The Gene Box
Clinical genomics

Clarity — Clinical-grade genomic intelligence

Whole exome sequencing covering 18 hereditary cancers, 3,000+ rare diseases, carrier screening, and pharmacogenomics — built for hospital-grade deployment with genetic counsellor review on every report.

Clinical scope

Four pillars of clinical genomics

From cancer risk to drug response — every report reviewed by qualified genetic counsellors before delivery.

Inherited cancer screening

BRCA1/2 + multigene panel covering breast, ovarian, colorectal, prostate, pancreatic, and 13 additional hereditary cancers. Cascade testing workflows built in.

  • BRCA1/2
  • Lynch syndrome
  • Li-Fraumeni
  • Hereditary diffuse gastric
  • 14 more panels

Rare disease diagnosis

Whole exome sequencing covering 3,000+ conditions. For the diagnostic odyssey patients — those who've seen five specialists and still have no answer.

  • 3,000+ conditions
  • Trio analysis (patient + parents)
  • Variant classification
  • ACMG guidelines
  • Clinical interpretation

Carrier screening

Preconception and prenatal risk assessment for 400+ inherited conditions. Designed for IVF clinics and obstetric practices.

  • 400+ conditions
  • Preconception planning
  • Prenatal risk
  • Family history integration
  • Cascade testing

Pharmacogenomics (PGx)

Drug-gene interaction analysis for 200+ medications. Bundled with Clarity — not sold standalone. Every report answers: will this drug work, at what dose, with what risk?

  • 200+ medications
  • Dosage guidance
  • Adverse reaction risk
  • FDA/CPIC annotations
  • CYP450 panel
Clinical workflow

From order to actionable report

1

Order

Clinician orders via partner portal. Kit dispatched to clinic or patient home.

2

Sequence

Whole exome sequencing at partner lab (Illumina/ThermoFisher validated).

3

Interpret

AI interpretation via Evolveme.ai knowledge graph + genetic counsellor review.

4

Deliver

Clinician report + patient summary + cascade testing follow-up workflow.

Platform preview

See a real Clarity report

Actual screenshots from the Clarity clinical reporting platform — including pharmacogenomics panels and drug interaction alerts.

Clarity clinical genomics overview
Clarity pharmacogenomics overview
Clarity PGx caution drugs panel
The business case

Why hospitals add Clarity

5-10% of ALL cancers are hereditary.

Offering NGS/WES + PGx gives your hospital a complete genomic service line. It's the highest clinical seriousness product — which makes it the highest trust builder for the entire brand. Partners see $50K-$500K annual value per hospital chain with a 4-8 month deployment cycle.

18
Hereditary cancers
3,000+
Rare diseases
200+
PGx medications

Integration & compliance

Systems integration

LIS/EHR integration via HL7/FHIR. Cascade testing workflows for family follow-up after positive findings. Genetic counselling summaries configurable from nutritionist to oncologist depth.

Credentials

NGS/WES validated. ISO 9001:2015 certified. GDPR compliant. Recommended by Illumina and ThermoFisher. Every report reviewed by qualified genetic counsellors.

Ready to add clinical genomics to your hospital?

See how Clarity deploys in your service line.