Non-replication and inconsistency in the genome-wide association setting
- PMID: 17551261
- DOI: 10.1159/000103512
Non-replication and inconsistency in the genome-wide association setting
Abstract
Non-replication and inconsistency had been common features in the search for common variants of candidate genes affecting the risk of complex diseases. They may continue to require attention in the current era, when massive hypothesis-free testing of genetic variants is feasible. An empirical evaluation of the early experience with genome-wide association (GWA) studies suggests several examples where proposed associations have failed to be replicated by subsequent investigations. Non-replication and inconsistency is defined here in the framework of cumulative meta-analysis. Ideally, associations exist, GWA finds them, and subsequent investigations should replicate them. However, a number of other possibilities need to be considered. No common genetic variants may associate with the phenotype of interest and GWA may find nothing; or associations may exist, but GWA may miss them. Associations that do not exist may be falsely selected by the GWA and subsequent studies may appropriately refute them or falsely replicate them. Finally, GWA may find true associations that are nevertheless falsely non-replicated in the subsequent studies; or associations may be genuinely inconsistent across study populations. A list of options is presented for consideration in each of these scenarios.
Copyright 2007 S. Karger AG, Basel.
Similar articles
-
Heterogeneity in meta-analyses of genome-wide association investigations.PLoS One. 2007 Sep 5;2(9):e841. doi: 10.1371/journal.pone.0000841. PLoS One. 2007. PMID: 17786212 Free PMC article.
-
Meta-analysis of genetic association studies: methodologies, between-study heterogeneity and winner's curse.J Hum Genet. 2009 Nov;54(11):615-23. doi: 10.1038/jhg.2009.95. Epub 2009 Oct 23. J Hum Genet. 2009. PMID: 19851339 Review.
-
Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease.Nat Genet. 2003 Feb;33(2):177-82. doi: 10.1038/ng1071. Epub 2003 Jan 13. Nat Genet. 2003. PMID: 12524541
-
Expectations and challenges stemming from genome-wide association studies.Mutagenesis. 2008 Nov;23(6):439-44. doi: 10.1093/mutage/gen042. Epub 2008 Sep 2. Mutagenesis. 2008. PMID: 18765424
-
Identifying genetic risk factors for osteoporosis.J Musculoskelet Neuronal Interact. 2006 Jan-Mar;6(1):16-26. J Musculoskelet Neuronal Interact. 2006. PMID: 16675886 Review.
Cited by
-
Importance of different types of prior knowledge in selecting genome-wide findings for follow-up.Genet Epidemiol. 2013 Feb;37(2):205-13. doi: 10.1002/gepi.21705. Genet Epidemiol. 2013. PMID: 23307621 Free PMC article.
-
Impact of phenotype definition on genome-wide association signals: empirical evaluation in human immunodeficiency virus type 1 infection.Am J Epidemiol. 2011 Jun 1;173(11):1336-42. doi: 10.1093/aje/kwr024. Epub 2011 Apr 13. Am J Epidemiol. 2011. PMID: 21490045 Free PMC article.
-
Evaluation of the potential excess of statistically significant findings in published genetic association studies: application to Alzheimer's disease.Am J Epidemiol. 2008 Oct 15;168(8):855-65. doi: 10.1093/aje/kwn206. Epub 2008 Sep 8. Am J Epidemiol. 2008. PMID: 18779388 Free PMC article.
-
Polymorphisms in AHI1 are not associated with type 2 diabetes or related phenotypes in Danes: non-replication of a genome-wide association result.Diabetologia. 2008 Apr;51(4):609-14. doi: 10.1007/s00125-008-0925-z. Epub 2008 Jan 29. Diabetologia. 2008. PMID: 18227995
-
Intermediate phenotypes in schizophrenia genetics redux: is it a no brainer?Mol Psychiatry. 2008 Mar;13(3):233-8. doi: 10.1038/sj.mp.4002145. Mol Psychiatry. 2008. PMID: 18285755 Review. No abstract available.
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
