To make the EGFRvIII mutant cell line in H9, gene editing was performed using CRISRP-CAS9 with two sgRNAs. This is the sequencing data for EGFR site for mutant cell line. Off-target position of each s
Genome sequencing data of Cryphonectria parasitica super hypovirus-donor strains SD82 and SD328 to show that there are not external genes left in the genome after gene manipulation.
In order to investigate changes upon ZBTB10 depletion, we used CRISPR/Cas9 to induce a ZBTB10 knockout in HEK293 and U2OS cells. Overall design: ZBTB10 knockouts were generated using three different g
