| Literature DB >> 35554906 |
Raphael Nyaruaba1,2,3, Xiohong Li1, Caroline Mwaliko2,3,4, Faith Ogolla1,2,3, Changchang Li1,2, Lu Zhao1,2, Hang Yang1, Junping Yu1, Honping Wei5.
Abstract
Droplet digital polymerase chain reaction (ddPCR) is a third generation of PCR that was recently developed to overcome the limitation of direct quantification observed in real-time quantification PCR (qPCR). Recent studies have shown that ddPCR is more sensitive than the gold standard reverse transcription real-time quantitative polymerase chain reaction (RT-qPCR) in detecting severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) samples. In combination with multiplexing, multiple RT-ddPCR assays can be developed to directly quantify different SARS-CoV-2 nucleic acid targets within a single sample, significantly saving on cost and time. Since ddPCR is tolerant to a number of inhibitors unlike qPCR, it can be used to detect and quantify samples from complex environments like wastewater. Here we present three one-step RT-ddPCR protocols on how to develop simplex (one target), duplex (two targets), and triplex probe mix (three targets) assays for SARS-CoV-2 detection and quantification. The assays can be used for diagnosis or other research-related SARS-CoV-2 applications.Entities:
Keywords: COVID-19; Detection; Droplet digital; Polymerase chain reaction; Quantification; RT-ddPCR; SARS-CoV-2; qPCR
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Year: 2022 PMID: 35554906 DOI: 10.1007/978-1-0716-2111-0_10
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745