PD CEN/TS 17981-2:2023 PDF
In vitro diagnostic Next Generation Sequencing (NGS) workflows - Human RNA examination
In vitro diagnostic Next Generation Sequencing (NGS) workflows - Human RNA examination
- Статус документа:
- Действующий
- Формат:
- Электронный (PDF)
- Дата публикации:
- 31 декабря 2023 г.
- ICS:
- 11.100.10
- SKU:
- PD CEN/TS 17981-2:2023
Abstract
1 Scope This document specifies requirements and gives recommendations for next generation sequencing ( NGS ) workflows for in vitro diagnostics and biomedical research. This document covers the pre-examination processes , human RNA isolation, sequencing library preparation, sequencing, sequence analysis and reporting of the examination of sequences for diagnostic purposes from isolated RNA from, e.g. formalin -fixed and paraffin embedded tissues, fresh frozen tissues, fine needle aspirates ( FNA ), whole blood, circulating tumour cells (CTCs), exosomes and other extracellular vesicles , and circulating cell free RNA from plasma.
NOTE 1 Typical applications include, but are not limited to, NGS for oncology and clinical genetics, certain single-cell analyses.
This document is applicable to molecular in vitro diagnostic examinations including laboratory developed tests performed by medical laboratories, molecular pathology laboratories and molecular genetic laboratories. This document is also applicable to laboratory customers, in vitro diagnostics developers and manufacturers, biobanks, institutions, and organisations performing biomedical research. This document is not applicable for in situ sequencing, forensic sequencing, sequencing of pathog...
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