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Biomedical Genomics Workbench

For analyzing, comparing and visualizing human hereditary and cancer NGS data for biomarker discovery

  • Quickly analyze complex data
  • High accuracy for low-frequency variant detection
  • Modify or personalize analysis workflows
  • Conveniently filter and visualize data
  • Compare results with relevant databases
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.
Cat No./ID: 832070
Biomedical Genomics WB, Desktop License
Biomedical Genomics Workbench is a comprehensive and accurate data analysis platform that enables you to find the signal in the noise in your cancer and hereditary disease NGS data. Includes 12 months of maintenance with purchase.
Performance

Performance
Intuitive and user-friendly
Biomedical Genomics Workbench offers advanced NGS data analysis tools in combination with an intuitive graphical user-interface, enabling rapid analysis and accurate interpretation of advanced next-generation sequencing data. The intuitive software interface allows users to customize workflows or even create new ones. Workflows can also be easily shared with collaborators and colleagues.

Cross-platform
Biomedical Genomics Workbench is a cross-platform desktop application and is compatible with Windows, Mac OS X, and Linux platforms.
 
Support for all major next-generation sequencing platforms
The workbench is compatible with data generated using all sequencing platforms, including whole genome, targeted amplicon, exome, transcriptome and epigenetic sequencing data.
 
A comprehensive analysis package
Biomedical Genomics Workbench is a comprehensive, human hereditary disease and cancer-focused informatics solution. It offers flexible, cancer-specific, ready-to-use analysis workflows that can be readily modified. It is also possible to build new personalized workflows for hypothesis-led discovery (see figure Build your own customized analysis workflows).

Applications
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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