| dc.rights.license | CC-BY-NC-ND | |
| dc.contributor.advisor | Cuppen, Edwin | |
| dc.contributor.author | Jongsma, Siem | |
| dc.date.accessioned | 2025-05-01T00:02:09Z | |
| dc.date.available | 2025-05-01T00:02:09Z | |
| dc.date.issued | 2025 | |
| dc.identifier.uri | https://studenttheses.uu.nl/handle/20.500.12932/48896 | |
| dc.description.sponsorship | Utrecht University | |
| dc.language.iso | EN | |
| dc.subject | This thesis explores how whole genome sequencing can be used to improve pharmacogenetic reporting in cancer care by expanding the number of analyzed genes, comparing analysis tools, and identifying new genetic variants to support more personalized and effective treatment recommendations. | |
| dc.title | Investigating the pharmacogenetic reporting potential of diagnostic whole genome sequencing data for cancer patients | |
| dc.type.content | Master Thesis | |
| dc.rights.accessrights | Open Access | |
| dc.subject.courseuu | Bioinformatics and Biocomplexity | |
| dc.thesis.id | 44881 | |
