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Table 1 Methodological comparison of RPA-PfAgo and nested PCR with Sanger sequencing

From: Rapid and supersensitive allele detection of Plasmodium falciparum chloroquine resistance via a Pyrococcus furiosus argonaute-triggered dual-signal biosensing platform

Haplotype

Method

Sensitivity (%)

Specificity (%)

False negative (%)

False positive (%)

Nested PCR with Sanger sequencing

RPA-PfAgo

N (%)

95% CI

N (%)

95% CI

CVMNK

55

55

100

0.9187–1

100

0.8587–1

0.00

0.00

CVIET

19

19

100

0.7908–1

100

0.9315–1

0.00

0.00

CV M/I N/E K/T

11

11

100

0.6786–1

100

0.9385–1

0.00

0.00

Total

85

85

100

0.9461–1

100

NaN

0.00

0.00