Spend your expertise where it matters in NGS testing
Qnomx revolutionizes case-level and variant interpretation to generate clinician-ready reports. Integrate within or replace your existing NGS pipeline - so your team can focus on science, not searching for sources.
Built for oncology diagnostic laboratories scaling NGS-based cancer diagnostics.
What Qnomx Does
Reduce expert workload per NGS case by up to 85%
Too much of your team's time goes to evidence gathering, formatting, and cross-checking, rather than applying their expert judgment. Qnomx handles the structured, repetitive steps so your experts can focus on the decisions that matter.
Qnomx Insight
Structured Variant-Level Interpretation
Consolidates evidence across leading clinical, population, and functional sources, in the context of each patient, into structured, reviewable variant-level annotations.
Filters and prioritises variants straight from your VCF
Consolidates evidence across leading sources including OncoKB, COSMIC, ClinVar, and the literature, in the context of each patient
Drafts patient-specific annotations from traceable evidence bases and methodologies, so your interpretation is reproducible across analysts and sites
Shows reasoning, confidence, and agreement across sources for every element, so variant analysts can quickly wrap up straightforward cases and focus their expertise on difficult ones
Your experts review, edit, and sign off. Interpretation and the final classification stay with them.
Integrated Evidence Sources
Qnomx Report
Clinician-Ready Report Generation
Transforms structured interpretations into standardized, defensible clinical reports following your lab's reporting standards, all in local languages.
Generates clear case-level clinical narratives
Applies your lab's configurable content standards and layout
Supports multilingual output, clinical trial references, and local conventions
Agentic chat enables you to edit outputs or provide custom instructions live, so you get the exact final output you need with no copy-paste or manual rework
Enables structured review and sign-off workflows
Reports stay fully editable. Qualified experts approve before anything is released.
Customizable Lab Context
Adaptable to your diagnostic scope
Built for somatic and germline. Configurable across tumor types, panel sizes, and reporting standards with constantly evolving support for the latest NGS innovations such as long-read sequencing. Implement our modules flexibly according to your needs. Start minimally to fit into workflows your team already trusts, or implement our entire solution to replace outdated products that don't work for your lab.
Operational Impact
Scale interpretation capacity and give your team's expertise back to them
Qnomx removes the manual burden between variant filtering and clinical sign-off - freeing your variant analysts, genomicists and pathologists to do more of the work that drew them to this field.
Scale test volumes without scaling headcount
Enable each expert to handle significantly more cases per day - without burnout from repetitive manual tasks, and without competing for scarce specialist hires.
Lighten the cognitive load
Your team reviews and refines - not assembles from scratch.
Automate what drains your team
Qnomx handles evidence lookup, database cross-referencing, report formatting, and consistency checks so your experts spend their energy on interpretation and judgment.
Faster turnaround for clinicians and patients
Deliver standardized reports more quickly, even as panel complexity and volumes grow.
Consistent and defensible across reviewers
Standardize documentation while retaining individual expert judgment. Reduce variability and make onboarding smoother for new team members.
Fits your current workflow
Deploy on top of your existing tertiary platform. No changes to validated upstream processes.
Workflow Integration
Solve the manual bottleneck in NGS
Qnomx operates after variant filtering and before clinical sign-off - exactly where the manual workload is heaviest and expert time is most constrained.
Your validated pipelines and existing tools stay in place. Works with any tertiary analysis platform.
Trust
Built for the standards your lab upholds every day
Expert control remains central
All outputs are reviewed and approved by qualified molecular experts. Qnomx supports your variant annotation and documentation process - it does not replace your team's expertise.
Transparent and traceable
Evidence sources, reasoning steps, and report outputs are transparent, documented and reviewable. When questions arise during audit or peer review, the trail is clear.
Workflow-safe deployment
Operates on top of existing tertiary platforms, minimizing validation effort and preserving established SOPs.
Data protection and compliance
Patient data handled under strict security and privacy standards, supporting GDPR-compliant deployment with EU/Swiss data residency. ISO 27001 certified.
Trusted by leading oncology laboratories
Qnomx is deployed and evaluated in clinical cancer centers and diagnostic laboratories across Europe.
“Qnomx delivers an outstanding solution for our workflow through the automatic capture and structured tabulation of variants and precise positional data, enabling time savings of up to 60 minutes per report. The collaboration is excellent - characterized by rapid, precise implementation of requested adaptations, deep domain and problem understanding, and a strong commitment to continuous development in the interest of users.”Dr. Frauke Bellos, Head of Genomics, LABOR BECKER MVZ
“What we value most about Qnomx is how easily and quickly it integrates all bioinformatics analysis, while significantly improving the report's turnaround time. This has been saving us 1.5 to 2 hours per case.”Marcela Gálvez, MD MSc, Medical Director, GENCELL
FAQ
Frequently Asked Questions
Get Started
Unlock your lab's full potential
Qnomx can be deployed on top of your current tertiary analysis platform and assessed within your established reporting process. Start with a limited evaluation using real cases in your environment.
Discuss a structured pilot tailored to your laboratory workflow.
Book a Demo