# rnaseq

**Repository Path**: xiekunwhy/rnaseq

## Basic Information

- **Project Name**: rnaseq
- **Description**: No description available
- **Primary Language**: Unknown
- **License**: MIT
- **Default Branch**: master
- **Homepage**: None
- **GVP Project**: No

## Statistics

- **Stars**: 0
- **Forks**: 0
- **Created**: 2020-03-11
- **Last Updated**: 2020-12-19

## Categories & Tags

**Categories**: Uncategorized

**Tags**: None

## README

# ![nf-core/rnaseq](docs/images/nf-core-rnaseq_logo.png)

[![Build Status](https://travis-ci.org/nf-core/rnaseq.svg?branch=master)](https://travis-ci.org/nf-core/rnaseq)
[![Nextflow](https://img.shields.io/badge/nextflow-%E2%89%A519.04.0-brightgreen.svg)](https://www.nextflow.io/)
[![DOI](https://zenodo.org/badge/127293091.svg)](https://zenodo.org/badge/latestdoi/127293091)

[![install with bioconda](https://img.shields.io/badge/install%20with-bioconda-brightgreen.svg)](http://bioconda.github.io/)
[![Docker](https://img.shields.io/docker/automated/nfcore/rnaseq.svg)](https://hub.docker.com/r/nfcore/rnaseq/)

### Introduction

**nf-core/rnaseq** is a bioinformatics analysis pipeline used for RNA sequencing data.

The workflow processes raw data from
 FastQ inputs ([FastQC](https://www.bioinformatics.babraham.ac.uk/projects/fastqc/),
 [Trim Galore!](https://www.bioinformatics.babraham.ac.uk/projects/trim_galore/)),
  aligns the reads
   ([STAR](https://github.com/alexdobin/STAR) or
    [HiSAT2](https://ccb.jhu.edu/software/hisat2/index.shtml)),
     generates counts relative to genes
      ([featureCounts](http://bioinf.wehi.edu.au/featureCounts/),
       [StringTie](https://ccb.jhu.edu/software/stringtie/)) or transcripts
        ([Salmon](https://combine-lab.github.io/salmon/),
         [tximport](https://bioconductor.org/packages/release/bioc/html/tximport.html)) and performs extensive quality-control on the results
          ([RSeQC](http://rseqc.sourceforge.net/),
           [Qualimap](http://qualimap.bioinfo.cipf.es/),
            [dupRadar](https://bioconductor.org/packages/release/bioc/html/dupRadar.html),
             [Preseq](http://smithlabresearch.org/software/preseq/),
              [edgeR](https://bioconductor.org/packages/release/bioc/html/edgeR.html),
               [MultiQC](http://multiqc.info/)). See the [output documentation](docs/output.md) for more details of the results.

The pipeline is built using [Nextflow](https://www.nextflow.io), a workflow tool to run tasks across multiple compute infrastructures in a very portable manner. It comes with docker containers making installation trivial and results highly reproducible.

## Quick Start

i. Install [`nextflow`](https://nf-co.re/usage/installation)

ii. Install one of [`docker`](https://docs.docker.com/engine/installation/), [`singularity`](https://www.sylabs.io/guides/3.0/user-guide/) or [`conda`](https://conda.io/miniconda.html)

iii. Download the pipeline and test it on a minimal dataset with a single command

```bash
nextflow run nf-core/rnaseq -profile test,<docker/singularity/conda>
```

iv. Start running your own analysis!

```bash
nextflow run nf-core/rnaseq -profile <docker/singularity/conda> --reads '*_R{1,2}.fastq.gz' --genome GRCh37
```

See [usage docs](docs/usage.md) for all of the available options when running the pipeline.

### Documentation

The nf-core/rnaseq pipeline comes with documentation about the pipeline, found in the `docs/` directory:

1. [Installation](https://nf-co.re/usage/installation)
2. Pipeline configuration
    * [Local installation](https://nf-co.re/usage/local_installation)
    * [Adding your own system config](https://nf-co.re/usage/adding_own_config)
    * [Reference genomes](https://nf-co.re/usage/reference_genomes)
3. [Running the pipeline](docs/usage.md)
4. [Output and how to interpret the results](docs/output.md)
5. [Troubleshooting](https://nf-co.re/usage/troubleshooting)

### Credits

These scripts were originally written for use at the [National Genomics Infrastructure](https://portal.scilifelab.se/genomics/), part of [SciLifeLab](http://www.scilifelab.se/) in Stockholm, Sweden, by Phil Ewels ([@ewels](https://github.com/ewels)) and Rickard Hammarén ([@Hammarn](https://github.com/Hammarn)).

Many thanks to other who have helped out along the way too, including (but not limited to):
[@Galithil](https://github.com/Galithil),
[@pditommaso](https://github.com/pditommaso),
[@orzechoj](https://github.com/orzechoj),
[@apeltzer](https://github.com/apeltzer),
[@colindaven](https://github.com/colindaven),
[@lpantano](https://github.com/lpantano),
[@olgabot](https://github.com/olgabot),
[@jburos](https://github.com/jburos),
[@drpatelh](https://github.com/drpatelh).

## Contributions and Support

If you would like to contribute to this pipeline, please see the [contributing guidelines](.github/CONTRIBUTING.md).

For further information or help, don't hesitate to get in touch on [Slack](https://nfcore.slack.com/channels/rnaseq) (you can join with [this invite](https://nf-co.re/join/slack)).

## Citation

If you use nf-core/rnaseq for your analysis, please cite it using the following doi: [10.5281/zenodo.1400710](https://doi.org/10.5281/zenodo.1400710)

You can cite the `nf-core` pre-print as follows:  

> Ewels PA, Peltzer A, Fillinger S, Alneberg JA, Patel H, Wilm A, Garcia MU, Di Tommaso P, Nahnsen S. **nf-core: Community curated bioinformatics pipelines**. *bioRxiv*. 2019. p. 610741. [doi: 10.1101/610741](https://www.biorxiv.org/content/10.1101/610741v1).