bedtools/bedtools_genomecov

genome coverage
BED
GFF
VCF
BAM

Description

Compute the coverage of a feature file among a genome.

Type

bash_script

License

MIT

Keywords

genome coverage
BED
GFF
VCF
BAM

Contributors

Run this component

Run the following command to execute this component with Nextflow:

cat > params.yaml <<'EOM'  
output: "$id.$key.output.bed"  
id: "run"  
publish_dir: "output/"  
EOM

nextflow run https://packages.viash-hub.com/vsh/biobox.git \  
  -revision v0.3.0 \  
  -main-script target/nextflow/bedtools/bedtools_genomecov/main.nf \  
  -params-file params.yaml  

Inputs

Name
Type & Properties
--input
-i
file
--input_bam
-ibam
file
--genome
-g
file

Outputs

Name
Type & Properties
--output
file
required
output

Options

Name
Type & Properties
--depth
-d
boolean_true
--depth_zero
-dz
boolean_true
--bed_graph
-bg
boolean_true
--bed_graph_zero_coverage
-bga
boolean_true
--split
boolean_true
--ignore_deletion
-ignoreD
boolean_true
--strand
string
--pair_end_coverage
-pc
boolean_true
--fragment_size
-fs
boolean_true
--du
boolean_true
--five_prime
-5
boolean_true
--three_prime
-3
boolean_true
--max
integer
--scale
double
--trackline
boolean_true
--trackopts
string
multiple

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