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move out of subreads directory and fix typos
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sainirmayi committed Jan 29, 2024
1 parent 22d02ec commit 986bd18
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functionality:
name: subread_featurecounts
name: featurecounts
description: |
featureCounts is a read summarization program for counting reads generated from either RNA or genomic DNA sequencing experiments by implementing highly efficient chromosome hashing and feature blocking techniques. It works with either single or paired-end reads and provides a wide range of options appropriate for different sequencing applications.
info:
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description: |
Name of an annotation file. GTF/GFF format by default. See -F option for more format information.
required: true
examples: annotation.gtf
example: annotation.gtf
- name: --input
alternatives: ["-i"]
type: file
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description: |
A comma-separated list of SAM or BAM format files. They can be either name or location sorted. Location-sorted paired-end reads are automatically sorted by read names.
required: true
examples: input_file1.bam
example: input_file1.bam

- name: Outputs
arguments:
- name: --output
alternative: ["-o"]
alternatives: ["-o"]
type: file
direction: output
description: |
Name of output file including read counts. A separate file including summary statistics of counting results is also included in the output ('<output>.summary'). Both files are in tab delimited format.
required: true
must_exist: true
example: features.txt
- name: --output_summary
type: file
direction: output
description: |
Summary statistics of counting results is also included in the output ('<output>.summary').
required: true
must_exist: true
example: features.txt.summary
- name: --output_junctions
type: file
direction: output
description: |
Count of number of reads supporting each exon-exon junction. See -J for more information.
required: false
must_exist: false
example: features.txt.jcounts
must_exist: false
- name: --r_path
type: file
direction: output
description: |
Directory to save the detailed assignment results. If unspecified, the directory where counting results are saved is used. See -R for more format information.
required: false
must_exist: false
example: detailed_results/
must_exist: false

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type: boolean_true
description: |
Output verbose information for debugging, such as un-matched chromosome/contig names.
- name: --version
alternatives: ["-v"]
type: boolean_true
description: |
Output version of the program.
resources:
- type: bash_script
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