The impact of improved microarray coverage and larger sample sizes on future genome-wide association studies.
Ontology highlight
ABSTRACT: Genome-wide association studies (GWAS) have identified many single nucleotide polymorphisms (SNPs) associated with complex traits. However, the genetic heritability of most of these traits remains unexplained. To help guide future studies, we address the crucial question of whether future GWAS can detect new SNP associations and explain additional heritability given the new availability of larger GWAS SNP arrays, imputation, and reduced genotyping costs. We first describe the pairwise and imputation coverage of all SNPs in the human genome by commercially available GWAS SNP arrays, using the 1000 Genomes Project as a reference. Next, we describe the findings from 6 years of GWAS of 172 chronic diseases, calculating the power to detect each of them while taking array coverage and sample siz
SUBMITTER: Lindquist KJ
PROVIDER: S-EPMC4291231 | biostudies-literature | 2013 May
REPOSITORIES: biostudies-literature
ACCESS DATA