Abstract
This chapter will broadly cover the newest genome editing technology, clustered regularly interspaced short palindromic repeats (CRISPR), and CRISPR-associated system (Cas), as a critical tool for a modern research laboratory. Multiplex gene mutagenesis, tissue-specific gene disruption, DNA insertions, transcriptional activation, transcriptional repression, megabase-sized deletions, translocations, and genetic screens are all possible with CRISPR/Cas technology. How CRISPR-genome editing works, its applications, and considerations for best use will be discussed.
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Freeman, K.W. (2019). Gene-Editing Techniques. In: Kennedy, G., Gosain, A., Kibbe, M., LeMaire, S. (eds) Success in Academic Surgery: Basic Science. Success in Academic Surgery. Springer, Cham. https://doi.org/10.1007/978-3-030-14644-3_11
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DOI: https://doi.org/10.1007/978-3-030-14644-3_11
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