{
  "decision_card_schema": "nmd-vcell-decision-card-set/1.0",
  "interface_build": "EA-20260817-57",
  "resource_release": "v1.2.0-measured-dmd-evidence",
  "ordering_policy": "Grouped by decision type and readiness; no target score, winner or numeric rank is generated.",
  "counts": {
    "decision_cards": 3,
    "registered_studies": 0,
    "registered_predictions": 0,
    "measured_outcomes": 0
  },
  "records": [
    {
      "decision_id": "DECISION:DMD:MYOGENIC:ZNF133-MON1A:1.0-DRAFT",
      "title": "Resolve whether ZNF133 or MON1A has a disease-context myogenic effect",
      "short_title": "ZNF133 + MON1A myogenic test",
      "decision_type": "discriminating_experiment",
      "lifecycle_state": "DRAFT_NOT_REGISTERED",
      "state": "myoblast_to_fusing_myocyte",
      "targets": [
        "ZNF133",
        "MON1A"
      ],
      "question": "Do ZNF133 or MON1A perturbations change a prespecified myogenic functional endpoint differently in DMD and matched-control cells?",
      "observed": [
        "Observed CRISPRi response exists in HepG2 for ZNF133 (84 cells) and MON1A (94 cells).",
        "Both targets were assessed in the GSE293514 human-myoblast fusion screen and neither met its FDR < 0.1 hit threshold.",
        "Both current candidate records retain source-conflicted DMD direction and recommend a muscle-context assay."
      ],
      "decision_blocking_gap": "Neither target has an independent perturbation repeated in a DMD muscle model.",
      "next_action": "Compare both targets in the same matched DMD/control human-myogenic assay, using qualified independent reagents and one frozen primary functional endpoint.",
      "result_changes": [
        "A reproducible DMD-specific effect would justify disease-context follow-up.",
        "A similar effect in DMD and control would support a broader myogenic—not DMD-specific—interpretation.",
        "A near-zero result inside a frozen equivalence margin would downgrade the hypothesis.",
        "Viability loss, differentiation blockade or reagent discordance would classify the result as toxic or inconclusive."
      ],
      "evidence_links": [
        {
          "label": "Compare ZNF133 and MON1A",
          "href": "/resource/compare?genes=ZNF133,MON1A"
        },
        {
          "label": "Open ZNF133 evidence",
          "href": "/resource/gene/ZNF133"
        },
        {
          "label": "Design the experiment",
          "href": "/resource/planner?gene=ZNF133"
        }
      ],
      "claim_boundary": "This card recommends a discriminating experiment. It does not predict that either target will improve DMD."
    },
    {
      "decision_id": "DECISION:EVIDENCE-AUDIT:GFOD2:1.0-DRAFT",
      "title": "Determine whether pending external evidence should change the GFOD2 record",
      "short_title": "GFOD2 evidence audit",
      "decision_type": "evidence_import_and_audit",
      "lifecycle_state": "PROVISIONAL_HOLD_IMPORT_PENDING",
      "state": "evidence_provenance",
      "targets": [
        "GFOD2"
      ],
      "question": "Does the author-reported external assessment provide traceable quantitative evidence that survives the released import and audit rules?",
      "observed": [
        "GFOD2 has an observed HepG2 CRISPRi response with 127 cells in the frozen aggregate.",
        "GFOD2 was not included in the GSE293514 human-myoblast fusion library.",
        "Its historical rank is preserved only for reproducibility; there is no current numeric rank."
      ],
      "decision_blocking_gap": "The reported external quantitative evidence, source provenance and analysis code have not been imported and audited.",
      "next_action": "Import the external result with source identifiers, quantitative values and analysis provenance, then run the released validation contract before changing status.",
      "result_changes": [
        "A complete, reproducible import can move the record from provisional hold to computational triage.",
        "An incomplete or incompatible import leaves the record on hold.",
        "Either outcome remains contextual evidence—not DMD perturbation efficacy."
      ],
      "evidence_links": [
        {
          "label": "Open GFOD2 evidence",
          "href": "/resource/gene/GFOD2"
        },
        {
          "label": "Read the evidence transition",
          "href": "/resource/evidence_transition"
        },
        {
          "label": "Download the import template",
          "href": "/resource/downloads/external_candidate_evidence_import_template.tsv"
        }
      ],
      "claim_boundary": "Audit resolution can change evidence status but cannot create a muscle, DMD or therapeutic validation claim."
    },
    {
      "decision_id": "DECISION:DMD:MINIMUM-PERTURBOME:24-SLOT:1.0-DRAFT",
      "title": "Freeze a balanced 24-slot DMD pilot before any outcome is visible",
      "short_title": "24-slot pilot freeze",
      "decision_type": "prospective_program_freeze",
      "lifecycle_state": "DRAFT_PANEL_ASSIGNED_SIGNOFF_PENDING",
      "state": "program_design",
      "targets": [],
      "question": "Which candidate, control and calibration conditions should occupy the 24 pilot slots under rules frozen before outcome access?",
      "observed": [
        "All 24 Stage A identities are provisionally assigned: 14 candidate genes and 10 calibration controls.",
        "The assignments remain editable; panel signoff and a frozen checksum are still pending.",
        "No study or prediction has been registered, no experiment has started and no outcome has been measured."
      ],
      "decision_blocking_gap": "Panel signoff, one primary endpoint, a minimally important effect and a negligible-effect margin remain unfrozen.",
      "next_action": "Sign off and checksum-freeze the assigned panel, endpoint and decision thresholds, then register an immutable truth-generation Study. Add a Prediction only when a condition is explicitly assigned to prediction validation.",
      "result_changes": [
        "A frozen panel makes future hit-rate and enrichment claims auditable.",
        "Controls allow calibration of false positives, nulls and toxicity.",
        "Pre-outcome registration prevents retrospective relabelling of successes and failures."
      ],
      "evidence_links": [
        {
          "label": "Open the 24-slot protocol",
          "href": "/resource/minimum-perturbome/"
        },
        {
          "label": "Review the no-wet-lab pack",
          "href": "/resource/no-wet-lab-evaluation/"
        },
        {
          "label": "Open the empty registry",
          "href": "/resource/registry"
        }
      ],
      "claim_boundary": "This is an assigned but unfrozen prospective design. It contains no registered experiment, measured outcome or efficacy result."
    }
  ],
  "claim_boundary": "Decision Cards identify evidence-resolving actions. They are not treatment recommendations or calibrated DMD perturbation predictions."
}
