Skip to content
New issue

Have a question about this project? Sign up for a free GitHub account to open an issue and contact its maintainers and the community.

By clicking “Sign up for GitHub”, you agree to our terms of service and privacy statement. We’ll occasionally send you account related emails.

Already on GitHub? Sign in to your account

Uniformize metadata #23

Merged
merged 3 commits into from
Feb 12, 2024
Merged
Show file tree
Hide file tree
Changes from all commits
Commits
File filter

Filter by extension

Filter by extension

Conversations
Failed to load comments.
Loading
Jump to
Jump to file
Failed to load files.
Loading
Diff view
Diff view
2 changes: 2 additions & 0 deletions CHANGELOG.md
Original file line number Diff line number Diff line change
Expand Up @@ -23,6 +23,8 @@

## MINOR CHANGES

* Uniformize component metadata (PR #23).

## DOCUMENTATION

## BUG FIXES
12 changes: 7 additions & 5 deletions src/arriba/config.vsh.yaml
Original file line number Diff line number Diff line change
Expand Up @@ -3,11 +3,13 @@ functionality:
description: Detect gene fusions from RNA-Seq data
info:
keywords: [Gene fusion, RNA-Seq]
homepage: https://arriba.readthedocs.io/en/latest/
documentation: https://arriba.readthedocs.io/en/latest/
repository: https://github.com/suhrig/arriba
reference: "doi:10.1101/gr.257246.119"
licence: MIT
links:
homepage: https://arriba.readthedocs.io/en/latest/
documentation: https://arriba.readthedocs.io/en/latest/
repository: https://github.com/suhrig/arriba
references:
doi: 10.1101/gr.257246.119
license: MIT
requirements:
cpus: 1
commands: [ arriba ]
Expand Down
11 changes: 6 additions & 5 deletions src/bgzip/config.vsh.yaml
Original file line number Diff line number Diff line change
Expand Up @@ -2,12 +2,13 @@ functionality:
name: bgzip
description: Block compression/decompression utility
info:
homepage: https://www.htslib.org/
documentation: https://www.htslib.org/doc/bgzip.html
repository: https://github.com/samtools/htslib
licence: MIT
reference:
links:
homepage: https://www.htslib.org/
documentation: https://www.htslib.org/doc/bgzip.html
repository: https://github.com/samtools/htslib
references:
doi: 10.1093/gigascience/giab007
license: MIT
requirements:
commands: [ bgzip ]
argument_groups:
Expand Down
13 changes: 7 additions & 6 deletions src/busco/busco_download_datasets/config.vsh.yaml
Original file line number Diff line number Diff line change
Expand Up @@ -3,12 +3,13 @@ functionality:
namespace: busco
description: Downloads available busco datasets
info:
keywords: [lineage datasets]
homepage: https://busco.ezlab.org/
documentation: https://busco.ezlab.org/busco_userguide.html
repository: https://gitlab.com/ezlab/busco
reference: "10.1007/978-1-4939-9173-0_14"
licence: MIT
links:
homepage: https://busco.ezlab.org/
documentation: https://busco.ezlab.org/busco_userguide.html
repository: https://gitlab.com/ezlab/busco
references:
doi: 10.1007/978-1-4939-9173-0_14
license: MIT
argument_groups:
- name: Inputs
arguments:
Expand Down
13 changes: 7 additions & 6 deletions src/busco/busco_list_datasets/config.vsh.yaml
Original file line number Diff line number Diff line change
Expand Up @@ -3,12 +3,13 @@ functionality:
namespace: busco
description: Lists the available busco datasets
info:
keywords: [lineage datasets]
homepage: https://busco.ezlab.org/
documentation: https://busco.ezlab.org/busco_userguide.html
repository: https://gitlab.com/ezlab/busco
reference: "10.1007/978-1-4939-9173-0_14"
licence: MIT
links:
homepage: https://busco.ezlab.org/
documentation: https://busco.ezlab.org/busco_userguide.html
repository: https://gitlab.com/ezlab/busco
references:
doi: 10.1007/978-1-4939-9173-0_14
license: MIT
argument_groups:
- name: Outputs
arguments:
Expand Down
12 changes: 7 additions & 5 deletions src/busco/busco_run/config.vsh.yaml
Original file line number Diff line number Diff line change
Expand Up @@ -4,11 +4,13 @@ functionality:
description: Assessment of genome assembly and annotation completeness with single copy orthologs
info:
keywords: [Genome assembly, quality control]
homepage: https://busco.ezlab.org/
documentation: https://busco.ezlab.org/busco_userguide.html
repository: https://gitlab.com/ezlab/busco
reference: "10.1007/978-1-4939-9173-0_14"
licence: MIT
links:
homepage: https://busco.ezlab.org/
documentation: https://busco.ezlab.org/busco_userguide.html
repository: https://gitlab.com/ezlab/busco
references:
doi: 10.1007/978-1-4939-9173-0_14
license: MIT
argument_groups:
- name: Inputs
arguments:
Expand Down
10 changes: 6 additions & 4 deletions src/fastp/config.vsh.yaml
Original file line number Diff line number Diff line change
Expand Up @@ -22,10 +22,12 @@ functionality:
- support ultra-fast FASTQ-level deduplication
info:
keywords: [RNA-Seq, Trimming, Quality control]
repository: https://github.com/OpenGene/fastp
documentation: https://github.com/OpenGene/fastp/blob/master/README.md
reference: "doi:10.1093/bioinformatics/bty560"
licence: MIT
links:
repository: https://github.com/OpenGene/fastp
documentation: https://github.com/OpenGene/fastp/blob/master/README.md
references:
doi: 10.1093/bioinformatics/bty560
license: MIT
argument_groups:
- name: Inputs
description: |
Expand Down
12 changes: 7 additions & 5 deletions src/featurecounts/config.vsh.yaml
Original file line number Diff line number Diff line change
Expand Up @@ -4,11 +4,13 @@ functionality:
featureCounts is a read summarization program for counting reads generated from either RNA or genomic DNA sequencing experiments by implementing highly efficient chromosome hashing and feature blocking techniques. It works with either single or paired-end reads and provides a wide range of options appropriate for different sequencing applications.
info:
keywords: ["Read counting", "Genomic features"]
homepage: https://subread.sourceforge.net/
documentation: https://subread.sourceforge.net/SubreadUsersGuide.pdf
repository: https://github.com/ShiLab-Bioinformatics/subread
reference: "doi:10.1093/bioinformatics/btt656"
licence: GPL-3.0
links:
homepage: https://subread.sourceforge.net/
documentation: https://subread.sourceforge.net/SubreadUsersGuide.pdf
repository: https://github.com/ShiLab-Bioinformatics/subread
references:
doi: 10.1093/bioinformatics/btt656
license: GPL-3.0
requirements:
commands: [ featureCounts ]

Expand Down
12 changes: 7 additions & 5 deletions src/pear/config.vsh.yaml
Original file line number Diff line number Diff line change
Expand Up @@ -6,11 +6,13 @@ functionality:
PEAR evaluates all possible paired-end read overlaps and without requiring the target fragment size as input. In addition, it implements a statistical test for minimizing false-positive results. Together with a highly optimized implementation, it can merge millions of paired end reads within a couple of minutes on a standard desktop computer.
info:
keywords: [ "pair-end", "read", "merge" ]
homepage: https://cme.h-its.org/exelixis/web/software/pear
repository: https://github.com/tseemann/PEAR
documentation: https://cme.h-its.org/exelixis/web/software/pear/doc.html
reference: doi:10.1093/bioinformatics/btt593
licence: "CC-BY-NC-SA-3.0"
links:
homepage: https://cme.h-its.org/exelixis/web/software/pear
repository: https://github.com/tseemann/PEAR
documentation: https://cme.h-its.org/exelixis/web/software/pear/doc.html
references:
doi: 10.1093/bioinformatics/btt593
license: "CC-BY-NC-SA-3.0"
requirements:
commands: [ pear , gzip ]
argument_groups:
Expand Down
Loading