Mercurial > repos > xuebing > sharplabtool
view tools/emboss_5/emboss_isochore.xml @ 2:c2a356708570
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author | xuebing |
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date | Fri, 09 Mar 2012 19:45:42 -0500 |
parents | 9071e359b9a3 |
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<tool id="EMBOSS: isochore47" name="isochore" version="5.0.0"> <description>Plots isochores in large DNA sequences</description> <requirements><requirement type="package" version="5.0.0">emboss</requirement></requirements> <command interpreter="perl">emboss_single_outputfile_wrapper.pl isochore -sequence $input1 -outfile $ofile2 -goutfile $ofile1 -graph png -window $window -shift $shift -auto</command> <!-- <command interpreter="perl">emboss_single_outputfile_wrapper.pl isochore -sequence $input1 -goutfile $ofile1 -graph png -window $window -shift $shift -auto</command>--> <inputs> <param format="fasta" name="input1" type="data"> <label>Sequences</label> </param> <param name="window" size="4" type="text" value="1000"> <label>Window size</label> </param> <param name="shift" size="4" type="text" value="100"> <label>Shift increment</label> </param> </inputs> <outputs> <data format="png" name="ofile1" /> <data format="isochore" name="ofile2" /> </outputs> <!-- <tests> <test> <param name="input1" value="2.fasta"/> <param name="window" value="1000"/> <param name="shift" value="100"/> <output name="ofile1" file="emboss_isochore_out.isochore"/> <output name="ofile2" file="emboss_isochore_out.isochore"/> </test> <test> <param name="input1" value="2.fasta"/> <param name="window" value="1000"/> <param name="shift" value="100"/> <output name="ofile2" file="emboss_isochore_out.isochore"/> </test> </tests>--> <help> .. class:: warningmark The input dataset needs to be sequences. ----- **Syntax** This application plots GC content over a sequence. It is intended for large sequences such as complete chromosomes or large genomic contigs, although interesting results can also be obtained from shorter sequences. You can view the original documentation here_. .. _here: http://emboss.sourceforge.net/apps/release/5.0/emboss/apps/isochore.html - Both **Window size** and **Shift increment** are intergers. ----- **Example** - Input sequences:: >hg18_dna range=chrX:151073054-151073376 5'pad=0 3'pad=0 revComp=FALSE strand=? repeatMasking=none TTTATGTCTATAATCCTTACCAAAAGTTACCTTGGAATAAGAAGAAGTCA GTAAAAAGAAGGCTGTTGTTCCGTGAAATACTGTCTTTATGCCTCAGATT TGGAGTGCTCAGAGCCTCTGCAGCAAAGATTTGGCATGTGTCCTAGGCCT GCTCAGAGCAGCAAATCCCACCCTCTTGGAGAATGAGACTCATAGAGGGA CAGCTCCCTCCTCAGAGGCTTCTCTAATGGGACTCCAAAGAGCAAACACT CAGCCCCATGAGGACTGGCCAGGCCAAGTGGTGTGTGGGAACAGGGAGCA GCGGTTTCCAAGAGGATACAGTA - Output data file:: Position Percent G+C 1 .. 323 80 0.422 112 0.460 144 0.509 176 0.534 208 0.553 240 0.553 - Output graphics file: .. image:: ./static/emboss_icons/isochore.png </help> </tool>