Researcher
Thierry Voet
- Disciplines:Analysis of next-generation sequence data, Single-cell data analysis, Cell division, Genetics, Transcription and translation
Affiliations
- Laboratory of Reproductive Genomics (Division)
Responsible
From1 Nov 2009 → Today - Laboratory for Cytogenetics and Genome Research (Division)
Member
From1 Apr 2009 → 30 Sep 2009 - Department of Human Genetics (Department)
Member
From1 Oct 1999 → Today
Projects
21 - 30 of 58
- Spectral flowcytometry (Cytek Aurora)From1 Jan 2021 → 31 Dec 2022Funding: BOF - scientific equipment program
- New CRISPR-dCas9 toolbox for diverse in vitro and in situ applications: from detecting cancer to cell heterogeneity during embryogenesisFrom1 Dec 2020 → 31 Oct 2021Funding: BOF - postdoctoral mandates
- The mutational landscape of in vivo and in vitro human embryogenesisFrom1 Oct 2020 → 30 Sep 2023Funding: FWO junior postdoctoral fellowship
- Charting non-small cell lung cancer evolution and heterogeneity through multi-omics analysis and deconvolutionFrom1 Oct 2020 → 1 Jul 2022Funding: FWO senior postdoctoral fellowship
- Resolving cellular heterogeneity and cooperation in human health and disease using highly multiplexed spatial (multi-)omics technologiesFrom25 Sep 2020 → TodayFunding: Own budget, for example: patrimony, inscription fees, gifts
- Development of single-cell multi-omics and spatial analysis pipelinesFrom12 Sep 2020 → 20 Jun 2021Funding: Own budget, for example: patrimony, inscription fees, gifts
- Leveraging droplet microfluidics and nucleic acid engineering for development of a CRISPR-based cell imaging toolboxFrom12 Aug 2020 → TodayFunding: FWO Strategic Basic Research Grant
- Integration of complementary, high throughput single-cell omics with spatial resolution.From1 May 2020 → TodayFunding: FWO Medium Size Research Infrastructure
- Translational research-oriented technology platform for single cell analysisFrom1 May 2020 → TodayFunding: BOF - scientific equipment program
- Understanding chromosome conformation, 3D nuclear DNA architecture and gene expression in human embryogenesis at single-cell resolutionFrom1 Jan 2020 → 31 Dec 2023Funding: FWO research project (including WEAVE projects)
Publications
1 - 10 of 130
- Adipose tissue macrophage dysfunction is associated with a breach of vascular integrity in NASH.(2024)
Authors: Matthias Lannoo, Ellen Deleus, Baki Topal, Tessa Ostyn, Lena Smets, Lukas Van Melkebeke, Tania Roskams, Jef Verbeek, Olivier Govaere, Alejandro Sifrim, et al.
Pages: 397 - 408 - A TCF4-dependent gene regulatory network confers resistance to immunotherapy in melanoma(2024)
Authors: Dennis Pedri, Ewout Landeloos, Yannick Van Herck, Katy Vandereyken, Thierry Voet, Wim Annaert, Diether Lambrechts, Veerle Boecxstaens, Joost van den Oord, Francesca Bosisio, et al.
- A multi-omics genome-plus-transcriptome single-cell atlas of human preimplantation development(2023)
Authors: Elia Fernandez Gallardo, Thierry Voet, Sophie Debrock, Joris Vermeesch
- SINGLE-NUCLEUS GENOME-PLUS-TRANSCRIPTOME SEQUENCING TO UNDERSTAND THE EXTENT AND CONSEQUENCES OF SOMATIC GENOME INSTABILITY IN NEUROTYPICAL AND TAUOPATHY BRAIN(2023)
Authors: Sarah Geurs, Thierry Voet, Bart Dermaut
- Development of novel methods for single-cell whole-genome amplification to study cancer heterogeneity.(2023)
Authors: Koen Theunis, Thierry Voet, Chris Marine
- Pharmacological targeting of netrin-1 inhibits EMT in cancer(2023)
Authors: Alejandro Sifrim, Thierry Voet
Pages: 402 - + - Methods and applications for single-cell and spatial multi-omics(2023)
Authors: Katy Vandereyken, Alejandro Sifrim, Bernard Thienpont, Thierry Voet
Pages: 494 - 515 - Dedicated macrophages organize and maintain the enteric nervous system(2023)
Authors: Elodie Modave, Marcello Delfini, Nathalie Stakenborg, Tobie Martens, Katy Vandereyken, Alejandro Sifrim, Gianluca Matteoli, Pieter Vanden Berghe, Thierry Voet, Guy Boeckxstaens
Pages: 818 - 826 - Exploring the possibility of non-invasive prenatal diagnosis using cervical cells(2023)
Authors: Margot van Riel, Joris Vermeesch, Thierry Voet, Dirk Timmerman
- Imaging the unimaginable: leveraging signal generation of CRISPR-Cas for sensitive genome imaging.(2023)
Authors: Charlotte Van Tricht, Thierry Voet, Jeroen Lammertyn, Dragana Spasic
Pages: 769 - 784
Patents
1 - 5 of 5
- High-throughput genotyping by sequencing low amounts of genetic material (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)