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| Funder | European Commission |
|---|---|
| Recipient Organization | Universite de Liege |
| Country | Belgium |
| Start Date | May 01, 2024 |
| End Date | Apr 30, 2026 |
| Duration | 729 days |
| Number of Grantees | 1 |
| Roles | Coordinator |
| Data Source | European Commission |
| Grant ID | 101155061 |
Inflammatory Bowel Disease, including Crohn’s disease and ulcerative colitis, now afflict close to 1/250 individuals in industrialized societies. There is a pressing need for effective preventive means as well as curative drugs.
Cis-eQTL analyses are uncovering a growing list of genes that are perturbed by IBD risk variants detected by GWAS, constituting a list of prime drug targets for the pharmaceutical industry.
Cis-eQTL effects trigger downstream effects – both within the same (intracellular) and other cell types (intercellular) – that culminate in disease declaration. Some of these downstream effects are accompanied by changes in transcript levels referred to as trans-eQTL effects.
The aim of the TRIQ project is to take advantage of the CEDAR-II dataset – transcriptome data for up to 400 individuals in > 75 IBD-relevant cell types – to identify trans-eQTL effects that mediate IBD predisposition.
The genes that are perturbed by these trans-effect will include druggable targets that constitute prime targets for the development of new IBD therapies.
Universite de Liege
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