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

When a family has a child with a rare undiagnosed condition,  a woman is diagnosed with an aggressive form of...

Around two decades ago, the amount of data about cancer genomes began to increase rapidly. Managing, viewing, and searching for...

Discover our new platform for exploring highly-curated single-cell RNA-seq data  Are you looking for highly curated single-cell (scRNA-seq) data to...

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

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

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

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...