Precision Nutrigenomics Platform

Your Genome.
Decoded.
OptimizedMappedSequencedUnlocked

Submit your raw genetic data and receive a clinically-informed supplement protocol — uniquely mapped to your SNPs, variants, and nutrient absorption factors.

700K+SNPs Analyzed
120+Genetic Markers
98.4%Call Accuracy
14Validated Labs

Built on the best available scientific evidence
from leading institutions

Methodology

From raw data to personalized protocol

Our engine cross-references your genetic variants against a curated database of peer-reviewed nutrigenomics research across 14 validated laboratory cohorts.

01 / INGEST

Upload raw genotype file

Export your raw DNA file from 23andMe, AncestryDNA, or any major genotyping provider. Parsing occurs entirely within your browser — your genome never traverses our servers.

02 / ANALYZE

Cross-reference 700K+ SNPs

Our variant calling engine scans your genotype against ClinVar, dbSNP, and our proprietary nutrigenomics variant database — flagging clinically-relevant SNPs for downstream analysis.

03 / REPORT

Receive your protocol

A ranked supplement protocol with precise dosing, the specific variants that triggered each recommendation, confidence intervals, and citations to primary literature.

Analysis Input

Begin your genomic analysis

Sign in to begin. Your DNA file is analysed in your browser and never uploaded.

Sign in to upload your DNA file

Your file is analysed in your browser — it is never uploaded to us

.TXT.ZIP.CSV.GZ23andMeAncestryDNAMyHeritageFamilyTreeDNA
genome_data.txt
Ready to analyze
FILE READY

This name appears on the generated report. On a Family plan, enter the family member this analysis belongs to.

Analysed in your browser
Raw DNA never uploaded
Verified account sign-in
Report saved to your account
Scientific Basis

Built on peer-reviewed nutrigenomics

We analyze the genetic variants most strongly linked to nutrient metabolism, absorption efficiency, and biochemical pathway function — then cross-reference against 4,200+ published studies from ClinVar, PubMed, and the Human Gene Mutation Database.

Methylation capacity (MTHFR)Folate · B12
Vitamin D receptor efficiency (VDR)Vit D3 · K2
Omega-3 metabolism (FADS1/2)DHA · EPA
Iron absorption (HFE gene)Iron · Vit C
Antioxidant capacity (SOD2, GPX)CoQ10 · ALA
Pricing

Choose your plan

Start free, upgrade when you're ready. Family plans cover up to five named profiles on a single account.

Free
$0 / forever

See what your genome can tell you.

  • Sample report walkthrough
  • See exactly what the full report covers
  • No DNA upload required
Family
$80 / per family

Everything in Regular — for the whole household.

  • Everything in the Regular plan
  • 5 full reports
  • 5 named profiles on one account
  • Each report personalized to its family member

Billing isn't live yet — selecting a plan saves your choice to your account so you can pick up where you left off at launch.

Your DNA stays yours — always

Your raw DNA file is parsed in your browser and is never sent to an AI provider. With your separate AI consent, matched SNPs and genotypes are sent to our AI provider for scoring; your saved report also syncs to your account. You can withdraw AI consent in Settings.

Raw file stays local
GDPR compliant
No data brokering
AI-Powered audited
GenoDyn Labs — Precision Nutrigenomics Platform