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. 2013 Apr 16;14:257. doi: 10.1186/1471-2164-14-257

Table 1.

Sequencing and coverage statistics for all paired-read libraries

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          

* The _b samples are retrieved from a replicate experiment using an independent DNA isolate from the same animal.

** Number of PCR cycles required to retrieve sufficient library molecules in the final adapter-mediated PCR.

*** Complexity is defined as minimal sequencing depth (in million clones) at which over half of the pairs are clonal.