Synthetic errors derived from chemically synthesized oligonucleotide is a critical factor that limits the length and cost of synthesized genes and genomes. To improve the quality of synthesized oligon
Control CRISPR gRNA against no target in HepG2 cells followed by RNA-seq. (NT-BGHcLV07-B) For data usage terms and conditions, please refer to http://www.genome.gov/27528022 and http://www.genome.gov
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
