Reproducible and reliable microarray results through quality control: good laboratory proficiency and appropriate data analysis practices are essential

被引：93

作者：

Shi, Leming ^{[1
]}

Perkins, Roger G. ^{[2
]}

Fang, Hong ^{[2
]}

Tong, Weida ^{[1
]}

机构：

[1] US FDA, Natl Ctr Toxicol Res, Jefferson, AR 72079 USA

[2] ICF Int Inc, Jefferson, AR 72079 USA

来源：

CURRENT OPINION IN BIOTECHNOLOGY | 2008年 / 19卷 / 01期

关键词：

D O I：

10.1016/j.copbio.2007.11.003

中图分类号：

Q5 [生物化学];

学科分类号：

071010 ; 081704 ;

摘要：

Over a few short years, microarray gene expression profiling has permeated most areas of biomedical research. Microarrays are now poised to enter the more demanding realm of clinical applications. The prospect of using microarray data to derive biomarkers of disease or toxicity, predict prognosis, or select treatments raises the validity and reliability bar substantially higher. The potential future payoffs are huge in terms of faster approval of more efficacious and safer medical interventions, and a more personalized implementation of them. Arriving at the future sooner rather than later is the motivation for the FDA-led MicroArray Quality Control (MAQC) project. The widespread collaboration aims to assess achievable technical performance of microarrays and capabilities and limitations of methods for microarray data analysis.

引用

页码：10 / 18

页数：9

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