| Popis: |
Supplementary Tables S1-S8 show the samples used for study (Table S1), the somatic single nucleotide variants, small insertions and small deletions (Table S2), the somatic copy number alterations anallyzed (Table S3), the gene list used to analyze somatic mutations (Table S4), putative driver genes, immunotherapy related genes, and mutation-targeted therapy genes affected by mutations in each case (Table S5), mutation signatures detected with a cosine score {greater than or equal to}0.80 (Table S6), Jaccard similarity coefficients (Table S7), and putative neoantigens in each case (Table S8). |
