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Digital polymerase chain reaction for characterisation of DNA reference materials

Accurate, reliable and reproducible quantification of nucleic acids (DNA/RNA) is important for many diagnostic applications and in routine laboratory testing, for example, for pathogen detection and detection of genetically modified organisms in food. To ensure reliable nucleic acid measurement, ref...

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Detalles Bibliográficos
Autores principales: Bhat, Somanath, Emslie, Kerry R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5154631/
https://www.ncbi.nlm.nih.gov/pubmed/27990349
http://dx.doi.org/10.1016/j.bdq.2016.04.001
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author Bhat, Somanath
Emslie, Kerry R.
author_facet Bhat, Somanath
Emslie, Kerry R.
author_sort Bhat, Somanath
collection PubMed
description Accurate, reliable and reproducible quantification of nucleic acids (DNA/RNA) is important for many diagnostic applications and in routine laboratory testing, for example, for pathogen detection and detection of genetically modified organisms in food. To ensure reliable nucleic acid measurement, reference materials (RM) that are accurately characterised for quantity of target nucleic acid sequences (in copy number or copy number concentration) with a known measurement uncertainty are needed. Recently developed digital polymerase chain reaction (dPCR) technology allows absolute and accurate quantification of nucleic acid target sequences without need for a reference standard. Due to these properties, this technique has the potential to not only improve routine quantitative nucleic acid analysis, but also to be used as a reference method for certification of nucleic acid RM. The article focuses on the use and application of both dPCR and RMs for accurate quantification.
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spelling pubmed-51546312016-12-16 Digital polymerase chain reaction for characterisation of DNA reference materials Bhat, Somanath Emslie, Kerry R. Biomol Detect Quantif Review Article Accurate, reliable and reproducible quantification of nucleic acids (DNA/RNA) is important for many diagnostic applications and in routine laboratory testing, for example, for pathogen detection and detection of genetically modified organisms in food. To ensure reliable nucleic acid measurement, reference materials (RM) that are accurately characterised for quantity of target nucleic acid sequences (in copy number or copy number concentration) with a known measurement uncertainty are needed. Recently developed digital polymerase chain reaction (dPCR) technology allows absolute and accurate quantification of nucleic acid target sequences without need for a reference standard. Due to these properties, this technique has the potential to not only improve routine quantitative nucleic acid analysis, but also to be used as a reference method for certification of nucleic acid RM. The article focuses on the use and application of both dPCR and RMs for accurate quantification. Elsevier 2016-05-03 /pmc/articles/PMC5154631/ /pubmed/27990349 http://dx.doi.org/10.1016/j.bdq.2016.04.001 Text en © 2016 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Review Article
Bhat, Somanath
Emslie, Kerry R.
Digital polymerase chain reaction for characterisation of DNA reference materials
title Digital polymerase chain reaction for characterisation of DNA reference materials
title_full Digital polymerase chain reaction for characterisation of DNA reference materials
title_fullStr Digital polymerase chain reaction for characterisation of DNA reference materials
title_full_unstemmed Digital polymerase chain reaction for characterisation of DNA reference materials
title_short Digital polymerase chain reaction for characterisation of DNA reference materials
title_sort digital polymerase chain reaction for characterisation of dna reference materials
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5154631/
https://www.ncbi.nlm.nih.gov/pubmed/27990349
http://dx.doi.org/10.1016/j.bdq.2016.04.001
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