Clinical genomics
without the infrastructure

GeneOps gives clinics and health providers access to a structured genomic knowledge base that supports clinical decision-making — without building or maintaining genomics infrastructure. Every output is evidence-graded and PubMed-citable.

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Where genomics changes
the clinical picture

The domains where genomic data most directly informs clinical decision-making — from pharmacogenomics to longevity protocols and patient engagement.

Pharmacogenomics

Drug-gene interaction intelligence

CYP450 metabolizer status, drug transporter variants, and adverse reaction risk profiles — surfaced before prescribing decisions. Coverage of the most clinically impactful drug-gene interactions with full citation traceability.

Longevity protocols

Genotype-specific health optimization

Across fitness, nutrition, supplements, sleep, and cardiovascular health — the GeneOps engine surfaces personalized protocols for each patient. Evidence-graded and continuously updated as research advances.

Nutritional genomics

Micronutrient and macronutrient optimization

MTHFR status, vitamin D metabolism, omega-3 conversion efficiency, and carbohydrate tolerance — the variants that shape nutritional needs and allow clinicians to move beyond generic dietary guidelines.

Cardiovascular risk

Lipid, blood pressure, and inflammation genetics

APOE, PCSK9, ACE, and inflammatory variant profiles — providing a genomic layer to cardiovascular risk stratification that complements traditional biomarker panels.

Mental health

Neurotransmitter and stress genetics

COMT, MAOA, SLC6A4, and BDNF variants — informing supplementation, lifestyle, and prescribing decisions for patients with mood, anxiety, and cognitive concerns.

Patient engagement

A genomic layer patients actually use

The white-label patient portal gives patients a conversational, evolving genomic health resource — driving retention, compliance, and the quality of clinical conversations.

The standard that clinical
environments require

Every finding in the GeneOps knowledge base meets the criteria a clinician would apply: peer-reviewed source, defined study design, quantified effect, and explicit confidence grade.

6,520+ peer-reviewed papers

The research substrate spans 6,520+ peer-reviewed publications. Every variant-phenotype association is sourced, graded, and linked to its primary citation. Nothing enters the knowledge base without a qualifying study.

Confidence grading on every finding

Each finding carries an explicit confidence grade based on replication, effect size, and study quality. Clinicians and patients see not just what the research says, but how strongly the evidence supports it.

dbSNP-verified variants

All 1477+ SNPs are verified against the dbSNP reference database, annotated in HGVS notation, and consistently cross-referenced to ensure identity across datasets and file formats.

Continuous re-evaluation

The knowledge base is not a static release. As new research is published, existing entries are reviewed, updated, or re-graded. Contradictory evidence is handled explicitly — not ignored. Read the methodology →

Clinical deployment
without clinical IT complexity

API
REST API for EHR and practice management integration
Portal
White-label patient portal, your branding, your domain
GDPR
GDPR/HIPAA-aligned data handling, encryption at rest and in transit
Weeks
Typical time from partnership to live deployment

Build a genomics offering
your patients will use

We'll walk through the clinical applications most relevant to your practice, the integration options, and what deployment looks like for your patient population.

Discuss Clinical Integration Review the Methodology