AI partner for genetic labs

Your sequencing. Our bioinformatics, reports and AI.

Add imputation, ancestry-informed risk scoring, white-label reports and an AI assistant to the data your lab already produces.

200M+

variants after imputation

35

ancestry reference populations

1,400+

polygenic risk models

API

raw and imputed data

Why it matters

What genetic labs get from OmicsEdge

01

Turn data into products

Sell interpreted reports, not just raw files, without building a bioinformatics team.

02

Accuracy across ancestries

Our Orchestra local-ancestry method and multi-ancestry PRS keep results accurate beyond European populations.

03

Your brand, your customers

Everything is white-label, from reports to the AI assistant your customers talk to.

For your lab

Interpretation for the data you already produce.

Send us arrays or whole genomes and get back imputed data, ancestry, risk scores and white-label reports, ready to sell.

Accepted: genotyping arrays and whole genomes from any sequencing platform

Custom pipelines and your own algorithms on our infrastructure

Extra capacity: 40X whole genome sequencing in our CLIA-certified, CAP-accredited lab

White-label genome-aware AI LLM, by iframe or MCP

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.

Analysis

Selphi imputationLocal ancestry (Orchestra)Global AncestryMitochondrial Ancestry

Reports

1,400+ polygenic risk modelsGene reports (MTHFR, COMT, APOE and more)PharmacogenomicsCarrier status

Tools for your geneticists

Gene lookup across 20,000 genesSNP lookup across 200M+ variantsCustom SNP reports

Browse the full report catalog →

Beyond 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

What data formats do you accept?

Good-quality genotyping arrays, consumer files, and whole genomes from any sequencing platform.

Can you run our own models?

Yes. Custom projects can run your algorithms on our pipeline, or our engine on your servers.

Is your science published?

Yes, in Nature Communications and Scientific Reports. See our research on the Why OmicsEdge page.

Let's plan your launch.

30 minutes with our team, with pricing and a demo account by the end of the call.