The rhAmpSeq™ CRISPR Analysis System
Wed, Mar 31
|Webinar
An end-to-end solution for genome editing quantification


Time & Location
Mar 31, 2021, 5:00 PM
Webinar
About the Event
CRISPR systems enable targeted editing in a wide variety of organisms by introducing single- or double-strand breaks (DSBs) to DNA, which can be leveraged to introduce genomic changes. However, unintended DSBs can occur off-target at genomic loci with partial complementarity to CRISPR-Cas guide RNA (gRNA) sequences, which can result in genotype/phenotype changes in the edited cells. Genome editing at on- and off-target sites can be quantified with multiplexed targeted next-generation sequencing (NGS) but requires bioinformatics expertise to analyze. Here we present the rhAmpSeq CRISPR Analysis System as a streamlined end-to-end solution for designing assays, generating sequencing libraries, and analyzing NGS data for quantifying CRISPR on- and off-target editing effects without the need for bioinformatics experience.
Objectives
Learn how rhAmpSeq CRISPR Analysis System can help you streamline your CRISPR genome editing analysis
Learn how to simultaneously quantify intended edits and evaluate off-target modifications with accuracy
Learn about reducing off-target effects without…