The Future of Precision Medicine

Leading Genomic Innovation Beyond Traditional Boundaries

Our groundbreaking technology is designed to fill essential gaps in genomics research, diagnostics, therapeutics, and drug development.

Our innovative method identifies genomic data and modifications inaccessible with other commercial technologies.

Our distinctive platform does not require DNA amplification, labels, or library preparation.

We Detect

What Others Cannot See

Missing Data

Current genomic analysis methods often miss critical epigenetic data and important genomic markers, leading to significant diagnostic gaps.

More Data

Detect of large structural variants, long range epigenetic mapping, and de novo genome assembly.
Sequence ultra-long, native nucleic acid molecules at single base resolution.
No labeling or amplification of target nucleic acid is required, and the sequence is read in real-time.

Professional physician interacting with futuristic holographic medical interface displayed on digital tablet. Innovative healthcare technology features blue icons representing DNA, heart health,

Research & Technology Using the Power of Machine Learning We Have:

Developed rapidly manufacturable metamaterial/plasmonic nanostructures with outstanding sensitivity for non-resonant SERS single nucleotide detection.

Demonstrated our detection of single nucleotides.

Integrated our structures into chips, where we control velocity with electric fields.

Epigenetic Sequencing

Revolutionizing today's sequencing technologies is essential to unlocking the full potential of precision medicine.

Nanochannels With Enhancement Structures

We created tiny channels (around 40nm wide) to improve Surface Enhanced Raman Spectroscopy (SERS) for precise single nucleotide detection. Our method can identify individual nucleotide structures and detect epigenetic and chemical changes accurately.

SERS - Surface Enhanced Raman Scattering

Surface-enhanced Raman spectroscopy (SERS) provides a clear view of molecular structures, making it possible to identify specific nucleotides and epigenetic markers easily. This method offers a simple yet powerful way to understand complex molecular details.