It’s a pleasure to announce the introduction of our new GeneReader NGS System. Now, we’re offering a complete product suite across all…

We are pleased to announce the introduction of the GeneReader NGS System. We are now offering a complete product suite across all…

Austin, here we come!  We’re getting AMPed up for the upcoming Association for Molecular Pathology 2015 annual meeting! Held at…

Simple, secure, and scalable interpretation workflow We are delighted to announce that we’ve expanded our QIAGEN® Clinical Insight™ (QCI™) solution to address…

PLoS Biology has published an interesting paper about big data in genomics from lead author Zachary Stephens, senior author Gene Robinson,…

Webinar: Learn about the key capabilities of QCITM, and get a QCI somatic cancer demonstration. Dr. Julie Deschênes, Associated manager, Integrated…

QIAGEN Clinical Insight is an integrated clinical decision support solution designed specifically for routine genomic testing laboratories assessing next-generation sequencing (NGS)…

An overview of the current NGS market Would you like to get an overview of the current NGS market? Our…

Webinar: POSSUMweb, HGMD®, and IVA allow you to combine genetics and morphology information.   This webinar demonstrates how to combine genetics and…

We are pleased to announce, in collaboration with 12 other leading life science organizations, the Allele Frequency Community (#AlleleFreq), a landmark initiative…

Our 2014 survey on the NGS market was completed by 529 respondents and provides a good summary of the current NGS…

Allele Frequency Community is an expansive, ethnically diverse, freely available community resource for allele frequency annotation Imagine Human Genome Interpretation minus…