OnpremBench.aiby Understand.tech

Help improve this record. Suggest a correction

Use cases

CLINICAL RESEARCH / BIOMEDICAL RESEARCH INSTITUTE · UNIVERSITY-HOSPITAL NETWORK

Rare-disease diagnosis support from dental photographs and radiographs, planned on an on-site appliance.

A six-month pilot of a vision-plus-retrieval pipeline that turns intra-oral images into standardised phenotypes and weighted, source-cited rare-disease hypotheses. Production is designed for a DGX Spark-class appliance on site, air-gap capable, for health-data sovereignty.

SectorPublic biomedical research with a university-hospital clinical network and rare-disease expert centres
StatusPlanned · Statement of work, May 2026; pilot start not yet published
EvidenceStatement of work
  • Story
  • Stack
  • Load
  • Measurements

THE SETTING

Who uses it, and where.

Public biomedical research with a university-hospital clinical network and rare-disease expert centres. Environment: clinical research.

Users. Up to 5 administrators and 20 end users (clinicians, geneticists, researchers, doctoral students); 100 to 300 annotated cases for validation.

THE STACK

What runs on the machine.

  • Vision model for per-tooth anomaly extraction in standard terminologies.
  • Retrieval-augmented reasoning over a structured rare-disease corpus.
  • Clinician report and plain-language patient summary generator.
  • Optional anonymised research registry.
  • Model IDs: not yet published.

Network posture. Pilot on the Understand Tech platform. Production designed with no public-cloud dependency and air-gap capability.

THE WORKLOADS

What it does, day to day.

  • Secure upload, automatic quality check and anonymisation of intra-oral photographs and radiographs.
  • Per-tooth phenotype extraction with confidence scores.
  • Weighted rare-disease hypotheses with suggested gene panels and cited sources.
  • Clinician report, patient summary, optional registry entry for retrospective research.

OUTCOME

What changed.

Planned scope

Planned scope: reproducible, traceable phenotyping; faster triage of complex cases to expert centres; a standardised phenotype registry for translational research. The system is explicitly non-binding: hypotheses, never a diagnosis; the clinician validates every output.

EVIDENCE & LIMITS

How to read this record.

The institute is not named. This is a planned deployment described in a statement of work; no result exists yet.

Measured figures (latency, throughput, concurrency, cost) are published only from a documented run on an identified machine. None is attached to this record yet.

LESSONS & FAILURES

What the team learned.

Not yet published. Three lessons from the project team, including what did not work, would complete this record.

RELATED RECORDS

Go deeper.

Author: Understand Tech · reviewed 2026-09-16. Customers are not named at their request.