NGS Assays - carefully designed assays to meet your needs.
Molecular Diagnostic Tests
Information
BioVendor Group offers powerful, user-friendly, hybridization-based NGS solutions designed as true all-in-one workflows. Our assays include everything required for library preparation, bioinformatic analysis, and report generation, supported by GENOVESA, our proprietary bioinformatics platform used across all BioVendor Group NGS solutions for automated data processing, variant calling, annotation, database management, and comprehensive reporting.
The epicGEN Solid Cancer & MSI Kit is a comprehensive solution for oncology diagnostics, combining solid tumor profiling with microsatellite instability (MSI) analysis. The MSI baseline is established using normal MS-Stable samples, ensuring robust and clinically relevant MSI assessment for precision oncology applications.
The Hereditary Cancer NGS Assay is designed for the detection of germline variants associated with inherited cancer predisposition syndromes. It covers the complete coding sequences (CDS) of clinically relevant genes and enables the detection of SNVs, InDels, CNVs, and MSI, supporting comprehensive hereditary cancer risk assessment and informed clinical decision-making.
The Clinical Exome Sequencing NGS Assay delivers broad coverage of clinically relevant genes across multiple disease areas, including oncology, enabling reliable variant detection and interpretation for clinical diagnostics and research.
