Built-in Beacon functionality for Cafe Variome installations. UMCG CardioKit variants - Cafe Cardio. Nature Protocols HGV2014 Blog Post. A data discovery platform for sequence variant data. Clean, intuitive interface for complete control over data discovery and subsequent data sharing. Installations can be hosted by Cafe Variome or installed locally.

A platform for people who work to cure diseases. The fastest path to new discoveries. Whether you have a population scale biobank, a large cohort or a collaboration project with 20 or more partners, we can help you. BC Platforms is an expert in understanding and advancing the science of life. Powerful and secure data right at your fingertips.

Is a centralized resource for cross-referenced information on disease mutations enriched in the Finnish population. FinDis provides up-to-date information on the 36 monogenic diseases belonging to the Finnish disease heritage. Prevalence or incidence and a short description of clinical symptoms. Genetic locus and a molecular description for identified mutations. Disease allele frequencies typically reported for Finnish mutations. Read About the FinDis project.

Welcome to the G2P Knowledge Centre. Welcome to the G2P Knowledge Centre - home of the GEN2PHEN project, a holistic approach to genotype-to-phenotype data. Find out more about GEN2PHEN. See a list of GEN2PHEN-supported activities, resources, platforms and initiatives. A simple gene search for G2P data. A listing of locus-specific databases.