Improving the accuracy of whole genome prediction for complex traits using the results of genome wide association studies.

Utilizing the whole genomic variation of complex traits to predict the yet-to-be observed phenotypes or unobserved genetic values via whole genome prediction (WGP) and to infer the underlying genetic architecture via genome wide association study (GWAS) is an interesting and fast developing area in...

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Main Authors: Zhe Zhang, Ulrike Ober, Malena Erbe, Hao Zhang, Ning Gao, Jinlong He, Jiaqi Li, Henner Simianer
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2014-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3963961?pdf=render
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author Zhe Zhang
Ulrike Ober
Malena Erbe
Hao Zhang
Ning Gao
Jinlong He
Jiaqi Li
Henner Simianer
author_facet Zhe Zhang
Ulrike Ober
Malena Erbe
Hao Zhang
Ning Gao
Jinlong He
Jiaqi Li
Henner Simianer
author_sort Zhe Zhang
collection DOAJ
description Utilizing the whole genomic variation of complex traits to predict the yet-to-be observed phenotypes or unobserved genetic values via whole genome prediction (WGP) and to infer the underlying genetic architecture via genome wide association study (GWAS) is an interesting and fast developing area in the context of human disease studies as well as in animal and plant breeding. Though thousands of significant loci for several species were detected via GWAS in the past decade, they were not used directly to improve WGP due to lack of proper models. Here, we propose a generalized way of building trait-specific genomic relationship matrices which can exploit GWAS results in WGP via a best linear unbiased prediction (BLUP) model for which we suggest the name BLUP|GA. Results from two illustrative examples show that using already existing GWAS results from public databases in BLUP|GA improved the accuracy of WGP for two out of the three model traits in a dairy cattle data set, and for nine out of the 11 traits in a rice diversity data set, compared to the reference methods GBLUP and BayesB. While BLUP|GA outperforms BayesB, its required computing time is comparable to GBLUP. Further simulation results suggest that accounting for publicly available GWAS results is potentially more useful for WGP utilizing smaller data sets and/or traits of low heritability, depending on the genetic architecture of the trait under consideration. To our knowledge, this is the first study incorporating public GWAS results formally into the standard GBLUP model and we think that the BLUP|GA approach deserves further investigations in animal breeding, plant breeding as well as human genetics.
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spelling doaj.art-c3c0b598dc504e1197e6bb811e12f3692022-12-22T03:36:31ZengPublic Library of Science (PLoS)PLoS ONE1932-62032014-01-0193e9301710.1371/journal.pone.0093017Improving the accuracy of whole genome prediction for complex traits using the results of genome wide association studies.Zhe ZhangUlrike OberMalena ErbeHao ZhangNing GaoJinlong HeJiaqi LiHenner SimianerUtilizing the whole genomic variation of complex traits to predict the yet-to-be observed phenotypes or unobserved genetic values via whole genome prediction (WGP) and to infer the underlying genetic architecture via genome wide association study (GWAS) is an interesting and fast developing area in the context of human disease studies as well as in animal and plant breeding. Though thousands of significant loci for several species were detected via GWAS in the past decade, they were not used directly to improve WGP due to lack of proper models. Here, we propose a generalized way of building trait-specific genomic relationship matrices which can exploit GWAS results in WGP via a best linear unbiased prediction (BLUP) model for which we suggest the name BLUP|GA. Results from two illustrative examples show that using already existing GWAS results from public databases in BLUP|GA improved the accuracy of WGP for two out of the three model traits in a dairy cattle data set, and for nine out of the 11 traits in a rice diversity data set, compared to the reference methods GBLUP and BayesB. While BLUP|GA outperforms BayesB, its required computing time is comparable to GBLUP. Further simulation results suggest that accounting for publicly available GWAS results is potentially more useful for WGP utilizing smaller data sets and/or traits of low heritability, depending on the genetic architecture of the trait under consideration. To our knowledge, this is the first study incorporating public GWAS results formally into the standard GBLUP model and we think that the BLUP|GA approach deserves further investigations in animal breeding, plant breeding as well as human genetics.http://europepmc.org/articles/PMC3963961?pdf=render
spellingShingle Zhe Zhang
Ulrike Ober
Malena Erbe
Hao Zhang
Ning Gao
Jinlong He
Jiaqi Li
Henner Simianer
Improving the accuracy of whole genome prediction for complex traits using the results of genome wide association studies.
PLoS ONE
title Improving the accuracy of whole genome prediction for complex traits using the results of genome wide association studies.
title_full Improving the accuracy of whole genome prediction for complex traits using the results of genome wide association studies.
title_fullStr Improving the accuracy of whole genome prediction for complex traits using the results of genome wide association studies.
title_full_unstemmed Improving the accuracy of whole genome prediction for complex traits using the results of genome wide association studies.
title_short Improving the accuracy of whole genome prediction for complex traits using the results of genome wide association studies.
title_sort improving the accuracy of whole genome prediction for complex traits using the results of genome wide association studies
url http://europepmc.org/articles/PMC3963961?pdf=render
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AT haozhang improvingtheaccuracyofwholegenomepredictionforcomplextraitsusingtheresultsofgenomewideassociationstudies
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