Basic pathway analysis has several limitations that can slow down research progress and hinder insights from biological data. One of…

We are very pleased to announce the latest QCI Interpret software release is now available. Expanding on the software’s current…

The recent plugin update to QIAGEN CLC Genomics version 21 (v21) includes new tools and database access within QIAGEN CLC…

On Thursday, May 20, join us for the Every Lab Summit, a free virtual event exploring how any lab, anywhere,…

COSMIC, the Catalogue Of Somatic Mutations In Cancer, is the world’s largest and most comprehensive resource for exploring the impact…

The Spring release of HGMD Professional is now available. Containing over 314,707 expert-curated disease-causing mutations, HGMD remains the largest, most…

During the current pandemic, the importance of continually monitoring viral genomes for new mutations has become fundamental to help guide…

It’s already happened: Several SARS-CoV-2 variants are upon us, lurking in various populations, bringing more uncertainty about how this pandemic…

How integrative analysis of multi-omics data accelerates biomarker and target discovery in inherited disease The analysis of multi-omics data has enabled unprecedented advances in discovering biomarkers…

Whole-exome sequencing (WES) using next-generation sequencing (NGS) technology is a powerful tool for investigating variants linked to genetic disease. It…

Next-generation sequencing (NGS) techniques allow high-throughput detection of a vast amount of genetic variations in a cost-effective manner. However, there…

Hint: The secret is in the biological context Today’s discovery scientists are challenged with identifying new biomarkers and therapeutic targets…