We are pleased to announce the introduction of the GeneReader NGS System. We are now offering a complete product suite across all…

HGMD® is widely accepted as the gold standard for information about published inherited disease mutations, but what makes it such…

Austin, here we come!  We’re getting AMPed up for the upcoming Association for Molecular Pathology 2015 annual meeting! Held at…

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

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…

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…

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