We incorporated 13 genome-wide deep sequencing techniques, including GUIDE-seq, CIRCLE-seq, SITE-seq, DISCOVER-seq, DISCOVER-seq+, CHANGE-seq, Digenome-seq, DIG-seq, HT-GTS, IDLV and BLESS to construc
Data illustrating how genetic variation may modify the genomic outcomes of therapeutic gene editing. We developed a tool called CRISPRme that explicitly and efficiently integrates human genetic varian
Rec-seq identifies bona fide recombinase substrates from a pool of randomized DNA sequences through in vitro selection and high-throughput sequencing. We used Rec-seq to study the DNA recombination pr