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kWIP: The k-mer weighted inner product, a de novo estimator of genetic similarity
Modern genomics techniques generate overwhelming quantities of data. Extracting population genetic variation demands computationally efficient methods to determine genetic relatedness between individuals (or “samples”) in an unbiased manner, preferably de novo. Rapid estimation of genetic relatednes...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5600398/ https://www.ncbi.nlm.nih.gov/pubmed/28873405 http://dx.doi.org/10.1371/journal.pcbi.1005727 |
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author | Murray, Kevin D. Webers, Christfried Ong, Cheng Soon Borevitz, Justin Warthmann, Norman |
author_facet | Murray, Kevin D. Webers, Christfried Ong, Cheng Soon Borevitz, Justin Warthmann, Norman |
author_sort | Murray, Kevin D. |
collection | PubMed |
description | Modern genomics techniques generate overwhelming quantities of data. Extracting population genetic variation demands computationally efficient methods to determine genetic relatedness between individuals (or “samples”) in an unbiased manner, preferably de novo. Rapid estimation of genetic relatedness directly from sequencing data has the potential to overcome reference genome bias, and to verify that individuals belong to the correct genetic lineage before conclusions are drawn using mislabelled, or misidentified samples. We present the k-mer Weighted Inner Product (kWIP), an assembly-, and alignment-free estimator of genetic similarity. kWIP combines a probabilistic data structure with a novel metric, the weighted inner product (WIP), to efficiently calculate pairwise similarity between sequencing runs from their k-mer counts. It produces a distance matrix, which can then be further analysed and visualised. Our method does not require prior knowledge of the underlying genomes and applications include establishing sample identity and detecting mix-up, non-obvious genomic variation, and population structure. We show that kWIP can reconstruct the true relatedness between samples from simulated populations. By re-analysing several published datasets we show that our results are consistent with marker-based analyses. kWIP is written in C++, licensed under the GNU GPL, and is available from https://github.com/kdmurray91/kwip. |
format | Online Article Text |
id | pubmed-5600398 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-56003982017-09-22 kWIP: The k-mer weighted inner product, a de novo estimator of genetic similarity Murray, Kevin D. Webers, Christfried Ong, Cheng Soon Borevitz, Justin Warthmann, Norman PLoS Comput Biol Research Article Modern genomics techniques generate overwhelming quantities of data. Extracting population genetic variation demands computationally efficient methods to determine genetic relatedness between individuals (or “samples”) in an unbiased manner, preferably de novo. Rapid estimation of genetic relatedness directly from sequencing data has the potential to overcome reference genome bias, and to verify that individuals belong to the correct genetic lineage before conclusions are drawn using mislabelled, or misidentified samples. We present the k-mer Weighted Inner Product (kWIP), an assembly-, and alignment-free estimator of genetic similarity. kWIP combines a probabilistic data structure with a novel metric, the weighted inner product (WIP), to efficiently calculate pairwise similarity between sequencing runs from their k-mer counts. It produces a distance matrix, which can then be further analysed and visualised. Our method does not require prior knowledge of the underlying genomes and applications include establishing sample identity and detecting mix-up, non-obvious genomic variation, and population structure. We show that kWIP can reconstruct the true relatedness between samples from simulated populations. By re-analysing several published datasets we show that our results are consistent with marker-based analyses. kWIP is written in C++, licensed under the GNU GPL, and is available from https://github.com/kdmurray91/kwip. Public Library of Science 2017-09-05 /pmc/articles/PMC5600398/ /pubmed/28873405 http://dx.doi.org/10.1371/journal.pcbi.1005727 Text en © 2017 Murray et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Murray, Kevin D. Webers, Christfried Ong, Cheng Soon Borevitz, Justin Warthmann, Norman kWIP: The k-mer weighted inner product, a de novo estimator of genetic similarity |
title | kWIP: The k-mer weighted inner product, a de novo estimator of genetic similarity |
title_full | kWIP: The k-mer weighted inner product, a de novo estimator of genetic similarity |
title_fullStr | kWIP: The k-mer weighted inner product, a de novo estimator of genetic similarity |
title_full_unstemmed | kWIP: The k-mer weighted inner product, a de novo estimator of genetic similarity |
title_short | kWIP: The k-mer weighted inner product, a de novo estimator of genetic similarity |
title_sort | kwip: the k-mer weighted inner product, a de novo estimator of genetic similarity |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5600398/ https://www.ncbi.nlm.nih.gov/pubmed/28873405 http://dx.doi.org/10.1371/journal.pcbi.1005727 |
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