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CLASS Introduction to Human Genetic Variant Databases - Somatic (Parnassus) In-Person
This 90-minute class will survey databases of human genetic variation with a focus on how to find and interpret knowledge linking somatic mutations and cancer. We will also review current best practices in human genetic variant interpretation and pathogenicity classification by examining a specific somatic mutation in the context of curated information available in:
- ClinVar http://www.ncbi.nlm.nih.gov/clinvar/
- cBioPortal http://www.cbioportal.org/
- MyCancerGenome http://www.mycancergenome.org/
- MD Anderson Knowledge Base for Precision Oncology https://pct.mdanderson.org/
- COSMIC http://cancer.sanger.ac.uk/cosmic
- 1000 Genomes, Exome Sequencing Project, and ExAC
- Date:
- Wednesday, Feb 24 2016
- Time:
- 2:00pm - 3:30pm
- Time Zone:
- Pacific Time - US & Canada (change)
- Location:
- CL231
- Campus:
- Parnassus
- Categories:
- Data Science Data Science > Data Management Special Event
Registration has closed.
Event Organizer
Micquel Little