Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
6133912 | Journal of Virological Methods | 2014 | 10 Pages |
Abstract
Luminex® technology, quantitative sequencing and quantitative RT-PCR (qRT-PCR) were compared in regard to specificity, sensitivity and accuracy for quantitation of wildtype and genetically marked viruses in mixed samples based on RNA obtained from samples of known viral titers. Although Luminex® technology and quantitative sequencing provided semi-quantitative or qualitative measurements, a sequence-specific primer extension approach using a specific reverse primer set in singleplex qRT-PCR demonstrated the best quantitation and specificity in the detection of RNA from wildtype and mutant viruses.
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Authors
Gabriella Worwa, Christy C. Andrade, Tara C. Thiemann, Bborie Park, Payal D. Maharaj, Michael Anishchenko, Aaron C. Brault, William K. Reisen,