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Bait‐ER: A Bayesian method to detect targets of selection in Evolve‐and‐Resequence experiments

For over a decade, experimental evolution has been combined with high‐throughput sequencing techniques. In so‐called Evolve‐and‐Resequence (E&R) experiments, populations are kept in the laboratory under controlled experimental conditions where their genomes are sampled and allele frequencies mon...

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Autores principales: Barata, Carolina, Borges, Rui, Kosiol, Carolin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10108205/
https://www.ncbi.nlm.nih.gov/pubmed/36544394
http://dx.doi.org/10.1111/jeb.14134
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author Barata, Carolina
Borges, Rui
Kosiol, Carolin
author_facet Barata, Carolina
Borges, Rui
Kosiol, Carolin
author_sort Barata, Carolina
collection PubMed
description For over a decade, experimental evolution has been combined with high‐throughput sequencing techniques. In so‐called Evolve‐and‐Resequence (E&R) experiments, populations are kept in the laboratory under controlled experimental conditions where their genomes are sampled and allele frequencies monitored. However, identifying signatures of adaptation in E&R datasets is far from trivial, and it is still necessary to develop more efficient and statistically sound methods for detecting selection in genome‐wide data. Here, we present Bait‐ER – a fully Bayesian approach based on the Moran model of allele evolution to estimate selection coefficients from E&R experiments. The model has overlapping generations, a feature that describes several experimental designs found in the literature. We tested our method under several different demographic and experimental conditions to assess its accuracy and precision, and it performs well in most scenarios. Nevertheless, some care must be taken when analysing trajectories where drift largely dominates and starting frequencies are low. We compare our method with other available software and report that ours has generally high accuracy even for trajectories whose complexity goes beyond a classical sweep model. Furthermore, our approach avoids the computational burden of simulating an empirical null distribution, outperforming available software in terms of computational time and facilitating its use on genome‐wide data. We implemented and released our method in a new open‐source software package that can be accessed at https://doi.org/10.5281/zenodo.7351736.
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spelling pubmed-101082052023-04-18 Bait‐ER: A Bayesian method to detect targets of selection in Evolve‐and‐Resequence experiments Barata, Carolina Borges, Rui Kosiol, Carolin J Evol Biol Methods Article For over a decade, experimental evolution has been combined with high‐throughput sequencing techniques. In so‐called Evolve‐and‐Resequence (E&R) experiments, populations are kept in the laboratory under controlled experimental conditions where their genomes are sampled and allele frequencies monitored. However, identifying signatures of adaptation in E&R datasets is far from trivial, and it is still necessary to develop more efficient and statistically sound methods for detecting selection in genome‐wide data. Here, we present Bait‐ER – a fully Bayesian approach based on the Moran model of allele evolution to estimate selection coefficients from E&R experiments. The model has overlapping generations, a feature that describes several experimental designs found in the literature. We tested our method under several different demographic and experimental conditions to assess its accuracy and precision, and it performs well in most scenarios. Nevertheless, some care must be taken when analysing trajectories where drift largely dominates and starting frequencies are low. We compare our method with other available software and report that ours has generally high accuracy even for trajectories whose complexity goes beyond a classical sweep model. Furthermore, our approach avoids the computational burden of simulating an empirical null distribution, outperforming available software in terms of computational time and facilitating its use on genome‐wide data. We implemented and released our method in a new open‐source software package that can be accessed at https://doi.org/10.5281/zenodo.7351736. John Wiley and Sons Inc. 2022-12-21 2023-01 /pmc/articles/PMC10108205/ /pubmed/36544394 http://dx.doi.org/10.1111/jeb.14134 Text en © 2022 The Authors. Journal of Evolutionary Biology published by John Wiley & Sons Ltd on behalf of European Society for Evolutionary Biology. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Methods Article
Barata, Carolina
Borges, Rui
Kosiol, Carolin
Bait‐ER: A Bayesian method to detect targets of selection in Evolve‐and‐Resequence experiments
title Bait‐ER: A Bayesian method to detect targets of selection in Evolve‐and‐Resequence experiments
title_full Bait‐ER: A Bayesian method to detect targets of selection in Evolve‐and‐Resequence experiments
title_fullStr Bait‐ER: A Bayesian method to detect targets of selection in Evolve‐and‐Resequence experiments
title_full_unstemmed Bait‐ER: A Bayesian method to detect targets of selection in Evolve‐and‐Resequence experiments
title_short Bait‐ER: A Bayesian method to detect targets of selection in Evolve‐and‐Resequence experiments
title_sort bait‐er: a bayesian method to detect targets of selection in evolve‐and‐resequence experiments
topic Methods Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10108205/
https://www.ncbi.nlm.nih.gov/pubmed/36544394
http://dx.doi.org/10.1111/jeb.14134
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