Table 2 Methods comparison for calculating sensitivity from empirical test based on Qvarnstrom real-time PCR-positive sample (as gold standard method).

From: Efficient nested-PCR-based method development for detection and genotype identification of Acanthamoeba from a small volume of aquatic environmental sample

Methods

Sensitivity

Specificity

Accuracy

D.C

Culture

Total

D.C

Culture

Total

D.C

Culture

Total

Genotyping PCR (M1)

52% (11/21)

62% (8/13)

54% (13/24)

91% (10/11)

95% (18/19)

85% (7/8)

66% (21/32)

81% (26/32)

63% (20/32)

Optimal modified genotyping nested PCR (M3)

95% (20/21)

100% (13/13)

96% (23/24)

64% (7/11)

95% (18/19)

50% (4/8)

84% (27/32)

97% (31/32)

84% (27/32)

Scheikl genotyping nested PCR (M4)

74% (17/23)

85% (11/13)

75% (18/24)

64% (7/11)

95% (18/19)

50% (4/8)

75% (24/32)

91% (29/32)

69% (22/32)

Genotyping semi-nested PCR (M5)

95% (20/21)

100% (13/13)

96% (23/24)

73% (8/11)

95% (18/19)

63% (5/8)

88% (28/32)

97% (31/32)

88% (28/32)