数字聚合酶链反应
计算机科学
过程(计算)
定量评估
数据科学
风险分析(工程)
生物
聚合酶链反应
医学
生物化学
基因
操作系统
作者
Jim F. Huggett,Carole A. Foy,Vladimı́r Beneš,Kerry R. Emslie,Jeremy A. Garson,Ross J. Haynes,Jan Hellemans,Mikael Kubista,Reinhold Mueller,Tania Nolan,Michael W. Pfaffl,Gregory L. Shipley,Jo Vandesompele,Carl T. Wittwer,Stephen A. Bustin
出处
期刊:Clinical Chemistry
[American Association for Clinical Chemistry]
日期:2013-04-10
卷期号:59 (6): 892-902
被引量:806
标识
DOI:10.1373/clinchem.2013.206375
摘要
There is growing interest in digital PCR (dPCR) because technological progress makes it a practical and increasingly affordable technology. dPCR allows the precise quantification of nucleic acids, facilitating the measurement of small percentage differences and quantification of rare variants. dPCR may also be more reproducible and less susceptible to inhibition than quantitative real-time PCR (qPCR). Consequently, dPCR has the potential to have a substantial impact on research as well as diagnostic applications. However, as with qPCR, the ability to perform robust meaningful experiments requires careful design and adequate controls. To assist independent evaluation of experimental data, comprehensive disclosure of all relevant experimental details is required. To facilitate this process we present the Minimum Information for Publication of Quantitative Digital PCR Experiments guidelines. This report addresses known requirements for dPCR that have already been identified during this early stage of its development and commercial implementation. Adoption of these guidelines by the scientific community will help to standardize experimental protocols, maximize efficient utilization of resources, and enhance the impact of this promising new technology.
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