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How we work

Built for each science.
Held to one standard.

A membrane free-energy calculation, a sweep of a million genomes and a crystal stability screen do not yield to the same machinery, and we do not pretend they do. Every domain gets its own harness, built around its own physics, data and controls. What they share is the part that decides whether a result can be trusted: the same rules of evidence, and the compute to apply them at scale.

The idea

Why each science gets its own harness

A single pipeline stretched over every field looks efficient on a slide. In practice it hides the decisions that settle whether a result is real, because those decisions are different in every field.

01

The physics is different

Molecular dynamics, genome-scale sequence search, density-functional theory and cohort statistics have almost nothing in common below the surface. Each harness is written around the method its field actually trusts.

02

The controls are different

What counts as a positive and a negative control is set by each field's own literature. We build them from primary sources for every domain and pin them, instead of borrowing a generic set.

03

The ways to be fooled are different

Thin statistics, database fields that disagree with their own papers, a candidate that turns out to be a published lookalike. Each harness is audited against the specific traps of its field.

04

The standard of proof is not

Negative controls, three-way verdicts, prior-art checks and provenance on every number apply everywhere. The code is separate; the rules a result must survive are the same.

When one harness teaches us a new way to be wrong, the lesson is written down as a rule and checked into the others by hand. We do not assume two pipelines agree until we have compared them.

For example

What goes in, what comes out

01

Drugs

Molecules in, binding and permeation energies out, ranked into the handful worth synthesising.

02

Proteins

A target surface in, sequences and backbones out, filtered before a single plasmid is ordered.

03

Biomarkers

Multi-omic cohorts in, signatures out, held to a site the model has never seen.

04

Materials

A property specification in, compositions and structures out, screened against physics before a furnace is switched on.

Layers

What we build with

01

Foundation Models

We use and develop foundation models capable of understanding molecular, biological, and scientific data.

Molecular structuresProtein sequencesGenomic dataScientific literatureClinical datasetsImagingMaterials structures
02

Generative Discovery

Instead of only predicting the properties of existing candidates, our models propose entirely new ones, optimized toward several objectives at once.

Novel moleculesProtein sequencesAntibodiesMaterial compositionsCandidate biomarkers
03

Simulation and Prediction

Physics and learned models estimate properties before expensive experiments begin.

Molecular bindingStructure predictionFree-energy landscapesToxicity and stabilitySolubilityProtein interactionsMaterial properties
04

Autonomous Research Agents

Agents run parts of the scientific workflow end to end, and keep a research memory across cycles.

Search literatureAnalyze datasetsGenerate hypothesesDesign experimentsRun computational workflowsCompare candidatesAudit their own results
05

Large-Scale Compute

Discovery needs scale. AI3 Discovery is built on the AI infrastructure and large-scale model serving expertise of AI3.

Large foundation modelsMassive candidate screeningGenerative simulationParallel agent fleetsHigh-throughput inference

Discovery loop

AI × Simulation × Experiment

Each experiment creates new data. Each new data point improves the next discovery cycle. The result is a research program that compounds.

1

Understand

Collect scientific knowledge and biological data.

2

Generate

AI proposes new hypotheses and candidates.

3

Predict

Models estimate likely properties and outcomes.

4

Select

The most promising candidates are prioritized.

5

Validate

Candidates are tested in simulation or in the laboratory.

6

Learn

Results return to the model, and the loop repeats.

Engineering

Built to be checked

A discovery system is only as good as the results it refuses to accept. Our pipelines are designed so that a wrong answer is caught by the system, not by a reader.

Negative controls by default

Every gate runs against a deliberately broken system. A gate that cannot fail is not a gate.

Three-way verdicts

Pass, fail, and indeterminate. A test that passes because the data is thin is reported as indeterminate, together with the smallest effect it could have resolved.

Cross-vendor adjudication

Independent model families score the same candidate. Disagreement raises priority instead of being averaged away.

Provenance on every number

Each reported value carries the system, force field, and run that produced it. Numbers without a track are not quotable.

Bring us a problem worth the computation.

Joint programs, platform access, and data collaborations.