System of Record for Genome Editing Decisions

Auditable decision infrastructure for genome editing programs.

Helix is the first Genome IDE designed to function as a system of record for genome editing decisions.

Omnis Helix is built for decisions you can defend: deterministic computation, explicit policy gates, and replayable evidence bundles that survive handoffs to QA, platform leads, and procurement.

Every system of record for genome editing is a Genome IDE. Not every Genome IDE deserves to be a system of record. What is a Genome IDE? →

What happens without a system of record?

Most genome editing decisions cannot be reconstructed six months later. The design may still exist, but the assumptions, policy gates, and evidence trail are gone.

Decisions can’t be reproduced
Assumptions drift silently
Risk assessments can’t be defended
Institutional memory evaporates

The unit of value: a governed decision workspace

Helix governs and audits at the level of a decision workspace: the program context, policies, evidence bundles, reviewer actions, and acceptance gates that must stay coherent over time.

A decision boundary
A regulatory surface
A long-lived artifact stream
Something that needs to be defended months or years later

Evidence, not insight

The goal is not to “predict biological truth”. The goal is to generate reviewable, reproducible outputs with Verified Cross-Host Reproducibility under explicit assumptions — and to enforce boundaries on what is and is not known.

Outcome simulation becomes Decision Evidence
Predicted outcomes become Implied Distributions (Assumption Bound)
Off-target analysis becomes Policy Gated Risk Enumeration

Pricing structure

Helix is sold through design partner pilots, enterprise pilots, and annual Teams/Governance packages. Compute and regulated deployment support are scoped separately.

See pricing →