Mercurial > repos > nilesh > rseqc

annotate geneBody_coverage.xml @ 3:71ed55a3515a draft

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planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/rseqc commit 37fb1988971807c6a072e1afd98eeea02329ee83
author iuc
date Tue, 14 Mar 2017 10:22:57 -0400
parents f92b87abef3d
children caaa120457bc
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1 <tool id="rseqc_geneBody_coverage" name="Gene Body Converage (BAM)" version="@WRAPPER_VERSION@">
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2 <description>
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3 Read coverage over gene body.
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4 </description>
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6 <macros>
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7 <import>rseqc_macros.xml</import>
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8 </macros>
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10 <expand macro="requirements" />
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12 <expand macro="stdio" />
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14 <version_command><![CDATA[geneBody_coverage.py --version]]></version_command>
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16 <command><![CDATA[
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17 #import re
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18 #set $input_list = []
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19 #for $i, $input in enumerate($inputs):
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20 #set $safename = re.sub('[^\w\-_]', '_', $input.element_identifier)
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21 #if $safename in $input_list:
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22 #set $safename = str($safename) + "." + str($i)
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23 #end if
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24 $input_list.append($safename)
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25 ln -sf '${input}' '${safename}.bam' &&
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26 ln -sf '${input.metadata.bam_index}' '${safename}.bam.bai' &&
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27 echo '${safename}.bam' >> 'input_list.txt' &&
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28 #end for
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29 geneBody_coverage.py -i 'input_list.txt' -r '${refgene}' --minimum_length ${minimum_length} -o output
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30 ]]>
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31 </command>
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33 <inputs>
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34 <param name="inputs" type="data" label="Input .bam file(s)" format="bam" help="(--input-file)" multiple="true"/>
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35 <expand macro="refgene_param" />
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36 <param name="minimum_length" type="integer" value="100" label="Minimum mRNA length (default: 100)" help="Minimum mRNA length in bp, mRNA that are shorter than this value will be skipped (--minimum_length)." />
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37 <expand macro="rscript_output_param" />
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38 </inputs>
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39
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40 <outputs>
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41 <data name="outputcurvespdf" format="pdf" from_work_dir="output.geneBodyCoverage.curves.pdf" label="${tool.name} on ${on_string} (Curves pdf)" />
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42 <data name="outputheatmappdf" format="pdf" from_work_dir="output.geneBodyCoverage.heatMap.pdf" label="${tool.name} on ${on_string} (HeatMap pdf)">
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43 <filter>len(inputs) >= 3</filter>
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44 </data>
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45 <expand macro="rscript_output_data" filename="output.geneBodyCoverage.r" />
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46 <data name="outputtxt" format="txt" from_work_dir="output.geneBodyCoverage.txt" label="${tool.name} on ${on_string} (text)" />
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47 </outputs>
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48
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49 <!-- PDF Files contain R version, must avoid checking for diff -->
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50 <tests>
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51 <test>
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52 <param name="inputs" value="pairend_strandspecific_51mer_hg19_chr1_1-100000.bam" />
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53 <param name="refgene" value="hg19_RefSeq_chr1_1-100000.bed" />
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54 <param name="rscript_output" value="true" />
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55 <output name="outputcurvespdf" file="output.geneBodyCoverage.curves.pdf" compare="sim_size" />
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56 <output name="outputr" file="output.geneBodyCoverage.r" />
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57 <output name="outputtxt" file="output.geneBodyCoverage.txt" />
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58 </test>
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59 <test>
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60 <param name="inputs" value="pairend_strandspecific_51mer_hg19_chr1_1-100000.bam,pairend_strandspecific_51mer_hg19_chr1_1-100000.bam,pairend_strandspecific_51mer_hg19_chr1_1-100000.bam" />
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61 <param name="refgene" value="hg19_RefSeq_chr1_1-100000.bed" />
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62 <param name="rscript_output" value="true" />
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63 <output name="outputcurvespdf" file="output2.geneBodyCoverage.curves.pdf" compare="sim_size" />
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64 <output name="outputheatmappdf" file="output2.geneBodyCoverage.heatMap.pdf" compare="sim_size" />
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65 <output name="outputr" file="output2.geneBodyCoverage.r" />
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66 <output name="outputtxt" file="output2.geneBodyCoverage.txt" />
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67 </test>
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68
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69 </tests>
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71 <help><![CDATA[
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72 ## geneBody_coverage.py
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74 Read coverage over gene body. This module is used to check if read coverage is uniform and if there is any 5\'/3\' bias. This module scales all transcripts to 100 nt and calculates the number of reads covering each nucleotide position. Finally, it generates plots illustrating the coverage profile along the gene body.
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75
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76 If 3 or more BAM files were provided. This program generates a lineGraph and a heatmap. If fewer than 3 BAM files were provided, only lineGraph is generated. See below for examples.
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77
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78 When heatmap is generated, samples are ranked by the "skewness" of the coverage: Sample with best (worst) coverage will be displayed at the top (bottom) of the heatmap.
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79 Coverage skewness was measured by `Pearson’s skewness coefficients <http://en.wikipedia.org/wiki/Skewness#Pearson.27s_skewness_coefficients>`_
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80
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81 .. image:: $PATH_TO_IMAGES/geneBody_workflow.png
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82 :width: 800 px
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83 :scale: 80 %
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84
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85
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86 ## Inputs
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88 Input BAM/SAM file
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89 Alignment file in BAM/SAM format.
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91 Reference gene model
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92 Gene Model in BED format.
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93
3
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94 Minimum mRNA length
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95 Minimum mRNA length (bp). mRNA that are shorter than this value will be skipped (default is 100).
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96
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97 ## Outputs
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98
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99 Text
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100 Table that includes the data used to generate the plots
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101
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102 R Script
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103 R script file that reads the data and generates the plot
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104
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105 PDF
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106 The final plot, in PDF format
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107
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108 Example plots:
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109 .. image:: $PATH_TO_IMAGES/Aug_26.geneBodyCoverage.curves.png
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110 :height: 600 px
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111 :width: 600 px
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112 :scale: 80 %
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113
3
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114 .. image:: $PATH_TO_IMAGES/Aug_26.geneBodyCoverage.heatMap.png
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115 :height: 600 px
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116 :width: 600 px
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117 :scale: 80 %
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118
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119 @ABOUT@
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120
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121 ]]>
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122 </help>
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123
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124 <expand macro="citations" />
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125
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126 </tool>