Literature DB >> 21104889

Using biological knowledge to discover higher order interactions in genetic association studies.

Gary K Chen1, Duncan C Thomas.   

Abstract

The recent successes of genome-wide association studies (GWAS) have revealed that many of the replicated findings have explained only a small fraction of the heritability of common diseases. One hypothesis that investigators have suggested is that higher order interactions between SNPs or SNPs and environmental risk factors may account for some of this missing heritability. Searching for these interactions poses great statistical and computational challenges. In this article, we propose a novel method that addresses these challenges by incorporating external biological knowledge into a fully Bayesian analysis. The method is designed to be scalable for high-dimensional search spaces (where it supports interactions of any order) because priors that use such knowledge focus the search in regions that are more biologically plausible and avoid having to enumerate all possible interactions. We provide several examples based on simulated data demonstrating how external information can enhance power, specificity, and effect estimates in comparison to conventional approaches based on maximum likelihood estimates. We also apply the method to data from a GWAS for breast cancer, revealing a set of interactions enriched for the Gene Ontology terms growth, metabolic process, and biological regulation.
© 2010 Wiley-Liss, Inc.

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Year:  2010        PMID: 21104889     DOI: 10.1002/gepi.20542

Source DB:  PubMed          Journal:  Genet Epidemiol        ISSN: 0741-0395            Impact factor:   2.135


  11 in total

1.  Gene-environment interactions in cancer epidemiology: a National Cancer Institute Think Tank report.

Authors:  Carolyn M Hutter; Leah E Mechanic; Nilanjan Chatterjee; Peter Kraft; Elizabeth M Gillanders
Journal:  Genet Epidemiol       Date:  2013-10-05       Impact factor: 2.135

2.  Modeling gene-covariate interactions in sparse regression with group structure for genome-wide association studies.

Authors:  Yun Li; George T O'Connor; Josée Dupuis; Eric Kolaczyk
Journal:  Stat Appl Genet Mol Biol       Date:  2015-06

3.  Mind the dbGAP: the application of data mining to identify biological mechanisms.

Authors:  Eric C Wooten; Gordon S Huggins
Journal:  Mol Interv       Date:  2011-04

4.  Analysis of exome sequences with and without incorporating prior biological knowledge.

Authors:  Junghyun Namkung; Paola Raska; Jia Kang; Yunlong Liu; Qing Lu; Xiaofeng Zhu
Journal:  Genet Epidemiol       Date:  2011       Impact factor: 2.135

5.  Evaluation of removable statistical interaction for binary traits.

Authors:  Jaya M Satagopan; Robert C Elston
Journal:  Stat Med       Date:  2012-09-27       Impact factor: 2.373

6.  Joint analysis for integrating two related studies of different data types and different study designs using hierarchical modeling approaches.

Authors:  Rui Li; David V Conti; David Diaz-Sanchez; Frank Gilliland; Duncan C Thomas
Journal:  Hum Hered       Date:  2013-01-18       Impact factor: 0.444

7.  Leveraging models of cell regulation and GWAS data in integrative network-based association studies.

Authors:  Andrea Califano; Atul J Butte; Stephen Friend; Trey Ideker; Eric Schadt
Journal:  Nat Genet       Date:  2012-07-27       Impact factor: 38.330

8.  Enhancing the discovery of rare disease variants through hierarchical modeling.

Authors:  Gary K Chen
Journal:  BMC Proc       Date:  2011-11-29

9.  Evaluating methods for modeling epistasis networks with application to head and neck cancer.

Authors:  Rajesh Talluri; Sanjay Shete
Journal:  Cancer Inform       Date:  2015-02-10

Review 10.  Detecting epistasis in human complex traits.

Authors:  Wen-Hua Wei; Gibran Hemani; Chris S Haley
Journal:  Nat Rev Genet       Date:  2014-09-09       Impact factor: 53.242

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