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

The Fall release of Ingenuity® Variant Analysis™ enriches the analysis functionality, adding speed and power, and offers new tools for the organization…

HGMD®, the Human Gene Mutation Database is used by scientists around the world to find information on reported genetic mutations. The…

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

Next-generation sequencing is quickly taking a more central spotlight in understanding both rare and common diseases. Every day there are…

Role of microRNA-mRNA interactions in Endometrioid Endometrial Carcinoma, a Sample to Insight biological exploration Endometrial adenoarcinoma is a common cause…

TRANSFAC 2015.3 release Get a brief overview of the new features for easier and more specific data analysis: Step-by-step, easy-to-use…

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

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

New NGS tools, ACMG variant data support, and more.   IsoProfiler – a new feature We’ve just put the finishing…

IPA Webinar: Part 1: Introduction to Ingenuity Pathway Analysis Learn how to quickly and easily identify significant pathways, discover potential…

Many great papers citing CLC Genomics Workbench have come out just in the last few months. To give you an…