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.
Workshop Guide: https://hsls.libguides.com/MolBioWorkshops/VarDet
Please register for:
You must also sign up for a Center for Research Computing HPC allocation and mention your intention to attend the HSLS-offered workshop on Variant Detection.