To identify potential off-target mutations generated by the NRT1.1 genome editing system, Illumina deep sequencing on T0 seedling leaf tissue from event 1 was performed. This sequencing run produced 7
S6 Table lists information regarding alleles, strain names and reagents that were generated and used, respectively, during this study for CRISPR/Cas9 mediated genome engineering. (XLSX)
RNA-seq on HepG2 cells treated with a CRISPR gRNA against RPS8. (RPS8-BGHcLV31) For data usage terms and conditions, please refer to http://www.genome.gov/27528022 and http://www.genome.gov/Pages/Res
Herein, we present the uncropped raw gel images associated with our manuscript titled " Enhancement of CRISPR-Cas12a System through Universal Circular RNA Design ," published in Cell Reports M