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NEWS

Whole Genome Sequencing is haalbaar in klinische praktijk

Op 19 september 2020 heeft dr. Kim Monkhorst, patholoog NKI/AVL de interimresultaten van WIDE, waarvan hij samen met prof.dr. Gerrit Meijer hoofdonderzoeker is, op ESMO 2020 gepresenteerd. Met deze resultaten in de hand heeft hij er alle vertrouwen in dat Whole Genome Sequencing (WGS) in de praktijk veilig, goed en snel uitvoerbaar is. De uitslag […]

20 September 2020

NEWS

SAGE: New algorithm for analysis of tumor DNA reveals mutations previously not found

At Hartwig we “analyse sequenced tumor DNA”. This is something we try to continuously improve. These analyses are shared with hospitals to help them find the best treatment for the patient. In addition, we aggregate all these analyses into our database from which we service researchers so that they can improve care for tomorrow’s patients.  […]

23 July 2020

NEWS

Whole genome sequencing to improve individual cancer treatment in Finland

Since August 2019, Docrates, a private cancer center in Finland, uses the whole genome sequencing test from Hartwig Medical Foundation to support personalised treatment for their patients. Juha Kononen, chief physician in personalized oncology at Docrates Cancer Center: ”Hearing Emile Voest speak at a scientific meeting it immediately made sense to me that instead of […]

10 July 2020

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