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One byte at a time: evidencing the quality of clinical service next-generation sequencing for germline and somatic variants
Next-generation sequencing (NGS) is replacing other molecular techniques to become the de facto gene diagnostics approach, transforming the speed of diagnosis for patients and expanding opportunities for precision medicine. Consequently, for accredited laboratories as well as those seeking accredita...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6974611/ https://www.ncbi.nlm.nih.gov/pubmed/31570784 http://dx.doi.org/10.1038/s41431-019-0515-1 |
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author | Gutowska-Ding, Maria Weronika Deans, Zandra C. Roos, Christophe Matilainen, Jukka Khawaja, Farrah Brügger, Kim Ahn, Jo Wook Boustred, Christopher Patton, Simon J. |
author_facet | Gutowska-Ding, Maria Weronika Deans, Zandra C. Roos, Christophe Matilainen, Jukka Khawaja, Farrah Brügger, Kim Ahn, Jo Wook Boustred, Christopher Patton, Simon J. |
author_sort | Gutowska-Ding, Maria Weronika |
collection | PubMed |
description | Next-generation sequencing (NGS) is replacing other molecular techniques to become the de facto gene diagnostics approach, transforming the speed of diagnosis for patients and expanding opportunities for precision medicine. Consequently, for accredited laboratories as well as those seeking accreditation, both objective measures of quality and external review of laboratory processes are required. External quality assessment (EQA), or Proficiency Testing (PT), can assess a laboratory’s service through an independent external agency, the EQA provider. The analysis of a growing number of genes and whole exome and genomes is now routine; therefore, an EQA must be delivered to enable all testing laboratories to participate. In this paper, we describe the development of a unique platform and gene target independent EQA scheme for NGS, designed to scale from current to future requirements of clinical diagnostic laboratories testing for germline and somatic variants. The EQA results from three annual rounds indicate that clinical diagnostic laboratories are providing an increasingly high-quality NGS service and variant calling abilities are improving. From an EQA provider perspective, challenges remain regarding delivery and performance criteria, as well as in analysing similar NGS approaches between cohorts with meaningful metrics, sample sourcing and data formats. |
format | Online Article Text |
id | pubmed-6974611 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-69746112020-01-24 One byte at a time: evidencing the quality of clinical service next-generation sequencing for germline and somatic variants Gutowska-Ding, Maria Weronika Deans, Zandra C. Roos, Christophe Matilainen, Jukka Khawaja, Farrah Brügger, Kim Ahn, Jo Wook Boustred, Christopher Patton, Simon J. Eur J Hum Genet Article Next-generation sequencing (NGS) is replacing other molecular techniques to become the de facto gene diagnostics approach, transforming the speed of diagnosis for patients and expanding opportunities for precision medicine. Consequently, for accredited laboratories as well as those seeking accreditation, both objective measures of quality and external review of laboratory processes are required. External quality assessment (EQA), or Proficiency Testing (PT), can assess a laboratory’s service through an independent external agency, the EQA provider. The analysis of a growing number of genes and whole exome and genomes is now routine; therefore, an EQA must be delivered to enable all testing laboratories to participate. In this paper, we describe the development of a unique platform and gene target independent EQA scheme for NGS, designed to scale from current to future requirements of clinical diagnostic laboratories testing for germline and somatic variants. The EQA results from three annual rounds indicate that clinical diagnostic laboratories are providing an increasingly high-quality NGS service and variant calling abilities are improving. From an EQA provider perspective, challenges remain regarding delivery and performance criteria, as well as in analysing similar NGS approaches between cohorts with meaningful metrics, sample sourcing and data formats. Springer International Publishing 2019-09-30 2020-02 /pmc/articles/PMC6974611/ /pubmed/31570784 http://dx.doi.org/10.1038/s41431-019-0515-1 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Gutowska-Ding, Maria Weronika Deans, Zandra C. Roos, Christophe Matilainen, Jukka Khawaja, Farrah Brügger, Kim Ahn, Jo Wook Boustred, Christopher Patton, Simon J. One byte at a time: evidencing the quality of clinical service next-generation sequencing for germline and somatic variants |
title | One byte at a time: evidencing the quality of clinical service next-generation sequencing for germline and somatic variants |
title_full | One byte at a time: evidencing the quality of clinical service next-generation sequencing for germline and somatic variants |
title_fullStr | One byte at a time: evidencing the quality of clinical service next-generation sequencing for germline and somatic variants |
title_full_unstemmed | One byte at a time: evidencing the quality of clinical service next-generation sequencing for germline and somatic variants |
title_short | One byte at a time: evidencing the quality of clinical service next-generation sequencing for germline and somatic variants |
title_sort | one byte at a time: evidencing the quality of clinical service next-generation sequencing for germline and somatic variants |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6974611/ https://www.ncbi.nlm.nih.gov/pubmed/31570784 http://dx.doi.org/10.1038/s41431-019-0515-1 |
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