Evidence map›Paper›PMID 18282271›Full record

ArticleBMC genomics2008

Multiplex-ready PCR: a new method for multiplexed SSR and SNP genotyping.

Matthew J Hayden, Thao M Nguyen, Amanda Waterman, Kenneth J Chalmers

Abstract read
In one paragraph

Article in BMC genomics, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

47 citing papers in PubMed.

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  5. Optimization of Breeding Tools in Quinoa (Plants (Basel, Switzerland) · 2024
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  13. Identification of molecular markers for the Pc39 gene conferring resistance to crown rust in oat.TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik · 2020
    Article
  14. Article
  15. Article
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  19. Development of 17 novel microsatellite markers forApplications in plant sciences · 2018
    Article
  20. Development of novel EST-SSR markers forApplications in plant sciences · 2018
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Matthew J HaydenMolecular Plant Breeding CRC, PMB 1, Glen Osmond, SA, 5064, Australia. matthew.hayden@adelaide.edu.au
Thao M Nguyen
Amanda Waterman
Kenneth J Chalmers

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMicrosatellite (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.

resultsWe 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.

conclusionMultiplex-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.

Indexed as

DNAFluorescenceGenome, PlantGenotypeHordeumMicrosatellite RepeatsPolymerase Chain ReactionPolymorphism, Single NucleotidePrunusReproducibility of ResultsTriticumDNA

Identifiers

PMID18282271
PMCPMC2275739

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.