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Fine-Scale Inference of Ancestry Segments Without Prior Knowledge of Admixing Groups
We present an algorithm for inferring ancestry segments and characterizing admixture events, which involve an arbitrary number of genetically differentiated groups coming together. This allows inference of the demographic history of the species, properties of admixing groups, identification of signa...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Genetics Society of America
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6614886/ https://www.ncbi.nlm.nih.gov/pubmed/31123038 http://dx.doi.org/10.1534/genetics.119.302139 |
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author | Salter-Townshend, Michael Myers, Simon |
author_facet | Salter-Townshend, Michael Myers, Simon |
author_sort | Salter-Townshend, Michael |
collection | PubMed |
description | We present an algorithm for inferring ancestry segments and characterizing admixture events, which involve an arbitrary number of genetically differentiated groups coming together. This allows inference of the demographic history of the species, properties of admixing groups, identification of signatures of natural selection, and may aid disease gene mapping. The algorithm employs nested hidden Markov models to obtain local ancestry estimation along the genome for each admixed individual. In a range of simulations, the accuracy of these estimates equals or exceeds leading existing methods. Moreover, and unlike these approaches, we do not require any prior knowledge of the relationship between subgroups of donor reference haplotypes and the unseen mixing ancestral populations. Our approach infers these in terms of conditional “copying probabilities.” In application to the Human Genome Diversity Project, we corroborate many previously inferred admixture events (e.g., an ancient admixture event in the Kalash). We further identify novel events such as complex four-way admixture in San-Khomani individuals, and show that Eastern European populations possess [Formula: see text] ancestry from a group resembling modern-day central Asians. We also identify evidence of recent natural selection favoring sub-Saharan ancestry at the human leukocyte antigen (HLA) region, across North African individuals. We make available an R and C++ software library, which we term MOSAIC (which stands for MOSAIC Organizes Segments of Ancestry In Chromosomes). |
format | Online Article Text |
id | pubmed-6614886 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Genetics Society of America |
record_format | MEDLINE/PubMed |
spelling | pubmed-66148862019-10-24 Fine-Scale Inference of Ancestry Segments Without Prior Knowledge of Admixing Groups Salter-Townshend, Michael Myers, Simon Genetics Investigations We present an algorithm for inferring ancestry segments and characterizing admixture events, which involve an arbitrary number of genetically differentiated groups coming together. This allows inference of the demographic history of the species, properties of admixing groups, identification of signatures of natural selection, and may aid disease gene mapping. The algorithm employs nested hidden Markov models to obtain local ancestry estimation along the genome for each admixed individual. In a range of simulations, the accuracy of these estimates equals or exceeds leading existing methods. Moreover, and unlike these approaches, we do not require any prior knowledge of the relationship between subgroups of donor reference haplotypes and the unseen mixing ancestral populations. Our approach infers these in terms of conditional “copying probabilities.” In application to the Human Genome Diversity Project, we corroborate many previously inferred admixture events (e.g., an ancient admixture event in the Kalash). We further identify novel events such as complex four-way admixture in San-Khomani individuals, and show that Eastern European populations possess [Formula: see text] ancestry from a group resembling modern-day central Asians. We also identify evidence of recent natural selection favoring sub-Saharan ancestry at the human leukocyte antigen (HLA) region, across North African individuals. We make available an R and C++ software library, which we term MOSAIC (which stands for MOSAIC Organizes Segments of Ancestry In Chromosomes). Genetics Society of America 2019-07 2019-05-23 /pmc/articles/PMC6614886/ /pubmed/31123038 http://dx.doi.org/10.1534/genetics.119.302139 Text en Copyright © 2019 Salter-Townshend and Myers Available freely online through the author-supported open access option. This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Investigations Salter-Townshend, Michael Myers, Simon Fine-Scale Inference of Ancestry Segments Without Prior Knowledge of Admixing Groups |
title | Fine-Scale Inference of Ancestry Segments Without Prior Knowledge of Admixing Groups |
title_full | Fine-Scale Inference of Ancestry Segments Without Prior Knowledge of Admixing Groups |
title_fullStr | Fine-Scale Inference of Ancestry Segments Without Prior Knowledge of Admixing Groups |
title_full_unstemmed | Fine-Scale Inference of Ancestry Segments Without Prior Knowledge of Admixing Groups |
title_short | Fine-Scale Inference of Ancestry Segments Without Prior Knowledge of Admixing Groups |
title_sort | fine-scale inference of ancestry segments without prior knowledge of admixing groups |
topic | Investigations |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6614886/ https://www.ncbi.nlm.nih.gov/pubmed/31123038 http://dx.doi.org/10.1534/genetics.119.302139 |
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