Q:DMD:DIFFERENTIATING_MYOBLAST:CRISPRI:ZNF133:48H:FUSION
Does CRISPRi of ZNF133 alter fusion after 48 h in differentiating DMD myoblasts?
NMD-VCell
Ask how a neuromuscular cell state could change after perturbation.
The platform turns a biological question into four answers: what is known, what is missing, whether computation is eligible and which experiment would change the conclusion.
Candidate provenance
Why these hypotheses exist.
Numbers are shown as provenance, not as defensive scorekeeping. The funnel explains how released evidence becomes a governed perturbation question.
- 17,921released genes
- 123evidence-enriched records
- 21governed hypotheses
- 14DMD candidate slots
- DMD Minimum Perturbomestudy-ready panel draft
Current value: the platform identifies the exact missing truth edge and returns the experiment that would make a DMD virtual-cell response claim eligible.
Data you can use now
Search opens pages, downloads and machine-readable records.
Start with a gene or dataset, then reuse the underlying TSV and JSON objects without hunting through the site.
Answer layerSearch a geneOpen evidence, planner and JSON from one result.
TSVAll-gene candidate tableFilter the released atlas offline.
DMD evidenceSource-specific effectsInspect direction by source before interpreting a gene.
IntegrityHosted resource manifestVerify the files that are directly served by this release.
Research View by default
Audit detail is available without overwhelming the first answer.
Use this path to decide what to inspect or test next.
Use this path for reviewers, reproducibility and machine contracts.
One scientific loop
Evidence → perturbation → experiment → outcome.
Positioning
Disease-specific evidence-to-experiment virtual cell.
Observed disease and target evidence.
Bounded same-context benchmark infrastructure.
Prospective DMD candidate perturbation outcomes.