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Meet us at PMWC 2016

Anja Lykkebak Wednesday, January 20, 2016

The 2016 Personalized Medicine World Conference (PMWC) takes place on January 24-27 in Silicon Valley, California. Within the three days…

Whole human genome analysis

QIAGEN Digital Insights Tuesday, November 3, 2015

Your $1,000 genome will only cost $22 to analyze We’re committed to enabling our customers to analyze vast amounts of…

Highlights from ASHG 2015

QIAGEN Digital Insights Thursday, October 22, 2015

ASHG 2015 was everything we hoped it would be: interesting and inspiring scientific presentations and a place to reconnect with friends and…

Detection of inherited disease mutations

QIAGEN Digital Insights Wednesday, October 7, 2015

This webinar highlights our highly accurate and integrated end-to-end NGS analysis solution for the discovery of novel, and clinically relevant, rare…

QIAGEN launches new bioinformatics solution for hereditary diseases

QIAGEN Digital Insights Wednesday, October 7, 2015

We are pleased to announce the launch of our new end-to-end solution for hereditary diseases; an offering including Biomedical Genomics Workbench, Biomedical…

Causal variants in hereditary diseases

QIAGEN Digital Insights Tuesday, September 8, 2015

We are pleased to announce the release of Biomedical Genomics Workbench version 2.5. Dr. Anika Joecker, Global Product Manager, presents…

Virtual conference and online events

QIAGEN Digital Insights Monday, September 7, 2015

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

PGMD feature update Spring 2015

QIAGEN Digital Insights Thursday, May 21, 2015

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

Launch of Biomedical Genomics Workbench

QIAGEN Digital Insights Thursday, April 16, 2015

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