Additional file 2: Table S2. List of copy number variation regions (CNVR) consistently detected with PennCNV and QuantiSNP in 1036 Murciano-Granadina goats.
Low coverage (~0.1X) whole genome sequencing from thymic lymphoma samples from Caph2nes/nes and Caph2nes/nes, P53-/- mice. Used to identify Copy Number Abberations.
D.SKY plot show the somatic copy number alterations (sCNAs) in cancer cell-line. For this breast cancer cell-line HCC1143, the D.SKY clearly showed the loss of chr8p and gain of chr8q, a pattern recur
Additional file 1: Table S1. Number of variants predicted for each individual. This table provides details on each sequenced animal: sequencing coverage, statistics about reads number, its parents if
