Labs
The biological workbench.
Separate the body's structures, explore a breathing or walking cycle, fold a protein, spin a double helix, transcribe and translate a gene, discover a real PubChem molecule in 3D, triage a discovery compound, or review a medication list. Choose an instrument to begin.
Methods and limitations
The anatomy studio uses male and female reference meshes with illustrative motion. Read the anatomy sources and simulation methods. The molecular instruments use the standard genetic code, Kyte–Doolittle hydropathy, Nussinov base-pair maximisation, Needleman–Wunsch alignment, Lennard-Jones dynamics, SpCas9 PAM scanning, structures retrieved from PubChem, and published Lipinski/Veber screening rules.
They are still teaching and exploration instruments, not research or clinical software. The folding model is coarse-grained and will not reproduce a crystal structure; a displayed PubChem structure is not a reaction pathway, docking result, or laboratory-safety model; property rules do not predict efficacy or toxicity; the RNA fold maximises base pairs rather than minimising free energy; guide scoring applies design rules but performs no genome-wide off-target search. Medication interaction output is an AI screening aid and must be verified against authoritative drug information by a pharmacist or prescribing clinician. Do not use any output here to make a therapeutic, diagnostic, or laboratory-safety decision. For real design work use validated tooling — AlphaFold, ViennaRNA, BLAST, and an off-target checker — and confirm at the bench.