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@@ -15,8 +15,7 @@ Learn more about contributing: [CONTRIBUTING.md](https://github.com/nf-core/rnas
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-[ ] This comment contains a description of changes (with reason).
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-[ ] If you've fixed a bug or added code that should be tested, add tests!
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-[ ] If you've added a new tool - have you followed the pipeline conventions in the [contribution docs](https://github.com/nf-core/rnaseq/tree/master/.github/CONTRIBUTING.md)
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-[ ] If necessary, also make a PR on the nf-core/rnaseq _branch_ on the [nf-core/test-datasets](https://github.com/nf-core/test-datasets) repository.
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-[ ] If you've added a new tool - have you followed the pipeline conventions in the [contribution docs](https://github.com/nf-core/rnaseq/tree/master/.github/CONTRIBUTING.md)- [] If necessary, also make a PR on the nf-core/rnaseq _branch_ on the [nf-core/test-datasets](https://github.com/nf-core/test-datasets) repository.
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-[ ] Make sure your code lints (`nf-core lint`).
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-[ ] Ensure the test suite passes (`nextflow run . -profile test,docker --outdir <OUTDIR>`).
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-[ ] Usage Documentation in `docs/usage.md` is updated.
-[[#746](https://github.com/nf-core/rnaseq/issues/746)] - Add `tin.py` output to MultiQC report
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-[[#841](https://github.com/nf-core/rnaseq/issues/841)] - Turn `--deseq2_vst` on by default
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-[[#853](https://github.com/nf-core/rnaseq/issues/853)] - Pipeline fails at email step: Failed to invoke `workflow.onComplete` event handler
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-[[#857](https://github.com/nf-core/rnaseq/issues/857)] - Missing parameter required by StringTie if using STAR as aligner
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-[[#862](https://github.com/nf-core/rnaseq/issues/862)] - Filter samples that have no reads after trimming
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-[[#864](https://github.com/nf-core/rnaseq/issues/864)] - Pre-process transcripts fasta when using `--gencode`
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- Expose additional arguments to UMI-tools as pipeline params: `--umitools_bc_pattern2` is required if the UMI is located on read 2. `--umitools_umi_separator` will often be needed in conjunction with `--skip_umi_extract` as most other tools such as Illumina's `BCL Convert` use a colon instead of an underscore to separate the UMIs. The `--umitools_grouping_method` allows to fine-tune handling of similar but non-identical UMIs.
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- Updated pipeline template to [nf-core/tools 2.5.1](https://github.com/nf-core/tools/releases/tag/2.5.1)
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### Parameters
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| Old parameter | New parameter |
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| ------------- | ---------------------------- |
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||`--umitools_bc_pattern2`|
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||`--umitools_umi_separator`|
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||`--umitools_grouping_method`|
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### Software dependencies
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Note, since the pipeline is now using Nextflow DSL2, each process will be run with its own [Biocontainer](https://biocontainers.pro/#/registry). This means that on occasion it is entirely possible for the pipeline to be using different versions of the same tool. However, the overall software dependency changes compared to the last release have been listed below for reference.
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| Dependency | Old version | New version |
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| ---------- | ----------- | ----------- |
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|`hisat2`| 2.2.0 | 2.2.1 |
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|`multiqc`| 1.11 | 1.13 |
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|`picard`| 2.26.10 | 2.27.4 |
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> **NB:** Dependency has been **updated** if both old and new version information is present.
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> **NB:** Dependency has been **added** if just the new version information is present.
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> **NB:** Dependency has been **removed** if version information isn't present.
[](https://github.com/nf-core/rnaseq/actions?query=workflow%3A%22nf-core+CI%22)
[](https://doi.org/10.5281/zenodo.1400710)
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[](https://nf-co.re/rnaseq/results)[](https://doi.org/10.5281/zenodo.1400710)
[](https://docs.conda.io/en/latest/)
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[](https://www.docker.com/)
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[](https://sylabs.io/docs/)
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[](https://docs.conda.io/en/latest/)
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[](https://www.docker.com/)
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[](https://sylabs.io/docs/)
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[](https://tower.nf/launch?pipeline=https://github.com/nf-core/rnaseq)
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[](https://nfcore.slack.com/channels/rnaseq)
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[](https://twitter.com/nf_core)
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[](https://www.youtube.com/c/nf-core)
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[](https://nfcore.slack.com/channels/rnaseq)[](https://twitter.com/nf_core)[](https://www.youtube.com/c/nf-core)
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## Introduction
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3. Download the pipeline and test it on a minimal dataset with a single command:
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```console
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```bash
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nextflow run nf-core/rnaseq -profile test,YOURPROFILE --outdir <OUTDIR>
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```
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@@ -82,13 +77,13 @@ The SRA download functionality has been removed from the pipeline (`>=3.2`) and
- An executable Python script called [`fastq_dir_to_samplesheet.py`](https://github.com/nf-core/rnaseq/blob/master/bin/fastq_dir_to_samplesheet.py) has been provided if you would like to auto-create an input samplesheet based on a directory containing FastQ files **before** you run the pipeline (requires Python 3 installed locally) e.g.
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