we also show that integrated networks, constructed by merging networks from multiple genomic profiles, demonstrate better topological properties and biological significance than individual networks.ConclusionsWe have developed a simple but powerful analysis tool that is able to detect gene-gene interactions associated with clinical outcome on multiple genomic profiles. By being network-based, our approach provides a better insight into the underlying gene-gene interaction mechanisms that affect the clinical outcome of cancer patients.

Highlights

  • Recent advances in high-throughput technology and the emergence of large-scale genomic datasets have enabled detection of genomic features that affect clinical outcomes

  • Mutual information for identifying gene-gene interactions associated with clinical outcome Using genomic profile data, we identify genomic interactions that are associated with clinical outcome, by utilizing an information-theoretic measure of mutual information [32]

  • Ethics statements All data related to human subjects used for this study is de-identified and publicly available from The Cancer Genome Atlas project

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Summary

Introduction

Recent advances in high-throughput technology and the emergence of large-scale genomic datasets have enabled detection of genomic features that affect clinical outcomes. Previous studies have often focused on the association between each single gene and clinical outcomes [16,17,18,19], and have not been able to detect the combined effects of multiple genomic features. The cox regression or sparse regression framework, like elastic net analysis, is effective in finding gene expression signatures associated with the overall survival of cancer patients [20]. These methods are limited to detection of the additive effect of multiple features on clinical outcome, and do not translate well for more general types of interaction effects

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