Why it matters
What hospitals & clinics get from OmicsEdge
01
From sequence to report, handled
We run 40X whole genome sequencing, bioinformatics and reporting, so your clinicians receive results they can use.
02
Risk beyond rare variants
Polygenic risk scores found 55–80× more true coronary cases than rare-variant tests in our published research.
03
Compliance built in
HIPAA BAAs, GDPR DPAs, accredited labs and in-region hosting for health systems.
Reference customer
Medicover: a consumer DNA service, built on OmicsEdge.
Medicover Genetics built mivano health, its direct-to-consumer genetic testing brand, on our white-label platform. Read the case study
Polygenic risk alongside blood-test results
White-label reports for consumers
Data processed and stored in the EU
What you can launch
Reports that fit your program
A starting point. Choose any of our reports, hide the ones you don't want, or build your own.
40X whole genome
Functional Rare VariantsDisease- and Risk-Associated VariantsLoss-of-Function-Associated VariantsACMG SF v3.3 Predisposition ReportAdvanced Pharmacogenomics (PGx)HLA & AntigenMedical Disease VariantsFamily Planning & FertilityMitochondrialWhole Genome Genius ReportClinical summaries
Clinical Overview ReportCardiovascular DiseasesCancerNeurodegenerative DisordersAutoimmune ConditionsClinical risk
Heart AttackHigh Blood PressureAlzheimer's DiseaseAPOEHeart ArrhythmiaArtery HardeningBeyond DNA
Lab Test Analyzer and Recommendations Engine
Lab Test Analyzer
Upload lab reports, with results extracted automatically, and track 4,000+ markers alongside genetics over time.
Recommendations Engine
20,000+ diet, lifestyle and supplement interventions ranked for each person, mapped to your products or protocols.
FAQ
Questions we hear
Are reports diagnostic?
No. OmicsEdge does not diagnose. Clinical reports such as ACMG findings and PGx are for clinician-led programs, and wellness reports show predisposition, not a diagnosis.
Where is patient data stored?
In the US for US partners and in the EU (Frankfurt) for European partners.
Can we use our own sequencing?
Yes. We accept whole genomes from any sequencing lab, and can partner with the lab of your choice, or run 40X whole genome sequencing in our own accredited labs.
Let's plan your launch.
30 minutes with our team, with pricing and a demo account by the end of the call.