Hartwig Medical Foundation analyses tumour biopsies by whole genome sequencing for precision medicine diagnostics. They generate and processes this data using state of the art bioinformatics and return actionable information to the treating specialist to support treatment decision making. In addition, the obtained genetic data is combined with clinical and treatment data into the largest database world wide of whole genome sequenced metastatic cancer patients and made available for research for improving future cancer care. Expertise: bioinformatics, whole genome sequencing, data science.