VariantIQ
variantiq.org
AI-powered genetic variant analysis
VariantIQ scores the biological impact of DNA mutations at study scale. Researchers upload a variant CSV and get ranked, tissue-aware effect scores in minutes instead of waiting on a multi-week bioinformatics queue — no pipeline engineering required.
What it does
CSV upload with column auto-detection
Smart mapping for ClinVar exports and custom variant formats, so files load without reshaping.
AI variant scoring
Every variant receives a 0–1 effect score powered by Google DeepMind's AlphaGenome.
Tissue specificity
Scores resolved across 18+ tissue types including lung, liver, brain, and blood.
Publication-ready export
Multi-page PDF reports and CSV exports with ranked results and interactive score distributions.
Who it is for
- Genomics researchers at universities and hospitals
- Clinical genetics labs
- Pharmaceutical R&D and target discovery teams
Where teams use it
- Prioritise which variants from a study justify wet-lab follow-up
- Screen a candidate gene panel for tissue-specific regulatory impact
- Give a lab a shared workspace for variant triage instead of per-analyst spreadsheets
Runs on the Chanova platform
VariantIQ shares its identity, billing, storage, and delivery layers with every other product in the portfolio. That is why it can be bundled under one agreement, and why a platform-level improvement reaches it without a migration.
Also in the portfolio
Evaluate VariantIQ with us
We will walk your team through it against your actual workflow, not a canned demo — and tell you plainly if it is the wrong fit.