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Clinical
QIAGEN Bioinformatics // Thursday, June 27, 2019

Discover more disease-causing mutations with the HGMD Summer ’19 release

  We are happy to announce the Summer ’19 Release of the Human Gene Mutation Database (HGMD) Professional is now…


Translational
QIAGEN Bioinformatics // Monday, June 24, 2019

New NGS panel for rare and inherited diseases with advanced bioinformatics

QIAseq Expanded Carrier Screening Panel and industry-leading software identify genetic variants responsible for more than 200 disease indications   Every…


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…


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 // Friday, July 7, 2017

Happy 25th, ISMB!

There are few meetings as important to the bioinformatics community as Intelligent Systems for Molecular Biology (ISMB), which is celebrating…


Clinical
Events
QIAGEN Bioinformatics // Tuesday, March 7, 2017

Join us at ACMG 2017 in Phoenix

Meet us at ACMG 2017 The American College of Medical Genetics and Genomics Annual Meeting (ACMG 2017) takes place on…


Discovery
QIAGEN Bioinformatics // Monday, February 6, 2017

Genomics England chooses HGMD

We’re excited to report that Genomics England has selected our Human Gene Mutation Database (HGMD) for its 100,000 Genomes Project….


Clinical
QIAGEN Bioinformatics // Monday, May 30, 2016

HGMD informs our understanding of rare inherited diseases

We often think of rare diseases as being rare, affecting only a small number of people. When looked at from…


Events
QIAGEN Bioinformatics // Thursday, May 19, 2016

Bioinformatics at ESHG

The European Human Genetics Conference 2016 is taking place in Barcelona, Spain, on May 21-24. We’ll be there and we…