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. 2022 Nov 3;9(3):e165. doi: 10.14440/jbm.2022.391

Table 1.

Consensus-making statistics for five dilutions of a D. magna gDNA-Seq library.

Dataset* Dilution (amol of DNA used as input)
10a 50a 100a 150a 1f Pooled**
Full Input read pairs (×106) 51.7 88.4 72.9 115.5 107.1 435.6
Total DCS 655072 902770 422378 493156 37860 2511236
Total DCS bases (×106) 77.0 114.0 45.0 57.0 46.0 339.0
Filtered DCS 148771 171002 152820 153884 9663 636140
(% of total DCS) (22.7) (18.9) (36.2) (31.2) (25.5) (25.3)
Filtered DCS bases (×106) 11.1 15.3 12.3 13.7 1.0 53.4
(% of total DCS bases) (14.4) (13.4) (27.3) (24.0) (2.2) (17.8)
Avg filtered DCS length (bp) 74 89 80 89 99 83
Filtered DCS bases in masked genome (×106) 4.79 6.71 5.30 6.00 0.39 23.19
Downsampled Input read pairs (×106) 50.0 50.0 50.0 nd 50.0 nd
Total DCS 644041 308193 191903 nd 8002 nd
Total DCS bases (×106) 42.8 24.2 14.0 nd 0.6 nd
Filtered DCS 147195 100136 76179 nd 1846 nd
(% of total DCS) (22.9) (32.5) (39.7) nd (23.1) nd
Filtered DCS bases (×106) 10.9 9.5 6.2 nd 0.2 nd
(% of total DCS bases) (25.5) (39.4) (44.3) nd (28.9) nd
Avg filtered DCS length (bp) 74 95 81 nd 100 nd
Filtered DCS bases in masked genome (×106) 4.71 4.15 2.64 nd 0.07 nd
Peak read family size 8 2 2 nd 2 nd

*Dataset: statistics are shown for the analysis pipeline run on the full set of read pairs generated per library (“Full”) or on libraries downsampled to 50 M read pairs each (“Downsampled”).

**Pooled: Reads from all five diluted libraries were combined and analyzed together (full datasets only). The pooled dataset was used to identify the final set of 14 putative somatic mutations described below.

nd, no data.