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Structure is more robust than other clustering methods in simulated mixed-ploidy populations

Analysis of population genetic structure has become a standard approach in population genetics. In polyploid complexes, clustering analyses can elucidate the origin of polyploid populations and patterns of admixture between different cytotypes. However, combining diploid and polyploid data can theor...

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Autores principales: Stift, Marc, Kolář, Filip, Meirmans, Patrick G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6781132/
https://www.ncbi.nlm.nih.gov/pubmed/31285566
http://dx.doi.org/10.1038/s41437-019-0247-6
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author Stift, Marc
Kolář, Filip
Meirmans, Patrick G.
author_facet Stift, Marc
Kolář, Filip
Meirmans, Patrick G.
author_sort Stift, Marc
collection PubMed
description Analysis of population genetic structure has become a standard approach in population genetics. In polyploid complexes, clustering analyses can elucidate the origin of polyploid populations and patterns of admixture between different cytotypes. However, combining diploid and polyploid data can theoretically lead to biased inference with (artefactual) clustering by ploidy. We used simulated mixed-ploidy (diploid-autotetraploid) data to systematically compare the performance of k-means clustering and the model-based clustering methods implemented in Structure, Admixture, FastStructure and InStruct under different scenarios of differentiation and with different marker types. Under scenarios of strong population differentiation, the tested applications performed equally well. However, when population differentiation was weak, Structure was the only method that allowed unbiased inference with markers with limited genotypic information (co-dominant markers with unknown dosage or dominant markers). Still, since Structure was comparatively slow, the much faster but less powerful FastStructure provides a reasonable alternative for large datasets. Finally, although bias makes k-means clustering unsuitable for markers with incomplete genotype information, for large numbers of loci (>1000) with known dosage k-means clustering was superior to FastStructure in terms of power and speed. We conclude that Structure is the most robust method for the analysis of genetic structure in mixed-ploidy populations, although alternative methods should be considered under some specific conditions.
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spelling pubmed-67811322019-10-09 Structure is more robust than other clustering methods in simulated mixed-ploidy populations Stift, Marc Kolář, Filip Meirmans, Patrick G. Heredity (Edinb) Article Analysis of population genetic structure has become a standard approach in population genetics. In polyploid complexes, clustering analyses can elucidate the origin of polyploid populations and patterns of admixture between different cytotypes. However, combining diploid and polyploid data can theoretically lead to biased inference with (artefactual) clustering by ploidy. We used simulated mixed-ploidy (diploid-autotetraploid) data to systematically compare the performance of k-means clustering and the model-based clustering methods implemented in Structure, Admixture, FastStructure and InStruct under different scenarios of differentiation and with different marker types. Under scenarios of strong population differentiation, the tested applications performed equally well. However, when population differentiation was weak, Structure was the only method that allowed unbiased inference with markers with limited genotypic information (co-dominant markers with unknown dosage or dominant markers). Still, since Structure was comparatively slow, the much faster but less powerful FastStructure provides a reasonable alternative for large datasets. Finally, although bias makes k-means clustering unsuitable for markers with incomplete genotype information, for large numbers of loci (>1000) with known dosage k-means clustering was superior to FastStructure in terms of power and speed. We conclude that Structure is the most robust method for the analysis of genetic structure in mixed-ploidy populations, although alternative methods should be considered under some specific conditions. Springer International Publishing 2019-07-08 2019-10 /pmc/articles/PMC6781132/ /pubmed/31285566 http://dx.doi.org/10.1038/s41437-019-0247-6 Text en © The Author(s) 2019 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Stift, Marc
Kolář, Filip
Meirmans, Patrick G.
Structure is more robust than other clustering methods in simulated mixed-ploidy populations
title Structure is more robust than other clustering methods in simulated mixed-ploidy populations
title_full Structure is more robust than other clustering methods in simulated mixed-ploidy populations
title_fullStr Structure is more robust than other clustering methods in simulated mixed-ploidy populations
title_full_unstemmed Structure is more robust than other clustering methods in simulated mixed-ploidy populations
title_short Structure is more robust than other clustering methods in simulated mixed-ploidy populations
title_sort structure is more robust than other clustering methods in simulated mixed-ploidy populations
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6781132/
https://www.ncbi.nlm.nih.gov/pubmed/31285566
http://dx.doi.org/10.1038/s41437-019-0247-6
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