Clinical Genomics Infrastructure · Romania
Precision medicine, built on clinical-grade genomic evidence.
Omnigenetica delivers ancestry-informed polygenic risk scoring, pharmacogenomics, and clinical-grade reporting to hospital networks, specialty clinics, and preventive-health programs across Europe.
Built for the institutions advancing precision medicine.
For 01
Hospital Networks
Enterprise-wide genomic integration, clinical reporting, and infrastructure scaled across multi-site healthcare systems.
Learn more →For 02
Specialty Clinics
Specialty-focused panels for oncology, cardiology, neurology, and rare disease centers, with deep phenotypic integration.
Learn more →For 03
Preventive-Health Programs
Longevity screening, lifestyle risk analysis, and carrier status for executive-health and protocol-driven preventive programs.
Learn more →Proprietary platform modules.
View technical architecture →PREDICT
Polygenic risk modeling across 650+ validated scores, ancestry-informed and clinically benchmarked.
Explore → 02INFORM
Pharmacogenomic profiles and dosing decision-support covering 100+ medications across 15+ drug classes.
Explore → 03INTEGRATE
Clinical decision-support delivered into hospital workflows, with 4,000+ lab markers and ACMG-aligned reporting.
Explore → 04TRANSLATE
Patient-readable reports with prioritized diet, lifestyle, and supplement recommendations from a 20,000+ intervention engine.
Explore →Clinically validated reports
Polygenic risk-score models
Variants imputed per sample
Patients validated
Whole-genome sequencing depth
EU data residency maintained
Data on File, Omnigenetica, 2026.
From sample to clinical decision — in three steps.
Collection kit
Clinical-grade DNA collection apparatus distributed to the clinical endpoint or directly to the patient, with chain-of-custody tracking.
European laboratory processing
Samples processed at a European laboratory in Denmark using clinical-grade short-read sequencing at 30× whole-genome depth.
Clinical dashboard
Encrypted reporting delivered into the physician’s portal with full diagnostic annotations and prioritized recommendations.
Peer-reviewed evidence underpinning the platform.
Tracing human genetic histories and natural selection with precise local ancestry inference.
Read paper →Empowering GWAS discovery through enhanced genotype imputation.
Read paper →Optimization of multi-ancestry polygenic risk score disease prediction models.
Read paper →Begin a clinical conversation.
Speak with the Omnigenetica team to evaluate clinical fit, integration, and operational scope for your organization.