Skip to main content

Table 1 Summary of the read mapping in DNA sequencing

From: Bacillus subtilis genome vector-based complete manipulation and reconstruction of genomic DNA for mouse transgenesis

 

BAC1

 

BAC2

 

Tg110CIBS

 

Tg220CISP

 

Tg250SB

 

# reads

%

# reads

%

# reads

%

# reads

%

# reads

%

Total reference length

114,183

 

220,003

 

115,372

 

222,532

 

254,658

 

Mapped reads

8,341,236

91.1

8,604,424

95.9

1,028,479

2.7

1,737,127

5.2

504,510

5.8

Unmapped reads

814,824

8.9

370,790

4.1

37,166,207

97.3

31,564,383

94.8

8,227,736

94.2

Reads in pairs

8,327,110

91.0

8,594,722

95.8

960,578

2.5

1,714,062

5.2

498,152

5.7

Broken paired reads

14,126

0.2

9,702

0.1

67,901

0.2

23,065

0.1

6,358

0.1

Total number of reads

9,156,060

 

8,975,214

 

38,194,686

 

33,301,510

 

8,732,246

 

Total read length (Mb)

915.6

 

897.5

 

3,819.5

 

3,330.2

 

873.2

 

Fraction of reference covered

1.00

 

1.00

 

1.00

 

1.00

 

1.00

 

Minimum coverage

241

 

125

 

28

 

22

 

6

 

Maximum coverage

15147

 

5631

 

2211

 

1514

 

574

 

Average coverage

7100.7

 

3812.3

 

851.5

 

752.2

 

191.0

 
  1. Reads obtained from the Illumina Genome Analyzer IIx were analyzed and mapped to each reference sequence using CLC Genomics Workbench 5.5 (CLC Bio). The number of mapped reads in each sample was enough to evaluate mutations. Analyzed DNA samples are follows: original BAC clones of BAC1 and BAC2 and BGM clones of Tg110CIBS, Tg220CISP and Tg250SB.