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Copy file name to clipboardExpand all lines: .github/CONTRIBUTING.md
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9. Update MultiQC config `assets/multiqc_config.yml` so relevant suffixes, file name clean up and module plots are in the appropriate order. If applicable, add a [MultiQC](https://https://multiqc.info/) module.
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10. Add a description of the output files and if relevant any appropriate images from the MultiQC report to `docs/output.md`.
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### Things to consider regarding displaying results for a new tool
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- If a MultiQC module exist for the tool, use the standard settings for it to start with.
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- If no Multiqc module exists, the results of the tool should be made available in the results directory.
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- If a tool doesn’t produce output files, the stdout should be channeled into a output file that can be accessible from the outdir of the pipeline.
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### Default values
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Parameters should be initialised / defined with default values within the `params` scope in `nextflow.config`.
Copy file name to clipboardExpand all lines: CITATIONS.md
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> Andrews, S. (2010). FastQC: A Quality Control Tool for High Throughput Sequence Data [Online].
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-[SeqFu](https://telatin.github.io/seqfu2/)
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> Telatin A, Fariselli P, Birolo G. SeqFu: A Suite of Utilities for the Robust and Reproducible Manipulation of Sequence Files. Bioengineering 2021, 8, 59. doi.org/10.3390/bioengineering8050059
> Wingett SW and Andrews S. FastQ Screen: A tool for multi-genome mapping and quality control [version 2; referees: 4 approved]. F1000Research 2018, 7:1338 (https://doi.org/10.12688/f1000research.15931.2)
> 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.
Copy file name to clipboardExpand all lines: README.md
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<!-- TODO nf-core: Include a figure that guides the user through the major workflow steps. Many nf-core
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workflows use the "tube map" design for that. See https://nf-co.re/docs/contributing/design_guidelines#examples for examples. -->
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<!-- TODO nf-core: Fill in short bullet-pointed list of the default steps in the pipeline -->1. Read QC ([`FastQC`](https://www.bioinformatics.babraham.ac.uk/projects/fastqc/))2. Present QC for raw reads ([`MultiQC`](http://multiqc.info/))
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<!-- TODO nf-core: Fill in short bullet-pointed list of the default steps in the pipeline -->
3. Present QC for raw reads ([`MultiQC`](http://multiqc.info/))
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## Usage
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> [!NOTE]
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> If you are new to Nextflow and nf-core, please refer to [this page](https://nf-co.re/docs/usage/installation) on how to set-up Nextflow. Make sure to [test your setup](https://nf-co.re/docs/usage/introduction#how-to-run-a-pipeline) with `-profile test` before running the workflow on actual data.
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<!-- TODO nf-core: Describe the minimum required steps to execute the pipeline, e.g. how to prepare samplesheets.
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Explain what rows and columns represent. For instance (please edit as appropriate):
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First, prepare a samplesheet with your input data that looks as follows:
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