Genoact
The science

Editorial calm. Clinical rigor.

Genoact sits on accredited sequencing, curated genomic evidence, and human clinical review. Here's how the work happens.

Research philosophy

We translate peer-reviewed genomics into preventive action. No hype, no fortune-telling, just curated evidence, ranked by clinical utility.

DNA methodology

Illumina SNP-array sequencing covers 700K+ curated variants. Polygenic risk scores are calibrated against population reference cohorts.

Lab standards

Processed by CAP-accredited and ISO 15189 certified partner labs with 99.9% concordance benchmarks across runs.

Scientific validation

Every trait card cites the underlying studies. Genoact's clinical board reviews evidence quarterly and retires low-quality claims.

Clinical process

Every report is reviewed and signed off by qualified consultants. AI assists, humans decide.

Data security

AES-256 at rest, TLS 1.3 in transit, regional storage, role-based access. We never sell your data. Deletion on request, always.

FAQ

Common questions, answered.

We use CAP-accredited Illumina SNP-array sequencing across 700K+ curated variants, processed by ISO 15189 partner labs.