Join the Qnomx Insight Early Access Programme

Too much of a genomicist's time goes to manually gathering evidence, reconciling databases, cross-checking, and copy-pasting — not to the expert judgment only you can apply. Qnomx Insight consolidates industry-leading sources (OncoKB, COSMIC, ClinVar, and more) and the latest literature into structured, reviewable variant-level interpretations.

Every result is tailored to each patient's specific disease context. No more manually filtering out results not relevant to your case.

Insight generates annotation drafts ready for you to review and lets you dive deep into reasoning, source agreement, and exact source data to back it up. You stay fully in control of every interpretation and final decision.