bwa_mem

Performs fastq alignment to a fasta reference using BWA. Adapted from the nf-core bwa-mem module.

mem
bwa
alignment
map
fastq
bam
sam
nf-core modules \
  --git-remote https://github.com/CCBR/nf-modules \
  install bwa/mem

https://github.com/CCBR/nf-modules/…/modules/CCBR/bwa/mem/

Input

name type description pattern
meta map Groovy Map containing sample information
e.g. [ id:‘test’, single_end:false ] NA
reads file List of input FastQ files of size 1 and 2 for single-end and paired-end data,
respectively. NA
index file BWA genome index files Directory containing BWA index *.{amb,ann,bwt,pac,sa}

Output

name type description pattern
bam file Output BAM file containing read alignments *.{bam}
bai file Output BAI index file *.{bai}
versions file File containing software versions versions.yml

Tools

bwa

Home Docs     GPL-3.0-or-later

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