Literature DB >> 32710418

CRISPR Guide RNA Design Guidelines for Efficient Genome Editing.

Patrick Schindele1, Felix Wolter1, Holger Puchta2.   

Abstract

The simple applicability and facile target programming of the CRISPR/Cas9-system abolish the major boundaries of previous genome editing tools, making it the tool of choice for generating site-specific genome alterations. Its versatility and efficacy have been demonstrated in various organisms; however, accurately predicting guide RNA efficiencies remains an organism-independent challenge. Thus, designing optimal guide RNAs is essential to maximize the experimental outcome. Here, we summarize the current knowledge for guide RNA design and highlight discrepancies between different experimental systems.

Keywords:  CRISPR; CRISPR prediction tool; Cas9; Genome editing; Mismatch tolerance; gRNA design; gRNA secondary structure

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Year:  2020        PMID: 32710418     DOI: 10.1007/978-1-0716-0712-1_19

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  2 in total

1.  Having a Same Type IIS Enzyme's Restriction Site on Guide RNA Sequence Does Not Affect Golden Gate (GG) Cloning and Subsequent CRISPR/Cas Mutagenesis.

Authors:  M Moniruzzaman; Yun Zhong; Zhifeng Huang; Guangyan Zhong
Journal:  Int J Mol Sci       Date:  2022-04-28       Impact factor: 6.208

2.  CRISPR/Cas9 mediated mutagenesis of MORE AXILLARY GROWTH 1 in tomato confers resistance to root parasitic weed Phelipanche aegyptiaca.

Authors:  Vinay Kumar Bari; Jackline Abu Nassar; Radi Aly
Journal:  Sci Rep       Date:  2021-02-16       Impact factor: 4.379

  2 in total

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