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Benchmarking small-variant genotyping in polyploids

Genotyping from sequencing is the basis of emerging strategies in the molecular breeding of polyploid plants. However, compared with the situation for diploids, in which genotyping accuracies are confidently determined with comprehensive benchmarks, polyploids have been neglected; there are no bench...

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Detalles Bibliográficos
Autores principales: Cooke, Daniel P., Wedge, David C., Lunter, Gerton
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8805713/
https://www.ncbi.nlm.nih.gov/pubmed/34965940
http://dx.doi.org/10.1101/gr.275579.121
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author Cooke, Daniel P.
Wedge, David C.
Lunter, Gerton
author_facet Cooke, Daniel P.
Wedge, David C.
Lunter, Gerton
author_sort Cooke, Daniel P.
collection PubMed
description Genotyping from sequencing is the basis of emerging strategies in the molecular breeding of polyploid plants. However, compared with the situation for diploids, in which genotyping accuracies are confidently determined with comprehensive benchmarks, polyploids have been neglected; there are no benchmarks measuring genotyping error rates for small variants using real sequencing reads. We previously introduced a variant calling method, Octopus, that accurately calls germline variants in diploids and somatic mutations in tumors. Here, we evaluate Octopus and other popular tools on whole-genome tetraploid and hexaploid data sets created using in silico mixtures of diploid Genome in a Bottle (GIAB) samples. We find that genotyping errors are abundant for typical sequencing depths but that Octopus makes 25% fewer errors than other methods on average. We supplement our benchmarks with concordance analysis in real autotriploid banana data sets.
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spelling pubmed-88057132022-02-07 Benchmarking small-variant genotyping in polyploids Cooke, Daniel P. Wedge, David C. Lunter, Gerton Genome Res Resource Genotyping from sequencing is the basis of emerging strategies in the molecular breeding of polyploid plants. However, compared with the situation for diploids, in which genotyping accuracies are confidently determined with comprehensive benchmarks, polyploids have been neglected; there are no benchmarks measuring genotyping error rates for small variants using real sequencing reads. We previously introduced a variant calling method, Octopus, that accurately calls germline variants in diploids and somatic mutations in tumors. Here, we evaluate Octopus and other popular tools on whole-genome tetraploid and hexaploid data sets created using in silico mixtures of diploid Genome in a Bottle (GIAB) samples. We find that genotyping errors are abundant for typical sequencing depths but that Octopus makes 25% fewer errors than other methods on average. We supplement our benchmarks with concordance analysis in real autotriploid banana data sets. Cold Spring Harbor Laboratory Press 2022-02 /pmc/articles/PMC8805713/ /pubmed/34965940 http://dx.doi.org/10.1101/gr.275579.121 Text en © 2022 Cooke et al.; Published by Cold Spring Harbor Laboratory Press https://creativecommons.org/licenses/by/4.0/This article, published in Genome Research, is available under a Creative Commons License (Attribution 4.0 International), as described at http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Resource
Cooke, Daniel P.
Wedge, David C.
Lunter, Gerton
Benchmarking small-variant genotyping in polyploids
title Benchmarking small-variant genotyping in polyploids
title_full Benchmarking small-variant genotyping in polyploids
title_fullStr Benchmarking small-variant genotyping in polyploids
title_full_unstemmed Benchmarking small-variant genotyping in polyploids
title_short Benchmarking small-variant genotyping in polyploids
title_sort benchmarking small-variant genotyping in polyploids
topic Resource
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8805713/
https://www.ncbi.nlm.nih.gov/pubmed/34965940
http://dx.doi.org/10.1101/gr.275579.121
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