Biomarker Discovery

Illuminating a new class of genomic biomarkers

Conventional approaches to identify biomarkers focus on expressed genes, missing critical effects of the non-coding regions. BreakSight goes beyond traditional methods by mapping DNA damage sites in and outside of gene regions, opening up the rest of the genome for biomarker discovery.

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Why BreakSight?

A complete workflow tailored for biomarker discovery

Genome-wide focus

BreakSight explores the entire genome, including non-coding regions and repetitive sequences, uncovering unique findings missed by other approaches.

Unparalleled data resolution

Our platform delivers high-resolution data on DNA break sites and their genomic contexts, offering insights that accelerate biomarker discovery and validation.

Enabling precision medicine

BreakSight bridges the gap between mechanistic insights and biomarker discovery to offer new information for clinical strategies that drive personalized treatment decisions.

Unique DNA damage insights

With BreakSight’s approach, map DNA double-strand breaks with precision and reveal patterns of genomic instability that may serve as key indicators for drug response and efficacy.

Accelerate your biomarker breakthroughs

Illuminate genome-wide landscapes of DNA damage with site-specific precision to increase your chances of discovering new sequence biomarkers.

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