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Table 1 Basic statistics of the whole genome sequences generated by the HiSeq 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

Read 2 %Q30: 100–150 cycles

Aligned bases (GB)

Mapping ratio (%)

SNPs

01

103

33.6

0.740

101

98

3,631,549

02

100

32.4

0.670

97.3

97

3,606,901

03

106

34.3

0.600

97.1

92

3,597,816

04

104

34.0

0.710

101

96

3,625,724

05

96

30.6

0.670

91.4

95

3,601,895

06

99

30.8

0.660

96.0

97

3,604,534

07

96

31.4

0.690

93.9

98

3,588,904

08

97

31.1

0.590

90.2

93

3,598,436

09

104

33.2

0.610

96.8

93

3,603,430

10

96

31.5

0.740

92.6

97

3,601,931

11

106

34.4

0.740

104

98

3,616,799

12

100

31.3

0.520

94.1

94

3,569,104

Mean

101

32.4

0.662

96.3

95.7

3603919

%CV

3.7

4.3

10

4.2

2.2

0.43