Journal
NATURE COMMUNICATIONS
Volume 9, Issue -, Pages -Publisher
NATURE PUBLISHING GROUP
DOI: 10.1038/s41467-018-04651-5
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Funding
- KU Leuven Research Council [PF/10/010, PDM/17/130, C1/17 3E170455]
- FWO [G047112N, G055517N, G0B2515N]
- VIB
- National Institutes of Health [R01GM48746, R01GM088653, NIH-GM079656, NIH-GM066099]
- National Science Foundation [NSF DBI-1356569]
- NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [R01GM048746, R01GM088653, R01GM066099, R01GM079656] Funding Source: NIH RePORTER
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CRISPR advances genome engineering by directing endonuclease sequence specificity with a guide RNA molecule (gRNA). For precisely targeting a gene for modification, each genetic construct requires a unique gRNA. By generating a gRNA against the flippase recognition target (FRT) site, a common genetic element shared by multiple genetic collections, CRISPRFRT circumvents this design constraint to provide a broad platform for fast, scarless, off-theshelf genome engineering.
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