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Client Portal
All reports and genomic findings in a single dashboard: actionable health priorities and full variant details.
NewAI Genetic Assistant Nome in Client Portal
Next-Generation
Genomic Medicine
Unlock the full clinical potential of your health with evidence-based whole exome sequencing and digital precision diagnostics.
Our mission is to make advanced clinical genomics actionable, accessible, and life-changing.
Irina Zhegulina, MDMedical Geneticist, Co-founder of OMNINOME
Evidence-Based
Genomic Diagnostics
We provide comprehensive clinical genomic sequencing and bioinformatics re-interpretations designed to deliver actionable answers for your health and medical care.
Whole Exome Sequencing
In-depth genomic sequencing of 3,600+ actionable genes for comprehensive inherited disease and cardiovascular risk profiling. Actionable insights for proactive longevity.
Hereditary Cancer Risk
Comprehensive hereditary cancer screening: NGS whole exome, chromosomal microarray exon-level CNVs, pharmacogenomics across 50+ syndromes with actionable guidelines.
Pharmacogenomics
Personalized drug-gene interaction profiling for 100+ medications. Exome-level ADME analysis helps physicians select safe and effective drug therapies.
Gut Microbiome Metagenomics
High-resolution metagenomic sequencing of 10,000+ gut bacterial species, diversity indices, and scientific dietary recommendations for immune and metabolic health.
Safe Anesthesia Genetics
Targeted screening of RYR1, CACNA1S, and BCHE genes to protect against malignant hyperthermia and perioperative complications before planned surgeries.
Carrier Screening
Comprehensive genetic carrier screening for individuals and couples planning a pregnancy. Analysis across severe recessive and X-linked conditions.
Patient & Clinical
Trust
Hundreds of patients and physicians rely on our precision genomics and actionable clinical reports
Omninome’s Whole Exome analysis provided the clarity my family needed. After uploading our raw genomic data, the clinical report identified key pharmacogenetic markers that immediately explained my prior adverse drug reactions to statins. The report is rigorous, beautifully presented, and actionable.
As a physician, I appreciate that Omninome follows strict ACMG and CPIC guidelines. The depth of oncogenetic variant classification and the digital portal interface make discussing hereditary risk profiles with patients seamless and scientifically grounded.
We completed whole exome sequencing as part of pre-pregnancy carrier screening. The team was extremely professional, and the comprehensive carrier report brought us peace of mind. Highly recommend their clinical genomics platform.
The pharmacogenomics panel was eye-opening. Having personal genomic data on how I metabolize cardiovascular medications gave my cardiologist the exact evidence needed to tailor my dosage safely. Invaluable medical intelligence.
Omninome’s Whole Exome analysis provided the clarity my family needed. After uploading our raw genomic data, the clinical report identified key pharmacogenetic markers that immediately explained my prior adverse drug reactions to statins. The report is rigorous, beautifully presented, and actionable.
As a physician, I appreciate that Omninome follows strict ACMG and CPIC guidelines. The depth of oncogenetic variant classification and the digital portal interface make discussing hereditary risk profiles with patients seamless and scientifically grounded.
We completed whole exome sequencing as part of pre-pregnancy carrier screening. The team was extremely professional, and the comprehensive carrier report brought us peace of mind. Highly recommend their clinical genomics platform.
The pharmacogenomics panel was eye-opening. Having personal genomic data on how I metabolize cardiovascular medications gave my cardiologist the exact evidence needed to tailor my dosage safely. Invaluable medical intelligence.
Omninome’s Whole Exome analysis provided the clarity my family needed. After uploading our raw genomic data, the clinical report identified key pharmacogenetic markers that immediately explained my prior adverse drug reactions to statins. The report is rigorous, beautifully presented, and actionable.
As a physician, I appreciate that Omninome follows strict ACMG and CPIC guidelines. The depth of oncogenetic variant classification and the digital portal interface make discussing hereditary risk profiles with patients seamless and scientifically grounded.
We completed whole exome sequencing as part of pre-pregnancy carrier screening. The team was extremely professional, and the comprehensive carrier report brought us peace of mind. Highly recommend their clinical genomics platform.
The pharmacogenomics panel was eye-opening. Having personal genomic data on how I metabolize cardiovascular medications gave my cardiologist the exact evidence needed to tailor my dosage safely. Invaluable medical intelligence.
Genomics Explained in Clear, Actionable Terms
All your clinical test results are synthesized in one secure portal, while our AI assistant clarifies complex terminology and variant annotations — empowering you to collaborate effectively with your healthcare providers.
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AI Genetic Assistant Nome
Context-aware answers tailored to your genomic data: clear clinical explanations and key questions for your physician.
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Interactive Reports Beyond Static PDFs
Engage dynamically with your findings: filter by clinical relevance, navigate risk profiles, and prepare for doctor visits.
The New Standard of
Clinical Practice
Integrate cutting-edge genomic intelligence into clinical workflows to elevate diagnostic precision, personalize pharmacotherapy, and drive patient trust.
EHR / EMR Integration
Seamless structured integration of genomic variant reports into leading electronic medical record systems. Complete patient data in a unified clinical view.
White Label Reporting
Provide patients with clinical reports under your hospital or laboratory branding with clear physician-ready layout.
Request Demo & PricingGet in touch with our team
Flexible Translational R&D
Open to clinical and academic collaboration. Order custom NGS panels designed for unique clinical research initiatives.
Evidence-Based Medicine
Variant interpretation and clinical management guidelines adhere strictly to global gold standards (CPIC, DPWG, FDA, ACMG).
Science You
Can Trust
Omninome is built upon world-class clinical genetics and bioinformatics expertise.
Our multidisciplinary team includes PhD scientists, medical geneticists, and bioinformaticians with track records at leading genomic research institutes worldwide.
We go beyond routine testing: we conduct clinical research, publish in peer-reviewed scientific journals, and continually refine our variant interpretation algorithms.
Our mission is to make precision clinical genomics
accessible and actionable for everyone
Denis Gudkov, PhDCEO, Omninome
Часто задаваемые вопросы
Answers to frequently asked questions about our tests and services