Population genomic screening

The platform built to reach everyone who needs to be reached.

Kinship is end-to-end infrastructure for population genomic screening programmes — built by a team that has already screened 45,000+ patients across Australia, and made available to the health systems, government programmes, and research institutions that need to do it at scale.

Talk to our team
45k+
patients screened on this platform
3
screening programme types in live operation
End-to-end
consent through to cascade screening
AU-built
for the Australian regulatory environment

The problem

Population screening programmes fail not from lack of intent — but lack of infrastructure.

01
The workforce shortage
A genetic counsellor can service hundreds of patients. National programmes need to reach tens of thousands. The gap cannot be closed by training alone — it requires a different model entirely.
02
The operational burden
Running a programme today means stitching together consent, sample logistics, lab connections, results delivery, and cascade coordination — often across spreadsheets and disconnected systems. Cost per participant is high. Throughput is low.
03
The build problem
Health systems that try to build this themselves spend years acquiring specialist capability. The result: programmes that should reach 45,000 people reach 5,000. Funding spent on overhead, not care.

The platform

Everything a programme needs. Nothing it doesn't.

Programme management suite
Configure gene panels, manage participant referrals, track samples, generate clinical reports, and coordinate cascade screening — in one purpose-built environment for administrators and clinicians.
Participant-facing app
Guided onboarding, consent, family health history, test kit management, and secure results delivery — a consumer-grade experience for the patients at the centre of every programme.
Lab-agnostic integration
Connect to your existing laboratory partners or leverage ours. Automated report generation from lab results, with delivery via HealthLink to referring providers — without manual intervention.
Cascade screening coordination
When a participant receives a significant result, the platform coordinates follow-up for at-risk relatives — maximising the clinical impact of every finding across the wider family over time.
Outcomes and efficiency analytics
Real-time dashboards covering programme throughput, turnaround times, result distributions, and population-level findings — the data your programme needs to demonstrate value and improve continuously.
Genetic counselling (optional)
Organisations with existing counsellors can use Kinship without ours. For those who want end-to-end support, Eugene's counselling team manages high-risk results and consultations as an add-on service.

Built for MRFF-funded and academic screening studies.

Research programmes face a unique challenge: the scientific rigour required to produce publishable outcomes demands clinical-grade infrastructure, ethics-compliant workflows, and clean longitudinal data — at a scale most academic teams cannot build themselves.

Kinship gives research teams the operational backbone to run a study at the scale the science demands, with the data architecture to support long-term analysis and reporting.

Ethics-compliant consent management
Configurable consent forms that meet HREC requirements, with a full audit trail from participant enrolment through to result delivery.
Longitudinal participant tracking
Follow cohorts across time — tracking results, follow-up actions, cascade outcomes, and clinical interventions in a single connected record.
Research-grade data exports
De-identified population-level datasets, outcome distributions, and programme analytics structured for research analysis and publication.
Scale without added headcount
Automate the operational burden — sample tracking, reporting, results delivery — so your research team focuses on the science, not the administration.

"Built to run our own programmes. Now available to run yours."

Kinship was not designed as a product first. It was built to operate real screening programmes — at scale, in a regulated Australian environment. The edge cases are solved. The integrations work. The compliance frameworks are in place.

Who it's for

Designed for the people who commission and run programmes at scale.

Government
Programme directors and population health leads
Commissioning national or state-level screening initiatives that need to demonstrate value to a procurement committee — and deliver on a public health mandate at genuine scale.
Health systems
CMOs and population health directors
Running condition-specific programmes across carrier, cancer, and cardiac risk. Need a platform that reduces operational burden, scales without adding headcount, and keeps clinicians focused on patients.
Research
MRFF-funded and academic research leads
Running genomic screening studies that require clinical-grade workflows, ethics-compliant consent, longitudinal data tracking, and the operational scale the study demands.

Get in touch

Tell us about your programme.

We work with a small number of partners at a time. If you're building or scaling a population screening programme, we'd like to hear from you.

Get in touch