Your Journey

From First Contact to
Living Intelligence

Whether you're seeking a personalized second opinion or accessing our philanthropic services, your journey follows a clear, transparent path designed to transform static genomic data into living intelligence.

High-Net-Worth Clients

Hyper-Personalized Genomic Intelligence

White-glove service with Helios-driven analysis, dedicated clinical team, and continuous living intelligence updates.

  • Dedicated clinical geneticist
  • 24/7 secure communication
  • Comprehensive multi-omics analysis
  • Lifetime living intelligence subscription

Philanthropic Clients

Accessible Genomic Second Opinions

The same rigorous analysis extended to underserved populations through our philanthropic mission.

  • Partner organization referral
  • Multi-language support
  • Plain-language reporting
  • Care coordination assistance

Institutional Partners

Enterprise-Scale Integration

Healthcare systems and laboratories seeking to enhance their genomic interpretation capabilities.

  • API integration options
  • White-label solutions
  • Volume-based agreements
  • Training and support

Philanthropic Client Journey

Accessible genomic second opinions with the same rigorous methodology.

1

Partner Referral

Varies

Referral through our network of philanthropic partners, community health centers, or advocacy organizations.

Partner organization referral
Eligibility verification
Consent and enrollment
Language support coordination
2

Accessible Data Collection

1-3 business days

Simplified data collection with support for various report formats and languages.

Multi-format report acceptance
Translation services available
Assisted data upload options
Quality verification
3

Standardized Analysis

7-10 business days

Same rigorous analysis methodology applied to all cases regardless of economic status.

Full Helios-grade analysis
Evidence-tier quantification
Risk assessment modeling
Clinical validation
4

Plain-Language Reporting

Scheduled delivery

Results delivered in accessible, plain-language format with visual aids and translations.

Plain-language summary
Visual risk communication
Multi-language support
Family-friendly explanations
5

Care Coordination

Ongoing support

Connection with local healthcare providers and support resources for follow-up care.

Provider communication support
Resource navigation assistance
Follow-up care coordination
Community health integration
6

Research Participation Option

Optional

Optional consent-driven participation in research to advance genomic medicine for all.

Fully informed consent process
Data sovereignty maintained
Contribution to global knowledge
Ongoing research updates

Begin Your Journey Today

Whether you're seeking a personalized second opinion or exploring partnership opportunities, we're here to guide you through every step.