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.

Helix Studio 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: an Edit Program

Helix prices, governs, and audits at the level of an Edit Program.

A target class or therapeutic objective
A bounded set of edit intents
A declared policy and calibration regime
A persistent decision history

Evidence, not insight

The goal is not to “predict biological truth”. The goal is to generate reviewable, reproducible computational evidence 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

How Helix is licensed

Helix is licensed per Edit Program with an annual governance license, plus optional compute and support tiers.

See licensing units →