Cancer Research

Advancing cancer research with precision genomics

BreakSight provides cutting-edge tools to map and sequence DNA double-strand breaks DNA double-strand breaks, shedding light on the genomic instability that drives cancer.

Get a complimentary
sample analysis

Why BreakSight?

Paving the way for personalized cancer treatments

Comprehensive genomic analysis

Captures data across the entire genome, including repetitive and non-coding sequences, for a holistic view of cancer biology.

Accelerated research timelines

Streamlines the identification of potentially new and synergistic therapeutic targets and corresponding genomic biomarkers, saving valuable time in the research process.

Data-driven decision making

Gain actionable insights on sequence vulnerabilities across the genome upon strategic molecular targeting.

Improved therapeutic targeting

Reveals DNA damage patterns that guide the development of more effective, personalized cancer treatments.

Ready to transform your cancer research?

Release the full potential of the genome to advance cancer research and improve patient outcomes.

Submit a sample link arrow icon