Genie Medical AIOne window for computational biology
A narrated walkthrough of the working platform. Every screen in it is real output on real molecules — nothing is mocked up — and every section explains what it does and who it is for.
What is covered
- 0:00The problemWhy the work is scattered across a dozen tools
- 0:41How the work flowsFour stages, eight sections, one window
- 1:33SequenceMass, charge, pI, and the number that turns A280 into mg/mL
- 2:44DNA and RNAReading frames, cloning sites, rare codons, primers
- 3:17StructureMeasured and computed shapes, and real secondary structure
- 3:50DynamicsFolding, binding, and testing whether an interface is electrostatic
- 4:25DevelopabilityLiabilities before cell-line development, and comparability
- 5:05CompoundsRanking by binding efficiency rather than raw potency
- 5:41Lab dataIC50 and enzyme kinetics fitted from your own numbers
- 6:09The recordEvery step, method and source — exportable
- 6:35The assistantReads the bench, cites the numbers, shows its evidence
- 7:09Who uses itSix kinds of company, six different reasons
- 7:52Where your data goesAnalysis in the browser, assistant on your hardware
- 8:27A worked passOne target, five minutes, one file at the end
- 9:05What it does not doThe limits, stated plainly
Who it is for
Biosimilar & biologics developers
Sequence liabilities found before cell-line development, and a comparability view that reports only what a candidate introduces relative to the originator.
Discovery & medicinal chemistry
Known actives ranked by binding efficiency rather than raw potency, so a series does not drift toward bigger, greasier compounds.
CROs & CDMOs
Every action timestamped with its method and its source, exportable as a single run record — the deliverable for the client and the evidence for the file.
Structural & molecular biology
Secondary structure computed from atom positions and cross-checked against the deposited annotation. Predictions always labelled as predictions.
Synthetic biology & diagnostics
Reading frames on both strands, unique cloning sites, rare codons that stall expression, and primer checks before you order.
Assay development
IC50 and Km fitted from your own numbers, with residuals shown and an explicit warning when the answer is an extrapolation.