Research use only · auditable by design

Pay for the workflow. Inspect the evidence.

GaiaLab turns biological context into source-linked, testable research hypotheses with visible uncertainty and reproducible records. Plans scale the research workflow—not unsupported claims about model superiority.

Source-linked evidenceExplicit uncertaintyReproducible recordsNo clinical-use claim

Start with the level of workflow you need.

Public exploration remains easy to try. Paid plans add durable research workflow, exports and programmatic access. Institutional teams begin with a bounded validation pilot before broader deployment.

Free
$0
for public research exploration

Evaluate the basic GaiaLab workflow before committing to a paid plan.

  • Gene-panel research exploration
  • Up to 50 genes per analysis
  • Source-linked evidence views
  • Visible limitations and uncertainty
  • Research-use outputs
Start exploring →
Use public or non-confidential inputs.
Pro
$99 / month

For advanced users who need higher-throughput, programmatic, and audit-oriented workflows.

  • Everything in Researcher
  • 200 analyses/day (vs. 50/day on Researcher)
  • API / developer workflow access subject to plan limits
  • Batch and structured export workflows
  • Evidence and lineage artifacts
  • Priority product support
Review developer workflow →
Capabilities remain subject to deployed feature and quota status.
Runtime contractFreeResearcherProInstitutional pilot
Analyses per day1050200Negotiated
Maximum genes per analysis50505050
Biotech · pharma · CRO · research groups

Institutional adoption starts with validation.

Rather than asking a scientific organization to buy a broad enterprise promise, GaiaLab begins with a bounded 4–6 week evaluation against the team's own review process and predefined success criteria.

Review the Validation Pilot →
✓ Agreed question family
✓ Criteria frozen before review
✓ Source-linked evidence package
✓ Negative findings retained
✓ Independent team review
✓ Final go / no-go decision memo
Institutional data boundary.

Initial validation pilots should use public, published, synthetic, or otherwise non-confidential inputs. GaiaLab does not currently represent the public workflow as ready for PHI, patient-identifiable data, regulated clinical data, trade-secret datasets, or confidential institutional information. Confidential-data use requires separately agreed terms and verified enterprise controls.

No agent-count theater

Plans are described by buyer value and workflow. Internal model or agent configurations may change and are not represented as evidence of scientific superiority.

No brittle source-count promise

Evidence availability depends on source health, credentials, query context, licensing and deployment status. GaiaLab should report provenance and availability rather than market a fixed count as a scientific guarantee.

No self-improvement efficacy claim

Calibration, evaluation and workflow updates are versioned. GaiaLab does not claim that every analysis automatically makes the scientific system more accurate.