Files
biobox/target/executable/umi_tools/umi_tools_dedup/.config.vsh.yaml
CI b17c19f92e Build branch main with version main (766ab6c)
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>
2024-08-21 11:54:23 +00:00

638 lines
20 KiB
YAML

name: "umi_tools_dedup"
namespace: "umi_tools"
version: "main"
authors:
- name: "Emma Rousseau"
roles:
- "author"
- "maintainer"
info:
links:
email: "emma@data-intuitive.com"
github: "emmarousseau"
linkedin: "emmarousseau1"
organizations:
- name: "Data Intuitive"
href: "https://www.data-intuitive.com"
role: "Bioinformatician"
argument_groups:
- name: "Inputs"
arguments:
- type: "file"
name: "--input"
alternatives:
- "--stdin"
description: "Input BAM or SAM file. Use --in_sam to specify SAM format."
info: null
must_exist: true
create_parent: true
required: true
direction: "input"
multiple: false
multiple_sep: ";"
- type: "boolean_true"
name: "--in_sam"
description: "By default, inputs are assumed to be in BAM format. Use this options\
\ to specify the use of SAM\nformat for input.\n"
info: null
direction: "input"
- type: "file"
name: "--bai"
description: "BAM index"
info: null
must_exist: true
create_parent: true
required: false
direction: "input"
multiple: false
multiple_sep: ";"
- type: "integer"
name: "--random_seed"
description: "Random seed to initialize number generator with."
info: null
required: false
direction: "input"
multiple: false
multiple_sep: ";"
- name: "Outputs"
arguments:
- type: "file"
name: "--output"
alternatives:
- "--stdout"
description: "Deduplicated BAM file."
info: null
must_exist: true
create_parent: true
required: true
direction: "output"
multiple: false
multiple_sep: ";"
- type: "boolean_true"
name: "--out_sam"
description: "By default, outputa are written in BAM format. Use this options\
\ to specify the use of SAM format\nfor output.\n"
info: null
direction: "input"
- type: "boolean_true"
name: "--paired"
description: "BAM is paired end - output both read pairs. This will also force\
\ the use of the template length\nto determine reads with the same mapping coordinates.\n"
info: null
direction: "input"
- type: "string"
name: "--output_stats"
description: "Generate files containing UMI based deduplication statistics files\
\ with this prefix in the file names.\n"
info: null
required: false
direction: "input"
multiple: false
multiple_sep: ";"
- type: "string"
name: "--extract_umi_method"
description: "Specify the method by which the barcodes were encoded in the read.\n\
The options are:\n * read_id (default) \n * tag\n * umis\n"
info: null
example:
- "read_id"
required: false
choices:
- "read_id"
- "tag"
- "umis"
direction: "input"
multiple: false
multiple_sep: ";"
- type: "string"
name: "--umi_tag"
description: "The tag containing the UMI sequence. This is only required if the\
\ extract_umi_method is set to tag.\n"
info: null
required: false
direction: "input"
multiple: false
multiple_sep: ";"
- type: "string"
name: "--umi_separator"
description: "The separator used to separate the UMI from the read sequence. This\
\ is only required if the\nextract_umi_method is set to id_read. Default: `_`.\n"
info: null
example:
- "_"
required: false
direction: "input"
multiple: false
multiple_sep: ";"
- type: "string"
name: "--umi_tag_split"
description: "Separate the UMI in tag by <SPLIT> and take the first element."
info: null
required: false
direction: "input"
multiple: false
multiple_sep: ";"
- type: "string"
name: "--umi_tag_delimiter"
description: "Separate the UMI in by <DELIMITER> and concatenate the elements."
info: null
required: false
direction: "input"
multiple: false
multiple_sep: ";"
- type: "string"
name: "--cell_tag"
description: "The tag containing the cell barcode sequence. This is only required\
\ if the extract_umi_method\nis set to tag.\n"
info: null
required: false
direction: "input"
multiple: false
multiple_sep: ";"
- type: "string"
name: "--cell_tag_split"
description: "Separate the cell barcode in tag by <SPLIT> and take the first element."
info: null
required: false
direction: "input"
multiple: false
multiple_sep: ";"
- type: "string"
name: "--cell_tag_delimiter"
description: "Separate the cell barcode in by <DELIMITER> and concatenate the\
\ elements."
info: null
required: false
direction: "input"
multiple: false
multiple_sep: ";"
- name: "Grouping Options"
arguments:
- type: "string"
name: "--method"
description: "The method to use for grouping reads. \nThe options are: \n * unique\n\
\ * percentile\n * cluster\n * adjacency\n * directional (default)\n"
info: null
example:
- "directional"
required: false
choices:
- "unique"
- "percentile"
- "cluster"
- "adjacency"
- "directional"
direction: "input"
multiple: false
multiple_sep: ";"
- type: "integer"
name: "--edit_distance_threshold"
description: "For the adjacency and cluster methods the threshold for the edit\
\ distance to connect two\nUMIs in the network can be increased. The default\
\ value of 1 works best unless the UMI is\nvery long (>14bp). Default: `1`.\n"
info: null
example:
- 1
required: false
direction: "input"
multiple: false
multiple_sep: ";"
- type: "boolean_true"
name: "--spliced_is_unique"
description: "Causes two reads that start in the same position on the same strand\
\ and having the same UMI\nto be considered unique if one is spliced and the\
\ other is not. (Uses the 'N' cigar operation\nto test for splicing).\n"
info: null
direction: "input"
- type: "integer"
name: "--soft_clip_threshold"
description: "Mappers that soft clip will sometimes do so rather than mapping\
\ a spliced read if there is only\na small overhang over the exon junction.\
\ By setting this option, you can treat reads with at\nleast this many bases\
\ soft-clipped at the 3' end as spliced. Default: `4`.\n"
info: null
example:
- 4
required: false
direction: "input"
multiple: false
multiple_sep: ";"
- type: "string"
name: "--multimapping_detection_method"
description: "If the sam/bam contains tags to identify multimapping reads, you\
\ can specify for use when selecting\nthe best read at a given loci. Supported\
\ tags are `NH`, `X0` and `XT`. If not specified, the read\nwith the highest\
\ mapping quality will be selected.\n"
info: null
required: false
direction: "input"
multiple: false
multiple_sep: ";"
- type: "boolean_true"
name: "--read_length"
description: "Use the read length as a criteria when deduping, for e.g. sRNA-Seq."
info: null
direction: "input"
- name: "Single-cell RNA-Seq Options"
arguments:
- type: "boolean_true"
name: "--per_gene"
description: "Reads will be grouped together if they have the same gene. This\
\ is useful if your library prep\ngenerates PCR duplicates with non identical\
\ alignment positions such as CEL-Seq. Note this option\nis hardcoded to be\
\ on with the count command. I.e. counting is always performed per-gene. Must\
\ be\ncombined with either --gene_tag or --per_contig option.\n"
info: null
direction: "input"
- type: "string"
name: "--gene_tag"
description: "Deduplicate per gene. The gene information is encoded in the bam\
\ read tag specified.\n"
info: null
required: false
direction: "input"
multiple: false
multiple_sep: ";"
- type: "string"
name: "--assigned_status_tag"
description: "BAM tag which describes whether a read is assigned to a gene. Defaults\
\ to the same value as given\nfor --gene_tag.\n"
info: null
required: false
direction: "input"
multiple: false
multiple_sep: ";"
- type: "string"
name: "--skip_tags_regex"
description: "Use in conjunction with the --assigned_status_tag option to skip\
\ any reads where the tag matches\nthis regex. Default (\"^[__|Unassigned]\"\
) matches anything which starts with \"__\" or \"Unassigned\".\n"
info: null
required: false
direction: "input"
multiple: false
multiple_sep: ";"
- type: "boolean_true"
name: "--per_contig"
description: "Deduplicate per contig (field 3 in BAM; RNAME). All reads with the\
\ sam contig will be considered to\nhave the same alignment position. This is\
\ useful if you have aligned to a reference transcriptome\nwith one transcript\
\ per gene. If you have aligned to a transcriptome with more than one transcript\n\
per gene, you can supply a map between transcripts and gene using the --gene_transcript_map\
\ option.\n"
info: null
direction: "input"
- type: "file"
name: "--gene_transcript_map"
description: "A file containing a mapping between gene names and transcript names.\
\ The file should be tab\nseparated with the gene name in the first column and\
\ the transcript name in the second column.\n"
info: null
must_exist: true
create_parent: true
required: false
direction: "input"
multiple: false
multiple_sep: ";"
- type: "boolean_true"
name: "--per_cell"
description: "Reads will only be grouped together if they have the same cell barcode.\
\ Can be combined with\n--per_gene.\n"
info: null
direction: "input"
- name: "SAM/BAM Options"
arguments:
- type: "integer"
name: "--mapping_quality"
description: "Minimium mapping quality (MAPQ) for a read to be retained. Default:\
\ `0`.\n"
info: null
example:
- 0
required: false
direction: "input"
multiple: false
multiple_sep: ";"
- type: "string"
name: "--unmapped_reads"
description: "How unmapped reads should be handled. \nThe options are:\n * \"\
discard\": Discard all unmapped reads. (default)\n * \"use\": If read2\
\ is unmapped, deduplicate using read1 only. Requires --paired.\n * \"output\"\
: Output unmapped reads/read pairs without UMI grouping/deduplication. Only\
\ available in umi_tools group.\n"
info: null
example:
- "discard"
required: false
direction: "input"
multiple: false
multiple_sep: ";"
- type: "string"
name: "--chimeric_pairs"
description: "How chimeric pairs should be handled. \nThe options are:\n * \"\
discard\": Discard all chimeric read pairs.\n * \"use\": Deduplicate using\
\ read1 only. (default)\n * \"output\": Output chimeric pairs without UMI\
\ grouping/deduplication. Only available in\n umi_tools group.\n"
info: null
example:
- "use"
required: false
choices:
- "discard"
- "use"
- "output"
direction: "input"
multiple: false
multiple_sep: ";"
- type: "string"
name: "--unpaired_reads"
description: "How unpaired reads should be handled. \nThe options are: \n * \"\
discard\": Discard all unmapped reads.\n * \"use\": If read2 is unmapped, deduplicate\
\ using read1 only. Requires --paired. (default)\n * \"output\": Output unmapped\
\ reads/read pairs without UMI grouping/deduplication. Only available\n \
\ 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"