High-throughput genotyping and sequencing technologies can generate dense sets of
genetic markers for large numbers of individuals. For most species, these data will contain …

We propose a multilocus version of F ST and a measure of haplotype diversity using
localized haplotype clusters. Specifically, we use haplotype clusters identified with BEAGLE …

Statistical methods for haplotype inference from multi‐site genotypes of unrelated
individuals have important application in association studies and population genetics …

In the 'indirect'method of detecting genetic associations between a trait and a DNA variant,
we type several markers in a gene or chromosome region of linkage disequilibrium. If there …

Abstract: Haplotypes defined by common single nucleotide polymorphisms (SNPs) have
important implications for mapping of disease genes and human traits. Often only a small …

Haplotype reconstruction is an important issue, both in population genetics and in the
identification of complex disease genes. Stephens et al.(2001) proposed a new statistical …

It is usually assumed that detection of a disease susceptability gene via marker
polymorphisms in linkage disequilibrium with it is facilitated by consideration of marker …

In the search for common genetic variants that contribute to prevalent human diseases,
patterns of linkage disequilibrium (LD) among linked markers should be considered when …

There is great interest in the use of tagging single nucleotide polymorphisms (tSNPs) to
facilitate association studies of complex diseases. This is based on the premise that a …

Association studies in populations that are genetically heterogeneous can yield large
numbers of spurious associations if population subgroups are unequally represented …