Standard

SN-CEN/TS 16827-3:2015

Aug 2015 Withdrawn

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Abstract

This Technical Specification gives recommendations for the handling, documentation and processing of FFPE tissue specimens intended for DNA analysis during the preanalytical phase before a molecular assay is performed. This Technical Specification is applicable to molecular in vitro diagnostic examinations (e.g., in vitro diagnostic laboratories, laboratory customers, developers and manufacturers of in vitro diagnostics, institutions and commercial organizations performing biomedical research, biobanks, and regulatory authorities). DNA integrity in tissues can change before and during formalin fixation, processing and storage. Chemical modifications introduced into DNA during tissue fixation might lead to fragmentation and sequence alterations [1], changes in the methylation status or even structural changes which can lead to e.g., spurious copy number changes in array-CGH profiles [2]. These modifications of the DNA molecules can impact the validity and reliability of the analytical test results. Therefore, it is essential to take special measures to minimize the described modifications for subsequent DNA analysis.

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Standard from SN
Published: 12 August 2015
Withdrawn: 1 April 2019
Edition: 2015-08
Version: 1
Document type: TS
ISBN:

ICS 11.100.10
National Committee SN/K 116

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Replaced by: NS-EN ISO 20166-3:2019
Refers: ISO 15190:2003
Refers: ISO 15190:2003
Adopted from: CEN/TS 16827-3:2015 , 0

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SN-CEN/TS 16827-3:2015
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NS-EN ISO 20166-3:2019

SN-CEN/TS 16827-3:2015

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Abstract

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