TP_experimental_biologists.md

title: "TP for experimental biologists"
author: Laurent Modolo [laurent.modolo@ens-lyon.fr](mailto:laurent.modolo@ens-lyon.fr)
date: 6 Jun 2018
output:
  pdf_document:
    toc: true
    toc_depth: 3
    number_sections: true
    highlight: tango
    latex_engine: xelatex

The Goal of this practical is to learn how to build your own pipeline with nextflow and using the tools already wrapped. For this we are going to build a small RNASeq analysis pipeline that should run the following steps:

• remove Illumina adaptors
• trim reads by quality
• build the index of a reference genome
• estimate the number of RNA fragments mapping to the transcript of this genome

Initialize your own project

You are going to build a pipeline for you or your team. So the first step is to create your own project.

Instead of reinventing the wheel, you can use the pipelines/nextflow as a template. To easily do so, go to the pipelines/nextflow repository and click on the fork button.

In git, the action of forking means that you are going to make your own private copy of a repository. You can then write modifications in your project, and if they are of interest for the source repository (here pipelines/nextflow) create a merge request. Merge request are send to the source repository to ask the maintainers to integrate modifications.