The aim of this course is designed for students without programming experience that want to process and analyse NGS data. In this course, we will use Galaxy, an open-source, web-based platform for accessible, reproducible, and transparent computational biomedical research. Even if we are only going to cover an NGS pipeline here (variant calling), this course will give students enough understanding on how Galaxy works, allowing them to easily run bioinformatics tools, setting up parameters and building larger workflows.
Before taking this course, it is important to understand the basics of NGS by taking the NGS: Introduction and pre-processing pipeline course.
This course is for you if:
Return to Catalogue