Are you looking to automate and streamline your data analysis workflows for next-generation sequencing (NGS) data? Join our Snakemake for Bioinformatics course to learn how to create scalable, reproducible workflows for RNA-seq analysis, variant calling, bacterial genome assembly, and more!
Course Dates: 24-27 March 2025
Location: Online (Cloud-based Linux environment provided)
Register here: https://genomics.ed.ac.uk/event/snakemake-2/
Why Snakemake?
Snakemake is a powerful, Python-based workflow management system that allows you to define and execute complex bioinformatics workflows efficiently. It avoids redundant computation and seamlessly scales from a personal workstation to high-performance computing
(HPC) environments.
What You’ll Learn:
Automate NGS data analysis with Snakemake
Create modular, scalable workflows
Integrate external tools and handle dependencies
Optimise workflow performance and share workflows online
Who Should Attend?
This course is designed for researchers who need to automate bioinformatics pipelines. A working knowledge of the Linux BASH command line is required (our Linux for Bioinformatics course provides a suitable background). No prior Python experience
is needed.
New to Linux?
If you're unfamiliar with the Linux command line, consider attending our Linux for Bioinformatics course first. This one-day workshop provides the essential skills needed to confidently navigate and operate within a Linux environment, preparing
you for workflow automation with Snakemake. More details are available here: Introduction to Linux for Genomics.
Interested in Variant Analysis?
We also offer a dedicated Variant Analysis course that covers essential methods for detecting and interpreting genetic variants in NGS data. Learn more and register here: Variant
Analysis.
Register Now!
Spaces are limited, so secure your place today. For more details and registration, visit
https://genomics.ed.ac.uk/event/snakemake-2/
Best regards,