We aim to develop personalized prediction models for disease progression and use these models as baseline in clinical trials
We aim to develop multi-omics data integration approaches to discover biomarker signatures and disease mechanisms.
We aim to develop computational pipelines for discovery of drug repurposing candidates.
We aim to develop FAIR data infrastructure for integration of molecular and clinical from heterogeneous and distributed resources.
Welcome to Research
We develop computational workflows for the integration of omics and clinical data to predict disease progression and identify drug repurposing candidates in myotonic dystrophy and other neuromuscular disorders.
Computational approaches to advance personalized medicine
Programs that are connected to this research group.
