Molecular diagnostics in routine practice: quality issues and application to complex disease

Author:

Ferns Gordon A.A.1,O'Dowd David2,Wark Gwen2,Collins Nadine2

Affiliation:

1. The Clinical and Molecular Diagnostics Laboratories, The Royal Surrey County Hospital, Egerton Road, Guildford GU2 7XX, UK

2. The Clinical and Molecular Diagnostics Laboratories The Royal Surrey County Hospital Egerton Road, Guildford GU2 7XX, UK

Abstract

The public already has concerns about 'the new genetics', and it is clear that confidence can only be maintained by scrupulous attention to quality. Standards can be improved by harmonization of methods, discouraging poor practice and using appropriate internal and external quality controls. At present, despite the profound implications of genetic test results, few genetic tests are subject to sufficient scrutiny. The Human Genome Project will lead to the identification of numerous genetic variations contributing to multifactorial diseases, and high-throughput technologies will permit the generation of disease-susceptibility profiles. Clinical laboratories will need to develop the wherewithal to handle these data and present them in a format that is clinically useful.

Publisher

SAGE Publications

Subject

Clinical Biochemistry,General Medicine

Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Genetic screening and diagnosis;Current Opinion in Obstetrics & Gynecology;2005-04

2. Molecular diagnostics in routine practice;Annals of Clinical Biochemistry: International Journal of Laboratory Medicine;2004-03-01

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