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PathOS: a decision support system for reporting high throughput sequencing of cancers in clinical diagnostic laboratories

BACKGROUND: The increasing affordability of DNA sequencing has allowed it to be widely deployed in pathology laboratories. However, this has exposed many issues with the analysis and reporting of variants for clinical diagnostic use. Implementing a high-throughput sequencing (NGS) clinical reporting...

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Autores principales: Doig, Kenneth D., Fellowes, Andrew, Bell, Anthony H., Seleznev, Andrei, Ma, David, Ellul, Jason, Li, Jason, Doyle, Maria A., Thompson, Ella R., Kumar, Amit, Lara, Luis, Vedururu, Ravikiran, Reid, Gareth, Conway, Thomas, Papenfuss, Anthony T., Fox, Stephen B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5404673/
https://www.ncbi.nlm.nih.gov/pubmed/28438193
http://dx.doi.org/10.1186/s13073-017-0427-z
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author Doig, Kenneth D.
Fellowes, Andrew
Bell, Anthony H.
Seleznev, Andrei
Ma, David
Ellul, Jason
Li, Jason
Doyle, Maria A.
Thompson, Ella R.
Kumar, Amit
Lara, Luis
Vedururu, Ravikiran
Reid, Gareth
Conway, Thomas
Papenfuss, Anthony T.
Fox, Stephen B.
author_facet Doig, Kenneth D.
Fellowes, Andrew
Bell, Anthony H.
Seleznev, Andrei
Ma, David
Ellul, Jason
Li, Jason
Doyle, Maria A.
Thompson, Ella R.
Kumar, Amit
Lara, Luis
Vedururu, Ravikiran
Reid, Gareth
Conway, Thomas
Papenfuss, Anthony T.
Fox, Stephen B.
author_sort Doig, Kenneth D.
collection PubMed
description BACKGROUND: The increasing affordability of DNA sequencing has allowed it to be widely deployed in pathology laboratories. However, this has exposed many issues with the analysis and reporting of variants for clinical diagnostic use. Implementing a high-throughput sequencing (NGS) clinical reporting system requires a diverse combination of capabilities, statistical methods to identify variants, global variant databases, a validated bioinformatics pipeline, an auditable laboratory workflow, reproducible clinical assays and quality control monitoring throughout. These capabilities must be packaged in software that integrates the disparate components into a useable system. RESULTS: To meet these needs, we developed a web-based application, PathOS, which takes variant data from a patient sample through to a clinical report. PathOS has been used operationally in the Peter MacCallum Cancer Centre for two years for the analysis, curation and reporting of genetic tests for cancer patients, as well as the curation of large-scale research studies. PathOS has also been deployed in cloud environments allowing multiple institutions to use separate, secure and customisable instances of the system. Increasingly, the bottleneck of variant curation is limiting the adoption of clinical sequencing for molecular diagnostics. PathOS is focused on providing clinical variant curators and pathology laboratories with a decision support system needed for personalised medicine. While the genesis of PathOS has been within cancer molecular diagnostics, the system is applicable to NGS clinical reporting generally. CONCLUSIONS: The widespread availability of genomic sequencers has highlighted the limited availability of software to support clinical decision-making in molecular pathology. PathOS is a system that has been developed and refined in a hospital laboratory context to meet the needs of clinical diagnostics. The software is available as a set of Docker images and source code at https://github.com/PapenfussLab/PathOS. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13073-017-0427-z) contains supplementary material, which is available to authorized users.
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spelling pubmed-54046732017-04-27 PathOS: a decision support system for reporting high throughput sequencing of cancers in clinical diagnostic laboratories Doig, Kenneth D. Fellowes, Andrew Bell, Anthony H. Seleznev, Andrei Ma, David Ellul, Jason Li, Jason Doyle, Maria A. Thompson, Ella R. Kumar, Amit Lara, Luis Vedururu, Ravikiran Reid, Gareth Conway, Thomas Papenfuss, Anthony T. Fox, Stephen B. Genome Med Software BACKGROUND: The increasing affordability of DNA sequencing has allowed it to be widely deployed in pathology laboratories. However, this has exposed many issues with the analysis and reporting of variants for clinical diagnostic use. Implementing a high-throughput sequencing (NGS) clinical reporting system requires a diverse combination of capabilities, statistical methods to identify variants, global variant databases, a validated bioinformatics pipeline, an auditable laboratory workflow, reproducible clinical assays and quality control monitoring throughout. These capabilities must be packaged in software that integrates the disparate components into a useable system. RESULTS: To meet these needs, we developed a web-based application, PathOS, which takes variant data from a patient sample through to a clinical report. PathOS has been used operationally in the Peter MacCallum Cancer Centre for two years for the analysis, curation and reporting of genetic tests for cancer patients, as well as the curation of large-scale research studies. PathOS has also been deployed in cloud environments allowing multiple institutions to use separate, secure and customisable instances of the system. Increasingly, the bottleneck of variant curation is limiting the adoption of clinical sequencing for molecular diagnostics. PathOS is focused on providing clinical variant curators and pathology laboratories with a decision support system needed for personalised medicine. While the genesis of PathOS has been within cancer molecular diagnostics, the system is applicable to NGS clinical reporting generally. CONCLUSIONS: The widespread availability of genomic sequencers has highlighted the limited availability of software to support clinical decision-making in molecular pathology. PathOS is a system that has been developed and refined in a hospital laboratory context to meet the needs of clinical diagnostics. The software is available as a set of Docker images and source code at https://github.com/PapenfussLab/PathOS. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13073-017-0427-z) contains supplementary material, which is available to authorized users. BioMed Central 2017-04-24 /pmc/articles/PMC5404673/ /pubmed/28438193 http://dx.doi.org/10.1186/s13073-017-0427-z Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Software
Doig, Kenneth D.
Fellowes, Andrew
Bell, Anthony H.
Seleznev, Andrei
Ma, David
Ellul, Jason
Li, Jason
Doyle, Maria A.
Thompson, Ella R.
Kumar, Amit
Lara, Luis
Vedururu, Ravikiran
Reid, Gareth
Conway, Thomas
Papenfuss, Anthony T.
Fox, Stephen B.
PathOS: a decision support system for reporting high throughput sequencing of cancers in clinical diagnostic laboratories
title PathOS: a decision support system for reporting high throughput sequencing of cancers in clinical diagnostic laboratories
title_full PathOS: a decision support system for reporting high throughput sequencing of cancers in clinical diagnostic laboratories
title_fullStr PathOS: a decision support system for reporting high throughput sequencing of cancers in clinical diagnostic laboratories
title_full_unstemmed PathOS: a decision support system for reporting high throughput sequencing of cancers in clinical diagnostic laboratories
title_short PathOS: a decision support system for reporting high throughput sequencing of cancers in clinical diagnostic laboratories
title_sort pathos: a decision support system for reporting high throughput sequencing of cancers in clinical diagnostic laboratories
topic Software
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5404673/
https://www.ncbi.nlm.nih.gov/pubmed/28438193
http://dx.doi.org/10.1186/s13073-017-0427-z
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