National network for establishing standardised bio informative and classification workflows, a joint variant database and joint data sharing
Received grant in 2017
DCCC has funded 175,000 DKK to the project.
The National Strategy for Personalised Medicine is currently establishing an infrastructure for storage and processing of genome sequencing. In the cancer area, this infrastructure can be used for saving the somatic variants of genome sequencing and in some cases treatment for these variants can be offered.
It is therefore necessary to establish a database for storing variants, linking clinical data at a national scale and ensuring anchorage in the entire healthcare system covering everything from bio informative competencies, medical insight and identification of important confounders to involvement of the system owners.
Multidisciplinary organisation
NEXT Bioinformatics
Project stakeholders
- Martin Bøgsted, Department of Clinical Medicine, Aalborg University. Primary contact, mail: martin.boegsted@rm.dk
- Jakob Pedersen, Department of Molecular Medicine (MOMA), Aarhus University Hospital
- Jens Winther Jensen, RKKP
- Inge Søkilde Pedersen, Section of Molecular Diagnostics/The Clinical Cancer Research Center, Aalborg University Hospital
- Britt Elmedal Laursen, Department of Molecular Medicine (MOMA), Aarhus University Hospital