Genodex

Name: Genodex
Author: Caferati Labs

By: Caferati Labs

Know Your Genes

Features & Capabilities

Genodex is a privacy-first educational data-visualization app for genomics. Explore 120 non-medical phenotypes against any imported genome, with transparent evidence, clear visualizations, and on-device processing — no raw genomic data leaves your phone.

Key features

• Private, on-device analysis — Import/manage up to 5 personal genomes (family plan). Data stays on your device; no genomic data leaves your phone • 120 phenotype visualizations — Non-medical traits (e.g., hair color, eye color, height, handedness, educational attainment) with clean data visualization • Evidence-based — Direct links to GWAS studies, plus RSIDs, alleles, and effect strengths for verification and deeper analysis • Compatibility — import raw data from major consumer DNA services (23andMe, AncestryDNA, MyHeritage, FamilyTreeDNA) and standard VCF (WGS). • Researcher Mode — Explorer for a large GWAS Catalog trait list at the population level, with advanced visualizations (never applied to uploaded genomes). • Population similarity (ethnicity) by distance — Estimates computed via distance to reference populations; presented strictly as informational insights.

Reference panels

• Built with 1000 Genomes Project populations at its core, with access to additional public reference panels from leading genomic projects.

Subscriptions

• Family Monthly Subscription — Unlocks all 120 phenotypes and supports up to 5 genomes on your personal list. • Researcher Monthly Subscription — For advanced learners and researchers: deeper population-level trait analysis, extended access to public GWAS Catalog traits, and advanced visualizations. • Subscriptions auto-renew unless canceled at least 24 hours before the end of the period. Manage subscriptions in your account settings.

Privacy & safety

• On-device by design — No raw genomic data are uploaded to servers. • Data control — In-app Data Export and Account Deletion.

Disclaimer

Genodex is strictly informational, built for educational purposes — not a medical device and does not provide medical interpretation, risk assessment, or diagnoses. It’s here to help you generate knowledge on genomics — clearly, privately, and responsibly.