Mercurial > repos > rnateam > viennarna_rnaplfold
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planemo upload for repository https://github.com/bgruening/galaxytools/tree/master/tools/rna_tools/vienna_rna commit 36681a08c6e44c663169caaefd964781c43d0d29
author | rnateam |
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date | Wed, 20 Dec 2017 08:30:44 -0500 |
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<tool id="viennarna_rnaplfold" name="@EXECUTABLE@" version="@VERSION@.0"> <description> predicts RNA secondary structures including pseudoknots</description> <macros> <token name="@EXECUTABLE@">RNAplfold</token> <import>macros.xml</import> </macros> <expand macro="requirements" /> <expand macro="stdio" /> <expand macro="version_command" /> <command> <![CDATA[ RNAplfold < '$input' -T$temperature --dangles=$dangling --cutoff=$cutoff --winsize=$winsize --span=$span $onthefly $openingenergies #if $varExists('$unpairedOption.ulength') --ulength=$unpairedOption.ulength #end if #if $varExists('$advancedOptions.nolp') $advancedOptions.noconversion $advancedOptions.nolp $advancedOptions.nogu $advancedOptions.noclosinggu $advancedOptions.notetra #end if && find -name '*_basepairs' -or -name '*_lunp' -or -name '*_openen*' > files.tmp && tar -cf '$outputf' --files-from=files.tmp ]]> </command> <inputs> <param format="fasta" name="input" type="data" label="Fasta file"/> <param name="temperature" type="float" value="37.0" label="temperature [°C]" help="-T"/> <param name="dangling" type="select" label="how to treat dangling end energies" help="-d"> <option value="2" selected="true">unpaired bases participate in all dangling ends (2)</option> <option value="0">ignore dangling ends (0)</option> <option value="1">unpaired bases participate in one dangling end only (1)</option> <option value="3">allow coaxial stacking (3)</option> </param> <param name="winsize" type="integer" value="70" label="Average pairing probabilities over this windowsize" help="--winsize"/> <param name="span" type="integer" value="70" label="Maximum seperation between base pairs" help="--span, -L"/> <param name="cutoff" type="float" value="0.01" label="Cutoff probability for report on base pairing" help="--cutoff"/> <param name="onthefly" type="boolean" truevalue="--print_onthefly" falsevalue="" checked="false" label="Print simplified base pair probabilities (_basepairs output)" help="--print_onthefly"/> <param name="openingenergies" type="boolean" truevalue="--opening_energies" falsevalue="" checked="false" label="Output in logarithm of the probabilities (_openen output)" help="--opening_energies"/> <param argument="--plex_output" type="boolean" truevalue="--plex_output" falsevalue="" checked="false" label="" help=""/> <conditional name="unpairedOption"> <param name="unpairedSelector" type="select" label="Compute probabilty that region is unpaired (_lunp output)"> <option value="no" selected="true">no</option> <option value="yes">yes</option> </param> <when value="yes"> <param name="ulength" type="integer" value="31" label="Maximal lenght of unpaired region" help="--ulength"/> </when> <when value="no"> </when> </conditional> <conditional name="advancedOptions"> <param name="advancedSelector" type="select" label="advanced options"> <option value="basic">basic Options</option> <option value="advanced">advanced Options</option> </param> <when value="advanced"> <param name="nolp" type="boolean" truevalue="" falsevalue="--noLP" checked="true" label="Allow lonely base-pairs" help="(--noLP)"/> <param name="nogu" type="boolean" truevalue="" falsevalue="--noGU" checked="true" label="Allow GU pairing" help="--noGU"/> <param name="noclosinggu" type="boolean" truevalue="" falsevalue="--noClosingGU" checked="true" label="Allow GU pairing at the ends" help="Allow pairing of G and U at the ends of helices. --noClosingGU"/> <param name="notetra" type="boolean" truevalue="" falsevalue="--noTetra" checked="true" label="Allow stabilization for loops, hairpins etc." help=" Include special tabulated stabilizing energies for tri-, tetra- and hexaloop hairpins. Mostly for testing. (--noTetra)"/> <param name="noconversion" type="boolean" truevalue="" falsevalue="--noconv" checked="true" label="Convert Thymine to Uracil (T -> U)" help="Avoids confusion with DNA sequences (--noconv)"/> </when> <when value="basic"> </when> </conditional> </inputs> <outputs> <collection name="matrix_outputs" type="list" label="rna_eps outputs"> <discover_datasets pattern="(?P<designation>.+)_dp\.ps" ext="rna_eps" visible="true"/> </collection> <data format="tar" name="outputf"/> </outputs> <tests> <test> <param name="input" value="rnaplfold_input1.fa"/> <output_collection name="matrix_outputs" type="list"> <element name="Anolis_caro_chrUn_GL343590.trna2-A"> <assert_contents> <has_text_matching expression="%%Creator: ViennaRNA-@VERSION@" /> </assert_contents> </element> </output_collection> </test> </tests> <help> <![CDATA[ **RNAplfold** Computes local pair probabilities for base pairs with a maximal span of L. The probabilities are averaged over all windows of size L that contain the base pair. For a sequence of length n and a window size of L the algorithm uses only O(n+L*L) memory and O(n*L*L) CPU time. Thus it is practical to "scan" very large genomes for short stable RNA structures. ----- **Input format** RNAPplfold requires one input file - Fasta file ------ **Outputs** For each structure in the Fasta input a postscript image with dot-plot of the pairing probabilities is generated. Different output is generated with the "--ulength", "--print_onthefly" and "--opening_energies" flags. The Dot Plot Matrices are stored in a Postscript file. The other output is packed in a tar file. ]]> </help> <expand macro="citations" /> </tool>