Evidence map›Paper›PMID 22957003›Full record

ArticlePloS one2012

High resolution melting analysis is a more sensitive and effective alternative to gel-based platforms in analysis of SSR--an example in citrus.

Gaetano Distefano, Marco Caruso, Stefano La Malfa, Alessandra Gentile, Shu-Biao Wu

Abstract read
In one paragraph

Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

24 citing papers in PubMed.

  1. Article
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  10. Cas9-Mediated Targeted Mutagenesis in Plants.Methods in molecular biology (Clifton, N.J.) · 2022
    Article
  11. Microsatellite Markers in Olives (Foods (Basel, Switzerland) · 2021
    Review
  12. Article
  13. Article
  14. Article
  15. Rapid detection and genotyping of ALK fusion variants by adapter multiplex PCR and high-resolution melting analysis.Laboratory investigation; a journal of technical methods and pathology · 2020
    Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. 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

5 authors.

Gaetano DistefanoDipartimento di Scienze delle Produzioni Agrarie e Alimentari, University of Catania, Catania, Italy.
Marco Caruso
Stefano La Malfa
Alessandra Gentile
Shu-Biao Wu

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

High resolution melting curve analysis (HRM) has been used as an efficient, accurate and cost-effective tool to detect single nucleotide polymorphisms (SNPs) or insertions or deletions (INDELs). However, its efficiency, accuracy and applicability to discriminate microsatellite polymorphism have not been extensively assessed. The traditional protocols used for SSR genotyping include PCR amplification of the DNA fragment and the separation of the fragments on electrophoresis-based platform. However, post-PCR handling processes are laborious and costly. Furthermore, SNPs present in the sequences flanking repeat motif cannot be detected by polyacrylamide-gel-electrophoresis based methods. In the present study, we compared the discriminating power of HRM with the traditional electrophoresis-based methods and provided a panel of primers for HRM genotyping in Citrus. The results showed that sixteen SSR markers produced distinct polymorphic melting curves among the Citrus spp investigated through HRM analysis. Among those, 10 showed more genotypes by HRM analysis than capillary electrophoresis owing to the presence of SNPs in the amplicons. For the SSR markers without SNPs present in the flanking region, HRM also gave distinct melting curves which detected same genotypes as were shown in capillary electrophoresis (CE) analysis. Moreover, HRM analysis allowed the discrimination of most of the 15 citrus genotypes and the resulting genetic distance analysis clustered them into three main branches. In conclusion, it has been approved that HRM is not only an efficient and cost-effective alternative of electrophoresis-based method for SSR markers, but also a method to uncover more polymorphisms contributed by SNPs present in SSRs. It was therefore suggested that the panel of SSR markers could be used in a variety of applications in the citrus biodiversity and breeding programs using HRM analysis. Furthermore, we speculate that the HRM analysis can be employed to analyse SSR markers in a wide range of applications in all other species.

Indexed as

Genotyping TechniquesMicrosatellite RepeatsTransition TemperatureAllelesBase SequenceCitrusGenes, PlantGenotypeMolecular Sequence DataMolecular TypingPhylogenyPolymorphism, GeneticSequence Analysis, DNA

Identifiers

PMID22957003
PMCPMC3431301

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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.