Dovetail Genomics utilizes proprietary proximity ligation technology to provide genome-wide and targeted insights into genetic variation and the three-dimensional regulatory landscape of genomes. This technology enables researchers to capture large structural rearrangements and variant phase information, enhancing the accuracy of genome assembly and advancing applications in epigenetics and oncology.
Funding
Funding not disclosed
Founders
Product
Problem
Researchers face challenges in fully understanding genetic variation and the three-dimensional structure of genomes, which limits insights into gene regulation, genome assembly, and applications in epigenetics and oncology. Traditional sequencing methods often fail to capture large structural rearrangements and variant phase information effectively.
Solution
Dovetail Genomics provides proximity ligation-based technology that enables comprehensive genome-wide and targeted analysis of genetic variation and the 3D regulatory landscape. Their solutions capture large structural rearrangements and variant phase information, enhancing the accuracy of genome assembly and providing a more complete picture of genome organization. This technology bridges the gap between genotype and phenotype, empowering researchers to unravel disease mechanisms, uncover drug modes of action, and identify biomarkers. Dovetail Genomics offers both kits and services to support a range of applications, from epigenetics to genome assembly.
Target Audience
The primary audience includes researchers in biopharmaceutical companies, academic institutions, and service labs focused on epigenetics, genome assembly, and oncology.
Features
- Proximity ligation technology for genome-wide and targeted analysis
- Kits for epigenetics, genome assembly, and microbial profiling
- Services for epigenetics and genome assembly
- Ability to capture large structural rearrangements and variant phase information
- Tools for diploid and polyploid genome assembly
- Expertise in 3D genomics, bridging the gap between genotype and phenotype
- LinkPrep NGS Technology for enhanced sensitivity in detecting structural variants and chromatin topology features in cancer
- AssemblyLink Assay for faster access to more accurate genomes for biodiversity research