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Home Pathology Portal Genetics and Genomics Omics techniques and their application to genomic medicine Overview of bioinformatics approaches to the analysis of genomic data.
Overview of bioinformatics approaches to the analysis of genomic data.
Pathology Portal

Annotating your own variation data with the Ensembl Variant Effect Predictor (VEP)

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The Ensembl VEP is a powerful tool that allows you to input a list of genetic variants and determines which genes are affected and how. In this webinar, you’ll learn how to use the online VEP tool, which is suitable for analysing short lists of genetic variants, and the offline tool, which allows you to annotate whole genome variant calls.

Who is this course for?

This webinar is suitable to any clinical or research scientists who areinterested in exploring geneticvariants and their effect. In this webinar we willuse examples fromhuman clinicaldatabut the VEPtool is available for other species too.

Outcomes

By the end of the webinar you will be able to:

  • Describe the application of VEP
  • Analyse short lists of genetic variants using VEP
  • Annotate variation data

Emily Perry (Pritchard)
EMBL-EBI, UK

Resource details

Contributed by: Pathology Portal
Authored by: Emily Perry (Pritchard), The European Molecular Biology Laboratory-European Bioinformatics Institute's (EMBL-EBI).
Licence: Creative Commons: Attribution-NonCommercial-NoDerivatives 4.0 International More information on licences
First contributed: 16 December 2022
Audience access level: Full user

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