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>
638 lines
20 KiB
YAML
638 lines
20 KiB
YAML
name: "umi_tools_dedup"
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namespace: "umi_tools"
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version: "main"
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authors:
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- name: "Emma Rousseau"
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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: "emma@data-intuitive.com"
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github: "emmarousseau"
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linkedin: "emmarousseau1"
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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: "Bioinformatician"
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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: "--input"
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alternatives:
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- "--stdin"
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description: "Input BAM or SAM file. Use --in_sam to specify SAM format."
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info: null
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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: "boolean_true"
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name: "--in_sam"
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description: "By default, inputs are assumed to be in BAM format. Use this options\
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\ to specify the use of SAM\nformat for input.\n"
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info: null
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direction: "input"
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- type: "file"
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name: "--bai"
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description: "BAM index"
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info: null
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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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- type: "integer"
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name: "--random_seed"
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description: "Random seed to initialize number generator with."
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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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- name: "Outputs"
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arguments:
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- type: "file"
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name: "--output"
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alternatives:
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- "--stdout"
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description: "Deduplicated BAM file."
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info: null
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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: "boolean_true"
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name: "--out_sam"
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description: "By default, outputa are written in BAM format. Use this options\
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\ to specify the use of SAM format\nfor output.\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: "--paired"
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description: "BAM is paired end - output both read pairs. This will also force\
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\ the use of the template length\nto determine reads with the same mapping coordinates.\n"
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info: null
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direction: "input"
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- type: "string"
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name: "--output_stats"
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description: "Generate files containing UMI based deduplication statistics files\
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\ with this prefix in the file names.\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: "string"
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name: "--extract_umi_method"
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description: "Specify the method by which the barcodes were encoded in the read.\n\
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The options are:\n * read_id (default) \n * tag\n * umis\n"
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info: null
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example:
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- "read_id"
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required: false
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choices:
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- "read_id"
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- "tag"
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- "umis"
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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: "--umi_tag"
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description: "The tag containing the UMI sequence. This is only required if the\
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\ extract_umi_method is set to tag.\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: "string"
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name: "--umi_separator"
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description: "The separator used to separate the UMI from the read sequence. This\
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\ is only required if the\nextract_umi_method is set to id_read. Default: `_`.\n"
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info: null
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example:
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- "_"
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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: "--umi_tag_split"
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description: "Separate the UMI in tag by <SPLIT> and take the first element."
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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: "string"
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name: "--umi_tag_delimiter"
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description: "Separate the UMI in by <DELIMITER> and concatenate the elements."
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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: "string"
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name: "--cell_tag"
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description: "The tag containing the cell barcode sequence. This is only required\
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\ if the extract_umi_method\nis set to tag.\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: "string"
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name: "--cell_tag_split"
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description: "Separate the cell barcode in tag by <SPLIT> and take the first element."
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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: "string"
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name: "--cell_tag_delimiter"
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description: "Separate the cell barcode in by <DELIMITER> and concatenate the\
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\ elements."
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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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- name: "Grouping Options"
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arguments:
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- type: "string"
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name: "--method"
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description: "The method to use for grouping reads. \nThe options are: \n * unique\n\
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\ * percentile\n * cluster\n * adjacency\n * directional (default)\n"
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info: null
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example:
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- "directional"
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required: false
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choices:
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- "unique"
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- "percentile"
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- "cluster"
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- "adjacency"
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- "directional"
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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: "--edit_distance_threshold"
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description: "For the adjacency and cluster methods the threshold for the edit\
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\ distance to connect two\nUMIs in the network can be increased. The default\
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\ value of 1 works best unless the UMI is\nvery long (>14bp). Default: `1`.\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: "boolean_true"
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name: "--spliced_is_unique"
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description: "Causes two reads that start in the same position on the same strand\
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\ and having the same UMI\nto be considered unique if one is spliced and the\
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\ other is not. (Uses the 'N' cigar operation\nto test for splicing).\n"
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info: null
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direction: "input"
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- type: "integer"
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name: "--soft_clip_threshold"
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description: "Mappers that soft clip will sometimes do so rather than mapping\
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\ a spliced read if there is only\na small overhang over the exon junction.\
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\ By setting this option, you can treat reads with at\nleast this many bases\
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\ soft-clipped at the 3' end as spliced. Default: `4`.\n"
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info: null
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example:
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- 4
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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: "--multimapping_detection_method"
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description: "If the sam/bam contains tags to identify multimapping reads, you\
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\ can specify for use when selecting\nthe best read at a given loci. Supported\
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\ tags are `NH`, `X0` and `XT`. If not specified, the read\nwith the highest\
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\ mapping quality will be selected.\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: "boolean_true"
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name: "--read_length"
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description: "Use the read length as a criteria when deduping, for e.g. sRNA-Seq."
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info: null
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direction: "input"
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- name: "Single-cell RNA-Seq Options"
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arguments:
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- type: "boolean_true"
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name: "--per_gene"
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description: "Reads will be grouped together if they have the same gene. This\
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\ is useful if your library prep\ngenerates PCR duplicates with non identical\
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\ alignment positions such as CEL-Seq. Note this option\nis hardcoded to be\
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\ on with the count command. I.e. counting is always performed per-gene. Must\
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\ be\ncombined with either --gene_tag or --per_contig option.\n"
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info: null
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direction: "input"
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- type: "string"
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name: "--gene_tag"
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description: "Deduplicate per gene. The gene information is encoded in the bam\
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\ read tag specified.\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: "string"
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name: "--assigned_status_tag"
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description: "BAM tag which describes whether a read is assigned to a gene. Defaults\
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\ to the same value as given\nfor --gene_tag.\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: "string"
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name: "--skip_tags_regex"
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description: "Use in conjunction with the --assigned_status_tag option to skip\
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\ any reads where the tag matches\nthis regex. Default (\"^[__|Unassigned]\"\
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) matches anything which starts with \"__\" or \"Unassigned\".\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: "boolean_true"
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name: "--per_contig"
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description: "Deduplicate per contig (field 3 in BAM; RNAME). All reads with the\
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\ sam contig will be considered to\nhave the same alignment position. This is\
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\ useful if you have aligned to a reference transcriptome\nwith one transcript\
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\ per gene. If you have aligned to a transcriptome with more than one transcript\n\
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per gene, you can supply a map between transcripts and gene using the --gene_transcript_map\
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\ option.\n"
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info: null
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direction: "input"
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- type: "file"
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name: "--gene_transcript_map"
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description: "A file containing a mapping between gene names and transcript names.\
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\ The file should be tab\nseparated with the gene name in the first column and\
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\ the transcript name in the second column.\n"
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info: null
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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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- type: "boolean_true"
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name: "--per_cell"
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description: "Reads will only be grouped together if they have the same cell barcode.\
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\ Can be combined with\n--per_gene.\n"
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info: null
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direction: "input"
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- name: "SAM/BAM Options"
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arguments:
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- type: "integer"
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name: "--mapping_quality"
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description: "Minimium mapping quality (MAPQ) for a read to be retained. Default:\
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\ `0`.\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: "string"
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name: "--unmapped_reads"
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description: "How unmapped reads should be handled. \nThe options are:\n * \"\
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discard\": Discard all unmapped reads. (default)\n * \"use\": If read2\
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\ is unmapped, deduplicate using read1 only. Requires --paired.\n * \"output\"\
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: Output unmapped reads/read pairs without UMI grouping/deduplication. Only\
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\ available in umi_tools group.\n"
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info: null
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example:
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- "discard"
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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: "--chimeric_pairs"
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description: "How chimeric pairs should be handled. \nThe options are:\n * \"\
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discard\": Discard all chimeric read pairs.\n * \"use\": Deduplicate using\
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\ read1 only. (default)\n * \"output\": Output chimeric pairs without UMI\
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\ grouping/deduplication. Only available in\n umi_tools group.\n"
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info: null
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example:
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- "use"
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required: false
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choices:
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- "discard"
|
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- "use"
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- "output"
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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: "--unpaired_reads"
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description: "How unpaired reads should be handled. \nThe options are: \n * \"\
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discard\": Discard all unmapped reads.\n * \"use\": If read2 is unmapped, deduplicate\
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\ using read1 only. Requires --paired. (default)\n * \"output\": Output unmapped\
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\ reads/read pairs without UMI grouping/deduplication. Only available\n \
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|
\ in umi_tools group.\n"
|
|
info: null
|
|
example:
|
|
- "use"
|
|
required: false
|
|
choices:
|
|
- "discard"
|
|
- "use"
|
|
- "output"
|
|
direction: "input"
|
|
multiple: false
|
|
multiple_sep: ";"
|
|
- type: "boolean_true"
|
|
name: "--ignore_umi"
|
|
description: "Ignore the UMI and group reads using mapping coordinates only."
|
|
info: null
|
|
direction: "input"
|
|
- type: "double"
|
|
name: "--subset"
|
|
description: "Only consider a fraction of the reads, chosen at random. This is\
|
|
\ useful for doing saturation\nanalyses.\n"
|
|
info: null
|
|
required: false
|
|
direction: "input"
|
|
multiple: false
|
|
multiple_sep: ";"
|
|
- type: "string"
|
|
name: "--chrom"
|
|
description: "Only consider a single chromosome. This is useful for debugging/testing\
|
|
\ purposes."
|
|
info: null
|
|
required: false
|
|
direction: "input"
|
|
multiple: false
|
|
multiple_sep: ";"
|
|
- name: "Group/Dedup Options"
|
|
arguments:
|
|
- type: "boolean_true"
|
|
name: "--no_sort_output"
|
|
description: "By default, output is sorted. This involves the use of a temporary\
|
|
\ unsorted file (saved in\n--temp_dir). Use this option to turn off sorting.\n"
|
|
info: null
|
|
direction: "input"
|
|
- type: "boolean_true"
|
|
name: "--buffer_whole_contig"
|
|
description: "Forces dedup to parse an entire contig before yielding any reads\
|
|
\ for deduplication. This is the\nonly way to absolutely guarantee that all\
|
|
\ reads with the same start position are grouped together\nfor deduplication\
|
|
\ since dedup uses the start position of the read, not the alignment coordinate\
|
|
\ on\nwhich the reads are sorted. However, by default, dedup reads for another\
|
|
\ 1000bp before outputting\nread groups which will avoid any reads being missed\
|
|
\ with short read sequencing (<1000bp).\n"
|
|
info: null
|
|
direction: "input"
|
|
- name: "Common Options"
|
|
arguments:
|
|
- type: "file"
|
|
name: "--log"
|
|
alternatives:
|
|
- "-L"
|
|
description: "File with logging information."
|
|
info: null
|
|
must_exist: true
|
|
create_parent: true
|
|
required: false
|
|
direction: "input"
|
|
multiple: false
|
|
multiple_sep: ";"
|
|
- type: "boolean_true"
|
|
name: "--log2stderr"
|
|
description: "Send logging information to stderr."
|
|
info: null
|
|
direction: "input"
|
|
- type: "integer"
|
|
name: "--verbose"
|
|
alternatives:
|
|
- "-v"
|
|
description: "Log level. The higher, the more output. Default: `0`.\n"
|
|
info: null
|
|
example:
|
|
- 0
|
|
required: false
|
|
direction: "input"
|
|
multiple: false
|
|
multiple_sep: ";"
|
|
- type: "file"
|
|
name: "--error"
|
|
alternatives:
|
|
- "-E"
|
|
description: "File with error information."
|
|
info: null
|
|
must_exist: true
|
|
create_parent: true
|
|
required: false
|
|
direction: "input"
|
|
multiple: false
|
|
multiple_sep: ";"
|
|
- type: "string"
|
|
name: "--temp_dir"
|
|
description: "Directory for temporary files. If not set, the bash environmental\
|
|
\ variable TMPDIR is used.\n"
|
|
info: null
|
|
required: false
|
|
direction: "input"
|
|
multiple: false
|
|
multiple_sep: ";"
|
|
- type: "integer"
|
|
name: "--compresslevel"
|
|
description: "Level of Gzip compression to use. Default=6 matches GNU gzip rather\
|
|
\ than python gzip default.\nDefault: `6`.\n"
|
|
info: null
|
|
example:
|
|
- 6
|
|
required: false
|
|
direction: "input"
|
|
multiple: false
|
|
multiple_sep: ";"
|
|
- type: "file"
|
|
name: "--timeit"
|
|
description: "Store timing information in file."
|
|
info: null
|
|
must_exist: true
|
|
create_parent: true
|
|
required: false
|
|
direction: "input"
|
|
multiple: false
|
|
multiple_sep: ";"
|
|
- type: "string"
|
|
name: "--timeit_name"
|
|
description: "Name in timing file for this class of jobs. Default: `all`.\n"
|
|
info: null
|
|
example:
|
|
- "all"
|
|
required: false
|
|
direction: "input"
|
|
multiple: false
|
|
multiple_sep: ";"
|
|
- type: "string"
|
|
name: "--timeit_header"
|
|
description: "Add header for timing information."
|
|
info: null
|
|
required: false
|
|
direction: "input"
|
|
multiple: false
|
|
multiple_sep: ";"
|
|
resources:
|
|
- type: "bash_script"
|
|
path: "script.sh"
|
|
is_executable: true
|
|
description: "Deduplicate reads based on the mapping co-ordinate and the UMI attached\
|
|
\ to the read.\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:
|
|
- "umi_tools"
|
|
- "deduplication"
|
|
- "dedup"
|
|
license: "MIT"
|
|
references:
|
|
doi:
|
|
- "10.1101/gr.209601.116"
|
|
links:
|
|
repository: "https://github.com/CGATOxford/UMI-tools"
|
|
homepage: "https://umi-tools.readthedocs.io/en/latest/"
|
|
documentation: "https://umi-tools.readthedocs.io/en/latest/reference/dedup.html"
|
|
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/umi_tools:1.1.5--py39hf95cd2a_1"
|
|
target_registry: "images.viash-hub.com"
|
|
target_tag: "main"
|
|
namespace_separator: "/"
|
|
setup:
|
|
- type: "docker"
|
|
run:
|
|
- "umi_tools -v | sed 's/ version//g' > /var/software_versions.txt\n"
|
|
entrypoint: []
|
|
cmd: null
|
|
- type: "native"
|
|
id: "native"
|
|
build_info:
|
|
config: "src/umi_tools/umi_tools_dedup/config.vsh.yaml"
|
|
runner: "executable"
|
|
engine: "docker|native"
|
|
output: "target/executable/umi_tools/umi_tools_dedup"
|
|
executable: "target/executable/umi_tools/umi_tools_dedup/umi_tools_dedup"
|
|
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"
|