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Haplotype and population structure inference using neural networks in whole-genome sequencing data
Accurate inference of population structure is important in many studies of population genetics. Here we present HaploNet, a method for performing dimensionality reduction and clustering of genetic data. The method is based on local clustering of phased haplotypes using neural networks from whole-gen...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Cold Spring Harbor Laboratory Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9435741/ https://www.ncbi.nlm.nih.gov/pubmed/35794006 http://dx.doi.org/10.1101/gr.276813.122 |
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author | Meisner, Jonas Albrechtsen, Anders |
author_facet | Meisner, Jonas Albrechtsen, Anders |
author_sort | Meisner, Jonas |
collection | PubMed |
description | Accurate inference of population structure is important in many studies of population genetics. Here we present HaploNet, a method for performing dimensionality reduction and clustering of genetic data. The method is based on local clustering of phased haplotypes using neural networks from whole-genome sequencing or dense genotype data. By using Gaussian mixtures in a variational autoencoder framework, we are able to learn a low-dimensional latent space in which we cluster haplotypes along the genome in a highly scalable manner. We show that we can use haplotype clusters in the latent space to infer global population structure using haplotype information by exploiting the generative properties of our framework. Based on fitted neural networks and their latent haplotype clusters, we can perform principal component analysis and estimate ancestry proportions based on a maximum likelihood framework. Using sequencing data from simulations and closely related human populations, we show that our approach is better at distinguishing closely related populations than standard admixture and principal component analysis software. We further show that HaploNet is fast and highly scalable by applying it to genotype array data of the UK Biobank. |
format | Online Article Text |
id | pubmed-9435741 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Cold Spring Harbor Laboratory Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-94357412023-02-01 Haplotype and population structure inference using neural networks in whole-genome sequencing data Meisner, Jonas Albrechtsen, Anders Genome Res Method Accurate inference of population structure is important in many studies of population genetics. Here we present HaploNet, a method for performing dimensionality reduction and clustering of genetic data. The method is based on local clustering of phased haplotypes using neural networks from whole-genome sequencing or dense genotype data. By using Gaussian mixtures in a variational autoencoder framework, we are able to learn a low-dimensional latent space in which we cluster haplotypes along the genome in a highly scalable manner. We show that we can use haplotype clusters in the latent space to infer global population structure using haplotype information by exploiting the generative properties of our framework. Based on fitted neural networks and their latent haplotype clusters, we can perform principal component analysis and estimate ancestry proportions based on a maximum likelihood framework. Using sequencing data from simulations and closely related human populations, we show that our approach is better at distinguishing closely related populations than standard admixture and principal component analysis software. We further show that HaploNet is fast and highly scalable by applying it to genotype array data of the UK Biobank. Cold Spring Harbor Laboratory Press 2022-08 /pmc/articles/PMC9435741/ /pubmed/35794006 http://dx.doi.org/10.1101/gr.276813.122 Text en © 2022 Meisner and Albrechtsen; Published by Cold Spring Harbor Laboratory Press https://creativecommons.org/licenses/by-nc/4.0/This article is distributed exclusively by Cold Spring Harbor Laboratory Press for the first six months after the full-issue publication date (see https://genome.cshlp.org/site/misc/terms.xhtml). After six months, it is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) . |
spellingShingle | Method Meisner, Jonas Albrechtsen, Anders Haplotype and population structure inference using neural networks in whole-genome sequencing data |
title | Haplotype and population structure inference using neural networks in whole-genome sequencing data |
title_full | Haplotype and population structure inference using neural networks in whole-genome sequencing data |
title_fullStr | Haplotype and population structure inference using neural networks in whole-genome sequencing data |
title_full_unstemmed | Haplotype and population structure inference using neural networks in whole-genome sequencing data |
title_short | Haplotype and population structure inference using neural networks in whole-genome sequencing data |
title_sort | haplotype and population structure inference using neural networks in whole-genome sequencing data |
topic | Method |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9435741/ https://www.ncbi.nlm.nih.gov/pubmed/35794006 http://dx.doi.org/10.1101/gr.276813.122 |
work_keys_str_mv | AT meisnerjonas haplotypeandpopulationstructureinferenceusingneuralnetworksinwholegenomesequencingdata AT albrechtsenanders haplotypeandpopulationstructureinferenceusingneuralnetworksinwholegenomesequencingdata |