Mercurial > repos > timpalpant > java_genomics_toolkit
view galaxy-conf/RollingReadLength.xml @ 22:727fbba02ef7 draft
Fix a bug in GeneTrackToWig where +/- strands were not merged correctly. Add option to vary the chunk size of tools that process chromosomes in chunks.
author | timpalpant |
---|---|
date | Tue, 19 Jun 2012 22:09:23 -0400 |
parents | 9d56b5b85740 |
children | b43c420a6135 |
line wrap: on
line source
<tool id="RollingReadLength" name="Compute mean fragment length" version="1.1.0"> <description>over each locus</description> <command interpreter="sh">galaxyToolRunner.sh ngs.RollingReadLength -i $input -a ${chromInfo} -o $output</command> <inputs> <param format="sam,bam,bed,bedgraph" name="input" type="data" label="Mapped reads" /> </inputs> <outputs> <data format="wig" name="output" /> </outputs> <help> This tool will compute the mean length of all fragments overlapping a given locus, and can be used to identify sites with exceptionally long or short reads. .. class:: warningmark This tool requires paired-end SAM, BAM, Bed, or BedGraph formatted data. Using single-end data will result in a constant read length. </help> </tool>