annotate rgFastQC.xml @ 7:ec73b7c83b2c draft

planemo upload for repository https://github.com/galaxyproject/tools-devteam/tree/master/tools/fastqc commit 8918618a5ef7bdca55a31cd919efa593044a376e
author devteam
date Wed, 02 Nov 2016 16:12:38 -0400
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1 <tool id="fastqc" name="FastQC" version="0.67">
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2 <description>Read Quality reports</description>
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3 <requirements>
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4 <requirement type="package" version="0.11.5">fastqc</requirement>
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5 </requirements>
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6 <stdio>
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7 <exit_code range="1:" />
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8 <exit_code range=":-1" />
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9 <regex match="Error:" />
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10 <regex match="Exception:" />
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11 </stdio>
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12 <command><![CDATA[
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13 python '$__tool_directory__'/rgFastQC.py
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14 -i "$input_file"
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15 -d "$html_file.files_path"
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16 -o "$html_file"
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17 -t "$text_file"
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18 -f "$input_file.ext"
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19 -j "$input_file.name"
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20 #if $contaminants.dataset and str($contaminants) > ''
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21 -c "$contaminants"
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22 #end if
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23 #if $limits.dataset and str($limits) > ''
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24 -l "$limits"
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25 #end if
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26 ]]></command>
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27 <inputs>
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28 <param format="fastqsanger,fastq,bam,sam" name="input_file" type="data" label="Short read data from your current history" />
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29 <param name="contaminants" type="data" format="tabular" optional="true" label="Contaminant list"
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30 help="tab delimited file with 2 columns: name and sequence. For example: Illumina Small RNA RT Primer CAAGCAGAAGACGGCATACGA"/>
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31 <param name="limits" type="data" format="txt" optional="true" label="Submodule and Limit specifing file"
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32 help="a file that specifies which submodules are to be executed (default=all) and also specifies the thresholds for the each submodules warning parameter" />
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33 </inputs>
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34 <outputs>
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35 <data format="html" name="html_file" label="${tool.name} on ${on_string}: Webpage" />
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36 <data format="txt" name="text_file" label="${tool.name} on ${on_string}: RawData" />
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37 </outputs>
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38 <tests>
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39 <test>
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40 <param name="input_file" value="1000gsample.fastq" />
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41 <param name="contaminants" value="fastqc_contaminants.txt" ftype="tabular" />
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42 <output name="html_file" file="fastqc_report.html" ftype="html" lines_diff="100"/>
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43 <output name="text_file" file="fastqc_data.txt" ftype="txt" lines_diff="100"/>
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44 </test>
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45 <test>
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46 <param name="input_file" value="1000gsample.fastq" />
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47 <param name="limits" value="fastqc_customlimits.txt" ftype="txt" />
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48 <output name="html_file" file="fastqc_report2.html" ftype="html" compare="sim_size" delta="4096"/>
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49 <output name="text_file" file="fastqc_data2.txt" ftype="txt" compare="sim_size"/>
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50 </test>
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51 <test>
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52 <param name="input_file" value="1000gsample.fastq.gz" />
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53 <param name="contaminants" value="fastqc_contaminants.txt" ftype="tabular" />
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54 <output name="html_file" file="fastqc_report.html" ftype="html" lines_diff="100"/>
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55 <output name="text_file" file="fastqc_data.txt" ftype="txt" lines_diff="100"/>
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56 </test>
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57 </tests>
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58 <help>
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59
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60 .. class:: infomark
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61
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62 **Purpose**
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63
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64 FastQC aims to provide a simple way to do some quality control checks on raw
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65 sequence data coming from high throughput sequencing pipelines.
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66 It provides a modular set of analyses which you can use to give a quick
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67 impression of whether your data has any problems of
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68 which you should be aware before doing any further analysis.
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69
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70 The main functions of FastQC are:
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71
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72 - Import of data from BAM, SAM or FastQ/FastQ.gz files (any variant),
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73 - Providing a quick overview to tell you in which areas there may be problems
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74 - Summary graphs and tables to quickly assess your data
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75 - Export of results to an HTML based permanent report
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76 - Offline operation to allow automated generation of reports without running the interactive application
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77
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78
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79 -----
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80
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81
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82 .. class:: infomark
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83
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84 **FastQC**
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85
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86 This is a Galaxy wrapper. It merely exposes the external package FastQC_ which is documented at FastQC_
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87 Kindly acknowledge it as well as this tool if you use it.
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88 FastQC incorporates the Picard-tools_ libraries for sam/bam processing.
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89
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90 The contaminants file parameter was borrowed from the independently developed
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91 fastqcwrapper contributed to the Galaxy Community Tool Shed by J. Johnson.
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92 Adaption to version 0.11.2 by T. McGowan.
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93
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94 -----
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95
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96 .. class:: infomark
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97
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98 **Inputs and outputs**
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99
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100 FastQC_ is the best place to look for documentation - it's very good.
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101 A summary follows below for those in a tearing hurry.
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102
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103 This wrapper will accept a Galaxy fastq, fastq.gz, sam or bam as the input read file to check.
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104 It will also take an optional file containing a list of contaminants information, in the form of
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105 a tab-delimited file with 2 columns, name and sequence. As another option the tool takes a custom
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106 limits.txt file that allows setting the warning thresholds for the different modules and also specifies
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107 which modules to include in the output.
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108
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109 The tool produces a basic text and a HTML output file that contain all of the results, including the following:
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110
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111 - Basic Statistics
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112 - Per base sequence quality
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113 - Per sequence quality scores
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114 - Per base sequence content
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115 - Per base GC content
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116 - Per sequence GC content
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117 - Per base N content
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118 - Sequence Length Distribution
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119 - Sequence Duplication Levels
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120 - Overrepresented sequences
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121 - Kmer Content
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122
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123 All except Basic Statistics and Overrepresented sequences are plots.
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124 .. _FastQC: http://www.bioinformatics.bbsrc.ac.uk/projects/fastqc/
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125 .. _Picard-tools: http://picard.sourceforge.net/index.shtml
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126
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127 </help>
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128 <citations>
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129 <citation type="bibtex">
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130 @ARTICLE{andrews_s,
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131 author = {Andrews, S.},
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132 keywords = {bioinformatics, ngs, qc},
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133 priority = {2},
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134 title = {{FastQC A Quality Control tool for High Throughput Sequence Data}},
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135 url = {http://www.bioinformatics.babraham.ac.uk/projects/fastqc/}
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136 }
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137 </citation>
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138 </citations>
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139 </tool>