Tracking human population structure through time from whole genome sequences.

The genetic diversity of humans, like many species, has been shaped by a complex pattern of population separations followed by isolation and subsequent admixture. This pattern, reaching at least as far back as the appearance of our species in the paleontological record, has left its traces in our ge...

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Main Authors: Ke Wang, Iain Mathieson, Jared O'Connell, Stephan Schiffels
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2020-03-01
Series:PLoS Genetics
Online Access:https://doi.org/10.1371/journal.pgen.1008552
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spelling doaj-3766b9294fd14387a062950bee2c7dc02021-04-21T13:51:27ZengPublic Library of Science (PLoS)PLoS Genetics1553-73901553-74042020-03-01163e100855210.1371/journal.pgen.1008552Tracking human population structure through time from whole genome sequences.Ke WangIain MathiesonJared O'ConnellStephan SchiffelsThe genetic diversity of humans, like many species, has been shaped by a complex pattern of population separations followed by isolation and subsequent admixture. This pattern, reaching at least as far back as the appearance of our species in the paleontological record, has left its traces in our genomes. Reconstructing a population's history from these traces is a challenging problem. Here we present a novel approach based on the Multiple Sequentially Markovian Coalescent (MSMC) to analyze the separation history between populations. Our approach, called MSMC-IM, uses an improved implementation of the MSMC (MSMC2) to estimate coalescence rates within and across pairs of populations, and then fits a continuous Isolation-Migration model to these rates to obtain a time-dependent estimate of gene flow. We show, using simulations, that our method can identify complex demographic scenarios involving post-split admixture or archaic introgression. We apply MSMC-IM to whole genome sequences from 15 worldwide populations, tracking the process of human genetic diversification. We detect traces of extremely deep ancestry between some African populations, with around 1% of ancestry dating to divergences older than a million years ago.https://doi.org/10.1371/journal.pgen.1008552
collection DOAJ
language English
format Article
sources DOAJ
author Ke Wang
Iain Mathieson
Jared O'Connell
Stephan Schiffels
spellingShingle Ke Wang
Iain Mathieson
Jared O'Connell
Stephan Schiffels
Tracking human population structure through time from whole genome sequences.
PLoS Genetics
author_facet Ke Wang
Iain Mathieson
Jared O'Connell
Stephan Schiffels
author_sort Ke Wang
title Tracking human population structure through time from whole genome sequences.
title_short Tracking human population structure through time from whole genome sequences.
title_full Tracking human population structure through time from whole genome sequences.
title_fullStr Tracking human population structure through time from whole genome sequences.
title_full_unstemmed Tracking human population structure through time from whole genome sequences.
title_sort tracking human population structure through time from whole genome sequences.
publisher Public Library of Science (PLoS)
series PLoS Genetics
issn 1553-7390
1553-7404
publishDate 2020-03-01
description The genetic diversity of humans, like many species, has been shaped by a complex pattern of population separations followed by isolation and subsequent admixture. This pattern, reaching at least as far back as the appearance of our species in the paleontological record, has left its traces in our genomes. Reconstructing a population's history from these traces is a challenging problem. Here we present a novel approach based on the Multiple Sequentially Markovian Coalescent (MSMC) to analyze the separation history between populations. Our approach, called MSMC-IM, uses an improved implementation of the MSMC (MSMC2) to estimate coalescence rates within and across pairs of populations, and then fits a continuous Isolation-Migration model to these rates to obtain a time-dependent estimate of gene flow. We show, using simulations, that our method can identify complex demographic scenarios involving post-split admixture or archaic introgression. We apply MSMC-IM to whole genome sequences from 15 worldwide populations, tracking the process of human genetic diversification. We detect traces of extremely deep ancestry between some African populations, with around 1% of ancestry dating to divergences older than a million years ago.
url https://doi.org/10.1371/journal.pgen.1008552
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AT jaredoconnell trackinghumanpopulationstructurethroughtimefromwholegenomesequences
AT stephanschiffels trackinghumanpopulationstructurethroughtimefromwholegenomesequences
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