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- W2403485205 endingPage "4824" @default.
- W2403485205 startingPage "4824" @default.
- W2403485205 abstract "The present review describes the current status of multiplex quantitative real time polymerase chain reaction (qPCR) assays developed and used globally for detection and subtyping of hepatitis viruses in body fluids. Several studies have reported the use of multiplex qPCR for the detection of hepatitis viruses, including hepatitis A virus (HAV), hepatitis B virus (HBV), hepatitis C virus (HCV), hepatitis D virus (HDV), and hepatitis E virus (HEV). In addition, multiplex qPCR has also been developed for genotyping HBV, HCV, and HEV subtypes. Although a single step multiplex qPCR assay for all six hepatitis viruses, i.e., A to G viruses, is not yet reported, it may be available in the near future as the technologies continue to advance. All studies use a conserved region of the viral genome as the basis of amplification and hydrolysis probes as the preferred chemistries for improved detection. Based on a standard plot prepared using varying concentrations of template and the observed threshold cycle value, it is possible to determine the linear dynamic range and to calculate an exact copy number of virus in the specimen. Advantages of multiplex qPCR assay over singleplex or other molecular techniques in samples from patients with co-infection include fast results, low cost, and a single step investigation process." @default.
- W2403485205 created "2016-06-24" @default.
- W2403485205 creator A5011122824 @default.
- W2403485205 creator A5012484486 @default.
- W2403485205 creator A5024050800 @default.
- W2403485205 creator A5064343307 @default.
- W2403485205 date "2016-01-01" @default.
- W2403485205 modified "2023-10-01" @default.
- W2403485205 title "Multiplex qPCR for serodetection and serotyping of hepatitis viruses: A brief review" @default.
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