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10.7717/peerj.9278

http://scihub22266oqcxt.onion/10.7717/peerj.9278
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32547882!7275676!32547882
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suck abstract from ncbi


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pmid32547882      PeerJ 2020 ; 8 (ä): e9278
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  • Real-time reverse transcription loop-mediated isothermal amplification for rapid detection of SARS-CoV-2 #MMPMID32547882
  • Lau YL; Ismail I; Mustapa NI; Lai MY; Tuan Soh TS; Hassan A; Peariasamy KM; Lee YL; Chong YM; Sam IC; Goh PP
  • PeerJ 2020[]; 8 (ä): e9278 PMID32547882show ga
  • BACKGROUND: Highly sensitive real-time reverse transcription polymerase chain reaction (RT-qPCR) methods have been developed for the detection of SARS-CoV-2. However, they are costly. Loop-mediated isothermal amplification (LAMP) assay has emerged as a novel alternative isothermal amplification method for the detection of nucleic acid. METHODS: A rapid, sensitive and specific real-time reverse transcription LAMP (RT-LAMP) assay was developed for SARS-CoV-2 detection. RESULTS: This assay detected one copy/reaction of SARS-CoV-2 RNA in 30 min. Both the clinical sensitivity and specificity of this assay were 100%. The RT-LAMP showed comparable performance with RT-qPCR. Combining simplicity and cost-effectiveness, this assay is therefore recommended for use in resource resource-limited settings.
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