QIAGEN powered by
Lab performing expanded carrier screening boosts efficiency by 80%

QIAGEN Bioinformatics 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 Bioinformatics 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…

Researching Rare Disease

QIAGEN Bioinformatics Wednesday, February 28, 2018

An estimated 300 million people worldwide live with some form of rare disease. In the US, a disease is considered…

ASHG Round up

QIAGEN Bioinformatics Tuesday, November 21, 2017

Bioinformatic Tools for Genome Analysis The dust has settled after a whirlwind annual meeting of the American Society of Human…

Join us at ACMG 2017 in Phoenix

QIAGEN Bioinformatics Tuesday, March 7, 2017

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

Rare Genomics Institute: Solving rare disease mysteries

QIAGEN Bioinformatics Friday, January 6, 2017

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

HGMD informs our understanding of rare inherited diseases

QIAGEN Bioinformatics Monday, May 30, 2016

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

Bioinformatics at ESHG

QIAGEN Bioinformatics Thursday, May 19, 2016

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

Efficient and accurate end-to-end solution for rare disease cases

QIAGEN Bioinformatics Thursday, May 12, 2016

Human Genome Variation Society (HGVS) is hosting a meeting on “Clinical Interpretation of Variants from Next-Generation Sequencing”. The meeting will…

Raising the profile of rare disease

QIAGEN Bioinformatics Monday, February 29, 2016

Living with a rare disease is often lonely and isolating for patients and caregivers alike. Through our work with researchers…