Description

Performs fastq alignment to a fasta reference using BWA

Input

name:type
description
pattern

meta:map

Groovy Map containing sample information e.g. [ id:‘test’, single_end

]

reads:file

List of input FastQ files of size 1 and 2 for single-end and paired-end data, respectively.

meta2:map

Groovy Map containing reference information. e.g. [ id:‘test’, single_end

]

index:file

BWA genome index files

Directory containing BWA index *.{amb,ann,bwt,pac,sa}

meta3:map

Groovy Map containing sample information e.g. [ id:‘test’, single_end

]

fasta:file

Reference genome in FASTA format

*.{fasta,fa}

sort_bam:boolean

use samtools sort (true) or samtools view (false)

true or false

Output

name:type
description
pattern

bam

meta:file

Output BAM file containing read alignments

*.{bam}

*.bam:file

Output BAM file containing read alignments

*.{bam}

cram

meta:file

Output CRAM file containing read alignments

*.{cram}

*.cram:file

Output CRAM file containing read alignments

*.{cram}

csi

meta:file

Optional index file for BAM file

*.{csi}

*.csi:file

Optional index file for BAM file

*.{csi}

crai

meta:file

Optional index file for CRAM file

*.{crai}

*.crai:file

Optional index file for CRAM file

*.{crai}

versions

versions.yml:file

File containing software versions

versions.yml

Tools

bwa
GPL-3.0-or-later

BWA is a software package for mapping DNA sequences against a large reference genome, such as the human genome.