Why it matters
What government & public health programs get from OmicsEdge
01
Accuracy for your population
Many risk scores are built on European data. Ours are calibrated across ancestries and validated in four ancestry groups.
02
Data stays where it belongs
Processing and storage in the region your program requires.
03
Results participants understand
White-label reports and a branded platform in your languages, so participants can act on their results.
Partnering with us
A scientific partner, not just a vendor.
Our PhD and MD team works with your program on study design, validation and reporting.
Published methods in Nature Communications and Scientific Reports
Custom pipelines and on-premises deployment options
Multi-language, white-label participant platform
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.
Program outputs
Polygenic risk for 1,400+ conditionsPharmacogenomicsCarrier statusAncestryPopulation-scale analysis
Imputation to 200M+ variantsLocal ancestry inferenceRaw and imputed data via APIBeyond 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
Can data stay in our country?
We host in the US or the EU today. Talk to us about in-country requirements for your program.
Can you work with our existing sequencing provider?
Yes. We accept array data and 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.