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- W4200369156 abstract "The global SARS-CoV-2 pandemic requires a rapid, reliable, and user-friendly diagnostic test to help control the spread of the virus. Reverse transcription and quantitative PCR (RT-qPCR) is currently the gold standard method for SARS-CoV-2 detection. Here, we develop a protocol based on reverse transcription loop-mediated isothermal amplification (RT-LAMP) and demonstrate increased sensitivity of this technique using fresh RNA extracts compared to RNA samples subjected to freezing/thawing cycles. We further compare RT-LAMP to RT-qPCR and demonstrate that the RT-LAMP approach has high sensitivity in fresh RNA extracts and can detect positive samples with Ct values between 8 and 35." @default.
- W4200369156 created "2021-12-31" @default.
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- W4200369156 date "2021-12-14" @default.
- W4200369156 modified "2023-10-18" @default.
- W4200369156 title "High-quality RNA improves sensitivity of SARS-CoV-2 detection by colorimetric RT-LAMP" @default.
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- W4200369156 doi "https://doi.org/10.1177/15353702211054768" @default.
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