Introduction to HGMD, the Human Gene Mutation Database

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Date and Time 
October 30, 2018
10:30am to 12:00pm
Location 
Robin Li and Melissa Ma Science Library, Sapp Center for Teaching and Learning, Training Room
Admission 

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.

Audience 
Faculty/Staff
Students
Event Sponsor 
Stanford University Libraries
Contact 
mnewman@stanford.edu
Michael Newman 650-723-1110

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.

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