Abstract
By using the 1.6 million single-nucleotide polymorphism (SNP) genotype data set from Perlegen Sciences [Hinds, D. A., Stuve, L. L., Nilsen, G. B., Halperin, E., Eskin, E., Ballinger, D. G., Frazer, K. A. & Cox, D. R. (2005) Science 307, 1072-1079], a probabilistic search for the landscape exhibited by positive Darwinian selection was conducted. By sorting each high-frequency allele by homozygosity, we search for the expected decay of adjacent SNP linkage disequilibrium (LD) at recently selected alleles, eliminating the need for inferring haplotype. We designate this approach the LD decay (LDD) test. By these criteria, 1.6% of Perlegen SNPs were found to exhibit the genetic architecture of selection. These results were confirmed on an independently generated data set of 1.0 million SNP genotypes (International Human Haplotype Map Phase I freeze). Simulation studies indicate that the LDD test, at the megabase scale used, effectively distinguishes selection from other causes of extensive LD, such as inversions, population bottlenecks, and admixture. The approximately 1,800 genes identified by the LDD test were clustered according to Gene Ontology (GO) categories. Based on overrepresentation analysis, several predominant biological themes are common in these selected alleles, including host-pathogen interactions, reproduction, DNA metabolism/cell cycle, protein metabolism, and neuronal function.
MeSH Terms
Alleles
Computational Biology/methods
Databases, Genetic
Genome, Human/genetics
Genomics/methods
Humans
Linkage Disequilibrium/genetics
Polymorphism, Single Nucleotide/genetics
Selection, Genetic
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Wang Eric T
Department of Biological Chemistry, College of Medicine, Donald Bren School of Information and Computer Sciences, and Institute of Genomics and Bioinformatics, University of California, Irvine, CA 92697, USA.
Kodama Greg
Baldi Pierre
Moyzis Robert K
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