Products

VarSeq is a robust genomic data analysis platform designed for efficient variant annotation, filtration, and interpretation. Built to meet the needs of clinical geneticists, molecular pathologists, and research scientists, VarSeq streamlines the entire next-generation sequencing (NGS) workflow—from raw data to clinical report.

VarSeq Dx is a clinical genomic analysis software designed and validated for diagnostic use. VarSeq Dx has received CE marking under European In Vitro Diagnostic Regulation (IVDR 2017/746) for use as a medical device in the European Economic Area (EEA).

VSWarehouse is a scalable multi-project warehouse for NGS variant call sets, clinical reports, and catalogs of variant assessments. VSWarehouse is flexible, scalable, and offers enterprise levels of genomic data security for labs of all sizes.

Clinical variant analysis software with automation of the ACMG (American College of Medical Genetics) and AMP (Association for Molecular Pathology) guidelines. VSClinical allows for the clinical interpretation of variants based on these guidelines for automated and enhance NGS analysis pipelines.

Industry leading Copy Number Variants (CNV) calling alogrithm for existing clinical NGS gene panel, exome, and whole genome NGS data. VS-CNV directly calls a CNV in target regions and avoids additional CMA or MLPA testing.

A pharmacogenomics interpretation software based on CPIC recommendations. Our PGx variant detection and recommendation algorithm identifies diplotypes and annotates them with drug recommendations.

Repeatable clinical workflows essential for CLIA and CAP certified analysis, creation of high throughput pipelines and access to curated annotation sources that are updated regularly.

With VSReports, you can easily convert the output of your tertiary analysis into a customized clinical report. After you've filtered down your imported variants, simply select variants to include in the report. You are then one click away from a report.

SVS is a powerful analytic tool created specifically to empower biologists and other researchers to easily perform complex analyses and visualizations on genomic and phenotypic data.

Bioinformatics secondary analysis tools that process genomics data with high computing efficiency, fast turnaround time, exceptional accuracy and 100% consistency.

This tool delivers stunning visualizations of your genomic data that give you the power to see what is occurring at each base pair in your samples.