MyOme

MyOme

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Private Company

Total funding raised: $35M

Overview

MyOme operates at the intersection of genetics, bioinformatics, and clinical care, offering a comprehensive whole-genome-based testing platform. Its core innovation is the integrated Polygenic Risk Score (iPRS™), which combines monogenic and polygenic risk data validated across diverse ancestries. The company targets multiple customer segments, including providers, patients, employers, and healthcare systems, with a focus on making precision medicine actionable in primary care settings. MyOme is a private, commercial-stage company with key partnerships, such as with Illumina and Broad Clinical Labs, enhancing its technological and distribution capabilities.

Cardiovascular DiseaseRare DiseasesOncologyPharmacogenomics

Technology Platform

Clinical whole genome sequencing and analysis platform featuring proprietary integrated Polygenic Risk Scores (iPRS™) that combine monogenic and polygenic data, validated across diverse ancestries.

Funding History

2
Total raised:$35M
Series A$25M
Seed$10M

Opportunities

The declining cost of whole genome sequencing and growing acceptance of genetic data in clinical care create a massive market for proactive health and diagnostic testing.
MyOme's single-sample, whole-genome approach positions it to capture lifetime value from patients and reduce redundant testing costs for health systems, a key value proposition for payers.

Risk Factors

Key risks include navigating an uncertain regulatory and insurance reimbursement landscape for polygenic risk scores, competing against larger diagnostic companies with established sales channels, and the ongoing need to clinically validate its models across diverse populations to ensure equity and maintain scientific credibility.

Competitive Landscape

MyOme competes with large commercial labs (e.g., Labcorp, Quest), specialized genetic testing companies (e.g., Invitae, Ambry Genetics, Color), and academic medical center labs. Its primary differentiation is the clinical application of integrated polygenic risk scores from whole genome data, validated for diverse ancestries, within a provider-focused workflow.