Introducing a novel myeloid gene panel for the GeneReader NGS System with integrated variant analysis, interpretation and reporting from QIAGEN...

Simple, secure, and scalable interpretation workflow We are delighted to announce that we’ve expanded our QIAGEN® Clinical Insight™ (QCI™) solution to address...

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