Build pipeline: viash-hub.biobox.main-lpdjj
Source commit: 766ab6c9c3
Source message: Qualimap rnaseq (#74)
* first version
* complete script for qualimap
* add escaping character before leading hashtag (#50)
* add escaping character before leading hashtag
* update changelog
* Update CHANGELOG.md
Co-authored-by: Robrecht Cannoodt <rcannood@gmail.com>
* replace escaping \ by \\
---------
Co-authored-by: Robrecht Cannoodt <rcannood@gmail.com>
* Samtools collate (#49)
* initial commit dedup
* Revert "initial commit dedup"
This reverts commit 38f586bec0ac9e4312b016e29c3aa0bd53f292b2.
* Initial commit, whole component is functional
* Update viash (#51)
* update viash
* update readme
* update changelog
* update changelog
* fix incorrect heading detection
* update again
* clean up readme
* Samtools view (#48)
* initial commit dedup
* Revert "initial commit dedup"
This reverts commit 38f586bec0ac9e4312b016e29c3aa0bd53f292b2.
* initial version with a few tests, script, and config file
* update changelog, add one test
* add a 4th test, fix option names in the script
* Fix name of component in config
* remove option named with a number
* add must_exist to input file argument
* removed "default: null" from one of the arguments in config
* remove utf8 characters from config
* Update CHANGELOG.md
---------
Co-authored-by: Robrecht Cannoodt <rcannood@gmail.com>
* Samtools fastq (#52)
* initial commit dedup
* Revert "initial commit dedup"
This reverts commit 38f586bec0ac9e4312b016e29c3aa0bd53f292b2.
* Initial commit, config, script, help and test_data
* Update changelog, add tests, fix argument naming errors, add test data
* update changelog, remove gffread namespace field
---------
Co-authored-by: Robrecht Cannoodt <rcannood@gmail.com>
* format URL in the description (#55)
* format URL in the description
* update changelog
* Change name in _viash.yaml (#60)
* Update operational code (#63)
* update readme
* switch ci to toolbox
* update to viash 0.9.0-RC6
* edit keywords
* fix version
* update biobox
* cutadapt (#7)
* First commit, clone of cutadapt in htrnaseq + help.txt
* Add config
* Don't allow multiple: true when providing a FASTA file with adapters
* First version of script
* Updates and fixes - se/pe
* Add tests and fix --json argument
* Add software version
* Better consistency in using snake_case
* Update src/cutadapt/config.vsh.yaml
Co-authored-by: Robrecht Cannoodt <rcannood@gmail.com>
* Update src/cutadapt/config.vsh.yaml
Co-authored-by: Robrecht Cannoodt <rcannood@gmail.com>
* Update src/cutadapt/config.vsh.yaml
Co-authored-by: Robrecht Cannoodt <rcannood@gmail.com>
* Specify --input and --input_r2 as separate arguments
* Avoid specifying default arg values
* Add more information to `--minimum_length` and `maximum_length`
* Add --cpus by means of $meta_cpus and set proper default
* Allow multiple for adapters/fasta and add test
* change multiple_sep to ';'
* add example
* simplify code with a helper function
* create directories in test
* use a different output extension if --fasta is provided
* decrease code duplication by separating optional outputs from paired/unpaired output arguments
* write custom tests for cutadapt
* fix _r2 arguments
* add debug flag as not to always print the cli command
* remove comment
* Update to Viash 0.9.0-RC4
* Ability to specify output globbing patterns
* Avoid the need for both output_dir and output
* Move fields from `info` to `links`
Co-authored-by: Robrecht Cannoodt <rcannood@gmail.com>
* Move references back to the info field
* apologies, I proposed a wrong syntax
---------
Co-authored-by: Robrecht Cannoodt <rcannood@gmail.com>
* update changelog
* update readme
* Update salmon quant arguments (#57)
* Make index an optional argument
* FIx argument type and add optional argument
* FEAT: add bedtools getfasta. (#59)
* FEAT: add bedtools getfasta.
* Add PR number to CHANGELOG
* Add star genomegenerate component (#58)
* Add star genomegenerate component
* Update changelog
* Rename component
* Update test
* Update CHANGELOG.md
---------
Co-authored-by: Robrecht Cannoodt <rcannood@gmail.com>
* fix package config (#65)
* Delete src/bgzip directory (#64)
It was moved to toolbox
* Output alignments to the transcriptome (#56)
* Output alignments to the transcriptome
* Change argument name
* BUG: pear component failure is ignored (#70)
* FEAT + BUG: cutadapt; allowing disabling demultiplexing and fix par_quality_cutoff_r2 (#69)
* FEAT: Disable cutadapt demultiplexing by default
* Cutadapt: fix --par_quality_cutoff_r2
* FEAT: update busco to 5.7.1 (#72)
* FEAT: update busco to 5.7.1
* Typo
* Samtools fasta (#53)
* initial commit dedup
* Revert "initial commit dedup"
This reverts commit 38f586bec0ac9e4312b016e29c3aa0bd53f292b2.
* Fasta component
* change script resource to samtools_fastq script, with dummy argument to specify the command
* add dummy argument to samtools_fastq to share the script with samtools_fasta
* fix path to script in config
* Update src/samtools/samtools_fastq/script.sh
Co-authored-by: Robrecht Cannoodt <rcannood@gmail.com>
* Change default fields to examples
* Two more default fields changed to examples
* Minor formatting changes
* Markdown formatting changes in configs
---------
Co-authored-by: Robrecht Cannoodt <rcannood@gmail.com>
* Umi tools dedup (#54)
* initial commit dedup
* Revert "initial commit dedup"
This reverts commit 38f586bec0ac9e4312b016e29c3aa0bd53f292b2.
* inital commit dedup
* Working component with one test
* Update test 1 and test data, fix some arg types in config and script
* test data files and changes to script
* Add third test and test data
* Fix typo in script
* remove utf8 characters in config
* Add choices fields and change default fields to exampels
* Minor formatting changes
* md formatting changes in config
* Fix typo (#79)
* add vscode to gitignore
* update multiple separator (#81)
* update multiple separator
* update changelog
* Update src/multiqc/config.vsh.yaml
Co-authored-by: Robrecht Cannoodt <rcannood@gmail.com>
* Update src/multiqc/config.vsh.yaml
Co-authored-by: Robrecht Cannoodt <rcannood@gmail.com>
* Update src/multiqc/config.vsh.yaml
Co-authored-by: Robrecht Cannoodt <rcannood@gmail.com>
* Update src/multiqc/config.vsh.yaml
Co-authored-by: Robrecht Cannoodt <rcannood@gmail.com>
* update ifs
---------
Co-authored-by: Robrecht Cannoodt <rcannood@gmail.com>
* add test data
* add tests
* update changelog
* remove unrequired test data
* update descriptions
* update changelog
* update help text
* Update src/qualimap/qualimap_rnaseq/script.sh
Co-authored-by: Robrecht Cannoodt <rcannood@gmail.com>
* update unit tests
* update unit tests
* addres pr changes request
* add version
* remove whitespace multiqc
* Apply suggestions from code review
Co-authored-by: Robrecht Cannoodt <rcannood@gmail.com>
* address pr comments
* Update CHANGELOG.md
* fix doi
* Fix name
* update version and container image
* write software version to file
---------
Co-authored-by: dorien-er <roosen.dorien@gmail.com>
Co-authored-by: Leila011 <leilapaquay@gmail.com>
Co-authored-by: Robrecht Cannoodt <rcannood@gmail.com>
Co-authored-by: emmarousseau <emmarou1@icloud.com>
Co-authored-by: Sai Nirmayi Yasa <92786623+sainirmayi@users.noreply.github.com>
Co-authored-by: Dries Schaumont <5946712+DriesSchaumont@users.noreply.github.com>
Co-authored-by: Dorien <41797896+dorien-er@users.noreply.github.com>
672 lines
21 KiB
YAML
672 lines
21 KiB
YAML
name: "featurecounts"
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version: "main"
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authors:
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- name: "Sai Nirmayi Yasa"
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roles:
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- "author"
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- "maintainer"
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info:
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links:
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email: "nirmayi@data-intuitive.com"
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github: "sainirmayi"
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linkedin: "sai-nirmayi-yasa"
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organizations:
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- name: "Data Intuitive"
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href: "https://www.data-intuitive.com"
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role: "Junior Bioinformatics Researcher"
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argument_groups:
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- name: "Inputs"
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arguments:
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- type: "file"
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name: "--annotation"
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alternatives:
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- "-a"
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description: "Name of an annotation file. GTF/GFF format by default. See '--format'\
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\ option for more format information.\n"
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info: null
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example:
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- "annotation.gtf"
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must_exist: true
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create_parent: true
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required: true
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direction: "input"
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multiple: false
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multiple_sep: ";"
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- type: "file"
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name: "--input"
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alternatives:
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- "-i"
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description: "A list of SAM or BAM format files separated by semi-colon (;). They\
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\ can be either name or location sorted. Location-sorted paired-end reads are\
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\ automatically sorted by read names.\n"
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info: null
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example:
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- "input_file1.bam"
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must_exist: true
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create_parent: true
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required: true
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direction: "input"
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multiple: true
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multiple_sep: ";"
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- name: "Outputs"
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arguments:
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- type: "file"
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name: "--counts"
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alternatives:
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- "-o"
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description: "Name of output file including read counts in tab delimited format.\n"
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info: null
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example:
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- "features.tsv"
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must_exist: true
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create_parent: true
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required: true
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direction: "output"
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multiple: false
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multiple_sep: ";"
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- type: "file"
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name: "--summary"
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description: "Summary statistics of counting results in tab delimited format.\n"
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info: null
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example:
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- "summary.tsv"
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must_exist: true
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create_parent: true
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required: false
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direction: "output"
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multiple: false
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multiple_sep: ";"
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- type: "file"
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name: "--junctions"
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description: "Count number of reads supporting each exon-exon junction. Junctions\
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\ were identified from those exon-spanning reads in the input (containing 'N'\
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\ in CIGAR string).\n"
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info: null
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example:
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- "junctions.txt"
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must_exist: true
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create_parent: true
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required: false
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direction: "output"
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multiple: false
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multiple_sep: ";"
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- name: "Annotation"
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arguments:
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- type: "string"
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name: "--format"
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alternatives:
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- "-F"
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description: "Specify format of the provided annotation file. Acceptable formats\
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\ include 'GTF' (or compatible GFF format) and 'SAF'. 'GTF' by default. \n"
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info: null
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example:
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- "GTF"
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required: false
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choices:
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- "GTF"
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- "GFF"
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- "SAF"
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direction: "input"
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multiple: false
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multiple_sep: ";"
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- type: "string"
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name: "--feature_type"
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alternatives:
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- "-t"
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description: "Specify feature type(s) in a GTF annotation. If multiple types are\
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\ provided, they should be separated by ';' with no space in between. 'exon'\
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\ by default. Rows in the annotation with a matched feature will be extracted\
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\ and used for read mapping.\n"
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info: null
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example:
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- "exon"
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required: false
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direction: "input"
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multiple: true
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multiple_sep: ";"
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- type: "string"
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name: "--attribute_type"
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alternatives:
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- "-g"
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description: "Specify attribute type in GTF annotation. 'gene_id' by default.\
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\ Meta-features used for read counting will be extracted from annotation using\
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\ the provided value.\n"
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info: null
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example:
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- "gene_id"
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required: false
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direction: "input"
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multiple: false
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multiple_sep: ";"
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- type: "string"
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name: "--extra_attributes"
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description: "Extract extra attribute types from the provided GTF annotation and\
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\ include them in the counting output. These attribute types will not be used\
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\ to group features. If more than one attribute type is provided they should\
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\ be separated by semicolon (;).\n"
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info: null
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required: false
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direction: "input"
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multiple: true
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multiple_sep: ";"
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- type: "file"
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name: "--chrom_alias"
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alternatives:
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- "-A"
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description: "Provide a chromosome name alias file to match chr names in annotation\
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\ with those in the reads. This should be a two-column comma-delimited text\
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\ file. Its first column should include chr names in the annotation and its\
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\ second column should include chr names in the reads. Chr names are case sensitive.\
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\ No column header should be included in the file.\n"
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info: null
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example:
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- "chrom_alias.csv"
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must_exist: true
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create_parent: true
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required: false
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direction: "input"
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multiple: false
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multiple_sep: ";"
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- name: "Level of summarization"
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arguments:
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- type: "boolean_true"
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name: "--feature_level"
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alternatives:
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- "-f"
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description: "Perform read counting at feature level (eg. counting reads for exons\
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\ rather than genes).\n"
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info: null
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direction: "input"
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- name: "Overlap between reads and features"
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arguments:
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- type: "boolean_true"
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name: "--overlapping"
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alternatives:
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- "-O"
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description: "Assign reads to all their overlapping meta-features (or features\
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\ if '--feature_level' is specified).\n"
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info: null
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direction: "input"
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- type: "integer"
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name: "--min_overlap"
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description: "Minimum number of overlapping bases in a read that is required for\
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\ read assignment. 1 by default. Number of overlapping bases is counted from\
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\ both reads if paired end. If a negative value is provided, then a gap of up\
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\ to specified size will be allowed between read and the feature that the read\
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\ is assigned to.\n"
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info: null
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example:
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- 1
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required: false
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direction: "input"
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multiple: false
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multiple_sep: ";"
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- type: "double"
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name: "--frac_overlap"
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description: "Minimum fraction of overlapping bases in a read that is required\
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\ for read assignment. Value should be within range [0,1]. 0 by default. Number\
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\ of overlapping bases is counted from both reads if paired end. Both this option\
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\ and '--min_overlap' option need to be satisfied for read assignment.\n"
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info: null
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example:
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- 0.0
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required: false
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min: 0.0
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max: 1.0
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direction: "input"
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multiple: false
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multiple_sep: ";"
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- type: "double"
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name: "--frac_overlap_feature"
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description: "Minimum fraction of overlapping bases in a feature that is required\
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\ for read assignment. Value should be within range [0,1]. 0 by default.\n"
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info: null
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example:
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- 0.0
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required: false
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min: 0.0
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max: 1.0
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direction: "input"
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multiple: false
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multiple_sep: ";"
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- type: "boolean_true"
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name: "--largest_overlap"
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description: "Assign reads to a meta-feature/feature that has the largest number\
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\ of overlapping bases.\n"
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info: null
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direction: "input"
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- type: "integer"
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name: "--non_overlap"
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description: "Maximum number of non-overlapping bases in a read (or a read pair)\
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\ that is allowed when being assigned to a feature. No limit is set by default.\n"
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info: null
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required: false
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direction: "input"
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multiple: false
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multiple_sep: ";"
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- type: "integer"
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name: "--non_overlap_feature"
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description: "Maximum number of non-overlapping bases in a feature that is allowed\
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\ in read assignment. No limit is set by default.\n"
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info: null
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required: false
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direction: "input"
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multiple: false
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multiple_sep: ";"
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- type: "integer"
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name: "--read_extension5"
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description: "Reads are extended upstream by <int> bases from their 5' end.\n"
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info: null
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required: false
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direction: "input"
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multiple: false
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multiple_sep: ";"
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- type: "integer"
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name: "--read_extension3"
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description: "Reads are extended upstream by <int> bases from their 3' end.\n"
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info: null
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required: false
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direction: "input"
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multiple: false
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multiple_sep: ";"
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- type: "integer"
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name: "--read2pos"
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description: "Reduce reads to their 5' most base or 3' most base. Read counting\
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\ is then performed based on the single base the read is reduced to.\n"
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info: null
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required: false
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choices:
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- 3
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- 5
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direction: "input"
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multiple: false
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multiple_sep: ";"
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- name: "Multi-mapping reads"
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arguments:
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- type: "boolean_true"
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name: "--multi_mapping"
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alternatives:
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- "-M"
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description: "Multi-mapping reads will also be counted. For a multi-mapping read,\
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\ all its reported alignments will be counted. The 'NH' tag in BAM/SAM input\
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\ is used to detect multi-mapping reads.\n"
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info: null
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direction: "input"
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- name: "Fractional counting"
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arguments:
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- type: "boolean_true"
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name: "--fraction"
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description: "Assign fractional counts to features. This option must be used together\
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\ with '--multi_mapping' or '--overlapping' or both. When '--multi_mapping'\
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\ is specified, each reported alignment from a multi-mapping read (identified\
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\ via 'NH' tag) will carry a fractional count of 1/x, instead of 1 (one), where\
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\ x is the total number of alignments reported for the same read. When '--overlapping'\
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\ is specified, each overlapping feature will receive a fractional count of\
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\ 1/y, where y is the total number of features overlapping with the read. When\
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\ both '--multi_mapping' and '--overlapping' are specified, each alignment will\
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\ carry a fractional count of 1/(x*y).\n"
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info: null
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direction: "input"
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- name: "Read filtering"
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arguments:
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- type: "integer"
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name: "--min_map_quality"
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alternatives:
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- "-Q"
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description: "The minimum mapping quality score a read must satisfy in order to\
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\ be counted. For paired-end reads, at least one end should satisfy this criteria.\
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\ 0 by default.\n"
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info: null
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example:
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- 0
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required: false
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direction: "input"
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multiple: false
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multiple_sep: ";"
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- type: "boolean_true"
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name: "--split_only"
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description: "Count split alignments only (ie. alignments with CIGAR string containing\
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\ 'N'). An example of split alignments is exon-spanning reads in RNA-seq data.\n"
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info: null
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direction: "input"
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- type: "boolean_true"
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name: "--non_split_only"
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description: "If specified, only non-split alignments (CIGAR strings do not contain\
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\ letter 'N') will be counted. All the other alignments will be ignored.\n"
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info: null
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direction: "input"
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- type: "boolean_true"
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name: "--primary"
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description: "Count primary alignments only. Primary alignments are identified\
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\ using bit 0x100 in SAM/BAM FLAG field.\n"
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info: null
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direction: "input"
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- type: "boolean_true"
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name: "--ignore_dup"
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description: "Ignore duplicate reads in read counting. Duplicate reads are identified\
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\ using bit Ox400 in BAM/SAM FLAG field. The whole read pair is ignored if one\
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\ of the reads is a duplicate read for paired end data.\n"
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info: null
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direction: "input"
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- name: "Strandedness"
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arguments:
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- type: "integer"
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name: "--strand"
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alternatives:
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- "-s"
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description: "Perform strand-specific read counting. A single integer value (applied\
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\ to all input files) should be provided. Possible values include: 0 (unstranded),\
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\ 1 (stranded) and 2 (reversely stranded). Default value is 0 (ie. unstranded\
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\ read counting carried out for all input files).\n"
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info: null
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example:
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- 0
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required: false
|
|
choices:
|
|
- 0
|
|
- 1
|
|
- 2
|
|
direction: "input"
|
|
multiple: false
|
|
multiple_sep: ";"
|
|
- name: "Exon-exon junctions"
|
|
arguments:
|
|
- type: "file"
|
|
name: "--ref_fasta"
|
|
alternatives:
|
|
- "-G"
|
|
description: "Provide the name of a FASTA-format file that contains the reference\
|
|
\ sequences used in read mapping that produced the provided SAM/BAM files.\n"
|
|
info: null
|
|
example:
|
|
- "reference.fasta"
|
|
must_exist: true
|
|
create_parent: true
|
|
required: false
|
|
direction: "input"
|
|
multiple: false
|
|
multiple_sep: ";"
|
|
- name: "Parameters specific to paired end reads"
|
|
arguments:
|
|
- type: "boolean_true"
|
|
name: "--paired"
|
|
alternatives:
|
|
- "-p"
|
|
description: "Specify that input data contain paired-end reads. To perform fragment\
|
|
\ counting (ie. counting read pairs), the '--countReadPairs' parameter should\
|
|
\ also be specified in addition to this parameter.\n"
|
|
info: null
|
|
direction: "input"
|
|
- type: "boolean_true"
|
|
name: "--count_read_pairs"
|
|
description: "Count read pairs (fragments) instead of reads. This option is only\
|
|
\ applicable for paired-end reads.\n"
|
|
info: null
|
|
direction: "input"
|
|
- type: "boolean_true"
|
|
name: "--both_aligned"
|
|
alternatives:
|
|
- "-B"
|
|
description: "Count read pairs (fragments) instead of reads. This option is only\
|
|
\ applicable for paired-end reads.\n"
|
|
info: null
|
|
direction: "input"
|
|
- type: "boolean_true"
|
|
name: "--check_pe_dist"
|
|
alternatives:
|
|
- "-P"
|
|
description: "Check validity of paired-end distance when counting read pairs.\
|
|
\ Use '--min_length' and '--max_length' to set thresholds.\n"
|
|
info: null
|
|
direction: "input"
|
|
- type: "integer"
|
|
name: "--min_length"
|
|
alternatives:
|
|
- "-d"
|
|
description: "Minimum fragment/template length, 50 by default.\n"
|
|
info: null
|
|
example:
|
|
- 50
|
|
required: false
|
|
direction: "input"
|
|
multiple: false
|
|
multiple_sep: ";"
|
|
- type: "integer"
|
|
name: "--max_length"
|
|
alternatives:
|
|
- "-D"
|
|
description: "Maximum fragment/template length, 600 by default.\n"
|
|
info: null
|
|
example:
|
|
- 600
|
|
required: false
|
|
direction: "input"
|
|
multiple: false
|
|
multiple_sep: ";"
|
|
- type: "boolean_true"
|
|
name: "--same_strand"
|
|
alternatives:
|
|
- "-C"
|
|
description: "Do not count read pairs that have their two ends mapping to different\
|
|
\ chromosomes or mapping to same chromosome but on different strands.\n"
|
|
info: null
|
|
direction: "input"
|
|
- type: "boolean_true"
|
|
name: "--donotsort"
|
|
description: "Do not sort reads in BAM/SAM input. Note that reads from the same\
|
|
\ pair are required to be located next to each other in the input.\n"
|
|
info: null
|
|
direction: "input"
|
|
- name: "Read groups"
|
|
arguments:
|
|
- type: "boolean_true"
|
|
name: "--by_read_group"
|
|
description: "Assign reads by read group. \"RG\" tag is required to be present\
|
|
\ in the input BAM/SAM files.\n"
|
|
info: null
|
|
direction: "input"
|
|
- name: "Long reads"
|
|
arguments:
|
|
- type: "boolean_true"
|
|
name: "--long_reads"
|
|
description: "Count long reads such as Nanopore and PacBio reads. Long read counting\
|
|
\ can only run in one thread and only reads (not read-pairs) can be counted.\
|
|
\ There is no limitation on the number of 'M' operations allowed in a CIGAR\
|
|
\ string in long read counting.\n"
|
|
info: null
|
|
direction: "input"
|
|
- name: "Assignment results for each read"
|
|
arguments:
|
|
- type: "file"
|
|
name: "--detailed_results"
|
|
description: "Directory to save the detailed assignment results. Use `--detailed_results_format`\
|
|
\ to determine the format of the detailed results.\n"
|
|
info: null
|
|
example:
|
|
- "detailed_results"
|
|
must_exist: true
|
|
create_parent: true
|
|
required: false
|
|
direction: "output"
|
|
multiple: false
|
|
multiple_sep: ";"
|
|
- type: "string"
|
|
name: "--detailed_results_format"
|
|
alternatives:
|
|
- "-R"
|
|
description: "Output detailed assignment results for each read or read-pair. Results\
|
|
\ are saved to a file that is in one of the following formats: CORE, SAM and\
|
|
\ BAM. See documentaiton for more info about these formats.\n"
|
|
info: null
|
|
required: false
|
|
choices:
|
|
- "CORE"
|
|
- "SAM"
|
|
- "BAM"
|
|
direction: "input"
|
|
multiple: false
|
|
multiple_sep: ";"
|
|
- name: "Miscellaneous"
|
|
arguments:
|
|
- type: "integer"
|
|
name: "--max_M_op"
|
|
description: "Maximum number of 'M' operations allowed in a CIGAR string. 10 by\
|
|
\ default. Both 'X' and '=' are treated as 'M' and adjacent 'M' operations are\
|
|
\ merged in the CIGAR string.\n"
|
|
info: null
|
|
example:
|
|
- 10
|
|
required: false
|
|
direction: "input"
|
|
multiple: false
|
|
multiple_sep: ";"
|
|
- type: "boolean_true"
|
|
name: "--verbose"
|
|
description: "Output verbose information for debugging, such as un-matched chromosome/contig\
|
|
\ names.\n"
|
|
info: null
|
|
direction: "input"
|
|
resources:
|
|
- type: "bash_script"
|
|
path: "script.sh"
|
|
is_executable: true
|
|
description: "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.\n"
|
|
test_resources:
|
|
- type: "bash_script"
|
|
path: "test.sh"
|
|
is_executable: true
|
|
- type: "file"
|
|
path: "test_data"
|
|
info: null
|
|
status: "enabled"
|
|
requirements:
|
|
commands:
|
|
- "ps"
|
|
keywords:
|
|
- "Read counting"
|
|
- "Genomic features"
|
|
license: "GPL-3.0"
|
|
references:
|
|
doi:
|
|
- "10.1093/bioinformatics/btt656"
|
|
links:
|
|
repository: "https://github.com/ShiLab-Bioinformatics/subread"
|
|
homepage: "https://subread.sourceforge.net/"
|
|
documentation: "https://subread.sourceforge.net/SubreadUsersGuide.pdf"
|
|
runners:
|
|
- type: "executable"
|
|
id: "executable"
|
|
docker_setup_strategy: "ifneedbepullelsecachedbuild"
|
|
- type: "nextflow"
|
|
id: "nextflow"
|
|
directives:
|
|
tag: "$id"
|
|
auto:
|
|
simplifyInput: true
|
|
simplifyOutput: false
|
|
transcript: false
|
|
publish: false
|
|
config:
|
|
labels:
|
|
mem1gb: "memory = 1000000000.B"
|
|
mem2gb: "memory = 2000000000.B"
|
|
mem5gb: "memory = 5000000000.B"
|
|
mem10gb: "memory = 10000000000.B"
|
|
mem20gb: "memory = 20000000000.B"
|
|
mem50gb: "memory = 50000000000.B"
|
|
mem100gb: "memory = 100000000000.B"
|
|
mem200gb: "memory = 200000000000.B"
|
|
mem500gb: "memory = 500000000000.B"
|
|
mem1tb: "memory = 1000000000000.B"
|
|
mem2tb: "memory = 2000000000000.B"
|
|
mem5tb: "memory = 5000000000000.B"
|
|
mem10tb: "memory = 10000000000000.B"
|
|
mem20tb: "memory = 20000000000000.B"
|
|
mem50tb: "memory = 50000000000000.B"
|
|
mem100tb: "memory = 100000000000000.B"
|
|
mem200tb: "memory = 200000000000000.B"
|
|
mem500tb: "memory = 500000000000000.B"
|
|
mem1gib: "memory = 1073741824.B"
|
|
mem2gib: "memory = 2147483648.B"
|
|
mem4gib: "memory = 4294967296.B"
|
|
mem8gib: "memory = 8589934592.B"
|
|
mem16gib: "memory = 17179869184.B"
|
|
mem32gib: "memory = 34359738368.B"
|
|
mem64gib: "memory = 68719476736.B"
|
|
mem128gib: "memory = 137438953472.B"
|
|
mem256gib: "memory = 274877906944.B"
|
|
mem512gib: "memory = 549755813888.B"
|
|
mem1tib: "memory = 1099511627776.B"
|
|
mem2tib: "memory = 2199023255552.B"
|
|
mem4tib: "memory = 4398046511104.B"
|
|
mem8tib: "memory = 8796093022208.B"
|
|
mem16tib: "memory = 17592186044416.B"
|
|
mem32tib: "memory = 35184372088832.B"
|
|
mem64tib: "memory = 70368744177664.B"
|
|
mem128tib: "memory = 140737488355328.B"
|
|
mem256tib: "memory = 281474976710656.B"
|
|
mem512tib: "memory = 562949953421312.B"
|
|
cpu1: "cpus = 1"
|
|
cpu2: "cpus = 2"
|
|
cpu5: "cpus = 5"
|
|
cpu10: "cpus = 10"
|
|
cpu20: "cpus = 20"
|
|
cpu50: "cpus = 50"
|
|
cpu100: "cpus = 100"
|
|
cpu200: "cpus = 200"
|
|
cpu500: "cpus = 500"
|
|
cpu1000: "cpus = 1000"
|
|
debug: false
|
|
container: "docker"
|
|
engines:
|
|
- type: "docker"
|
|
id: "docker"
|
|
image: "quay.io/biocontainers/subread:2.0.6--he4a0461_0"
|
|
target_registry: "images.viash-hub.com"
|
|
target_tag: "main"
|
|
namespace_separator: "/"
|
|
setup:
|
|
- type: "docker"
|
|
run:
|
|
- "featureCounts -v 2>&1 | sed 's/featureCounts v\\([0-9.]*\\)/featureCounts:\
|
|
\ \\1/' > /var/software_versions.txt\n"
|
|
entrypoint: []
|
|
cmd: null
|
|
- type: "native"
|
|
id: "native"
|
|
build_info:
|
|
config: "src/featurecounts/config.vsh.yaml"
|
|
runner: "executable"
|
|
engine: "docker|native"
|
|
output: "target/executable/featurecounts"
|
|
executable: "target/executable/featurecounts/featurecounts"
|
|
viash_version: "0.9.0-RC6"
|
|
git_commit: "766ab6c9c3059004c7c3f205621909b2d8b0b26d"
|
|
git_remote: "https://github.com/viash-hub/biobox"
|
|
package_config:
|
|
name: "biobox"
|
|
version: "main"
|
|
description: "A collection of bioinformatics tools for working with sequence data.\n"
|
|
info: null
|
|
viash_version: "0.9.0-RC6"
|
|
source: "src"
|
|
target: "target"
|
|
config_mods:
|
|
- ".requirements.commands := ['ps']\n"
|
|
- ".engines += { type: \"native\" }"
|
|
- ".engines[.type == 'docker'].target_registry := 'images.viash-hub.com'"
|
|
- ".engines[.type == 'docker'].target_tag := 'main'"
|
|
keywords:
|
|
- "bioinformatics"
|
|
- "modules"
|
|
- "sequencing"
|
|
license: "MIT"
|
|
organization: "vsh"
|
|
links:
|
|
repository: "https://github.com/viash-hub/biobox"
|
|
issue_tracker: "https://github.com/viash-hub/biobox/issues"
|