Table 1.
Depth of coverage a | Read length b | Insert size c | Reference covered d | |
---|---|---|---|---|
Breeding panel 1 red | 24.72 x | 150 | 500 | 66.5 |
Breeding panel 1 green | 23.60 x | 150 | 500 | 62.0 |
Breeding panel 2 red | 25.60 x | 150 | 500 | 64.4 |
Breeding panel 2 green | 25.08 x | 150 | 500 | 63.0 |
Breeding panel 3 red | 19.41 x | 150 | 500 | 47.2 |
Breeding panel 3 green | 23.45 x | 150 | 500 | 62.9 |
Breeding panel 2 red total | 73.27 x | 100/150 | 450/500 | 90.0 |
Breeding panel 2 green total | 69.69 x | 100/150 | 450/500 | 89.3 |
Superpool red | 76.14 x | 100/150 | 450/500 | 91.7 |
Superpool green | 78.41 x | 100/150 | 450/500 | 91.9 |
a Mean number of uniquely mapped reads covering each base of the reference sequence
b Length of the sequenced reads in base pairs; if more than one number is shown, two datasets with differing read length were merged; all generated as paired ends (PE)
c Targeted length of the PE sequenced fragments in base pairs; if more than one number is shown, two datasets with differing read length were merged
d Percentage of the reference sequence with more than 15 fold read coverage