exploring cost-effective, genotype-first, population-wide genomic sequencing.
The Idea
PREDiSPOSED runs on combinatorial batching. Two times over, we take individual DNA samples, batch them, sequence them and then, bioinformatically, pin-point rare pathogenic mutations in individuals. This "trick" cuts costs up to 20-fold.
The Team
PREDiSPOSED has a multi-disciplinary team. Monogenic diseases exist in every medical specialty. With outset in oncogenetics, PREDiSPOSED involves experts from across medicine and anthropology, data science, epidemiology, etc.
The Plan
PREDiSPOSED finds rare, genetic disease. Despite the name, rare diseases are common; present in approx. 1 in 16 individuals. PREDiSPOSED explores whether earlier cost-effective diagnosis is, firstly, possible, secondly, meaningful for 100s of conditions.
Funders
10.000.000 DKK or more
1,000,000 DKK to 10,000,000 DKK
This is an early version of the website for the PREDiSPOSED project. The website is not yet completed and may contain inaccuracies or errors. The website was created by Ulrik Stoltze, and any feedback, comments and question can be directed to him at ulrik.kristoffer.stoltze@regionh.dk