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Merge pull request #812 from jfy133/pipeline-diagram
Add Pipeline diagram
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CHANGELOG.md

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- [[#799](https://github.com/nf-core/rnaseq/issues/799)] - Issue with using `--retain_unpaired` with the `FASTQC_UMITOOLS_TRIMGALORE:TRIMGALORE` module
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- [[#802](https://github.com/nf-core/rnaseq/issues/802)] - `--bam_csi_index` error generated if `--skip_alignment` specified
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- [[#808](https://github.com/nf-core/rnaseq/issues/808)] - Auto-detect usage of Illumina iGenomes reference
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- [[#809](https://github.com/nf-core/rnaseq/issues/809)] - Add metro map for pipeline
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- [[#814](https://github.com/nf-core/rnaseq/issues/814)] - Use decimal values for `--min_mapped_reads`
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- Updated pipeline template to [nf-core/tools 2.3.2](https://github.com/nf-core/tools/releases/tag/2.3.2)
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README.md

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## Pipeline summary
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![nf-core/RNASeq Workflow Diagram](docs/images/pipeline_diagram_grey.png)
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The SRA download functionality has been removed from the pipeline (`>=3.2`) and ported to an independent workflow called [nf-core/fetchngs](https://nf-co.re/fetchngs). You can provide `--nf_core_pipeline rnaseq` when running nf-core/fetchngs to download and auto-create a samplesheet containing publicly available samples that can be accepted directly as input by this pipeline.
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1. Merge re-sequenced FastQ files ([`cat`](http://www.linfo.org/cat.html))
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The pipeline was re-written in Nextflow DSL2 and is primarily maintained by Harshil Patel ([@drpatelh](https://github.com/drpatelh)) from [Seqera Labs, Spain](https://seqera.io/).
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The pipeline workflow diagram was designed by Sarah Guinchard ([@G-Sarah](https://github.com/G-Sarah)) and James Fellows Yates ([@jfy133](https://github.com/jfy133)).
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Many thanks to other who have helped out along the way too, including (but not limited to):
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[@Galithil](https://github.com/Galithil),
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[@pditommaso](https://github.com/pditommaso),
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