You’ve been looking for a better way to understand the underlying genomics of human disease. It’s here now.

Dovetail Genomics has proven technology that can accelerate your research into human diseases such as oncology, neurodegenerative and developmental diseases.

From a single NGS library prep, capture a broad range of genetic variants and chromosomal 3D architecture.

Power translational research studies by unlocking valuable FFPE material with Fix-C™ technology.

Whether you prefer to bring our technology in-house or rely on our world-class service team – Dovetail Genomics has you covered.

The All-In-One Library Prep

Sequencing is a major cost in every NGS study. Maximize your return on that investment with our Omni-C™ technology.
Omni-C™ libraries capture SNPs, structural variants and 3-D genome conformation in a single sequencing run.

The Omni-C™ Kit offers the following benefits:

  • “Shotgun-like” genome coverage
  • Long-range information from Illumina short reads
  • Capture SNP and structural variants in a single library
Learn More about Omni-C™

FFPE is the de facto archival material for biopsy specimens. Access this challenging sample type with Dovetail Fix-C™ Services.

Capture valuable long-range 3-D genomic information from Illumina generated short reads

Explore large structural variants, such as insertions, deletions and translocations

Leverage the industry leading proximity ligation services of Dovetail Genomics

We can help you advance research into human disease. Just ask.

Contact us to discover more about this breakthrough technology and how it can help you see further into human disease.

Reach out to get started