Description

ataqv function of a corresponding ataqv tool

Input

name:type
description
pattern

meta:map

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

]

bam:file

BAM file

*.bam

bai:file

BAM index file with the same prefix as bam file. Required if tss_file input is provided.

*.bam.bai

peak_file:file

A BED file of peaks called for alignments in the BAM file

*.bed

organism:string

The subject of the experiment, which determines the list of autosomes (see “Reference Genome Configuration” section at https://github.com/ParkerLab/ataqv).

mito_name:string

Name of the mitochondrial sequence.

tss_file:file

A BED file of transcription start sites for the experiment organism. If supplied, a TSS enrichment score will be calculated according to the ENCODE data standards. This calculation requires that the BAM file of alignments be indexed.

*.bed

excl_regs_file:file

A BED file containing excluded regions. Peaks or TSS overlapping these will be ignored.

*.bed

autosom_ref_file:file

A file containing autosomal reference names, one per line. The names must match the reference names in the alignment file exactly, or the metrics based on counts of autosomal alignments will be wrong.

Output

name:type
description
pattern

json

meta:map

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

]

*.ataqv.json:file

The JSON file to which metrics will be written.

problems

meta:map

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

]

*.problems:file

If given, problematic reads will be logged to a file per read group, with names derived from the read group IDs, with “.problems” appended. If no read groups are found, the reads will be written to one file named after the BAM file.

*.problems

versions

versions.yml:file

File containing software versions

versions.yml

Tools

ataqv
GPL v3

ataqv is a toolkit for measuring and comparing ATAC-seq results. It was written to help understand how well ATAC-seq assays have worked, and to make it easier to spot differences that might be caused by library prep or sequencing.