Digital PCR-An Emerging Technology with Broad Applications in Microbiology

被引:111
|
作者
Salipante, Stephen J. [1 ]
Jerome, Keith R. [1 ,2 ]
机构
[1] Univ Washington, Dept Lab Med, Seattle, WA 98195 USA
[2] Fred Hutchinson Canc Res Ctr, Vaccine & Infect Dis Div, 1124 Columbia St, Seattle, WA 98104 USA
关键词
REAL-TIME PCR; POLYMERASE-CHAIN-REACTION; ABSOLUTE QUANTIFICATION; ACCURATE QUANTIFICATION; INTERNATIONAL STANDARD; VIRAL LOAD; QUANTITATIVE DETECTION; INFECTIOUS-DISEASES; VIRUS POPULATIONS; DROPLET;
D O I
10.1373/clinchem.2019.304048
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
BACKGROUND: The PCR and its variant, quantitative PCR (qPCR), have revolutionized the practice of clinical microbiology. Continued advancements in PCR have led to a new derivative, digital PCR (dPCR), which promises to address certain limitations inherent to qPCR. CONTENT: Here we highlight the important technical differences between qPCR and dPCR, and the potential advantages and disadvantages of each. We then review specific situations in which dPCR has been implemented in clinical microbiology and the results of such applications. Finally, we attempt to place dPCR in the context of other emerging technologies relevant to the clinical laboratory, including next-generation sequencing. SUMMARY: dPCR offers certain dear advantages over traditional qPCR, but these are to some degree offset by limitations of the technology, at least as currently practiced. Laboratories considering implementation of dPCR should carefully weigh the potential advantages and disadvantages of this powerful technique for each specific application planned. (C) 2019 American Association for Clinical Chemistry
引用
收藏
页码:117 / 123
页数:7
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