Align reads to a reference genome using YARA
meta
Groovy Map containing sample information e.g. [ id:‘test’, single_end
reads
List of input FastQ files of size 1 and 2 for single-end and paired-end data, respectively.
index
YARA genome index files
versions
File containing software versions
versions.yml
bam
Sorted BAM file
*.{bam}
bai
Sorted BAM file index
*.{bai}
Yara is an exact tool for aligning DNA sequencing reads to reference genomes.
