Mercurial > repos > nilesh > rseqc

annotate geneBody_coverage.xml @ 49:6b33e31bda10 draft

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Uploaded tar based on https://github.com/lparsons/galaxy_tools/tree/master/tools/rseqc 1a3c419bc0ded7c40cb2bc3e7c87bfb01ddfeba2
author lparsons
date Thu, 16 Jul 2015 17:43:43 -0400
parents 2e6190c29c54
children f242ee103277
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49
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1 <tool id="rseqc_geneBody_coverage" name="Gene Body Converage (BAM)" version="2.4galaxy1">
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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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9
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10 <requirements>
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11 <expand macro="requirement_package_r" />
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12 <expand macro="requirement_package_numpy" />
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13 <expand macro="requirement_package_rseqc" />
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14 </requirements>
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16 <expand macro="stdio" />
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18 <version_command><![CDATA[geneBody_coverage.py --version]]></version_command>
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20 <command><![CDATA[
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21 #set $safename = ''.join(c in '_0123456789abcdefghijklmnopqrstuvwxyzABCDEFGHIJKLMNOPQRSTUVWXYZ' and c or '_' for c in $input.display_name)
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22 #set $fname = "d1_" + str($safename) + ".bam"
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23 ln -s '${input}' '${fname}' &&
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24 ln -s '${input.metadata.bam_index}' '${fname}.bai' &&
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25 echo '${fname}' > input_list.txt &&
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26 #for $i, $additional_input in enumerate($additionalinputs):
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27 #set $index = $i+2
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28 #set $safename = ''.join(c in '_0123456789abcdefghijklmnopqrstuvwxyzABCDEFGHIJKLMNOPQRSTUVWXYZ' and c or '_' for c in $additional_input.file.display_name)
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29 #set $fname = 'd' + str($index) + '_' + str($safename) + ".bam"
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30 ln -s '$additional_input.file' '${fname}' &&
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31 ln -s '$additional_input.file.metadata.bam_index' '${fname}.bai' &&
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32 echo '${fname}' >> input_list.txt &&
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33 #end for
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34 geneBody_coverage.py -i input_list.txt -r $refgene --minimum_length $minimum_length -o output
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35 ]]>
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36 </command>
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37
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38 <inputs>
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39 <param name="input" type="data" label="Input .bam File" format="bam" help="(--input-file)"/>
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40 <repeat name="additionalinputs" title="Additional input .bam files">
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41 <param name="file" type="data" label="Additional input .bam file" format="bam" />
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42 </repeat>
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43 <param name="refgene" type="data" format="bed" label="reference gene model" help="(--refgene)"/>
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44 <param name="minimum_length" type="integer" value="100" label="Minimum mRNA length in bp (default: 100)" help="mRNA that are shorter than this value will be skipped (--minimum_length)." />
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45 </inputs>
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46
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47 <outputs>
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48 <data name="outputcurvespdf" format="pdf" from_work_dir="output.geneBodyCoverage.curves.pdf" label="${tool.name} on ${on_string} (Curves PDF)" />
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49 <data name="outputheatmappdf" format="pdf" from_work_dir="output.geneBodyCoverage.heatMap.pdf" label="${tool.name} on ${on_string} (HeatMap PDF)">
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50 <filter>len(additionalinputs) >= 2</filter>
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51 </data>
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52 <data name="outputr" format="txt" from_work_dir="output.geneBodyCoverage.r" label="${tool.name} on ${on_string} (R Script)" />
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53 <data name="outputtxt" format="txt" from_work_dir="output.geneBodyCoverage.txt" label="${tool.name} on ${on_string} (Text)" />
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54 </outputs>
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56 <tests>
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57 <test>
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58 <param name="input" value="pairend_strandspecific_51mer_hg19_chr1_1-100000.bam"/>
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59 <param name="refgene" value="hg19_RefSeq_chr1_1-100000.bed"/>
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60 <output name="outputcurvespdf" file="output.geneBodyCoverage.curves.pdf"/>
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61 <output name="outputr" file="output.geneBodyCoverage.r"/>
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62 <output name="outputtxt" file="output.geneBodyCoverage.txt"/>
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63 </test>
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64 <test>
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65 <param name="input" value="pairend_strandspecific_51mer_hg19_chr1_1-100000.bam"/>
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66 <param name="file_0" value="pairend_strandspecific_51mer_hg19_chr1_1-100000.bam"/>
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67 <param name="file_1" value="pairend_strandspecific_51mer_hg19_chr1_1-100000.bam"/>
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68 <param name="refgene" value="hg19_RefSeq_chr1_1-100000.bed"/>
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69 <output name="outputcurvespdf" file="output2.geneBodyCoverage.curves.pdf"/>
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70 <output name="outputcurvespdf" file="output2.geneBodyCoverage.heatMap.pdf"/>
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71 <output name="outputr" file="output2.geneBodycoverage.r"/>
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72 <output name="outputtxt" file="output2.geneBodyCoverage.txt"/>
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73 </test>
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74
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75 </tests>
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77 <help><![CDATA[
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78 geneBody_coverage.py
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79 ++++++++++++++++++++
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80
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81 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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82
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83 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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84
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85 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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86 Coverage skewness was measured by `Pearson’s skewness coefficients <http://en.wikipedia.org/wiki/Skewness#Pearson.27s_skewness_coefficients>`_
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87
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88 .. image:: http://rseqc.sourceforge.net/_images/geneBody_workflow.png
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89 :width: 800 px
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90 :scale: 80 %
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91
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92
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93 Inputs
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94 ++++++++++++++
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95
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96 Input BAM/SAM file
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97 Alignment file in BAM/SAM format.
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98
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99 Reference gene model
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100 Gene Model in BED format.
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101
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102 Minimum mRNA length
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103 Minimum mRNA length (bp). mRNA that are shorter than this value will be skipped (default is 100).
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104
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105 Outputs
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106 ++++++++++++++
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107 Text
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108 Table that includes the data used to generate the plots
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109
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110 R Script
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111 R script file that reads the data and generates the plot
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112
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113 PDF
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114 The final plot, in PDF format
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115
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116 Example plots:
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117 .. image:: http://rseqc.sourceforge.net/_images/Aug_26.geneBodyCoverage.curves.png
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118 :height: 600 px
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119 :width: 600 px
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120 :scale: 80 %
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121
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122 .. image:: http://rseqc.sourceforge.net/_images/Aug_26.geneBodyCoverage.heatMap.png
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123 :height: 600 px
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124 :width: 600 px
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125 :scale: 80 %
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126
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127 -----
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128
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129 About RSeQC
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130 +++++++++++
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131
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132 The RSeQC_ package provides a number of useful modules that can comprehensively evaluate high throughput sequence data especially RNA-seq data. "Basic modules" quickly inspect sequence quality, nucleotide composition bias, PCR bias and GC bias, while "RNA-seq specific modules" investigate sequencing saturation status of both splicing junction detection and expression estimation, mapped reads clipping profile, mapped reads distribution, coverage uniformity over gene body, reproducibility, strand specificity and splice junction annotation.
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133
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134 The RSeQC package is licensed under the GNU GPL v3 license.
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135
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136 .. image:: http://rseqc.sourceforge.net/_static/logo.png
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137
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138 .. _RSeQC: http://rseqc.sourceforge.net/
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139 ]]>
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140 </help>
48
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141
49
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142 <expand macro="citations" />
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143
48
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144 </tool>