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Automation and standardisation of clinical molecular testing using PCR.Ai – A comparative performance study
BACKGROUND: We undertook a prospective clinical study to evaluate PCR.Ai’s (www.pcr.ai) accuracy and impact when automating the manual data-analysis and quality control steps associated with routine clinical pathogen testing using real-time PCR (qPCR). OBJECTIVES: We evaluated the impact of PCR.Ai w...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier B.V.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7172212/ https://www.ncbi.nlm.nih.gov/pubmed/31563652 http://dx.doi.org/10.1016/j.jcv.2019.08.005 |
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author | MacLean, A.R. Gunson, R. |
author_facet | MacLean, A.R. Gunson, R. |
author_sort | MacLean, A.R. |
collection | PubMed |
description | BACKGROUND: We undertook a prospective clinical study to evaluate PCR.Ai’s (www.pcr.ai) accuracy and impact when automating the manual data-analysis and quality control steps associated with routine clinical pathogen testing using real-time PCR (qPCR). OBJECTIVES: We evaluated the impact of PCR.Ai when used as the final interpretation/verification step for routine in-house qPCR tests for respiratory pathogens and for norovirus for a total of 22,200 interpretations. STUDY DESIGN: We compared PCR.Ai to our existing manual interpretation, to determine accuracy and hands-on time savings. PCR.Ai was accurate. RESULTS AND CONCLUSIONS: There was 100% concurrence between validated respiratory virus and norovirus detection by our manual routine analysis method and PCR.Ai. Furthermore, there were significant routine savings with PCR.Ai of 45 min/respiratory run and 32 min/norovirus run. Our conclusion is that PCR.Ai is a highly accurate time-saving tool that reduces complexity of qPCR analysis and hence the need for specialists and hands-on time. It demonstrated capabilities to enable us to get results out more quickly with lower costs and less risk of errors. |
format | Online Article Text |
id | pubmed-7172212 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71722122020-04-22 Automation and standardisation of clinical molecular testing using PCR.Ai – A comparative performance study MacLean, A.R. Gunson, R. J Clin Virol Article BACKGROUND: We undertook a prospective clinical study to evaluate PCR.Ai’s (www.pcr.ai) accuracy and impact when automating the manual data-analysis and quality control steps associated with routine clinical pathogen testing using real-time PCR (qPCR). OBJECTIVES: We evaluated the impact of PCR.Ai when used as the final interpretation/verification step for routine in-house qPCR tests for respiratory pathogens and for norovirus for a total of 22,200 interpretations. STUDY DESIGN: We compared PCR.Ai to our existing manual interpretation, to determine accuracy and hands-on time savings. PCR.Ai was accurate. RESULTS AND CONCLUSIONS: There was 100% concurrence between validated respiratory virus and norovirus detection by our manual routine analysis method and PCR.Ai. Furthermore, there were significant routine savings with PCR.Ai of 45 min/respiratory run and 32 min/norovirus run. Our conclusion is that PCR.Ai is a highly accurate time-saving tool that reduces complexity of qPCR analysis and hence the need for specialists and hands-on time. It demonstrated capabilities to enable us to get results out more quickly with lower costs and less risk of errors. Elsevier B.V. 2019-11 2019-08-14 /pmc/articles/PMC7172212/ /pubmed/31563652 http://dx.doi.org/10.1016/j.jcv.2019.08.005 Text en © 2019 Elsevier B.V. All rights reserved. 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 MacLean, A.R. Gunson, R. Automation and standardisation of clinical molecular testing using PCR.Ai – A comparative performance study |
title | Automation and standardisation of clinical molecular testing using PCR.Ai – A comparative performance study |
title_full | Automation and standardisation of clinical molecular testing using PCR.Ai – A comparative performance study |
title_fullStr | Automation and standardisation of clinical molecular testing using PCR.Ai – A comparative performance study |
title_full_unstemmed | Automation and standardisation of clinical molecular testing using PCR.Ai – A comparative performance study |
title_short | Automation and standardisation of clinical molecular testing using PCR.Ai – A comparative performance study |
title_sort | automation and standardisation of clinical molecular testing using pcr.ai – a comparative performance study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7172212/ https://www.ncbi.nlm.nih.gov/pubmed/31563652 http://dx.doi.org/10.1016/j.jcv.2019.08.005 |
work_keys_str_mv | AT macleanar automationandstandardisationofclinicalmoleculartestingusingpcraiacomparativeperformancestudy AT gunsonr automationandstandardisationofclinicalmoleculartestingusingpcraiacomparativeperformancestudy |