We generated paired-end panel seq data from 89 ccRCC patients, including two spatially separated primary tumor biopsies, and a matched normal sample per patient. A selection of 826 genes frequently mu
In order to determine the mutational burden in highly variable and lowly variable breast cancer cells, we quantified single-nucleotide variant and insertion-deletion mutation frequencies from populati
Sequencing of LCM-derived microbiopsies from 10 women who underwent reduction mammoplasty. Goal to assess the mutational burden, spectrum, and clonal dynamics within the tissue. Exome data will be use
