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Developing best practices for genotyping-by-sequencing analysis in the construction of linkage maps

BACKGROUND: Genotyping-by-sequencing (GBS) provides affordable methods for genotyping hundreds of individuals using millions of markers. However, this challenges bioinformatic procedures that must overcome possible artifacts such as the bias generated by polymerase chain reaction duplicates and sequ...

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Autores principales: Taniguti, Cristiane Hayumi, Taniguti, Lucas Mitsuo, Amadeu, Rodrigo Rampazo, Lau, Jeekin, Gesteira, Gabriel de Siqueira, Oliveira, Thiago de Paula, Ferreira, Getulio Caixeta, Pereira, Guilherme da Silva, Byrne, David, Mollinari, Marcelo, Riera-Lizarazu, Oscar, Garcia, Antonio Augusto Franco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10603770/
https://www.ncbi.nlm.nih.gov/pubmed/37889010
http://dx.doi.org/10.1093/gigascience/giad092
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author Taniguti, Cristiane Hayumi
Taniguti, Lucas Mitsuo
Amadeu, Rodrigo Rampazo
Lau, Jeekin
Gesteira, Gabriel de Siqueira
Oliveira, Thiago de Paula
Ferreira, Getulio Caixeta
Pereira, Guilherme da Silva
Byrne, David
Mollinari, Marcelo
Riera-Lizarazu, Oscar
Garcia, Antonio Augusto Franco
author_facet Taniguti, Cristiane Hayumi
Taniguti, Lucas Mitsuo
Amadeu, Rodrigo Rampazo
Lau, Jeekin
Gesteira, Gabriel de Siqueira
Oliveira, Thiago de Paula
Ferreira, Getulio Caixeta
Pereira, Guilherme da Silva
Byrne, David
Mollinari, Marcelo
Riera-Lizarazu, Oscar
Garcia, Antonio Augusto Franco
author_sort Taniguti, Cristiane Hayumi
collection PubMed
description BACKGROUND: Genotyping-by-sequencing (GBS) provides affordable methods for genotyping hundreds of individuals using millions of markers. However, this challenges bioinformatic procedures that must overcome possible artifacts such as the bias generated by polymerase chain reaction duplicates and sequencing errors. Genotyping errors lead to data that deviate from what is expected from regular meiosis. This, in turn, leads to difficulties in grouping and ordering markers, resulting in inflated and incorrect linkage maps. Therefore, genotyping errors can be easily detected by linkage map quality evaluations. RESULTS: We developed and used the Reads2Map workflow to build linkage maps with simulated and empirical GBS data of diploid outcrossing populations. The workflows run GATK, Stacks, TASSEL, and Freebayes for single-nucleotide polymorphism calling and updog, polyRAD, and SuperMASSA for genotype calling, as well as OneMap and GUSMap to build linkage maps. Using simulated data, we observed which genotype call software fails in identifying common errors in GBS sequencing data and proposed specific filters to better handle them. We tested whether it is possible to overcome errors in a linkage map using genotype probabilities from each software or global error rates to estimate genetic distances with an updated version of OneMap. We also evaluated the impact of segregation distortion, contaminant samples, and haplotype-based multiallelic markers in the final linkage maps. Through our evaluations, we observed that some of the approaches produce different results depending on the dataset (dataset dependent) and others produce consistent advantageous results among them (dataset independent). CONCLUSIONS: We set as default in the Reads2Map workflows the approaches that showed to be dataset independent for GBS datasets according to our results. This reduces the number of required tests to identify optimal pipelines and parameters for other empirical datasets. Using Reads2Map, users can select the pipeline and parameters that best fit their data context. The Reads2MapApp shiny app provides a graphical representation of the results to facilitate their interpretation.
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spelling pubmed-106037702023-10-28 Developing best practices for genotyping-by-sequencing analysis in the construction of linkage maps Taniguti, Cristiane Hayumi Taniguti, Lucas Mitsuo Amadeu, Rodrigo Rampazo Lau, Jeekin Gesteira, Gabriel de Siqueira Oliveira, Thiago de Paula Ferreira, Getulio Caixeta Pereira, Guilherme da Silva Byrne, David Mollinari, Marcelo Riera-Lizarazu, Oscar Garcia, Antonio Augusto Franco Gigascience Technical Note BACKGROUND: Genotyping-by-sequencing (GBS) provides affordable methods for genotyping hundreds of individuals using millions of markers. However, this challenges bioinformatic procedures that must overcome possible artifacts such as the bias generated by polymerase chain reaction duplicates and sequencing errors. Genotyping errors lead to data that deviate from what is expected from regular meiosis. This, in turn, leads to difficulties in grouping and ordering markers, resulting in inflated and incorrect linkage maps. Therefore, genotyping errors can be easily detected by linkage map quality evaluations. RESULTS: We developed and used the Reads2Map workflow to build linkage maps with simulated and empirical GBS data of diploid outcrossing populations. The workflows run GATK, Stacks, TASSEL, and Freebayes for single-nucleotide polymorphism calling and updog, polyRAD, and SuperMASSA for genotype calling, as well as OneMap and GUSMap to build linkage maps. Using simulated data, we observed which genotype call software fails in identifying common errors in GBS sequencing data and proposed specific filters to better handle them. We tested whether it is possible to overcome errors in a linkage map using genotype probabilities from each software or global error rates to estimate genetic distances with an updated version of OneMap. We also evaluated the impact of segregation distortion, contaminant samples, and haplotype-based multiallelic markers in the final linkage maps. Through our evaluations, we observed that some of the approaches produce different results depending on the dataset (dataset dependent) and others produce consistent advantageous results among them (dataset independent). CONCLUSIONS: We set as default in the Reads2Map workflows the approaches that showed to be dataset independent for GBS datasets according to our results. This reduces the number of required tests to identify optimal pipelines and parameters for other empirical datasets. Using Reads2Map, users can select the pipeline and parameters that best fit their data context. The Reads2MapApp shiny app provides a graphical representation of the results to facilitate their interpretation. Oxford University Press 2023-10-27 /pmc/articles/PMC10603770/ /pubmed/37889010 http://dx.doi.org/10.1093/gigascience/giad092 Text en © The Author(s) 2023. Published by Oxford University Press GigaScience. 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 reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Technical Note
Taniguti, Cristiane Hayumi
Taniguti, Lucas Mitsuo
Amadeu, Rodrigo Rampazo
Lau, Jeekin
Gesteira, Gabriel de Siqueira
Oliveira, Thiago de Paula
Ferreira, Getulio Caixeta
Pereira, Guilherme da Silva
Byrne, David
Mollinari, Marcelo
Riera-Lizarazu, Oscar
Garcia, Antonio Augusto Franco
Developing best practices for genotyping-by-sequencing analysis in the construction of linkage maps
title Developing best practices for genotyping-by-sequencing analysis in the construction of linkage maps
title_full Developing best practices for genotyping-by-sequencing analysis in the construction of linkage maps
title_fullStr Developing best practices for genotyping-by-sequencing analysis in the construction of linkage maps
title_full_unstemmed Developing best practices for genotyping-by-sequencing analysis in the construction of linkage maps
title_short Developing best practices for genotyping-by-sequencing analysis in the construction of linkage maps
title_sort developing best practices for genotyping-by-sequencing analysis in the construction of linkage maps
topic Technical Note
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10603770/
https://www.ncbi.nlm.nih.gov/pubmed/37889010
http://dx.doi.org/10.1093/gigascience/giad092
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