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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),...

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Autores principales: Krishnan, Sidaswar, DeMaere, Matthew Z., Beck, Dominik, Ostrowski, Martin, Seymour, Justin R., Darling, Aaron E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2023
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.
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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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