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Ianthe van Belzen

PhD student
Ianthe van Belzen
Somatic structural variant detection in cancer
Phone 088 97 25 188

We aim to improve the detection of somatic structural variants in cancer with advanced computational techniques. Integration of RNA-seq, WES (whole exome sequencing) and WGS (whole genome sequencing) data from tumor-normal paired samples should improve sensitivity and precision of detection as well as the interpretation of variants for diagnostics and follow-up research.