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