Causal variants in hereditary diseases


QIAGEN Digital Insights

Causal variants in hereditary diseases

We are pleased to announce the release of Biomedical Genomics Workbench version 2.5.

Dr. Anika Joecker, Global Product Manager, presents some of the new features including

  • Highly accurate end-to-end analysis workflows to identify causal variants in hereditary and rare diseases
  • Major update of the Ingenuity® Variant Analysis™ plugin for best in class data interpretation
  • Mouse, rat as well as human genome assembly hg38 available as direct download
  • New capabilities to analyze epigenomics data as bisulphite sequencing and ChIP-Seq data

A full list of all new features and improvements of the workbench can be found here.