nf-core_modules/modules/fgbio/fastqtobam/meta.yml
Matthias De Smet 36049bf544
Fgbio/fastqtobam (#1980)
* fix samtools stats thread usage

* fix samtools stats thread usage (#1975)

* fix samtools stats thread usage

* fix checksums

* Fix/samtools flagstat (#1979)

* fix samtools stats thread usage

* flagstat: fix threads

* Update busco to v5.4.3 and tar small files (#1970)

* Update busco to v5.4.3 and tar small files

* Fix file contain strings

* Swap md5sums to contains for variable files

* Simplify and generalize module

* add test.yml

* Update modules/fgbio/fastqtobam/meta.yml

Co-authored-by: Moritz E. Beber <midnighter@posteo.net>

* add support + tests for cram output

* more tweaks

* update test.yml

* prettier

* try to fix tests

* fix tests

* prettier

* drop checksum for cram

Co-authored-by: Mahesh Binzer-Panchal <mahesh.binzer-panchal@nbis.se>
Co-authored-by: Moritz E. Beber <midnighter@posteo.net>
2022-09-05 11:57:55 +02:00

43 lines
1.2 KiB
YAML

name: fgbio_fastqtobam
description: |
Using the fgbio tools, converts FASTQ files sequenced into unaligned BAM or CRAM files possibly moving the UMI barcode into the RX field of the reads
keywords:
- fastqtobam
- fgbio
tools:
- fgbio:
description: A set of tools for working with genomic and high throughput sequencing data, including UMIs
homepage: http://fulcrumgenomics.github.io/fgbio/
documentation: http://fulcrumgenomics.github.io/fgbio/tools/latest/
tool_dev_url: https://github.com/fulcrumgenomics/fgbio
doi: ""
licence: ["MIT"]
input:
- reads:
type: file
description: pair of reads to be converted into BAM file
pattern: "*.{fastq.gz}"
output:
- meta:
type: map
description: |
Groovy Map containing sample information
e.g. [ id:'test', single_end:false ]
- version:
type: file
description: File containing software version
pattern: "*.{version.yml}"
- bam:
type: file
description: Unaligned, unsorted BAM file
pattern: "*.{bam}"
- cram:
type: file
description: Unaligned, unsorted CRAM file
pattern: "*.{cram}"
authors:
- "@lescai"
- "@matthdsm"