Base Editing

CRISPR-derived editors that chemically convert individual DNA bases without requiring double-strand DNA breaks.

Core metadata

Prerequisites

Dependents

Fields

Field lanes

Node sources

Prerequisite edge evidence

Edge/source evidence summary:

Prerequisite Type Confidence Evidence level Note Sources
CRISPR-Cas9 Genome Editing (crispr_gene_editing) historical_predecessor 78% primary_source CRISPR-Cas9 genome editing established the programmable Cas9 editing platform that base editing adapted to install base conversions without double-strand DNA cleavage.
Programmable Cas9 Nuclease (cas9_programmable_nuclease) required 92% primary_source Cytosine base editors use catalytically impaired Cas9 as the programmable DNA-targeting component fused to a deaminase.
Protein Engineering (protein_engineering) required 90% primary_source Base editors are engineered protein fusions, such as deaminase domains joined to catalytically impaired Cas9 variants, making protein engineering a direct component dependency.

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