ChIP-seq analysis using R
ChIP-seq analysis using R
Keywords
ChIP-Seq, Experimental-design, QC, Data-format, Alignment, Peak-calling, Differential-binding, Visualisation, Annotation
Authors
- Anna Poetsch
- based partially on material from Bori Mifsud and Ernest Turro
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Description
ChIP-seq is the most commonly used technique to study binding profiles of chromatin proteins, such as TFs or histone modification patterns. This course is an introduction to ChIP-seq data, and data analysis mainly using R, some command line based peak-callers and online software. It provides a theoretical background and the means to perform peak calling and differential binding analysis.
Aims
The aim of the course is to draw biologists' attention to the impact of experimental design, and the pitfalls of ChIP-seq data analysis, and to give them the tools to do their own preliminary data analysis.
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Prerequisites
- R-programming
- Unix
- HTS-introduction
- Preprocessing
- Alignment
Target audience
- Biologist
- Programming experience
Learning objectives
- Define approriate experimental design
- Describe and perform steps of the ChIP-Seq workflow
- Visualise raw and processed data
- Annotate and interpret results
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Materials
- [material 1; see (instructions)[https://microasp.upsc.se/ngs_trainers/Materials/wikis/Templates#documenting-new-material] and guidelines(https://microasp.upsc.se/ngs_trainers/Materials/wikis/Git-Repos#guide
Quality control of three sequencing data sets, two from ChiP-Seq experiments, one RNA-Seq.
Availability
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Technical requirements
- Bowtie
- MGA (https://github.com/crukci-bioinformatics/MGA/blob/master/README)
- FastQC (http://www.bioinformatics.babraham.ac.uk/projects/fastqc/)
- firefox
Literature references
- Hadfield J, Eldridge MD (2014) Multi-genome alignment for quality control and contamination screening of next-generation sequencing data. Frontiers in Genetics 5:31.
- Morgan M, Anders S, Lawrence M, Aboyoun P, Pagès H and Gentleman R (2009) ShortRead: a Bioconductor package for input, quality assessment and exploration of high-throughput sequence data. Bioinformatics 25:2607-2608.
Top | Keywords | Authors | Description | Aims | Prerequisites | Target audience | Learning objectives | Materials | Data | Technical requirements | Literature references
Keywords: ChIP-Seq, Experimental-design, QC, Data-format, Alignment, Peak-calling, Differential-binding, Visualisation, Annotation
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