Preventive & longevity care
For longevity clinics, preventive medicine, executive health, and longitudinal health programmes.
PRS screening · prevention · longitudinal follow-upPolygenic Scores as a Service
From request and sample to validated scoring, interpretation, reporting, and integration — delivered under your brand or ours for preventive, clinical, and research settings.
One service layer
Built around care
Starling adapts the same controlled polygenic-score service to the way each organisation requests, delivers, and uses probabilistic PRS information.
For longevity clinics, preventive medicine, executive health, and longitudinal health programmes.
PRS screening · prevention · longitudinal follow-upFor general medicine, primary-care groups, and multidisciplinary clinics incorporating polygenic scores into prevention and risk-stratification pathways.
Prevention pathways · risk stratification · professional reportingFor hospitals, laboratories, private providers, biobanks, and translational research teams.
PRS validation · cohort analysis · integrated reportingFrom request to report
Every PRS programme follows the same traceable operating model, while data intake, scoring, interpretation, delivery, and integrations remain configurable.
Clinical, research, portal, or API-led intake.
Consent, logistics, activation, and tracking.
Fit-for-purpose platform and laboratory route.
Quality control, bioinformatics, and versioned pipelines.
Evidence and context translated for the intended setting.
Reports, structured data, and system integration.
One focused service
The public portfolio is focused on PRS and PGS. Each module supports a different part of the same controlled path from programme design to reporting and integration.
Define population, intended use, evidence boundaries, consent, reporting roles, and implementation requirements before scoring begins.
Work from a qualified genotyping route or controlled customer genotype data, with identity, format, coverage, and sample-quality checks.
Versioned reference panels and controlled harmonisation create the variant coverage required by the selected score models.
Selected models run through transparent, versioned pipelines with allele alignment, model checks, score calculation, and traceable provenance.
Scores are interpreted against calibration, ancestry, reference populations, published evidence, and the clinical or research context.
Recipient, professional, technical, and structured outputs can be delivered under your brand and returned to the systems your organisation uses.
Configurable reporting
See how Starling translates polygenic scores into a visual recipient layer, professional interpretation, model-level QC, and structured output for your organisation.
Heart & circulation · at a glance
Of 100 people, about 94 have a lower or equal inherited predisposition and 6 have a higher predisposition.
Of 100 people, about 93 have a lower or equal inherited predisposition and 7 have a higher predisposition.
Of 100 people, about 39 have a lower or equal inherited predisposition and 61 have a higher predisposition.
Of 100 people, about 17 have a lower or equal inherited predisposition and 83 have a higher predisposition.
Detailed results
Read the result in three steps: percentile shows relative position, model comparison summarises the published association, and coverage confirms whether the required variants passed pipeline checks. None of these is a diagnosis.
Of 100 people, about 93 have a lower or equal inherited predisposition and 7 have a higher predisposition.
This fictional result places the individual near the 93rd percentile of the stated reference population. It indicates relatively higher inherited predisposition and should be interpreted alongside age, blood pressure, cholesterol, family history, and the intended care pathway.
Reporting and white label
The same PRS result can be explained differently for recipients, care professionals, technical reviewers, and connected systems without changing the underlying model output.
A percentile visual, plain-language meaning, and an explicit reminder that PRS describes probability rather than diagnosis.
Score position, model comparison, family and clinical context, and considerations for qualified follow-up.
Model identifier, genome build, ancestry context, coverage, validation metrics, pipeline version, and traceability.
Selected PRS fields can return to an EHR, LIMS, data warehouse, or research environment through controlled interfaces.
The same controlled layers can be presented in your brand, language, portal, and reporting workflow.
Risk stratification, prevention, research, or another clearly scoped PRS pathway.
Concise explanations for recipients, professional interpretation for care providers, and technical detail for authorised teams.
In a report, portal, customer system, dataset, or a combination of these.
Professional appendix
Transparent model-level metrics for professional review.
All checks passed| Condition / model | PRS | Effect | Validation | Coverage | QC |
|---|---|---|---|---|---|
| HypertensionPRS_BP · v2026.1 | 94z +1.56 | 1.72xper SD | 0.716AUC | 100% | Pass |
| Coronary artery diseasePRS_CAD · v2026.1 | 93z +1.48 | 2.12xper SD | 0.735AUC | 100% | Pass |
| StrokePRS_STR · v2026.1 | 39z -0.27 | 0.96xper SD | 0.701AUC | 100% | Pass |
| Atrial fibrillationPRS_AF · v2026.1 | 17z -1.15 | 0.63xper SD | 0.759AUC | 100% | Pass |
Under your brand or ours
The experience can be visibly Starling, co-branded, or embedded behind the customer brand while the scientific and operational foundation remains controlled.
Starling-branded reports and service experience.
A shared clinical or programme identity.
Customer-branded portals, reports, and delivery.