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. 2017 Feb 13;12(2):e0171435. doi: 10.1371/journal.pone.0171435

Table 1. Sequencing information and total number of SNVs found in the variant calling analysis for the different cell line experiments.

Cell line Replicates Read design Total reads Total SNVs SNVs per 106 reads
COLO205 3 50 x 1 89 964 067 38 777 431
DLD1 2 69 x 1 37 087 864 72 203 1947
HCT116a 3 100 x 2 98 756 403 177 948 1802
HCT116b 3 50 x 1 96 249 743 44 231 460
HCT15 3 50 x 1 97 492 596 55 195 566
HKE3 4 125 x 2 255 394 483 670 153 2624
HT29 3 50 x 1 87 846 283 38 456 438
RKO 3 100 x 2 103 479 468 250 042 2416