Recombination rates in admixed individuals identified by ancestry-based inference

被引:85
|
作者
Wegmann, Daniel [1 ]
Kessner, Darren E. [2 ]
Veeramah, Krishna R. [1 ]
Mathias, Rasika A. [3 ]
Nicolae, Dan L. [4 ,5 ,6 ]
Yanek, Lisa R. [3 ]
Sun, Yan V. [7 ,8 ]
Torgerson, Dara G. [6 ]
Rafaels, Nicholas [9 ]
Mosley, Thomas [10 ]
Becker, Lewis C. [3 ]
Ruczinski, Ingo [9 ]
Beaty, Terri H. [11 ]
Kardia, Sharon L. R. [7 ]
Meyers, Deborah A. [12 ]
Barnes, Kathleen C. [3 ]
Becker, Diane M. [3 ]
Freimer, Nelson B. [13 ]
Novembre, John [1 ,2 ]
机构
[1] Univ Calif Los Angeles, Dept Ecol & Evolutionary Biol, Los Angeles, CA 90024 USA
[2] Univ Calif Los Angeles, Interdept Program Bioinformat, Los Angeles, CA USA
[3] Johns Hopkins Univ, Dept Med, Baltimore, MD USA
[4] Univ Chicago, Dept Med, Chicago, IL 60637 USA
[5] Univ Chicago, Dept Stat, Chicago, IL 60637 USA
[6] Univ Chicago, Dept Human Genet, Chicago, IL 60637 USA
[7] Univ Michigan, Dept Epidemiol, Ann Arbor, MI 48109 USA
[8] Emory Univ, Dept Epidemiol, Atlanta, GA 30322 USA
[9] Johns Hopkins Bloomberg Sch Publ Hlth, Dept Biostat, Baltimore, MD USA
[10] Univ Mississippi, Dept Med, Jackson, MS 39216 USA
[11] Johns Hopkins Bloomberg Sch Publ Hlth, Dept Epidemiol, Baltimore, MD USA
[12] Wake Forest Univ, Bowman Gray Sch Med, Ctr Human Genom, Winston Salem, NC USA
[13] Univ Calif Los Angeles, Ctr Neurobehav Genet, Semel Inst Neurosci & Human Behav, Los Angeles, CA USA
基金
美国国家卫生研究院;
关键词
STRUCTURAL VARIATION; HUMAN GENOME; COPY NUMBER; INVERSION POLYMORPHISMS; POPULATION-STRUCTURE; ADMIXTURE; PATTERNS; LINKAGE; SELECTION; SEQUENCE;
D O I
10.1038/ng.894
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
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.
引用
收藏
页码:847 / U53
页数:9
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