PleioGRiP: genetic risk prediction with pleiotropy.
basic_science · Level V
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- Record sourced from PubMed, PMID 23419378.
- Also identified by DOI 10.1093/bioinformatics/btt081 and PMC identifier 3624803.
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Abstract
Although several studies have used Bayesian classifiers for risk prediction using genome-wide single nucleotide polymorphism (SNP) datasets, no software can efficiently perform these analyses on massive genetic datasets and can accommodate multiple traits. We describe the program PleioGRiP that performs a genome-wide Bayesian model search to identify SNPs associated with a discrete phenotype and uses SNPs ranked by Bayes factor to produce nested Bayesian classifiers. These classifiers can be used for genetic risk prediction, either selecting the classifier with optimal number of features or using an ensemble of classifiers. In addition, PleioGRiP implements an extension to the Bayesian search and classification and can search for pleiotropic relationships in which SNPs are simultaneously associated with two or more distinct phenotypes. These relationships can be used to generate connected Bayesian classifiers to predict the phenotype of interest either using genetic data alone or in combination with the secondary phenotype(s). PleioGRiP is implemented in Java, and it is available from http://hdl.handle.net/2144/4367. Supplementary data are available at Bioinformatics online.
Medical subject headings
- Genome-Wide Association Study
- Phenotype
- Polymorphism, Single Nucleotide
- Software