Learning objectives
- Understand what structural variations are and why they are difficult to detect
- Learn about the available tools for detecting structural variation using long reads, and how to use them
- Learn how to inspect and visualise structural variation calls
Related lessons
Related content
- Analysis solutions for nanopore sequencing
- Structural variation sample-to-analysis workflow
- Structural variation white paper
- Shruti Iyer - Understanding genetic variation in cancer, using targeted nanopore sequencing
- Poster: Resolving structural variants in genomic disorders
- Poster: Using Pore-C to investigate the spatial organisation of the human genome