We are the only scientifically validated genetic prediction technology for consumers. Read more
The world’s most advanced genomics infrastructure for Precision Health, supporting clinical services, health systems, and clinical labs with secure cloud deployment. White-labeled, scalable, scientifically validated, HIPAA & GDPR-compliant.
OmicsEdge was spun out from SelfDecode to independently focus on R&D, genomic analysis, and reporting using large-scale genomic data.
Launch and grow precision health products with industry-leading polygenic risk scores, global sequencing & fulfillment, and customizable genomic reports built for accuracy, patient care, and real-world disease prevention.
Platform includes:
1,500+ genetic reports, fully customizable white-label genetic reports, Nutrigenomics, Rare Variants, Pathway reports, Pharmacogenomics, ACMG, Functional health reports, genotyping, exome sequencing, genetic imputation, turnkey solutions, and API workflows.
Start easily with no minimum volume required, creating a scalable white-label product for clinical usage and digital health providers.
The global genealogy and genetic testing pioneer trusts us for powering MyHeritage DNA Traits using validated genomic analysis.
Leading EU healthcare & diagnostics provider relies on our genomics and blood test analysis for D2C initiatives.
The Middle East’s largest healthcare provider trusts us for advanced genomics and blood testing services for preventive patient care.
The global leader in functional health & nutrition partners with us to power their genetic testing offerings.
Built by a multidisciplinary team of more than 60 experts in software engineering, data science, medicine, clinical research, and genetics, delivering enterprise-grade services.
Our platform generates portable, multi-ancestry polygenic risk scores that perform reliably across diverse and admixed populations, improving clinical decision-making and patient outcomes.
The only consumer technology with published benchmark studies, peer-reviewed publications, and polygenic risk scores proven to outperform competing models in clinical environments.
200M variants and 1,500 genetic reports, giving clinical labs and healthcare providers the deepest catalog in the industry for consumer and clinical genomics solutions.
Deliver fully branded genomic reports from layout to insights — without building internal genomics infrastructure. Deliver instantly or integrate our models into your workflows through API, or turnkey solutions.
PRS, rare variants, nutrigenomics, functional health, PGx, ACMG, pathway reports, genotype imputation, and sequencing – no other genomics platform delivers this breadth of clinical services.
True, full-genome coverage with consistent depth, accurate variant calls, and rigorous QC, supporting clinical care, cancer research, and disease risk assessment.
Access worldwide sequencing, fulfillment, and logistics services – start immediately with zero minimum volume and fully white-label solution.
OmicsEdge provides a complete suite of precision health and bioinformatics capabilities with flexible integration options.
Connect via API or choose one of our fully managed white-labeled turnkey solutions delivering scalable clinical and research-ready services.
Generate polygenic risk scores, genetic and ancestry reports, genotype imputation, carrier status, pharmacogenomics insights, lifestyle recommendations, and actionable patient insights.
Process large-scale genomic and phenotypic datasets quickly and accurately for consumer, research, or clinical applications across global health systems.
OmicsEdge supports a wide range of precision health and genomics-driven businesses, including:
Researchers and biotech organizations working with large genomic datasets and disease models
We provide the infrastructure needed to launch scientifically validated personalized health features and clinical services without building complex pipelines internally.
Our PRS models deliver strong predictive power across multiple ancestries, improving risk assessment accuracy in diverse populations.
Our proprietary AI-powered pipeline converts genotyping data into 200M variants with 99.9% accuracy for large-scale genomic analysis.
Access 1,500+ validated reports and features covering every major genomics domain for clinical, research, and commercial services. Get the full catalogue here.
Building an internal bioinformatics platform requires deep genetics expertise, advanced engineering, and constant scientific updates. OmicsEdge gives you:
Your team can focus on product innovation while we handle the scientific and technical complexity.
Book a call to learn how OmicsEdge can help you deliver precise, personalized genetic insights at scale through white-labeled reports and advanced bioinformatics. See why leading health-tech companies rely on our platform.