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. 2021 Mar 19;59(4):e02403-20. doi: 10.1128/JCM.02403-20

FIG 1.

FIG 1

(A) PEARL workflow. (B) Comparative RT-qPCR analysis of the levels of SARS-CoV-2 nucleocapsid (N1) and RNase P RNA sequences in deidentified SARS-CoV-2-positive and -negative clinical specimen samples after RNA extraction using PEARL or an RNA extraction kit (QIAamp Mini Elute virus spin kit) in nasopharyngeal swab samples. Dotted lines indicate a limit of detection of 36 cycles. We obtained Cq values for N1 below our limit of detection in 9 negative samples out of 67. No Cq values were obtained for N1 in the remaining 58 samples. Data points correspond to the reciprocal of the Cq value (1/Cq), which is directly proportional to input RNA. P values and Spearman’s correlation coefficient (ρ) are shown.