Biomedical Genomics Workbench
For analyzing, comparing and visualizing human hereditary and cancer NGS data for biomarker discovery
Biomedical Genomics Workbench is a highly accurate and comprehensive NGS data analysis platform. It provides a user-friendly and customizable human hereditary disease and cancer analysis solution for biomarker discovery and validation. Its ready-to-use analysis workflows can be easily modified for hypothesis-led discovery.
Biomedical Genomics Workbench provides human hereditary disease and cancer researchers with the tools to discover prognostic markers, identify subclonal somatic mutations, detect inherited traits, find biomarkers for drug response and determine if protein modification is deleterious by visualizing the protein in 3D – and all results can be filtered, visualized and compared with relevant databases.
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