With version 5, a new powerful plugin redefines accuracy and ease of use for analyzing targeted DNA and RNA panel data.
The plugin expands the capabilities of Biomedical Genomics Workbench and, best of all, comes free of charge.
Are you ready to uncover the signals that lead to breakthrough discoveries in your human disease research? 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. With its broad selection of end-to-end analysis workflows, tools, and visualization modules, it enables easy and accurate discovery, verification, and validation of novel disease biomarkers.
Discover novel insights with greater than 95% sensitivity and unsurpassed accuracy. Biomedical Genomics Workbench guides you through a complete analysis of your genome, exome, targeted amplicon, transcriptome, and epigenetic NGS sequencing data for results you can trust.
Modify workflows and discovery parameters for hypothesis-led analysis that guides you to the most promising breakthroughs.
Simplicity, flexibility, and accuracy combine to provide you with a solution that is more than 50% faster than open-source alternatives.
With the help of Biomedical Genomics Workbench and it’s clearly laid out and intuitive user interface, I was able to prototype, develop, and validate a custom targeted amplicon NGS data analysis pipeline in a matter of a few weeks. Any roadblock I would come across in this process was resolved either with the detailed documentation available or with a quick email to their responsive technical support team.
Steven Lockton, Biological Dynamics
We frequently release updates and improvements such as new functionalities, bug fixes or plugins. To get a complete overview, please read the latest improvements.
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