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Lab performing expanded carrier screening boosts efficiency by 80%

QIAGEN Digital Insights Saturday, June 1, 2019

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

HGMD 2019.1 hits major milestone

QIAGEN Digital Insights Wednesday, April 3, 2019

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

Structural Variant Detection using CLC Genomics Workbench

Thomas Poulsen Tuesday, March 19, 2019

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

QIAGEN Digital Insights Wednesday, November 7, 2018

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

HGMD® Professional 2018.3 Has Arrived!

QIAGEN Digital Insights Monday, October 1, 2018

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…

ESHG 50th Anniversary

QIAGEN Digital Insights Tuesday, May 2, 2017

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

Rare Genomics Institute: Solving rare disease mysteries

QIAGEN Digital Insights Friday, January 6, 2017

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

A look back at ASHG 2016

QIAGEN Digital Insights Tuesday, November 8, 2016

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

AGBT Precision Health meeting

QIAGEN Digital Insights Monday, August 8, 2016

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

Most accurate solution for solving clinical hereditary disease cases

QIAGEN Digital Insights Tuesday, April 19, 2016

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

Detection of inherited disease mutations

QIAGEN Digital Insights Wednesday, October 7, 2015

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

Causal variants in hereditary diseases

QIAGEN Digital Insights Tuesday, September 8, 2015

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