Description

Computes read coverage for genomic regions (bins) across the entire genome.

Input

name:type
description
pattern

meta:map

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

]

bams:file

One or more BAM files

*.{bam}

bais:file

Corresponding BAM file indexes

*.bam.bai

labels:string

User specified labels instead of default labels (file names).

Output

name:type
description
pattern

matrix

meta:map

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

]

*.npz:file

compressed numpy array of read coverage data used by plotCorrelation and plotPCA deeptool utilities

all_bam.bamSummary.npz

versions

versions.yml:file

File containing software versions

versions.yml

Tools

deeptools
GPL v3

A set of user-friendly tools for normalization and visualization of deep-sequencing data