annotate pyCRAC/pyBinCollector.xml @ 1:7c9574213c0a draft default tip

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author swebb
date Thu, 20 Jun 2013 12:13:43 -0400
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1 <tool id ="pyBinCollector" name="pyBinCollector">
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2 <requirements>
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3 <requirement type="package">pyCRAC</requirement>
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4 </requirements>
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5 <command interpreter="perl">
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6 pyBinCollector.pl
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7 -f $input
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8 --gtf $addGTF.gtf
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9 #if $addGTF.gtfFile == "default" and $addGTF.annotate.annotations == "auto":
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10 --annotation $addGTF.annotate.scan.annotation
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11 #else:
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12 --annotation $addGTF.annotate.annotation
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13 #end if#
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14 #if $addOpt.options == "edit":
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15 --options
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16 --range $addOpt.range
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17 --min_length $addOpt.min_length
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18 --max_length $addOpt.max_length
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19 --numberofbins $addOpt.numberofbins
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20 -s $addOpt.sequence
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21 #if $addOpt.limitBins.binselect == "yes":
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22 --bins1 $addOpt.limitBins.bs_first
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23 --bins2 $addOpt.limitBins.bs_last
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24 #end if#
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25 $addOpt.ignore
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26 $addOpt.oall.outputall
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27 #end if#
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28 -o "$input.name"
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29 #if $addOpt.options == "edit" and $addOpt.oall.outputall == "--outputall":
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30 --id $sd.id
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31 --sd $sd
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32 --ssub $ssub
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33 --sdel $sdel
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34 --asd $asd
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35 --assub $assub
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36 --asdel $asdel
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37 #else:
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38 --out $out
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39 --id $out.id
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40 #end if#
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41 </command>
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42 <version_command>/usr/local/bin/pyBinCollector.py --version</version_command>
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43 <inputs>
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44 <param format="gtf" name="input" type="data" label="Input File -f" help="pyReadCounters or pyMotif gtf output files" />
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45
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46 <conditional name="addGTF">
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47 <param name="gtfFile" type="select" label="Choose GTF File from">
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48 <option value="default" selected="true">Defaults</option>
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49 <option value="other">History</option>
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50 </param>
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51 <when value="default">
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52 <param name="gtf" type="select" label="GTF File --gtf" help="GTF file containing gene ID co-ordinates">
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53 <options from_data_table="pycrac_gtf"/>
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54 </param>
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55
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56 <conditional name="annotate">
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57 <param name="annotations" type="select" label="Select annotation">
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58 <option value="all" selected="true">All</option>
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59 <option value="manual">Enter in text box</option>
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60 <option value="auto">Scan pyGetGTFSources file</option>
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61 </param>
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62 <when value="all">
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63 <param name="annotation" type="hidden" format="txt" size="10" value="all"/>
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64 </when>
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65 <when value="manual">
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66 <param name="annotation" type="text" format="txt" size="100" value="protein_coding" label="Select which annotation to focus search on --annotation" help="To find a list of available annotations please use pyGetGTFSources tool">
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67 <validator type="empty_field" message="Please enter a value"/>
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68 </param>
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69 </when>
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70 <when value="auto">
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71 <param format="tabular" name="gtf_annotation" type="data" label="GTF annotation File (pyGetGTFSources output)" help="Tabular file containing unique list of annotations/sources in selected GTF file. Refer to pyGetGTFSources"/>
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72 <conditional name="scan">
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73 <param name="annotations" type="select" label="Scan this file for annotations" help="Choose the correct GTF file then choose GO">
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74 <option value="wait" selected="true">Waiting</option>
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75 <option value="scanning">Go</option>
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76 </param>
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77 <when value="wait">
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78 </when>
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79 <when value="scanning">
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80 <param name="annotation" type="select" multiple="false" label="Select which annotation to focus search on --annotation">
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81 <options from_dataset="gtf_annotation">
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82 <column name="name" index="0"/>
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83 <column name="value" index="0"/>
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84 </options>
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85 </param>
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86 </when>
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87 </conditional>
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88 </when>
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89 </conditional>
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90
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91 </when>
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92 <when value="other">
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93 <param format="gtf" name="gtf" type="data" label="GTF File --gtf" help="GTF file containing gene ID co-ordinates"/>
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94 <conditional name="annotate">
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95 <param name="annotations" type="select" label="Select annotation">
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96 <option value="all" selected="true">All</option>
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97 <option value="manual">Enter in text box</option>
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98 <option value="auto">Scan selected file</option>
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99 </param>
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100 <when value="all">
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101 <param name="annotation" type="hidden" format="txt" size="10" value="all"/>
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102 </when>
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103 <when value="manual">
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104 <param name="annotation" type="text" format="txt" size="100" value="protein_coding" label="Select which annotation to focus search on --annotation" help="To find a list of available annotations please use pyGetGTFSources tool">
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105 <validator type="empty_field" message="Please enter a value"/>
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106 </param>
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107 </when>
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108 <when value="auto">
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109 <param name="annotation" type="select" multiple="false" label="Select which annotation to focus search on --annotation">
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110 <options from_dataset="gtf">
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111 <column name="name" index="1"/>
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112 <column name="value" index="1"/>
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113 <filter type="unique_value" name="unique" column="1"/>
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114 </options>
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115 </param>
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116 </when>
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117 </conditional>
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118 </when>
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119 </conditional>
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120
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121
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122 <conditional name="addOpt">
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123 <param name="options" type="select" label="Options">
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124 <option value="default" selected="true">Default</option>
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125 <option value="edit">Edit</option>
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126 </param>
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127 <when value="edit">
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128 <param format="integer" name="range" type="integer" label="Range --range" value="0" size="5" help="Manually set the length of the 5' and 3' UTRs 0>50000">
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129 <validator type="in_range" min="0" max="50000" message="Please enter a value between 0 and 50000"/>
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130 </param>
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131 <param format="integer" name="numberofbins" type="integer" label="Set the number of bins --numberofbins" value="20" size="7" help="Set the number of bins you want to divide the genes into">
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132 <validator type="in_range" min="20" max="1000" message="Please enter a value between 20 and 1000"/>
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133 </param>
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134 <param format="integer" name="min_length" type="integer" label="Set the minimum gene length (nt) --min_length" value="50" size="7" help="To filter the data for gene length (nucleotides)" >
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135 <validator type="in_range" min="20" message="Please enter a value greater than 20"/>
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136 </param>
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137 <param format="integer" name="max_length" type="integer" label="Set the maximum gene length (nt) --max_length" help="Default = 100000000" value="100000000" size="10" >
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138 <validator type="in_range" min="50" max="100000000" message="Please enter a value between 50 and 100000000"/>
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139 </param>
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140 <param name="sequence" type="select" label="What sequences do you want to run pyBinCollector on? --sequence">
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141 <option value="genomic" selected="true">Genomic Sequence</option>
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142 <option value="coding">Coding Sequence</option>
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143 <option value="intron">Introns</option>
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144 <option value="exon">Exons</option>
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145 <option value="CDS">CDS</option>
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146 <option value="5UTR">5UTR</option>
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147 <option value="3UTR">3UTR</option>
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148 </param>
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149 <conditional name="limitBins">
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150 <param name="binselect" type="select" label="Select sequences that map to specific bins --binselect">
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151 <option value="no" selected="true">No</option>
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152 <option value="yes">Yes</option>
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153 </param>
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154 <when value="yes">
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155 <param format="integer" name="bs_first" type="integer" label="Select First Bin" value="1" size="7">
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156 <validator type="in_range" min="1" message="Please enter a value greater than 0"/>
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157 </param>
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158 <param format="integer" name="bs_last" type="integer" label="Select Last Bin" value="2" size="7">
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159 <validator type="in_range" min="2" message="Please enter a value greater than 0"/>
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160 </param>
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161 </when>
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162 <when value="no">
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163 </when>
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164 </conditional>
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165 <param name="ignore" type="select" label="Ignore strand information? --ignorestrand">
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166 <option value="" selected="true">No</option>
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167 <option value="--ignorestrand">Yes</option>
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168 </param>
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169 <conditional name="oall">
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170 <param name="outputall" type="select" label="Output all genes --outputall" help="output the normalized distribution for each individual gene, rather than making a cumulative coverage plot">
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171 <option value="" selected="true">No</option>
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172 <option value="--outputall">Yes</option>
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173 </param>
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174 <when value="--outputall"/>
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175 <when value=""/>
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176 </conditional>
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177 </when>
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178 <when value="default">
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179 </when>
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180 </conditional>
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181 <param name="label" type="text" format="txt" size="30" value="pyBinCollector" label="Enter output file label -o" />
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182 </inputs>
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183
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184 <outputs>
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185 <data format="gtf" name="out" label="${label.value}.gtf">
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186 <filter>addOpt['oall']['outputall'] == ""</filter>
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187 </data>
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188 <data format="txt" name="sd" label="sense_data_${label.value}.txt">
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189 <filter>addOpt['options'] == "edit" and addOpt['oall']['outputall'] == "--outputall"</filter>
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190 </data>
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191 <data format="txt" name="ssub" label="sense_subs_${label.value}.txt">
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192 <filter>addOpt['options'] == "edit" and addOpt['oall']['outputall'] == "--outputall"</filter>
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193 </data>
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194 <data format="txt" name="sdel" label="sense_dels_${label.value}.txt">
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195 <filter>addOpt['options'] == "edit" and addOpt['oall']['outputall'] == "--outputall"</filter>
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196 </data>
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197 <data format="txt" name="asd" label="anti_sense_data_${label.value}.txt">
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198 <filter>addOpt['options'] == "edit" and addOpt['oall']['outputall'] == "--outputall"</filter>
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199 </data>
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200 <data format="txt" name="assub" label="anti_sense_subs_${label.value}.txt">
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201 <filter>addOpt['options'] == "edit" and addOpt['oall']['outputall'] == "--outputall"</filter>
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202 </data>
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203 <data format="txt" name="asdel" label="anti_sense_dels_${label.value}.txt">
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204 <filter>addOpt['options'] == "edit" and addOpt['oall']['outputall'] == "--outputall"</filter>
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205 </data>
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206 </outputs>
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207 <help>
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208
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209
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210 .. class:: infomark
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211
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212 **pyBinCollector**
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213
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214 pyBinCollector is part of the pyCRAC_ package. Allows the user to generate genome-wide coverage plots. Normalises gene lengths by dividing genes into a
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215 fixed number of bins and then calculates the hit density in each bin. The program also allows the user to input specific bin numbers to extract
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216 blocks/clusters present in these bins.
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217
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218
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219 .. _pyCRAC: http://sandergranneman.bio.ed.ac.uk/Granneman_Lab/pyCRAC_software.html
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220
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221 ------
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222
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223 **Parameter list**
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224
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225 File input options::
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226
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227 -f FILE, --input_file=FILE
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228 Provide the path and name of the pyReadCounters.py or
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229 pyMotif.py GTF file. By default the program expects
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230 data from the standard input.
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231 -o OUTPUT_FILE, --output_file=OUTPUT_FILE
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232 To set an output file name. Do not add a file
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233 extension. By default, if the --outputall flag is not
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234 used, the program writes to the standard output.
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235 --gtf=yeast.gtf
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236 type the path to the gtf annotation file that you want
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237 to use. Default is /usr/local/pyCRAC/db/Saccharomyces_
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238 cerevisiae.EF2.59.1.2.gtf
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239
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240 pyBinCollector.py specific options::
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241
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242 -a protein_coding, --annotation=protein_coding
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243 select which annotation (i.e. protein_coding, ncRNA,
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244 sRNA, rRNA, tRNA, snoRNA, all) you would like to focus
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245 your search on. Default = all
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246 --min_length=20
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247 to set a minimum length threshold for genes. Genes
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248 shorter than the minimal length will be discarded.
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249 Default = 1
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250 --max_length=10000
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251 to set a maximum length threshold for genes. Genes
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252 larger than the maximum length will be discarded.
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253 Default = 100000000
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254 -n 20, --numberofbins=20
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255 select the number of bins you want to generate.
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256 Default=20
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257 --binselect=2 4
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258 allows selection of sequences that were mapped to
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259 specific bins. This option expects two numbers, one
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260 for each bin, separated by a space. For example:
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261 --binselect 20 30.
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262 --outputall
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263 use this flag to output the normalized distribution
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264 for each individual gene, rather than making a
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265 cumulative coverage plot. Useful for making box plots
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266 or for making heat maps.
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267
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268 Common options::
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269
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270 -r 100, --range=100
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271 allows you to set the length of the UTR regions. If
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272 you set '-r 50' or '--range=50', then the program will
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273 set a fixed length (50 bp) regardless of whether the
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274 GTF file has genes with annotated UTRs.
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275 -s intron, --sequence=intron
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276 with this option you can select whether you want to
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277 generate bins from the coding or genomic sequence or
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278 introns,exon,CDS, or UTR coordinates. Default =
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279 genomic
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280 --ignorestrand
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281 To ignore strand information and all reads overlapping
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282 with genomic features will be considered sense reads.
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283 Useful for analysing ChIP or RIP data
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284
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285
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286
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287
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288
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289 </help>
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290 </tool>