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nf-core/gatk4/collectreadcounts @ 0.0.0-6c4ed3a

Collects read counts at specified intervals. The count for each interval is calculated by counting the number of read starts that lie in the interval.

Latest version: 0.0.0-6c4ed3a
Total downloads: 6
Source: nf-core/modules
Authors: @nvnieuwk
Maintainers: @nvnieuwk

Summary

Collects read counts at specified intervals. The count for each interval is calculated by counting the number of read starts that lie in the interval.

Get started

Add the following snippet to your workflow script to include this module.

include { GATK4_COLLECTREADCOUNTS } from 'nf-core/gatk4/collectreadcounts'

License

MIT License

Process
Name GATK4_COLLECTREADCOUNTS
Input 4 channels
#1 tuple
meta map

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

input file

BAM/CRAM/SAM file

*.{bam,cram,sam}
input_index file

BAM/CRAM/SAM index file

*.{bai,crai,sai}
intervals file

A file containing the specified intervals

*.{bed,intervals}
#2 tuple
meta2 map

Groovy Map containing reference information e.g. [ id:'test' ]

fasta file

Optional - Reference FASTA

*.{fasta,fa}
#3 tuple
meta3 map

Groovy Map containing reference information e.g. [ id:'test' ]

fai file

Optional - Index of the reference FASTA file

*.fai
#4 tuple
meta4 map

Groovy Map containing reference information e.g. [ id:'test' ]

dict file

Optional - Sequence dictionary of the reference FASTA file

*.dict
Output 3 channels
#1 tsv tuple
meta map

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

*.tsv file

The read counts in TSV format

*.tsv
#2 hdf5 tuple
meta map

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

*.hdf5 file

The read counts in hdf5 format

*.hdf5
#3 versions_gatk4 tuple
${task.process} string

The name of the process

gatk4 string

The name of the tool

gatk --version | sed -n '/GATK.*v/s/.*v//p' eval

The expression to obtain the version of the tool

Tool Description Homepage
gatk4 Genome Analysis Toolkit (GATK4). Developed in the Data Sciences Platform at the Broad Institute, the toolkit offers a wide variety of tools with a primary focus on variant discovery and genotyping. Its powerful processing engine and high-performance computing features make it capable of taking on projects of any size. https://gatk.broadinstitute.org/hc/en-us
Version 0.0.0-6c4ed3a
Commit ID 6c4ed3a220310b905a1fc9d04f05be2e0837142b
Release Date 23 Apr 2026 15:18:30 (UTC)
Download URL https://registry.nextflow.io/api/v1/modules/nf-core%2Fgatk4%2Fcollectreadcounts/0.0.0-6c4ed3a/download
OCI Store URL https://public.cr.seqera.io/v2/nextflow/plugin/modules/nf-core/gatk4/collectreadcounts/blobs/sha256:e0851021ee7ad1e7f0d91566d5a864124a2e935c4734af3c9391c0b0ac26bc2b
Size 3.5 KB
Checksum sha256:e0851021ee7ad1e7f0d91566d5a864124a2e935c4734af3c9391c0b0ac26bc2b
Downloads 3
Version Date Status Downloads Size
0.0.0-6c4ed3a