Clinical
QIAGEN Bioinformatics // Monday, February 8, 2016

Challenges of variant analysis in genetic testing

The February 2016 issue of Medical Lab Observer features a story co-authored by two QIAGEN Bioinformatics executives, Ramon Felciano and…


Clinical
QIAGEN Bioinformatics // Tuesday, January 31, 2017

Clinical oncology testing

QCI Interpret’s integration of highly curated knowledge and rules enables automation for much of the interpretation and reporting process for…


Clinical
Events
QIAGEN Bioinformatics // Tuesday, February 14, 2017

Attending HIMSS17?

This year at HIMSS17 We’ll be joining Intel in their booth #2661 to share insights on NGS-based genetic testing across a range…


Clinical
QIAGEN Bioinformatics // Tuesday, May 9, 2017

A collective push for change

Looking ahead: the future bioinformatics of genetic testing and precision medicine The next big medical frontier is on the horizon….


Clinical
QIAGEN Bioinformatics // Friday, July 7, 2017

Five Trends Shaping Precision Medicine

How QIAGEN Clinical Insight is leading the way for predictive and preventative care   Next-generation sequencing, bolstered by powerful data…


Clinical
QIAGEN Bioinformatics // Monday, June 25, 2018

Announcing HGMD® Professional 2018.2!

The latest HGMD® Professional release is now available! Version 2018.2 contains a total of 232,443 mutation entries—that’s 7,801 more mutation…


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
QIAGEN Bioinformatics // Saturday, December 1, 2018

QIAGEN launches QCI Interpret bioinformatics features for blood cancers

Introducing a novel myeloid gene panel for the GeneReader NGS System with integrated variant analysis, interpretation and reporting from QIAGEN…


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 // 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 leading…


Clinical
QIAGEN Bioinformatics // Monday, June 24, 2019

QIAGEN Clinical Insight surpasses 1 million patient test cases analyzed and interpreted

READ PRESS RELEASE   We are proud to announce that QIAGEN Clinical Insight (QCI®), QIAGEN’s clinical decision support platform has…


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…

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