A CRISPR enhanced Viral Integration Site detection method in genome level
We describe CReVIS-seq, a highly efficient, genome-wide method for detecting viral insertion sites using high-throughput sequencing, which is based on in vitro circularization and subsequent cleavage of genomic DNAs in a CRISPR guide RNA-specific manner.
Citation info: Kim HS. et al. CReVIS-seq: a highly accurate and multiplexable method for genome-wide mapping of lentiviral integration sites
Please input your data in below form, or download an example.
(blue: indicator sequences at each ends of comparision range, green: LTR sequence in data)
|Comparison range (R) [?]||Minimum frequency (n) [?]|