—Ready. Start the molecular reader or choose any token directly.
A text figure projected from the generated 3D coordinates.
Start the reader to project the current pyPept window.
Evidence becomes an audible layer, not molecular authority.
- No external enrichment attached to this residue/window yet.
The mapping is deterministic interface sonification. It is not a physical vibrational spectrum and does not encode clinical truth by itself.
The displayed fragment is written as it is heard.
Each BILN token is a readable unit with biologically meaningful numbering. Prominent residues or regions stay visually distinct; connection annotations such as oxytocin's shared disulfide label receive a separate cue; terminal chemistry remains visible and audible.
FoldSense base score: deterministic BILN/pyPept context.
UniProt/HPA/Biohub: structured context layers with evidence class preserved.
Exa: retrieval arrival cue.
Apify: selected-source snapshot cue.
GMI/Gemini: inference layer over a frozen reader event.
Vapi: agent/control cue only.
ElevenLabs: speech/audio artifact cue only.
Generated fragment: pyPept/RDKit conformer used for 2D/3D representation.
Experimental PDB: fallback structural context; no exact BILN cursor mapping is claimed unless known.
Discordance: an attention cue. It must never be read as a diagnosis.
Consonance: source agreement/coherence, not “healthy” or “beneficial.”