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Table 2 Basic statistics of whole exome sequences generated by the Ion Proton sequencer

From: Validation of multiple single nucleotide variation calls by additional exome analysis with a semiconductor sequencer to supplement data of whole-genome sequencing of a human population

Samples

Total bases (GB)

Average depth

Average read length (bp)

Aligned bases (GB)

Aligned bases (%)

SNPs

01_1

6.77

65.9

121

6.40

96

58037

01_2

8.37

85.1

127

7.90

95

02

10.8

122

142

10.4

98

69667

03_1

8.24

78.5

144

8.00

97

67493

03_2

8.93

93.0

139

8.60

97

04

11.2

126

149

10.8

97

53811

05

12.2

147

148

11.9

98

46923

06

9.25

94.5

149

9.00

98

52516

07

12.1

135

149

11.8

98

53993

08

10.7

103

138

10.3

96

52243

09

10.9

121

137

10.5

97

50166

10

11.6

136

142

11.3

97

50781

11

10.4

85.5

134

10.0

97

67810

12

11.3

133

146

10.9

97

54335

Mean

10.2

109

140

9.84

97.0

56481.25

%CV

15

23

5.9

16

0.87

12.94

  1. Two independent runs (indicated as _1 and 2) were performed for Samples 01 and 03.