Mercurial > repos > bgruening > hicexplorer_hiccorrectmatrix
diff hicCorrectMatrix.xml @ 0:d5bf8c60d661 draft
planemo upload for repository https://github.com/maxplanck-ie/HiCExplorer/tree/master/galaxy/wrapper/ commit 2f347b0756d720114f037ed1ff9ba4836e1b3b04
author | bgruening |
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date | Thu, 30 Mar 2017 02:21:47 -0400 |
parents | |
children | ecf11dda45f7 |
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--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/hicCorrectMatrix.xml Thu Mar 30 02:21:47 2017 -0400 @@ -0,0 +1,163 @@ +<tool id="hicexplorer_hiccorrectmatrix" name="@BINARY@" version="@WRAPPER_VERSION@.0"> + <description>Runs Dekker's iterative correction over a hic matrix.</description> + <macros> + <token name="@BINARY@">hicCorrectMatrix</token> + <import>macros.xml</import> + </macros> + <expand macro="requirements" /> + <command> +<![CDATA[ + ln -s '$matrix' temp_matrix.npz.h5 && + + hicCorrectMatrix + $mode.mode_selector + --matrix temp_matrix.npz.h5 + + ## special: --chromosomes is optional, but if given needs at least one argument + #set chroms = '" "'.join([ str($var.chromosome) for $var in $chromosomes ]) + #if chroms + --chromosomes "$chroms" + #end if + + #if $mode.mode_selector == 'correct': + + --iterNum $mode.iterNum + --outFileName corrected_matrix.npz.h5 + + #if $mode.filterThreshold_low and $mode.filterThreshold_large: + --filterThreshold $mode.filterThreshold_low $mode.filterThreshold_large + #end if + + #if $mode.inflationCutoff: + --inflationCutoff $mode.inflationCutoff + #end if + + #if $mode.transCutoff: + --transCutoff $mode.transCutoff + #end if + + #if $mode.sequencedCountCutoff: + --sequencedCountCutoff $mode.sequencedCountCutoff + #end if + + $mode.skipDiagonal + $mode.perchr + + #elif $mode.mode_selector == 'merge_failed': + --plotName diagnostic_plot.png + --outMatrixFile corrected_matrix.npz.h5 + #if $mode.xMax: + --xMax $mode.xMax + #end if + #if $mode.filterThreshold_low and $mode.filterThreshold_large: + --filterThreshold $mode.filterThreshold_low $mode.filterThreshold_large + #end if + #else: + --plotName diagnostic_plot.png + #if $mode.xMax: + --xMax $mode.xMax + #end if + #end if + +]]> + </command> + <inputs> + <param argument="--matrix" name="matrix" type="data" format="h5" + label="Hi-C matrix" /> + + <conditional name="mode"> + <param name="mode_selector" type="select" label="Range restriction (in bp)" argument="--range"> + <option value="diagnostic_plot">Diagnostic plot</option> + <option value="correct">Correct matrix</option> + </param> + <when value="diagnostic_plot"> + <expand macro="xMax" /> + </when> + <when value="correct"> + <param argument="--iterNum" name="iterNum" type="integer" optional="true" value="500" + label="Number of iterations" /> + + <param argument="--inflationCutoff" name="inflationCutoff" type="float" optional="true" + label="Inflation cutoff" value="" + help="Value corresponding to the maximum number of times a bin can be scaled up during the iterative correction. + For example, a inflationCutoff of 3 will filter out all bins that were expanded 3 times or more during the iterative correction."/> + + <param argument="--transCutoff" name="transCutoff" type="float" optional="true" + label="Trans region cutoff" value="" + help="Clip high counts in the top -transcut trans regions (i.e. between chromosomes). A usual value is 0.05."/> + + <param argument="--sequencedCountCutoff" name="sequencedCountCutoff" optional="true" type="float" + label="Sequenced count cutoff" + help="Each bin receives a value indicating the fraction that is covered by reads. + A cutoff of 0.5 will discard all those bins that have less than half of the bin covered."/> + + <param argument="--skipDiagonal" name="skipDiagonal" type="boolean" truevalue="--skipDiagonal" falsevalue="" checked="false" + label="Skip diagonal counts"/> + + <param argument="--perchr" name="perchr" type="boolean" truevalue="--perchr" falsevalue="" checked="false" + label="Normalize each chromosome separately" /> + <expand macro="filterThreshold" /> + + </when> + </conditional> + + <repeat name="chromosomes" min="1" + title="Include chromosomes" help="List of chromosomes to be included in the iterative correction. + The order of the given chromosomes will be kept for the resulting corrected matrix"> + <param name="chromosome" type="text" value="" /> + </repeat> + + </inputs> + <outputs> + <data name="outFileName" from_work_dir="corrected_matrix.npz.h5" format="h5"> + <filter>mode['mode_selector'] == "correct"</filter> + </data> + <data name="diagnostic_plot" from_work_dir="diagnostic_plot.png" format="png"> + <filter>mode['mode_selector'] == "diagnostic_plot"</filter> + </data> + </outputs> + <tests> + <test> + <param name="matrix" value="hicBuildMatrix_result1.h5" ftype="h5"/> + <param name="mode_selector" value="correct"/> + <repeat name="chromosomes"> + <param name="chromosome" value="chrUextra"/> + </repeat> + <repeat name="chromosomes"> + <param name="chromosome" value="chr3LHet"/> + </repeat> + <output name="outFileName" file="hicCorrectMatrix_result1.npz.h5" ftype="h5" compare="sim_size"/> + </test> + <test> + <param name="matrix" ftype="h5" value="hicBuildMatrix_result1.h5"/> + <param name="mode_selector" value="diagnostic_plot"/> + <repeat name="chromosomes"> + <param name="chromosome" value="chrUextra"/> + </repeat> + <repeat name="chromosomes"> + <param name="chromosome" value="chr3LHet"/> + </repeat> + <output name="diagnostic_plot" file="diagnostic_plot.png" ftype="png" compare="sim_size"/> + </test> + </tests> + <help><![CDATA[ + +**What it does** + +Runs Dekker's iterative correction over a hic matrix. + + + correct Run the iterative correction. + diagnostic_plot + Plots a histogram of the coverage per bin together with the + modified z-score based on the median absolute deviation + method (see Boris Iglewicz and David Hoaglin 1993, Volume + 16: How to Detect and Handle Outliers The ASQC Basic + References in Quality Control: Statistical Techniques, + Edward F. Mykytka, Ph.D., Editor. + + +]]></help> + <expand macro="citations" /> +</tool> +