EPIVISION™ — One Platform. Multiple Markets. Breakthrough Impact.
Early Cancer Detection

One Platform. Multiple Markets.
Breakthrough Impact.

DNA mutations tell you what previously changed for patients.
Our tests reveal what's happening now — reading the layered epigenetic signatures conventional tests cannot see. Detect earlier. Monitor smarter. Power richer trials.

A New Layer of Cancer Detection

Reading the biological signals in blood that conventional liquid biopsies miss — from less than 1 mL of plasma.

Today's Blind Spot

Most liquid biopsies look for one thing: genetic mutations shed by tumors into the bloodstream. But in early-stage cancer, those mutations are often too rare to find — like searching for a handful of typos in a library. By the time the signal is strong enough to detect, the disease has often progressed.

✗ The Gap

At Stage 0 and Stage I — when treatment outcomes are best — mutation-based tests frequently come up empty.

The Signal Others Miss

Cancer doesn't just rewrite the genetic code — it changes how that code is packaged and controlled. We read these regulatory changes one molecule at a time, capturing a far richer picture of the disease. Crucially, this signal remains visible even when mutation-based tests go silent.

✓ Validated in Nature Biotechnology

Peer-reviewed evidence shows our approach delivers accurate cancer detection — independent of DNA sequencing.
(Fedyuk et al., Nature Biotechnology, 2022)

Seed Round Now Open

Invest in the next generation of cancer diagnostics.

We're raising our Seed Round to accelerate clinical validation, regulatory milestones, and BioPharma partnerships — and we're inviting a select group of mission-aligned investors to join us at the ground floor.

$15B+
Addressable Market
Across liquid biopsy, early screening, and companion diagnostics.
Nature
Peer-Reviewed Validation
Foundational science published in Nature Biotechnology.
1st
In Category
A defensible new diagnostic layer no competitor can read today.

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