Today genetic innovation is advancing at breakneck pace. Since the first whole genome was sequenced in 2003, a feat that…

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

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

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

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…

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…

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

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

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

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

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