Description

converts FASTQ files to unmapped SAM/BAM/CRAM

Input

name:type
description
pattern

meta{:bash}

:map

Groovy Map containing sample information e.g. [ id:'test', single_end:false ]

reads{:bash}

:file

fastq data to be converted to SAM/BAM/CRAM

*.{fastq,fq,fastq.gz,fq.gz}

Output

name:type
description
pattern

sam{:bash}

meta{:bash}

:map

Groovy Map containing sample information e.g. [ id:'test', single_end:false ]

*.sam{:bash}

:file

SAM file

*.sam

bam{:bash}

meta{:bash}

:map

Groovy Map containing sample information e.g. [ id:'test', single_end:false ]

*.bam{:bash}

:file

Unaligned BAM file

*.bam

cram{:bash}

meta{:bash}

:map

Groovy Map containing sample information e.g. [ id:'test', single_end:false ]

*.cram{:bash}

:file

Unaligned CRAM file

*.cram

versions{:bash}

versions.yml{:bash}

:file

File containing software versions

versions.yml

Tools

samtools
MIT

SAMtools is a set of utilities for interacting with and post-processing short DNA sequence read alignments in the SAM, BAM and CRAM formats, written by Heng Li. These files are generated as output by short read aligners like BWA.