Evaluation and utilization of preassembled frozen commercial fast real-time qPCR master mixes for detection of cytomegalovirus and BK virus
Author:
Affiliation:
1. Department of Laboratory Medicine; Molecular Virology Laboratory; University of Washington; Seattle Washington
2. Vaccine and Infectious Diseases Division; Fred Hutchinson Cancer Research Center; Seattle Washington
Funder
University of Washington Postdoctoral Fellowship in Clinical and Public Health Microbiology (to W.A.G.) in partnership with the University of Washington Molecular Virology Laboratory
Publisher
Wiley
Subject
Infectious Diseases,Virology
Reference13 articles.
1. Optimization of quantitative detection of cytomegalovirus DNA in plasma by real-time PCR;Boeckh;J Clin Microbiol,2004
2. Automation in the virology laboratory: Contribution to improve the viral diagnosis;Cobo;Open Virol J,2012
3. Use of the MagNA pure LC automated nucleic acid extraction system followed by real-time reverse transcription-PCR for ultrasensitive quantitation of hepatitis C virus RNA;Cook;J Clin Microbiol,2004
4. Development of an internal positive control for rapid diagnosis of avian influenza virus infections by real-time reverse transcription-PCR with lyophilized reagents;Das;J Clin Microbiol,2006
5. Marked variability of BK virus load measurement using quantitative real-time PCR among commonly used assays;Hoffman;J Clin Microbiol,2008
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1. The effect of a genetic variant on quantitative real-time PCR in a case of disseminated adenovirus infection;Diagnostic Microbiology and Infectious Disease;2017-09
2. Sample Processing Effect on BK Virus Detection by Real-Time PCR in Urine Samples;Clinical Laboratory;2016
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