Will you be joining our workshop? Throughout SOT 2017 you can find us in booth #1812, Exhibit Hall E. You’re also…

Research to beat rare diseases With Rare Disease Day 2017 approaching on February 28, we want to show our support. As…

This year at HIMSS17 We’ll be joining Intel in their booth #2661 to share insights on NGS-based genetic testing across a range…

We’re excited to report that Genomics England has selected our Human Gene Mutation Database (HGMD) for its 100,000 Genomes Project….

We were delighted to read about the success of a former PhD student who spent three years working in our…

QCI Interpret’s integration of highly curated knowledge and rules enables automation for much of the interpretation and reporting process for…

Research scientist Dr. Margarete Odenthal leads the translational molecular pathology group at University Hospital Cologne, putting new technologies through their…

January is National Glaucoma Awareness Month, the time of year when the Glaucoma Research Foundation seeks to raise awareness about…

We are very pleased to announce QIAGEN’s acquisition of OmicSoft, a market-leading provider of biomarker data management, visualization and analysis…

Nearly 250 million people around the world are affected by rare diseases, which are typically genetic in nature. Their rarity…

We love to know how our tools are being used in the field. Ingenuity Pathway Analysis (IPA) is a popular…

Bioinformatics expansion strengthens our metagenomics solutions We’ve launched a new metagenomics analysis plugin for our QIAGEN CLC Genomics ProSuite and…