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Table 2 Effects of submitting multiple and individual pooled BAM files to each program

From: Evaluation of variant detection software for pooled next-generation sequence data

a

Group Size

Sen%

FP%

BA%

SD%

CRISP-2 pools

97.8

10.5

93.7

95.3

CRISP-4 pools

96.1

7.5

94.3

91.6

CRISP-8 pools

97.2

7.4

94.9

94.1

SNVer-1 pool

72.4

3.3

84.6

52.9

SNVer-2 pools

71.4

3.3

84.1

51

SNVer-4 pools

70.4

3.3

83.6

49

SNVer-8 pools

69.4

3.2

83.1

47.1

VarScan-1 pool

29.3

0.1

64.6

0.1

VarScan-2 pools

29.3

0.1

64.6

0.1

VarScan-4 pools

29.3

0.1

64.6

0.1

VarScan-8 pools

29.2

0.1

64.5

0.1

GATK-1 pool

98.2

9.1

94.6

95.9

GATK-2 pools

98.2

9

94.6

95.8

GATK-4 pools

98.1

8.6

94.7

95.5

GATK-8 pools

98

8.5

94.7

95.1

b

Group Size

Sen%

FP%

BA%

SD%

CRISP-2 pools

97.1

4.1

96.5

93.2

CRISP-4 pools

92.2

4

94.1

83.4

SNVer-1 pool

74.4

1

86.7

53.6

SNVer-2 pools

73.7

1

86.3

52.5

SNVer-4 pools

72.8

1

85.9

50.8

VarScan-1 pool

41

0

70.5

3.1

VarScan-2 pools

41

0

70.5

3.1

VarScan-4 pools

40.9

0

70.5

3.1

GATK-1 pool

98

0.2

98.9

95.2

GATK-2 pools

97.9

0.2

98.9

95.1

GATK-4 pools

97.9

0.2

98.9

95

  1. In (a), all values were calculated using eight ClinSeq samples per pool with 35.1x average total coverage (50 % of typical full coverage for each sample). In (b), all values were calculated using four Thousand Genomes samples per pool with 21.0x average total coverage (50 % of typical full coverage for each sample)