Genomic data governance
Pseudonymised subjects, consent, samples, genomic metadata, provenance and traceability in one governed environment.
RESEARCH USE ONLY · RUO
UESE LIFE SCIENCES & PRECISION MEDICINE
Secure genomic research for precision medicine.
A digital platform for hospitals, research institutes, universities, NGS laboratories, biotech and consortia that need to govern data, samples, bioinformatics workflows and AI activities with traceability, security and human scientific oversight.
Synthetic DEMO data
Security by design
AI with human review
Research workflows
Sequencing, analyses, HLA, RNA expression, normalisation and bioinformatics pipelines with transparent states and accountability.
Secure collaboration
Multi-organisation workspace for centres, laboratories, universities and consortia with project- and role-based segregation.
AI with scientific review
RUO orchestration of AI and bioinformatics with versioning, provenance and mandatory human scientific oversight.
Security & governance
2FA, activity logging, access controls and governance support for GDPR, EHDS and responsible AI.
Controlled DEMO access
Evaluation environment using synthetic data only, time-limited access and Superadmin approval for meaningful due diligence.
Built for healthcare and scientific organisations
Medical leadershipHospitals and healthcare organisations
Research institutesClinical and translational research
UniversitiesAcademic and translational science
NGS laboratoriesGenomics and molecular biology
Biotech & PharmaR&D and strategic partnerships
Public & consortiaPublic health and research programmes
WHY ADOPT IT
A governance layer between science, data and accountability.
UESE Precision Bio AI is not designed to replace clinical or laboratory systems. It is designed to make the research journey readable, traceable and governable when multiple datasets, roles and organisations need to work together.
Reduce fragmentation
Connect work currently spread across files, email and vertical systems without replacing existing specialist tools.
Make data verifiable
Link subjects, samples, analyses, pipelines, outputs and reviews to a coherent and auditable history.
Collaborate without losing control
Share work across organisations, sites and partners while preserving segregation, accountability and selective visibility.
Adopt proportionately
Start with a controlled pilot and expand only after multidisciplinary validation of utility, risk and integration.
OPERATING WORKFLOW
From sample to scientific review without losing provenance.
Each step remains linked to project, organisation, user, version and purpose. This supports controlled pilots, multicentre studies and structured collaborations.
Ingest
Register pseudonymised subjects, consent, samples and sequencing metadata.
Analyse
Connect files, variants, molecular profiles and versioned bioinformatics pipelines.
Review
Submit RUO outputs and candidates to documented human scientific review.
Collaborate
Share evidence and progress with authorised teams, partners and consortia.
GDPREHDS2FARUO
SECURITY, COMPLIANCE & GOVERNANCE
✓ ✓ ✓ ✓ ✓
Controls designed for highly sensitive data.
Research Use Only
The current configuration is RUO: it does not provide diagnosis, prescriptions or autonomous therapeutic decisions.
Human scientific review
Research outputs remain subject to authorised and qualified personnel.
Traceability & integrity
Events, versions, provenance, hashes and reviews support auditability and accountability.
Privacy & security by design
Pseudonymisation, minimisation, access segregation and 2FA are built into the architecture.
European governance
The platform supports organisational governance of applicable GDPR, EHDS and responsible-AI requirements.
EVALUATE BEFORE ADOPTION
Explore the platform with synthetic data before deciding.
The DEMO environment is pre-populated with projects, synthetic subjects, samples, sequencing, variants, HLA, RNA expression, pipelines, RUO jobs and reviews. Access is temporary, verified and approved so prospective users can meaningfully assess the workflow without exposing real data.
- No real patient data
- Controlled time-limited credentials
- Pre-populated evaluation dataset
- Guided paths for professional roles
DEMO / SYNTHETIC DATA
3Synthetic subjects
8+Demo variants
RUOPipelines & review
0Real patient data
Subject→Sample→Analysis→Pipeline→Review
DUE DILIGENCE
Questions to clarify before adoption.
Is it a medical device?
The published configuration is intended for research use (RUO) and is not presented as a medical device or diagnostic system. Any future regulated intended use would require a separate qualification and compliance pathway.
Where is genomic data stored?
The Control Plane governs metadata, roles, workflows and auditability. Large files may remain on institutional infrastructure or authorised storage according to the agreed architecture.
Can it integrate with existing systems?
Yes. The platform is designed as a governance and orchestration layer and can be prepared for API integrations with LIS, information systems, storage, laboratories and bioinformatics engines.
How can I assess it before adoption?
A controlled DEMO using synthetic data only is available. Requests are verified and approved before temporary credentials are activated.
UESE ITALIA S.p.A. · LIFE SCIENCES & PRECISION MEDICINE
A platform to assess methodically, not just look at.
Request a DEMO or a technical discussion with UESE to assess scope, security, integrations and the adoption model.