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Validating Real-Time Polymerase Chain Reaction (PCR) Assays

For many years, the development of assays took place in the laboratories where the test was required. Whilst more and more commercially developed tests have become available, novel assays continue to be developed in academic hospital laboratories. Although commercial kits are more expensive than LDT...

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Detalles Bibliográficos
Autor principal: Smith, Melvyn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7834634/
http://dx.doi.org/10.1016/B978-0-12-814515-9.00053-9
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author Smith, Melvyn
author_facet Smith, Melvyn
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description For many years, the development of assays took place in the laboratories where the test was required. Whilst more and more commercially developed tests have become available, novel assays continue to be developed in academic hospital laboratories. Although commercial kits are more expensive than LDTs, they enable the rapid introduction of assays, with the advantage of being CE marked or FDA approved. However, this approval does not necessarily guarantee the rigorous validation of the assay. Furthermore, commercial assays have to be commercially attractive, which is unlikely for small-scale, specialist tests targeting rarely occurring infectious pathogens and thus there will continue to be a need for laboratory-developed tests.
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spelling pubmed-78346342021-01-26 Validating Real-Time Polymerase Chain Reaction (PCR) Assays Smith, Melvyn Encyclopedia of Virology Article For many years, the development of assays took place in the laboratories where the test was required. Whilst more and more commercially developed tests have become available, novel assays continue to be developed in academic hospital laboratories. Although commercial kits are more expensive than LDTs, they enable the rapid introduction of assays, with the advantage of being CE marked or FDA approved. However, this approval does not necessarily guarantee the rigorous validation of the assay. Furthermore, commercial assays have to be commercially attractive, which is unlikely for small-scale, specialist tests targeting rarely occurring infectious pathogens and thus there will continue to be a need for laboratory-developed tests. 2021 2021-03-01 /pmc/articles/PMC7834634/ http://dx.doi.org/10.1016/B978-0-12-814515-9.00053-9 Text en Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Smith, Melvyn
Validating Real-Time Polymerase Chain Reaction (PCR) Assays
title Validating Real-Time Polymerase Chain Reaction (PCR) Assays
title_full Validating Real-Time Polymerase Chain Reaction (PCR) Assays
title_fullStr Validating Real-Time Polymerase Chain Reaction (PCR) Assays
title_full_unstemmed Validating Real-Time Polymerase Chain Reaction (PCR) Assays
title_short Validating Real-Time Polymerase Chain Reaction (PCR) Assays
title_sort validating real-time polymerase chain reaction (pcr) assays
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7834634/
http://dx.doi.org/10.1016/B978-0-12-814515-9.00053-9
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