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ABSTRACT: Background
The distribution of human disease-associated mutations is not random across the human genome. Despite the fact that natural selection continually removes disease-associated mutations, an enrichment of these variants can be observed in regions of low recombination. There are a number of mechanisms by which such a clustering could occur, including genetic perturbations or demographic effects within different populations. Recent genome-wide association studies (GWAS) suggest that single nucleotide polymorphisms (SNPs) associated with complex disease traits are not randomly distributed throughout the genome, but tend to cluster in regions of low recombination.Principal findings
Here we investigated whether deleterious mutations have accumulated in regions of low reco
SUBMITTER: Preuss C
PROVIDER: S-EPMC3351447 | biostudies-literature | 2012
REPOSITORIES: biostudies-literature