Please use this identifier to cite or link to this item:
https://hdl.handle.net/2440/52492
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dc.contributor.author | Hayden, M. | - |
dc.contributor.author | Nguyen, T. | - |
dc.contributor.author | Waterman, A. | - |
dc.contributor.author | Chalmers, K. | - |
dc.date.issued | 2008 | - |
dc.identifier.citation | BMC Genomics, 2008; 9(1):WWW 1-WWW 12 | - |
dc.identifier.issn | 1471-2164 | - |
dc.identifier.issn | 1471-2164 | - |
dc.identifier.uri | http://hdl.handle.net/2440/52492 | - |
dc.description | © 2008 Hayden et al; licensee BioMed Central Ltd. 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. | - |
dc.description.abstract | Background Microsatellite (SSR) and single nucleotide polymorphism (SNP) markers are widely used in plant breeding and genomic research. Thus, methods to improve the speed and efficiency of SSR and SNP genotyping are highly desirable. Here we describe a new method for multiplex PCR that facilitates fluorescence-based SSR genotyping and the multiplexed preparation of DNA templates for SNP assays. Results We show that multiplex-ready PCR can achieve a high (92%) success rate for the amplification of published sequences under standardised reaction conditions, with a PCR specificity comparable to that of conventional PCR methods. We also demonstrate that multiplex-ready PCR supports an improved level of multiplexing in plant genomes of varying size and ploidy, without the need to carefully optimize assay conditions. Several advantages of multiplex-ready PCR for SSR and SNP genotyping are demonstrated and discussed. These include the uniform amplification of target sequences within multiplexed reactions and between independent assays, and the ability to label amplicons during PCR with specialised moieties such fluorescent dyes and biotin. Conclusion Multiplex-ready PCR provides several technological advantages that can facilitate fluorescence-based SSR genotyping and the multiplexed preparation of DNA templates for SNP assays. These advantages can be captured at several points in the genotyping process, and offer considerable cost and labour savings. Multiplex-ready PCR is broadly applicable to plant genomics and marker assisted breeding, and should be transferable to any animal or plant species. | - |
dc.description.statementofresponsibility | Matthew J Hayden, Thao M Nguyen, Amanda Waterman and Kenneth J Chalmers | - |
dc.language.iso | en | - |
dc.publisher | BioMed Central Ltd. | - |
dc.rights | © 2008 Hayden et al; licensee BioMed Central Ltd. 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. | - |
dc.source.uri | http://dx.doi.org/10.1186/1471-2164-9-80 | - |
dc.subject | Hordeum | - |
dc.subject | Triticum | - |
dc.subject | Prunus | - |
dc.subject | DNA | - |
dc.subject | Reproducibility of Results | - |
dc.subject | Polymerase Chain Reaction | - |
dc.subject | Microsatellite Repeats | - |
dc.subject | Genotype | - |
dc.subject | Polymorphism, Single Nucleotide | - |
dc.subject | Genome, Plant | - |
dc.subject | Fluorescence | - |
dc.title | Multiplex-ready PCR: A new method for multiplexed SSR and SNP genotyping | - |
dc.type | Journal article | - |
dc.identifier.doi | 10.1186/1471-2164-9-80 | - |
pubs.publication-status | Published | - |
dc.identifier.orcid | Nguyen, T. [0000-0001-9066-6962] | - |
dc.identifier.orcid | Chalmers, K. [0000-0002-9687-8680] | - |
Appears in Collections: | Agriculture, Food and Wine publications Aurora harvest 5 |
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hdl_52492.pdf | Published version | 683.68 kB | Adobe PDF | View/Open |
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