Description

Performs fastq alignment to a fasta reference using SNAP

Input

name:type
description
pattern

meta{:bash}

:map

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

reads{:bash}

:file

List of input fastq files of size 2 for paired fastq or 1 for bam or single fastq

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

meta2{:bash}

:map

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

index{:bash}

:file

List of SNAP genome index files

{Genome,GenomeIndex,GenomeIndexHash,OverflowTable}

Output

name:type
description
pattern

bam{:bash}

meta{:bash}

:map

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

*.bam{:bash}

:file

Aligned BAM file

*.{bam}

bai{:bash}

meta{:bash}

:map

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

*.bai{:bash}

:file

Optional aligned BAM file index

*.{bai}

versions{:bash}

versions.yml{:bash}

:file

File containing software versions

versions.yml

Tools

snapaligner
Apache v2

Scalable Nucleotide Alignment Program -- a fast and accurate read aligner for high-throughput sequencing data