Description

command line tool for CNV/CNA analysis. This step imports the read depth data into a root pytor file.

Input

name:type
description
pattern

meta

:map

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

input_file

:file

BAM/CRAM/SAM file

*.{bam,cram}

index

:file

bam file index

*.{bai,crai}

meta2

:map

Groovy Map containing genome information e.g. [ id:‘genome’ ]

fasta

:file

specifies reference genome file (only for cram file without reference genome)

*.{fasta,fasta.gz,fa,fa.gz}

fai

:file

Index of reference fasta file

*.fai

Output

name:type
description
pattern

pytor

meta

:map

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

*.pytor

:file

read depth root file in which read depth data binned to 100 base pair bins will be stored.

*.{pytor}

versions_cnvpytor

${task.process}

:string

The name of the process

cnvpytor

:string

The name of the tool

cnvpytor --version 2>&1 | sed -n 's/.*CNVpytor //p'

:eval

The expression to obtain the version of the tool

Topics

name:type
description
pattern

versions

${task.process}

:string

The name of the process

cnvpytor

:string

The name of the tool

cnvpytor --version 2>&1 | sed -n 's/.*CNVpytor //p'

:eval

The expression to obtain the version of the tool

Tools

cnvpytor -rd
MIT

calling CNVs using read depth