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美国临床分子遗传学实验室的质量保证与质量改进。

Quality assurance and quality improvement in U.S. clinical molecular genetic laboratories.

作者信息

Chen Bin, Richards C Sue, Wilson Jean Amos, Lyon Elaine

机构信息

Centers for Disease Control and Prevention, Atlanta, Georgia, USA.

出版信息

Curr Protoc Hum Genet. 2011 Apr;Chapter 9:Unit9.2. doi: 10.1002/0471142905.hg0902s69.

Abstract

A robust quality-assurance program is essential for laboratories that perform molecular genetic testing to maintain high-quality testing and be able to address challenges associated with performance or delivery of testing services as the use of molecular genetic tests continues to expand in clinical and public health practice. This unit discusses quality-assurance and quality-improvement considerations that are critical for molecular genetic testing performed for heritable diseases and conditions. Specific discussion is provided on applying regulatory standards and best practices in establishing/verifying test performance, ensuring quality of the total testing process, monitoring and maintaining personnel competency, and continuing quality improvement. The unit provides a practical reference for laboratory professionals to use in recognizing and addressing essential quality-assurance issues in human molecular genetic testing. It should also provide useful information for genetics researchers, trainees, and fellows in human genetics training programs, as well as others who are interested in quality assurance and quality improvement for molecular genetic testing.

摘要

对于进行分子基因检测的实验室而言,一个健全的质量保证计划至关重要,以便在临床和公共卫生实践中,随着分子基因检测的使用持续扩大,保持高质量检测并能够应对与检测服务的性能或交付相关的挑战。本单元讨论了对遗传性疾病和病症进行分子基因检测至关重要的质量保证和质量改进考量。具体讨论了在建立/验证检测性能、确保整个检测过程的质量、监测和维持人员能力以及持续质量改进方面应用监管标准和最佳实践。本单元为实验室专业人员在识别和解决人类分子基因检测中的基本质量保证问题时提供了实用参考。它还应为遗传学研究人员、学员以及人类遗传学培训项目中的研究员,以及其他对分子基因检测的质量保证和质量改进感兴趣的人员提供有用信息。

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