Meet us at ACMG 2017 The American College of Medical Genetics and Genomics Annual Meeting (ACMG 2017) takes place on...

We’re happy to announce that new releases of our products are now available. These releases offer a number of new features and improvements. You can...

We were pleased to see this Oncotarget report includes our software CLC Genomics Workbench as an important tool in identifying and characterizing cervical...

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...

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...

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

Not too long ago, we returned from Oxford Global’s 8th Annual NGS Congress. While the majestic host city of London was...

Fast, accurate, and easy-to-use solutions encompassing variant identification and interpretation are critical for identifying pathogenic and disease driver variants successfully....