Article on PGMD: a comprehensive manually curated pharmacogenomic database The PharmacoGenomic Mutation Database (PGMD) is a manually curated database of…

Learn about added content and features of PGMD, the PharmacoGenomic Mutation Database, which are making it even easier to look…

Hands-on training courses on Genomics Workbench, Biomedical Genomics Workbench, and Ingenuity Variant Analysis, June 16th-18th at the LMU Biocenter  …

Conference Presentation: A Systems Biology Approach to Viral Research (West Nile Virus Case Study) QIAGEN scientists, Jean-Noel Billaud, Ph.D. and…

Learn about the latest TRANSFAC features which make it easier to identify transcription factors causing expression patterns observed in microarray…

Webinar: Unraveling the genomic complexity of common and rare genetic disorders NGS bioinformatics for the discovery of causal variants   Rajini…

TGF-β3 Protein Structure Demonstrates Variant-to-3D Structure Function A new functionality in QIAGEN® Biomedical Genomics Workbench can be used in conjunction…

We would like to invite you to join our live online seminar, Optimize ligand binding with CLC Drug Discovery Workbench,…

Biomedical Genomics Workbench enables you to find the signal in noise in your cancer and hereditary disease NGS data with…

Later this month, we will head to Boston for the annual Bio-IT World Conference & Expo.  This year some 3,000 life…

Later this week we’ll be heading to the annual meeting of the American Association for Cancer Research (AACR 2015), held…

Webinar Want to learn how to find the whole truth in your cancer and hereditary diseases NGS data? Anika Joecker, PhD,…