Clinical
QIAGEN Bioinformatics // Monday, July 8, 2019

Using liquid biopsy to guide clinical trial enrollment for patients with cancer

Investigators in the UK are using QIAGEN Clinical Insight (QCI) to identify clinically actionable mutations from blood-based sequencing results On…


Clinical
QIAGEN Bioinformatics // Thursday, June 27, 2019

Discover more disease-causing mutations with the HGMD Summer ’19 release

  We are happy to announce the Summer ’19 Release of the Human Gene Mutation Database (HGMD) Professional is now…


Clinical
QIAGEN Bioinformatics // Monday, June 24, 2019

QIAGEN Clinical Insight surpasses 1 million patient test cases analyzed and interpreted

READ PRESS RELEASE   We are proud to announce that QIAGEN Clinical Insight (QCI®), QIAGEN’s clinical decision support platform has…


Translational
QIAGEN Bioinformatics // Monday, June 24, 2019

New NGS panel for rare and inherited diseases with advanced bioinformatics

QIAseq Expanded Carrier Screening Panel and industry-leading software identify genetic variants responsible for more than 200 disease indications   Every…


Clinical
QIAGEN Bioinformatics // Saturday, June 1, 2019

Lab performing expanded carrier screening boosts efficiency by 80%

A high-throughput population screening laboratory sees significant scale-up with implementation of QIAGEN Clinical Insight (QCI®)   INTRODUCTION Genetic disease is the…


Clinical
QIAGEN Bioinformatics // Wednesday, May 29, 2019

Curating the Clinical Genome 2019, Washington, DC

2019 Curating the Clinical Genome Wrap-Up The 2019 Curating the Clinical Genome Conference was a remarkable event this year. A…


Clinical
Discovery
Leif Schauser // Tuesday, May 21, 2019

How to accurately quantify miRNAs and increase fraction of annotated reads

Introduction to the QIAseq miRNA library kit support in the Biomedical Genomics Analysis plugin for CLC Genomics Workbench The QIAseq…


Discovery
Paula Tataru // Thursday, May 16, 2019

Comparative Analysis of Whole Genomes using CLC Workbenches

  Introducing the Whole Genome Alignment Plugin Paula Tataru, Ph.D, Senior Bioinformatics Scientist   The new Whole Genome Alignment plugin,…


Clinical
QIAGEN Bioinformatics // Wednesday, April 3, 2019

HGMD 2019.1 hits major milestone

Over a quarter million germline mutations catalogued   HGMD now contains 256,070 germline mutations As of March 29, 2019, HGMD…


Discovery
Winnie Ridderberg // Wednesday, March 20, 2019

Detecting antimicrobial resistance causing mutations using a custom-designed variant database

In a recent blog post we shared exciting news on new functionalities for detecting antimicrobial resistance (AMR) implemented within CLC…


Discovery
Thomas Poulsen // Tuesday, March 19, 2019

Structural Variant Detection using CLC Genomics Workbench

Introduction to the Advanced Structural Variant Detection plugin for the CLC Genomics Workbench Structural variants affect large regions of the…


Discovery
Leif Schauser // Friday, February 15, 2019

Transcript Discovery using CLC Genomics Workbench

Introduction to the Transcript Discovery Plugin Leif Schauser, PhD, Director Product Management Genome Analysis Bioinformatics – CLC Transcript discovery using…

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