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 are interested in exploring genetic variants and their effect. In this webinar we will use examples from human clinical data but the VEP tool is available for other species too.
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
This webinar took place on 03 March 2021. Please click the 'Watch video' button to view the recording.