annotate stacks_shortreads.xml @ 1:1974fee35ca7 draft

"planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/stacks2 commit c300b84615660459bb0020fa74ccd3b874d329a4"
author iuc
date Mon, 30 Sep 2019 14:16:13 -0400
parents ad7a60726fc3
children 43e3eeb2e0ec
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ad7a60726fc3 planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/stacks2 commit b395fa36fa826e26085820ba3a9faacaeddcb460
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1 <!-- this is essentially a copy of stacks_procrad minus the unsupported options -->
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2 <tool id="stacks2_shortreads" name="Stacks2: process shortreads" profile="@PROFILE@" version="@STACKS_VERSION@+galaxy@WRAPPER_VERSION@">
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3 <description>fast cleaning of randomly sheared genomic or transcriptomic data</description>
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4 <macros>
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5 <import>macros.xml</import>
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6 <import>macros_process.xml</import>
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7 </macros>
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8 <expand macro="requirements"/>
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9 <expand macro="version_cmd"/>
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10 <command detect_errors="aggressive"><![CDATA[
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11 @FASTQ_INPUT_FUNCTIONS@
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13 mkdir stacks_inputs stacks_outputs &&
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1
1974fee35ca7 "planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/stacks2 commit c300b84615660459bb0020fa74ccd3b874d329a4"
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15 #if $output_log
1974fee35ca7 "planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/stacks2 commit c300b84615660459bb0020fa74ccd3b874d329a4"
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16 ln -s '$output_log' stacks_outputs/process_shortreads.log &&
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17 #end if
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18
0
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19 #set ($link_command, $inputype) = $fastq_input_nonbatch( $input_type.fqinputs, $input_type.input_type_select, "_R%d_0" )
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20 $link_command
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ad7a60726fc3 planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/stacks2 commit b395fa36fa826e26085820ba3a9faacaeddcb460
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ad7a60726fc3 planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/stacks2 commit b395fa36fa826e26085820ba3a9faacaeddcb460
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23 process_shortreads
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25 @PROCESS_IOOPTIONS@
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26 @PROCESS_FILTER@
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27 @COMMON_ADVANCED@
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28 @RESCUE_BARCODE@
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29 @PROCESS_ADAPTER@
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31 ## advanced options not shared between shortreads and radtags
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32 $options_advanced.no_read_trimming
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33 $options_advanced.mate_pair
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34 $options_advanced.no_overhang
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36 @PROCESS_FASTQ_POSTPROC@
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37 ]]></command>
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38
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39 <inputs>
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40 <expand macro="fastq_input_bc_file" multiple="true" listtype="list:paired"/>
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41 <section name="options_advanced" title="advanced options" expanded="False">
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42 <expand macro="common_advanced"/>
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43 <param argument="--no_read_trimming" type="boolean" checked="false" truevalue="--no_read_trimming" falsevalue="" label="Do not trim low quality reads, just discard them" />
ad7a60726fc3 planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/stacks2 commit b395fa36fa826e26085820ba3a9faacaeddcb460
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44 <param argument="--mate-pair" name="mate_pair" type="boolean" checked="false" truevalue="--mate-pair" falsevalue="" label="Raw reads are circularized mate-pair data, first read will be reverse complemented" />
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45 <param argument="--no_overhang" type="boolean" checked="false" truevalue="--no_overhang" falsevalue="" label="Data does not contain an overhang nucleotide between barcode and seqeunce" />
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46 <expand macro="rescue_barcode"/>
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47 <expand macro="process_adapter"/>
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48 </section>
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49 <expand macro="process_filter"/>
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50 <expand macro="process_output_types"/>
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51 </inputs>
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52
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53 <outputs>
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54 <data format="txt" name="output_log" label="${tool.name} on ${on_string} log file" from_work_dir="stacks_outputs/process_shortreads.log" />
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55 <expand macro="process_outputs"/>
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56 </outputs>
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57
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58 <tests>
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59 <!-- test single end, default options -->
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60 <test>
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61 <param name="input_type|input_type_select" value="single"/>
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62 <param name="input_type|fqinputs" ftype="fastqsanger" value="procrad/R1.fq"/>
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63 <param name="input_type|barcode_encoding" value="--inline_null"/>
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64 <param name="barcode" value="procrad/barcodes"/>
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65 <param name="add_log" value="yes" />
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66 <output name="output_log" file="shortreads/process_shortreads.out" lines_diff="4"/>
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67 <output_collection name="demultiplexed" count="40">
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68 <element name="PopA_01" file="shortreads/PopA_01.fq" ftype="fastqsanger" />
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69 </output_collection>
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70 </test>
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71 <!-- test single end, default options -->
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72 <test>
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73 <param name="input_type|input_type_select" value="paired"/>
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74 <param name="input_type|fqinputs">
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75 <collection type="list:paired">
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76 <element name="reads">
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77 <collection type="paired">
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78 <element name="forward" value="procrad/R1.fq" ftype="fastqsanger" />
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79 <element name="reverse" value="procrad/R2.fq" ftype="fastqsanger"/>
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80 </collection>
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81 </element>
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82 </collection>
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83 </param>
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84 <param name="input_type|barcode_encoding" value="--inline_null"/>
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85 <param name="barcode" value="procrad/barcodes"/>
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86 <param name="capture" value="-D"/>
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87 <param name="no_read_trimming" value="--no_read_trimming" />
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88 <param name="mate_pair" value="--mate-pair" />
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89 <param name="no_overhang" value="--no_overhang" />
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90 <param name="outype" value="gzfastq"/>
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91 <param name="add_log" value="yes" />
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92 <assert_command>
1
1974fee35ca7 "planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/stacks2 commit c300b84615660459bb0020fa74ccd3b874d329a4"
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93 <has_text text="-D" />
0
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94 <has_text text="--no_read_trimming" />
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95 <has_text text="--mate-pair" />
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96 <has_text text="--no_overhang" />
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97 </assert_command>
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98 <output name="output_log" file="shortreads/process_shortreads.out" compare="sim_size"/>
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99 <output_collection name="demultiplexed_paired" type="list:paired" count="40">
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100 <element name="PopA_01">
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101 <element name="forward" value="shortreads/PopA_01.forward.fq.gz" ftype="fastqsanger.gz" compare="sim_size"/>
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102 <element name="reverse" value="shortreads/PopA_01.reverse.fq.gz" ftype="fastqsanger.gz" compare="sim_size"/>
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103 </element>
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104 </output_collection>
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105 <output_collection name="remaining" type="list:paired" count="40">
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106 <element name="PopA_01">
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107 <element name="forward" file="shortreads/PopA_01.rem.forward.fq.gz" ftype="fastqsanger.gz"/>
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108 <element name="reverse" file="shortreads/PopA_01.rem.reverse.fq.gz" ftype="fastqsanger.gz"/>
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109 </element>
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110 </output_collection>
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111 <output_collection name="discarded_paired" type="list:paired" count="1">
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112 <element name="reads">
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113 <element name="forward" file="shortreads/reads.forward.fq" ftype="fastqsanger"/>
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114 <element name="reverse" file="shortreads/reads.forward.fq" ftype="fastqsanger"/>
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115 </element>
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116 </output_collection>
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117 </test>
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118 </tests>
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119 <help>
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120 <![CDATA[
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121 .. class:: infomark
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122
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123 **What it does**
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124
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125 Performs the same task as process_radtags for fast cleaning of randomly sheared genomic or transcriptomic data, not for RAD data.
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126
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127 **Help**
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128
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129 Input files:
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130
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131 - FASTQ
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132
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133 - Barcode File Format
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134
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135 The barcode file is a very simple format:
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136
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137 ======= ===========
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138 Barcode Sample name
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139 ======= ===========
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140 ATGGGG PopA_01
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141 GGGTAA PopA_02
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142 AGGAAA PopA_03
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143 TTTAAG PopA_04
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144 GGTGTG PopA_05
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145 TGATGT PopA_06
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146 ======= ===========
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147
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148 Combinatorial barcodes are specified, one per column, separated by a tab:
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149
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150 ======== ======== ===========
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151 Barcode1 Barcode2 Sample name
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152 ======== ======== ===========
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153 CGATA ACGTA PopA_01
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154 CGGCG CGTA PopA_02
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155 GAAGC CGTA PopA_03
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156 GAGAT CGTA PopA_04
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157 CGATA AGCA PopA_05
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158 CGGCG AGCA PopA_06
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159 ======== ======== ===========
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160
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161 @STACKS_INFOS@
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162 ]]>
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163 </help>
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164 <expand macro="citation" />
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165 </tool>