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SNPSelect: A scalable and flexible targeted sequence-based genotyping solution

In plant breeding the use of molecular markers has resulted in tremendous improvement of the speed with which new crop varieties are introduced into the market. Single Nucleotide Polymorphism (SNP) genotyping is routinely used for association studies, Linkage Disequilibrium (LD) and Quantitative Tra...

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Autores principales: Hogers, René C. J., de Ruiter, Marjo, Huvenaars, Koen H. J., van der Poel, Hein, Janssen, Antoine, van Eijk, Michiel J. T., van Orsouw, Nathalie J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6185863/
https://www.ncbi.nlm.nih.gov/pubmed/30312324
http://dx.doi.org/10.1371/journal.pone.0205577
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author Hogers, René C. J.
de Ruiter, Marjo
Huvenaars, Koen H. J.
van der Poel, Hein
Janssen, Antoine
van Eijk, Michiel J. T.
van Orsouw, Nathalie J.
author_facet Hogers, René C. J.
de Ruiter, Marjo
Huvenaars, Koen H. J.
van der Poel, Hein
Janssen, Antoine
van Eijk, Michiel J. T.
van Orsouw, Nathalie J.
author_sort Hogers, René C. J.
collection PubMed
description In plant breeding the use of molecular markers has resulted in tremendous improvement of the speed with which new crop varieties are introduced into the market. Single Nucleotide Polymorphism (SNP) genotyping is routinely used for association studies, Linkage Disequilibrium (LD) and Quantitative Trait Locus (QTL) mapping studies, marker-assisted backcrosses and validation of large numbers of novel SNPs. Here we present the KeyGene SNPSelect technology, a scalable and flexible multiplexed, targeted sequence-based, genotyping solution. The multiplex composition of SNPSelect assays can be easily changed between experiments by adding or removing loci, demonstrating their content flexibility. To demonstrate this versatility, we first designed a 1,056-plex maize assay and genotyped a total of 374 samples originating from an F2 and a Recombinant Inbred Line (RIL) population and a maize germplasm collection. Next, subsets of the most informative SNP loci were assembled in 384-plex and 768-plex assays for further genotyping. Indeed, selection of the most informative SNPs allows cost-efficient yet highly informative genotyping in a custom-made fashion, with average call rates between 88.1% (1,056-plex assay) and 99.4% (384-plex assay), and average reproducibility rates between duplicate samples ranging from 98.2% (1056-plex assay) to 99.9% (384-plex assay). The SNPSelect workflow can be completed from a DNA sample to a genotype dataset in less than three days. We propose SNPSelect as an attractive and competitive genotyping solution to meet the targeted genotyping needs in fields such as plant breeding.
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spelling pubmed-61858632018-10-26 SNPSelect: A scalable and flexible targeted sequence-based genotyping solution Hogers, René C. J. de Ruiter, Marjo Huvenaars, Koen H. J. van der Poel, Hein Janssen, Antoine van Eijk, Michiel J. T. van Orsouw, Nathalie J. PLoS One Research Article In plant breeding the use of molecular markers has resulted in tremendous improvement of the speed with which new crop varieties are introduced into the market. Single Nucleotide Polymorphism (SNP) genotyping is routinely used for association studies, Linkage Disequilibrium (LD) and Quantitative Trait Locus (QTL) mapping studies, marker-assisted backcrosses and validation of large numbers of novel SNPs. Here we present the KeyGene SNPSelect technology, a scalable and flexible multiplexed, targeted sequence-based, genotyping solution. The multiplex composition of SNPSelect assays can be easily changed between experiments by adding or removing loci, demonstrating their content flexibility. To demonstrate this versatility, we first designed a 1,056-plex maize assay and genotyped a total of 374 samples originating from an F2 and a Recombinant Inbred Line (RIL) population and a maize germplasm collection. Next, subsets of the most informative SNP loci were assembled in 384-plex and 768-plex assays for further genotyping. Indeed, selection of the most informative SNPs allows cost-efficient yet highly informative genotyping in a custom-made fashion, with average call rates between 88.1% (1,056-plex assay) and 99.4% (384-plex assay), and average reproducibility rates between duplicate samples ranging from 98.2% (1056-plex assay) to 99.9% (384-plex assay). The SNPSelect workflow can be completed from a DNA sample to a genotype dataset in less than three days. We propose SNPSelect as an attractive and competitive genotyping solution to meet the targeted genotyping needs in fields such as plant breeding. Public Library of Science 2018-10-12 /pmc/articles/PMC6185863/ /pubmed/30312324 http://dx.doi.org/10.1371/journal.pone.0205577 Text en © 2018 Hogers et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Hogers, René C. J.
de Ruiter, Marjo
Huvenaars, Koen H. J.
van der Poel, Hein
Janssen, Antoine
van Eijk, Michiel J. T.
van Orsouw, Nathalie J.
SNPSelect: A scalable and flexible targeted sequence-based genotyping solution
title SNPSelect: A scalable and flexible targeted sequence-based genotyping solution
title_full SNPSelect: A scalable and flexible targeted sequence-based genotyping solution
title_fullStr SNPSelect: A scalable and flexible targeted sequence-based genotyping solution
title_full_unstemmed SNPSelect: A scalable and flexible targeted sequence-based genotyping solution
title_short SNPSelect: A scalable and flexible targeted sequence-based genotyping solution
title_sort snpselect: a scalable and flexible targeted sequence-based genotyping solution
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6185863/
https://www.ncbi.nlm.nih.gov/pubmed/30312324
http://dx.doi.org/10.1371/journal.pone.0205577
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