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Genome-scale engineering of Saccharomyces cerevisiae with single-nucleotide precision

Journal Article · · Nature Biotechnology
DOI:https://doi.org/10.1038/nbt.4132· OSTI ID:1486877

We developed a CRISPR–Cas9- and homology-directed-repairassisted genome-scale engineering method named CHAnGE that can rapidly output tens of thousands of specific genetic variants in yeast. More than 98% of target sequences were efficiently edited with an average frequency of 82%. We validate the single-nucleotide resolution genome-editing capability of this technology by creating a genome-wide gene disruption collection and apply our method to improve tolerance to growth inhibitors.

Research Organization:
Univ. of Illinois at Urbana-Champaign, IL (United States)
Sponsoring Organization:
USDOE Office of Science (SC)
DOE Contract Number:
SC0018260
OSTI ID:
1486877
Journal Information:
Nature Biotechnology, Vol. 36, Issue 6; ISSN 1087-0156
Publisher:
Springer Nature
Country of Publication:
United States
Language:
English

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A gRNA-tRNA array for CRISPR-Cas9 based rapid multiplexed genome editing in Saccharomyces cerevisiae March 2019
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Double Selection Enhances the Efficiency of Target-AID and Cas9-Based Genome Editing in Yeast August 2018
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