Bio-Rad Laboratories, Inc., Pleasanton, California 94566, United States.
Anal Chem. 2011 Nov 15;83(22):8604-10. doi: 10.1021/ac202028g. Epub 2011 Oct 28.
Digital PCR enables the absolute quantitation of nucleic acids in a sample. The lack of scalable and practical technologies for digital PCR implementation has hampered the widespread adoption of this inherently powerful technique. Here we describe a high-throughput droplet digital PCR (ddPCR) system that enables processing of ~2 million PCR reactions using conventional TaqMan assays with a 96-well plate workflow. Three applications demonstrate that the massive partitioning afforded by our ddPCR system provides orders of magnitude more precision and sensitivity than real-time PCR. First, we show the accurate measurement of germline copy number variation. Second, for rare alleles, we show sensitive detection of mutant DNA in a 100,000-fold excess of wildtype background. Third, we demonstrate absolute quantitation of circulating fetal and maternal DNA from cell-free plasma. We anticipate this ddPCR system will allow researchers to explore complex genetic landscapes, discover and validate new disease associations, and define a new era of molecular diagnostics.
数字 PCR 可实现样本中核酸的绝对定量。由于缺乏可扩展且实用的数字 PCR 实施技术,该强大技术的广泛应用受到阻碍。本文介绍了一种高通量液滴数字 PCR(ddPCR)系统,该系统可使用 96 孔板工作流程对 ~200 万个 PCR 反应进行处理,同时使用常规 TaqMan 分析。三种应用表明,ddPCR 系统提供的大规模分区比实时 PCR 具有更高的精度和灵敏度。首先,我们展示了对种系拷贝数变异的准确测量。其次,对于稀有等位基因,我们展示了在 10 万倍野生型背景中对突变 DNA 的敏感检测。第三,我们证明了从无细胞血浆中循环胎儿和母体 DNA 的绝对定量。我们预计该 ddPCR 系统将使研究人员能够探索复杂的遗传景观,发现和验证新的疾病关联,并开创分子诊断的新时代。