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Publication roundup: Ingenuity Variant Analysis

QIAGEN Digital Insights Friday, August 7, 2015

Over the years, scientists around the world have been using our bioinformatics solutions in their research. We feel privileged that…

Family studies on brain malformation

QIAGEN Digital Insights Tuesday, June 30, 2015

Oxford scientists uncover rare mutations in neurological disorder At the Oxford Biomedical Research Center, scientists used Ingenuity Variant Analysis from…

7,000+ ethnically and phenotypically diverse whole genomes

QIAGEN Digital Insights Tuesday, June 9, 2015

Inova Genomes It’s a pleasure to introduce the launch of Inova Genomes, a unique compendium of ethnically and phenotypically diverse…

The PharmacoGenomic Mutation Database

QIAGEN Digital Insights Monday, June 1, 2015

Article on PGMD: a comprehensive manually curated pharmacogenomic database The PharmacoGenomic Mutation Database (PGMD) is a manually curated database of…

PGMD feature update Spring 2015

QIAGEN Digital Insights Thursday, May 21, 2015

Learn about added content and features of PGMD, the PharmacoGenomic Mutation Database, which are making it even easier to look…

NGS data analysis training at LMU

QIAGEN Digital Insights Tuesday, May 12, 2015

Hands-on training courses on Genomics Workbench, Biomedical Genomics Workbench, and Ingenuity Variant Analysis, June 16th-18th at the LMU Biocenter  …

Understanding the genomic complexity of human genetic disorders

QIAGEN Digital Insights Monday, May 4, 2015

Webinar: Unraveling the genomic complexity of common and rare genetic disorders NGS bioinformatics for the discovery of causal variants   Rajini…

Discovery of causal variants in NGS data leads to appreciation of changes in protein function in 3D

QIAGEN Digital Insights Tuesday, April 28, 2015

TGF-β3 Protein Structure Demonstrates Variant-to-3D Structure Function A new functionality in QIAGEN® Biomedical Genomics Workbench can be used in conjunction…

Launch of Biomedical Genomics Workbench

QIAGEN Digital Insights Thursday, April 16, 2015

Biomedical Genomics Workbench enables you to find the signal in noise in your cancer and hereditary disease NGS data with…

Cancer, hereditary, and rare diseases data analysis

QIAGEN Digital Insights Thursday, April 16, 2015

Webinar Want to learn how to find the whole truth in your cancer and hereditary diseases NGS data? Anika Joecker, PhD,…

NGS variant discovery

QIAGEN Digital Insights Wednesday, April 15, 2015

Webinar: Sourcing multiple databases for NGS variant discovery   Correct identification of actionable variants has always been the most challenging…

Human variation studies at Stanford

QIAGEN Digital Insights Friday, April 10, 2015

CNV Expert Rajini Haraksingh Studies Human Variation at Stanford, Rare Genomics Institute Rajini Haraksingh aims for a broad understanding of…