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《下一代测序技术在基因组诊断应用中的最佳实践指南:荷兰基因组诊断实验室的国家合作研究》。

Best practice guidelines for the use of next-generation sequencing applications in genome diagnostics: a national collaborative study of Dutch genome diagnostic laboratories.

机构信息

Department of Clinical Genetics, VU University Medical Centre, Amsterdam, The Netherlands.

出版信息

Hum Mutat. 2013 Oct;34(10):1313-21. doi: 10.1002/humu.22368. Epub 2013 Aug 19.

DOI:10.1002/humu.22368
PMID:23776008
Abstract

Next-generation sequencing (NGS) methods are being adopted by genome diagnostics laboratories worldwide. However, implementing NGS-based tests according to diagnostic standards is a challenge for individual laboratories. To facilitate the implementation of NGS in Dutch laboratories, the Dutch Society for Clinical Genetic Laboratory Diagnostics (VKGL) set up a working group in 2012. The results of their discussions are presented here. We provide best practice guidelines and criteria for implementing and validating NGS applications in a clinical setting. We introduce the concept of "diagnostic yield" as the main performance characteristic for evaluating diagnostic tests. We recommend that the laboratory procedures, including the tested genes, should be recorded in a publicly available document describing the complete "diagnostic routing." We also propose that laboratories should use a list of "core disease genes" for specific genetic diseases. This core list contains the essential genes for each disease, and they should all be included in a diagnostic test to establish a reliable and accurate molecular diagnosis. The guidelines will ensure a clear and standardized quality of care provided by genetic diagnostic laboratories. The best practice guidelines and criteria that are presented here were adopted by the VKGL in January 2013.

摘要

下一代测序(NGS)方法正在被全球的基因组诊断实验室所采用。然而,根据诊断标准来实施基于 NGS 的检测对于各个实验室而言是一项挑战。为了促进荷兰实验室采用 NGS,荷兰临床遗传实验室诊断学会(VKGL)于 2012 年成立了一个工作组。他们的讨论结果在此呈现。我们提供了在临床环境中实施和验证 NGS 应用的最佳实践指南和标准。我们引入了“诊断收益”的概念,作为评估诊断测试的主要性能特征。我们建议将包括测试基因在内的实验室程序记录在一份公开的文件中,描述完整的“诊断路径”。我们还建议实验室应针对特定的遗传疾病使用“核心疾病基因”列表。这个核心列表包含每个疾病的基本基因,所有这些基因都应包含在诊断测试中,以建立可靠和准确的分子诊断。这些指南将确保遗传诊断实验室提供清晰和标准化的护理质量。VKGL 于 2013 年 1 月采用了这里提出的最佳实践指南和标准。

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