Research philosophy
We translate peer-reviewed genomics into preventive action. No hype, no fortune-telling, just curated evidence, ranked by clinical utility.
Genoact sits on accredited sequencing, curated genomic evidence, and human clinical review. Here's how the work happens.
We translate peer-reviewed genomics into preventive action. No hype, no fortune-telling, just curated evidence, ranked by clinical utility.
Illumina SNP-array sequencing covers 700K+ curated variants. Polygenic risk scores are calibrated against population reference cohorts.
Processed by CAP-accredited and ISO 15189 certified partner labs with 99.9% concordance benchmarks across runs.
Every trait card cites the underlying studies. Genoact's clinical board reviews evidence quarterly and retires low-quality claims.
Every report is reviewed and signed off by qualified consultants. AI assists, humans decide.
AES-256 at rest, TLS 1.3 in transit, regional storage, role-based access. We never sell your data. Deletion on request, always.