Laurens Beerepoot
19-04-2023
In our profession, we need to know everything about the patient, but we also want to know as much as possible about the patient’s tumor.
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Whole genome sequencing to improve individual cancer treatment in Finland
10-07-2020
Since August 2019, Docrates, a private cancer center in Finland, uses the whole genome sequencing test from Hartwig Medical Foundation to …
Erasmus MC Cancer Institute introduces comprehensive DNA testing for CUP cancer patients in EMBRAZE region
01-08-2021
The Erasmus MC Cancer Institute has started using comprehensive DNA testing for carcinoma of unknown primary (CUP) cancer patients in …
Towards a learning healthcare system by broad collaboration
15-09-2022
Developing a new drug is expensive and takes a long time. In addition, there is only a slim chance that …
The number of WGS samples Hartwig Medical Foundation has is quite unique in the research field and is rapidly growing. It amounted to 3.500 samples when we started and it’s already over 5.000 now.
Research Professor ICREA, Barcelona