| Literature DB >> 27818047 |
Lei Cao1, Xingye Cui1, Jie Hu1, Zedong Li1, Jane Ru Choi1, Qingzhen Yang1, Min Lin1, Li Ying Hui2, Feng Xu3.
Abstract
Since the invention of polymerase chain reaction (PCR) in 1985, PCR has played a significant role in molecular diagnostics for genetic diseases, pathogens, oncogenes and forensic identification. In the past three decades, PCR has evolved from end-point PCR, through real-time PCR, to its current version, which is the absolute quantitive digital PCR (dPCR). In this review, we first discuss the principles of all key steps of dPCR, i.e., sample dispersion, amplification, and quantification, covering commercialized apparatuses and other devices still under lab development. We highlight the advantages and disadvantages of different technologies based on these steps, and discuss the emerging biomedical applications of dPCR. Finally, we provide a glimpse of the existing challenges and future perspectives for dPCR.Entities:
Keywords: Absolute quantification; Beads; Deoxyribonucleic acid; Digital PCR; Droplet; Microfluidics; Microwell
Mesh:
Year: 2016 PMID: 27818047 DOI: 10.1016/j.bios.2016.09.082
Source DB: PubMed Journal: Biosens Bioelectron ISSN: 0956-5663 Impact factor: 10.618