Developers

Interactive API reference

Run the UNMIRI API in your browser. Every request below executes live against api.unmiri.com. No key, no signup. The endpoints shown here are the synthetic-data sandbox: they accept literal variant triples and pre-loaded sample IDs, never a real patient report, so nothing you send is PHI.

What you can run here

  • POST /v1/parse/sample: cross-vendor NGS parsing on a pre-loaded synthetic report. Call GET /v1/samples first for the list of sample IDs.
  • POST /v1/lookup: variant evidence join across CIViC, ClinVar, openFDA, ClinicalTrials.gov, and CPIC for a literal (gene, variant, tumor) triple.
  • POST /v2/recommendations/sample: Engine 2 genomics-aware CDS recommendations on a synthetic parsed report. GET /v2/recommendations/samples lists the IDs.
  • POST /v4/trials/match/sample: Tier 1B variant-grounded trial matching on a synthetic sample. GET /v4/trials/samples lists the IDs; GET /v4/trials/search runs a text-and-filter search across the trial corpus.
  • POST /v4/pa/decide/sample: Tier 2C prior-authorization decision on a synthetic tuple, returned with the source policy excerpt and citation. GET /v4/pa/samples lists the IDs.

Production access is partner tier: uploading real reports, the full /v2/recommendations endpoint, higher rate limits, and a signed BAA. See the NGS API and CDS API pages for what that includes, or get in touch.

Educational use only. Synthetic data, demonstration only. Not a medical device. Not for unsupervised clinical decision-making.

Related references

Product

NGS Interpretation API

The Engine 1 product page. Cross-vendor parsing, evidence join, FHIR Genomics output.

Product

CDS API

Engine 2. Five reasoning categories. FDA CDS-exempt under FD&C Act §520(o)(1)(E).

Product

Trial Matching API

Tier 1B. Variant-grounded matching that won't conflate L858R with T790M.

Product

PA Decision Engine

Tier 2C. FDA-label-aligned prior-auth decisions with citations.

Reference

Open FHIR Genomics schema

The data contract behind every response. Apache 2.0 on GitHub.

Reference

FHIR Genomics validator

Paste a synthetic Bundle, get a per-issue diagnostic. Useful in CI.

Live demo

Vendor coverage matrix

Honest list of what we parse today and what we don't.

Case study

EGFR L858R walkthrough

One synthetic sample, end-to-end, with citations intact.