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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)

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