Clinician Portal
Secure clinician-facing interpretation and follow-up support environment.
Starling Genomics delivers clinically robust polygenic risk scores designed for scalable deployment across European healthcare systems.
Starling Genomics develops and deploys validated polygenic risk score solutions for healthcare systems, laboratories, and clinical partners across Europe.
We combine scalable PRS engine infrastructure with regulatory-aware implementation strategies to enable responsible integration of genomic risk insights into clinical pathways.
The platform follows a structured five-stage PRS engine flow designed for clinical traceability and operational deployment in healthcare environments.
Starling Genomics provides a deployment-oriented architecture built for healthcare institutions that require reproducibility, data security, and interoperability.
The operating model is built for institutional adoption: transparent score generation logic, auditable reporting pipelines, and governance controls compatible with European clinical and data frameworks.
Starling Genomics delivers the full chain: test kit distribution, laboratory analysis and genotyping, then structured reporting for clinical use.
The portfolio is organized by clinical domain to support phased deployment, evidence review, and country-specific implementation planning.
Core oncology-focused PRS modules are available for staged clinical program design.
Risk models are available for integration into broader neurological and psychiatric pathway assessments.
Domain modules support investigation of inflammatory and immune-mediated risk stratification.
Polygenic modules support risk profiling in bone density and fracture-related contexts.
Selected PRS modules are designed for gastroenterology-oriented risk characterization.
Quantitative trait models support research-to-clinic transition and integrated risk interpretation.
Polygenic risk scores provide probabilistic risk information and are not diagnostic tests.
Starling Genomics is deploying its PRS platform across selected European markets, beginning with the Netherlands.
The platform structure is prepared for additional modules as implementation programs expand.
Secure clinician-facing interpretation and follow-up support environment.
Standardized onboarding interfaces for laboratory integration workflows.
Evidence summaries and technical documentation publication module.
Governance and compliance artifact repository for local jurisdictions.