Bioinformatics for Precision Medicine: From Reads to Disease Variants. A GATK Workshop
Date: 20 - 24 April 2020
This 5-day course, with instructors from the Broad Institute (Boston, USA), covers all the steps from raw sequencing data to the obtention of lists of variants using the popular GATK4 software. The 4-day GATK workshop is followed by a last day covering topics on germline and somatic disease variant prioritization instructed by experts from the Unit of Bioinformatics for Precision Oncology (Catalan Institute of Oncology) and the Clinical Bioinformatics Area (Fundación Progreso y Salud).
GATK workshops are designed to provide a comprehensive onboarding experience to new users, as well as access to more advanced understanding for users who are already familiar with the toolkit.
Keywords: GATK, Variant detection, Variant calling, Variant discovery, disease variant, priorization, genomics, oncology
Venue: Institut Català d'Oncologia - L'Hospitalet de Llobregat, 203, Avinguda de la Granvia de l’Hospitalet
City: L'Hospitalet de Llobregat
Region: Barcelona
Country: Spain
Organizer: Catalan Institute of Oncology (ICO), Broad Institute, Bellvitge Biomedical Research Institute (IDIBELL), Fundación Progreso y Salud (FPS) and Spanish National Bioinformatics Institute (INB/ELIXIR-ES)
Host institutions: Catalan Institute of Oncology (ICO)
Eligibility:
- First come first served
Target audience: mixed audience, GATK newbies, GATK experts, GATK users, variant discovery newbies
Capacity: 40
Event types:
- Workshops and courses
Activity log

Spain