Dovetail Genomics Showcases New VariLink™ Assay Findings at AGBT Conference
A Groundbreaking Assay Using Short-Read Sequencers to Comprehensively Detect Large Structural Variants
"Detection of large structural variants has been a challenge using short-read platforms. We have solved this problem using VariLink, our single-day library preparation workflow. By generating high-quality, unbiased Hi-C libraries, we capture the full spectrum of genetic variants enabling oncology researchers to more fully understand the drivers of human cancer," said
Using a clinical ovarian serous adenocarcinoma sample, the authors compared the performance of the VariLink assay for detecting a continuum of large and small structural variants compared to whole genome shotgun sequencing (WGS) and RNA-seq. Compared to WGS, the VariLink assay demonstrated enhanced sensitivity and precision for SV detection while maintaining a high concordance for capturing SNVs and indels.
The VariLink data demonstrated increased sensitivity for breakpoint detection while reducing the number of false positives that plague short-read WGS data. Illustrating this capability, three translocations linked to known oncogenes known to drive oncogenesis were discovered with high confidence and confirmed by PCR and
"In the past, we have seen interest in using Hi-C for detecting large structural variants, however, the assay complexity, multiday workflow, and sequence coverage gaps associated with traditional Hi-C have limited its broad adoption. Our LinkPrep technology on which the VariLink assay is built addresses these shortcomings," stated
The detailed findings will be presented in the poster titled "VariLink: a novel assay for comprehensive variant detection and genome characterization" (Poster Number: 506) on
Dovetail Genomics is seeking additional projects that highlight the unique sensitivity and precision offered by the VariLink assay for inclusion in the early access program. Researchers interested in being considered for this program are encouraged to contact Dovetail Genomics at dovetailgenomics.com.
About Dovetail Genomics
Dovetail Genomics, a subsidiary of Cantata Bio and an Edenroc Sciences company, is a leading provider of genomics solutions focused on understanding the complex organization of the genome. Through Dovetail Genomics' proprietary proximity ligation technologies, the 3D architecture of the genome is captured alongside primary sequence information using standard next-generation sequencing (NGS) approaches. Researchers are using Dovetail Genomics' unique methods to solve complex problems including chromatin topology analysis, small and large structural variant detection, de novo chromosome assembly, haplotype phasing, and microbiome analysis in the fields of epigenetics, developmental biology, cancer research, evolutionary biology and more. For more information on Dovetail, its technology, and service offerings, visit www.dovetailgenomics.com. Follow Dovetail on X/Twitter: @DTGenomics.
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SOURCE Dovetail Genomics
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