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Making standards for quantitative real-time pneumococcal PCR
Quantitative lytA PCR is often performed using in-house standards. We hypothesised equivalence when measuring a standard suspension of Streptococcus pneumoniae by colony-forming-units (CFU) or genome-copies. Median (IQR) ratio of CFU/genome-copies was 0.19 (0.1–1.2). Genome-copies were less variable...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5121202/ https://www.ncbi.nlm.nih.gov/pubmed/27896138 http://dx.doi.org/10.1016/j.bdq.2014.11.003 |
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author | Morpeth, Susan C. Huggett, Jim F. Murdoch, David R. Scott, J. Anthony G. |
author_facet | Morpeth, Susan C. Huggett, Jim F. Murdoch, David R. Scott, J. Anthony G. |
author_sort | Morpeth, Susan C. |
collection | PubMed |
description | Quantitative lytA PCR is often performed using in-house standards. We hypothesised equivalence when measuring a standard suspension of Streptococcus pneumoniae by colony-forming-units (CFU) or genome-copies. Median (IQR) ratio of CFU/genome-copies was 0.19 (0.1–1.2). Genome-copies were less variable than CFU, but the discrepancy between the methods highlights challenges with absolute quantification. |
format | Online Article Text |
id | pubmed-5121202 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-51212022016-11-28 Making standards for quantitative real-time pneumococcal PCR Morpeth, Susan C. Huggett, Jim F. Murdoch, David R. Scott, J. Anthony G. Biomol Detect Quantif Short Communication Quantitative lytA PCR is often performed using in-house standards. We hypothesised equivalence when measuring a standard suspension of Streptococcus pneumoniae by colony-forming-units (CFU) or genome-copies. Median (IQR) ratio of CFU/genome-copies was 0.19 (0.1–1.2). Genome-copies were less variable than CFU, but the discrepancy between the methods highlights challenges with absolute quantification. Elsevier 2014-12-04 /pmc/articles/PMC5121202/ /pubmed/27896138 http://dx.doi.org/10.1016/j.bdq.2014.11.003 Text en © 2014 The Authors http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/3.0/). |
spellingShingle | Short Communication Morpeth, Susan C. Huggett, Jim F. Murdoch, David R. Scott, J. Anthony G. Making standards for quantitative real-time pneumococcal PCR |
title | Making standards for quantitative real-time pneumococcal PCR |
title_full | Making standards for quantitative real-time pneumococcal PCR |
title_fullStr | Making standards for quantitative real-time pneumococcal PCR |
title_full_unstemmed | Making standards for quantitative real-time pneumococcal PCR |
title_short | Making standards for quantitative real-time pneumococcal PCR |
title_sort | making standards for quantitative real-time pneumococcal pcr |
topic | Short Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5121202/ https://www.ncbi.nlm.nih.gov/pubmed/27896138 http://dx.doi.org/10.1016/j.bdq.2014.11.003 |
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