/In-depth-NGS-Data-Analysis-Course

Materials for 12-day course on analyzing RNA-Seq, ChIP-Seq and variant calling data.

Primary LanguageHTMLOtherNOASSERTION

**NOTE: This is the "master" branch of the repository, the May2017 branch contains the latest materials for this course.

In-depth NGS Data Analysis Course

This branch (May 2017) of the NGS course repo contains all course materials for the Summer 2017 version of HBC's In-depth NGS Data Analysis Course, a 12-day course run over 6 weeks (May 31 through July 7, 2017).

The course is aimed at bench biologists who are interested in learning about NGS-based genomic analysis. The topics covered in-depth during this course are analysis of RNA-Seq and ChIP-Seq data, with an optional Variant Calling session. The sessions will also include functional analysis downstream of sequence data processing. During this course, participants will gain skills in the areas of:

  • UNIX and basic shell scripting
  • high-performance compute clusters, and
  • R for statistical analysis and data visualization.

At the end of this course, participants can expect to have the expertise to independently run data analysis for sequencing experiments.

No prior programming experience or command-line training is required.

This repo contains the materials for the six sessions of the course. The six sessions are described below:

NOTE: Additional materials are included in this repo but are not part of the main course.

These materials have been developed by members of the teaching team at the Harvard Chan Bioinformatics Core (HBC). These are open access materials distributed under the terms of the Creative Commons Attribution license (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.