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RNA-Seq Analysis

This course provides an introduction to the QC, processing and analysis of RNA-Seq data. It focuses on a workflow where RNA-Seq is performed on a large eukaryotic genome for which there is a reference genome available. The course starts with a comprehensive lecture covering the theory of RNA-Seq data generation and analysis and is then followed by hands-on practical sessions which run though the entire RNA-Seq analysis pipeline from raw fastq files to a list of differentially expressed candidate genes.
NGS courses

Quality Control in Sequencing Experiments

This course looks at the different ways in which sequencing based studies can fail and the options for visualisation and QC which allow you to identify and diagnose these failures at an early stage. It is designed to be of use to anyone who is using sequencing as part of their research, not just those who are running sequencing facilities.
NGS courses

ChIP-Seq Analysis

This course provides a complete introduction to the theory and practice of the analysis of ChIP-Seq data. It is designed for biologists who may have limited practical bioinformatics skills, but who would like to use ChIP-Seq as part of their work. By the end of the course students should be able to process and analyse their own data. Students on this course would benefit from having attended the SeqMonk or Unix introduction courses, but these are not required in order to attend.
NGS courses

Analysing Mapped Sequence Data with SeqMonk

SeqMonk is a program which can analyse large data sets of mapped genomic positions. It is most commonly used to work with data coming from high-throughput sequencing pipelines. The program allows you to view your reads against an annotated genome and to quantitate and filter your data to let you identify regions of interest. It is a friendly way to explore and analyse very large datasets. This course provides an introduction to the main features of SeqMonk and will run through the analysis of a couple of different datasets to show what sort of analysis options it provides.
NGS courses

Analysing bisulfite methylation sequencing data

This course builds on the core skills introduced in the Introduction to R, Introduction to Unix and Introduction to SeqMonk courses to provide a more in depth look at the analysis of bisulfite sequencing data. The course is a mix of theoretical lectures and hands-on practicals which go through the whole analysis pipeline, starting from raw sequence data and covering QC, visualisation, quantitation and differential methylation analysis.
NGS courses

10X Single Cell RNA-Seq Analysis

This course gives a practical introduction to the processing, qc and analysis of a simple single cell RNA-Seq experiment performed on the 10X platform. It explains the technology used to create the data and goes through some common analysis tools. The course also goes through the theory and practice of the dimension reduction techniques which are very often used to present this kind of data.
NGS courses

Centre for Genomic Regulation

The Centre for Genomic Regulation (CRG) is an international biomedical
research institute of excellence, created in July 2000. It is a
non-profit foundation funded by the Catalan Government through the
Department of Business & Knowledge and the Department of Health, the
Spanish Ministry of Science & Innovation, the "la Caixa" Banking
Foundation, and includes the participation of Pompeu Fabra University.

CRG

  • https://www.crg.eu/
  • training@crg.eu
  • +34 93 316 01 00
    https://www.facebook.com/centreforgenomicregulation https://twitter.com/CRGenomica?ref_src=twsrc%5Egoogle%7Ctwcamp%5Eserp%7Ctwgr%5Eauthor https://es.linkedin.com/company/center-for-genomic-regulation-crg- https://www.crg.eu
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