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. 2018 Jul 17;4:39. doi: 10.1038/s41421-018-0047-9

Fig. 1. Highly efficient base editing using ABE system in rats.

Fig. 1

a Summary of the base editing experiments in rats. b The representative sequence chromatogram of Hemgn targeting sequence (potential founder #1). The conversion of A to G at target site was marked with red star. c Summary of the targeted deep sequencing of on-target site for Hemgn (potential founders #1, #8, #10, and #12). The conversion efficiency of every A was indicated. The PAM was highlight in red. d The representative sequence chromatogram of Ndst4-A targeting sequence (clone #4 of potential founder #32). The conversion of T to C at target site was marked with red star. e The representative sequence chromatogram of Ndst4-B targeting sequence (clone #4 of potential founder #32). The conversion of T to C at target site was marked with red star. f Summary of the targeted deep sequencing of on-target site for Ndst4-A (potential founders #7, #15, #22, and #32). The conversion efficiency of every A was indicated. The PAM was highlight in red. g Summary of the targeted deep sequencing of on-target site for Ndst4-A (potential founders #7, #15, #22, and #32). The conversion efficiency of every A was indicated. The PAM was highlight in red