Access
To read this article in full you may need to log in, make a payment or gain access through a site license (see right).
Letter
Nature Genetics 38, 663–667 (1 June 2006) | doi:10.1038/ng1816
Evaluating and improving power in whole-genome association studies using fixed marker sets
&
Abstract
Emerging technologies make it possible for the first time to genotype hundreds of thousands of SNPs simultaneously, enabling whole-genome association studies. Using empirical genotype data from the International HapMap Project, we evaluate the extent to which the sets of SNPs contained on three whole-genome genotyping arrays capture common SNPs across the genome, and we find that the majority of common SNPs are well captured by these products either directly or through linkage disequilibrium.
To read this article in full you may need to log in, make a payment or gain access through a site license (see right).
