Skip to main content

Table 1 Sequencing and coverage statistics for all paired-read libraries

From: Improving mammalian genome scaffolding using large insert mate-pair next-generation sequencing

Library name*

Sequenced pairs

Non-duplicate pairs (%)

Unique, consistently mapped pairs (%)

Median insert size (bp)

Physical coverage (x-fold)

5 M reads coverage (x-fold)

PCR cycles **

Relative complexity ***

inconsistent pairs forming clusters

inconsistent inter-chromosomal pairs forming clusters

PE

160 M

151 M (95%)

131 M (87%)

166

8.5

0.34

5

>131 M

9.5%

2.0%

3 kb

17.7 M

16.3 M (92%)

15.2 M (93%)

3,208

50

6

14

4.6 M

24.0%

3.2%

5 kb_a

11.9 M

6.0 M (51%)

5.5 M (92%)

5,696

11

10.1

18

4.7 M

46.5%

3.7%

5 kb_b

16.7 M

14.7 M (88%)

14.0 M (95%)

5,811

28

10.1

13

>16.7 M

47.5%

4.6%

8 kb_a

20.8 M

8.6 M (41%)

7.8 M (91%)

8,293

25

16.2

14

5.7 M

58.4%

6.9%

8 kb_b

11.8 M

11.2 M (95%)

10.6 M (95%)

8,160

34

16.2

13

>11.8 M

50.6%

5.5%

15 kb_a

31.7 M

1.7 M (5%)

1.0 M (60%)

14,561

6

30.3

21

0.6 M

60.8%

7.6%

15 kb_b

11.6 M

1.6 M (14%)

1.2 M (73%)

13,556

7

30.3

21

0.7 M

23.2%

3.2%

20 kb

13.3 M

6.7 M (51%)

5.9 M (87%)

19,375

48

40.5

14

4.9 M

41.8%

4.7%

25 kb

56.9 M

2.3 M (4%)

1.1 M (49%)

25,871

11

50.6

17

0.7 M

51.9%

5.4%

TOTAL

352.4 M

220.1 M (62%)

193.3 M (88%)

 

228.5

     
  1. * The _b samples are retrieved from a replicate experiment using an independent DNA isolate from the same animal.
  2. ** Number of PCR cycles required to retrieve sufficient library molecules in the final adapter-mediated PCR.
  3. *** Complexity is defined as minimal sequencing depth (in million clones) at which over half of the pairs are clonal.