Consented, de-identified, and actually usable.
A research workspace that pairs consented patient-journey data with live public oncology sources — queryable in a conversational assistant, explorable in a simulator, exportable in the formats your pipeline already speaks.
Live integrations
4 public sources
Oncology data bank
15 curated sources
Export formats
CSV · JSON · FHIR R4
Consent
Re-checked at download
What you get
Built around how you actually work
Research Assistant
A conversational assistant powered by Calanthe that queries live sources mid-answer — ClinicalTrials.gov, PubMed, cBioPortal, and NCI GDC — and shows you exactly what it queried.
Tumor-state simulator
Run the platform's rule engine on fully synthetic profiles — cancer type, stage, biomarkers, progression, recurrence — with zero patient data involved.
Cohort insights
De-identified aggregates across consented records: cancer-type and stage distributions, biomarker frequencies, treatment-response mix, mean tumor-state scores.
De-identified exports
Download CSV, JSON, or FHIR R4 bundles with pseudonymized ids that still group into cohorts. Consent is re-verified at download time and every export is audited.
Oncology data bank
15 curated public sources — registries, genomics portals, trial databases — ranked by cancer type, with evidence cards surfacing inside the analysis tools.
Consent-first by design
Patients opt in explicitly and can withdraw at any time. Names, emails, dates of birth, MRNs, and exact dates never enter the research plane.
From question to cohort
Explore public data
Ask the Research Assistant — it pulls live trials, literature, and genomics studies. No patient data required to start.
Simulate and aggregate
Test hypotheses against synthetic profiles, then check de-identified cohort distributions across consented records.
Export for your pipeline
Pull consented cohorts as CSV, JSON, or FHIR R4 — pseudonymized, audited, consent-checked.
De-identification you can defend
A research plane that never sees identity
Research access is architecturally separated from care access. The researcher role can never open an identified record — the API enforces it, and the audit log proves it.
- ✓Stripped before export: names, emails, DOB, MRN, exact dates, free-text identifiers
- ✓Preserved for science: diagnoses, biomarkers with values, treatment lines and responses, labs, symptom trajectories
- ✓Pseudonymized ids remain stable within an export so rows join into cohorts
- ✓Research consent is separate from care-team sharing and revocable independently
- ✓Every export creation and download is written to an append-only audit log
Put a live oncology workspace behind your next study
Explore the research tools on the demo environment, or contact us for researcher access to consented cohorts.
Not a researcher? Teloma for clinicians · Teloma for patients · Teloma for caregivers