Description
Create flanking intervals for each genomic feature.
This tool generates new intervals representing the regions immediately
upstream and/or downstream of existing genomic features. Unlike slop which
extends existing intervals, flank creates entirely new intervals from the
flanking regions.
Type
bash_script
License
MIT
Keywords
Contributors
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 v0.4.2 \
-main-script target/nextflow/bedtools/bedtools_flank/main.nf \
-params-file params.yaml Name | Type & Properties |
|---|---|
--input -i | file required |
--genome -g | file required |
Name | Type & Properties |
|---|---|
--output | file required output |
Name | Type & Properties |
|---|---|
--both -b | string |
--left -l | string |
--right -r | string |
Name | Type & Properties |
|---|---|
--strand -s | boolean_true |
--percent -pct | boolean_true |
Name | Type & Properties |
|---|---|
--header | boolean_true |