Genomics and rare diseases
Genomic data reveal information about individuals and their relatives, which makes sharing them across sites especially sensitive. We design privacy-preserving methods for genome-wide association studies that scale with cohort size and for querying whole-genome variant databases, and we support rare disease research across institutions: identifying disease-causing variants, analyzing rare disease variants under homomorphic encryption and detecting disease-associated cell subsets in single-cell data.
Key papers
- arXiv preprint 2026 Privacy-Preserving Detection of Rare Disease-Associated Cell Subsets via Secure Multi-Party Computation
- Nature Communications 2025 PP-GWAS: Privacy Preserving Multi-Site Genome-wide Association Studies
- Bioinformatics 2025 PRISM: Privacy-preserving Rare Disease Analysis using Fully Homomorphic Encryption
- Bioinformatics 2022 Efficient privacy-preserving whole-genome variant queries
- Bioinformatics 2020 Identifying disease-causing mutations with privacy protection
- Balkan Journal of Electrical and Computer Engineering 2019 An Active Genomic Data Recovery Attack