Two expert-curated databases exclusively licensed through QIAGEN link sequence-level somatic mutation data to detailed molecular information about functional and clinical...

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

Interpretation of genomic variants in tumor samples still presents a challenge in clinical settings. Variant interpretation is fragmented across disparate...

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

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,...

Experts forecast this year’s cancer research advances In cancer research, the focus has shifted to precision medicine and much progress...