Variant Detection & Analysis: CLC Genomics & IVA
by Ansuman Chattopadhyay, PhD
Wednesday, 7th February 2018
1-4 pm
Falk Library Classroom 2 (upstairs)
Register here.
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, Correlation Engine, COSMIC, Broad Tumor Portal, gnomAD Browser, RegulomeDb). The workshop teaches how to use bioinformatics tools for functional analysis of mutations and covers web tools such as EBI Variant Effect Predictor, Ingenuity Variant Analysis (IVA), and PredictSNP2.
Please register for the following tools: CLC Genomics Workbench, Biomedical Genomics Workbench, Correlation Engine, and IVA.
You must also sign up for a Center for Research Computing HPC allocation.
This class is approved for AMA Category 2 CME credit.
HSLS Winter/Spring 2018 MolBio Info Service Training Workshops schedule