Analysis of chromosomal radiosensitivity/instability in triple negative and/or young breast cancer patients and patients with Fanconi anemia from South Africa

Cofunding core facility - UGent NGS Core

CONDITIONAL: COvid-19: iNterplay between genetic preDisposITION and immunologicAl Landscape

Development of an in vivo functional assay to determine the pathogenicity of variants in breast cancer genes

Diagnosing HEreditary predisposition syndromes for Childhood cancer: Implementation in clinical PRactice (DHECIPR)

Familial pancreatic cancer: identifying predisposition genes and developing a clinical path for prevention and treatment exploration

HBOC (Hereditary Breast and Ovarian Cancer), a paradigm shift for counseling and treatment of patients with defects in homologous recombination - an explorative study

Heading towards an in vivo predictive test for personalized ovarian cancer treatment: application of novel therapies in zebrafish patient derived xenografts

In vivo functional evaluation of unclassified variants, found in the breast cancer gene BRCA2, using CRISPR-mediated genome editing in zebrafish

Joint Action on Networks of Expertise

miRNAs as alternative second hits and potential therapeutic targets in hereditary breast cancer

Multi-omics approach to identify pancreatic cancer biomarkers in liquid biopsies of advanced stage patients by pioneering single cell mass spectrometry of CTCs and (epi)genetics characterization of cfDNA

Next generation sequencing in molecular genetics for hereditary breast cancer, an emerging new strategy

Pancreatic cancer: hope to improve prognosis through thorough analysis of DNA and RNA biomarkers for detection and therapy monitoring in liquid biopsies

Pancreatic cancer: hope to improve prognosis through thorough analysis of DNA and RNA markers for diagnosis and therapy monitoring in liquid biopsies

Towards improved genetic diagnosis for hereditary breast and ovarian cancer: evolution and challenges

Unraveling genetic mechanisms in early onset breast cancer

Zebrafish as a model system to evaluate the causality of variants of unknown clinical significance in hereditary breast cancer

Belgian Genome Biobank

Personalized functional genomics in Mendelian diseases: from DNA variants to clinical and bioethical implications

RAPID - Radiosensitivity Analysis for patients with a Primary Immunodeficiency Disease

Immunomonitoring of patients with non-small cell lung carcinoma treated with a tumor mutanome-targeted dendritic cell vaccine