Additional file 2 of Deep whole genome sequencing identifies recurrent genomic alterations in commonly used breast cancer cell lines and patient-derived xenograft models

Additional file 2: Table S1. Summary of total number of variants in difference cell line models and PDXs from whole genome sequencing. Table S2. List of the 635 additional missense mutations in MCF7 compared to Ben-David et al. Table S3. The complete list of variants in the non-coding regions in these cell lines models. Table S4. Weights of mutational signatures identified from DeconstructSigs for each of the cell lines. Table S5. List of structural variants identified in the cell line models.