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Abstract
Base and prime editors enable precise modifications in the genome without introducing double-strand breaks.
- Base and prime editing platforms systematically annotate clinical variants.
- These technologies reveal mechanisms of drug resistance and immune evasion.
- Functional screens using these editors can dissect fundamental biological processes at the level of single nucleotides.
- Challenges and future perspectives for precision editing screens are addressed.
- Causal genotype-to-phenotype mapping is facilitated, potentially redefining genomic variation interpretation.
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