Large-scale studies of linkage disequilibrium (LD) have shown considerable variation in the extent and distribution of pairwise LD within and between populations. Taken at face value, these results suggest that genomewide LD maps for one population may not be generalizable to other populations. However, at least part of this diversity is due to some undesirable features of pairwise LD measures, which are well documented for the D′ and r2 measures. In this report, we compare patterns of LD derived from pairwise measures with statistical estimates of population recombination rates (ρ) along a 10-Mb stretch of chromosome 20 in four population samples, comprising East Asians, African Americans, and U.K. and U.S. individuals of western European ...
AbstractThe International HapMap Consortium has determined the linkage disequilibrium (LD) patterns ...
Genetic association studies of common disease often rely on linkage disequilibrium (LD) along the hu...
Both the optimal marker density for genome scans in case-control association studies and the appropr...
Large-scale studies of linkage disequilibrium (LD) have shown considerable variation in the extent a...
The prospect of using linkage disequilibrium (LD) for fine-scale mapping in humans has attracted con...
High-throughput genotyping technologies for SNPs have enabled the recent completion of the Internati...
In this review, we describe recent empirical and theoretical work on the extent of linkage disequili...
The extent and patterns of linkage disequilibrium (LD) determine the feasibility of association stud...
The extent and patterns of linkage disequilibrium (LD) determine the feasibility of association stud...
To characterize linkage disequilibrium (LD) levels in human populations, we have analyzed 10 indepen...
Understanding the pattern of linkage disequilibrium (LD) in the human genome is important both for s...
High-throughput genotyping technologies for single nucleotide polymorphisms (SNP) have enabled the r...
The extent and patterns of linkage disequilibrium (LD) determine the feasibility of association stud...
The prospect of using linkage disequilibrium (LD) for fine-scale mapping in humans has attracted con...
Linkage disequilibrium (LD) refers to the statistical dependency of the DNA content at nearby locat...
AbstractThe International HapMap Consortium has determined the linkage disequilibrium (LD) patterns ...
Genetic association studies of common disease often rely on linkage disequilibrium (LD) along the hu...
Both the optimal marker density for genome scans in case-control association studies and the appropr...
Large-scale studies of linkage disequilibrium (LD) have shown considerable variation in the extent a...
The prospect of using linkage disequilibrium (LD) for fine-scale mapping in humans has attracted con...
High-throughput genotyping technologies for SNPs have enabled the recent completion of the Internati...
In this review, we describe recent empirical and theoretical work on the extent of linkage disequili...
The extent and patterns of linkage disequilibrium (LD) determine the feasibility of association stud...
The extent and patterns of linkage disequilibrium (LD) determine the feasibility of association stud...
To characterize linkage disequilibrium (LD) levels in human populations, we have analyzed 10 indepen...
Understanding the pattern of linkage disequilibrium (LD) in the human genome is important both for s...
High-throughput genotyping technologies for single nucleotide polymorphisms (SNP) have enabled the r...
The extent and patterns of linkage disequilibrium (LD) determine the feasibility of association stud...
The prospect of using linkage disequilibrium (LD) for fine-scale mapping in humans has attracted con...
Linkage disequilibrium (LD) refers to the statistical dependency of the DNA content at nearby locat...
AbstractThe International HapMap Consortium has determined the linkage disequilibrium (LD) patterns ...
Genetic association studies of common disease often rely on linkage disequilibrium (LD) along the hu...
Both the optimal marker density for genome scans in case-control association studies and the appropr...