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Flexible and scalable genotyping-by-sequencing strategies for population studies

BACKGROUND: Many areas critical to agricultural production and research, such as the breeding and trait mapping in plants and livestock, require robust and scalable genotyping platforms. Genotyping-by-sequencing (GBS) is a one such method highly suited to non-human organisms. In the GBS protocol, ge...

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Autores principales: Heffelfinger, Christopher, Fragoso, Christopher A, Moreno, Maria A, Overton, John D, Mottinger, John P, Zhao, Hongyu, Tohme, Joe, Dellaporta, Stephen L
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4253001/
https://www.ncbi.nlm.nih.gov/pubmed/25406744
http://dx.doi.org/10.1186/1471-2164-15-979
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author Heffelfinger, Christopher
Fragoso, Christopher A
Moreno, Maria A
Overton, John D
Mottinger, John P
Zhao, Hongyu
Tohme, Joe
Dellaporta, Stephen L
author_facet Heffelfinger, Christopher
Fragoso, Christopher A
Moreno, Maria A
Overton, John D
Mottinger, John P
Zhao, Hongyu
Tohme, Joe
Dellaporta, Stephen L
author_sort Heffelfinger, Christopher
collection PubMed
description BACKGROUND: Many areas critical to agricultural production and research, such as the breeding and trait mapping in plants and livestock, require robust and scalable genotyping platforms. Genotyping-by-sequencing (GBS) is a one such method highly suited to non-human organisms. In the GBS protocol, genomic DNA is fractionated via restriction digest, then reduced representation is achieved through size selection. Since many restriction sites are conserved across a species, the sequenced portion of the genome is highly consistent within a population. This makes the GBS protocol highly suited for experiments that require surveying large numbers of markers within a population, such as those involving genetic mapping, breeding, and population genomics. We have modified the GBS technology in a number of ways. Custom, enzyme specific adaptors have been replaced with standard Illumina adaptors compatible with blunt-end restriction enzymes. Multiplexing is achieved through a dual barcoding system, and bead-based library preparation protocols allows for in-solution size selection and eliminates the need for columns and gels. RESULTS: A panel of eight restriction enzymes was selected for testing on B73 maize and Nipponbare rice genomic DNA. Quality of the data was demonstrated by identifying that the vast majority of reads from each enzyme aligned to restriction sites predicted in silico. The link between enzyme parameters and experimental outcome was demonstrated by showing that the sequenced portion of the genome was adaptable by selecting enzymes based on motif length, complexity, and methylation sensitivity. The utility of the new GBS protocol was demonstrated by correctly mapping several in a maize F(2) population resulting from a B73 × Country Gentleman test cross. CONCLUSIONS: This technology is readily adaptable to different genomes, highly amenable to multiplexing and compatible with over forty commercially available restriction enzymes. These advancements represent a major improvement in genotyping technology by providing a highly flexible and scalable GBS that is readily implemented for studies on genome-wide variation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1471-2164-15-979) contains supplementary material, which is available to authorized users.
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spelling pubmed-42530012014-12-04 Flexible and scalable genotyping-by-sequencing strategies for population studies Heffelfinger, Christopher Fragoso, Christopher A Moreno, Maria A Overton, John D Mottinger, John P Zhao, Hongyu Tohme, Joe Dellaporta, Stephen L BMC Genomics Methodology Article BACKGROUND: Many areas critical to agricultural production and research, such as the breeding and trait mapping in plants and livestock, require robust and scalable genotyping platforms. Genotyping-by-sequencing (GBS) is a one such method highly suited to non-human organisms. In the GBS protocol, genomic DNA is fractionated via restriction digest, then reduced representation is achieved through size selection. Since many restriction sites are conserved across a species, the sequenced portion of the genome is highly consistent within a population. This makes the GBS protocol highly suited for experiments that require surveying large numbers of markers within a population, such as those involving genetic mapping, breeding, and population genomics. We have modified the GBS technology in a number of ways. Custom, enzyme specific adaptors have been replaced with standard Illumina adaptors compatible with blunt-end restriction enzymes. Multiplexing is achieved through a dual barcoding system, and bead-based library preparation protocols allows for in-solution size selection and eliminates the need for columns and gels. RESULTS: A panel of eight restriction enzymes was selected for testing on B73 maize and Nipponbare rice genomic DNA. Quality of the data was demonstrated by identifying that the vast majority of reads from each enzyme aligned to restriction sites predicted in silico. The link between enzyme parameters and experimental outcome was demonstrated by showing that the sequenced portion of the genome was adaptable by selecting enzymes based on motif length, complexity, and methylation sensitivity. The utility of the new GBS protocol was demonstrated by correctly mapping several in a maize F(2) population resulting from a B73 × Country Gentleman test cross. CONCLUSIONS: This technology is readily adaptable to different genomes, highly amenable to multiplexing and compatible with over forty commercially available restriction enzymes. These advancements represent a major improvement in genotyping technology by providing a highly flexible and scalable GBS that is readily implemented for studies on genome-wide variation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1471-2164-15-979) contains supplementary material, which is available to authorized users. BioMed Central 2014-11-18 /pmc/articles/PMC4253001/ /pubmed/25406744 http://dx.doi.org/10.1186/1471-2164-15-979 Text en © Heffelfinger et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. 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
Heffelfinger, Christopher
Fragoso, Christopher A
Moreno, Maria A
Overton, John D
Mottinger, John P
Zhao, Hongyu
Tohme, Joe
Dellaporta, Stephen L
Flexible and scalable genotyping-by-sequencing strategies for population studies
title Flexible and scalable genotyping-by-sequencing strategies for population studies
title_full Flexible and scalable genotyping-by-sequencing strategies for population studies
title_fullStr Flexible and scalable genotyping-by-sequencing strategies for population studies
title_full_unstemmed Flexible and scalable genotyping-by-sequencing strategies for population studies
title_short Flexible and scalable genotyping-by-sequencing strategies for population studies
title_sort flexible and scalable genotyping-by-sequencing strategies for population studies
topic Methodology Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4253001/
https://www.ncbi.nlm.nih.gov/pubmed/25406744
http://dx.doi.org/10.1186/1471-2164-15-979
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