Developing centrifugal force real-time digital PCR for detecting extremely low DNA concentration

Author:

Shin Jong Cheol,Jeong Jeong-Yeon,Son Seon Gyu,Choi Sang-Haeng,Nam Ho-Chul,Yoon Tae-Ho,Kim Hyo-Jun,Choi Dong-Geun,Lee Hwarang,Lee Ukyeol,Yang Seon-Mo,Kang Il,Jung Dae-Young,Lee Han Woo,Lee Moon-Keun,Lee Tae Jae,Kim Geehong,Park Han-Oh,Lee Sung-Woon

Abstract

AbstractDigital PCR (dPCR) is a technique for absolute quantification of nucleic acid molecules. To develop a dPCR technique that enables more accurate nucleic acid detection and quantification, we established a novel dPCR apparatus known as centrifugal force real-time dPCR (crdPCR). This system is efficient than other systems with only 2.14% liquid loss by dispensing samples using centrifugal force. Moreover, we applied a technique for analyzing the real-time graph of the each micro-wells and distinguishing true/false positives using artificial intelligence to mitigate the rain, a persistent issue with dPCR. The limits of detection and quantification were 1.38 and 4.19 copies/μL, respectively, showing a two-fold higher sensitivity than that of other comparable devices. With the integration of this new technology, crdPCR will significantly contribute to research on next-generation PCR targeting absolute micro-analysis.

Publisher

Springer Science and Business Media LLC

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