22 – 26 February 2027
Virtual, UK time zone
Applications now open until 22 November 2026.
Full programme and application details.
This course is aimed at life science researchers, wet and/or dry lab, wanting to learn more about processing RNA-seq data and later downstream analysis. It will help you if you want a basic introduction to handling RNA-seq data. We'll guide you through several common approaches that can be applied to your own datasets. The course features taught and practical sessions that cover how to interpret gene expression data and learn more about the biological significance of certain results.
Some experience with R and the Linux-based command line is beneficial, but not essential. During the course, some of the practicals will make use of a Linux-based command line interface and R statistical packages. We recommend completing some basic tutorials on this topic in preparation for the upcoming course.
In this course, we will guide you through the core technology, data analysis approaches, tools, and resources used in RNA sequencing (RNA-seq) and transcriptomics. Our goal is to support you as you build a shared understanding of the field, whether your background is in biology, computer science, or data analysis. We will introduce the fundamental concepts behind transcriptomic workflows and help you gain confidence with basic command‑line analysis.
Together, we'll explore key public data repositories and outline the main methodologies that can help you begin the biological interpretation of gene expression data. Throughout the course, a mix of learning through lectures, practical exercises, and open discussions will create an environment where you can engage with the material from your own disciplinary perspective.
All computational work will use small example data sets so that you can focus on learning the concepts and workflows. Please note that there will be no opportunity to analyse personal data during the course.
During this course, you will learn about:
- High throughput sequencing technologies for RNA-Seq
- Basics of experimental design
- RNA-seq file formats
- RNA-seq bioinformatics workflow steps following sequence generation
- Methods for transcriptomics; QC, mapping, and visualisation tools
- Data resources to assist in the functional analysis and interpretation of transcriptomic data
- Introduction to long read analysis
- Fundamentals of pipeline implementation (with Nextflow) for bulk RNA-seq analysis
- Data resources covered: Expression Atlas and g:Profiler
- Sequencing repositories: ENA, GEO, SRA
After the course, you should be able to:
- Describe a variety of applications and workflow approaches for NGS technologies
- Apply bioinformatics software and tools to undertake analysis of RNA-seq data
- Evaluate the advantages and limitations of NGS analyses
- Interpret and annotate data with functional information using public resources
Applications close 22 November 2026
Course fee: £250.00 (academia) / £350.00 (industry). Financial assistance is available.
Open application with selection: 35 places
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