IT
- Algorithms
- Billing code
- Biomarker
- Cancer of Unknown Primary
- cfDNA
- DNA
- Education
- End of Treatment
- GENAYA project
- Hartwig Medical Database
- Hartwig Medical Foundation
- Innovation
- IT
- Lab process
- Learning healthcare system
- Molecular diagnostics
- OncoAct
- oncoanalyser
- Participating hospitals
- Patients' stories
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- Quality
- Rare cancers
- Re-use data
- Research
- Scientific publications
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- Uncategorized
- Whole genome sequencing
- Working in the cloud
Catalog makes Hartwig Medical Database easily searchable
29-09-2023
Hartwig Medical Foundation maintains a catalog of the Hartwig Medical Database with whole-genome data on full tumor genomes: https://catalog.hartwigmedicalfoundation.nl. The …
Collaboration between Hartwig and CKB makes both parties stronger
13-06-2023
Hartwig Medical Foundation has worked with The Jackson Laboratory (JAX) Clinical Knowledgebase (CKB) team since 2020, to the benefit of …
Blogs
Expansion of the Hartwig Client Portal: registration becomes easier, safer, and smarter
07-08-2026
The expansion of the Hartwig Client Portal marks another important step in further digitizing the collaboration between Hartwig Medical Foundation …
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How do you analyze 8,000 Tumor/Normal genomes in under two months?
06-03-2026
It has been a long time coming: Hartwig Medical Foundation has transitioned to the GRCh38 (hg38) reference genome! For years, …
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It is important to unravel the DNA in rare types of cancer; 21% of patients with cancer have a rare form.
Internist-oncologist and Professor of Rare Cancers at Radboudumc