Mercurial > repos > bgruening > deeptools_plot_coverage
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planemo upload for repository https://github.com/deeptools/deepTools/tree/master/galaxy/wrapper/ commit 4a4029b5c2e725b7cebc27217b76d23910508412
author | bgruening |
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date | Wed, 27 Sep 2023 20:21:56 +0000 |
parents | 9368fbc49c8b |
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<tool id="deeptools_plot_coverage" name="plotCoverage" version="@TOOL_VERSION@+galaxy0" profile="@GALAXY_VERSION@"> <description>assesses the sequencing depth of BAM/CRAM files </description> <macros> <token name="@BINARY@">plotCoverage</token> <import>deepTools_macros.xml</import> </macros> <expand macro="requirements"/> <command> <![CDATA[ #set files=[] #set labels=[] @multiple_input_bams@ @BINARY@ @THREADS@ --plotFile '$outFileName' --bamfiles #echo " ".join($files)# --labels #echo " ".join($labels)# --plotFileFormat '$outFileFormat' #if $outRawCounts: --outRawCounts '$outFileRawCounts' #end if #if ' '.join(map(str, $BED)) != 'None': #set bedFileList=[] #for $f in $BED: #silent $bedFileList.append("'%s'" % $f) #end for #if $bedFileList != ["'None'"]: --BED #echo ' '.join($bedFileList)# #end if #end if #if $coverageOpt.showCoverageOpt == "yes": --outCoverageMetrics '$outFileCoverageMetrics' #for $t in $coverageOpt.thresholds: -ct $t.coverageThreshold #end for #end if #if $advancedOpt.showAdvancedOpt == "yes": --numberOfSamples '$advancedOpt.numberOfSamples' $advancedOpt.skipZeros #if str($advancedOpt.region).strip() != '': --region '$advancedOpt.region' #end if --numberOfSamples $advancedOpt.numberOfSamples #if $advancedOpt.plotTitle and str($advancedOpt.plotTitle.value) != "": --plotTitle '$advancedOpt.plotTitle' #end if @ADVANCED_OPTS_READ_PROCESSING@ @PLOTWIDTHHEIGHT@ @blacklist@ #end if ]]> </command> <inputs> <expand macro="multiple_input_bams" MIN="1"/> <expand macro="custom_sample_labels" /> <param argument="--BED" type="data" format="bed,gtf" multiple="true" optional="true" min="0" label="Regions of interest" help="Limits the coverage analysis to the regions specified in these files. This overrides --numberOfSamples. It is inadvisable to combine this with saving the raw counts." /> <conditional name="coverageOpt"> <param name="showCoverageOpt" type="select" label="Show coverage metrics options"> <option value="no" selected="true">No</option> <option value="yes">Yes</option> </param> <when value="no" /> <when value="yes"> <param argument="--outCoverageMetrics" type="boolean" label="Save per-threshold coverage metrics?"/> <repeat name="thresholds" title="Coverage Thresholds"> <param argument="--coverageThreshold" type="integer" min="0" label="Coverage Threshold" value="0"/> </repeat> </when> </conditional> <conditional name="advancedOpt"> <param name="showAdvancedOpt" type="select" label="Show advanced options" > <option value="no" selected="true">No</option> <option value="yes">Yes</option> </param> <when value="no" /> <when value="yes"> <param argument="--numberOfSamples" type="integer" value="100000" min="1" label="Number of samples" help="Number of samples taken from the genome to compute the scaling factors."/> <expand macro="plotWidthHeight" PLOTWIDTH="15.0" PLOTHEIGHT="5.0" /> <expand macro="region_limit_operation" /> <expand macro="read_processing_options" /> <expand macro="skipZeros" /> <expand macro="plotTitle" /> <expand macro="blacklist" /> </when> </conditional> <expand macro="input_image_file_format" /> <param argument="--outRawCounts" type="boolean" label="Save raw counts (coverages) to a file" help=""/> </inputs> <outputs> <expand macro="output_image_file_format_not_nested" /> <data format="tabular" name="outFileRawCounts" label="${tool.name} on ${on_string}: bin counts"> <filter>outRawCounts is True</filter> </data> <data format="tabular" name="outFileCoverageMetrics" label="${tool.name} on ${on_string}: Threshold Metrics"> <filter>coverageOpt.outCoverageMetrics is True</filter> </data> </outputs> <tests> <test> <param name="bamfiles" value="bowtie2 test1.bam,bowtie2 test1.bam" ftype="bam" /> <!--param name="outFileFormat" value="png" /--> <param name="showAdvancedOpt" value="yes" /> <param name="plotTitle" value="Test Title from Galaxy" /> <param name="outRawCounts" value="True" /> <output name="outFileRawCounts" file="plotCoverage_result1.tabular" ftype="tabular" /> <output name="outFileName" file="plotCoverage_result1.png" ftype="png" compare="sim_size" delta="2400" /> </test> <test> <param name="bamfiles" value="bowtie2 test1.bam,bowtie2 test1.bam" ftype="bam" /> <param name="showAdvancedOpt" value="yes" /> <param name="plotTitle" value="Test Title from Galaxy" /> <param name="showCoverageOpt" value="yes" /> <param name="coverageThreshold" value="0" /> <param name="coverageThreshold" value="5" /> <param name="coverageThreshold" value="10" /> <param name="coverageThreshold" value="20" /> <output name="outFileName" file="plotCoverage_result1.png" ftype="png" compare="sim_size" delta="2400" /> <output name="outFileCoverageMetrics" file="plotCoverage.metrics" ftype="tabular" /> </test> </tests> <help> <![CDATA[ What it does ------------- This tool is useful to **assess the sequencing depth** of a given sample. It samples 1 million bp, counts the number of overlapping reads and reports a coverage histogram that tells you how many bases are covered how many times. **Note:** Multiple BAM files are accepted but all should correspond to the same genome assembly. Output --------- The default output is a **panel of two plots** (see below for an example): One is a density plot visualizing the frequencies of read coverages, the other one lets you estimate what fraction of the genome has a depth of sequencing of, for example, 2 overlapping reads or more. The optional output is a table where each row represents the number of reads overlapping with a sampled bp. .. image:: $PATH_TO_IMAGES/plotCoverage_output.png :width: 600 :height: 345 Example plot ----------------- .. image:: $PATH_TO_IMAGES/plotCoverage_annotated.png :width: 600 :height: 291 @REFERENCES@ ]]> </help> <expand macro="citations" /> </tool>