Webinar: Variation


August 6, 2019, 1-2 pm Eastern/10-11 am Pacific (USA time): You can click here for a link to the webinar start time in your timezone. Learn how to find and visualize variation data, Single Nucleotide Polymorphism (SNP) and Insertion/Deletion (INDEL) calls, with the Genotype Explorer and the Genome Browser. There are also tools to analyze your own variation data or data from GenBank and other databases, using the Variant Effect Predictor (VEP) and Galaxy.

webinar materials: slides (includes six demos with videos).

Sign up is required but attendance is free. Registration ends the day before each webinar session. Each registered participant will receive an email with connection details. Follow this link to sign up (or here if Google products are blocked in your location).


For more details follow this link.
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