Files
biobox/target/executable/bcl_convert/.config.vsh.yaml
CI 6f2f840fd9 Build branch main with version main (7f8bcc2)
Build pipeline: viash-hub.biobox.main-zp6tq

Source commit: 7f8bcc2b3e

Source message: BD rhapsody sequence analysis (#96)

* wip

* fix test

* add help

* update 2.2 args

* fix bug

* extend test data

* output separate files

* analyse missing args

* tweaks to test

* fix script

* fix test

* fix test

* move small reference

* wip generate wta test data

* don't forget about umi in r1

* remove unneeded pkg

* load reference in memory just once

* fix random choices

* extend test

* add abc immunediscoverypanel

* wip abc testing code

* fix abc test; need unique instrument, run and flowcell ids for each sample

* add smk data

* add entry to changelog

* remove old test file

* adapt test for missing read

* update description

* add comment

* ensure cwl files are absolute

* Apply suggestions from code review

Co-authored-by: Dries Schaumont <5946712+DriesSchaumont@users.noreply.github.com>

* fix suggestion

* newer pipelines have docker requirements as a hint instead of a strict requirement

* rename str to content

* remove deleted resources

* fix containers

* fix script

* fix suggestion

* fix suggestion...

* fix test

* fix component name

* fix test

* apply suggestions

* fix test

* added note

* fix changelog

* fix changelog again

* splitting hairs here

---------

Co-authored-by: Dries Schaumont <5946712+DriesSchaumont@users.noreply.github.com>
2024-09-17 10:13:18 +00:00

446 lines
12 KiB
YAML

name: "bcl_convert"
version: "main"
authors:
- name: "Toni Verbeiren"
roles:
- "author"
- "maintainer"
info:
links:
github: "tverbeiren"
linkedin: "verbeiren"
organizations:
- name: "Data Intuitive"
href: "https://www.data-intuitive.com"
role: "Data Scientist and CEO"
- name: "Dorien Roosen"
roles:
- "author"
info:
links:
email: "dorien@data-intuitive.com"
github: "dorien-er"
linkedin: "dorien-roosen"
organizations:
- name: "Data Intuitive"
href: "https://www.data-intuitive.com"
role: "Data Scientist"
argument_groups:
- name: "Input arguments"
arguments:
- type: "file"
name: "--bcl_input_directory"
alternatives:
- "-i"
description: "Input run directory"
info: null
example:
- "bcl_dir"
must_exist: true
create_parent: true
required: true
direction: "input"
multiple: false
multiple_sep: ";"
- type: "file"
name: "--sample_sheet"
alternatives:
- "-s"
description: "Path to SampleSheet.csv file (default searched for in --bcl_input_directory)"
info: null
example:
- "bcl_dir/sample_sheet.csv"
must_exist: true
create_parent: true
required: false
direction: "input"
multiple: false
multiple_sep: ";"
- type: "file"
name: "--run_info"
description: "Path to RunInfo.xml file (default root of BCL input directory)"
info: null
example:
- "bcl_dir/RunInfo.xml"
must_exist: true
create_parent: true
required: false
direction: "input"
multiple: false
multiple_sep: ";"
- name: "Lane and tile settings"
arguments:
- type: "integer"
name: "--bcl_only_lane"
description: "Convert only specified lane number (default all lanes)"
info: null
example:
- 1
required: false
direction: "input"
multiple: false
multiple_sep: ";"
- type: "boolean"
name: "--first_tile_only"
description: "Only convert first tile of input (for testing & debugging)"
info: null
example:
- true
required: false
direction: "input"
multiple: false
multiple_sep: ";"
- type: "string"
name: "--tiles"
description: "Process only a subset of tiles by a regular expression"
info: null
example:
- "s_[0-9]+_1"
required: false
direction: "input"
multiple: false
multiple_sep: ";"
- type: "string"
name: "--exclude_tiles"
description: "Exclude set of tiles by a regular expression"
info: null
example:
- "s_[0-9]+_1"
required: false
direction: "input"
multiple: false
multiple_sep: ";"
- name: "Resource arguments"
arguments:
- type: "boolean"
name: "--shared_thread_odirect_output"
description: "Use linux native asynchronous io (io_submit) for file output (Default=false)"
info: null
example:
- true
required: false
direction: "input"
multiple: false
multiple_sep: ";"
- type: "integer"
name: "--bcl_num_parallel_tiles"
description: "\\# of tiles to process in parallel (default 1)"
info: null
example:
- 1
required: false
direction: "input"
multiple: false
multiple_sep: ";"
- type: "integer"
name: "--bcl_num_conversion_threads"
description: "\\# of threads for conversion (per tile, default # cpu threads)"
info: null
example:
- 1
required: false
direction: "input"
multiple: false
multiple_sep: ";"
- type: "integer"
name: "--bcl_num_compression_threads"
description: "\\# of threads for fastq.gz output compression (per tile, default\
\ # cpu threads, or HW+12)"
info: null
example:
- 1
required: false
direction: "input"
multiple: false
multiple_sep: ";"
- type: "integer"
name: "--bcl_num_decompression_threads"
description: "\\# of threads for bcl/cbcl input decompression (per tile, default\
\ half # cpu threads, or HW+8). Only applies when preloading files"
info: null
example:
- 1
required: false
direction: "input"
multiple: false
multiple_sep: ";"
- name: "Run arguments"
arguments:
- type: "boolean"
name: "--bcl_only_matched_reads"
description: "For pure BCL conversion, do not output files for 'Undetermined'\
\ [unmatched] reads (output by default)"
info: null
example:
- true
required: false
direction: "input"
multiple: false
multiple_sep: ";"
- type: "boolean"
name: "--no_lane_splitting"
description: "Do not split FASTQ file by lane (false by default)"
info: null
example:
- true
required: false
direction: "input"
multiple: false
multiple_sep: ";"
- type: "integer"
name: "--num_unknown_barcodes_reported"
description: "\\# of Top Unknown Barcodes to output (1000 by default)"
info: null
example:
- 1000
required: false
direction: "input"
multiple: false
multiple_sep: ";"
- type: "boolean"
name: "--bcl_validate_sample_sheet_only"
description: "Only validate RunInfo.xml & SampleSheet files (produce no FASTQ\
\ files)"
info: null
example:
- true
required: false
direction: "input"
multiple: false
multiple_sep: ";"
- type: "boolean"
name: "--strict_mode"
description: "Abort if any files are missing (false by default)"
info: null
example:
- true
required: false
direction: "input"
multiple: false
multiple_sep: ";"
- type: "boolean"
name: "--sample_name_column_enabled"
description: "Use sample sheet 'Sample_Name' column when naming fastq files &\
\ subdirectories"
info: null
example:
- true
required: false
direction: "input"
multiple: false
multiple_sep: ";"
- name: "Output arguments"
arguments:
- type: "file"
name: "--output_directory"
alternatives:
- "-o"
description: "Output directory containig fastq files"
info: null
example:
- "fastq_dir"
must_exist: true
create_parent: true
required: true
direction: "output"
multiple: false
multiple_sep: ";"
- type: "boolean"
name: "--bcl_sampleproject_subdirectories"
description: "Output to subdirectories based upon sample sheet 'Sample_Project'\
\ column"
info: null
example:
- true
required: false
direction: "input"
multiple: false
multiple_sep: ";"
- type: "integer"
name: "--fastq_gzip_compression_level"
description: "Set fastq output compression level 0-9 (default 1)"
info: null
example:
- 1
required: false
direction: "input"
multiple: false
multiple_sep: ";"
- type: "file"
name: "--reports"
description: "Reports directory"
info: null
example:
- "reports_dir"
must_exist: true
create_parent: true
required: false
direction: "output"
multiple: false
multiple_sep: ";"
- type: "file"
name: "--logs"
description: "Reports directory"
info: null
example:
- "logs_dir"
must_exist: true
create_parent: true
required: false
direction: "output"
multiple: false
multiple_sep: ";"
resources:
- type: "bash_script"
path: "script.sh"
is_executable: true
description: "Convert bcl files to fastq files using bcl-convert.\nInformation about\
\ upgrading from bcl2fastq via\n[Upgrading from bcl2fastq to BCL Convert](https://emea.support.illumina.com/bulletins/2020/10/upgrading-from-bcl2fastq-to-bcl-convert.html)\n\
and [BCL Convert Compatible Products](https://support.illumina.com/sequencing/sequencing_software/bcl-convert/compatibility.html)\n"
test_resources:
- type: "bash_script"
path: "test.sh"
is_executable: true
info: null
status: "enabled"
requirements:
commands:
- "ps"
keywords:
- "demultiplex"
- "fastq"
- "bcl"
- "illumina"
license: "Proprietary"
links:
repository: "https://github.com/viash-hub/biobox"
homepage: "https://support.illumina.com/sequencing/sequencing_software/bcl-convert.html"
documentation: "https://support.illumina.com/downloads/bcl-convert-user-guide.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: "debian:trixie-slim"
target_registry: "images.viash-hub.com"
target_tag: "main"
namespace_separator: "/"
setup:
- type: "apt"
packages:
- "wget"
- "gdb"
- "which"
- "hostname"
- "alien"
- "procps"
interactive: false
- type: "docker"
run:
- "wget https://s3.amazonaws.com/webdata.illumina.com/downloads/software/bcl-convert/bcl-convert-4.2.7-2.el8.x86_64.rpm\
\ -O /tmp/bcl-convert.rpm && \\\nalien -i /tmp/bcl-convert.rpm && \\\nrm -rf\
\ /var/lib/apt/lists/* && \\\nrm /tmp/bcl-convert.rpm\n"
- type: "docker"
run:
- "echo \"bcl-convert: \\\"$(bcl-convert -V 2>&1 >/dev/null | sed -n '/Version/\
\ s/^bcl-convert\\ Version //p')\\\"\" > /var/software_versions.txt\n"
entrypoint: []
cmd: null
- type: "native"
id: "native"
build_info:
config: "src/bcl_convert/config.vsh.yaml"
runner: "executable"
engine: "docker|native"
output: "target/executable/bcl_convert"
executable: "target/executable/bcl_convert/bcl_convert"
viash_version: "0.9.0"
git_commit: "7f8bcc2b3e1ffaac9778b6acb42420b19660d1a1"
git_remote: "https://x-access-token:ghs_aSDBedV4vU66pddFDN6d8UEy0ZQApn08RAsh@github.com/viash-hub/biobox"
git_tag: "v0.2.0-3-g7f8bcc2"
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"
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"