Viral diagnostics in the era of digital polymerase chain reaction.

Diagn Microbiol Infect Dis

Department of Laboratory Medicine, University of Washington, Seattle, WA, USA.

Published: January 2013

AI Article Synopsis

  • Digital PCR (dPCR) allows for precise measurement of DNA without needing a standard curve, unlike traditional qPCR.
  • dPCR works by splitting a single reaction into many separate ones, using Poisson statistics to determine the quantity of DNA based on positive and negative signals.
  • The rising popularity of dPCR platforms is opening new opportunities in clinical diagnostics, especially for detecting low viral loads and rare mutations.

Article Abstract

Unlike quantitative polymerase chain reaction (qPCR), digital PCR (dPCR) achieves sensitive and accurate absolute quantitation of a DNA sample without the need for a standard curve. A single PCR reaction is divided into many separate reactions that each have a positive or negative signal. By applying Poisson statistics, the number of DNA molecules in the original sample is directly calculated from the number of positive and negative reactions. The recent availability of multiple commercial dPCR platforms has led to increased interest in clinical diagnostic applications, such as low viral load detection and low abundance mutant detection, where dPCR could be superior to traditional qPCR. Here we review current literature that demonstrates dPCR's potential utility in viral diagnostics, particularly through absolute quantification of target DNA sequences and rare mutant allele detection.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3519953PMC
http://dx.doi.org/10.1016/j.diagmicrobio.2012.10.009DOI Listing

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