Bioinformatics Training Platform (BTP) Module: Copy Number Variation
- Topic
- Copy Number Variation
- Target Audience
- Biologists
- Non-bioinformaticians
- Little to no programming expereience
- Prerequisites
- None
- Key Learning Outcomes
- Understand and perform a simple copy number variation analysis on NGS data
- Become familiar with Sequenza
- Understand the CNV inference process as an interplay between depth of sequencing, cellularity and B-allele frequency
- Visualize CNV events by manual inspection
- Time Required *
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