Skip to main content

Table 1 Comparison of different variant callers using real data on chromosome 21

From: vi-HMM: a novel HMM-based method for sequence variant identification in short-read data

 

SNP

INDEL

Caller

Sensitivity (%)

Precision (%)

F1 score (%)

Sensitivity (%)

Precision (%)

F1 score (%)

15 ×

 vi-HMM

95.11

99.62

97.31

91.95

90.18

91.06

 FreeBayes

94.82

91.61

93.18

88.93

74.79

81.25

 Platypus

90.97

99.84

95.20

93.74

70.03

80.17

 SAMtools

98.66

99.56

99.11

83.79

95.45

89.24

 VarScan

76.31

99.87

86.51

74.00

99.44

84.85

30 ×

 vi-HMM

99.81

99.44

99.63

95.22

95.62

95.42

 FreeBayes

95.80

95.48

95.64

90.36

76.41

82.80

 Platypus

92.92

99.73

96.21

95.67

69.54

80.54

 SAMtools

99.64

99.62

99.62

87.84

93.23

90.46

 VarScan

97.93

99.82

98.86

88.59

99.37

93.67

54 ×

 vi-HMM

99.95

99.18

99.56

95.61

96.09

95.85

 FreeBayes

95.88

96.90

96.39

90.77

77.27

83.48

 Platypus

92.97

99.63

96.18

96.06

69.11

80.38

 SAMtools

99.70

99.61

99.65

88.99

90.53

89.75

 VarScan

99.53

99.77

99.65

91.67

99.24

95.31