Description

Lofreq subcommand to call low frequency variants from alignments when tumor-normal paired samples are available

Input

name:type
description
pattern

meta

:map

Groovy Map containing sample information e.g. [ id:'sample1', single_end:false ]

bam

:file

Sorted BAM file

*.{bam}

meta2

:map

Groovy Map containing sample information about the reference fasta e.g. [ id:‘reference’ ]

fasta

:file

Reference genome FASTA file

*.{fasta}

Output

name:type
description
pattern

bam

meta

:map

Groovy Map containing sample information e.g. [ id:'sample1', single_end:false ]

*.bam

:file

Realignment and sorted BAM file

*.{bam}

versions_lofreq

${task.process}

:string

Process which generated the version

lofreq

:string

Tool name

lofreq version | sed -n '1s/^.* //p'

:eval

The expression to obtain the version of the tool

Topics

name:type
description
pattern

versions

${task.process}

:string

Process which generated the version

lofreq

:string

Tool name

lofreq version | sed -n '1s/^.* //p'

:eval

The expression to obtain the version of the tool

Tools

lofreq
MIT

A fast and sensitive variant-caller for inferring SNVs and indels from next-generation sequencing data