Dovetail^®LinkPrep™ Kit

Accelerate Your Linked-Read Library Prep

Ideal For:

Genetic Variation, 3D Genomics, and Genome Assembly

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Dovetail^®LinkPrep™ Technology Video

One Assay, Multiple Solutions

Generate a comprehensive whole genome view of the chromatin topology, genetic variation including structural variants, SNVs, InDels, and CNVs, and genome assemblies with high senstivity. LinkPrep technology enables your short-read sequencer to capture long-range information across the genome.

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Do More with a Single Assay, In Less Time

Uniform Coverage Across The Genome

The Dovetail^® LinkPrep™ technology delivers improved genome coverage and data quality compared to traditional short-read sequencing approaches. The enhanced signal-to-noise ratio (green curve) underscores the assay’s ability to achieve higher resolution and more accurate detection of structural variations and chromatin interactions. This offers a clearer understanding of complex genomic regions, enabling you to extract more meaningful insights from your data.

An Integrated Solution

Dovetail^® LinkPrep™ technology expands the capabilities of short-read sequencers to capture long-range genetic information. It enables base pair-resolved genetic variation detection, high-resolution 3D genome characterization, and rapid haplotype-aware assemblies. Utilizing standard NGS workflows, the LinkPrep™ Assay generates linked-read data, enhancing sensitivity and improving accuracy across a broad range of applications to advance your research.

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Customer Testimonials

"Our lab is excited about the potential of LinkPrep™ data. We currently use a range of NGS-based assays to catalog genetic variations spanning from SNVs up to large SVs. LinkPrep™ has the potential to become a key tool in our oncology research, offering powerful capabilities for the de novo detection of the full spectrum of somatic variants that we focus on."

Brian Walker, Ph.D.

Professor of Medical and Molecular Genetics at Indiana University School of Medicine