Sequence variations in the public human genome data reflect a bottlenecked population history.

ABSTRACT: Single-nucleotide polymorphisms (SNPs) constitute the great majority of variations in the human genome, and as heritable variable landmarks they are useful markers for disease mapping and resolving population structure. Redundant coverage in overlaps of large-insert genomic clones, sequenced as part of the Human Genome Project, comprises a quarter of the genome, and it is representative in terms of base compositional and functional sequence features. We mined these regions to produce 500,000 high-confidence SNP candidates as a uniform resource for describing nucleotide diversity and its regional variation within the genome. Distributions of marker density observed at different overlap length scales under a model of recombination and population size change show that the history of the popul

SUBMITTER: Marth G 

PROVIDER: S-EPMC140982 | biostudies-literature | 2003 Jan

REPOSITORIES: biostudies-literature