Variant Detection & Analysis: CLC Genomics workbench, dbSNP, COSMIC, & more
by Ansuman Chattopadhyay, PhD
Wednesday, 16th November 2016
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.