Mercurial > repos > iuc > bedtools
view clusterBed.xml @ 41:7ab85ac5f64b draft
"planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/bedtools commit 500a03281ea704abc7a16d9af63d67dbdcc5cd0b"
author | iuc |
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date | Thu, 04 Nov 2021 11:36:55 +0000 |
parents | 3e38c9b3214f |
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<tool id="bedtools_clusterbed" name="bedtools ClusterBed" version="@TOOL_VERSION@" profile="@PROFILE@"> <description>cluster overlapping/nearby intervals</description> <macros> <import>macros.xml</import> </macros> <expand macro="bio_tools" /> <expand macro="requirements" /> <expand macro="stdio" /> <command><![CDATA[ bedtools cluster $strand -d $distance -i '$inputA' > '$output' ]]></command> <inputs> <param name="inputA" argument="-i" type="data" format="@STD_BEDTOOLS_INPUTS@" label="@STD_BEDTOOLS_INPUT_LABEL@ file"/> <param name="strand" argument="-s" type="boolean" truevalue="-s" falsevalue="" checked="false" label="Force strandedness." help="That is, only cluster features that are the same strand. By default, this is disabled." /> <param name="distance" argument="-d" type="integer" value="0" label="Maximum distance between features allowed for features to be clustered" help="Default is 0. That is, overlapping and/or book-ended features are clustered." /> </inputs> <outputs> <data name="output" format_source="inputA" metadata_source="inputA"/> </outputs> <tests> <test> <param name="inputA" value="mergedBed1.bed" ftype="bed" /> <output name="output" file="clusterBed_result.bed" ftype="bed" /> </test> </tests> <help><![CDATA[ **What it does** Similar to merge, cluster report each set of overlapping or “book-ended” features in an interval file. In contrast to merge, cluster does not flatten the cluster of intervals into a new meta-interval; instead, it assigns an unique cluster ID to each record in each cluster. This is useful for having fine control over how sets of overlapping intervals in a single interval file are combined. .. image:: $PATH_TO_IMAGES/cluster-glyph.png .. class:: warningmark bedtools cluster requires that you presort your data by chromosome and then by start position (e.g., sort -k1,1 -k2,2n in.bed > in.sorted.bed for BED files). @REFERENCES@ ]]></help> <expand macro="citations" /> </tool>