Clinical Decision Support

Identify disease risks early

The CDS identifies lifetime risks of disease, enabling earlier detection and proactive intervention before symptoms arise.

Triage patients accurately

The CDS differentiates complex conditions with overlapping symptoms, enabling accurate diagnoses and differential triage.

Predict disease trajectory

The CDS analyzes genetic mechanisms to predict disease progression, guiding personalized monitoring and care pathways.

Select the right treatment

The CDS can match therapies to individual genetic profiles, guiding precision treatments for better patient outcomes.

Seamless integration

Our clinical decision support system seamlessly deploys inside multiple HIPAA/GDPR protected clinical environments, integrating into existing workflows.

Trust & transparency

Our reports are based on a simple count of genotypic signatures identified by our mechnostic tests. There's no complex polygenic risk score models or black box AI – our findings are reproducible and explainable.

We remove the bias of machine learning software and avoid the main issues of concern to regulators around software interpretation and AI.

Simple workflow delivering actionable insights

Sample collection

Minimally invasive buccal swab or blood sample taken by the patient at home or in their primary care setting.

Genotyping & analysis

The sample is tested against a well-known genotyping array using industry standard equipment to generate a comprehensive genetic profile.

Mechanistic interpretation

Our clinical decision support platform interprets the results, identifying disease-associated mechanisms and generating a clear report for the clinician.