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. 2020 Oct 21;10:17912. doi: 10.1038/s41598-020-74960-7

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© The Author(s) 2020

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

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Comparison of pronuclear microinjection versus electroporation (live pups). (a) Table summarizing editing efficiency at 5 gene loci in live pups after pronuclear microinjection (PNI) or electroporation (EP) of CRISPR reagents into wild-type C57BL/6J zygotes. (b) Total mutagenesis rate at 4 gene loci in live pups obtained from pronuclear microinjection (PNI) or electroporation (EP WT) of CRISPR reagents into wild-type C57BL/6J zygotes. (c) Rate of homology directed repair at 3 gene loci. Colours representing individual target loci are consistent across the figures (Supplementary Table 4).