Skip to main content

MolBio Licensed Tools: Biomedical Genomics

Registration & Access Info

Register here.

  • Must have Pitt or UPMC email address
  • Limited to on-campus computers
  • Runs on PC & Mac & Linux

System requirements

About Biomedical Genomics Workbench

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.

  • Complete end-to-end and customizable analysis workflows for the comprehensive discovery, verification, and validation of novel biomarkers
  • Specialized functionalities such as primer & 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

(from Biomedical Genomics Workbench)

The Health Sciences Library System supports the Health Sciences at the University of Pittsburgh.

© 1996 - 2014 Health Sciences Library System, University of Pittsburgh. All rights reserved.
Contact the Webmaster

University of Pittsburgh Libraries