Biomedical Genomics Workbench 4 is here!

With version 4, your RNA-seq experience is further strengthened by achieving faster run times,
and delivering even more accurate results than before.

› Explore more release highlights


Biomedical Genomics Workbench

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.

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Find the signals in the noise with ease!

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.

  • Complete end-to-end and customizable analysis workflows for the comprehensive discovery, verification, and validation of novel biomarkers
  • Specialized functionalities such as primer and primer-dimer removal for highly accurate targeted amplicon sequencing results
  • High sensitivity detection of germline and low frequency variants from DNA-seq and RNA-seq data
  • Unsurpassed accuracy for copy number detection in exome and targeted amplicon sequencing data
  • Easy viewing of findings such as dynamic protein structures in 3D, and sequencing reads afford faster discovery

 

 


Lead your own discovery

Modify workflows and discovery parameters for hypothesis-led analysis that guides you to the most promising breakthroughs.

 

Discover more faster

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


Try Biomedical Genomics Workbench today!

QIAGEN Bioinformatics provides a portfolio of NGS solutions that integrate seamlessly to aid researchers in the fight against hereditary disease and cancer.

Start your 30-day no obligation trial of Biomedical Genomics Workbench today and take a look at our tutorials to see how you can use the software for your research.

 

 

 


System requirements

  • Windows 7, Windows 8, Windows 10 or Windows Server 2012.
  • Mac OS X 10.9, 10.10, 10.11 and 10.12.
  • Linux: RHEL 6.0 and later, Suse 13.1 and later. (The software is expected to run without problem on other recent Linux systems, but we do not guarantee this.)
  • 64 bit operating system
  • 16 GB RAM required
  • 24 GB RAM recommended
  • 1024 x 768 display required
  • 1600 x 1200 display recommended
  • Intel or AMD CPU required
  • Minimum 100 GB free disk space in the tmp directory
  • Minimum 90 GB free disc space required in the CLC_References directory (if you are not connected to a server and wish to work with either hg19 or hg38). For more information about reference data size, please refer to the user manual. If you have less free disc space available it is possible to change the reference data location. How to do this is described in Download and configure reference data

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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