Table 2 Sensitivity, specificity, predictive agreement and DOR characterizations of SHERLOCK detection of SARS-CoV-2 RNA compared with RT–qPCR

From: Clinical validation of a Cas13-based assay for the detection of SARS-CoV-2 RNA

  

All samples

Samples within SHERLOCK LoD

SHERLOCK lateral-flow readout

Sensitivity

87.65%

97.14%

(95% CI)

(78.47–93.92)

(90.06–99.65)

Specificity

100.00%

100.00%

(95% CI)

(95.07–100.00)

(95.07–100.00)

PPA

100.00%

100.00%

(95% CI)

(94.94–100.00)

(94.72–100.00)

NPA

87.95%

97.33%

(95% CI)

(78.96–94.04)

(90.70–99.68)

ln(DOR)

6.91

8.30

(95% CI)

(4.05–9.76)

(5.25–11.40)

SHERLOCK fluorescence readout

Sensitivity

96.30%

100.00%

(95% CI)

(89.56–99.23)

(94.87–100.00)

Specificity

100.00%

100.00%

(95% CI)

(95.07–100.00)

(95.07–100.00)

PPA

100.00%

100.00%

(95% CI)

(95.38–100.00)

(94.87–100.00)

NPA

96.05%

100.00%

(95% CI)

(88.89–99.18)

(95.07–100.00)

ln(DOR)

8.10

9.94

(95% CI)

(5.12–11.08)

(6.01–13.87)

  1. Values calculated from 154 samples used for clinical validation. CI, confidence interval; PPA, positive predictive agreement; NPA, negative predictive agreement; ln(DOR), the natural logarithm of diagnostic odds ratio.