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rhAmpSeq™ CRISPR Analysis Tool

Flexible, cloud-based interrogation of CRISPR-mediated, double-strand break repair

  • Analyze on- and off-target CRISPR edit sites without having bioinformatics expertise
  • Characterize Cas 9 or Cas12a (Cpf1) edits (contact us for other nucleases)   
  • Batch analyze singleplex or multiplex samples (≤500 targets) simultaneously
  • Interpret results with supported, validated, versioned workflows
  • Streamline analysis with the same-day data delivery
  • Access with purchase of rhAmpSeq CRISPR Library Kit

* This service is not currently available in China or Russia

Research-friendly UX

An advanced, accessible, and rapid analysis tool for CRISPR results validation.

  • Stream or drag-and-drop FASTQ files
  • Annotation of repair mechanisms (NHEJ, MMEJ, HDR)
  • Interactive graphics with high-resolution downloads
  • Secure and GDPR-compliant
Cloud-Hosted UI screenshot

Advanced genome editing analysis tool with a friendly graphical user interface

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High throughput
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Same-day delivery
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Advanced yet accessible

Tailored to your research

Using the rhAmpSeq™ CRISPR Analysis Tool

Get started

rhAmpSeq™ CRISPR Analysis Tool tutorial

This tutorial will guide you though the process of using the rhAmpSeq™ CRISPR Analysis Tool, and several of its features.

Resources

Brochures and flyers

Frequently asked questions

Sample data

The tool combines a user-friendly interface with powerful readouts of different types of genome editing including imprecise HDR and MMEJ. The ability to quickly analyze multiplexed reads makes it all the more better.

Eric Aird
Posdoctoral Researcher
ETH Zurich