Table 3

Read-depth coverage in the whole dataset and in the significant sets of exons

Single-copy

Duplicated

All




HS

MMU

Both

HS

MMU

Both

HS

MMU

Both


Initial set (178,295 exons)

Exon

4.18

4.23

8.41

17.16

11.53

28.69

4.96

4.66

9.62

Intron

4.19

3.94

8.13

16.84

10.82

27.67

4.95

4.35

9.29

Total

4.2

4.03

8.23

17

11.16

28.16

4.96

4.45

9.42

Significant set (74 exons)

Exon

4.23

7.38

11.61

36.39

24.04

60.43

22.05

16.61

38.66

Intron

4.17

5.66

9.83

35.22

18.75

53.97

21.37

12.91

34.29

Total

4.16

6.01

10.18

35.96

20.01

55.97

21.78

13.77

35.55


Coverage is defined as the average number of high-quality reads aligned per nucleotide. HS corresponds to the human reads, while MMU to macaque reads.

Lorente-Galdos et al. Genome Biology 2013 14:R9   doi:10.1186/gb-2013-14-1-r9

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