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Rhometa: Population recombination rate estimation from metagenomic read datasets
Prokaryotic evolution is influenced by the exchange of genetic information between species through a process referred to as recombination. The rate of recombination is a useful measure for the adaptive capacity of a prokaryotic population. We introduce Rhometa (https://github.com/sid-krish/Rhometa),...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10079220/ https://www.ncbi.nlm.nih.gov/pubmed/36972309 http://dx.doi.org/10.1371/journal.pgen.1010683 |
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author | Krishnan, Sidaswar DeMaere, Matthew Z. Beck, Dominik Ostrowski, Martin Seymour, Justin R. Darling, Aaron E. |
author_facet | Krishnan, Sidaswar DeMaere, Matthew Z. Beck, Dominik Ostrowski, Martin Seymour, Justin R. Darling, Aaron E. |
author_sort | Krishnan, Sidaswar |
collection | PubMed |
description | Prokaryotic evolution is influenced by the exchange of genetic information between species through a process referred to as recombination. The rate of recombination is a useful measure for the adaptive capacity of a prokaryotic population. We introduce Rhometa (https://github.com/sid-krish/Rhometa), a new software package to determine recombination rates from shotgun sequencing reads of metagenomes. It extends the composite likelihood approach for population recombination rate estimation and enables the analysis of modern short-read datasets. We evaluated Rhometa over a broad range of sequencing depths and complexities, using simulated and real experimental short-read data aligned to external reference genomes. Rhometa offers a comprehensive solution for determining population recombination rates from contemporary metagenomic read datasets. Rhometa extends the capabilities of conventional sequence-based composite likelihood population recombination rate estimators to include modern aligned metagenomic read datasets with diverse sequencing depths, thereby enabling the effective application of these techniques and their high accuracy rates to the field of metagenomics. Using simulated datasets, we show that our method performs well, with its accuracy improving with increasing numbers of genomes. Rhometa was validated on a real S. pneumoniae transformation experiment, where we show that it obtains plausible estimates of the rate of recombination. Finally, the program was also run on ocean surface water metagenomic datasets, through which we demonstrate that the program works on uncultured metagenomic datasets. |
format | Online Article Text |
id | pubmed-10079220 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-100792202023-04-07 Rhometa: Population recombination rate estimation from metagenomic read datasets Krishnan, Sidaswar DeMaere, Matthew Z. Beck, Dominik Ostrowski, Martin Seymour, Justin R. Darling, Aaron E. PLoS Genet Methods Prokaryotic evolution is influenced by the exchange of genetic information between species through a process referred to as recombination. The rate of recombination is a useful measure for the adaptive capacity of a prokaryotic population. We introduce Rhometa (https://github.com/sid-krish/Rhometa), a new software package to determine recombination rates from shotgun sequencing reads of metagenomes. It extends the composite likelihood approach for population recombination rate estimation and enables the analysis of modern short-read datasets. We evaluated Rhometa over a broad range of sequencing depths and complexities, using simulated and real experimental short-read data aligned to external reference genomes. Rhometa offers a comprehensive solution for determining population recombination rates from contemporary metagenomic read datasets. Rhometa extends the capabilities of conventional sequence-based composite likelihood population recombination rate estimators to include modern aligned metagenomic read datasets with diverse sequencing depths, thereby enabling the effective application of these techniques and their high accuracy rates to the field of metagenomics. Using simulated datasets, we show that our method performs well, with its accuracy improving with increasing numbers of genomes. Rhometa was validated on a real S. pneumoniae transformation experiment, where we show that it obtains plausible estimates of the rate of recombination. Finally, the program was also run on ocean surface water metagenomic datasets, through which we demonstrate that the program works on uncultured metagenomic datasets. Public Library of Science 2023-03-27 /pmc/articles/PMC10079220/ /pubmed/36972309 http://dx.doi.org/10.1371/journal.pgen.1010683 Text en © 2023 Krishnan et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://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 | Methods Krishnan, Sidaswar DeMaere, Matthew Z. Beck, Dominik Ostrowski, Martin Seymour, Justin R. Darling, Aaron E. Rhometa: Population recombination rate estimation from metagenomic read datasets |
title | Rhometa: Population recombination rate estimation from metagenomic read datasets |
title_full | Rhometa: Population recombination rate estimation from metagenomic read datasets |
title_fullStr | Rhometa: Population recombination rate estimation from metagenomic read datasets |
title_full_unstemmed | Rhometa: Population recombination rate estimation from metagenomic read datasets |
title_short | Rhometa: Population recombination rate estimation from metagenomic read datasets |
title_sort | rhometa: population recombination rate estimation from metagenomic read datasets |
topic | Methods |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10079220/ https://www.ncbi.nlm.nih.gov/pubmed/36972309 http://dx.doi.org/10.1371/journal.pgen.1010683 |
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