Want easy analysis of your own variant calls? The Ensembl Variant Effect Predictor (VEP) allows you to annotate variants with the genes and regulatory features they hit and what effect they have on them. It can also tell you if your variant is known or novel, and give you more information about known variants, such as population frequencies. You can use data from the VEP to prioritise variants from GWAS and whole variant calling studies, or from smaller scale single gene sequencing.
This webinar will guide you through using the easy web interface for the VEP - suitable for annotating small numbers of variants, and using the standalone script - suitable for fast analysis of genome-wide variant calls. VEP developers will be on hand to answer your questions on using the VEP, and on the data behind this powerful tool.
Familiarity with Ensembl is useful, but not essential. You don't need to have used the VEP before, but regular VEP users may find it useful to find out new tricks and ask the developers questions.