Discover more about the latest QCI update and how the platform simplifies and accelerates NGS variant analysis, interpretation, and reporting…

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

We are excited to announce the general availability of the Fall 2020 Release of QIAGEN Clinical Insight (QCI) Interpret. This…

Introducing QCI Interpret Translational, a new software solution for NGS variant assessment Whole-exome sequencing (WES) using next-generation sequencing (NGS) technology…

Recently, there have been many noteworthy papers citing QIAGEN CLC Genomics Workbench, a comprehensive, easy-to-use toolbox that ensures continuity in…

Are you a scientist or public health lab professional studying viral host response? Do you find it challenging to find…

Using viral reference databases for phylogeny construction and taxonomic profiling of samples with low viral load This blog tutorial highlights…

Imagine this scenario: You are working on a high profile scientific finding (for example the Nevada SARS-CoV-2 reinfection case), and you…

The Human Gene Mutation Database (HGMD®) Professional has over 298,000 inherited disease-relevant mutations and polymorphisms–nearly 40% more than in the…

We’ve got a useful tip that will help you get even more value out of QIAGEN CLC Microbial Genomics Module…

Read about how researchers across the world are using QIAGEN Digital Insights solutions to accelerate their work in a variety…

‘Omics research has made it easy to gather large volumes of data on differentially expressed genes in various conditions. Changes…