Sequence + assay design
Choose the candidate sequence, reporter reference, supported construct configuration and target tissue or panel.
From model capability to virtual assay
A Zero-Shot Virtual Assay Harness for Multi-Omics Foundation Models
Turn multi-omics foundation models into virtual reporter assays. VirDLA extracts assay-relevant signals from model representations to compare promoter activity across tissues and power iterative sequence design.
Sequence representations and molecular predictions.
Construct assembly, model calls and assay readout.
Relative reporter activity in a defined context.
Candidate search, optimization and compression.
How does this candidate behave relative to its reporter reference in the selected tissue or cell context?
Choose the candidate sequence, reporter reference, supported construct configuration and target tissue or panel.
VirDLA assembles the construct, locates reporter regions and invokes the selected model through its registered adapter.
The adapter maps predictions or representations to a relative reporter readout. Panel analysis compares target and reference contexts.
VirDLA estimates relative reporter activity and compares target and reference contexts to prioritize candidates.
VirDLA brings AlphaGenome, APenformer and Borzoi into one virtual assay workflow, connecting model capability to promoter comparison and sequence design.
The full-readout route gains accuracy by expanding the input window, making repeated evaluation expensive. V3c extracts trunk activation signals directly: compact inputs deliver strong agreement at a fraction of the evaluation time.
27 ms per V3c evaluation
0.666 Pearson r
Trunk activation extraction makes repeated virtual assays practical for sequence search. v11 carries this approach forward, powering VirDLA as the evaluation oracle in the VirEvo design loop.
VirDLA / APromoter
Computation requires an authorized API key.
Please contact the administrator at contact@apromoter.bio from your institutional email for access.