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 and software that can accelerate your research into human diseases such as oncology, inherited, and undiagnosed diseases.
With the combination of our industry leading proximity ligation techniques and analysis software we can now reveal all classes of large structural variants and 3D features in the human genome.
FFPE is the de facto archival material for biopsy specimens. For the first time, we can help you see structural variants and 3D features on a genome-wide scale in FFPE.
Think of how many decades of paraffin-embedded biopsy specimens are available in research facilities. How much further could you advance disease research if there was a way to learn more from them? We’re giving you the ability to do just that with Fix-C™ and Selva™ analysis. Reveal previously undetectable structural variants and 3D chromatin features in FFPE samples, and take your research—and our global understanding of the genome—to a whole new level.
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.