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.
Guided intake — what to do next
Step 1: Choose a synthetic or de-identified file below. Selecting a file does not upload it to the server.
- Choose a file in the File input below. Verify that the filename and preview appear.
- Run checks using Classify file, PHI precheck, Eligibility and Run check. The result will appear below with feedback.
- Choose your next path: Create review-ready package for a safe demo, or for a governed upload sign in to an authorized workspace, confirm the appropriate attestation, then use the separate PDF or VCF upload button.
- Continue review using the Case Detail / Review Package link shown after a successful server operation. Human review is always required before clinical release.
Ready to select a file. Nothing has been uploaded to the server yet.
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.
Governed PDF report intake · P197
Upload a synthetic or de-identified PDF report into the existing governed case/vault path. Embedded PDF text is extracted and passed to the existing P197 report interpretation engine. OCR is not claimed; image-only PDFs remain stored but require a separate extraction/review step.
Choose a .pdf file above, then sign in with an authorized workspace account.
Saved reference-VCF case · governed upload
This is a separate, authenticated nonclinical reference workflow within the existing intake page. Use only an explicitly public reference or fully invented synthetic VCF containing eight site-only columns. No sample IDs, genotype columns, personal VCF, reports or phenotype notes. Your workspace session determines access; selecting a role above does not grant access.
This public-reference declaration is not independently verified. Clinical upload remains unavailable through this workflow.
Choose a .vcf file above, then sign in with a workspace-authorized account.
| Chromosome | Position | REF | ALT |
|---|
Genomic site identity only. Gene, transcript, clinical significance and real evidence have not been established by this upload.
Return to workspaceThese links preserve the exact workspace/case identity. A room remains blocked until its required evidence/agent receipts exist.
G3 · Public source evidence for the saved reference case
Only a saved public or invented synthetic VCF with up to two single-base sites is eligible for this limited source check. NCBI RefSeq verifies the genomic reference allele; exact matching NCBI ClinVar records, if any, are external source claims and NOT a diagnosis, ACMG classification, gene assignment or clinical sign-off.
This evidence view reuses your signed-in authorized workspace and existing saved case. It does not transfer patient data or use an AI agent. An absent ClinVar exact match is reported as absent; no result will be invented.
Open an existing saved G2 case to inspect the G3 public source ledger.
Reference allele matching and source assertions do not satisfy evidence sufficiency or qualified human review. Clinical release remains blocked.
G3 · Source-bound five-agent execution audit
This view displays execution metadata for the five real synthetic-only agent roles already approved for this saved case. Unreviewed model text is withheld; it is NOT scientific source evidence, ACMG classification, diagnosis, clinical recommendation, or human sign-off.
A signed-in workspace account and existing synthetic case are required.
Exact source-backed clinical evidence and qualified human review remain insufficient for a clinical conclusion. Clinical release is blocked.
Operational journey status
This is a projection of existing intake/upload/review states. It does not create a second workflow state store.
Current state
Not started
Start with PHI precheck or a governed upload.
Next action
Start intake
No corrective action required yet.
Human review remains required. Qualified signoff and clinical release are not inferred from this status.
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.