Introduction to HGMD, the Human Gene Mutation Database
This workshop is limited to current students, faculty, and staff at Stanford. Advance registration required. Click on "more info" link to register for this workshop.
Having been cited in more than 10,000 scientific publications, HGMD is the gold standard industry-leading resource for comprehensive coverage of published human inherited disease mutations. Whether searching for an overview of known mutations associated with a particular disease, interpreting clinical test results, looking for the likely causal mutation in a list of variants, or seeking to integrate mutation content into your custom NGS pipeline or data repository – HGMD is a flexible resource that can be adapted to a broad range of applications.