Biomedical Genomics Workbench

Start your search for cancer and hereditary disease biomarkers today!

Discover the signals that lead to answers

Complete end-to-end customizable analysis workflows for the comprehensive discovery, verification, and validation of novel biomarkers.

Unsurpassed, greater than 95% sensitivity for the detection of low frequency variants

Specialized functionalities such as primer, and primer-dimer removal for highly accurate targeted amplicon sequencing results.

Unsurpassed, greater than 95% sensitivity for the detection of low frequency variants

Integrated visualization, validation, and filtering tools
Variant visualization on protein 3D structure for pathogenicity detectionResults viewable in a simple and easy to read genome browser format
Filtering and annotation with dbSNP, ClinVar, COSMIC, and others

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Request your no obligation, 30-day trial of Biomedical Genomics Workbench today!

Interested in a tutorial and learning more? Visit the Biomedical Genomics Workbench website.

For up-to-date information and product-specific disclaimers, see the respective QIAGEN kit handbooks or user manual. QIAGEN kit handbooks and user manuals are avaliable at www.qiagen.com or can be requested from QIAGEN Technical Services or your locale distributer.