ISO/DIS 22692

Indisponible en français

Projet

Projet de Norme internationale au stade enquête auprès des membres de l’ISO.

Remplacera ISO/TS 22692:2020

ISO/DIS 22692

CHF 67

Convertir les francs suisses (CHF) dans une autre devise

Résumé

This document identifies quality metrics for the detection of DNA variants using next generation sequencing (NGS) technology. It also defines the data types, relationships, optionality, cardinalities and terminology bindings of the data.

This document provides a basis for sharing and for the application of "high quality" genomic data and contributes to the realization of the precision medicine and the development of relevant industries.

This document is intended to serve as a catalogue of sequencing data elements used to address quality metrics for various clinical, industrial and commercial applications. The exchange of these data allows researchers, commercial entities, and regulatory bodies to assess for the purpose of selective utilization of the data by setting application-specific quality criteria

This document is not intended for

— sequencing methods other than NGS, such as the Sanger sequencing,

— targets other than genome, such as transcriptome or proteome, or

— specimens of species other than humans.

Informations générales

État actuel
: Projet

Vous pouvez contribuer à l’élaboration de ce projet de Norme internationale en contactant le membre national

Stade
: Mise au vote du DIS: 12 semaines [40.20]
Edition
: 1
Comité technique :
ISO/TC 215/SC 1

ICS :
35.240.80
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