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

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Scales from

discovery to IND

Support guide screening, optimization, and downstream characterization

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Works across cell

types & editors

Use one approach across diverse cell models and nuclease systems

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Reproducible

standardized data

Generate decision-ready outputs you can trust across programs

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Single

unified workflow

Replace fragmented assays with one consistent approach

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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.

From edited cells to genome-wide insights in a single workflow

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Cell editing &
immobilization


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DNA break labeling
& library prep


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Sequencing


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Data analysis


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Reporting

Reduce program risk with confident genome-wide on- and off-target insights

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Identify the best-performing guides in days

Avoid late-stage failures caused by hidden off-targets

Build robust regulatory packages with empirical data

Translate sequencing data into clear, ranked on- and off-target insights

Simplify workflows and reduce dependence on bespoke assays

Identify and characterize new editing tools

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