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10.1016/j.jviromet.2021.114185

http://scihub22266oqcxt.onion/10.1016/j.jviromet.2021.114185
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34051244!8149472!34051244
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suck abstract from ncbi


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pmid34051244      J+Virol+Methods 2021 ; 295 (ä): 114185
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  • Digital PCR assay for the effective detection of COVID-19 patients with SARS-CoV-2 low viral load #MMPMID34051244
  • Sun Y; Ding C; Chen Q; Xie J; Yu J; Shi Y; Jiang C; Zhang Z; He H; Ge Y; Li W; He J; Gao Y
  • J Virol Methods 2021[Sep]; 295 (ä): 114185 PMID34051244show ga
  • OBJECTIVE: Viral nucleic acid detection by real-time reverse transcription polymerase chain reaction (qPCR) is the current standard method for diagnosis of SARS-CoV-2 infection. However, due to low viral load in some COVID-19 patients, false negative results from this method have been repeatedly reported. METHOD: In this study, we compared the sensitivity and specificity of digital PCR (dPCR) in simulated samples and clinical samples with qPCR assay through a series of vigorous tests. RESULTS: The results showed that dPCR was more sensitive than qPCR especially for samples with low viral load (
  • |*Viral Load[MESH]
  • |COVID-19 Nucleic Acid Testing/*methods[MESH]
  • |COVID-19/*diagnosis/virology[MESH]
  • |Humans[MESH]
  • |RNA, Viral/genetics[MESH]
  • |Real-Time Polymerase Chain Reaction/*methods[MESH]
  • |Recurrence[MESH]
  • |SARS-CoV-2/genetics/*isolation & purification[MESH]


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