NMD-VCellNeuromuscular Virtual Cell Research PlatformDigital Tissue hypothesis workspace · Evidence → perturbation → experiment → outcomeNMD = neuromuscular disorders

Evidence Release 2026.08DMD context observedDMD candidate-conditioned prediction locked

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Evidence freeze: 3 August 2026 P59 hold · scorer failure retained · no target score NAR working package · 6 main + 31 supplementary figures Resource: v1.2.0-measured-dmd-evidence Schema: 1.1 Open platform state → Open Trust Center → Open evidence dashboard → Open claim registry → Open release status →

Digital Tissue · local V201 candidate

Map tissue-scale evidence without pretending to simulate it.

Released cell-context, physical-time and spatial-reference objects now share one multiscale evidence map. Every unsupported jump—from perturbation to neighboring cells, tissue function or patient trajectory—remains visibly locked.

Hypothesis workspace, not a cell-cell simulator. V201 adds no dataset, model run, synthetic tissue state or patient forecast. It links what has actually been measured to the exact evidence needed before a cross-scale edge may open.

Available reference substrate

Three bounded views are available; none is a perturbation-conditioned tissue truth.

Counts below resolve from released context, trajectory and spatial-task objects. Statistical units and transfer limits remain attached to their sources.

Open trajectory contract →
Cell context registry10 contexts

9 observed or measured; 0 candidate-conditioned DMD outcomes.

Physical-time reference271 cells

GSE52529 at 0 / 24 / 48 / 72 h; unperturbed human myoblast reference only.

Spatial representation7,509 spots × 128 dimensions across 4 sections

two mdx strain backgrounds; not DMD versus wild type Random feature-dropout stability does not establish gene-panel transfer.

Evidence planes

Three bounded references; three missing or locked planes.

Each plane declares its permitted use and boundary. Visual adjacency never creates a causal or simulated interaction.

Open cell contexts →
CELL_CONTEXTBOUNDED OBSERVED CONTEXT

Disease and cell context

Inspect measured or explicitly missing disease/cell contexts with their statistical units.

Context proximity is descriptive and does not create a candidate-conditioned response.
PHYSICAL_TIMEMEASURED REFERENCE ONLY

Physical-time myogenic reference

Inspect the unperturbed human myoblast reference at physical sampling times.

This is not a longitudinal DMD trajectory or perturbation-conditioned fate.
SPATIAL_REFERENCEBOUNDED SPATIAL REFERENCE

Spatial tissue representation

Inspect registered section-level representation stability and its sensitivity requirements.

The released mdx comparison lacks a wild-type arm and confirmed animal-level identity; nonspatial objects cannot enter the spatial task.
DMD_PERTURBATIONMISSING REQUIRED OUTCOME

Candidate-conditioned DMD response

Expose the missing truth and route users to a governed experiment plan.

Zero measured candidate outcomes is absence of evidence, not a null or negative effect.
CROSS_CELL_OUTCOMELOCKED NO MATCHED CROSS CELL TRUTH

Cross-cell and tissue outcome

Form a falsifiable multicellular hypothesis only.

No matched perturbation, neighboring-cell response and tissue-level functional outcome are jointly observed.
PATIENT_SCALELOCKED NO LONGITUDINAL CALIBRATION

Patient-scale calibration

Document which longitudinal and calibration evidence is missing.

No patient digital twin, clinical trajectory forecast or therapeutic recommendation is supported.

Cross-scale bridge

These are falsifiable handoffs between scales. Their labels describe missing evidence, not a generated biological effect.

Open Experiment OS →

Tissue admission ledger

1 ready · 3 partial · 4 open.

LOCK_UNSUPPORTED_CROSS_SCALE_INFERENCE. A cross-scale claim remains locked until its exact context, unit, geometry, perturbation, outcome, calibration and execution objects are jointly present.

  1. CONTEXT_IDENTITYDisease, species, tissue and cell-state identityPARTIAL
  2. INDEPENDENT_UNITSIndependent-unit and nested-cell structurePARTIAL
  3. PHYSICAL_TIMEPhysical-time reference rather than pseudotime substitutionREADY
  4. SPATIAL_GEOMETRYCoordinates, section/animal identity and spatial negative controlsPARTIAL
  5. DMD_RESPONSECandidate-conditioned DMD responseOPEN
  6. CROSS_CELL_OUTCOMEMatched sender/receiver and tissue outcomeOPEN
  7. PATIENT_CALIBRATIONLongitudinal patient calibrationOPEN
  8. REGISTERED_EXECUTIONRegistered multiscale task, model and receiptOPEN

Claim boundary

Zero new datasets · zero new runs · zero new scientific claims.

The Digital Tissue workspace links measured context, time and spatial references to explicit cross-scale gaps. It is a hypothesis and experiment-design layer, not a multicellular simulator, patient twin or efficacy model.

Does not imply: cell-cell simulation · perturbation-conditioned spatial prediction · tissue-level rescue · patient trajectory forecasting · clinical or therapeutic validity.