Table 1.
reference genome | number of aligned reads, millions | per cent endogenous reads aligned | length of aligned reads, bp | average coverage depth | number of genome positions covered, ≥1× | number of variant sites | duplication, % of original aligned read pool |
---|---|---|---|---|---|---|---|
nuclear | 2.58 (2.63) | 16.77 (17.27) | 56.34 (11.21) | 0.136 (0.141) | 123 755 026 (117 895 958) | 13 883 (26 877) | 4.74 (2.85) |
mitochondrial | 0.01 (0.01) | 0.06 (0.06) | 58.23 (11.90) | 33.39 (37.18) | 16 104 (3649) | 38.09 (20.41) | 20.13 (16.46) |