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      Modeling Human Population Separation History Using Physically Phased Genomes

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          Abstract

          Phased haplotype sequences are a key component in many population genetic analyses since variation in haplotypes reflects the action of recombination, selection, and changes in population size. In humans, haplotypes are typically estimated from unphased sequence or genotyping data using statistical models applied to large reference panels. To assess the importance of correct haplotype phase on population history inference, we performed fosmid pool sequencing and resolved phased haplotypes of five individuals from diverse African populations (including Yoruba, Esan, Gambia, Maasai, and Mende). We physically phased 98% of heterozygous SNPs into haplotype-resolved blocks, obtaining a block N50 of 1 Mbp. We combined these data with additional phased genomes from San, Mbuti, Gujarati, and Centre de’Etude du Polymorphism Humain European populations and analyzed population size and separation history using the pairwise sequentially Markovian coalescent and multiple sequentially Markovian coalescent models. We find that statistically phased haplotypes yield a more recent split-time estimation compared with experimentally phased haplotypes. To better interpret patterns of cross-population coalescence, we implemented an approximate Bayesian computation approach to estimate population split times and migration rates by fitting the distribution of coalescent times inferred between two haplotypes, one from each population, to a standard isolation-with-migration model. We inferred that the separation between hunter-gatherer populations and other populations happened ∼120–140 KYA, with gene flow continuing until 30–40 KYA; separation between west-African and out-of-African populations happened ∼70–80 KYA; while the separation between Maasai and out-of-African populations happened ∼50 KYA.

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          Author and article information

          Journal
          Genetics
          Genetics
          genetics
          genetics
          genetics
          Genetics
          Genetics Society of America
          0016-6731
          1943-2631
          January 2017
          8 November 2016
          8 November 2016
          : 205
          : 1
          : 385-395
          Affiliations
          [* ]Department of Computational Medicine and Bioinformatics, University of Michigan Medical School, Ann Arbor, Michigan 48109
          []Department of Human Genetics, University of Michigan Medical School, Ann Arbor, Michigan 48109
          Author notes
          [1 ]Corresponding author: 3726 Medical Science II Building, University of Michigan, 1241 E. Catherine St., Ann Arbor, MI 48109. E-mail: jmkidd@ 123456umich.edu
          Article
          PMC5223516 PMC5223516 5223516 192963
          10.1534/genetics.116.192963
          5223516
          28049708
          8f6e8ca7-782c-4f76-b53a-7447c7a46a19
          Copyright © 2017 by the Genetics Society of America
          History
          : 21 June 2016
          : 02 November 2016
          Page count
          Figures: 5, Tables: 3, Equations: 3, References: 35, Pages: 11
          Categories
          Investigations
          Population and Evolutionary Genetics

          MSMC,approximate Bayesian computation,fosmid pool sequencing,haplotype,PSMC,population split time

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