This information is over 2 years old. Information was current at time of publication.{"id":2131,"date":"2016-11-03T13:26:59","date_gmt":"2016-11-03T18:26:59","guid":{"rendered":"http:\/\/info.hsls.pitt.edu\/molbio\/?p=2131"},"modified":"2016-11-03T13:26:59","modified_gmt":"2016-11-03T18:26:59","slug":"variant-detection-wksp-1116","status":"publish","type":"post","link":"https:\/\/info.hsls.pitt.edu\/molbio\/2016\/11\/03\/variant-detection-wksp-1116\/","title":{"rendered":"Variant Detection wksp 11\/16"},"content":{"rendered":"

Variant Detection & Analysis: CLC Genomics workbench, dbSNP, COSMIC, & more<\/big><\/span><\/strong>
\nby Ansuman Chattopadhyay, PhD
\n<\/span><\/strong>
\nWednesday, 16th November 2016
\n1-4 pm
\nFalk Library Classroom 2 (upstairs)<\/span><\/strong><\/p>\n

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).<\/p>\n

This class is approved for AMA Category 2 CME credit.<\/p>\n

HSLS Fall 2016 Bioinformatics Training Workshops schedule<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"

Variant Detection & Analysis: CLC Genomics workbench, dbSNP, COSMIC, & more<\/span><\/strong>
\nby Ansuman Chattopadhyay, PhD
\n<\/span><\/strong>
\nWednesday, 16th November 2016
\n1-4 pm
\nFalk Library Classroom 2 (upstairs)<\/span><\/strong><\/p>\n

This hands-on workshop focuses on human genetic variations and cancer mutations.<\/p>\n