Statistical correction of the Winner's Curse explains replication variability in quantitative trait genome-wide association studies.

Genome-wide association studies (GWAS) have identified hundreds of SNPs responsible for variation in human quantitative traits. However, genome-wide-significant associations often fail to replicate across independent cohorts, in apparent inconsistency with their apparent strong effects in discovery...

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Main Authors: Cameron Palmer, Itsik Pe'er
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2017-07-01
Series:PLoS Genetics
Online Access:http://europepmc.org/articles/PMC5536394?pdf=render
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spelling doaj-036fffa4414f4787969636e8fe466d972020-11-25T02:25:27ZengPublic Library of Science (PLoS)PLoS Genetics1553-73901553-74042017-07-01137e100691610.1371/journal.pgen.1006916Statistical correction of the Winner's Curse explains replication variability in quantitative trait genome-wide association studies.Cameron PalmerItsik Pe'erGenome-wide association studies (GWAS) have identified hundreds of SNPs responsible for variation in human quantitative traits. However, genome-wide-significant associations often fail to replicate across independent cohorts, in apparent inconsistency with their apparent strong effects in discovery cohorts. This limited success of replication raises pervasive questions about the utility of the GWAS field. We identify all 332 studies of quantitative traits from the NHGRI-EBI GWAS Database with attempted replication. We find that the majority of studies provide insufficient data to evaluate replication rates. The remaining papers replicate significantly worse than expected (p < 10-14), even when adjusting for regression-to-the-mean of effect size between discovery- and replication-cohorts termed the Winner's Curse (p < 10-16). We show this is due in part to misreporting replication cohort-size as a maximum number, rather than per-locus one. In 39 studies accurately reporting per-locus cohort-size for attempted replication of 707 loci in samples with similar ancestry, replication rate matched expectation (predicted 458, observed 457, p = 0.94). In contrast, ancestry differences between replication and discovery (13 studies, 385 loci) cause the most highly-powered decile of loci to replicate worse than expected, due to difference in linkage disequilibrium.http://europepmc.org/articles/PMC5536394?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Cameron Palmer
Itsik Pe'er
spellingShingle Cameron Palmer
Itsik Pe'er
Statistical correction of the Winner's Curse explains replication variability in quantitative trait genome-wide association studies.
PLoS Genetics
author_facet Cameron Palmer
Itsik Pe'er
author_sort Cameron Palmer
title Statistical correction of the Winner's Curse explains replication variability in quantitative trait genome-wide association studies.
title_short Statistical correction of the Winner's Curse explains replication variability in quantitative trait genome-wide association studies.
title_full Statistical correction of the Winner's Curse explains replication variability in quantitative trait genome-wide association studies.
title_fullStr Statistical correction of the Winner's Curse explains replication variability in quantitative trait genome-wide association studies.
title_full_unstemmed Statistical correction of the Winner's Curse explains replication variability in quantitative trait genome-wide association studies.
title_sort statistical correction of the winner's curse explains replication variability in quantitative trait genome-wide association studies.
publisher Public Library of Science (PLoS)
series PLoS Genetics
issn 1553-7390
1553-7404
publishDate 2017-07-01
description Genome-wide association studies (GWAS) have identified hundreds of SNPs responsible for variation in human quantitative traits. However, genome-wide-significant associations often fail to replicate across independent cohorts, in apparent inconsistency with their apparent strong effects in discovery cohorts. This limited success of replication raises pervasive questions about the utility of the GWAS field. We identify all 332 studies of quantitative traits from the NHGRI-EBI GWAS Database with attempted replication. We find that the majority of studies provide insufficient data to evaluate replication rates. The remaining papers replicate significantly worse than expected (p < 10-14), even when adjusting for regression-to-the-mean of effect size between discovery- and replication-cohorts termed the Winner's Curse (p < 10-16). We show this is due in part to misreporting replication cohort-size as a maximum number, rather than per-locus one. In 39 studies accurately reporting per-locus cohort-size for attempted replication of 707 loci in samples with similar ancestry, replication rate matched expectation (predicted 458, observed 457, p = 0.94). In contrast, ancestry differences between replication and discovery (13 studies, 385 loci) cause the most highly-powered decile of loci to replicate worse than expected, due to difference in linkage disequilibrium.
url http://europepmc.org/articles/PMC5536394?pdf=render
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