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AllCoPol: inferring allele co-ancestry in polyploids

BACKGROUND: Inferring phylogenetic relationships of polyploid species and their diploid ancestors (leading to reticulate phylogenies in the case of an allopolyploid origin) based on multi-locus sequence data is complicated by the unknown assignment of alleles found in polyploids to diploid subgenome...

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Autores principales: Lautenschlager, Ulrich, Wagner, Florian, Oberprieler, Christoph
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7542712/
https://www.ncbi.nlm.nih.gov/pubmed/33028201
http://dx.doi.org/10.1186/s12859-020-03750-9
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author Lautenschlager, Ulrich
Wagner, Florian
Oberprieler, Christoph
author_facet Lautenschlager, Ulrich
Wagner, Florian
Oberprieler, Christoph
author_sort Lautenschlager, Ulrich
collection PubMed
description BACKGROUND: Inferring phylogenetic relationships of polyploid species and their diploid ancestors (leading to reticulate phylogenies in the case of an allopolyploid origin) based on multi-locus sequence data is complicated by the unknown assignment of alleles found in polyploids to diploid subgenomes. A parsimony-based approach to this problem has been proposed by Oberprieler et al. (Methods Ecol Evol 8:835–849, 2017), however, its implementation is of limited practical value. In addition to previously identified shortcomings, it has been found that in some cases, the obtained results barely satisfy the applied criterion. To be of better use to other researchers, a reimplementation with methodological refinement appears to be indispensable. RESULTS: We present the AllCoPol package, which provides a heuristic method for assigning alleles from polyploids to diploid subgenomes based on the Minimizing Deep Coalescences (MDC) criterion in multi-locus sequence datasets. An additional consensus approach further allows to assess the confidence of phylogenetic reconstructions. Simulations of tetra- and hexaploids show that under simplifying assumptions such as completely disomic inheritance, the topological errors of reconstructed phylogenies are similar to those of MDC species trees based on the true allele partition. CONCLUSIONS: AllCoPol is a Python package for phylogenetic reconstructions of polyploids offering enhanced functionality as well as improved usability. The included methods are supplied as command line tools without the need for prior programming knowledge.
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spelling pubmed-75427122020-10-08 AllCoPol: inferring allele co-ancestry in polyploids Lautenschlager, Ulrich Wagner, Florian Oberprieler, Christoph BMC Bioinformatics Software BACKGROUND: Inferring phylogenetic relationships of polyploid species and their diploid ancestors (leading to reticulate phylogenies in the case of an allopolyploid origin) based on multi-locus sequence data is complicated by the unknown assignment of alleles found in polyploids to diploid subgenomes. A parsimony-based approach to this problem has been proposed by Oberprieler et al. (Methods Ecol Evol 8:835–849, 2017), however, its implementation is of limited practical value. In addition to previously identified shortcomings, it has been found that in some cases, the obtained results barely satisfy the applied criterion. To be of better use to other researchers, a reimplementation with methodological refinement appears to be indispensable. RESULTS: We present the AllCoPol package, which provides a heuristic method for assigning alleles from polyploids to diploid subgenomes based on the Minimizing Deep Coalescences (MDC) criterion in multi-locus sequence datasets. An additional consensus approach further allows to assess the confidence of phylogenetic reconstructions. Simulations of tetra- and hexaploids show that under simplifying assumptions such as completely disomic inheritance, the topological errors of reconstructed phylogenies are similar to those of MDC species trees based on the true allele partition. CONCLUSIONS: AllCoPol is a Python package for phylogenetic reconstructions of polyploids offering enhanced functionality as well as improved usability. The included methods are supplied as command line tools without the need for prior programming knowledge. BioMed Central 2020-10-07 /pmc/articles/PMC7542712/ /pubmed/33028201 http://dx.doi.org/10.1186/s12859-020-03750-9 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Software
Lautenschlager, Ulrich
Wagner, Florian
Oberprieler, Christoph
AllCoPol: inferring allele co-ancestry in polyploids
title AllCoPol: inferring allele co-ancestry in polyploids
title_full AllCoPol: inferring allele co-ancestry in polyploids
title_fullStr AllCoPol: inferring allele co-ancestry in polyploids
title_full_unstemmed AllCoPol: inferring allele co-ancestry in polyploids
title_short AllCoPol: inferring allele co-ancestry in polyploids
title_sort allcopol: inferring allele co-ancestry in polyploids
topic Software
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7542712/
https://www.ncbi.nlm.nih.gov/pubmed/33028201
http://dx.doi.org/10.1186/s12859-020-03750-9
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