Why it matters
What clinical practices get from OmicsEdge
01
Separate genetic from lifestyle risk
See whether a patient's risk is mainly genetic or driven by habits, and decide where to focus.
02
Make labs mean more
Read every blood test in the context of the patient's genetics, and track it over time.
03
Save time on plans
Generate personalized health plans from DNA, labs and lifestyle, with your own notes applied across patients.
Tools for your team
Everything a precision clinic needs, in one platform.
The same tools our practitioners use every day, branded as yours.
Lab Test Analyzer: upload lab reports and track trends over time
Personalized health action plans and meal plans
Lifestyle Risk Analyzer with 150+ scientific assessments
Custom intake forms and questionnaires
Gene and SNP lookup tools for deep case work
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.
Functional & pathway
Methylation PathwayDetox PathwayMTHFRCOMTPhase I & Phase II DetoxMitochondrial SupportLongevity & prevention
Longevity & Healthy AgingCardiovascular HealthInflammation & AutoimmunityHormone HealthCognitionClinical
Clinical Overview ReportCardiovascular DiseasesNeurodegenerative DisordersAPOEBeyond 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
I'm an individual practitioner. Is this for me?
For single practitioners, our PromicsEdge platform lets you order kits and reports with no setup. OmicsEdge is for clinic groups that want their own brand.
Can we add our own protocols?
Yes. Recommendations can be mapped to your protocols and products, and custom notes apply across patients.
Which test should we offer?
Genotyping covers wellness, nutrition and risk. 40X whole genome adds rare functional and rare medical variants, ACMG findings and clinical PGx.
Let's plan your launch.
30 minutes with our team, with pricing and a demo account by the end of the call.