Discovery
QIAGEN Bioinformatics // Tuesday, January 10, 2017

Welcoming OmicSoft to the team

We are very pleased to announce QIAGEN’s acquisition of OmicSoft, a market-leading provider of biomarker data management, visualization and analysis…


Clinical
QIAGEN Bioinformatics // Friday, January 6, 2017

Rare Genomics Institute: Solving rare disease mysteries

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


Discovery
QIAGEN Bioinformatics // Friday, January 6, 2017

Publications citing IPA

We love to know how our tools are being used in the field. Ingenuity Pathway Analysis (IPA) is a popular…


Discovery
QIAGEN Bioinformatics // Thursday, December 8, 2016

New plugin for metagenomics analysis

Bioinformatics expansion strengthens our metagenomics solutions   We’ve launched a new metagenomics analysis plugin for our Microbial Genomics Pro Suite…


Discovery
QIAGEN Bioinformatics // Thursday, December 8, 2016

Publications citing CLC Genomics Workbench

Genome research scientists want a powerful, end-to-end solution that easily integrates into their existing NGS analysis workflows. CLC Genomics Workbench…


Discovery
QIAGEN Bioinformatics // Wednesday, December 7, 2016

IPA sheds light on mosquito-borne viruses

For Zika and West Nile studies, longitudinal sample collection and in-depth analysis prove crucial to new insights Our Principal Scientist,…


Discovery
Events
QIAGEN Bioinformatics // Tuesday, December 6, 2016

PAG 2017 activities

We’ll be attending PAG XXV, the largest ag-genomics meeting in the world, January 14-18 in San Diego, CA, USA. PAG is…


Clinical
QIAGEN Bioinformatics // Thursday, November 24, 2016

Highlights from London

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


Discovery
QIAGEN Bioinformatics // Thursday, November 10, 2016

Building an automated high throughput analysis pipeline

Cost effective high volume bioinformatics solutions for high volume bacterial strain typing and quantification As demand for next-generation sequencing (NGS)…


Clinical
QIAGEN Bioinformatics // Wednesday, November 9, 2016

Enhanced solution for analysis of ccfDNA and hereditary diseases

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


Events
QIAGEN Bioinformatics // Tuesday, November 8, 2016

A look back at ASHG 2016

ASHG 2016 was an exciting event for us. We loved the beautiful city of Vancouver, BC, and our calendars were…


Clinical
Events
Charlotte Rasmussen // Tuesday, November 1, 2016

AMP 2016

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

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