Update docs for trimgalore

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drpatelh 2020-08-07 12:10:42 +01:00
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name: Trim Galore!
name: trimgalore
description: Trim FastQ files using Trim Galore!
keywords:
- trimming
- adapters
- sequencing adapters
- trimming
- adapters
- sequencing adapters
tools:
- fastqc:
description: |
A wrapper tool around Cutadapt and FastQC to consistently apply quality
and adapter trimming to FastQ files, with some extra functionality for
MspI-digested RRBS-type (Reduced Representation Bisufite-Seq) libraries.
homepage: https://www.bioinformatics.babraham.ac.uk/projects/trim_galore/
documentation: https://github.com/FelixKrueger/TrimGalore/blob/master/Docs/Trim_Galore_User_Guide.md
- trimgalore:
description: |
A wrapper tool around Cutadapt and FastQC to consistently apply quality
and adapter trimming to FastQ files, with some extra functionality for
MspI-digested RRBS-type (Reduced Representation Bisufite-Seq) libraries.
homepage: https://www.bioinformatics.babraham.ac.uk/projects/trim_galore/
documentation: https://github.com/FelixKrueger/TrimGalore/blob/master/Docs/Trim_Galore_User_Guide.md
params:
- outdir:
type: string
description: |
The pipeline's output directory. By default, the module will
output files into `$params.outdir/<SOFTWARE>`
- publish_dir_mode:
type: string
description: |
Value for the Nextflow `publishDir` mode parameter.
Available: symlink, rellink, link, copy, copyNoFollow, move.
- conda:
type: boolean
description: |
Run the module with Conda using the software specified
via the `conda` directive
- clip_r1:
type: integer
description: |
Instructs Trim Galore to remove bp from the 5' end of read 1
(or single-end reads)
- clip_r2:
type: integer
description: |
Instructs Trim Galore to remove bp from the 5' end of read 2
(paired-end reads only)
- three_prime_clip_r1:
type: integer
description: |
Instructs Trim Galore to remove bp from the 3' end of read 1
AFTER adapter/quality trimming has been performed
- three_prime_clip_r2:
type: integer
description: |
Instructs Trim Galore to re move bp from the 3' end of read 2
AFTER adapter/quality trimming has been performed
input:
-
- sample_id:
type: string
description: Sample identifier
- reads:
type: file
description: Input FastQ file, or pair of files
- meta:
type: map
description: |
Groovy Map containing sample information
e.g. [ id:'test', single_end:false ]
- reads:
type: file
description: |
List of input FastQ files of size 1 and 2 for single-end and paired-end data,
respectively.
- options:
type: map
description: |
Groovy Map containing module options for passing command-line arguments and
output file paths.
output:
-
- sample_id:
type: string
description: Sample identifier
- trimmed_fastq:
type: file
description: Trimmed FastQ files
pattern: "*fq.gz"
-
- report:
type: file
description: Trim Galore! trimming report
pattern: "*trimming_report.txt"
- meta:
type: map
description: |
Groovy Map containing sample information
e.g. [ id:'test', single_end:false ]
- reads:
type: file
description: |
List of input adapter trimmed FastQ files of size 1 and 2 for
single-end and paired-end data, respectively.
pattern: "*.fq.gz"
- html:
type: file
description: FastQC report (optional)
pattern: "*_fastqc.html"
- zip:
type: file
description: FastQC report archive (optional)
pattern: "*_fastqc.zip"
- log:
type: file
description: Trim Galore! trimming report
pattern: "*report.txt"
- version:
type: file
description: File containing software version
pattern: "*.version.txt"
authors:
- "@drpatelh"
- "@ewels"
- "@FelixKrueger"