The QCI Interpret Winter 2023 Release brings new variant assessment tools, functionality improvements, and expanded bibliographic coverage for carrier screening…

Nearly two dozen new fully curated somatic genes and 387 clinical trials included in COSMIC Actionability v8 release We are…

In 2022, the world crossed a sobering new threshold. Over 20 million people were diagnosed with cancer, and 10 million…

A new balancing act: How do clinical cancer geneticists and genetic counselors manage more patients with less time? The COVID-19…

Why manually curated data is essential to convert data into knowledge Are you a researcher or data scientist working in…

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

Discover how our new LightSpeed feature changes the world of whole genome sequencing analysis We’re excited to reveal many new…

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

Introducing a new way to improve bioinformatics efficiency in your high-throughput NGS setting It’s exciting that advancements in high-throughput sequencing…

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

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

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