TY - JOUR
T1 - Genomic inflation factors under polygenic inheritance
AU - Yang, Jian
AU - Weedon, Michael N.
AU - Purcell, Shaun
AU - Lettre, Guillaume
AU - Estrada, Karol
AU - Willer, Cristen J.
AU - Smith, Albert V.
AU - Ingelsson, Erik
AU - O'Connell, Jeffrey R.
AU - Mangino, Massimo
AU - Mägi, Reedik
AU - Madden, Pamela A.
AU - Heath, Andrew C.
AU - Nyholt, Dale R.
AU - Martin, Nicholas G.
AU - Montgomery, Grant W.
AU - Frayling, Timothy M.
AU - Hirschhorn, Joel N.
AU - McCarthy, Mark I.
AU - Goddard, Michael E.
AU - Visscher, Peter M.
N1 - Funding Information:
We thank all three reviewers for helpful comments. We acknowledge funding from the Australian National Health and Medical Research Council (NHMRC Grants 389891, 389892, 613672 and 613601), the Australian Research Council (ARC Grants DP0770096 and DP1093900) and the US National Institute of Health (NIH Grants AA13320, AA13321 and DA12854).
PY - 2011/7
Y1 - 2011/7
N2 - Population structure, including population stratification and cryptic relatedness, can cause spurious associations in genome-wide association studies (GWAS). Usually, the scaled median or mean test statistic for association calculated from multiple single-nucleotide-polymorphisms across the genome is used to assess such effects, and genomic control can be applied subsequently to adjust test statistics at individual loci by a genomic inflation factor. Published GWAS have clearly shown that there are many loci underlying genetic variation for a wide range of complex diseases and traits, implying that a substantial proportion of the genome should show inflation of the test statistic. Here, we show by theory, simulation and analysis of data that in the absence of population structure and other technical artefacts, but in the presence of polygenic inheritance, substantial genomic inflation is expected. Its magnitude depends on sample size, heritability, linkage disequilibrium structure and the number of causal variants. Our predictions are consistent with empirical observations on height in independent samples of ∼4000 and ∼133 000 individuals.
AB - Population structure, including population stratification and cryptic relatedness, can cause spurious associations in genome-wide association studies (GWAS). Usually, the scaled median or mean test statistic for association calculated from multiple single-nucleotide-polymorphisms across the genome is used to assess such effects, and genomic control can be applied subsequently to adjust test statistics at individual loci by a genomic inflation factor. Published GWAS have clearly shown that there are many loci underlying genetic variation for a wide range of complex diseases and traits, implying that a substantial proportion of the genome should show inflation of the test statistic. Here, we show by theory, simulation and analysis of data that in the absence of population structure and other technical artefacts, but in the presence of polygenic inheritance, substantial genomic inflation is expected. Its magnitude depends on sample size, heritability, linkage disequilibrium structure and the number of causal variants. Our predictions are consistent with empirical observations on height in independent samples of ∼4000 and ∼133 000 individuals.
KW - genome-wide association study
KW - genomic inflation factor
KW - polygenic inheritance
UR - http://www.scopus.com/inward/record.url?scp=79959241413&partnerID=8YFLogxK
U2 - 10.1038/ejhg.2011.39
DO - 10.1038/ejhg.2011.39
M3 - Article
C2 - 21407268
AN - SCOPUS:79959241413
SN - 1018-4813
VL - 19
SP - 807
EP - 812
JO - European Journal of Human Genetics
JF - European Journal of Human Genetics
IS - 7
ER -