Demo

Take the tour

Five stops, about ten minutes, no signup. Each step links to a live page on the demo. The disclaimer below is the canonical one. It appears on every result surface.

Educational use only. UNMIRI is a developer preview, not a medical device, and is not for clinical decision-making.

  1. 1

    Pick a synthetic vendor sample

    Foundation Medicine F1CDx, Tempus xT, Caris MI Profile. Every sample is synthetic, watermarked, and never accepts uploads.

    Why this matters: Buyers want to see the actual input. Click into any sample and the source PDF is right there.

    Open the sample showcase →
  2. 2

    See the canonical schema output

    The same patient situation, parsed into HL7 FHIR Genomics Reporting STU3 with mCODE 4.0. Identical shape across every vendor.

    Why this matters: Cross-vendor normalization is the core promise. The compare view stacks two vendors side by side.

    Compare two vendors →
  3. 3

    Look up variant evidence

    CIViC, ClinVar, openFDA, ClinicalTrials.gov, and CPIC joined on (gene, variant, tumor type), with the AMP/ASCO/CAP tier.

    Why this matters: Every claim links back to its source. The example link prefills EGFR L858R in NSCLC.

    Try the lookup →
  4. 4

    View CDS recommendations

    Genomics-aware suggestions, deterministic templates, no LLM in the final clinical surface. Educational use only.

    Why this matters: The same sample from step 1 flows end-to-end. The disclaimer banner stays sticky.

    See the recommendations →
  5. 5

    Search the literature

    PubMed plus a paraphrased summary on top of the same evidence graph. Curated for medical-affairs use.

    Why this matters: Closes the loop between variant call, evidence, and the underlying papers.

    Open literature search →

Done with the tour?

The honest matrix of what we extract today and what we don't yet is at /coverage. The interactive API reference is at /api-explorer. For pilot conversations, email partnerships@unmiri.com.