Multiplexed digital polymerase chain reaction as a powerful diagnostic tool

被引:40
作者
Ganova, Martina [1 ]
Zhang, Haoqing [2 ]
Zhu, Hanliang [2 ]
Korabecna, Marie [3 ,4 ]
Neuzil, Pavel [1 ,2 ,5 ]
机构
[1] Brno Univ Technol, Cent European Inst Technol, Brno 61200, Czech Republic
[2] Northwestern Polytech Univ, Sch Mech Engn, Xian 710072, Peoples R China
[3] Charles Univ Prague, Fac Med 1, Inst Biol & Med Genet, Prague 12800, Czech Republic
[4] Gen Univ Hosp, Prague 12800, Czech Republic
[5] Brno Univ Technol, Fac Elect Engn & Commun, Brno 61600, Czech Republic
关键词
Digital polymerase chain reaction; Absolute quantification; Multiplexing strategies; Duplex multiplexing; Higher order multiplexing; Clinical applications; REAL-TIME PCR; POINT-OF-CARE; GIARDIA-LAMBLIA; DNA; QUANTIFICATION; SENSITIVITY; PLASMA; ELECTROPHORESIS; IDENTIFICATION; AMPLIFICATION;
D O I
10.1016/j.bios.2021.113155
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
The digital polymerase chain reaction (dPCR) multiplexing method can simultaneously detect and quantify closely related deoxyribonucleic acid sequences in complex mixtures. The dPCR concept is continuously improved by the development of microfluidics and micro- and nanofabrication, and different complex techniques are introduced. In this review, we introduce dPCR techniques based on sample compartmentalization, droplet-and chip-based systems, and their combinations. We then discuss dPCR multiplexing methods in both laboratory research settings and advanced or routine clinical applications. We focus on their strengths and weaknesses with regard to the character of biological samples and to the required precision of such analysis, as well as showing recently published work based on those methods. Finally, we envisage possible future achievements in this field.
引用
收藏
页数:12
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