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Ianthe van Belzen

PhD student
Ianthe van Belzen
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.

  • Systematic discovery of gene fusions in pediatric cancer by integrating RNA-seq and WGS

    • jul. 2023
    • Ianthe A E M, van Belzen, et al
    • BMC Cancer
  • NTRK rearrangements in a subset of NF1-related malignant peripheral nerve sheath tumors as novel actionable target

    • jan. 2023
    • L S, Hiemcke-Jiwa, et al
    • Acta Neuropathologica
  • Molecular Characterization Reveals Subclasses of 1q Gain in Intermediate Risk Wilms Tumors

    • okt. 2022
    • Ianthe A.E.M., van Belzen, et al
    • Cancers
  • Structural variant detection in cancer genomes

    • mrt. 2021
    • Ianthe A E M, van Belzen, et al
    • NPJ precision oncology
  • Chromatin accessibility landscape of pediatric T-lymphoblastic leukemia and human T-cell precursors

    • sep. 2020
    • Büşra, Erarslan-Uysal, et al
    • EMBO Molecular Medicine
View all publications