What to do when your genomics software platform needs a content boost   When it comes to NGS variant interpretation,…

New content, clinical trials, and analysis categories added to the world’s largest expert-curated somatic mutation database The latest release of…

Peer-reviewed study compares accuracy and consistency of variant assessments from commercial CDS software to the variant interpretation of 8 laboratories…

Build confidence and efficiency into your preclinical pipeline with traceable and high-quality cell line ‘omics data from a trusted source…

Looking for flexible ways to integrate high-quality ‘omics data? Execute detailed queries via API, download flat files or use the…

More mutations, better annotations, confident classifications HGMD Professional 2022.3 is now available, expanding the world’s largest collection of human inherited disease…

In oncology research, identifying potentially actionable gene alterations and exploiting cancer’s molecular vulnerabilities is becoming increasingly difficult. Due to the…

The latest version of the Human Somatic Mutation Database (HSMD) is now available. HSMD 2.0 includes over 140,000 new alterations,…

QCI Interpret Translational’s latest software update comes with several new features, including a new workflow for comprehensive cancer panels and…

QCI Interpret’s latest software update comes with several new features, including a new workflow for comprehensive cancer panels and greater…

Many labs struggle with prioritizing clinically- and biologically-relevant variants among the millions of variants detected using NGS. Labs are starting…

Explore an easy way to extend your in-house resources to include integrated single-cell data and analysis Single-cell sequencing is a…