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利用未混合的外群检测古老的基因渗入。

Detecting archaic introgression using an unadmixed outgroup.

机构信息

Bioinformatics Research Centre, Aarhus University, Aarhus C., Denmark.

Department of Genetics, University of Cambridge, Cambridge United Kingdom.

出版信息

PLoS Genet. 2018 Sep 18;14(9):e1007641. doi: 10.1371/journal.pgen.1007641. eCollection 2018 Sep.

DOI:10.1371/journal.pgen.1007641
PMID:30226838
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6161914/
Abstract

Human populations outside of Africa have experienced at least two bouts of introgression from archaic humans, from Neanderthals and Denisovans. In Papuans there is prior evidence of both these introgressions. Here we present a new approach to detect segments of individual genomes of archaic origin without using an archaic reference genome. The approach is based on a hidden Markov model that identifies genomic regions with a high density of single nucleotide variants (SNVs) not seen in unadmixed populations. We show using simulations that this provides a powerful approach to identifying segments of archaic introgression with a low rate of false detection, given data from a suitable outgroup population is available, without the archaic introgression but containing a majority of the variation that arose since initial separation from the archaic lineage. Furthermore our approach is able to infer admixture proportions and the times both of admixture and of initial divergence between the human and archaic populations. We apply the model to detect archaic introgression in 89 Papuans and show how the identified segments can be assigned to likely Neanderthal or Denisovan origin. We report more Denisovan admixture than previous studies and find a shift in size distribution of fragments of Neanderthal and Denisovan origin that is compatible with a difference in admixture time. Furthermore, we identify small amounts of Denisova ancestry in South East Asians and South Asians.

摘要

非洲以外的人类群体至少经历了两次来自古人类(尼安德特人和丹尼索瓦人)的基因渗入。在巴布亚人中,这两种基因渗入都有先前的证据。在这里,我们提出了一种新的方法,可以在不使用古人类参考基因组的情况下,检测个体基因组中具有古人类起源的片段。该方法基于隐马尔可夫模型,该模型可以识别出具有高密度单核苷酸变异(SNV)的基因组区域,而这些变异在未混合的人群中是看不到的。我们通过模拟表明,在有合适的外群数据的情况下,这种方法可以有效地识别出具有低假阳性率的古人类基因渗入片段,而无需古人类基因渗入,但包含了自与古人类谱系最初分离以来出现的大部分变异。此外,我们的方法还可以推断出混合比例以及人类和古人类群体之间的混合时间和初始分化时间。我们将该模型应用于 89 名巴布亚人中,以确定古人类基因渗入的情况,并将鉴定出的片段分配到可能的尼安德特人和丹尼索瓦人起源。我们报告的丹尼索瓦人混合比例比以前的研究多,并发现尼安德特人和丹尼索瓦人起源的片段的大小分布发生了变化,这与混合时间的差异是一致的。此外,我们还在东南亚人和南亚人中发现了少量的丹尼索瓦人遗传。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54dd/6161914/e43e4faf7f33/pgen.1007641.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54dd/6161914/2d1d8be72571/pgen.1007641.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54dd/6161914/01ea43010ffc/pgen.1007641.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54dd/6161914/e43e4faf7f33/pgen.1007641.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54dd/6161914/2d1d8be72571/pgen.1007641.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54dd/6161914/01ea43010ffc/pgen.1007641.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54dd/6161914/e43e4faf7f33/pgen.1007641.g003.jpg

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