annotate je-markdupes.xml @ 8:a79f67128fc3 draft

planemo upload for repository https://git.embl.de/grp-gbcs/Je/tree/master/src/galaxy commit bc2365188e0dd0f20925884276a27914bb714280
author gbcs-embl-heidelberg
date Mon, 23 Apr 2018 05:47:37 -0400
parents e2d1b5e1eb11
children
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4ccf1406832d planemo upload for repository https://git.embl.de/grp-gbcs/Je/tree/master/src/galaxy commit dd9e62bdb01d1252a90ce778103ce9b6b4a8cd52-dirty
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1 <tool id="je_markdupes" name="Je-MarkDuplicates" version="@VERSION_STRING@">
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2 <description>to filter BAM files for read duplicates taking UMIs into account</description>
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3 <macros>
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4 <import>macros.xml</import>
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5 </macros>
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6 <expand macro="requirements" />
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7 <stdio>
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8 <exit_code range="1:" level="fatal" description="Tool exception" />
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9 </stdio>
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10 <expand macro="version_command" />
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11 <command>
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12 <![CDATA[
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13 je markdupes
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14
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15 ## picard MarkDuplicates defaults
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16 INPUT="${inputFile}"
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17 OUTPUT="${outFile}"
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18
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19 METRICS_FILE="${metrics_file}"
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20
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21 REMOVE_DUPLICATES="${remove_duplicates}"
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22 ASSUME_SORTED="${assume_sorted}"
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23
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24 #for $element in $adv_options.comments:
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25 COMMENT="${element.comment}"
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26 #end for
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27
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28 DUPLICATE_SCORING_STRATEGY="${adv_options.duplicate_scoring_strategy}"
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29
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30 #import pipes
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31 READ_NAME_REGEX=${ pipes.quote( str( $adv_options.read_name_regex ) ) or "''" }
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32 OPTICAL_DUPLICATE_PIXEL_DISTANCE="${adv_options.optical_duplicate_pixel_distance}"
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33
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34 VALIDATION_STRINGENCY="${adv_options.validation_stringency}"
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35 QUIET=true
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36 VERBOSITY=ERROR
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37
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38 ## Je Markdupes Specific
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39 MM=${MM}
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40 #if str($MAX_N) != "":
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41 MAX_N=${MAX_N}
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42 #end if
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43 @barcode_option_cmd@
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44
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45 #for $i, $option in enumerate( $repeat_slots )
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46 #if str($option.SLOTS) != "":
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47 SLOTS=${option.SLOTS}
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48 #end if
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49 #end for
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50
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51 #if str($trim_conditional.T) == "true":
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52 T=${trim_conditional.T}
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53 #for $i, $option in enumerate( $trim_conditional.repeat_tslots )
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54 #if str($option.TSLOTS) != "":
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55 TSLOTS=${option.TSLOTS}
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56 #end if
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57 #end for
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58 #end if
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59 ]]>
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60 </command>
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61 <configfiles>
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62 <expand macro="barcode_config_file"></expand>
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63 </configfiles>
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64
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65 <inputs>
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66 <param format="bam,sam" name="inputFile" type="data" label="Select SAM/BAM dataset"
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67 help="If empty, upload or import a SAM/BAM dataset"/>
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68 <param name="remove_duplicates" type="boolean" label="If true do not write duplicates to the output file
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69 instead of writing them with appropriate flags set" help="REMOVE_DUPLICATES; default=False"/>
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70 <param name="assume_sorted" type="boolean" label="Assume the input file is already sorted" checked="true"
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71 truevalue="true" falsevalue="false" help="ASSUME_SORTED; default=True"/>
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72 <conditional name="barcodes">
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73 <param name="barcode_list_type_con" type="select" label="Do you have a predefined list of UMIs">
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74 <option value="file" selected="true">A one column txt file from the history</option>
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75 <option value="text">Paste the UMI list in a text field</option>
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76 <option value="no_barcodes">No predefined list</option>
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77 </param>
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78
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79 <when value="file">
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80 <param name="BARCODE_FILE" type="data" format="tabular,txt" label="UMI file"
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81 help="BARCODE_FILE. Pre-defined list of Unique Molecular Identifiers that can be expected.
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82 Format: one column text file, one UMI per line. All UMIs MUST have the same length."/>
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83 </when>
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84
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85 <when value="text">
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86 <param name="barcode_text" type="text" area="True" size="10x30"
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87 value="barcode\n" label="Barcode file"
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88 help="BARCODE_FILE. Pre-defined list of Unique Molecular Identifiers that can be expected.
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89 Format: one column text file, one UMI per line. All UMIs MUST have the same length.">
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90 <sanitizer>
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91 <valid initial="string.printable"></valid>
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92 <mapping initial="none"/>
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93 </sanitizer>
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94 </param>
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95 </when>
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96 <when value="no_barcodes"/>
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97 </conditional>
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98 <repeat name="repeat_slots" min="1" title="Unique Molecular Identifier location">
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99 <param name="SLOTS" type="text" value="-1" label="Where to find the UMIs in the read name"
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100 help="SLOTS. The last position is considered by default (-1). See help below."/>
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101 </repeat>
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102 <param name="MM" type="integer" value="1" min="0"
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103 label="Number of maximum mismatches to consider two Unique Molecular Identifiers (UMIs) similar"
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104 help="MISMATCHES"/>
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105 <param name="MAX_N" type="text" value="" label="Maximum number of Ns a UMI can contain"
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106 help="MAX_NUMBER_OF_N. Above this value, reads are placed in a 'undefined' group.
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107 Default value is the MISMATCHES number."/>
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108 <param name="SPLIT" type="text" value=":" label="Character to split up the header" help="SPLIT"/>
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109 <conditional name="trim_conditional">
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110 <param name="T" type="select"
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111 label="Should barcode information be removed from read names in the output BAM" help="TRIM_HEADERS">
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112 <option value="true">Yes</option>
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113 <option value="false" selected="true">No</option>
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114 </param>
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115 <when value="true">
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116 <repeat name="repeat_tslots" min="1" title="Unique Molecular Identifier location for trimming">
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117 <param name="TSLOTS" type="text" value="-1"
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118 label="Where to find the UMIs in the read name that should be removed from the header"
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119 help="TSLOTS. Value for SLOTS is considered by default. See help below"/>
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120 </repeat>
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121 </when>
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122 <when value="false"/>
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123 </conditional>
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124 <section name="adv_options" title="Advanced Options" expanded="False">
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125 <repeat name="comments" title="Comment" min="0" help="You can provide multiple comments">
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126 <param name="comment" type="text" label="Add this comment to BAM dataset"/>
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127 </repeat>
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128
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129 <param name="duplicate_scoring_strategy" type="select" label="The scoring strategy for choosing the
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130 non-duplicate among candidates" help="DUPLICATE_SCORING_STRATEGY; default=SUM_OF_BASE_QUALITIES">
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131 <option value="SUM_OF_BASE_QUALITIES">SUM_OF_BASE_QUALITIES</option>
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132 <option value="TOTAL_MAPPED_REFERENCE_LENGTH">TOTAL_MAPPED_REFERENCE_LENGTH</option>
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133 </param>
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134
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135 <param name="read_name_regex" type="text" value="[a-zA-Z0-9]+:[0-9]:([0-9]+):([0-9]+):([0-9]+).*."
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136 label="Regular expression that can be used to parse read names in the incoming SAM/BAM dataset"
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137 help="READ_NAME_REGEX; Read names are parsed to extract three variables: tile/region, x coordinate and
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138 y coordinate. These values are used to estimate the rate of optical duplication in order to give a more
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139 accurate estimated library size. See help below for more info;
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140 default=[a-zA-Z0-9]+:[0-9]:([0-9]+):([0-9]+):([0-9]+).*.">
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141 <sanitizer>
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142 <valid initial="string.printable">
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143 </valid>
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144 </sanitizer>
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145 </param>
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146 <param name="optical_duplicate_pixel_distance" type="integer" value="100" min="0" max="500"
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147 label="The maximum offset between two duplicte clusters in order to consider them optical duplicates"
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148 help="OPTICAL_DUPLICATE_PIXEL_DISTANCE; default=100"/>
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149
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150 <param name="validation_stringency" type="select" label="Select validation stringency"
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151 help="Setting stringency to SILENT can improve performance when processing a BAM file in which
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152 variable-length data (read, qualities, tags) do not otherwise need to be decoded.">
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153 <option value="LENIENT" selected="True">Lenient</option>
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154 <option value="SILENT">Silent</option>
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155 <option value="STRICT">Strict</option>
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156 </param>
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157 </section>
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158 </inputs>
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159 <outputs>
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160 <data format="bam" name="outFile" label="${tool.name} on ${on_string}: Je-MarkDuplicates BAM output"/>
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161 <data format="txt" name="metrics_file" label="${tool.name} on ${on_string}: Je-MarkDuplicate metrics"/>
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162 </outputs>
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163
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164 <tests>
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165 <test>
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166 <!-- picard markduplicates default test -->
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167 <param name="inputFile" value="markdupes_DNase_sorted.bam" ftype="bam"/>
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168 <param name="barcode_list_type_con" value="file"/>
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169 <param name="BARCODE_FILE" value="markdupes_umis.txt" ftype="txt"/>
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170 <param name="repeat_slots_0|SLOTS" value="-1"/>
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171 <param name="repeat_slots_1|SLOTS" value="-2"/>
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172 <param name="MM" value="2"/>
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173 <param name="MAX_N" value="1"/>
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174 <param name="comment" value="test-run"/>
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175 <param name="assume_sorted" value="True"/>
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176 <param name="remove_duplicates" value="True"/>
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177 <param name="read_name_regex" value="[a-zA-Z0-9]+:[0-9]:([0-9]+):([0-9]+):([0-9]+).*."/>
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178 <param name="optical_duplicate_pixel_distance" value="100"/>
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179 <param name="duplicate_scoring_strategy" value="SUM_OF_BASE_QUALITIES"/>
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180 <param name="validation_stringency" value="LENIENT"/>
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181 <output name="outFile" file="markdupes_DNase_sorted_marked.bam" ftype="bam" lines_diff="2"/>
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182 <output name="metrics_file" file="markdupes_metrics.txt" ftype="txt" lines_diff="4"/>
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183 </test>
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184 </tests>
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185
5
e2d1b5e1eb11 planemo upload for repository https://git.embl.de/grp-gbcs/Je/tree/master/src/galaxy commit 0eefd837333dae6fbecaf4f55b053268d844eff6
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186 <help>
0
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187 <![CDATA[
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188 **What it does**
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189
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190 Je MarkDupes: Examines aligned records in the supplied SAM or BAM file to locate duplicate molecules taking into account
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191 molecular barcodes (Unique Molecular Identifiers or UMIs) found in read header.
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192 All records are then either written to the output file with the duplicate records flagged or trashed.
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193
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194 Input file is a bam file.
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195
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196 Author: Charles Girardot (charles.girardot@embl.de).
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197
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198 Wrapper by: Jelle Scholtalbers (jelle.scholtalbers@embl.de).
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199
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200 ------
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201
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202 **Know what you are doing**
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203
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204 .. class:: warningmark
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205
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206 You will want to read the `documentation`__.
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207
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208 .. __: http://gbcs.embl.de/portal/Je
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209
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210 ------
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211
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212 **Parameter list**
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213
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214 This is an exhaustive list of options::
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215
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216 INPUT=String
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217 I=String
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218
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219 One or more input SAM or BAM files to analyze. Must be coordinate sorted.
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220
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221 Default value: null. This option may be specified 0 or more times.
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222
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223 OUTPUT=File
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224 O=File
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225
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226 The output file to write marked records to
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227
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228 Required.
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229
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230 MISMATCHES=Integer
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231 MM=Integer
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232
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233 Number of MisMatches (inclusive) to still consider two Unique Molecular Identifiers
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234 (UMIs) the same i.e. this option buffers for sequencing errors.
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235 Indeed, in case of a sequencing error, 2 duplicate reads would not be considered
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236 duplicates anymore.
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237 Note that N are not considered mismatches during comparison ie ATTNGG and NTTANG are seen
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238 as the same barcode and these two reads would be flagged duplicates.
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239 This option takes a single value even when several barcodes are present (see SLOTS).
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240 Note that when declaring several barcodes (see SLOTS) AND providing a predefined set
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241 of barcodes (see BC option), the MM value is applicable in each lookup. When a predefined
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242 set of barcodes is NOT given, the different barcodes (SLOTS) are concatenated first and
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243 the MM value is therefore considered *overall* as the concatenated code is seen as a
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244 unique code.
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245 MM=null is like MM=0
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246 Use the minimum Hamming distance of the original barcode set (if applicable).
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247
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248 Required.
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249
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250 MAX_NUMBER_OF_N=Integer
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251 MAX_N=Integer
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252
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253 Maximum number of Ns a molecular code can contain (inclusive). Above this value, reads
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254 are placed in a UNDEF group.
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255 More precisely, these 'too degenarate' codes will not :
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256 * be compared to the list of predefined codes [predefined code list situation ie BC
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257 option given] nor
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258 * be considered as a potential independent code [no predefined code list situation ie
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259 BC option not given]
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260 Default value is the MISMATCHES number.
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261 Note that when declaring several barcodes (see SLOTS) AND providing a predefined set
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262 of barcodes (see BC option), the MAX_N value is applicable to each barcode. When a
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263 predefined set
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264 of barcodes is NOT given, the different barcodes (SLOTS) are concatenated first and the
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265 MAX_N value
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266 is therefore considered *overall*.
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267
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268 Default value: null.
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269
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270
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271 SLOTS=Integer
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272 SLOTS=Integer
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273
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274 Where to find the UMIs (and only the UMIs) in the read name once read name has been
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275 tokenized using the SPLIT character (e.g. ':').
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276 By default, the UMI is considered to be found at the end of the read header i.e. after
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277 the last ':'. Use this option to indicate other or additional UMI positions (e.g.
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278 multiple UMIs present in read header.
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279 IMPORTANT: counting starts at 1 and negative numbers can be used to start counting from
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280 the end.
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281 For example, consider the following read name that lists 3 different barcodes in the end:
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282 HISEQ:44:C6KC0ANXX:8:2112:20670:79594:CGATGTTT:GATCCTAG:AAGGTACG
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283 to indicate that the three barcodes are molecular codes, use
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284 SLOTS=-1 SLOTS=-2 SLOTS=-3
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285 if only the 2 last ones should be considered (the third one being a sample encoding
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286 barcode), use
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287 SLOTS=-1 SLOTS=-2
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288
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289 Default value: null. This option may be specified 0 or more times.
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290
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291 BARCODE_FILE=File
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292 BC=File
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293
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294 Pre-defined list of UMIs that can be expected. Format: one column text file, one barcode
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295 per line. All UMIs MUST have the same length.
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296
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297 Default value: null.
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298
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299 TRIM_HEADERS=Boolean
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300 T=Boolean
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301
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302 Should barcode information be removed from read names in the output BAM?
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303
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304 Default value: false. This option can be set to 'null' to clear the default value.
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305 Possible values: {true, false}
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306
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307 TSLOTS=Integer
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308 TSLOTS=Integer
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309
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310 Where to find *all* barcode(s) (i.e. sample encoding and UMIs) in the read name once has
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311 been tokenized using the SPLIT character (e.g. ':').
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312 This option is only considered when TRIM_HEADERS=true. When TSLOTS is ommited while
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313 TRIM_HEADERS=true, the values of SLOTS apply.
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314 IMPORTANT : counting starts at 1 and negative numbers can be used to start counting from
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315 the end.
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316 See SLOT help for examples.
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317
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318 Default value: null. This option may be specified 0 or more times.
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319
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320 SPLIT_CHAR=String
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321 SPLIT=String
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322
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323 Character to use to split up the read header line, default is ':'.
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324
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325 Default value: ':'. This option can be set to 'null' to clear the default value.
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326
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327 INPUT=String
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328 I=String
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329
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330 One or more input SAM or BAM files to analyze. Must be coordinate sorted.
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331
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332 Default value: null. This option may be specified 0 or more times.
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333
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334 OUTPUT=File
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335 O=File
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336
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337 The output file to write marked records to Required.
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338
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339 METRICS_FILE=File
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340 M=File
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341
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342 File to write duplication metrics to Required.
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343
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344 COMMENT=String
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345 CO=String
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346
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347 Comment(s) to include in the output file's header.
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348
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349 Default value: null. This option may be specified 0 or more times.
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350
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351 REMOVE_DUPLICATES=Boolean
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352
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353 If true do not write duplicates to the output file instead of writing them with
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354 appropriate flags set.
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355
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356 Default value: false. This option can be set to 'null' to clear
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357 the default value.
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358 Possible values: {true, false}
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359
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360 ASSUME_SORTED=Boolean
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361 AS=Boolean
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362
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363 If true, assume that the input file is coordinate sorted even if the header says
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364 otherwise.
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365
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366 Default value: false. This option can be set to 'null' to clear the default
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367 value.
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368 Possible values: {true, false}
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369
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370 DUPLICATE_SCORING_STRATEGY=ScoringStrategy
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371 DS=ScoringStrategy
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372
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373 The scoring strategy for choosing the non-duplicate among candidates.
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374
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375 Default value: SUM_OF_BASE_QUALITIES. This option can be set to 'null' to clear the default value.
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376 Possible values: {SUM_OF_BASE_QUALITIES, TOTAL_MAPPED_REFERENCE_LENGTH}
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377
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378 READ_NAME_REGEX=String
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379
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380 Regular expression that can be used to parse read names in the incoming SAM file. Read
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381 names are parsed to extract three variables: tile/region, x coordinate and y coordinate.
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382 These values are used to estimate the rate of optical duplication in order to give a more
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383 accurate estimated library size. Set this option to null to disable optical duplicate
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384 detection. The regular expression should contain three capture groups for the three
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385 variables, in order. It must match the entire read name. Note that if the default regex
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386 is specified, a regex match is not actually done, but instead the read name is split on
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387 colon character. For 5 element names, the 3rd, 4th and 5th elements are assumed to be
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388 tile, x and y values. For 7 element names (CASAVA 1.8), the 5th, 6th, and 7th elements
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389 are assumed to be tile, x and y values.
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390
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391 Default value:
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392 [a-zA-Z0-9]+:[0-9]:([0-9]+):([0-9]+):([0-9]+).*. This option can be set to 'null' to
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393 clear the default value.
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394
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395 OPTICAL_DUPLICATE_PIXEL_DISTANCE=Integer
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396
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397 The maximum offset between two duplicte clusters in order to consider them optical
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398 duplicates. This should usually be set to some fairly small number (e.g. 5-10 pixels)
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399 unless using later versions of the Illumina pipeline that multiply pixel values by 10, in
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400 which case 50-100 is more normal.
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401
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402 Default value: 100. This option can be set to 'null'
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403 to clear the default value.
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404
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405 ]]>
5
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406 </help>
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407 <expand macro="citations"/>
0
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408 </tool>