dualrnaseq

Analysis of Dual RNA-seq data - an experimental method for interrogating host-pathogen interactions through simultaneous RNA-seq.

https://github.com/nf-core/dualrnaseq

Science Score: 77.0%

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    Found 4 DOI reference(s) in README
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Keywords

dualrna-seq host-pathogen nextflow nf-core pipeline quantification readmapping rna-seq workflow
Last synced: 6 months ago · JSON representation ·

Repository

Analysis of Dual RNA-seq data - an experimental method for interrogating host-pathogen interactions through simultaneous RNA-seq.

Basic Info
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  • Stars: 22
  • Watchers: 133
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  • Open Issues: 46
  • Releases: 1
Topics
dualrna-seq host-pathogen nextflow nf-core pipeline quantification readmapping rna-seq workflow
Created over 5 years ago · Last pushed 8 months ago
Metadata Files
Readme Changelog Contributing License Code of conduct Citation

README.md

nf-core/dualrnaseq

GitHub Actions CI Status GitHub Actions Linting Status Nextflow DOI

install with bioconda Docker Get help on Slack

Dual RNA-seq pipeline

nf-core/dualrnaseq is a bioinformatics pipeline built using Nextflow, 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.

Introduction

nf-core/dualrnaseq is specifically used for the analysis of Dual RNA-seq data, interrogating host-pathogen interactions through simultaneous RNA-seq.

This pipeline has been initially tested with eukaryotic host's including Human and Mouse, and pathogens including Salmonella enterica, Orientia tsutsugamushi, Streptococcus penumoniae, Escherichia coli and Mycobacterium leprae. The workflow should work with any eukaryotic and bacterial organisms with an available reference genome and annotation.

Method

The workflow merges host and pathogen genome annotations taking into account differences in annotation conventions, then processes raw data from FastQ inputs (FastQC, BBDuk), quantifies gene expression (STAR and HTSeq; STAR, Salmon and tximport; or Salmon in quasimapping mode and tximport), and summarises the results (MultiQC), as well as generating a number of custom summary plots and separate results tables for the pathogen and host. See the output documentation for more details.

Workflow

The workflow diagram below gives a simplified visual overview of how dualrnaseq has been designed.

nf-core/dualrnaseq

Documentation

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

  1. Installation
  2. Pipeline configuration
  3. Running the pipeline
  4. Output and how to interpret the results
  5. Troubleshooting

Credits

nf-core/dualrnaseq was coded and written by Bozena Mika-Gospodorz and Regan Hayward.

We thank the following people for their extensive assistance in the development of this pipeline:

Contributions and Support

If you would like to contribute to this pipeline, please see the contributing guidelines.

For further information or help, don't hesitate to get in touch on the Slack #dualrnaseq channel (you can join with this invite).

Citations

You can cite the nf-core publication as follows:

The nf-core framework for community-curated bioinformatics pipelines.

Philip Ewels, Alexander Peltzer, Sven Fillinger, Harshil Patel, Johannes Alneberg, Andreas Wilm, Maxime Ulysse Garcia, Paolo Di Tommaso & Sven Nahnsen.

Nat Biotechnol. 2020 Feb 13. doi: 10.1038/s41587-020-0439-x. ReadCube: Full Access Link

An extensive list of references for the tools used by the pipeline can be found in the CITATIONS.md file.

Owner

  • Name: nf-core
  • Login: nf-core
  • Kind: organization
  • Email: core@nf-co.re

A community effort to collect a curated set of analysis pipelines built using Nextflow.

Citation (CITATIONS.md)

# nf-core/dualrnaseq: Citations

## [nf-core](https://pubmed.ncbi.nlm.nih.gov/32055031/)

> Ewels PA, Peltzer A, Fillinger S, Patel H, Alneberg J, Wilm A, Garcia MU, Di Tommaso P, Nahnsen S. The nf-core framework for community-curated bioinformatics pipelines. Nat Biotechnol. 2020 Mar;38(3):276-278. doi: 10.1038/s41587-020-0439-x. PubMed PMID: 32055031.

## [Nextflow](https://pubmed.ncbi.nlm.nih.gov/28398311/)

> Di Tommaso P, Chatzou M, Floden EW, Barja PP, Palumbo E, Notredame C. Nextflow enables reproducible computational workflows. Nat Biotechnol. 2017 Apr 11;35(4):316-319. doi: 10.1038/nbt.3820. PubMed PMID: 28398311.

## Pipeline tools

* [BBTools](https://jgi.doe.gov/data-and-tools/bbtools/)

* [Cutadapt](https://doi.org/10.14806/ej.17.1.200)
  > Martin, M. (2011). Cutadapt removes adapter sequences from high-throughput sequencing reads. EMBnet.journal, 17(1), pp. 10-12

* [FastQC](https://www.bioinformatics.babraham.ac.uk/projects/fastqc/)

* [GffRead](https://pubmed.ncbi.nlm.nih.gov/32489650/)
  > Pertea G, Pertea M. GFF Utilities: GffRead and GffCompare. F1000Res. 2020 Apr 28;9:ISCB Comm J-304. doi: 10.12688/f1000research.23297.2. eCollection 2020. PubMed PMID: 32489650; PubMed Central PMCID: PMC7222033.

* [HTSeq](https://pubmed.ncbi.nlm.nih.gov/25260700/)
  > Anders S, Pyl PT, Huber W. HTSeq--a Python framework to work with high-throughput sequencing data. Bioinformatics. 2015 Jan 15;31(2):166-9. doi: 10.1093/bioinformatics/btu638. Epub 2014 Sep 25. PMID: 25260700; PMCID: PMC4287950.

* [MultiQC](https://pubmed.ncbi.nlm.nih.gov/27312411/)
  > Ewels P, Magnusson M, Lundin S, Käller M. MultiQC: summarize analysis results for multiple tools and samples in a single report. Bioinformatics. 2016 Oct 1;32(19):3047-8. doi: 10.1093/bioinformatics/btw354. Epub 2016 Jun 16. PubMed PMID: 27312411; PubMed Central PMCID: PMC5039924.

* [Salmon](https://pubmed.ncbi.nlm.nih.gov/28263959/)
  > Patro R, Duggal G, Love MI, Irizarry RA, Kingsford C. Salmon provides fast and bias-aware quantification of transcript expression Nat Methods. 2017 Apr;14(4):417-419. doi: 10.1038/nmeth.4197. Epub 2017 Mar 6. PubMed PMID: 28263959; PubMed Central PMCID: PMC5600148.

* [STAR](https://pubmed.ncbi.nlm.nih.gov/23104886/)
  > Dobin A, Davis CA, Schlesinger F, Drenkow J, Zaleski C, Jha S, Batut P, Chaisson M, Gingeras TR. STAR: ultrafast universal RNA-seq aligner Bioinformatics. 2013 Jan 1;29(1):15-21. doi: 10.1093/bioinformatics/bts635. Epub 2012 Oct 25. PubMed PMID: 23104886; PubMed Central PMCID: PMC3530905.

## R packages

* [R](https://www.R-project.org/)
  > R Core Team (2017). R: A language and environment for statistical computing. R Foundation for Statistical Computing, Vienna, Austria.

* [ggplot2](https://cran.r-project.org/web/packages/ggplot2/index.html)
  > H. Wickham. ggplot2: Elegant Graphics for Data Analysis. Springer-Verlag New York, 2016.

* [rtracklayer](https://pubmed.ncbi.nlm.nih.gov/19468054/)
  > Lawrence M, Gentleman R, Carey V (2009). “rtracklayer: an R package for interfacing with genome browsers.” Bioinformatics, 25, 1841-1842.

* [Tximport](https://f1000research.com/articles/4-1521/v2)
  > Soneson C, Love MI and Robinson MD. Differential analyses for RNA-seq: transcript-level estimates improve gene-level inferences [version 2; peer review: 2 approved]. F1000Research 2016, 4:1521

## Python packages

* [Python](http://www.python.org)
  > van Rossum, G. Python tutorial, Technical Report CS-R9526, Centrum voor Wiskunde en Informatica (CWI), Amsterdam, May 1995.

* [Biopython](https://academic.oup.com/bioinformatics/article/25/11/1422/330687)
  > Peter J. A. Cock, Tiago Antao, Jeffrey T. Chang, Brad A. Chapman, Cymon J. Cox, Andrew Dalke, Iddo Friedberg, Thomas Hamelryck, Frank Kauff, Bartek Wilczynski, Michiel J. L. de Hoon, Biopython: freely available Python tools for computational molecular biology and bioinformatics, Bioinformatics, Volume 25, Issue 11, 1 June 2009, Pages 1422–1423

* [pysam](https://github.com/pysam-developers/pysam)

* [matplotlib](https://matplotlib.org/3.1.0/citing.html)
  > J. D. Hunter, "Matplotlib: A 2D Graphics Environment", Computing in Science & Engineering, vol. 9, no. 3, pp. 90-95, 2007

* [seaborn](http://seaborn.pydata.org/index.html)
  > Waskom, M. et al., 2017. mwaskom/seaborn: v0.8.1

## Software packaging/containerisation tools

* [Anaconda](https://anaconda.com)
  > Anaconda Software Distribution. Computer software. Vers. 2-2.4.0. Anaconda, Nov. 2016. Web.

* [Bioconda](https://pubmed.ncbi.nlm.nih.gov/29967506/)
  > Grüning B, Dale R, Sjödin A, Chapman BA, Rowe J, Tomkins-Tinch CH, Valieris R, Köster J; Bioconda Team. Bioconda: sustainable and comprehensive software distribution for the life sciences. Nat Methods. 2018 Jul;15(7):475-476. doi: 10.1038/s41592-018-0046-7. PubMed PMID: 29967506.

* [BioContainers](https://pubmed.ncbi.nlm.nih.gov/28379341/)
  > da Veiga Leprevost F, Grüning B, Aflitos SA, Röst HL, Uszkoreit J, Barsnes H, Vaudel M, Moreno P, Gatto L, Weber J, Bai M, Jimenez RC, Sachsenberg T, Pfeuffer J, Alvarez RV, Griss J, Nesvizhskii AI, Perez-Riverol Y. BioContainers: an open-source and community-driven framework for software standardization. Bioinformatics. 2017 Aug 15;33(16):2580-2582. doi: 10.1093/bioinformatics/btx192. PubMed PMID: 28379341; PubMed Central PMCID: PMC5870671.

* [Docker](https://dl.acm.org/doi/10.5555/2600239.2600241)

* [Singularity](https://pubmed.ncbi.nlm.nih.gov/28494014/)
  > Kurtzer GM, Sochat V, Bauer MW. Singularity: Scientific containers for mobility of compute. PLoS One. 2017 May 11;12(5):e0177459. doi: 10.1371/journal.pone.0177459. eCollection 2017. PubMed PMID: 28494014; PubMed Central PMCID: PMC5426675.

GitHub Events

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Last Year
  • Create event: 7
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  • Watch event: 4
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  • Member event: 2
  • Issue comment event: 19
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  • Fork event: 3

Committers

Last synced: over 2 years ago

All Time
  • Total Commits: 489
  • Total Committers: 6
  • Avg Commits per committer: 81.5
  • Development Distribution Score (DDS): 0.603
Past Year
  • Commits: 0
  • Committers: 0
  • Avg Commits per committer: 0.0
  • Development Distribution Score (DDS): 0.0
Top Committers
Name Email Commits
reganhayward r****d@g****m 194
bozmik b****1@g****m 151
Bozena Mika-Gospodorz b****z@h****e 137
Lars Barquist l****t@g****m 4
nf-core-bot c****e@n****e 2
Alexander Peltzer a****r@u****m 1
Committer Domains (Top 20 + Academic)

Issues and Pull Requests

Last synced: 6 months ago

All Time
  • Total issues: 52
  • Total pull requests: 78
  • Average time to close issues: 3 months
  • Average time to close pull requests: 18 days
  • Total issue authors: 19
  • Total pull request authors: 16
  • Average comments per issue: 0.42
  • Average comments per pull request: 0.79
  • Merged pull requests: 45
  • Bot issues: 0
  • Bot pull requests: 0
Past Year
  • Issues: 22
  • Pull requests: 15
  • Average time to close issues: N/A
  • Average time to close pull requests: 8 days
  • Issue authors: 3
  • Pull request authors: 3
  • Average comments per issue: 0.0
  • Average comments per pull request: 0.33
  • Merged pull requests: 10
  • Bot issues: 0
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Pull Request Authors
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Dependencies

.github/workflows/awsfulltest.yml actions
  • conda-incubator/setup-miniconda v2 composite
.github/workflows/awstest.yml actions
  • conda-incubator/setup-miniconda v2 composite
.github/workflows/branch.yml actions
  • mshick/add-pr-comment v1 composite
.github/workflows/ci.yml actions
  • actions/checkout v2 composite
  • technote-space/get-diff-action v4 composite
.github/workflows/linting.yml actions
  • actions/checkout v2 composite
  • actions/checkout v1 composite
  • actions/setup-node v1 composite
  • actions/setup-python v1 composite
  • actions/upload-artifact v2 composite
.github/workflows/linting_comment.yml actions
  • dawidd6/action-download-artifact v2 composite
  • marocchino/sticky-pull-request-comment v2 composite
.github/workflows/push_dockerhub_dev.yml actions
  • actions/checkout v2 composite
.github/workflows/push_dockerhub_release.yml actions
  • actions/checkout v2 composite
Dockerfile docker
  • nfcore/base 1.12.1 build
environment.yml pypi