Author:
De La Vega Francisco M.,Isaac Hadar,Collins Andrew,Scafe Charles R.,Halldórsson Bjarni V.,Su Xiaoping,Lippert Ross A.,Wang Yu,Laig-Webster Marion,Koehler Ryan T.,Ziegle Janet S.,Wogan Lewis T.,Stevens Junko F.,Leinen Kyle M.,Olson Sheri J.,Guegler Karl J.,You Xiaoqing,Xu Lily H.,Hemken Heinz G.,Kalush Francis,Itakura Mitsuo,Zheng Yi,de Thé Guy,O'Brien Stephen J.,Clark Andrew G.,Istrail Sorin,Hunkapiller Michael W.,Spier Eugene G.,Gilbert Dennis A.
Abstract
The extent and patterns of linkage disequilibrium (LD) determine the feasibility of association studies to map genes that underlie complex traits. Here we present a comparison of the patterns of LD across four major human populations (African-American, Caucasian, Chinese, and Japanese) with a high-resolution single-nucleotide polymorphism (SNP) map covering almost the entire length of chromosomes 6, 21, and 22. We constructed metric LD maps formulated such that the units measure the extent of useful LD for association mapping. LD reaches almost twice as far in chromosome 6 as in chromosomes 21 or 22, in agreement with their differences in recombination rates. By all measures used, out-of-Africa populations showed over a third more LD than African-Americans, highlighting the role of the population's demography in shaping the patterns of LD. Despite those differences, the long-range contour of the LD maps is remarkably similar across the four populations, presumably reflecting common localization of recombination hot spots. Our results have practical implications for the rational design and selection of SNPs for disease association studies.
Publisher
Cold Spring Harbor Laboratory
Subject
Genetics (clinical),Genetics
Cited by
82 articles.
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