deCODE is a global leader in analyzing and understanding the human genome. Using its unique expertise and population resources, deCODE has discovered key genetic risk factors for dozens of common diseases ranging from cardiovascular disease to cancer.
Role within Neuromics
deCODE will perform whole exome sequencing and sequence RNA samples from partners and develop bioinformatics solutions for analysing of data.
Workpackage 13 - Research infrastructure
Workpackage 9 - Omics-assisted therapy development
Workpackage 10 - Elucidation of pathogenesis and monitoring of treatment
Workpackage 2 - Identification of novel disease genes in NDD/NMD patients
Workpackage 3 - Identification of modifying factors in cohorts enriched by deep phenotyping
Workpackage 4 - Identification of hypothesis-driven biomarkers for disease progression
Workpackage 11 - Modifier gene identification, prioritization and study