My Genome.
My Health.
MyOme.

Empowering individuals to take control of their health through actionable genomic insights

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Genomic Analysis for Personalized Healthcare

Using whole genome sequencing and state-of-the-art bioinformatics, MyOme analyzes a single patient sample to produce comprehensive and clinically actionable reports that allow patients and their providers to make personalized lifestyle, prevention, and treatment choices.

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An expanding selection of actionable tests

With just one sample, MyOme provides access to proactive and diagnostic tests that can be ordered by a healthcare provider.

Proactive Health Tests

Assess personal health risks to guide prevention and treatment decisions.

  • Single-Gene Risk™
  • Medication Response™
  • Integrated Polygenic Risk Score™ (iPRS™)
Proactive Health Tests

Diagnostic Tests

Comprehensive testing to uncover diagnostic answers

  • Rare Disease Genome
  • Rare Disease Exome
  • Rare Disease Copy Number Analysis
Diagnostic Tests

Advancing personalized health together

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Broad Clinical Labs
Novi Health
Southern Research

A comprehensive approach

MyOme offers comprehensive genomic sequencing that goes beyond limited gene panels, delivering actionable insights for screening, medication decisions, lifestyle adjustments, and diagnostics—all from a single sample.

Our proprietary integrated polygenic risk scores (iPRS) combine clinical factors and are validated across diverse ancestries including individuals of mixed ancestry, ensuring the most personalized and precise risk assessment.

We prioritize data security with uncompromising standards— information is never sold or used without explicit consent.

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Who we serve

We make genomic testing and precision medicine more accessible across care settings, including primary care. Our seamless, end-to-end support model integrates effortlessly into busy clinics, reducing the burden on providers and their staff.

We also empower patients with the resources they need to understand and act on their genomic insights. From easy test ordering and actionable reports to clear clinical summaries, education, and optional genetic counseling, we provide comprehensive support for both providers and patients.

Learn how genetics can help inform your health decisions

Patient

Industry-leading and clinically-relevant genetic insights to guide patient care

Provider

What our partners say

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"In my practice in the Philadelphia area, I see patients of diverse ancestries for whom current ASCVD tools do not assess risk equitably or adequately consider other genetic factors for CAD. There are steps someone can take once we accurately identify those at risk, whether it is common medications such as statins, imaging or changes to lifestyle that can reduce heart-related events."

"Broad Clinical Labs has always been at the forefront of deploying the most advanced genomic sequencing technologies and together with MyOme’s bioinformatics and analysis pipeline, we can bring this power to the clinic, seamlessly providing patients and providers individual risk assessments powered by an individual’s whole genome."

"Communities in Alabama and across the nation have waited too long for advances in healthcare technologies—specifically genetics—to benefit them in clinical practices. Providing these patients and their providers with personalized health insights using MyOme’s industry-leading, clinical risk assessments will allow providers to identify potentially life-saving interventions, lifestyle and medication changes, imaging, and early cancer detection tests for their patients. "

The latest from MyOme

Events

Join us at our Advancing Rare Disease session at ACMG on March 19th in the LA Convention Center

News

MyOme Announces Launch of CAD iPRS and Beginning Enrollment in the COMPASS-CAD Prospective Trial

We're Hiring

Frontend Design and Development Lead

Ordering a test

With flexible billing options and an easy ordering process, MyOme makes ordering a test simple.

ordering a test
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