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…

How to easily create, manage and share adverse outcome pathways to accelerate drug discovery programs Scientists working in drug discovery…

COSMIC v96 adds new oncogene that may be beneficial to diagnose HNSCC Head and neck cancers are a heterogeneous collection…

Have you reserved your in-person or virtual spot at the European Human Genetics Conference (ESHG) held June 11-14, 2022, in…

Do you ever struggle to formulate hypotheses based on your experimental expression data? You may be comparing results from healthy…

The latest COSMIC Actionability release is here with a focus on the ERBB2 gene. Before we delve into the trove…