SERVICE

Genetic Variant Services

Leverage our scientists' expertise to take on your somatic variation project. From large SVs down to single-nucleotide mutations, we’re here to help unravel the cancer genome.

Build a Comprehensive View of Genetic Variation

Simplify your somatic variation analysis—just send us your samples, and we’ll handle the rest! No need to onboard new technology or learn new NGS data types. Once your samples are submitted, we’ll provide a comprehensive report with standard deliverables, including SNVs/InDels (VCF file with ensemble variant effect predictor annotation), CNVs (SEG file), and SVs (BEDPE file), all ready to integrate into your existing variant analysis workflow.

Our team will work closely with you to set clear goals and customize the project to meet your needs. From full project management to targeted support, our experts are here to make your research easier.

Dovetail^® Genetic Variant Service

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For those seeking robust and accurate somatic variation detection, our linked-read assay offers high-sensitivity detection of SVs with base-pair breakpoint resolution, along with comprehensive capture of SNVs, InDels, and CNVs. Gain a complete view of somatic variation with unmatched precision and reliability.

Translational human sample types including, cells, tissue,

blood, and FFPE are supported

Performance that holds up, even in FFPE

Strong agreement in SV Calls between FFPE fresh frozen samples
SV detection with high sensitivity and specificity
Robust Performance across DIN ranges and tumor types

Summarize Genetic Variation with Clear, Actionable Reporting

The Dovetail^® linked-read service provides a customized genetic report, summarizing variant calls with clear, accessible insights.

Alongside sample information, the genomic analysis report features an at-a-glance overview with a Circos plot and a breakdown of variant counts by type.

For deeper analysis, it includes a ranked list of SNVs and InDels annotated with variant effect predictors, a summary table of large structural variants, and a CNV plot highlighting gains and losses.

This report is designed to pinpoint genetic aberrations most likely to influence or drive oncogenic phenotypes, guiding you toward key insights for your research.

Clear, Actionable Reports—Built for Discovery

Interactive Circos plot and variant class tables
SV, CNV, and SNV/InDel visualization
Variant annotation with cancer relevance
Easily exportable for downstream use