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Updated: May 26, 2026

A Duplex Digital PCR Assay for Simultaneous Quantification of the Enterococcus spp. and the Human Fecal-associated HF183 Marker in Waters
Published on: March 9, 2016
Quantitative polymerase chain reaction (PCR) for detection of aquatic animal pathogens in a diagnostic laboratory
Maureen K Purcell1, Rodman G Getchell, Carol A McClure
1U.S. Geological Survey, Western Fisheries Research Center 6505 North East 65th Street, Seattle, Washington 98115, USA. mpurcell@usgs.gov
Abstract:
Real-time, or quantitative, polymerase chain reaction (qPCR) is quickly supplanting other molecular methods for detecting the nucleic acids of human and other animal pathogens owing to the speed and robustness of the technology. As the aquatic animal health community moves toward implementing national diagnostic testing schemes, it will need to evaluate how qPCR technology should be employed. This review outlines the basic principles of qPCR technology, considerations for assay development, standards and controls, assay performance, diagnostic validation, implementation in the diagnostic laboratory, and quality assurance and control measures. These factors are fundamental for ensuring the validity of qPCR assay results obtained in the diagnostic laboratory setting.
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