Whole-Genome Foundation
Clinical-grade sequencing uncovers health risks that may be missed by standard clinical assessments.

MyOme Atlas uses clinically integrated whole-genome sequencing to map comprehensive health risks and guide personalized care.
delivers whole-genome data
powers lifelong health insights
map distinct risks
from sample to results
A patient's risk profile can be reanalyzed throughout their lifetime, revealing new insights as their health journey evolves and technology advances. Results help guide personalized screening, medication, and lifestyle recommendations that can reduce risks and prevent disease — even before symptoms arise.
Clinical-grade sequencing uncovers health risks that may be missed by standard clinical assessments.
Clinician-designed reports translate genomic risk into guideline-aligned metrics and clear next steps, with interpretation support and patient genetic counseling included.
Genomic datasets can be reanalyzed over a patient’s lifetime, revealing new insights as health, science, and technology evolve.

Uncover actionable risk variants across a curated, rigorously evidenced set of genes linked to 40+ health conditions.
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Reveal pharmacogenomic variants that guide safer, more effective prescribing across 70+ medications.
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Map integrated risk for coronary artery disease and type 2 diabetes with cross-ancestry accuracy.
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Detect elevated risk early for breast and prostate cancer with whole-genome risk mapping.
Learn MoreReady to bring proactive, genomics-informed care to your patients? Get started with MyOme Atlas today.