annotate bowtie2_wrapper.xml @ 4:1fc845afa3ac draft

planemo upload for repository https://github.com/galaxyproject/tools-devteam/tree/master/tools/bowtie2 commit 32fe80982b5c59687eece667f0372002588566f8-dirty
author devteam
date Tue, 21 Jul 2015 13:00:51 -0400
parents ceb6467e276c
children 42bb952b4e3c
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1fc845afa3ac planemo upload for repository https://github.com/galaxyproject/tools-devteam/tree/master/tools/bowtie2 commit 32fe80982b5c59687eece667f0372002588566f8-dirty
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1 <tool id="bowtie2" name="Bowtie2" version="0.5">
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2 <!-- Wrapper compatible with Bowtie version 2.2.4 -->
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3 <description>- map reads against reference genome</description>
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4 <version_command>bowtie2 --version</version_command>
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5 <requirements>
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6 <requirement type="package" version="2.2.4">bowtie2</requirement>
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7 <requirement type="package" version="0.1.18">samtools</requirement>
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8 </requirements>
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9 <command>
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10
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11 ## prepare bowtie2 index
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12 #set index_path = ''
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13 #if str($reference_genome.source) == "history":
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14 bowtie2-build "$reference_genome.own_file" genome &amp;&amp;
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15 ln -s "$reference_genome.own_file" genome.fa &amp;&amp;
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16 #set index_path = 'genome'
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17 #else:
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18 #set index_path = $reference_genome.index.fields.path
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19 #end if
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20
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21 ## execute bowtie2
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22
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23 bowtie2
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24
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25 ## number of threads
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26 -p \${GALAXY_SLOTS:-4}
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27
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28 ## index file path
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29 -x $index_path
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30
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31
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32 ## Fastq inputs
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33 #if str( $library.type ) == "single":
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34 -U "${library.input_1}"
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35 #if str( $library.unaligned_file ) == "true":
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36 --un $output_unaligned_reads_l
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37 #end if
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38 #elif str( $library.type ) == "paired":
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39 -1 "${library.input_1}"
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40 -2 "${library.input_2}"
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41 #if str( $library.paired_options.paired_options_selector ) == "yes":
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42 -I "${library.paired_options.I}"
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43 -X "${library.paired_options.X}"
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44 ${library.paired_options.fr_rf_ff}
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45 ${library.paired_options.no_mixed}
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46 ${library.paired_options.no_discordant}
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47 ${library.paired_options.dovetail}
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48 ${library.paired_options.no_contain}
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49 ${library.paired_options.no_overlap}
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50 #end if
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51 #if str( $library.unaligned_file ) == "true":
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52 --un-conc $output_unaligned_reads_l
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53 #end if
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54 #else
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55 ## prepare collection
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56 -1 $library.input_1.forward
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57 -2 $library.input_1.reverse
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58 #if str( $library.paired_options.paired_options_selector ) == "yes":
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59 -I "${library.paired_options.I}"
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60 -X "${library.paired_options.X}"
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61 ${library.paired_options.fr_rf_ff}
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62 ${library.paired_options.no_mixed}
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63 ${library.paired_options.no_discordant}
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64 ${library.paired_options.dovetail}
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65 ${library.paired_options.no_contain}
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66 ${library.paired_options.no_overlap}
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67 #end if
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68 #if str( $library.unaligned_file ) == "true":
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69 --un-conc $output_unaligned_reads_l
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70 #end if
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71 #end if
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72
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73 ## Readgroups
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74 #if str( $read_group.read_group_selector ) == "yes":
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75 --rg-id "${read_group.rgid}"
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76 --rg "SM:${read_group.rgsm}"
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77 --rg "LB:${read_group.rglb}"
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78 --rg "PL:${read_group.rgpl}"
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79 #end if
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80
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81 ## Analysis type
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82 #if ( str( $analysis_type.analysis_type_selector ) == "simple" and str( $analysis_type.presets ) != "no_presets" ):
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83 $analysis_type.presets
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84 #elif str( $analysis_type.analysis_type_selector ) == "full":
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85 #if str( $analysis_type.input_options.input_options_selector ) == "yes":
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86 --skip "${analysis_type.input_options.skip}"
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87 --qupto "${analysis_type.input_options.qupto}"
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88 --trim5 "${analysis_type.input_options.trim5}"
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89 --trim3 "${analysis_type.input_options.trim3}"
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90 ${analysis_type.input_options.qv_encoding}
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91 ${analysis_type.input_options.solexa_quals}
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92 ${analysis_type.input_options.int_quals}
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93 #end if
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94
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95 #if str( $analysis_type.alignment_options.alignment_options_selector ) == "yes":
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96 -N "${analysis_type.alignment_options.N}"
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97 -L "${analysis_type.alignment_options.L}"
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98 -i "${analysis_type.alignment_options.i}"
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99 --n-ceil "${analysis_type.alignment_options.n_ceil}"
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100 --dpad "${analysis_type.alignment_options.dpad}"
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101 --gbar "${analysis_type.alignment_options.gbar}"
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102 ${analysis_type.alignment_options.ignore_quals}
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103 ${analysis_type.alignment_options.nofw}
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104 ${analysis_type.alignment_options.norc}
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105 ${analysis_type.alignment_options.no_1mm_upfront}
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106 #if str( $analysis_type.alignment_options.align_mode.align_mode_selector ) == "end-to-end":
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107 --end-to-end
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108 --score-min "${analysis_type.alignment_options.align_mode.score_min_ete}"
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109 #elif str( $analysis_type.alignment_options.align_mode.align_mode_selector ) == "local":
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110 --local
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111 --score-min "${analysis_type.alignment_options.align_mode.score_min_loc}"
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112 #end if
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113 #end if
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114
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115 #if str( $analysis_type.scoring_options.scoring_options_selector ) == "yes":
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116 #if ( str( $analysis_type.alignment_options.alignment_options_selector ) == "yes" and str( $analysis_type.alignment_options.align_mode.align_mode_selector ) == "local" ):
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117 --ma "${analysis_type.scoring_options.ma}"
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118 #end if
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119 --mp "${analysis_type.scoring_options.mp}"
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120 --np "${analysis_type.scoring_options.np}"
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121 --rdg "${analysis_type.scoring_options.rdg_read_open},${analysis_type.scoring_options.rdg_read_extend}"
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122 --rfg "${analysis_type.scoring_options.rfg_ref_open},${analysis_type.scoring_options.rfg_ref_extend}"
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123 #end if
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124
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125 #if str( $analysis_type.reporting_options.reporting_options_selector ) == "k":
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126 -k "${analysis_type.reporting_options.k}"
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127 #elif str( $analysis_type.reporting_options.reporting_options_selector ) == "a":
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128 -a
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129 #end if
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130
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131 #if str( $analysis_type.effort_options.effort_options_selector ) == "yes":
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132 -D "${analysis_type.effort_options.D}"
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133 -R "${analysis_type.effort_options.R}"
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134 #end if
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135
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136 #if str( $analysis_type.sam_options.sam_options_selector ) == "yes":
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137 ${analysis_type.sam_options.no_unal}
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138 ${analysis_type.sam_options.omit_sec_seq}
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139 #end if
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140
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141 #if str( $analysis_type.other_options.other_options_selector ) == "yes":
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142 ${analysis_type.other_options.non_deterministic}
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143 --seed "${analysis_type.other_options.seed}"
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144 #end if
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145
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146 #elif str( $analysis_type.analysis_type_selector ) == "cline":
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147 ${analysis_type.cline}
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148 #end if
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149
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150 -S "galaxy_bowtie_2_output.sam" &amp;&amp;
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151
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152 ## view/sort and output BAM file
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153 ( samtools view -Su "galaxy_bowtie_2_output.sam" | samtools sort -o - - > $output )
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154
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155 ## rename unaligned sequence files
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156 #if $library.type == "paired" and $output_unaligned_reads_l and $output_unaligned_reads_r:
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157 #from os.path import splitext
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158 #set _unaligned_root, _unaligned_ext = splitext( str( $output_unaligned_reads_l ) )
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159 &amp;&amp; mv "${ _unaligned_root }.1${_unaligned_ext}" "${ output_unaligned_reads_l }"
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160 &amp;&amp; mv "${ _unaligned_root }.2${_unaligned_ext}" "${ output_unaligned_reads_r }"
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161 #end if
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162
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163 </command>
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164
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165 <!-- basic error handling -->
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166 <stdio>
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167 <exit_code range="1:" level="fatal" description="Tool exception" />
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168 </stdio>
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169
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170 <inputs>
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171 <!-- single/paired -->
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172 <conditional name="library">
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173 <param name="type" type="select" label="Is this single or paired library">
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174 <option value="single">Single-end</option>
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175 <option value="paired">Paired-end</option>
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176 <option value="paired_collection">Paired-end Dataset Collection</option>
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177 </param>
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178
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179 <when value="single">
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180 <param name="input_1" format="fastqsanger" type="data" label="FASTQ file" help="Nucleotide-space: Must have Sanger-scaled quality values with ASCII offset 33"/>
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181 <param name="unaligned_file" type="boolean" truevalue="true" falsevalue="false" checked="False" label="Write unaligned reads (in fastq format) to separate file(s)" help="--un/--un-conc; This triggers --un parameter for single reads and --un-conc for paired reads" />
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182 </when>
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183 <when value="paired">
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184 <param name="input_1" format="fastqsanger" type="data" label="FASTQ file" help="Nucleotide-space: Must have Sanger-scaled quality values with ASCII offset 33" />
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185 <param name="input_2" format="fastqsanger" type="data" label="FASTQ file" help="Nucleotide-space: Must have Sanger-scaled quality values with ASCII offset 33" />
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186 <param name="unaligned_file" type="boolean" truevalue="true" falsevalue="false" checked="False" label="Write unaligned reads (in fastq format) to separate file(s)" help="--un/--un-conc; This triggers --un parameter for single reads and --un-conc for paired reads" />
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187 <conditional name="paired_options">
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188 <param name="paired_options_selector" type="select" label="Do you want to set paired-end options?" help="See &quot;Alignment Options&quot; section of Help below for information">
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189 <option value="no" selected="True">No</option>
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190 <option value="yes">Yes</option>
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191 </param>
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192 <when value="yes">
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193 <param name="I" type="integer" value="0" min="0" label="Set the minimum fragment length for valid paired-end alignments" help="-I/--minins; E.g. if `-I 60` is specified and a paired-end alignment consists of two 20-bp alignments in the appropriate orientation with a 20-bp gap between them, that alignment is considered valid (as long as `-X` is also satisfied). A 19-bp gap would not be valid in that case. If trimming options `-3` or `-5` are also used, the `-I` constraint is applied with respect to the untrimmed mates. The larger the difference between `-I` and `-X`, the slower Bowtie 2 will run. This is because larger differences bewteen `-I` and `-X` require that Bowtie 2 scan a larger window to determine if a concordant alignment exists. For typical fragment length ranges (200 to 400 nucleotides), Bowtie 2 is very efficient. Default=0"/>
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194 <param name="X" type="integer" value="500" min="0" label="Set the maximum fragment length for valid paired-end alignments" help="-X/--maxins; E.g. if `-X 100` is specified and a paired-end alignment consists of two 20-bp alignments in the proper orientation with a 60-bp gap between them, that alignment is considered valid (as long as `-I` is also satisfied). A 61-bp gap would not be valid in that case. If trimming options `-3` or `-5` are also used, the `-X` constraint is applied with respect to the untrimmed mates, not the trimmed mates; Default=500"/>
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195 <param name="fr_rf_ff" type="select" display="radio" label="Select the upstream/downstream mate orientations for a valid paired-end alignment against the forward reference strand" help="--fr, --rf, or --ff; E.g., if `--fr` is specified and there is a candidate paired-end alignment where mate 1 appears upstream of the reverse complement of mate 2 and the fragment length constraints (`-I` and `-X`) are met, that alignment is valid. Also, if mate 2 appears upstream of the reverse complement of mate 1 and all other constraints are met, that too is valid. `--rf` likewise requires that an upstream mate1 be reverse-complemented and a downstream mate2 be forward-oriented. `--ff` requires both an upstream mate 1 and a downstream mate 2 to be forward-oriented; Default=--fr (appropriate for Illumina's Paired-end Sequencing Assay)">
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196 <option value="--fr" selected="True">--fr</option>
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197 <option value="--rf">--rf</option>
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198 <option value="--ff">--ff</option>
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199 </param>
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200 <param name="no_mixed" type="boolean" truevalue="--no-mixed" falsevalue="" checked="False" label="Disable no-mixed behavior" help="--no-mixed; By default, when `bowtie2` cannot find a concordant or discordant alignment for a pair, it then tries to find alignments for the individual mates; default=False"/>
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201 <param name="no_discordant" type="boolean" truevalue="--no-discordant" falsevalue="" checked="False" label="Disable no-discordant behavior" help="--no-discordant; By default, `bowtie2` looks for discordant alignments if it cannot find any concordant alignments. A discordant alignment is an alignment where both mates align uniquely, but that does not satisfy the paired-end constraints (`--fr`/`--rf`/`--ff`, `-I`, `-X`); default=False"/>
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202 <param name="dovetail" type="boolean" truevalue="--dovetail" falsevalue="" checked="False" label="Allow mate dovetailing" help="--dovetail; If the mates `dovetail`, that is if one mate alignment extends past the beginning of the other such that the wrong mate begins upstream, consider that to be concordant. Default=False"/>
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203 <param name="no_contain" type="boolean" truevalue="--no-contain" falsevalue="" checked="False" label="Allow one mate alignment to contain another" help="--no-contain; If one mate alignment contains the other, consider that to be non-concordant. Default=False"/>
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204 <param name="no_overlap" type="boolean" truevalue="--no-overlap" falsevalue="" checked="False" label="Allow mate alignments to overlap" help="--no-overlap; If one mate alignment overlaps the other at all, consider that to be non-concordant. Default=False"/>
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205 </when>
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206 <when value="no">
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207 <!-- do nothing -->
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208 </when>
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209 </conditional>
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210 </when>
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211 <when value="paired_collection">
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212 <param name="input_1" format="fastqsanger" type="data_collection" collection_type="paired" label="FASTQ Paired Dataset" help="Nucleotide-space: Must have Sanger-scaled quality values with ASCII offset 33" />
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213 <param name="unaligned_file" type="boolean" truevalue="true" falsevalue="false" checked="False" label="Write unaligned reads (in fastq format) to separate file(s)" help="--un/--un-conc; This triggers --un parameter for single reads and --un-conc for paired reads" />
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214 <conditional name="paired_options">
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215 <param name="paired_options_selector" type="select" label="Do you want to set paired-end options?" help="See &quot;Alignment Options&quot; section of Help below for information">
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216 <option value="no" selected="True">No</option>
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217 <option value="yes">Yes</option>
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218 </param>
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219 <when value="yes">
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220 <param name="I" type="integer" value="0" min="0" label="Set the minimum fragment length for valid paired-end alignments" help="-I/--minins; E.g. if `-I 60` is specified and a paired-end alignment consists of two 20-bp alignments in the appropriate orientation with a 20-bp gap between them, that alignment is considered valid (as long as `-X` is also satisfied). A 19-bp gap would not be valid in that case. If trimming options `-3` or `-5` are also used, the `-I` constraint is applied with respect to the untrimmed mates. The larger the difference between `-I` and `-X`, the slower Bowtie 2 will run. This is because larger differences bewteen `-I` and `-X` require that Bowtie 2 scan a larger window to determine if a concordant alignment exists. For typical fragment length ranges (200 to 400 nucleotides), Bowtie 2 is very efficient. Default=0"/>
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221 <param name="X" type="integer" value="500" min="0" label="Set the maximum fragment length for valid paired-end alignments" help="-X/--maxins; E.g. if `-X 100` is specified and a paired-end alignment consists of two 20-bp alignments in the proper orientation with a 60-bp gap between them, that alignment is considered valid (as long as `-I` is also satisfied). A 61-bp gap would not be valid in that case. If trimming options `-3` or `-5` are also used, the `-X` constraint is applied with respect to the untrimmed mates, not the trimmed mates; Default=500"/>
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222 <param name="fr_rf_ff" type="select" display="radio" label="Select the upstream/downstream mate orientations for a valid paired-end alignment against the forward reference strand" help="--fr, --rf, or --ff; E.g., if `--fr` is specified and there is a candidate paired-end alignment where mate 1 appears upstream of the reverse complement of mate 2 and the fragment length constraints (`-I` and `-X`) are met, that alignment is valid. Also, if mate 2 appears upstream of the reverse complement of mate 1 and all other constraints are met, that too is valid. `--rf` likewise requires that an upstream mate1 be reverse-complemented and a downstream mate2 be forward-oriented. `--ff` requires both an upstream mate 1 and a downstream mate 2 to be forward-oriented; Default=--fr (appropriate for Illumina's Paired-end Sequencing Assay)">
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223 <option value="--fr" selected="True">--fr</option>
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224 <option value="--rf">--rf</option>
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225 <option value="--ff">--ff</option>
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226 </param>
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227 <param name="no_mixed" type="boolean" truevalue="--no-mixed" falsevalue="" checked="False" label="Disable no-mixed behavior" help="--no-mixed; By default, when `bowtie2` cannot find a concordant or discordant alignment for a pair, it then tries to find alignments for the individual mates; default=False"/>
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228 <param name="no_discordant" type="boolean" truevalue="--no-discordant" falsevalue="" checked="False" label="Disable no-discordant behavior" help="--no-discordant; By default, `bowtie2` looks for discordant alignments if it cannot find any concordant alignments. A discordant alignment is an alignment where both mates align uniquely, but that does not satisfy the paired-end constraints (`--fr`/`--rf`/`--ff`, `-I`, `-X`); default=False"/>
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229 <param name="dovetail" type="boolean" truevalue="--dovetail" falsevalue="" checked="False" label="Allow mate dovetailing" help="--dovetail; If the mates `dovetail`, that is if one mate alignment extends past the beginning of the other such that the wrong mate begins upstream, consider that to be concordant. Default=False"/>
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230 <param name="no_contain" type="boolean" truevalue="--no-contain" falsevalue="" checked="False" label="Allow one mate alignment to contain another" help="--no-contain; If one mate alignment contains the other, consider that to be non-concordant. Default=False"/>
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231 <param name="no_overlap" type="boolean" truevalue="--no-overlap" falsevalue="" checked="False" label="Allow mate alignments to overlap" help="--no-overlap; If one mate alignment overlaps the other at all, consider that to be non-concordant. Default=False"/>
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232 </when>
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233 <when value="no">
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234 <!-- do nothing -->
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235 </when>
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236 </conditional>
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237 </when>
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238 </conditional>
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239
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240 <!-- reference genome -->
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241 <conditional name="reference_genome">
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242 <param name="source" type="select" label="Will you select a reference genome from your history or use a built-in index?" help="Built-ins were indexed using default options. See `Indexes` section of help below">
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243 <option value="indexed">Use a built-in genome index</option>
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244 <option value="history">Use a genome from the history and build index</option>
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245 </param>
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246 <when value="indexed">
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247 <param name="index" type="select" label="Select reference genome" help="If your genome of interest is not listed, contact the Galaxy team">
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248 <options from_data_table="bowtie2_indexes">
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249 <filter type="sort_by" column="2"/>
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250 <validator type="no_options" message="No indexes are available for the selected input dataset"/>
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251 </options>
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252 </param>
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253 </when>
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254 <when value="history">
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255 <param name="own_file" type="data" format="fasta" metadata_name="dbkey" label="Select reference genome" />
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256 </when>
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257 </conditional>
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258
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259 <!-- read group settings -->
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260 <conditional name="read_group">
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261 <param name="read_group_selector" type="select" label="Specify the read group for this file?" help="Specifying readgroup information can greatly simplify your downstream analyses by allowing combining multiple datasets. See help below for more details">
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262 <option value="yes">Yes</option>
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263 <option value="no" selected="True">No</option>
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264 </param>
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265 <when value="yes">
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266 <param name="rgid" type="text" size="25" label="Read group identifier (ID). Each @RG line must have a unique ID. The value of ID is used in the RG tags of alignment records. Must be unique among all read groups in header section." help="--rg-id; Required if RG specified. Read group IDs may be modified when merging SAM files in order to handle collisions." />
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267 <param name="rglb" type="text" size="25" label="Library name (LB)" help="--rg; Required if RG specified" />
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268 <param name="rgpl" type="text" size="25" label="Platform/technology used to produce the reads (PL)" help="--rg; Required if RG specified. Valid values : CAPILLARY, LS454, ILLUMINA, SOLID, HELICOS, IONTORRENT and PACBIO" />
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269 <param name="rgsm" type="text" size="25" label="Sample (SM)" help="--rg; Required if RG specified. Use pool name where a pool is being sequenced" />
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270 </when>
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271 <when value="no" />
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272 </conditional>
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273
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274 <conditional name="analysis_type">
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275 <param name="analysis_type_selector" type="select" label="Select analysis mode">
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276 <option value="simple">1: Default setting only</option>
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277 <option value="full">2: Full parameter list</option>
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278 </param>
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279 <when value="simple">
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280 <param name="presets" type="select" display="radio" label="Do you want to use presets?" help="Allow selecting among several preset parameter settings. Choosing between these will result in dramatic changes in runtime. See help below to understand effects of these presets.">
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281 <option value="no_presets" selected="True">No, just use defaults</option>
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282 <option value="--very-fast">Very fast end-to-end (--very-fast)</option>
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283 <option value="--fast">Fast end-to-end (--fast)</option>
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284 <option value="--sensitive">Sensitive end-to-end (--sensitive)</option>
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285 <option value="--very-sensitive">Very sensitive end-to-end (--very-sensitive)</option>
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286 <option value="--very-fast-local">Very fast local (--very-fast-local)</option>
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287 <option value="--fast-local">Fast local (--fast-local)</option>
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288 <option value="--sensitive-local">Sensitive local (--sensitive-local)</option>
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289 <option value="--very-sensitive-local">Very sensitive local (--very-sensitive-local)</option>
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290 </param>
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291 </when>
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292 <when value="full">
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293 <conditional name="input_options">
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294 <param name="input_options_selector" type="select" label="Do you want to tweak input options?" help="See &quot;Input Options&quot; section of Help below for information">
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295 <option value="yes">Yes</option>
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296 <option value="no" selected="true">No</option>
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297 </param>
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298 <when value="yes">
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299 <param name="skip" type="integer" min="0" value="0" label="Skip (i.e. do not align) the first that many reads or pairs in the input" help="-s/--skip; default=0"/>
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300 <param name="qupto" type="integer" min="1" value="100000000" label="Align the first that many reads or read pairs from the input (after the -s/--skip reads or pairs have been skipped), then stop" help="-u/--qupto; for default behavior (no limit) leave this value very large"/>
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301 <param name="trim5" type="integer" min="0" value="0" label="Trim that many bases from 5' (left) end of each read before alignment" help="-5/--trim5; default=0"/>
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302 <param name="trim3" type="integer" min="0" value="0" label="Trim that many bases from 3' (right) end of each read before alignment" help="-3/--trim3; default=0"/>
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303 <param name="qv_encoding" type="select" display="radio" label="Select quality score encoding" help="See help below for more details">
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304 <option value="--phred33" selected="True">Input qualities are ASCII chars equal to the Phred quality plus 33. This is also called the "Phred+33" encoding, which is used by the very latest Illumina pipelines (--phred33)</option>
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305 <option value="--phred64">Input qualities are ASCII chars equal to the Phred quality plus 64. This is also called the "Phred+64" encoding (--phred64)</option>
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306 </param>
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307 <param name="solexa_quals" type="boolean" truevalue="--solexa-quals" falsevalue="" checked="False" label="Convert input qualities from Solexa (which can be negative) to Phred (which can't). This scheme was used in older Illumina GA Pipeline versions (prior to 1.3)" help="--solexa-quals; default=False"/>
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308 <param name="int_quals" type="boolean" truevalue="--int-quals" falsevalue="" checked="False" label="Quality values are represented in the read input file as space-separated ASCII integers, e.g., 40 40 30 40..., rather than ASCII characters, e.g., II?I.... Integers are treated as being on the Phred quality scale unless --solexa-quals is also specified" help="--int-quals; default=False"/>
2
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309 </when>
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310 <when value="no">
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311 <!-- do nothing -->
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312 </when>
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313 </conditional>
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314 <conditional name="alignment_options">
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315 <param name="alignment_options_selector" type="select" label="Do you want to tweak alignment options?" help="See &quot;Alignment Options&quot; section of Help below for information">
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316 <option value="yes">Yes</option>
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317 <option value="no" selected="true">No</option>
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318 </param>
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319 <when value="yes">
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320 <param name="N" type="integer" min="0" max="1" value="0" label="Set the number of mismatches to be allowed in a seed alignment during multiseed alignment (see `Multiseed alignment` section of help below)" help="-N; Can be set to 0 or 1. Setting this higher makes alignment slower (often much slower) but increases sensitivity; default=0"/>
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321 <param name="L" type="integer" min="0" max="32" value="22" label="Sets the length of the seed substrings to align during multiseed alignment (see `Multiseed alignment` section of help below)" help="-L; Smaller values make alignment slower but more sensitive. Default=22"/>
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322 <param name="i" type="text" value="S,1,1.15" size="10" label="Set a function governing the interval between seed substrings to use during multiseed alignment (see `Multiseed alignment` section of help below). Also see description of this option below in the help section" help="-i; Since it's best to use longer intervals for longer reads, this parameter sets the interval as a function of the read length, rather than a single one-size-fits-all number. For instance, specifying `-i S,1,2.5` sets the interval function `f` to `f(x) = 1 + 2.5 * sqrt(x)`, where x is the read length. If the function returns a result less than 1, it is rounded up to 1. Default=`S,1,1.15`"/>
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323 <param name="n_ceil" type="text" value="L,0,0.15" label="Set a function governing the maximum number of ambiguous characters (usually `N`s and/or `.`s) allowed in a read as a function of read length" help="--n-ceil; For instance, specifying `L,0,0.15` sets the N-ceiling function `f` to `f(x) = 0 + 0.15 * x`, where x is the read length. Reads exceeding this ceiling are filtered out. Default=`L,0,0.15`"/>
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324 <param name="dpad" type="integer" min="0" value="15" label="Pad dynamic programming problems by that many columns on either side to allow gaps" help="--dpad; default=15"/>
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325 <param name="gbar" type="integer" min="0" value="4" label="Disallow gaps within that many positions of the beginning or end of the read" help="--gbar; default=4"/>
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326 <param name="ignore_quals" type="boolean" truevalue="--ignore-quals" falsevalue="" selected="False" label="When calculating a mismatch penalty, always consider the quality value at the mismatched position to be the highest possible, regardless of the actual value" help="--ignore-quals; input is treated as though all quality values are high; default=False"/>
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327 <param name="nofw" type="boolean" truevalue="--nofw" falsevalue="" selected="False" label="Do not attempt to align unpaired reads to the forward (Watson) reference strand" help="In paired-end mode, `--nofw` and `--norc` pertain to the fragments; i.e. specifying `--nofw` causes `bowtie2` to explore only those paired-end configurations corresponding to fragments from the reverse-complement (Crick) strand. Default=False"/>
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328 <param name="norc" type="boolean" truevalue="--norc" falsevalue="" selected="False" label="Do not attempt to align unpaired reads to the reverse (Crick) reference strand" help="In paired-end mode, `--nofw` and `--norc` pertain to the fragments; i.e. specifying `--nofw` causes `bowtie2` to explore only those paired-end configurations corresponding to fragments from the reverse-complement (Crick) strand. Default=False"/>
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329 <param name="no_1mm_upfront" type="boolean" truevalue="--no-1mm-upfront" falsevalue="" selected="False" label="Prevent searching for 1-mismatch end-to-end alignments before using the multiseed heuristic (see `Multiseed alignment` section of help below)" help="--no-1mm-upfront; By default, Bowtie 2 will attempt to find either an exact or a 1-mismatch end-to-end alignment for the read *before* trying the multiseed heuristic. Such alignments can be found very quickly, and many short read alignments have exact or near-exact end-to-end alignments. However, this can lead to unexpected alignments when the user also sets options governing the multiseed heuristic, like `-L` and `-N`. For instance, if the user specifies `-N 0` and `-L` equal to the length of the read, the user will be surprised to find 1-mismatch alignments reported. This option prevents Bowtie 2 from searching for 1-mismatch end-to-end alignments before using the multiseed heuristic, which leads to the expected behavior when combined with options such as `-L` and `-N`. This comes at the expense of speed; Default=False"/>
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330 <conditional name="align_mode">
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331 <param name="align_mode_selector" type="select" display="radio" label="Select between `--local` and `--end-to-end` alignment modes" help="--local and --end-to-end; see help below for detailed explanation; default=--end-to-end">
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332 <option value="end-to-end" selected="True">End to End (--end-to-end)</option>
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333 <option value="local">Local (--local)</option>
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334 </param>
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335 <when value="end-to-end">
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336 <param name="score_min_ete" type="text" value="L,-0.6,-0.6" label="Set a function governing the minimum alignment score needed for an alignment to be considered `valid` (i.e. good enough to report)" help="--score-min; This is a function of read length. For instance, specifying `L,0,-0.6` sets the minimum-score function `f` to `f(x) = 0 + -0.6 * x`, where `x` is the read length. The default in `--end-to-end` mode is `L,-0.6,-0.6` and the default in `--local` mode is `G,20,8`"/>
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337 </when>
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338 <when value="local">
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339 <param name="score_min_loc" type="text" value="G,20,8" label="Set a function governing the minimum alignment score needed for an alignment to be considered `valid` (i.e. good enough to report)" help="--score-min; This is a function of read length. For instance, specifying `L,0,-0.6` sets the minimum-score function `f` to `f(x) = 0 + -0.6 * x`, where `x` is the read length. The default in `--end-to-end` mode is `L,-0.6,-0.6` and the default in `--local` mode is `G,20,8`"/>
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340 </when>
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341 </conditional>
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342 </when>
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343 <when value="no">
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344 <!-- do nothing -->
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345 </when>
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346 </conditional>
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347 <conditional name="scoring_options">
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348 <param name="scoring_options_selector" type="select" label="Do you want to tweak scoring options?" help="See &quot;Scoring Options&quot; section of Help below for information">
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349 <option value="yes">Yes</option>
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350 <option value="no" selected="true">No</option>
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351 </param>
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352 <when value="yes">
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353 <param name="ma" type="integer" value="2" label="Set the match bonus" help="--ma; In `--local` mode match bonus is added to the alignment score for each position where a read character aligns to a reference character and the characters match. Not used in `--end-to-end` mode; Default=2"/>
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354 <param name="mp" type="text" size="10" value="6,2" label="Set the maximum (`MX`) and minimum (`MN`) mismatch penalties, both integers" help="--mp; A number less than or equal to `MX` and greater than or equal to `MN` is subtracted from the alignment score for each position where a read character aligns to a reference character, the characters do not match, and neither is an `N`. If `--ignore-quals` is specified, the number subtracted quals `MX`. Otherwise, the number subtracted is `MN + floor( (MX-MN)(MIN(Q, 40.0)/40.0) )` where Q is the Phred quality value; Default=6,2"/>
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355 <param name="np" type="integer" value="1" label="Sets penalty for positions where the read, reference, or both, contain an ambiguous character such as `N`" help="--np; Default=1"/>
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356 <param name="rdg_read_open" type="integer" value="5" label="Set the read gap opening penalty" help="--rdg; this is the first component of --rdg flag - opening penalty; Default=5"/>
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357 <param name="rdg_read_extend" type="integer" value="3" label="Set the read gap extension penalty" help="--rdg; this is the second component of --rdg flag - extension penalty; Default=3"/>
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358 <param name="rfg_ref_open" type="integer" value="5" label="Set the reference gap opening penalty" help="--rfg; this is the first component of --rfg flag - opening penalty; Default=5"/>
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359 <param name="rfg_ref_extend" type="integer" value="3" label="Set the reference gap extension penalty" help="--rfg; this is the second component of --rfg flag - extension penalty; Default=3"/>
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360 </when>
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361 <when value="no">
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362 <!-- do nothing -->
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363 </when>
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364 </conditional>
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365 <conditional name="reporting_options">
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366 <param name="reporting_options_selector" type="select" label="Do you want to use -a or -k options" help="Make sure you understand implications of setting -k and -a. See &quot;Reporting Options&quot; section of Help below for information on -k and -a options">
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367 <option value="no" selected="true">No, do not set</option>
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368 <option value="k">Set -k option and enter -k value</option>
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369 <option value="a">Set -a option</option>
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370 </param>
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371 <when value="no">
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372 <!-- do nothing -->
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373 </when>
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374 <when value="k">
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375 <param name="k" type="integer" min="1" value="1" label="Searches for at most that many distinct, valid alignments for each read" help="-k; see detailed description of this option in the help section below. Note: Bowtie 2 is not designed with large values for `-k` in mind, and when aligning reads to long, repetitive genomes large `-k` can be very, very slow"/>
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376 </when>
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377 <when value="a">
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378 <!-- do nothing here; set -a flag on the command line-->
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379 </when>
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380 </conditional>
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381 <conditional name="effort_options">
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382 <param name="effort_options_selector" type="select" label="Do you want to tweak effort options?" help="See &quot;Effort Options&quot; section of Help below for information">
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383 <option value="yes">Yes</option>
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384 <option value="no" selected="true">No</option>
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385 </param>
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386 <when value="yes">
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387 <param name="D" type="integer" value="15" min="0" label="Attempt that many consecutive seed extension attempts to `fail` before Bowtie 2 moves on, using the alignments found so far" help="-D; A seed extension `fails` if it does not yield a new best or a new second-best alignment. This limit is automatically adjusted up when -k or -a are specified. Default=15"/>
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388 <param name="R" type="integer" value="2" min="0" label="Set the maximum number of times Bowtie 2 will `re-seed` reads with repetitive seeds" help="When `re-seeding`, Bowtie 2 simply chooses a new set of reads (same length, same number of mismatches allowed) at different offsets and searches for more alignments. A read is considered to have repetitive seeds if the total number of seed hits divided by the number of seeds that aligned at least once is greater than 300. Default=2"/>
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389 </when>
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390 <when value="no">
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391 <!-- do nothing -->
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392 </when>
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393 </conditional>
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394
2
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395 <conditional name="sam_options">
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396 <param name="sam_options_selector" type="select" label="Do you want to tweak SAM/BAM Options?" help="See &quot;Output Options&quot; section of Help below for information">
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397 <option value="yes">Yes</option>
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398 <option value="no" selected="true">No</option>
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399 </param>
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400 <when value="yes">
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401 <param name="no_unal" type="boolean" truevalue="--no-unal" falsevalue="" label="Suppress SAM records for reads that failed to align" help="--no-unal; Default=False"/>
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402 <param name="omit_sec_seq" type="boolean" truevalue="--omit-sec-seq" falsevalue="" label="Suppress SEQ and QUAL strings for secondary alignments" help="--omit-sec-seq; Default=False"/>
2
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403 </when>
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404 <when value="no">
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405 <!-- do nothing -->
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406 </when>
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407 </conditional>
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408 <conditional name="other_options">
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409 <param name="other_options_selector" type="select" label="Do you want to tweak Other Options?" help="See &quot;Other Options&quot; section of Help below for information">
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410 <option value="yes">Yes</option>
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411 <option value="no" selected="true">No</option>
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412 </param>
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413 <when value="yes">
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414 <param name="seed" type="integer" value="0" min="0" label="Use this number as the seed for pseudo-random number generator" help="--seed; Default=0"/>
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415 <param name="non_deterministic" type="boolean" truevalue="--non-deterministic" falsevalue="" label="Re-initialize the pseudo-random generator for each read using the current time" help="--non-deterministic; see Help below for explanation of this option; default=False"/>
2
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416 </when>
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417 <when value="no">
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418 <!-- do nothing -->
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419 </when>
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420 </conditional>
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421 </when>
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422 </conditional>
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423 </inputs>
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424
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425 <!-- define outputs -->
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426
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427 <outputs>
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428
0
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429 <data format="fastqsanger" name="output_unaligned_reads_l" label="${tool.name} on ${on_string}: unaligned reads (L)" >
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430 <filter>library['unaligned_file'] is True</filter>
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431 <actions>
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432 <action type="format">
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433 <option type="from_param" name="library.input_1" param_attribute="ext" />
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434 </action>
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435 </actions>
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436 </data>
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437 <data format="fastqsanger" name="output_unaligned_reads_r" label="${tool.name} on ${on_string}: unaligned reads (R)">
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438 <filter>( library['type'] == "paired" or library['type'] == "paired_collection" ) and library['unaligned_file'] is True</filter>
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439 <actions>
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440 <action type="format">
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441 <option type="from_param" name="library.input_1" param_attribute="ext" />
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442 </action>
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443 </actions>
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444 </data>
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445
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446 <data format="bam" name="output" label="${tool.name} on ${on_string}: aligned reads (sorted BAM)">
0
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447 <actions>
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448 <conditional name="reference_genome.source">
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449 <when value="indexed">
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450 <action type="metadata" name="dbkey">
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451 <option type="from_data_table" name="bowtie2_indexes" column="1" offset="0">
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452 <filter type="param_value" column="0" value="#" compare="startswith" keep="False"/>
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453 <filter type="param_value" ref="reference_genome.index" column="0"/>
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454 </option>
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455 </action>
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456 </when>
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457 <when value="history">
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458 <action type="metadata" name="dbkey">
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459 <option type="from_param" name="reference_genome.own_file" param_attribute="dbkey" />
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460 </action>
96d2e31a3938 Imported from capsule None
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461 </when>
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462 </conditional>
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463 </actions>
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464 </data>
3
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465
0
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466 </outputs>
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467
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468 <tests>
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469 <test>
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470 <!-- basic test on single paired default run -->
2
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471 <param name="type" value="paired"/>
0
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472 <param name="selection" value="no"/>
2
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473 <param name="paired_options_selector" value="no"/>
0
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474 <param name="unaligned_file" value="false"/>
2
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475 <param name="analysis_type_selector" value="simple"/>
0
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476 <param name="source" value="history" />
2
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477 <param name="input_1" value="bowtie2-fq1.fq" ftype="fastqsanger"/>
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478 <param name="input_2" value="bowtie2-fq2.fq" ftype="fastqsanger"/>
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479 <param name="own_file" value="bowtie2-ref.fasta" />
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480 <output name="output" file="bowtie2-test1.bam" ftype="bam" lines_diff="2"/>
0
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481 </test>
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482 </tests>
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483
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484 <help>
2
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485
0
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486 **Bowtie2 Overview**
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487
2
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488 Bowtie2_ is an ultrafast and memory-efficient tool for aligning sequencing reads to long reference sequences. It is particularly good at aligning reads of about 50 up to 100s or 1,000s of characters to relatively long (e.g. mammalian) genomes. Bowtie 2 supports gapped, local, and paired-end alignment modes. Galaxy wrapper for Bowtie 2 outputs alignments in `BAM format`_, enabling interoperation with a large number of other tools available at this site.
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489 Majority of information in this page is derived from an excellent `Bowtie2 manual`_ written by Ben Langmead.
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490
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491 .. _Bowtie2: http://bowtie-bio.sourceforge.net/bowtie2/
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492 .. _`Bowtie2 manual`: http://bowtie-bio.sourceforge.net/bowtie2/manual.shtml
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493 .. _`BAM format`: http://samtools.github.io/hts-specs/SAMv1.pdf
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494
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495 -----
0
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496
2
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497 **Selecting reference genomes for Bowtie2**
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498
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499 Galaxy wrapper for Bowtie2 allows you select between precomputed and user-defined indices for reference genomes using **Will you select a reference genome from your history or use a built-in index?** flag. This flag has two options:
0
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500
2
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501 1. **Use a built-in genome index** - when selected (this is default), Galaxy provides the user with **Select reference genome index** dropdown. Genomes listed in this dropdown have been pre-indexed with bowtie2-build utility and are ready to be mapped against.
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502 2. **Use a genome from the history and build index** - when selected, Galaxy provides the user with **Select reference genome sequence** dropdown. This dropdown is populated by all FASTA formatted files listed in your current history. If your genome of interest is uploaded into history it will be shown there. Selecting a genome from this dropdown will cause Galaxy to first transparently index it using bowtie2-build command, and then run mapping with bowtie2.
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503
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504 If your genome of interest is not listed here you have two choices:
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505
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506 1. Contact galaxy team using **Help->Support** link at the top of the interface and let us know that an index needs to be added
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507 2. Upload your genome of interest as a FASTA file to Galaxy history and selected **Use a genome from the history and build index** option.
0
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508
96d2e31a3938 Imported from capsule None
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509 ------
96d2e31a3938 Imported from capsule None
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510
2
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511 .. class:: infomark
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512
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diff changeset
513 **Bowtie2 options**
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514
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515 Galaxy wrapper for Bowtie2 implements most but not all options available through the command line. Supported options are described below.
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516
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517 -----
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518
0
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519 **Inputs**
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520
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521 Bowtie 2 accepts files in Sanger FASTQ format (single or pair-end). Use the FASTQ Groomer to prepare your files.
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522
96d2e31a3938 Imported from capsule None
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523 ------
96d2e31a3938 Imported from capsule None
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524
2
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525 **Input options**::
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526
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527 -s/--skip &lt;int&gt;
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diff changeset
528 Skip (i.e. do not align) the first `&lt;int&gt;` reads or pairs in the input.
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529
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530 -u/--qupto &lt;int&gt;
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diff changeset
531 Align the first `&lt;int&gt;` reads or read pairs from the input (after the
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532 `-s`/`--skip` reads or pairs have been skipped), then stop. Default: no limit.
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533
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534 -5/--trim5 &lt;int&gt;
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535 Trim `&lt;int&gt;` bases from 5' (left) end of each read before alignment (default: 0).
0
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536
2
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537 -3/--trim3 &lt;int&gt;
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diff changeset
538 Trim `&lt;int&gt;` bases from 3' (right) end of each read before alignment (default: 0).
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539
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540 --phred33
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diff changeset
541 Input qualities are ASCII chars equal to the Phred quality plus 33. This is
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542 also called the "Phred+33" encoding, which is used by the very latest Illumina
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543 pipelines.
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544
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545 --phred64
3
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diff changeset
546 Input qualities are ASCII chars equal to the Phred quality plus 64. This is
2
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547 also called the "Phred+64" encoding.
0
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548
2
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549 --solexa-quals
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550 Convert input qualities from Solexa Phred quality (which can be negative) to
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551 Phred Phred quality (which can't). This scheme was used in older Illumina GA
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552 Pipeline versions (prior to 1.3). Default: off.
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553
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554 --int-quals
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555 Quality values are represented in the read input file as space-separated ASCII integers, e.g., `40 40 30 40`..., rather than ASCII characters, e.g., `II?I`....
3
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556 Integers are treated as being on the Phred quality scale unless
2
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557 `--solexa-quals` is also specified. Default: off.
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558
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559 ------
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560
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561 **Presets in `--end-to-end` mode**::
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562
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563 --very-fast
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564 Same as: `-D 5 -R 1 -N 0 -L 22 -i S,0,2.50`
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565
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566 --fast
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567 Same as: `-D 10 -R 2 -N 0 -L 22 -i S,0,2.50`
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568
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569 --sensitive
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570 Same as: `-D 15 -R 2 -L 22 -i S,1,1.15` (default in `--end-to-end` mode)
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571
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572 --very-sensitive
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573 Same as: `-D 20 -R 3 -N 0 -L 20 -i S,1,0.50`
0
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574
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575 ------
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576
2
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577 **Presets options in `--local` mode**::
0
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578
2
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579 --very-fast-local
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580 Same as: `-D 5 -R 1 -N 0 -L 25 -i S,1,2.00`
0
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581
2
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582 --fast-local
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diff changeset
583 Same as: `-D 10 -R 2 -N 0 -L 22 -i S,1,1.75`
0
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584
2
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585 --sensitive-local
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586 Same as: `-D 15 -R 2 -N 0 -L 20 -i S,1,0.75` (default in `--local` mode)
0
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587
2
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588 --very-sensitive-local
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589 Same as: `-D 20 -R 3 -N 0 -L 20 -i S,1,0.50`
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diff changeset
590
0
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591 ------
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592
2
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593 **Alignment options**::
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diff changeset
594
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diff changeset
595 -N &lt;int&gt;
3
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diff changeset
596 Sets the number of mismatches to allowed in a seed alignment during multiseed
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597 alignment. Can be set to 0 or 1. Setting this higher makes alignment slower
2
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598 (often much slower) but increases sensitivity. Default: 0.
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599
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diff changeset
600 -L &lt;int&gt;
3
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diff changeset
601 Sets the length of the seed substrings to align during multiseed alignment.
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diff changeset
602 Smaller values make alignment slower but more sensitive. Default: the
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603 `--sensitive` preset is used by default, which sets `-L` to 22 in
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diff changeset
604 `--end-to-end` mode and to 20 in `--local` mode.
2
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605
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diff changeset
606 -i &lt;func&gt;
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diff changeset
607 Sets a function governing the interval between seed substrings to use during
3
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diff changeset
608 multiseed alignment. For instance, if the read has 30 characers, and seed
2
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diff changeset
609 length is 10, and the seed interval is 6, the seeds extracted will be:
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diff changeset
610
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diff changeset
611 Read: TAGCTACGCTCTACGCTATCATGCATAAAC
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diff changeset
612 Seed 1 fw: TAGCTACGCT
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diff changeset
613 Seed 1 rc: AGCGTAGCTA
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diff changeset
614 Seed 2 fw: CGCTCTACGC
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diff changeset
615 Seed 2 rc: GCGTAGAGCG
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diff changeset
616 Seed 3 fw: ACGCTATCAT
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diff changeset
617 Seed 3 rc: ATGATAGCGT
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diff changeset
618 Seed 4 fw: TCATGCATAA
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diff changeset
619 Seed 4 rc: TTATGCATGA
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diff changeset
620
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diff changeset
621 Since it's best to use longer intervals for longer reads, this parameter sets
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diff changeset
622 the interval as a function of the read length, rather than a single
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diff changeset
623 one-size-fits-all number. For instance, specifying `-i S,1,2.5` sets the
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diff changeset
624 interval function `f` to `f(x) = 1 + 2.5 * sqrt(x)`, where x is the read length.
3
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diff changeset
625 If the function returns a result less than
2
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diff changeset
626 1, it is rounded up to 1. Default: the `--sensitive` preset is used by
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diff changeset
627 default, which sets `-i` to `S,1,1.15` in `--end-to-end` mode to `-i S,1,0.75`
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diff changeset
628 in `--local` mode.
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diff changeset
629
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diff changeset
630 --n-ceil &lt;func&gt;
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diff changeset
631 Sets a function governing the maximum number of ambiguous characters (usually
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diff changeset
632 `N`s and/or `.`s) allowed in a read as a function of read length. For instance,
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diff changeset
633 specifying `-L,0,0.15` sets the N-ceiling function `f` to `f(x) = 0 + 0.15 * x`,
3
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diff changeset
634 where x is the read length. Reads exceeding this ceiling are filtered out.
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diff changeset
635 Default: `L,0,0.15`.
2
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diff changeset
636
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diff changeset
637 --dpad &lt;int&gt;
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diff changeset
638 "Pads" dynamic programming problems by `&lt;int&gt;` columns on either side to allow
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639 gaps. Default: 15.
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diff changeset
640
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diff changeset
641 --gbar &lt;int&gt;
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diff changeset
642 Disallow gaps within `&lt;int&gt;` positions of the beginning or end of the read.
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diff changeset
643 Default: 4.
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diff changeset
644
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645 --ignore-quals
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diff changeset
646 When calculating a mismatch penalty, always consider the quality value at the
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647 mismatched position to be the highest possible, regardless of the actual value.
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648 I.e. input is treated as though all quality values are high. This is also the
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diff changeset
649 default behavior when the input doesn't specify quality values (e.g. in `-f`,
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650 `-r`, or `-c` modes).
0
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651
2
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diff changeset
652 --nofw/--norc
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diff changeset
653 If `--nofw` is specified, `bowtie2` will not attempt to align unpaired reads to
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diff changeset
654 the forward (Watson) reference strand. If `--norc` is specified, `bowtie2` will
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diff changeset
655 not attempt to align unpaired reads against the reverse-complement (Crick)
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diff changeset
656 reference strand. In paired-end mode, `--nofw` and `--norc` pertain to the
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diff changeset
657 fragments; i.e. specifying `--nofw` causes `bowtie2` to explore only those
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diff changeset
658 paired-end configurations corresponding to fragments from the reverse-complement
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diff changeset
659 (Crick) strand. Default: both strands enabled.
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660
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diff changeset
661 --no-1mm-upfront
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diff changeset
662 By default, Bowtie 2 will attempt to find either an exact or a 1-mismatch
3
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diff changeset
663 end-to-end alignment for the read *before* trying the multiseed heuristic. Such
2
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diff changeset
664 alignments can be found very quickly, and many short read alignments have exact or
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diff changeset
665 near-exact end-to-end alignments. However, this can lead to unexpected
3
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diff changeset
666 alignments when the user also sets options governing the multiseed heuristic,
2
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diff changeset
667 like `-L` and `-N`. For instance, if the user specifies `-N 0` and `-L` equal
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diff changeset
668 to the length of the read, the user will be surprised to find 1-mismatch alignments
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diff changeset
669 reported. This option prevents Bowtie 2 from searching for 1-mismatch end-to-end
3
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parents: 2
diff changeset
670 alignments before using the multiseed heuristic, which leads to the expected
2
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diff changeset
671 behavior when combined with options such as `-L` and `-N`. This comes at the
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diff changeset
672 expense of speed.
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673
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diff changeset
674 --end-to-end
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diff changeset
675 In this mode, Bowtie 2 requires that the entire read align from one end to the
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diff changeset
676 other, without any trimming (or "soft clipping") of characters from either end.
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diff changeset
677 The match bonus `--ma` always equals 0 in this mode, so all alignment scores
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diff changeset
678 are less than or equal to 0, and the greatest possible alignment score is 0.
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679 This is mutually exclusive with `--local`. `--end-to-end` is the default mode.
0
96d2e31a3938 Imported from capsule None
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680
2
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diff changeset
681 --local
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diff changeset
682 In this mode, Bowtie 2 does not require that the entire read align from one end
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683 to the other. Rather, some characters may be omitted ("soft clipped") from the
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684 ends in order to achieve the greatest possible alignment score. The match bonus
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diff changeset
685 `--ma` is used in this mode, and the best possible alignment score is equal to
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parents: 0
diff changeset
686 the match bonus (`--ma`) times the length of the read. Specifying `--local`
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parents: 0
diff changeset
687 and one of the presets (e.g. `--local --very-fast`) is equivalent to specifying
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688 the local version of the preset (`--very-fast-local`). This is mutually
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689 exclusive with `--end-to-end`. `--end-to-end` is the default mode.
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parents: 0
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690
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parents: 0
diff changeset
691 -----
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parents: 0
diff changeset
692
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parents: 0
diff changeset
693 **Scoring options**::
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694
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parents: 0
diff changeset
695 --ma &lt;int&gt;
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parents: 0
diff changeset
696 Sets the match bonus. In `--local` mode `&lt;int&gt;` is added to the alignment
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parents: 0
diff changeset
697 score for each position where a read character aligns to a reference character
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parents: 0
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698 and the characters match. Not used in `--end-to-end` mode. Default: 2.
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parents: 0
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699
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diff changeset
700 --mp MX,MN
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diff changeset
701 Sets the maximum (`MX`) and minimum (`MN`) mismatch penalties, both integers. A
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diff changeset
702 number less than or equal to `MX` and greater than or equal to `MN` is
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703 subtracted from the alignment score for each position where a read character
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parents: 0
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704 aligns to a reference character, the characters do not match, and neither is an
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diff changeset
705 `N`. If `--ignore-quals` is specified, the number subtracted quals `MX`.
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706 Otherwise, the number subtracted is `MN + floor( (MX-MN)(MIN(Q, 40.0)/40.0) )`
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diff changeset
707 where Q is the Phred quality value. Default: `MX` = 6, `MN` = 2.
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708
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709 --np &lt;int&gt;
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parents: 0
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710 Sets penalty for positions where the read, reference, or both, contain an
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711 ambiguous character such as `N`. Default: 1.
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parents: 0
diff changeset
712
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713 --rdg &lt;int1&gt;,&lt;int2&gt;
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parents: 0
diff changeset
714 Sets the read gap open (`&lt;int1&gt;`) and extend (`&lt;int2&gt;`) penalties. A read gap of
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715 length N gets a penalty of `&lt;int1&gt;` + N * `&lt;int2&gt;`. Default: 5, 3.
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716
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717 --rfg &lt;int1&gt;,&lt;int2&gt;
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diff changeset
718 Sets the reference gap open (`&lt;int1&gt;`) and extend (`&lt;int2&gt;`) penalties. A
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parents: 0
diff changeset
719 reference gap of length N gets a penalty of `&lt;int1&gt;` + N * `&lt;int2&gt;`. Default:
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parents: 0
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720 5, 3.
0
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721
2
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722 --score-min &lt;func&gt;
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723 Sets a function governing the minimum alignment score needed for an alignment to
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724 be considered "valid" (i.e. good enough to report). This is a function of read
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725 length. For instance, specifying `L,0,-0.6` sets the minimum-score function `f`
3
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diff changeset
726 to `f(x) = 0 + -0.6 * x`, where `x` is the read length. The default in `--end-to-end` mode is `L,-0.6,-0.6` and
2
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727 the default in `--local` mode is `G,20,8`.
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diff changeset
728
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parents: 0
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729 -----
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parents: 0
diff changeset
730
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731 **Reporting options**::
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732
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733 -k &lt;int&gt;
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parents: 0
diff changeset
734 By default, `bowtie2` searches for distinct, valid alignments for each read.
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735 When it finds a valid alignment, it continues looking for alignments that are
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736 nearly as good or better. The best alignment found is reported (randomly
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737 selected from among best if tied). Information about the best alignments is
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738 used to estimate mapping quality and to set SAM optional fields, such as
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parents: 0
diff changeset
739 `AS:i` and `XS:i`.
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740
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diff changeset
741 When `-k` is specified, however, `bowtie2` behaves differently. Instead, it
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742 searches for at most `&lt;int&gt;` distinct, valid alignments for each read. The
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diff changeset
743 search terminates when it can't find more distinct valid alignments, or when it
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744 finds `&lt;int&gt;`, whichever happens first. All alignments found are reported in
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parents: 0
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745 descending order by alignment score. The alignment score for a paired-end
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746 alignment equals the sum of the alignment scores of the individual mates. Each
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diff changeset
747 reported read or pair alignment beyond the first has the SAM 'secondary' bit
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parents: 0
diff changeset
748 (which equals 256) set in its FLAGS field. For reads that have more than
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diff changeset
749 `&lt;int&gt;` distinct, valid alignments, `bowtie2` does not guarantee that the
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diff changeset
750 `&lt;int&gt;` alignments reported are the best possible in terms of alignment score.
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751 `-k` is mutually exclusive with `-a`.
0
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752
2
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753 Note: Bowtie 2 is not designed with large values for `-k` in mind, and when
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diff changeset
754 aligning reads to long, repetitive genomes large `-k` can be very, very slow.
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diff changeset
755
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diff changeset
756 -a
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diff changeset
757 Like `-k` but with no upper limit on number of alignments to search for. `-a`
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diff changeset
758 is mutually exclusive with `-k`.
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759
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760 Note: Bowtie 2 is not designed with `-a` mode in mind, and when
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diff changeset
761 aligning reads to long, repetitive genomes this mode can be very, very slow.
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parents: 0
diff changeset
762
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763 -----
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parents: 0
diff changeset
764
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765 **Effort options**::
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diff changeset
766
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parents: 0
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767 -D &lt;int&gt;
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parents: 0
diff changeset
768 Up to `&lt;int&gt;` consecutive seed extension attempts can "fail" before Bowtie 2
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parents: 0
diff changeset
769 moves on, using the alignments found so far. A seed extension "fails" if it
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parents: 0
diff changeset
770 does not yield a new best or a new second-best alignment. This limit is
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parents: 0
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771 automatically adjusted up when -k or -a are specified. Default: 15.
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parents: 0
diff changeset
772
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parents: 0
diff changeset
773 -R &lt;int&gt;
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parents: 0
diff changeset
774 `&lt;int&gt;` is the maximum number of times Bowtie 2 will "re-seed" reads with
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diff changeset
775 repetitive seeds. When "re-seeding," Bowtie 2 simply chooses a new set of reads
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parents: 0
diff changeset
776 (same length, same number of mismatches allowed) at different offsets and
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parents: 0
diff changeset
777 searches for more alignments. A read is considered to have repetitive seeds if
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parents: 0
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778 the total number of seed hits divided by the number of seeds that aligned at
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779 least once is greater than 300. Default: 2.
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parents: 0
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780
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parents: 0
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781 -----
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782
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783 **Paired-end options**::
0
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784
2
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785 -I/--minins &lt;int&gt;
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parents: 0
diff changeset
786 The minimum fragment length for valid paired-end alignments. E.g. if `-I 60` is
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parents: 0
diff changeset
787 specified and a paired-end alignment consists of two 20-bp alignments in the
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parents: 0
diff changeset
788 appropriate orientation with a 20-bp gap between them, that alignment is
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parents: 0
diff changeset
789 considered valid (as long as `-X` is also satisfied). A 19-bp gap would not
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parents: 0
diff changeset
790 be valid in that case. If trimming options `-3` or `-5` are also used, the
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parents: 0
diff changeset
791 `-I` constraint is applied with respect to the untrimmed mates.
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parents: 0
diff changeset
792
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parents: 0
diff changeset
793 The larger the difference between `-I` and `-X`, the slower Bowtie 2 will
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parents: 0
diff changeset
794 run. This is because larger differences bewteen `-I` and `-X` require that
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parents: 0
diff changeset
795 Bowtie 2 scan a larger window to determine if a concordant alignment exists.
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parents: 0
diff changeset
796 For typical fragment length ranges (200 to 400 nucleotides), Bowtie 2 is very
c1ec08cb34f9 Uploaded
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parents: 0
diff changeset
797 efficient.
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798
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799 Default: 0 (essentially imposing no minimum)
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800
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parents: 0
diff changeset
801 -X/--maxins &lt;int&gt;
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parents: 0
diff changeset
802 The maximum fragment length for valid paired-end alignments. E.g. if `-X 100`
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parents: 0
diff changeset
803 is specified and a paired-end alignment consists of two 20-bp alignments in the
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parents: 0
diff changeset
804 proper orientation with a 60-bp gap between them, that alignment is considered
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diff changeset
805 valid (as long as `-I` is also satisfied). A 61-bp gap would not be valid in
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parents: 0
diff changeset
806 that case. If trimming options `-3` or `-5` are also used, the `-X`
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parents: 0
diff changeset
807 constraint is applied with respect to the untrimmed mates, not the trimmed
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parents: 0
diff changeset
808 mates.
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parents: 0
diff changeset
809
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parents: 0
diff changeset
810 The larger the difference between `-I` and `-X`, the slower Bowtie 2 will
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parents: 0
diff changeset
811 run. This is because larger differences bewteen `-I` and `-X` require that
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parents: 0
diff changeset
812 Bowtie 2 scan a larger window to determine if a concordant alignment exists.
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parents: 0
diff changeset
813 For typical fragment length ranges (200 to 400 nucleotides), Bowtie 2 is very
c1ec08cb34f9 Uploaded
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parents: 0
diff changeset
814 efficient.
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parents: 0
diff changeset
815
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parents: 0
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816 Default: 500.
0
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parents:
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817
2
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diff changeset
818 --fr/--rf/--ff
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parents: 0
diff changeset
819 The upstream/downstream mate orientations for a valid paired-end alignment
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parents: 0
diff changeset
820 against the forward reference strand. E.g., if `--fr` is specified and there is
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parents: 0
diff changeset
821 a candidate paired-end alignment where mate 1 appears upstream of the reverse
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parents: 0
diff changeset
822 complement of mate 2 and the fragment length constraints (`-I` and `-X`) are
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parents: 0
diff changeset
823 met, that alignment is valid. Also, if mate 2 appears upstream of the reverse
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parents: 0
diff changeset
824 complement of mate 1 and all other constraints are met, that too is valid.
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parents: 0
diff changeset
825 `--rf` likewise requires that an upstream mate1 be reverse-complemented and a
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parents: 0
diff changeset
826 downstream mate2 be forward-oriented. ` --ff` requires both an upstream mate 1
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parents: 0
diff changeset
827 and a downstream mate 2 to be forward-oriented. Default: `--fr` (appropriate
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parents: 0
diff changeset
828 for Illumina's Paired-end Sequencing Assay).
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parents: 0
diff changeset
829
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diff changeset
830 --no-mixed
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831 By default, when `bowtie2` cannot find a concordant or discordant alignment for
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832 a pair, it then tries to find alignments for the individual mates. This option
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833 disables that behavior.
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834
2
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835 --no-discordant
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836 By default, `bowtie2` looks for discordant alignments if it cannot find any
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837 concordant alignments. A discordant alignment is an alignment where both mates
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838 align uniquely, but that does not satisfy the paired-end constraints
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839 (`--fr`/`--rf`/`--ff`, `-I`, `-X`). This option disables that behavior.
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840
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841 --dovetail
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842 If the mates "dovetail", that is if one mate alignment extends past the
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843 beginning of the other such that the wrong mate begins upstream, consider that
3
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844 to be concordant. Default: mates cannot dovetail in a concordant alignment.
2
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845
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846 --no-contain
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847 If one mate alignment contains the other, consider that to be non-concordant.
3
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848 Default: a mate can contain the other in a concordant alignment.
2
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849
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850 --no-overlap
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851 If one mate alignment overlaps the other at all, consider that to be
3
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852 non-concordant. Default: mates can overlap in a concordant alignment.
2
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853
0
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854 ------
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855
2
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856 **SAM options**::
0
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857
2
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858 --rg-id &lt;text&gt;
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859 Set the read group ID to `&lt;text&gt;`. This causes the SAM `@RG` header line to be
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860 printed, with `&lt;text&gt;` as the value associated with the `ID:` tag. It also
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861 causes the `RG:Z:` extra field to be attached to each SAM output record, with
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862 value set to `&lt;text&gt;`.
0
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863
2
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864 --rg &lt;text&gt;
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865 Add `&lt;text&gt;` (usually of the form `TAG:VAL`, e.g. `SM:Pool1`) as a field on the
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866 `@RG` header line. Note: in order for the `@RG` line to appear, `--rg-id`
3
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867 must also be specified. This is because the `ID` tag is required by the SAM
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868 Specification. Specify `--rg` multiple times to set multiple fields. See the
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869 SAM Specification for details about what fields are legal.
0
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870
2
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871 --omit-sec-seq
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872 When printing secondary alignments, Bowtie 2 by default will write out the `SEQ`
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873 and `QUAL` strings. Specifying this option causes Bowtie 2 to print an asterix
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874 in those fields instead.
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875
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876 -----
0
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877
2
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878 **Other options**::
0
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879
2
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880 --reorder
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881 Guarantees that output SAM records are printed in an order corresponding to the
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882 order of the reads in the original input file, even when `-p` is set greater
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883 than 1. Specifying `--reorder` and setting `-p` greater than 1 causes Bowtie
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884 2 to run somewhat slower and use somewhat more memory then if `--reorder` were
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885 not specified. Has no effect if `-p` is set to 1, since output order will
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886 naturally correspond to input order in that case.
0
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887
2
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888 --seed &lt;int&gt;
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889 Use `&lt;int&gt;` as the seed for pseudo-random number generator. Default: 0.
0
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890
2
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891 --non-deterministic
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892 Normally, Bowtie 2 re-initializes its pseudo-random generator for each read. It
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893 seeds the generator with a number derived from (a) the read name, (b) the
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894 nucleotide sequence, (c) the quality sequence, (d) the value of the `--seed`
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895 option. This means that if two reads are identical (same name, same
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896 nucleotides, same qualities) Bowtie 2 will find and report the same alignment(s)
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897 for both, even if there was ambiguity. When `--non-deterministic` is specified,
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898 Bowtie 2 re-initializes its pseudo-random generator for each read using the
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899 current time. This means that Bowtie 2 will not necessarily report the same
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900 alignment for two identical reads. This is counter-intuitive for some users,
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901 but might be more appropriate in situations where the input consists of many
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902 identical reads.
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903
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904 </help>
2
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905 <citations>
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906 <citation type="doi">10.1186/gb-2009-10-3-r25</citation>
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907 <citation type="doi">10.1038/nmeth.1923</citation>
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908 </citations>
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909 </tool>