A high-throughput population screening laboratory sees significant scale-up with implementation of QIAGEN Clinical Insight (QCI®) INTRODUCTION Genetic disease is the leading…

Over a quarter million germline mutations catalogued HGMD now contains 256,070 germline mutations As of March 29, 2019, HGMD contains…

Introduction to the Advanced Structural Variant Detection plugin for the CLC Genomics Workbench Structural variants affect large regions of the…

Publication Roundup: Biomedical Genomics Workbench Check out these recent articles citing Biomedical Genomics Workbench, a comprehensive, highly accurate NGS data…

HGMD® Professional version 2018.3 contains a total of 240,269 mutations entries—that’s 7,826 more mutation entries than the previous release! Human…

This year ESHG is celebrating it’s 50th anniversary in beautiful Copenhagen! Come and meet us at booths 540 and 542 and…

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

ASHG 2016 was an exciting event for us. We loved the beautiful city of Vancouver, BC, and our calendars were…

Advances in Genome Biology and Technology The AGBT Precision Health meeting will take place in Scottsdale, Arizona on September 22-24,…

Our hereditary disease solution performs best in terms of clinical accuracy at the Critical Assessment of Genome Interpretation (CAGI) conference….

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 release of Biomedical Genomics Workbench version 2.5. Dr. Anika Joecker, Global Product Manager, presents…