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,...

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

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