Literature DB >> 22053078

Detecting genome-wide epistases based on the clustering of relatively frequent items.

Minzhu Xie1, Jing Li, Tao Jiang.   

Abstract

MOTIVATION: In genome-wide association studies (GWAS), up to millions of single nucleotide polymorphisms (SNPs) are genotyped for thousands of individuals. However, conventional single locus-based approaches are usually unable to detect gene-gene interactions underlying complex diseases. Due to the huge search space for complicated high order interactions, many existing multi-locus approaches are slow and may suffer from low detection power for GWAS.
RESULTS: In this article, we develop a simple, fast and effective algorithm to detect genome-wide multi-locus epistatic interactions based on the clustering of relatively frequent items. Extensive experiments on simulated data show that our algorithm is fast and more powerful in general than some recently proposed methods. On a real genome-wide case-control dataset for age-related macular degeneration (AMD), the algorithm has identified genotype combinations that are significantly enriched in the cases. AVAILABILITY: http://www.cs.ucr.edu/~minzhux/EDCF.zip CONTACT: minzhux@cs.ucr.edu; jingli@cwru.edu SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.

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Mesh:

Year:  2011        PMID: 22053078      PMCID: PMC3244765          DOI: 10.1093/bioinformatics/btr603

Source DB:  PubMed          Journal:  Bioinformatics        ISSN: 1367-4803            Impact factor:   6.937


  33 in total

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Authors:  W Li; J Reich
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8.  Detecting epistatic effects in association studies at a genomic level based on an ensemble approach.

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  16 in total

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Review 7.  Detecting epistasis in human complex traits.

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10.  HiSeeker: Detecting High-Order SNP Interactions Based on Pairwise SNP Combinations.

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