Description

The rhAmpSeq CRISPR Analysis System allows quick and accurate quantification of CRISPR-Cas edits. Our proprietary RNAse H2-dependent PCR technology generates amplicon libraries for targeted sequencing on Illumina® NGS platforms. The system also includes an advanced but accessible cloud-based data analysis pipeline for quantification of on- and off-target edits.

• Best-in-class insertion/deletion (indel) quantification of genome editing
• Batch analysis of your results (multiplex up to 500 targets)
• High sequencing coverage uniformity and percentage of mapped reads
• Intuitive data analysis that requires no bioinformatics expertise
• Sample-to-analysis in under a week