Table 2. Genome-wide coverage at each sampling proportion for the 29 datasets after Novoalign mapping and subsequent read filtering.
Proportion of reads sampled | Average number of reads | Range | Mean fold coverage |
original | 26,174,727 | 18,832,054–32,733,023 | 0.42X |
0.75 | 19,719,795 | 14,172,672–24,677,526 | 0.31X |
0.5 | 13,206,439 | 9,483,101–16,539,568 | 0.21X |
0.25 | 6,635,982 | 4,761,496–8,317,675 | 0.11X |
0.125 | 3,328,165 | 2,387,989–4,173,351 | 0.053X |
0.0625 | 1,667,889 | 1,196,946–2,091,602 | 0.026X |
0.0312 | 854,222 | 613,083–1,071,927 | 0.014X |