Prioritization of variants and genes: BiERapp

These exercises show how to analyze exome data for different families or groups.
Goal is to detect associated mutations to Mendelian disease.
Input data is a set of VCF files. Output analysis will be a selection of candidate variants.

We are working from BiERapp. Two steps:

  1. Uploading VCF files in BiERapp and automatically these files will be indexed and annotated.
  2. Now you can use different filtering options to refine your variant selection strategy.


Let's go to BiERapp!
We have uploaded several VCF files for you. Now these files are indexed and annotated. So it is prepared to work.
You can check this data with user: gda password: gda