Researcher
Joris Vermeesch
- Disciplines:Genetics, Systems biology, Medical imaging and therapy, Molecular and cell biology, Other paramedical sciences
Affiliations
- Laboratory for Cytogenetics and Genome Research (Division)
Responsible
From1 Jan 2008 → Today - Department of Human Genetics (Department)
Member
From27 Sep 2004 → Today
Infrastructure
1 - 3 of 3
- PACBIO; third -generation sequencing platform with Single Molecule Real Time technology (SMRT) (Consortium coordinator)
- EU-Genomics: EU Infrastructure for genomic analysis. (Consortium coordinator)
- Belgian Genome Biobank (Consortium coordinator)
Projects
1 - 10 of 63
- Impact of ccfDNA on clinical decision making in NEN patientsFrom8 Jan 2024 → TodayFunding: Own budget, for example: patrimony, inscription fees, gifts
- Towards a better understanding of incidental cancer detection upon non-invasive prenatal testingFrom17 Sep 2023 → TodayFunding: Own budget, for example: patrimony, inscription fees, gifts
- Mapping the functional role of the low copy repeats in the phenotypic variability of the 22q11.2 Deletion SyndromeFrom27 Jan 2023 → TodayFunding: Own budget, for example: patrimony, inscription fees, gifts
- Impact of ccfDNA on clinical decision making in NEN patientsFrom1 Jan 2023 → TodayFunding: Foundations, funds and other with scientific goal
- Sabbatical Joris Vermeesch: Computational analyses of large sequencing data setsFrom1 Oct 2022 → 30 Apr 2023Funding: BOF - mobility
- SymBioSys: Computationally mapping genomic heterogeneity from long read sequencing dataFrom1 Oct 2022 → TodayFunding: BOF - projects
- Implementation and validation of liquid biopsies as a diagnostic tool for early breast cancer detection in South African black womenFrom1 Sep 2022 → TodayFunding: VLIR-UOS South Initiatives
- Belgian Genome BiobankFrom1 May 2022 → TodayFunding: FWO Large scale research infrastructure
- Remote allograft rejection diagnosis by epigenetic changes in circulating cell-free DNA in kidney transplanted patients.From1 Feb 2022 → TodayFunding: FWO Strategic Basic Research Grant
- Mapping the role of the low copy repeats in the phenotypic variability of the 22q11 Deletion SyndromeFrom1 Jan 2022 → TodayFunding: FWO research project (including WEAVE projects)
Publications
31 - 40 of 400
- Machine learning-based detection of immune-mediated diseases from genome-wide cell-free DNA sequencing datasets(2022)
Authors: Huiwen Che, Lore Lannoo, Nathalie Brison, Kris Van Den Bogaert, Koenraad Devriendt, Ellen De Langhe, Séverine Vermeire, Bram Verstockt, Kristel Van Calsteren, Joris Vermeesch
- ESHRE survey results and good practice recommendations on managing chromosomal mosaicism(2022)
Authors: Joris Vermeesch
- Pan-Cancer Detection and Typing by Mining Patterns in Large Genome-Wide Cell-Free DNA Sequencing Datasets(2022)
Authors: Huiwen Che, Tatjana Jatsenko, Liesbeth Lenaerts, Nathalie Brison, Kris Van Den Bogaert, Ruben Heremans, Agnieszka Wozniak, Christophe Dooms, Els Wauters, Sigrid Hatse, et al.
Pages: 1164 - 1176 - A normative chart for cognitive development in a genetically selected population.(2022)
Authors: Ann Swillen, Joris Vermeesch, Maude Schneider
Pages: 1379 - 1386 - A review of normative documents on preimplantation genetic testing: Recommendations for PGT-P(2022)
Authors: Maria Siermann, Olga Tsuiko, Joris Vermeesch, Pascal Borry
Pages: 1165 - 1175 - Augmenting THerapeutic Effectiveness Through Novel Analytics (ATHENA) - A Public and Private Partnership Project Funded by the Flemish Government (VLAIO).(2022)
Authors: Ashkan Pirmani, Edward De Brouwer, Murat Akand, Frank Van der Aa, Joris Vermeesch, Roel Wuyts, Yves Moreau
Pages: 829 - 833 - Commentary on Multiple Copy Number Variants Detected by Noninvasive Prenatal Testing Comment(2022)
Authors: Joris Vermeesch, Liesbeth Lenaerts
Pages: 634 - 634 - Genomic profiling of cell-free DNA(2022)
Authors: Huiwen Che, Joris Vermeesch, Frédéric Amant, Bernard Thienpont
- Optimizing the diagnostic workflow for acute lymphoblastic leukemia by optical genome mapping(2022)
Authors: Jolien De Bie, Sofie Demeyer, Jan Cools, Kim De Keersmaecker, Joris Vermeesch, Johan Maertens, Heidi Segers, Lucienne Michaux, Barbara Dewaele
Pages: 548 - 561 - The Hunt for the Chromosome 22q11.2 Deletion Syndrome Schizophrenia Genes(2022)
Authors: Joris Vermeesch
Pages: 692 - 693
Patents
1 - 8 of 8
- Method for analysing cell-free nucleic acids (Inventor)
- Method for analysing cell-free nucleic acids (Inventor)
- High-throughput genotyping by sequencing low amounts of genetic material (Inventor)
- Method for analysing cell-free nucleic acids (Inventor)
- Haplotyping and copy number typing using polymorphic variant allelic frequencies (Inventor)
- Methods for haplotyping single cells (Inventor)
- HAPLOTYPING AND COPY NUMBER TYPING USING POLYMORPHIC VARIANT ALLELIC FREQUENCIES (Inventor)
- HIGH-THROUGHPUT GENOTYPING BY SEQUENCING LOW AMOUNTS OF GENETIC MATERIAL (Inventor)