Abstract

BackgroundDetecting and visualizing nonlinear interaction effects of single nucleotide polymorphisms (SNPs) or epistatic interactions are important topics in bioinformatics since they play an important role in unraveling the mystery of “missing heritability”. However, related studies are almost limited to pairwise epistatic interactions due to their methodological and computational challenges.ResultsWe develop CINOEDV (Co-Information based N-Order Epistasis Detector and Visualizer) for the detection and visualization of epistatic interactions of their orders from 1 to n (n ≥ 2). CINOEDV is composed of two stages, namely, detecting stage and visualizing stage. In detecting stage, co-information based measures are employed to quantify association effects of n-order SNP combinations to the phenotype, and two types of search strategies are introduced to identify n-order epistatic interactions: an exhaustive search and a particle swarm optimization based search. In visualizing stage, all detected n-order epistatic interactions are used to construct a hypergraph, where a real vertex represents the main effect of a SNP and a virtual vertex denotes the interaction effect of an n-order epistatic interaction. By deeply analyzing the constructed hypergraph, some hidden clues for better understanding the underlying genetic architecture of complex diseases could be revealed.ConclusionsExperiments of CINOEDV and its comparison with existing state-of-the-art methods are performed on both simulation data sets and a real data set of age-related macular degeneration. Results demonstrate that CINOEDV is promising in detecting and visualizing n-order epistatic interactions. CINOEDV is implemented in R and is freely available from R CRAN: http://cran.r-project.org and https://sourceforge.net/projects/cinoedv/files/.Electronic supplementary materialThe online version of this article (doi:10.1186/s12859-016-1076-8) contains supplementary material, which is available to authorized users.

Highlights

  • Detecting and visualizing nonlinear interaction effects of single nucleotide polymorphisms (SNPs) or epistatic interactions are important topics in bioinformatics since they play an important role in unraveling the mystery of “missing heritability”

  • All detected n-order epistatic interactions are used to construct a hypergraph, where a real vertex represents the main effect of a SNP and a virtual vertex denotes the interaction effect of an n-order epistatic interaction

  • CINOEDV is applied on a real data set of age-related macular degeneration (AMD), and results of which provide several new clues for the exploration of causative factors of AMD

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Summary

Introduction

Detecting and visualizing nonlinear interaction effects of single nucleotide polymorphisms (SNPs) or epistatic interactions are important topics in bioinformatics since they play an important role in unraveling the mystery of “missing heritability”. Genome-wide association studies (GWAS) have become a routine tool in investigating the genetic architectures of complex diseases, such as cancer, heart disease, diabetes and many others. With these studies, hundreds of thousands of SNPs speculated to associate with. It is widely believed that nonlinear interaction effects of multiple SNPs or epistatic interactions could unveil a large portion of unexplained heritability of complex diseases [8,9,10,11]. Detection of epistatic interactions has already been a compelling step in GWAS [12]

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