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Spiked GBS: a unified, open platform for single marker genotyping and whole-genome profiling

BACKGROUND: In plant breeding, there are two primary applications for DNA markers in selection: 1) selection of known genes using a single marker assay (marker-assisted selection; MAS); and 2) whole-genome profiling and prediction (genomic selection; GS). Typically, marker platforms have addressed o...

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Autores principales: Rife, Trevor W, Wu, Shuangye, Bowden, Robert L, Poland, Jesse A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4404221/
https://www.ncbi.nlm.nih.gov/pubmed/25880848
http://dx.doi.org/10.1186/s12864-015-1404-9
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author Rife, Trevor W
Wu, Shuangye
Bowden, Robert L
Poland, Jesse A
author_facet Rife, Trevor W
Wu, Shuangye
Bowden, Robert L
Poland, Jesse A
author_sort Rife, Trevor W
collection PubMed
description BACKGROUND: In plant breeding, there are two primary applications for DNA markers in selection: 1) selection of known genes using a single marker assay (marker-assisted selection; MAS); and 2) whole-genome profiling and prediction (genomic selection; GS). Typically, marker platforms have addressed only one of these objectives. RESULTS: We have developed spiked genotyping-by-sequencing (sGBS), which combines targeted amplicon sequencing with reduced representation genotyping-by-sequencing. To minimize the cost of targeted assays, we utilize a small percent of sequencing capacity available in runs of GBS libraries to “spike” amplified targets of a priori alleles tagged with a different set of unique barcodes. This open platform allows multiple, single-target loci to be assayed while simultaneously generating a whole-genome profile. This dual-genotyping approach allows different sets of samples to be evaluated for single markers or whole genome-profiling. Here, we report the application of sGBS on a winter wheat panel that was screened for converted KASP markers and newly-designed markers targeting known polymorphisms in the leaf rust resistance gene Lr34. CONCLUSIONS: The flexibility and low-cost of sGBS will enable a range of applications across genetics research. Specifically in breeding applications, the sGBS approach will allow breeders to obtain a whole-genome profile of important individuals while simultaneously targeting specific genes for a range of selection strategies across the breeding program. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-015-1404-9) contains supplementary material, which is available to authorized users.
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spelling pubmed-44042212015-04-21 Spiked GBS: a unified, open platform for single marker genotyping and whole-genome profiling Rife, Trevor W Wu, Shuangye Bowden, Robert L Poland, Jesse A BMC Genomics Methodology Article BACKGROUND: In plant breeding, there are two primary applications for DNA markers in selection: 1) selection of known genes using a single marker assay (marker-assisted selection; MAS); and 2) whole-genome profiling and prediction (genomic selection; GS). Typically, marker platforms have addressed only one of these objectives. RESULTS: We have developed spiked genotyping-by-sequencing (sGBS), which combines targeted amplicon sequencing with reduced representation genotyping-by-sequencing. To minimize the cost of targeted assays, we utilize a small percent of sequencing capacity available in runs of GBS libraries to “spike” amplified targets of a priori alleles tagged with a different set of unique barcodes. This open platform allows multiple, single-target loci to be assayed while simultaneously generating a whole-genome profile. This dual-genotyping approach allows different sets of samples to be evaluated for single markers or whole genome-profiling. Here, we report the application of sGBS on a winter wheat panel that was screened for converted KASP markers and newly-designed markers targeting known polymorphisms in the leaf rust resistance gene Lr34. CONCLUSIONS: The flexibility and low-cost of sGBS will enable a range of applications across genetics research. Specifically in breeding applications, the sGBS approach will allow breeders to obtain a whole-genome profile of important individuals while simultaneously targeting specific genes for a range of selection strategies across the breeding program. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-015-1404-9) contains supplementary material, which is available to authorized users. BioMed Central 2015-03-28 /pmc/articles/PMC4404221/ /pubmed/25880848 http://dx.doi.org/10.1186/s12864-015-1404-9 Text en © Rife et al.; licensee BioMed Central. 2015 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 work is properly credited. 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.
spellingShingle Methodology Article
Rife, Trevor W
Wu, Shuangye
Bowden, Robert L
Poland, Jesse A
Spiked GBS: a unified, open platform for single marker genotyping and whole-genome profiling
title Spiked GBS: a unified, open platform for single marker genotyping and whole-genome profiling
title_full Spiked GBS: a unified, open platform for single marker genotyping and whole-genome profiling
title_fullStr Spiked GBS: a unified, open platform for single marker genotyping and whole-genome profiling
title_full_unstemmed Spiked GBS: a unified, open platform for single marker genotyping and whole-genome profiling
title_short Spiked GBS: a unified, open platform for single marker genotyping and whole-genome profiling
title_sort spiked gbs: a unified, open platform for single marker genotyping and whole-genome profiling
topic Methodology Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4404221/
https://www.ncbi.nlm.nih.gov/pubmed/25880848
http://dx.doi.org/10.1186/s12864-015-1404-9
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