AuraOne
Domain Lab

You're editing life. That demands proof.
Your sequences need safety review before synthesis. AI scores every one. You get the regulatory evidence.
For teams that answer to regulators before they answer to investors.

Upload FASTA or CSV. AI runs off-target scoring, pathway simulation, variant triage, and ADMET screening. Results ship with FDA/EU AI Act evidence packs.

Your first run

50 sequences. 2 weeks. Your first evidence pack.

AI LabsRegression BankDomain Labs
Accepted formats
FASTA / CSV / GenBank

Upload sequences in the formats your lab already uses.

Compliance frameworks
FDA / EU AI Act

Evidence packs structured for regulatory submission and audit.

Pre-built agent
sequence-analyst

Off-target scoring, ORF analysis, and pathway simulation out of the box.

Focus Areas

What this lab is built for.

Surfaces designed for scientists, operators, and executives. Every output is versioned with provenance so no work is lost.

Automated QC

Safety checks before synthesis.

  • Off-target motif probability scoring on upload
  • ORF summary, GC content, and codon analysis
  • Risky sequences flagged and routed for expert review

Pathway Simulation

Predict flux before the bench.

  • Simulate downstream impacts on metabolic pathways
  • Estimate flux shifts and reagent requirements
  • Link predictions to lab assay files with provenance

Evidence that compounds

Your decisions, captured.

  • Every approved decision strengthens regression coverage
  • Structured JSONL exports with audit-friendly metadata
  • Evidence packages reviewers and procurement will accept

Variant Review & Screening

Genomics and drug-discovery in one loop.

  • Variant triage with scoring, adjudication, and reviewer sign-off
  • ADMET-relevant property scoring for molecular screening
  • Adjudication workflows that keep disputed calls documented
Signature Workflow

How Biology runs.

Automated evaluation. Expert routing. Regression-tested releases.

Step 1

Upload

Drop your sequences.

  • Upload FASTA, CSV, or GenBank batches
  • Automatic parsing and validation of DNA/RNA strings
  • Link to project constraints and reagent specifications
Step 2

Score

Safety and efficacy signals.

  • Off-target motif scans and structural checks on every sequence
  • Edge cases routed to domain experts via Workforce
  • Risk factors visualized on a unified timeline
Step 3

Export

Lab-ready handoff with evidence.

  • Export accepted guides to synthesis partners
  • Generate FDA/EU AI Act evidence packs tied to runs and reviewers
  • Edge cases sent to review with full context attached

Overview

Upload your sequences and get structured safety scoring before anything reaches the bench. AuraOne Biology runs off-target motif analysis, ORF checks, pathway simulation, variant triage, and ADMET screening — then packages the results into evidence your regulators will accept.

Biology capsule

Your sequences need safety review before synthesis. AI scores every one. You get the regulatory evidence.

  • Upload FASTA or CSV. AI runs off-target scoring, pathway simulation, variant triage, and ADMET screening. Results ship with FDA/EU AI Act evidence packs.
  • FASTA / CSV / GenBank Accepted formats
  • Focus: Automated QC
  • Workflow: Upload

Score before you synthesize

Upload FASTA or CSV files and receive structured safety summaries. The system flags higher-risk motifs for expert review so bench work starts from a cleaner set of assumptions. Variant triage and molecular screening follow the same pattern: score, route, decide, record.

Biology capsule

Your sequences need safety review before synthesis. AI scores every one. You get the regulatory evidence.

  • Upload FASTA or CSV. AI runs off-target scoring, pathway simulation, variant triage, and ADMET screening. Results ship with FDA/EU AI Act evidence packs.
  • FASTA / CSV / GenBank Accepted formats
  • Focus: Automated QC
  • Workflow: Upload

Evidence that survives audit

Every decision is captured with provenance. Approved results strengthen regression coverage, so what you learned once is reusable. Export FDA/EU AI Act evidence packs when regulators or procurement ask.

Biology capsule

Your sequences need safety review before synthesis. AI scores every one. You get the regulatory evidence.

  • Upload FASTA or CSV. AI runs off-target scoring, pathway simulation, variant triage, and ADMET screening. Results ship with FDA/EU AI Act evidence packs.
  • FASTA / CSV / GenBank Accepted formats
  • Focus: Automated QC
  • Workflow: Upload

Proof hooks

Evidence that stays attached

This is what the system is designed to record for Biology workflows. Metrics and outcomes depend on your deployment and must be validated in staging and production.

FDA / EU AI Act
Evidence packs structured for regulatory submission and audit review.
Borderline routing
Edge cases route to experts with full sequence context attached.
Regression coverage
Approved decisions compound into reusable regression tests.
Want the security and evidence model? Start in the Trust Center.
Visit Trust Center

Start your Biology Lab.

One session. First lab running.