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Overlap between the number of sites nominated by the three genome-wide assays and sites sequence-confirmed as edited in HEK293T/Cas9 cells following hybrid capture sequencing in the 5 MM 0 gap, 3 MM 1 gap homology space. Sites sequenced with an average depth of more than 500 reads and with <30% indel frequency in the untreated samples are included. MM, mismatch; indel: insertions and deletions.
