Clinical
QIAGEN Bioinformatics // Saturday, June 1, 2019

Lab performing expanded carrier screening boosts efficiency by 80%

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


Clinical
QIAGEN Bioinformatics // Wednesday, April 3, 2019

HGMD 2019.1 hits major milestone

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


Discovery
Thomas Poulsen // Tuesday, March 19, 2019

Structural Variant Detection using CLC Genomics Workbench

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


Discovery
QIAGEN Bioinformatics // Wednesday, November 7, 2018

Publication Roundup: Biomedical Genomics Workbench

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


Clinical
QIAGEN Bioinformatics // Monday, October 1, 2018

HGMD® Professional 2018.3 Has Arrived!

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…


Clinical
Discovery
Events
QIAGEN Bioinformatics // Tuesday, May 2, 2017

ESHG 50th Anniversary

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


Clinical
QIAGEN Bioinformatics // Friday, January 6, 2017

Rare Genomics Institute: Solving rare disease mysteries

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


Events
QIAGEN Bioinformatics // Tuesday, November 8, 2016

A look back at ASHG 2016

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


Clinical
Events
QIAGEN Bioinformatics // Monday, August 8, 2016

AGBT Precision Health meeting

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


Clinical
QIAGEN Bioinformatics // Tuesday, April 19, 2016

Most accurate solution for solving clinical hereditary disease cases

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


Translational
Webinar
QIAGEN Bioinformatics // Wednesday, October 7, 2015

Detection of inherited disease mutations

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


Translational
Webinar
QIAGEN Bioinformatics // Tuesday, September 8, 2015

Causal variants in hereditary diseases

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

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