The main objectives are to comprehensively characterize the genomic diversity of the Swiss
population, identify variants of medical relevance, and support the development of
personalized medicine strategies. By collecting high-quality reference genomes, the project
creates a benchmark for interpreting genomic information in both rare and common
diseases. Moreover, it aims to strengthen national research infrastructures and contribute to
broader European genomic initiatives, such as “Genome of Europe,” while maintaining strict
ethical and data protection standards.
Swiss Biobanking Platform (SBP) is an independent association, initiated by the Swiss
National Science Foundation (SNSF) in 2016. An important part if it is the Biobanque
Génomique du CHUV (BGC, established in 2013). Both serve as a long-term resource for
storing biological specimens and clinical information from patients who consent to research
use. Governed by strict ethical and legal frameworks, SBP and BGC support numerous
biomedical studies across disciplines. The Genome of Switzerland pilot project builds upon
this infrastructure, integrating advanced sequencing technologies and expertise from the
PHRT co-funded Health 2030 Genome Center — Switzerland’s national hub for large-scale
genomic analysis and part of SMOC. The project is supported by institutions from multiple
linguistic regions, emphasizing its commitment to inclusive and representative research.