Scientific Reports (May 2024)

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

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

DOI
https://doi.org/10.1038/s41598-024-62199-5
Journal volume & issue
Vol. 14, no. 1
pp. 1 – 13

Abstract

Read online

Abstract Digital 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.