Table 6 Comparison of sensitivity and specificity of SARS-CoV 2 detection in respiratory samples using Emergency Use Authorization (EUA) PCR kits and the assay developed in this study.

From: Validation of real-time RT-PCR for detection of SARS-CoV-2 in the early stages of the COVID-19 outbreak in the Republic of Korea

This study

PowerCheck 2019-nCoV

Allplex 2019-nCoVAssay

DiaPlexQ Novel Coronavirus

STANDARD M nCoV Real-Time Detection kit

Real-Q 2019-nCoV Detection kit

Pos

Neg

Inc

Pos

Neg

Inc

Pos

Neg

Inc

Pos

Neg

Inc

Pos

Neg

Inc

Pos

54

53

 

1*

54

  

54

  

54

  

54

  

Neg

50

 

50

  

50

  

50

  

50

  

50

 

Inc

1

  

1

  

1

  

1

  

1

  

1

Sensitivity¶ (%)

 

98.2

98.2

98.2

98.2

98.2

Specificity# (%)

 

100

100

100

100

100

  1. *Inconsistent (Inc) results in one kit were confirmed by further examination to be an inconclusive case and not a false case.
  2. ¶95% confidence interval: 90.4 ~ 99.7%.
  3. #95% confidence interval: 92.9 ~ 100%.