Powering the future of gene editing development
The next generation of genome-wide on- and off-target analysis in your own hands
The new standard for rapid detection of gene editing-induced breaks
Scales from
discovery to IND
Support guide screening, optimization, and downstream characterization
Works across cell
types & editors
Use one approach across diverse cell models and nuclease systems
Reproducible
standardized data
Generate decision-ready outputs you can trust across programs
Single
unified workflow
Replace fragmented assays with one consistent approach
No outsourcing.
No black-box services.
Full control of your data.
The BreakMap platform powered by INDUCE-seq® delivers fast, unbiased on- and off-target analysis entirely in-house, replacing fragmented legacy workflows with a single standardized assay.
Integrated bioinformatics converts complex genome-wide sequencing data into clear, ranked outputs, for confident decision-making.

