APPLICATION

Powering Genetic Variation

Capture the full extent of genetic variation from a single sequencing run including SNVs, variant phasing, CNVs, and large structural variants.

Powering Genetic Variation

Discover the power of Dovetail^® LinkPrep™ technology—your new go-to solution for somatic variant detection. With the LinkPrep™ Assay, you can easily create linked-read libraries, enabling highly sensitive detection of structural variants (SVs) while capturing the full range of somatic variation. That means one assay delivers SVs, SNVs, InDels, and CNVs with ease.

Best of all, the workflow is streamlined to fit into your day—it takes just a single day from sample to sequence-ready library, requires no specialized equipment, and works seamlessly with any Illumina sequencer. It’s innovation made simple.

Variant Phasing

The ability to resolve variant phase information is highly limited using standard NGS platforms due to the short reads they produce. While long read sequencing platforms do much better, they are not accessible to all. The lack of variant phase information for many datasets limits their utility in being able to:

• Distinguish compound heterozygotes
• Understand linkage disequilibrium patterns
• Identify disease causing variants
• Determine haplotypes

Dovetail proximity ligation libraries enable short read sequencers to capture long-range phase information alongside traditional genotypes. Break though the limits of your short read sequencer with the Dovetail^® VariLink™ assay.

HLA Typing

The 3 Mbp human leukocyte antigen region (HLA) on chromosome 6 is responsible for encoding protein markers that enable the immune system to distinguish self from non-self. HLA plays key roles in:

• Infectious disease
• Transplant rejection
• Cancer
• Autoimmune disease

As the most highly polymorphic region in the human genome (containing over 30,000 possible alleles), the ability to capture phase information is key to being able to match haplotypes between individuals, tailor drugs to specific disease causing haplotypes and better prime the immune system to fight infection.

Dovetail Genomics is currently working with external partners for HLA typing and are open to solving your specific needs.

Genetic Variant Detection

Chromosomal large structural rearrangements are associated with a variety of diseases from cancer to rare inherited diseases. These variants can take the form of translocations, inversions, duplications, and deletions. By their very nature, they are challenging to detect using today’s next generation sequencing platforms due to limited read length and continue to be a missing component to most NGS datasets.

Powered by our proprietory LinkPrep™ technology, the Dovetail^® VariLink™ assay offers a unique solution enabling the detection of known and unknown structural variants on short read sequencers. The VariLink assay, currently in early access, enables the user to go from sample to sequencer in a single day and is amenable to automation.

Application

Chromatin Topology

Whole Genome Ultra
High-Resolution Topology

Whole Genome Rapid
High-Resolution Topology

Protein Anchored Topology

Enhancer Promoter Interactions

Genetic Variation

Large Structural
Variant Detection

Genotyping

Haplotype Phasing

Genetic Genome Assembly

Genome Scafolding

Hybrid Capture Compatible

Dovetail Assay

Micro-C

TopoLink

HiChIP

Pan Promoter

VariLink

Omni-C

* Workflow also requires the Dovetail Micro-C Kit