We are the only scientifically validated genetic prediction technology for consumers. Read more

White-Label Genetic Testing & Custom Reports for Precision Medicine

Launch clinically validated genetic reports under your brand. We handle the science, you own the customer experience.

DNA Data In
1
Impute 200M+ Variants
2
Analyze & Score
3
White-Label Reports Out
4
Your brand. Our science. Zero minimums.
Trusted by industry leaders
Medicover
Pure Health
Designs for Health
GenomeLink
Life X DNA
The build vs buy question

Why not build it yourself?

BUILD IN-HOUSE

The hard way

Hire geneticists, bioinformaticians & data scientists
Build imputation, PRS & ancestry pipelines from scratch
Achieve CLIA/CAP lab certification
Validate across multiple ancestries (years of R&D)
Maintain HIPAA/GDPR compliance infrastructure
Publish peer-reviewed research for credibility
$35M+
Estimated investment & years of development
USE OMICSEDGE

The smart way

1,500+ validated reports, ready to white-label
200M variant imputation at 99.9% accuracy
Multi-ancestry PRS for 1,400 conditions
HIPAA & GDPR compliant out of the box
Published in Nature Scientific Reports
Launch in weeks with zero minimum volume
Start Building Today
200M+
Variants Imputed
1,500+
Genetic Reports
1,400+
Conditions Scored
2M+
Validation Dataset
Complete platform

Everything from DNA in to reports out

One platform replaces dozens of tools. No other provider delivers this breadth.

01

Polygenic Risk Scores

Ancestry-informed PRS for 1,400 conditions with peer-reviewed validation.

02

Genetic Imputation

Expand genotyping arrays to 200M+ variants at 99.9% accuracy.

03

Ancestry Analysis

Sub-continental resolution across 35+ populations with Orchestra.

04

Pharmacogenomics

Personalized medication guidance based on genetic drug metabolism.

05

Longevity Screener

Risk assessment for 26 of 30 top causes of non-accidental mortality.

06

Recommendations Engine

20,000+ diet, lifestyle & supplement interventions ranked by impact.

07

Lab Test Analyzer

Interpret 4,000+ biomarkers integrated with genetic context.

08

Custom White-Label Reports

1,500+ report types fully branded to your company.

09

Precision Health GPT

AI chatbot that answers health questions using personal genetic data.

Built for your industry

One platform, tailored to your industry

Proven science

We don't just claim accuracy.
We proved it.

OmicsEdge is the only consumer-facing genetics company with polygenic risk scores validated in a peer-reviewed Nature journal publication. Our models outperform competing academic and industry approaches across diverse populations.

Read the Research 6 Peer-Reviewed Papers
Imputation accuracy benchmarkn = 2M
OmicsEdge (Selphi)99.9%
Beagle 5.487%
Minimac485%
IMPUTE584%
Based on rare variant imputation accuracy across multi-ancestry cohorts
Case study

Powering Precision Health for Medicover

One of Europe's leading healthcare and diagnostics providers integrated OmicsEdge's polygenic risk scoring and blood test analysis to deliver personalized genomics across their direct-to-consumer health initiatives.

Read Case Study
20+
Countries served by Medicover
Multi-Ancestry
PRS accuracy across all populations
Weeks
Integration timeline to live reports
Common questions

Frequently Asked Questions

We accept raw genotyping data from all major array platforms (Illumina, Affymetrix, etc.), VCF files from whole genome or exome sequencing, and 23andMe/AncestryDNA consumer export files. Our imputation pipeline expands any of these into 200M+ variants automatically.

API integrations typically go live in 2 to 4 weeks depending on your team's availability. The turnkey platform can launch in 1 to 2 weeks since no development is required. WordPress store setups can be live in days. Custom built solutions are scoped per project and timelines vary based on complexity.

No. That's the core value of OmicsEdge. We handle all genomic analysis, imputation, scoring, and report generation. Your team focuses on the customer experience and product decisions. Our 60+ scientists and engineers are your bioinformatics team.

No. You can start with zero minimums and scale as you grow. This applies to all integration models: API, Turnkey, WordPress, and Custom Built. Volume discounts are available as your usage increases.

You and your customers own the data. OmicsEdge processes and analyzes data on your behalf but does not sell, share, or commercialize genetic information. We can also host data in your country if required.

This is one of our key differentiators. Our PRS models are ancestry-informed and validated across multiple populations. Our Orchestra ancestry tool covers 35+ population groups, and our models are specifically designed to perform reliably in diverse and admixed populations, not just European cohorts.

Yes. Every report is fully white-labeled. You control the layout, branding, colors, logo, and content. You can choose from 1,500+ existing report templates or commission completely custom reports for specific conditions or markets.

OmicsEdge is HIPAA and GDPR compliant. We use AES-256 encryption for genomic data storage, support dedicated infrastructure, and offer in-country data hosting for partners with residency requirements. Our lab partners are CLIA/CAP certified.

Ready to add genomics
to your product?

Start with zero minimums. Choose your integration model. Launch in weeks.