Fundamentals of multiplexing with digital PCR

Q1 Biochemistry, Genetics and Molecular Biology Biomolecular Detection and Quantification Pub Date : 2016-12-01 DOI:10.1016/j.bdq.2016.05.002
Alexandra S. Whale , Jim F. Huggett , Svilen Tzonev
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引用次数: 146

Abstract

Over the past decade numerous publications have demonstrated how digital PCR (dPCR) enables precise and sensitive quantification of nucleic acids in a wide range of applications in both healthcare and environmental analysis. This has occurred in parallel with the advances in partitioning fluidics that enable a reaction to be subdivided into an increasing number of partitions. As the majority of dPCR systems are based on detection in two discrete optical channels, most research to date has focused on quantification of one or two targets within a single reaction. Here we describe ‘higher order multiplexing’ that is the unique ability of dPCR to precisely measure more than two targets in the same reaction. Using examples, we describe the different types of duplex and multiplex reactions that can be achieved. We also describe essential experimental considerations to ensure accurate quantification of multiple targets.

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数字PCR的多路复用基础
在过去的十年中,许多出版物已经证明了数字PCR (dPCR)如何在医疗保健和环境分析的广泛应用中实现精确和敏感的核酸定量。这与分割流体的进步同时发生,这些进步使反应能够被细分为越来越多的分割。由于大多数dPCR系统是基于两个离散光通道的检测,迄今为止大多数研究都集中在单个反应中的一个或两个靶标的定量上。在这里,我们描述了“高阶多路复用”,这是dPCR在同一反应中精确测量两个以上目标的独特能力。通过实例,我们描述了可以实现的不同类型的双工和多工反应。我们还描述了必要的实验考虑,以确保准确量化多个目标。
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来源期刊
Biomolecular Detection and Quantification
Biomolecular Detection and Quantification Biochemistry, Genetics and Molecular Biology-Biochemistry
CiteScore
14.20
自引率
0.00%
发文量
0
审稿时长
8 weeks
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