Variant Detection & Analysis: CLC Genomics workbench, dbSNP, COSMIC, & more
by Ansuman Chattopadhyay, PhD
Wednesday, 1st June 2016 NOT 27th April
1-4 pm
Falk Library Classroom 2 (upstairs)
This hands-on workshop focuses on human genetic variations and cancer mutations. It covers identification of variants using CLC Genomics Workbench software and introduces variation databases (dbSNP, ClinVar, OMIM, DGV, PheGenI, HGMD, NextBio, COSMIC, Broad Tumor Portal, ExAc Browser, RegulomeDb). The workshop will also teach how to use bioinformatics tools for functional analysis of mutations (EBI Variant Effect Predictor).
This class is approved for AMA Category 2 CME credit.
HSLS early Summer 2016 Bioinformatics Training Workshops schedule