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Screening of a Brassica napus bacterial artificial chromosome library using highly parallel single nucleotide polymorphism assays

BACKGROUND: Efficient screening of bacterial artificial chromosome (BAC) libraries with polymerase chain reaction (PCR)-based markers is feasible provided that a multidimensional pooling strategy is implemented. Single nucleotide polymorphisms (SNPs) can be screened in multiplexed format, therefore...

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Autores principales: Cao, Hieu Xuan, Schmidt, Renate
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3846124/
https://www.ncbi.nlm.nih.gov/pubmed/24010766
http://dx.doi.org/10.1186/1471-2164-14-603
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author Cao, Hieu Xuan
Schmidt, Renate
author_facet Cao, Hieu Xuan
Schmidt, Renate
author_sort Cao, Hieu Xuan
collection PubMed
description BACKGROUND: Efficient screening of bacterial artificial chromosome (BAC) libraries with polymerase chain reaction (PCR)-based markers is feasible provided that a multidimensional pooling strategy is implemented. Single nucleotide polymorphisms (SNPs) can be screened in multiplexed format, therefore this marker type lends itself particularly well for medium- to high-throughput applications. Combining the power of multiplex-PCR assays with a multidimensional pooling system may prove to be especially challenging in a polyploid genome. In polyploid genomes two classes of SNPs need to be distinguished, polymorphisms between accessions (intragenomic SNPs) and those differentiating between homoeologous genomes (intergenomic SNPs). We have assessed whether the highly parallel Illumina GoldenGate® Genotyping Assay is suitable for the screening of a BAC library of the polyploid Brassica napus genome. RESULTS: A multidimensional screening platform was developed for a Brassica napus BAC library which is composed of almost 83,000 clones. Intragenomic and intergenomic SNPs were included in Illumina’s GoldenGate® Genotyping Assay and both SNP classes were used successfully for screening of the multidimensional BAC pools of the Brassica napus library. An optimized scoring method is proposed which is especially valuable for SNP calling of intergenomic SNPs. Validation of the genotyping results by independent methods revealed a success of approximately 80% for the multiplex PCR-based screening regardless of whether intra- or intergenomic SNPs were evaluated. CONCLUSIONS: Illumina’s GoldenGate® Genotyping Assay can be efficiently used for screening of multidimensional Brassica napus BAC pools. SNP calling was specifically tailored for the evaluation of BAC pool screening data. The developed scoring method can be implemented independently of plant reference samples. It is demonstrated that intergenomic SNPs represent a powerful tool for BAC library screening of a polyploid genome.
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spelling pubmed-38461242013-12-03 Screening of a Brassica napus bacterial artificial chromosome library using highly parallel single nucleotide polymorphism assays Cao, Hieu Xuan Schmidt, Renate BMC Genomics Methodology Article BACKGROUND: Efficient screening of bacterial artificial chromosome (BAC) libraries with polymerase chain reaction (PCR)-based markers is feasible provided that a multidimensional pooling strategy is implemented. Single nucleotide polymorphisms (SNPs) can be screened in multiplexed format, therefore this marker type lends itself particularly well for medium- to high-throughput applications. Combining the power of multiplex-PCR assays with a multidimensional pooling system may prove to be especially challenging in a polyploid genome. In polyploid genomes two classes of SNPs need to be distinguished, polymorphisms between accessions (intragenomic SNPs) and those differentiating between homoeologous genomes (intergenomic SNPs). We have assessed whether the highly parallel Illumina GoldenGate® Genotyping Assay is suitable for the screening of a BAC library of the polyploid Brassica napus genome. RESULTS: A multidimensional screening platform was developed for a Brassica napus BAC library which is composed of almost 83,000 clones. Intragenomic and intergenomic SNPs were included in Illumina’s GoldenGate® Genotyping Assay and both SNP classes were used successfully for screening of the multidimensional BAC pools of the Brassica napus library. An optimized scoring method is proposed which is especially valuable for SNP calling of intergenomic SNPs. Validation of the genotyping results by independent methods revealed a success of approximately 80% for the multiplex PCR-based screening regardless of whether intra- or intergenomic SNPs were evaluated. CONCLUSIONS: Illumina’s GoldenGate® Genotyping Assay can be efficiently used for screening of multidimensional Brassica napus BAC pools. SNP calling was specifically tailored for the evaluation of BAC pool screening data. The developed scoring method can be implemented independently of plant reference samples. It is demonstrated that intergenomic SNPs represent a powerful tool for BAC library screening of a polyploid genome. BioMed Central 2013-09-06 /pmc/articles/PMC3846124/ /pubmed/24010766 http://dx.doi.org/10.1186/1471-2164-14-603 Text en Copyright © 2013 Cao and Schmidt; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Methodology Article
Cao, Hieu Xuan
Schmidt, Renate
Screening of a Brassica napus bacterial artificial chromosome library using highly parallel single nucleotide polymorphism assays
title Screening of a Brassica napus bacterial artificial chromosome library using highly parallel single nucleotide polymorphism assays
title_full Screening of a Brassica napus bacterial artificial chromosome library using highly parallel single nucleotide polymorphism assays
title_fullStr Screening of a Brassica napus bacterial artificial chromosome library using highly parallel single nucleotide polymorphism assays
title_full_unstemmed Screening of a Brassica napus bacterial artificial chromosome library using highly parallel single nucleotide polymorphism assays
title_short Screening of a Brassica napus bacterial artificial chromosome library using highly parallel single nucleotide polymorphism assays
title_sort screening of a brassica napus bacterial artificial chromosome library using highly parallel single nucleotide polymorphism assays
topic Methodology Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3846124/
https://www.ncbi.nlm.nih.gov/pubmed/24010766
http://dx.doi.org/10.1186/1471-2164-14-603
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