Go beyond the score. See the exact biological features—exons, TF motifs, protein structures—that drive a prediction and understand *why* a variant is disruptive.
From feature attribution to activation steering
We simulate the extraction of active SAE features for a given sequence and calculate the change in log-likelihood (ΔLL) caused by a variant.
Connects the model's internal logic to human-readable biological concepts (RUO).
DynamicOracleExplain component. Detect low‑complexity repeats and other pathological attractors; flag viral/sensitive content (aligned with Forge safety gates).
Reduces junk outputs and improves the reliability of generative demos.
Expose endpoints to nudge/target feature activations (e.g., chromatin patterns, motif presence) with compute‑aware beam search.
Maps CrisPRO.ai‑style inference‑time scaling to controllable design objectives.
See SAE Intelligence in action
High Impact
High Impact
Medium Impact
Low Impact
The ΔLL (Delta Log-Likelihood) score quantifies how much a variant disrupts each biological feature. Negative values indicate disruption, with more negative values showing greater impact.
Transcription factor binding motifs
Accessible chromatin regions
Protein secondary structure
Activation steering is currently in development. This demo shows the planned interface for controlling feature activations during generation, with compute-aware beam search and predictable quality scaling.