The usage of expressed somatic mutations may have a unique advantage in identifying active cancer driver mutations. However, accurately calling mutations from RNA-seq data is difficult due to confound
Table with read numbers for each clone for experiment 5 shown in Table 1 of the paper. Further Tabs in the file include the respective DeSeq2 statistics for each sampled timepoint.
The contents of this dataset were created de novo starting from RNA-seq data downloaded from Gene Expression Omnibus (GEO), with a pipeline specifically written to generate results starting with seque
