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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2020-03-01
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Series: | PLoS Genetics |
Online Access: | https://doi.org/10.1371/journal.pgen.1008552 |
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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 |
work_keys_str_mv |
AT kewang trackinghumanpopulationstructurethroughtimefromwholegenomesequences AT iainmathieson trackinghumanpopulationstructurethroughtimefromwholegenomesequences AT jaredoconnell trackinghumanpopulationstructurethroughtimefromwholegenomesequences AT stephanschiffels trackinghumanpopulationstructurethroughtimefromwholegenomesequences |
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