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Merge pull request #1032 from nf-core/patch
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DSL1: Release 2.5.0 - Bopfingen
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TCLamnidis authored Nov 7, 2023
2 parents 631f18e + f3cde49 commit a2c9f87
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23 changes: 13 additions & 10 deletions .github/workflows/ci.yml
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Expand Up @@ -23,7 +23,7 @@ jobs:
strategy:
matrix:
# Nextflow versions: check pipeline minimum and current latest
nxf_ver: ['20.07.1', '22.10.6']
nxf_ver: ["20.07.1", "22.10.6"]
steps:
- name: Check out pipeline code
uses: actions/checkout@v2
Expand All @@ -37,13 +37,13 @@ jobs:
- name: Build new docker image
if: env.MATCHED_FILES
run: docker build --no-cache . -t nfcore/eager:2.4.7
run: docker build --no-cache . -t nfcore/eager:2.5.0

- name: Pull docker image
if: ${{ !env.MATCHED_FILES }}
run: |
docker pull nfcore/eager:dev
docker tag nfcore/eager:dev nfcore/eager:2.4.7
docker tag nfcore/eager:dev nfcore/eager:2.5.0
- name: Install Nextflow
env:
Expand All @@ -58,7 +58,7 @@ jobs:
run: |
git clone --single-branch --branch eager https://github.com/nf-core/test-datasets.git data
- name: DELAY to try address some odd behaviour with what appears to be a conflict between parallel htslib jobs leading to CI hangs
run: |
run: |
if [[ $NXF_VER = '' ]]; then sleep 1200; fi
- name: BASIC Run the basic pipeline with directly supplied single-end FASTQ
run: |
Expand All @@ -74,7 +74,7 @@ jobs:
nextflow run ${GITHUB_WORKSPACE} -profile test,docker --save_reference
- name: REFERENCE Basic workflow, with supplied indices
run: |
nextflow run ${GITHUB_WORKSPACE} -profile test,docker --bwa_index 'results/reference_genome/bwa_index/BWAIndex/' --fasta_index 'https://github.com/nf-core/test-datasets/blob/eager/reference/Mammoth/Mammoth_MT_Krause.fasta.fai'
nextflow run ${GITHUB_WORKSPACE} -profile test,docker --bwa_index 'results/reference_genome/bwa_index/BWAIndex/' --fasta_index 'https://github.com/nf-core/test-datasets/blob/eager/reference/Mammoth/Mammoth_MT_Krause.fasta.fai'
- name: REFERENCE Run the basic pipeline with FastA reference with `fna` extension
run: |
nextflow run ${GITHUB_WORKSPACE} -profile test_tsv_fna,docker
Expand Down Expand Up @@ -107,7 +107,7 @@ jobs:
nextflow run ${GITHUB_WORKSPACE} -profile test,docker --clip_adapters_list 'https://github.com/nf-core/test-datasets/raw/eager/databases/adapters/adapter-list.txt'
- name: ADAPTER LIST Run the basic pipeline using an adapter list, skipping adapter removal
run: |
nextflow run ${GITHUB_WORKSPACE} -profile test,docker --clip_adapters_list 'https://github.com/nf-core/test-datasets/raw/eager/databases/adapters/adapter-list.txt' --skip_adapterremoval
nextflow run ${GITHUB_WORKSPACE} -profile test,docker --clip_adapters_list 'https://github.com/nf-core/test-datasets/raw/eager/databases/adapters/adapter-list.txt' --skip_adapterremoval
- name: POST_AR_FASTQ_TRIMMING Run the basic pipeline post-adapterremoval FASTQ trimming
run: |
nextflow run ${GITHUB_WORKSPACE} -profile test,docker --run_post_ar_trimming
Expand Down Expand Up @@ -141,6 +141,9 @@ jobs:
- name: BEDTOOLS Test bedtools feature annotation
run: |
nextflow run ${GITHUB_WORKSPACE} -profile test,docker --run_bedtools_coverage --anno_file 'https://github.com/nf-core/test-datasets/raw/eager/reference/Mammoth/Mammoth_MT_Krause.gff3'
- name: MAPDAMAGE2 damage calculation
run: |
nextflow run ${GITHUB_WORKSPACE} -profile test,docker --damage_calculation_tool 'mapdamage'
- name: GENOTYPING_HC Test running GATK HaplotypeCaller
run: |
nextflow run ${GITHUB_WORKSPACE} -profile test_tsv_fna,docker --run_genotyping --genotyping_tool 'hc' --gatk_hc_out_mode 'EMIT_ALL_ACTIVE_SITES' --gatk_hc_emitrefconf 'BP_RESOLUTION'
Expand Down Expand Up @@ -193,11 +196,11 @@ jobs:
nextflow run ${GITHUB_WORKSPACE} -profile test,docker --run_bam_filtering --bam_unmapped_type 'fastq' --run_metagenomic_screening --metagenomic_tool 'malt' --database "/home/runner/work/eager/eager/databases/malt/" --metagenomic_complexity_filter
- name: MALTEXTRACT Download resource files
run: |
mkdir -p databases/maltextract
for i in ncbi.tre ncbi.map; do wget https://github.com/rhuebler/HOPS/raw/0.33/Resources/"$i" -P databases/maltextract/; done
mkdir -p databases/maltextract
for i in ncbi.tre ncbi.map; do wget https://github.com/rhuebler/HOPS/raw/0.33/Resources/"$i" -P databases/maltextract/; done
- name: MALTEXTRACT Basic with MALT plus MaltExtract
run: |
nextflow run ${GITHUB_WORKSPACE} -profile test,docker --run_bam_filtering --bam_unmapped_type 'fastq' --run_metagenomic_screening --metagenomic_tool 'malt' --database "/home/runner/work/eager/eager/databases/malt" --run_maltextract --maltextract_ncbifiles "/home/runner/work/eager/eager/databases/maltextract/" --maltextract_taxon_list 'https://raw.githubusercontent.com/nf-core/test-datasets/eager/testdata/Mammoth/maltextract/MaltExtract_list.txt'
nextflow run ${GITHUB_WORKSPACE} -profile test,docker --run_bam_filtering --bam_unmapped_type 'fastq' --run_metagenomic_screening --metagenomic_tool 'malt' --database "/home/runner/work/eager/eager/databases/malt" --run_maltextract --maltextract_ncbifiles "/home/runner/work/eager/eager/databases/maltextract/" --maltextract_taxon_list 'https://raw.githubusercontent.com/nf-core/test-datasets/eager/testdata/Mammoth/maltextract/MaltExtract_list.txt'
- name: METAGENOMIC Run the basic pipeline but with unmapped reads going into Kraken
run: |
nextflow run ${GITHUB_WORKSPACE} -profile test_tsv_kraken,docker --run_bam_filtering --bam_unmapped_type 'fastq'
Expand All @@ -216,4 +219,4 @@ jobs:
nextflow run ${GITHUB_WORKSPACE} -profile test_tsv_humanbam,docker --skip_fastqc --skip_adapterremoval --skip_deduplication --skip_qualimap --skip_preseq --skip_damage_calculation --run_mtnucratio
- name: RESCALING Run basic pipeline with basic pipeline but with mapDamage rescaling of BAM files. Note this will be slow
run: |
nextflow run ${GITHUB_WORKSPACE} -profile test,docker --run_mapdamage_rescaling --run_genotyping --genotyping_tool hc --genotyping_source 'rescaled'
nextflow run ${GITHUB_WORKSPACE} -profile test,docker --run_mapdamage_rescaling --run_genotyping --genotyping_tool hc --genotyping_source 'rescaled'
19 changes: 19 additions & 0 deletions CHANGELOG.md
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Expand Up @@ -3,6 +3,25 @@
The format is based on [Keep a Changelog](http://keepachangelog.com/en/1.0.0/)
and this project adheres to [Semantic Versioning](http://semver.org/spec/v2.0.0.html).

## [2.5.0] - Bopfingen - 2023-11-03

### `Added`

- [#1020](https://github.com/nf-core/eager/issues/1020) Added mapDamage2 as an alternative for damage calculation.

### `Fixed`

- [#1017](https://github.com/nf-core/eager/issues/1017) Fixed file name collision in niche cases with multiple libraries of multiple UDG treatments.
- [#1024](https://github.com/nf-core/eager/issues/1024) `multiqc_general_stats.txt` is now generated even if the table is a beeswarm plot in the report.
- [#655](https://github.com/nf-core/eager/issues/655) Updated RG tags for all mappers. RG-id now includes Sample as well as Library ID. Added `LB:` tag with the library ID.
- [#1031](https://github.com/nf-core/eager/issues/1031) Always index fasta regardless of mapper. This ensures that DamageProfiler and genotyping processes get submitted when using bowtie2 and not providing a fasta index.

### `Dependencies`

- `multiqc`: 1.14 -> 1.16

### `Deprecated`

## [2.4.7] - 2023-05-16

### `Added`
Expand Down
4 changes: 2 additions & 2 deletions Dockerfile
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Expand Up @@ -7,7 +7,7 @@ COPY environment.yml /
RUN conda env create --quiet -f /environment.yml && conda clean -a

# Add conda installation dir to PATH (instead of doing 'conda activate')
ENV PATH /opt/conda/envs/nf-core-eager-2.4.7/bin:$PATH
ENV PATH /opt/conda/envs/nf-core-eager-2.5.0/bin:$PATH

# Dump the details of the installed packages to a file for posterity
RUN conda env export --name nf-core-eager-2.4.7 > nf-core-eager-2.4.7.yml
RUN conda env export --name nf-core-eager-2.5.0 > nf-core-eager-2.5.0.yml
15 changes: 9 additions & 6 deletions README.md
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Expand Up @@ -15,6 +15,9 @@

[![Get help on Slack](http://img.shields.io/badge/slack-nf--core%20%23eager-4A154B?logo=slack)](https://nfcore.slack.com/channels/eager)

>[!IMPORTANT]
> nf-core/eager versions 2.* are only compatible with Nextflow versions up to 22.10.6!
## Introduction

<!-- nf-core: Write a 1-2 sentence summary of what data the pipeline is for and what it does -->
Expand All @@ -28,7 +31,7 @@ The pipeline is built using [Nextflow](https://www.nextflow.io), a workflow tool

## Quick Start

1. Install [`nextflow`](https://nf-co.re/usage/installation) (`>=20.07.1`)
1. Install [`nextflow`](https://nf-co.re/usage/installation) (`>=20.07.1` && `<=22.10.6`)

2. Install any of [`Docker`](https://docs.docker.com/engine/installation/), [`Singularity`](https://www.sylabs.io/guides/3.0/user-guide/), [`Podman`](https://podman.io/), [`Shifter`](https://nersc.gitlab.io/development/shifter/how-to-use/) or [`Charliecloud`](https://hpc.github.io/charliecloud/) for full pipeline reproducibility _(please only use [`Conda`](https://conda.io/miniconda.html) as a last resort; see [docs](https://nf-co.re/usage/configuration#basic-configuration-profiles))_

Expand All @@ -52,7 +55,7 @@ The pipeline is built using [Nextflow](https://www.nextflow.io), a workflow tool
nextflow clean -f -k
```

See [usage docs](https://nf-co.re/eager/docs/usage.md) for all of the available options when running the pipeline.
See [usage docs](https://nf-co.re/eager/usage) for all of the available options when running the pipeline.

**N.B.** You can see an overview of the run in the MultiQC report located at `./results/MultiQC/multiqc_report.html`

Expand All @@ -69,7 +72,7 @@ By default the pipeline currently performs the following:
* Sequencing adapter removal, paired-end data merging (`AdapterRemoval`)
* Read mapping to reference using (`bwa aln`, `bwa mem`, `CircularMapper`, or `bowtie2`)
* Post-mapping processing, statistics and conversion to bam (`samtools`)
* Ancient DNA C-to-T damage pattern visualisation (`DamageProfiler`)
* Ancient DNA C-to-T damage pattern visualisation (`DamageProfiler` or `mapDamage`)
* PCR duplicate removal (`DeDup` or `MarkDuplicates`)
* Post-mapping statistics and BAM quality control (`Qualimap`)
* Library Complexity Estimation (`preseq`)
Expand Down Expand Up @@ -133,9 +136,9 @@ The nf-core/eager pipeline comes with documentation about the pipeline: [usage](
* [Pipeline 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](https://nf-co.re/eager/docs/usage.md)
3. [Running the pipeline](https://nf-co.re/eager/usage)
* This includes tutorials, FAQs, and troubleshooting instructions
4. [Output and how to interpret the results](https://nf-co.re/eager/docs/output.md)
4. [Output and how to interpret the results](https://nf-co.re/eager/output)

## Credits

Expand Down Expand Up @@ -246,7 +249,7 @@ In addition, references of tools and data used in this pipeline are as follows:
* **Bowtie2** Langmead, B. and Salzberg, S. L. 2012 Fast gapped-read alignment with Bowtie 2. Nature methods, 9(4), p. 357–359. doi: [10.1038/nmeth.1923](https:/dx.doi.org/10.1038/nmeth.1923).
* **sequenceTools** Stephan Schiffels (Unpublished). Download: [https://github.com/stschiff/sequenceTools](https://github.com/stschiff/sequenceTools)
* **EigenstratDatabaseTools** Thiseas C. Lamnidis (Unpublished). Download: [https://github.com/TCLamnidis/EigenStratDatabaseTools.git](https://github.com/TCLamnidis/EigenStratDatabaseTools.git)
* **mapDamage2** Jónsson, H., et al 2013. mapDamage2.0: fast approximate Bayesian estimates of ancient DNA damage parameters. Bioinformatics , 29(13), 1682–1684. [https://doi.org/10.1093/bioinformatics/btt193](https://doi.org/10.1093/bioinformatics/btt193)
* **mapDamage** Jónsson, H., et al 2013. mapDamage2.0: fast approximate Bayesian estimates of ancient DNA damage parameters. Bioinformatics , 29(13), 1682–1684. [https://doi.org/10.1093/bioinformatics/btt193](https://doi.org/10.1093/bioinformatics/btt193)
* **BBduk** Brian Bushnell (Unpublished). Download: [https://sourceforge.net/projects/bbmap/](sourceforge.net/projects/bbmap/)
## Data References
Expand Down
18 changes: 15 additions & 3 deletions assets/multiqc_config.yaml
Original file line number Diff line number Diff line change
Expand Up @@ -17,6 +17,7 @@ run_modules:
- gatk
- kraken
- malt
- mapdamage
- mtnucratio
- multivcfanalyzer
- picard
Expand Down Expand Up @@ -91,6 +92,7 @@ top_modules:
path_filters:
- "*.preseq"
- "damageprofiler"
- "mapdamage"
- "mtnucratio"
- "qualimap"
- "sexdeterrmine"
Expand Down Expand Up @@ -155,6 +157,11 @@ table_columns_visible:
3 Prime2: False
mean_readlength: True
median: True
mapDamage:
5 Prime1: True
5 Prime2: True
3 Prime1: False
3 Prime2: False
mtnucratio:
mt_nuc_ratio: True
QualiMap:
Expand Down Expand Up @@ -240,10 +247,15 @@ table_columns_placement:
3 Prime2: 730
mean_readlength: 740
median: 750
mapDamage:
5 Prime1: 760
5 Prime2: 765
3 Prime1: 770
3 Prime2: 775
mtnucratio:
mtreads: 760
mt_cov_avg: 770
mt_nuc_ratio: 780
mtreads: 780
mt_cov_avg: 785
mt_nuc_ratio: 790
QualiMap:
mapped_reads: 800
mean_coverage: 805
Expand Down
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