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United StatesHealthcare and life sciences2025 – ongoing

Scribe Therapeutics

DeepXE model for predicting guide RNA editing efficiency

Scribe Therapeutics said its in-house DeepXE model doubled the hit rate and cut guide RNA screening by more than half

In progressCompany's own claimOfficial ↗

Problem

Designing potent guide RNAs for the company's CasXE gene editors normally needs large screening runs in the lab. Scribe wanted to speed up the design of potent editing molecules.

Approach

Scribe built DeepXE, a proprietary machine learning model that predicts the on-target editing efficiency of guide RNAs for its XE variant of CRISPR-CasX. The company unveiled it in September 2025 at a Cold Spring Harbor Laboratory genome engineering meeting. It said it tested the model across several engineered XE variants, target genes and assay conditions.

Results

2xhigher hit rate with the model, per ScribeCompany's own claim[1]
under 10%false negatives, per ScribeCompany's own claim[1]
more than 50%reduction in screening size, per ScribeCompany's own claim[1]

Takeaway

The results are company-reported and preclinical. Scribe gave no training data or independent validation.

Categories

Business function
IT and R&D
Innovation type
Process innovation
Evidence
Company's own claim

Sources

Source summaries

[1]Scribe Therapeutics9 Sep 2025

Scribe's release introduced DeepXE, which it called the first machine learning model able to accurately predict on-target editing efficiency for XE. It reported a 2x higher hit rate, under 10% false negatives, sensitivity above 90% and a screening size cut of more than 50%. It said the model beat conventional Cas9-based models.

Full details are in the original sources.

Added 3 Nov 2026 · Updated 3 Nov 2026
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