Performs fastq alignment to a fasta reference using BWA-MEME
meta
:map
Groovy Map containing sample information e.g. [ id:‘test’, single_end:false ]
reads
:file
List of input FastQ files of size 1 and 2 for single-end and paired-end data, respectively.
meta2
Groovy Map containing reference/index information e.g. [ id:‘test’ ]
index
BWA genome index files
Directory containing BWA index *.{0132,amb,ann,bwt.2bit.64,pac}
meta3
Groovy Map containing reference information e.g. [ id:‘genome’ ]
fasta
Reference genome in FASTA format
*.{fa,fasta,fna}
sort_bam
:boolean
use samtools sort (true) or samtools view (false)
true or false
output
${prefix}.{sam,bam,cram}
Output alignment file (SAM, BAM, or CRAM)
*.{sam,bam,cram}
${prefix}.{csi,crai}
Index file for BAM (.csi) or CRAM (.crai) output
*.{csi,crai}
versions_bwameme
${task.process}
:string
The name of the process
bwameme
The name of the tool
1.0.6
The expression to obtain the version of the tool
versions_samtools
samtools
Name of the tool
samtools version | sed "1!d;s/.* //"
:eval
versions_mbuffer
mbuffer
mbuffer --version 2>&1 | sed -n 's/mbuffer version //p'
versions
Faster BWA-MEM2 using learned-index
