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.
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