One byte at a time: evidencing the quality of clinical service next-generation sequencing for germline and somatic variants.


Journal

European journal of human genetics : EJHG
ISSN: 1476-5438
Titre abrégé: Eur J Hum Genet
Pays: England
ID NLM: 9302235

Informations de publication

Date de publication:
02 2020
Historique:
received: 20 03 2019
accepted: 29 08 2019
revised: 03 07 2019
pubmed: 2 10 2019
medline: 3 2 2021
entrez: 2 10 2019
Statut: ppublish

Résumé

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.

Identifiants

pubmed: 31570784
doi: 10.1038/s41431-019-0515-1
pii: 10.1038/s41431-019-0515-1
pmc: PMC6974611
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

202-212

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Auteurs

Maria Weronika Gutowska-Ding (MW)

European Molecular Genetics Quality Network (EMQN), Manchester Centre for Genomic Medicine, St Mary's Hospital, Manchester, UK.

Zandra C Deans (ZC)

Genomics Quality Assessment (GenQA), Department of Laboratory Medicine, Royal Infirmary of Edinburgh, Little France Crescent, Edinburgh, UK.

Christophe Roos (C)

Euformatics Oy, Tekniikantie 12, Espoo, Finland.

Jukka Matilainen (J)

Euformatics Oy, Tekniikantie 12, Espoo, Finland.

Farrah Khawaja (F)

Genomics Quality Assessment (GenQA), Department of Laboratory Medicine, Royal Infirmary of Edinburgh, Little France Crescent, Edinburgh, UK.

Kim Brügger (K)

Department of Informatics, University of Bergen, Bergen, Norway.

Jo Wook Ahn (JW)

Genetics Laboratories, Guy's and St Thomas' NHS Foundation Trust, London, UK.

Christopher Boustred (C)

Genomics England, London, UK.

Simon J Patton (SJ)

European Molecular Genetics Quality Network (EMQN), Manchester Centre for Genomic Medicine, St Mary's Hospital, Manchester, UK. office@emqn.org.

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Classifications MeSH