CRISPR-Cas9 and related technologies can efficiently alter genomic DNA at targeted positions and have far-reaching implications for functional screening and therapeutic gene editing. Understanding and unlocking this potential requires accurate evaluation of editing efficiency. Here, we show that methodological decisions for analyzing sequencing data can significantly affect mutagenesis efficiency estimates and we provide a comprehensive R-based toolkit, CrispRVariants and an accompanying web tool CrispRVariantsLite, that resolve and localize individual mutant alleles with respect to the endonuclease cut site. CrispRVariantsenabled analyses of newly generated and existing genome editing datasets underscore how careful consideration of the full variant spectrum gives insight toward effective guide and amplicon design as well as the mutagenic process.
CRISPR-Cas9 and related technologies efficiently alter genomic DNA at targeted positions and have far-reaching implications for functional screening and therapeutic gene editing.Understanding and unlocking this potential requires accurate evaluation of editing efficiency.
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