Case details
1. Enter or upload2. Run checks3. Create package
Run precheck before creating a review package.Start a case or run a safe report check
Use synthetic/de-identified content to run readiness, PHI precheck, eligibility, and review package creation. Doctor and patient roles receive safe explanations and questions, not final diagnosis.
Upload PDF / VCF
Select a local PDF, VCF, TXT, JSON, or CSV. The demo reads safe preview text in-browser where possible and sends synthetic/de-identified precheck metadata to existing APIs.
After selecting a file, run check. Do not upload PHI in this demo.
Result
Run check to see readiness, PHI status, missing evidence, safety boundaries, and next actions.
Advanced technical audit JSON
No technical result yet.
Case intake and readiness check
What this page does
Upload or paste synthetic/de-identified genomic input and check whether it is ready for review.
Who should use it
Lab users and demo users preparing a VCF, PDF-like summary, text report, or case description for review.
What you get
Input type classification, PHI precheck, readiness score, missing fields, and recommended next step.
What is not allowed
No final diagnosis. Do not submit PHI or patient identifiers in the demo. Intake does not finalize diagnosis or classification.
Example in practice
A synthetic BRCA1 VCF passes PHI precheck, receives a readiness score, and moves to review package creation.
Next step
If eligible, create a review-ready package or send the case to reviewer workflow.
Case intake value moments
The intake workflow turns raw synthetic/de-identified input into a clear readiness decision before review-package creation.
Readiness Score
The user sees whether the case has enough structure to continue.
Basis: readiness-score API
PHI Safety Check
The demo confirms that the input is synthetic/de-identified before processing.
Basis: PHI precheck API
Missing Inputs
Missing fields and recommended next steps are shown before package generation.
Basis: eligibility and missing-input checks
Safety: These value moments are event-based and review-context-only. They do not claim autonomous diagnosis, final ACMG classification, treatment decisions, clinical performance approval, regulatory approval, unsupervised clinical automation, same-visit final clinical decisions, or clinical release without qualified human sign-off.