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10.1016/j.bios.2021.113218

http://scihub22266oqcxt.onion/10.1016/j.bios.2021.113218
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33878591!8052607!33878591
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suck abstract from ncbi


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pmid33878591      Biosens+Bioelectron 2021 ; 184 (ä): 113218
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  • Sensitive quantitative detection of SARS-CoV-2 in clinical samples using digital warm-start CRISPR assay #MMPMID33878591
  • Ding X; Yin K; Li Z; Sfeir MM; Liu C
  • Biosens Bioelectron 2021[Jul]; 184 (ä): 113218 PMID33878591show ga
  • Quantifying severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in clinical samples is crucial for early diagnosis and timely medical treatment of coronavirus disease 2019. Here, we describe a digital warm-start CRISPR (dWS-CRISPR) assay for sensitive quantitative detection of SARS-CoV-2 in clinical samples. The dWS-CRISPR assay is initiated at above 50 degrees C and overcomes undesired premature target amplification at room temperature, enabling accurate and reliable digital quantification of SARS-CoV-2. By targeting SARS-CoV-2's nucleoprotein gene, the dWS-CRISPR assay is able to detect down to 5 copies/mul SARS-CoV-2 RNA in the chip. It is clinically validated by quantitatively determining 32 clinical swab samples and three clinical saliva samples. Moreover, it has been demonstrated to directly detect SARS-CoV-2 in heat-treated saliva samples without RNA extraction. Thus, the dWS-CRISPR method, as a sensitive and reliable CRISPR assay, facilitates accurate SARS-CoV-2 detection toward digitized quantification.
  • |*Biosensing Techniques[MESH]
  • |*COVID-19[MESH]
  • |CRISPR-Cas Systems/genetics[MESH]
  • |Clustered Regularly Interspaced Short Palindromic Repeats[MESH]
  • |Humans[MESH]
  • |Nucleic Acid Amplification Techniques[MESH]
  • |RNA, Viral[MESH]


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