Failure to replicate a genetic association may provide important clues about genetic architecture.

Replication has become the gold standard for assessing statistical results from genome-wide association studies. Unfortunately this replication requirement may cause real genetic effects to be missed. A real result can fail to replicate for numerous reasons including inadequate sample size or variab...

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Main Authors: Casey S Greene, Nadia M Penrod, Scott M Williams, Jason H Moore
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2009-06-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC2685469?pdf=render
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spelling doaj-f4ef53a8701d428ebd7cd3b0aef7ae992020-11-24T20:50:41ZengPublic Library of Science (PLoS)PLoS ONE1932-62032009-06-0146e563910.1371/journal.pone.0005639Failure to replicate a genetic association may provide important clues about genetic architecture.Casey S GreeneNadia M PenrodScott M WilliamsJason H MooreReplication has become the gold standard for assessing statistical results from genome-wide association studies. Unfortunately this replication requirement may cause real genetic effects to be missed. A real result can fail to replicate for numerous reasons including inadequate sample size or variability in phenotype definitions across independent samples. In genome-wide association studies the allele frequencies of polymorphisms may differ due to sampling error or population differences. We hypothesize that some statistically significant independent genetic effects may fail to replicate in an independent dataset when allele frequencies differ and the functional polymorphism interacts with one or more other functional polymorphisms. To test this hypothesis, we designed a simulation study in which case-control status was determined by two interacting polymorphisms with heritabilities ranging from 0.025 to 0.4 with replication sample sizes ranging from 400 to 1600 individuals. We show that the power to replicate the statistically significant independent main effect of one polymorphism can drop dramatically with a change of allele frequency of less than 0.1 at a second interacting polymorphism. We also show that differences in allele frequency can result in a reversal of allelic effects where a protective allele becomes a risk factor in replication studies. These results suggest that failure to replicate an independent genetic effect may provide important clues about the complexity of the underlying genetic architecture. We recommend that polymorphisms that fail to replicate be checked for interactions with other polymorphisms, particularly when samples are collected from groups with distinct ethnic backgrounds or different geographic regions.http://europepmc.org/articles/PMC2685469?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Casey S Greene
Nadia M Penrod
Scott M Williams
Jason H Moore
spellingShingle Casey S Greene
Nadia M Penrod
Scott M Williams
Jason H Moore
Failure to replicate a genetic association may provide important clues about genetic architecture.
PLoS ONE
author_facet Casey S Greene
Nadia M Penrod
Scott M Williams
Jason H Moore
author_sort Casey S Greene
title Failure to replicate a genetic association may provide important clues about genetic architecture.
title_short Failure to replicate a genetic association may provide important clues about genetic architecture.
title_full Failure to replicate a genetic association may provide important clues about genetic architecture.
title_fullStr Failure to replicate a genetic association may provide important clues about genetic architecture.
title_full_unstemmed Failure to replicate a genetic association may provide important clues about genetic architecture.
title_sort failure to replicate a genetic association may provide important clues about genetic architecture.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2009-06-01
description Replication has become the gold standard for assessing statistical results from genome-wide association studies. Unfortunately this replication requirement may cause real genetic effects to be missed. A real result can fail to replicate for numerous reasons including inadequate sample size or variability in phenotype definitions across independent samples. In genome-wide association studies the allele frequencies of polymorphisms may differ due to sampling error or population differences. We hypothesize that some statistically significant independent genetic effects may fail to replicate in an independent dataset when allele frequencies differ and the functional polymorphism interacts with one or more other functional polymorphisms. To test this hypothesis, we designed a simulation study in which case-control status was determined by two interacting polymorphisms with heritabilities ranging from 0.025 to 0.4 with replication sample sizes ranging from 400 to 1600 individuals. We show that the power to replicate the statistically significant independent main effect of one polymorphism can drop dramatically with a change of allele frequency of less than 0.1 at a second interacting polymorphism. We also show that differences in allele frequency can result in a reversal of allelic effects where a protective allele becomes a risk factor in replication studies. These results suggest that failure to replicate an independent genetic effect may provide important clues about the complexity of the underlying genetic architecture. We recommend that polymorphisms that fail to replicate be checked for interactions with other polymorphisms, particularly when samples are collected from groups with distinct ethnic backgrounds or different geographic regions.
url http://europepmc.org/articles/PMC2685469?pdf=render
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