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.

The LinkPrep™ Service provides a customized genetic report, summarizing variant calls with clear, accessible insights. Alongside sample information, the LinkPrep™ 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.