Mercurial > repos > timpalpant > java_genomics_toolkit
annotate 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 |
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date | Tue, 19 Jun 2012 22:09:23 -0400 |
parents | 9d56b5b85740 |
children | b43c420a6135 |
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1 <tool id="RollingReadLength" name="Compute mean fragment length" version="1.1.0"> |
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2 <description>over each locus</description> |
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3 <command interpreter="sh">galaxyToolRunner.sh ngs.RollingReadLength -i $input -a ${chromInfo} -o $output</command> |
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4 <inputs> |
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5 <param format="sam,bam,bed,bedgraph" name="input" type="data" label="Mapped reads" /> |
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6 </inputs> |
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7 <outputs> |
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8 <data format="wig" name="output" /> |
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9 </outputs> |
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10 |
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11 <help> |
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12 |
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13 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. |
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14 |
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15 .. class:: warningmark |
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16 |
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17 This tool requires paired-end SAM, BAM, Bed, or BedGraph formatted data. Using single-end data will result in a constant read length. |
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18 |
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19 </help> |
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20 </tool> |