Mercurial > repos > timpalpant > java_genomics_toolkit
diff galaxy-conf/IntervalToBed.xml @ 24:a77e126ae856 draft
Reupload since last upload did not load correctly
author | timpalpant |
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date | Tue, 19 Jun 2012 22:15:09 -0400 |
parents | 9d56b5b85740 |
children | b43c420a6135 |
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--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/galaxy-conf/IntervalToBed.xml Tue Jun 19 22:15:09 2012 -0400 @@ -0,0 +1,19 @@ +<tool id="IntervalToBed" name="SAM/BAM/GFF/BedGraph/BigBed/VCF to Bed" version="1.0.0"> + <description>converter</description> + <command interpreter="sh">galaxyToolRunner.sh converters.IntervalToBed -i $input -o $output</command> + <inputs> + <param name="input" type="data" format="sam,bam,gff,bigbed,bedgraph,vcf" label="Input" /> + </inputs> + <outputs> + <data name="output" format="bed" metadata_source="input" /> + </outputs> +<help> + +This tool will convert any file in SAM, BAM, GFF, BedGraph, BigBed, or VCF format to Bed format. + +.. class:: warningmark + +For SAM/BAM data, paired-end reads are converted to Bed format as the entire fragment (5' end of mate 1 to the 5' end of mate 2). Single-end reads are converted to Bed format as the read itself, with strand information. If your SAM/BAM file contains both mate alignments from a paired-end sequencing run (i.e. two entries for each fragment), you should first filter out reads from either the + or - strand with the SAM Tools -> Filter SAM tool to avoid producing redundant entries in the output Bed file. + +</help> +</tool>