In the coming months, we have a number of webinars prepared for you. You can meet our experts and get…

PLoS Biology has published an interesting paper about big data in genomics from lead author Zachary Stephens, senior author Gene Robinson,…

Over the years, scientists around the world have been using our bioinformatics solutions in their research. We feel privileged that…

Oxford scientists uncover rare mutations in neurological disorder At the Oxford Biomedical Research Center, scientists used Ingenuity Variant Analysis from…

Inova Genomes It’s a pleasure to introduce the launch of Inova Genomes, a unique compendium of ethnically and phenotypically diverse…

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  …

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…

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

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