Description

Perform merging of mate paired-end sequencing reads

Input

name:type
description
pattern

meta

:map

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

reads

:file

List of input FastQ files of size 2; i.e., paired-end data.

*fastq.gz

Output

name:type
description
pattern

merged

meta

:map

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

${prefix}.extendedFrags.fastq.gz

:file

The merged fastq reads

.extendedFrags.fastq.gz

notcombined

meta

:map

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

${prefix}.notCombined_*.fastq.gz

:file

Not combined reads from flash

.notCombined_*.fastq.gz

histogram

meta

:map

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

${prefix}.hist

:file

HistogramNumeric histogram of merged read lengths.

.hist

versions_flash

${task.process}

:string

The name of the process

flash

:string

The name of the tool

flash --version |& sed '1!d;s/^.*FLASH v//'

:eval

The expression to obtain the version of the tool

Topics

name:type
description
pattern

versions

${task.process}

:string

The name of the process

flash

:string

The name of the tool

flash --version |& sed '1!d;s/^.*FLASH v//'

:eval

The expression to obtain the version of the tool

Tools

flash
GPL v3+

Merge mates from fragments that are shorter than twice the read length