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Friday, June 19, 2026
🇺🇸 Americas · Directory profile

Broken String

Gene Editing Safety Platform

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Company overview

Broken String Biosciences offers the INDUCE-seq® platform for unbiased, genome-wide detection of on- and off-target DNA double-strand breaks in gene editing therapies. This PCR-free, cell-based technology enables precise safety assessments in days, supporting cell and gene therapy developers from discovery to commercialization. They provide lab services, in-house kits via the Catalyst Early Access Program, and bioinformatics analysis for actionable insights.

Broken String is listed in the NovaPharmaNews Supplier Hub in the life-science supply chain serving United States & Americas. Core focus areas include gene editing safety, induce-seq, off-target detection, crispr analysis, cell gene therapy.

Structured facts

Website
https://www.brokenstringbio.com
Markets served
United States & Americas
Keywords
gene editing safety, induce-seq, off-target detection, crispr analysis, cell gene therapy

Products & technologies

  • Gene Editing Safety
  • Induce-Seq
  • Off-Target Detection
  • Crispr Analysis
  • Cell Gene Therapy

Therapeutic areas

  • Gene Therapy

Markets served

  • United States & Americas

Company timeline

  1. — Profile published on NovaPharmaNews
  2. — Profile last updated

Frequently asked questions

What is INDUCE-seq® and how does it work?
INDUCE-seq® is a scalable, PCR-free platform that directly labels and captures DNA breaks in cells using next-generation sequencing, enabling genome-wide detection of on- and off-target edits from any nuclease-based system in days.
What products and services are available for gene editing safety?
Products include BreakMap™ with cloud-based bioinformatics and reporting; services encompass lab-based analysis and the Catalyst Early Access Program for in-house use of INDUCE-seq® kits in clinically relevant cells.
What are the key capabilities and regulatory benefits?
The platform is cell- and nuclease-agnostic, measures editing kinetics and repair pathways, supports patient-specific genotypes, and addresses regulatory scrutiny by providing precise, quantitative safety data early in development.