Operationalizing genome editing across a broad range of genomic and cellular targets

Since 2013, the CRISPR/Cas9 system has become a widely used tool for genome editing due to its simplicity. Since that time, CRISPR technology has been adapted for diverse applications aside from genome editing, providing versatility comparable to preceding techniques. With ongoing attempts to unlock the full potential of this technology, the future of CRISPR technology is promising.

In this SelectScience CRISPR webinar series, produced in partnership with GenScript, we explore topics ranging from creating double-strand breakages, to targeting animal model and building tools to support your work. This series features presentations from expert speakers with a variety of scientific backgrounds and consists of three webinars, starting on Thursday, August 12.

Operationalizing genome editing across a broad range of genomic and cellular targets

Thursday, August 12, at 16:00 BST / 17:00 CEST / 11:00 EDT / 08:00 PDT

Targeted DNA integration without double-strand breaks using CRISPR RNA-guided transposons

Thursday, August 26, at 16:00 BST / 17:00 CEST / 11:00 EDT / 08:00 PDT

Building more useful CRISPR/Cas technologies

Wednesday, September 1, at 16:00 BST / 17:00 CEST / 11:00 EDT / 08:00 PDT