Objective: The aim of this course was to provide information and hands-on training on processing exome and human whole genome data for the identification, annotation and filtering of small (SNP) and structural variants (SV) including inversions, duplications, deletions and translocations.
Duration: 30 hours
Type: Personalized for clinical geneticists
Trainers: Riccardo Aiese Cigliano, Andreu Paytuví, Rosa Barcelona