BioSignature Discoverer: New release and publication
This post is authored by Gnosis Data Analysis I.K.E. New release We are proud to announce a new release for BioSignature…
Unique Sample to Insight solutions for liquid biopsies and hereditary diseases
We are thrilled to be part of the announcement at ASHG 2016, detailing the new QIAseq® cfDNA All-in-One Kit — including…
QIAGEN teams up with 10x Genomics
At the AGBT conference in Orlando we announced a new collaboration with 10x Genomics to co-market and co-develop NGS, single-cell…
Looking back at 2015 and ahead to 2016
In this post, we share some of the trends and milestones that mattered most to us in 2015, and dust…
Evaluation of GeneReader NGS System
It’s a pleasure to announce the introduction of our new GeneReader NGS System. Now, we’re offering a complete product suite across all…
QIAGEN introduces GeneReader NGS System
We are pleased to announce the introduction of the GeneReader NGS System. We are now offering a complete product suite across all…
HGMD: A view into comprehensive coverage
HGMD® is widely accepted as the gold standard for information about published inherited disease mutations, but what makes it such…
Looking ahead to AMP 2015
Austin, here we come! We’re getting AMPed up for the upcoming Association for Molecular Pathology 2015 annual meeting! Held at…
Whole human genome analysis
Your $1,000 genome will only cost $22 to analyze We’re committed to enabling our customers to analyze vast amounts of…
Data analysis with greater efficiency
The Fall release of Ingenuity® Variant Analysis™ enriches the analysis functionality, adding speed and power, and offers new tools for the organization…
Publication roundup: HGMD
HGMD®, the Human Gene Mutation Database is used by scientists around the world to find information on reported genetic mutations. The…
Discover the genetic basis of disease
Next-generation sequencing is quickly taking a more central spotlight in understanding both rare and common diseases. Every day there are…
