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,…

Webinar: Sourcing multiple databases for NGS variant discovery   Correct identification of actionable variants has always been the most challenging…

RNA-Seq, a path to biological insight Are you getting the most our of your RNA-Seq data from plant, animal, or…

CNV Expert Rajini Haraksingh Studies Human Variation at Stanford, Rare Genomics Institute Rajini Haraksingh aims for a broad understanding of…