4.8 Article

Recombination rates in admixed individuals identified by ancestry-based inference

Journal

NATURE GENETICS
Volume 43, Issue 9, Pages 847-U53

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/ng.894

Keywords

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Funding

  1. Searle Scholar Program
  2. US National Institutes of Health (NIH) [R01HL087679, RL1MH083268]
  3. NIH [HL072518, M01-RR00052, U01 HL49596, R01 HL072414, R01 HL087665, RC2 HL101651, HL087660, HL49612, AI50024, AI44840, HL075417, HL072433, AI41040, ES09606, RR03048]
  4. US Environmental Protection Agency [83213901]
  5. National Institute of General Medical Sciences (NIGMS) [S06GM08015]
  6. Johns Hopkins University
  7. NHLBI STAMPEED

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Studies of recombination and how it varies depend crucially on accurate recombination maps. We propose a new approach for constructing high-resolution maps of relative recombination rates based on the observation of ancestry switch points among admixed individuals. We show the utility of this approach using simulations and by applying it to SNP genotype data from a sample of 2,565 African Americans and 299 African Caribbeans and detecting several hundred thousand recombination events. Comparison of the inferred map with high-resolution maps from non-admixed populations provides evidence of fine-scale differentiation in recombination rates between populations. Overall, the admixed map is well predicted by the average proportion of admixture and the recombination rate estimates from the source populations. The exceptions to this are in areas surrounding known large chromosomal structural variants, specifically inversions. These results suggest that outside of structurally variable regions, admixture does not substantially disrupt the factors controlling recombination rates in humans.

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