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Rare Genomics Institute: Solving rare disease mysteries

QIAGEN Digital Insights Friday, January 6, 2017

Nearly 250 million people around the world are affected by rare diseases, which are typically genetic in nature. Their rarity…

Highlights from London

QIAGEN Digital Insights Thursday, November 24, 2016

Not too long ago, we returned from Oxford Global’s 8th Annual NGS Congress. While the majestic host city of London was…

Enhanced solution for analysis of ccfDNA and hereditary diseases

QIAGEN Digital Insights Wednesday, November 9, 2016

Fast, accurate, and easy-to-use solutions encompassing variant identification and interpretation are critical for identifying pathogenic and disease driver variants successfully….

AMP 2016

QIAGEN Digital Insights Tuesday, November 1, 2016

The Association for Molecular Pathology (AMP) 2016 Annual Meeting is held in Charlotte, North Carolina, from November 10-12. The theme of…

New white paper: Challenges in Clinical NGS Testing

QIAGEN Digital Insights Monday, October 31, 2016

Clinical lab managers are constantly under pressure to do more with less. Launch more tests, review more information – in…

BioSignature Discoverer: New release and publication

QIAGEN Digital Insights Friday, October 28, 2016

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

QIAGEN Digital Insights Wednesday, October 19, 2016

We are thrilled to be part of the announcement at ASHG 2016, detailing the new QIAseq® cfDNA All-in-One Kit — including…

ASHG 2016

QIAGEN Digital Insights Thursday, October 13, 2016

Sample to insight solutions for liquid biopsy, hereditary diseases, and RNA-seq Meet us at ASHG 2016 Together with leading scientists and…

Low frequency variant detection with increased accuracy

QIAGEN Digital Insights Friday, October 7, 2016

Using new QIAseq DNA Targeted Panels with Biomedical Genomics Workbench increases the accuracy of detecting low frequency variants. We are…

Publication roundup: Ingenuity Variant Analysis in the literature

QIAGEN Digital Insights Tuesday, October 4, 2016

As a provider of bioinformatics tools designed to provide insight and accelerate scientific analysis and interpretation, we love to read…

Publication roundup: HGMD

QIAGEN Digital Insights Monday, August 8, 2016

Scientists often turn to HGMD, the Human Gene Mutation Database, as their first stop for learning about reported genetic mutations….

European Society of Pathology

QIAGEN Digital Insights Monday, August 8, 2016

On September 25-29, 2016, the 28th Congress of the European Society of Pathology will take place in Cologne, Germany. For…