A method for genome-wide genealogy estimation for thousands of samples

被引:245
|
作者
Speidel, Leo [1 ]
Forest, Marie [2 ]
Shi, Sinan [1 ]
Myers, Simon R. [1 ,3 ]
机构
[1] Univ Oxford, Dept Stat, Oxford, England
[2] Univ Quebec Montreal, Montreal, PQ, Canada
[3] Univ Oxford, Wellcome Ctr Human Genet, Oxford, England
基金
英国工程与自然科学研究理事会; 英国惠康基金; 加拿大自然科学与工程研究理事会;
关键词
LINKAGE-DISEQUILIBRIUM; POPULATION HISTORY; POSITIVE SELECTION; HUMAN ADAPTATION; INFERENCE; RECOMBINATION; EVOLUTION; SEQUENCES; NEANDERTHAL; ALLELE;
D O I
10.1038/s41588-019-0484-x
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Knowledge of genome-wide genealogies for thousands of individuals would simplify most evolutionary analyses for humans and other species, but has remained computationally infeasible. We have developed a method, Relate, scaling to >10,000 sequences while simultaneously estimating branch lengths, mutational ages and variable historical population sizes, as well as allowing for data errors. Application to 1,000 Genomes Project haplotypes produces joint genealogical histories for 26 human populations. Highly diverged lineages are present in all groups, but most frequent in Africa. Outside Africa, these mainly reflect ancient introgression from groups related to Neanderthals and Denisovans, while African signals instead reflect unknown events unique to that continent. Our approach allows more powerful inferences of natural selection than has previously been possible. We identify multiple regions under strong positive selection, and multi-allelic traits including hair color, body mass index and blood pressure, showing strong evidence of directional selection, varying among human groups.
引用
收藏
页码:1321 / +
页数:11
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