annotate bowtie2_wrapper.xml @ 14:85f0e9edb32d draft

planemo upload for repository https://github.com/galaxyproject/tools-devteam/tree/master/tools/bowtie2 commit 954b2052cb74a0bc88f65df37f429ff27c45ea8f
author devteam
date Wed, 12 Apr 2017 17:09:24 -0400
parents 55dcd6aad1ab
children 7e0b333f39e1
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14
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1 <tool id="bowtie2" name="Bowtie2" version="2.3.0.1" profile="17.01">
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2 <description>- map reads against reference genome</description>
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3 <macros>
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4 <import>read_group_macros.xml</import>
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5 </macros>
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6 <requirements>
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7 <requirement type="package" version="2.3.0">bowtie2</requirement>
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8 <requirement type="package" version="1.3.1">samtools</requirement>
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9 </requirements>
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10 <version_command>bowtie2 --version</version_command>
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11 <command detect_errors="exit_code"><![CDATA[
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12 ## prepare bowtie2 index
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13 #set index_path = ''
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14 #if str($reference_genome.source) == "history":
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15 bowtie2-build --threads \${GALAXY_SLOTS:-4} '$reference_genome.own_file' genome &&
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16 ln -s -f '$reference_genome.own_file' genome.fa &&
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17 #set index_path = 'genome'
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18 #else:
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19 #set index_path = $reference_genome.index.fields.path
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20 #end if
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21
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22 ## Link in the input files, so bowtie2 can tell their type
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24 #set compressed="False"
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25 #if str($library.type) == 'paired':
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26 #if $library.input_1.is_of_type("fastq.gz", "fastqsanger.gz"):
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27 #set read1 = "input_f.fastq.gz"
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28 #set compressed = "GZ"
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29 #else if $library.input_1.is_of_type("fastq.bz2", "fastqsanger.bz2"):
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30 #set read1 = "input_f.fastq.bz2"
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31 #set compressed = "BZ2"
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32 #else:
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33 #set read1 = "input_f.fastq"
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34 #end if
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35 ln -f -s '${library.input_1}' ${read1} &&
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36
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37 #if $library.input_2.is_of_type("fastq.gz", "fastqsanger.gz"):
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38 #set read2 = "input_r.fastq.gz"
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39 #set compressed = "GZ"
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40 #else if $library.input_2.is_of_type("fastq.bz2", "fastqsanger.bz2"):
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41 #set read2 = "input_r.fastq.bz2"
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42 #set compressed = "BZ2"
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43 #else:
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44 #set read2 = "input_r.fastq"
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45 #end if
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46 ln -f -s '${library.input_2}' ${read2} &&
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47 #else if str($library.type) == 'paired_collection':
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48 #if $library.input_1.forward.is_of_type("fastq.gz", "fastqsanger.gz"):
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49 #set read1 = "input_f.fastq.gz"
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50 #set compressed = "GZ"
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51 #else if $library.input_1.forward.is_of_type("fastq.bz2", "fastqsanger.bz2"):
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52 #set read1 = "input_f.fastq.bz2"
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53 #set compressed = "BZ2"
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54 #else:
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55 #set read1 = "input_f.fastq"
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56 #end if
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57 ln -s '${library.input_1.forward}' ${read1} &&
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58
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59 #if $library.input_1.reverse.is_of_type("fastq.gz", "fastqsanger.gz"):
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60 #set read2 = "input_r.fastq.gz"
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61 #set compressed = "GZ"
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62 #else if $library.input_1.reverse.is_of_type("fastq.bz2", "fastqsanger.bz2"):
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63 #set read2 = "input_r.fastq.bz2"
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64 #set compressed = "BZ2"
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65 #else:
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66 #set read2 = "input_r.fastq"
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67 #end if
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68 ln -s '${library.input_1.reverse}' ${read2} &&
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69 #else:
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70 #if $library.input_1.is_of_type("fastq.gz", "fastqsanger.gz"):
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71 #set read1 = "input_f.fastq.gz"
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72 #set compressed = "GZ"
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73 #else if $library.input_1.is_of_type("fastq.bz2", "fastqsanger.bz2"):
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74 #set read1 = "input_f.fastq.bz2"
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75 #set compressed = "BZ2"
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76 #else:
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77 #set read1 = "input_f.fastq"
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78 #end if
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79 ln -s '${library.input_1}' ${read1} &&
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80 #end if
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81
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82 ## execute bowtie2
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83
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84 bowtie2
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85
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86 ## number of threads
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87 -p \${GALAXY_SLOTS:-4}
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88
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89 ## index file path
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90 -x '$index_path'
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91
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92 ## Fastq inputs
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93 #if str( $library.type ) == "single":
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94 -U '${read1}'
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95 #if str( $library.unaligned_file ) == "true":
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96 #if $compressed == "GZ":
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97 --un-gz '${output_unaligned_reads_l}'
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98 #else if $compressed == "BZ2":
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99 --un-bz2 '${output_unaligned_reads_l}'
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100 #else:
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101 --un '${output_unaligned_reads_l}'
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102 #end if
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103 #end if
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104 #if str( $library.aligned_file ) == "true":
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105 #if $compressed == "GZ":
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106 --al-gz '${output_aligned_reads_l}'
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107 #else if $compressed == "BZ2":
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108 --al-bz2 '${output_aligned_reads_l}'
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109 #else:
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110 --al '${output_aligned_reads_l}'
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111 #end if
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112 #end if
14
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113 #else:
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114 -1 '${read1}'
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115 -2 '${read2}'
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116 #if str( $library.unaligned_file ) == "true":
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117 #if $compressed == "GZ":
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118 --un-conc-gz '${output_unaligned_reads_l}'
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119 #else if $compressed == "BZ2":
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120 --un-conc-bz2 '${output_unaligned_reads_l}'
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121 #else:
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122 --un-conc '${output_unaligned_reads_l}'
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123 #end if
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124 #end if
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125 #if str( $library.aligned_file ) == "true":
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126 #if $compressed == "GZ":
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127 --al-conc-gz '${output_aligned_reads_l}'
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128 #else if $compressed == "BZ2":
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129 --al-conc-bz2 '${output_aligned_reads_l}'
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130 #else:
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131 --al-conc '${output_aligned_reads_l}'
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132 #end if
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133 #end if
2
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134 #if str( $library.paired_options.paired_options_selector ) == "yes":
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135 -I "${library.paired_options.I}"
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136 -X "${library.paired_options.X}"
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137 ${library.paired_options.fr_rf_ff}
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138 ${library.paired_options.no_mixed}
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139 ${library.paired_options.no_discordant}
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140 ${library.paired_options.dovetail}
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141 ${library.paired_options.no_contain}
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142 ${library.paired_options.no_overlap}
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143 #end if
0
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144 #end if
5
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145
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146 ## Read group information.
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147 @define_read_group_helpers@
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148 #if str( $library.type ) == "single":
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149 #set $rg_auto_name = $read_group_name_default($library.input_1)
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150 #elif str( $library.type ) == "paired":
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151 #set $rg_auto_name = $read_group_name_default($library.input_1, $library.input_2)
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152 #else
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153 #set $rg_auto_name = $read_group_name_default($library.input_1)
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154 #end if
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155 @set_use_rg_var@
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156 @set_read_group_vars@
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157 #if $use_rg
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158 $format_read_group("", $rg_id, '"', arg='--rg-id ')
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159 $format_read_group("SM:", $rg_sm, '"', arg='--rg ')
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160 $format_read_group("PL:", $rg_pl, '"', arg='--rg ')
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161 $format_read_group("LB:", $rg_lb, '"', arg='--rg ')
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162 $format_read_group("CN:", $rg_cn, '"', arg='--rg ')
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163 $format_read_group("DS:", $rg_ds, '"', arg='--rg ')
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164 $format_read_group("DT:", $rg_dt, '"', arg='--rg ')
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165 $format_read_group("FO:", $rg_fo, '"', arg='--rg ')
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166 $format_read_group("KS:", $rg_ks, '"', arg='--rg ')
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167 $format_read_group("PG:", $rg_pg, '"', arg='--rg ')
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168 $format_read_group("PI:", $rg_pi, '"', arg='--rg ')
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169 $format_read_group("PU:", $rg_pu, '"', arg='--rg ')
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170 #end if
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171
2
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172 ## Analysis type
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173 #if ( str( $analysis_type.analysis_type_selector ) == "simple" and str( $analysis_type.presets ) != "no_presets" ):
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174 $analysis_type.presets
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175 #elif str( $analysis_type.analysis_type_selector ) == "full":
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176 #if str( $analysis_type.input_options.input_options_selector ) == "yes":
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177 --skip "${analysis_type.input_options.skip}"
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178 --qupto "${analysis_type.input_options.qupto}"
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179 --trim5 "${analysis_type.input_options.trim5}"
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180 --trim3 "${analysis_type.input_options.trim3}"
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181 ${analysis_type.input_options.qv_encoding}
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182 ${analysis_type.input_options.solexa_quals}
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183 ${analysis_type.input_options.int_quals}
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184 #end if
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185
2
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186 #if str( $analysis_type.alignment_options.alignment_options_selector ) == "yes":
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187 -N "${analysis_type.alignment_options.N}"
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188 -L "${analysis_type.alignment_options.L}"
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189 -i "${analysis_type.alignment_options.i}"
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190 --n-ceil "${analysis_type.alignment_options.n_ceil}"
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191 --dpad "${analysis_type.alignment_options.dpad}"
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192 --gbar "${analysis_type.alignment_options.gbar}"
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193 ${analysis_type.alignment_options.ignore_quals}
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194 ${analysis_type.alignment_options.nofw}
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195 ${analysis_type.alignment_options.norc}
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196 ${analysis_type.alignment_options.no_1mm_upfront}
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197 #if str( $analysis_type.alignment_options.align_mode.align_mode_selector ) == "end-to-end":
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198 --end-to-end
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199 --score-min "${analysis_type.alignment_options.align_mode.score_min_ete}"
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200 #elif str( $analysis_type.alignment_options.align_mode.align_mode_selector ) == "local":
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201 --local
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202 --score-min "${analysis_type.alignment_options.align_mode.score_min_loc}"
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203 #end if
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204 #end if
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205
2
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206 #if str( $analysis_type.scoring_options.scoring_options_selector ) == "yes":
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207 #if ( str( $analysis_type.alignment_options.alignment_options_selector ) == "yes" and str( $analysis_type.alignment_options.align_mode.align_mode_selector ) == "local" ):
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208 --ma "${analysis_type.scoring_options.ma}"
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209 #end if
2
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210 --mp "${analysis_type.scoring_options.mp}"
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211 --np "${analysis_type.scoring_options.np}"
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212 --rdg "${analysis_type.scoring_options.rdg_read_open},${analysis_type.scoring_options.rdg_read_extend}"
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213 --rfg "${analysis_type.scoring_options.rfg_ref_open},${analysis_type.scoring_options.rfg_ref_extend}"
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214 #end if
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215
2
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216 #if str( $analysis_type.reporting_options.reporting_options_selector ) == "k":
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217 -k "${analysis_type.reporting_options.k}"
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218 #elif str( $analysis_type.reporting_options.reporting_options_selector ) == "a":
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219 -a
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220 #end if
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221
2
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222 #if str( $analysis_type.effort_options.effort_options_selector ) == "yes":
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223 -D "${analysis_type.effort_options.D}"
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224 -R "${analysis_type.effort_options.R}"
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225 #end if
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226
2
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227 #if str( $analysis_type.sam_options.sam_options_selector ) == "yes":
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228 ${analysis_type.sam_options.no_unal}
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229 ${analysis_type.sam_options.omit_sec_seq}
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230 #end if
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231
2
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232 #if str( $analysis_type.other_options.other_options_selector ) == "yes":
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233 ${analysis_type.other_options.reorder}
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234 ${analysis_type.other_options.non_deterministic}
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235 --seed "${analysis_type.other_options.seed}"
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236 #end if
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237
2
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238 #elif str( $analysis_type.analysis_type_selector ) == "cline":
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239 ${analysis_type.cline}
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240 #end if
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241
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242 ## mapping stats (i.e. stderr from bowtie2)
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243 #if $save_mapping_stats
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244 2> '$mapping_stats'
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245 #end if
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246
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247 ## output file
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248 #if ( str( $analysis_type.analysis_type_selector ) != "full" or str( $analysis_type.sam_opt ) != "true" ):
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249 | samtools sort -O bam -o '$output'
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250 #else
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251 > '$output_sam'
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252 #end if
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253
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254 ## rename unaligned sequence files
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255 #if $library.type == "paired" and $output_unaligned_reads_l and $output_unaligned_reads_r:
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256 #from os.path import splitext
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257 #set _unaligned_root, _unaligned_ext = splitext( str( $output_unaligned_reads_l ) )
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258 && mv "${ _unaligned_root }.1${_unaligned_ext}" '$output_unaligned_reads_l'
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259 && mv "${ _unaligned_root }.2${_unaligned_ext}" '$output_unaligned_reads_r'
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260 #end if
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261 #if $library.type == "paired" and $output_aligned_reads_l and $output_aligned_reads_r:
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262 #from os.path import splitext
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263 #set _aligned_root, _aligned_ext = splitext( str( $output_aligned_reads_l ) )
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264 && mv "${ _aligned_root }.1${_aligned_ext}" '$output_aligned_reads_l'
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265 && mv "${ _aligned_root }.2${_aligned_ext}" '$output_aligned_reads_r'
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266 #end if
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267
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268 ]]></command>
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269 <inputs>
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270 <!-- single/paired -->
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271 <conditional name="library">
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272 <param name="type" type="select" label="Is this single or paired library">
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273 <option value="single">Single-end</option>
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274 <option value="paired">Paired-end</option>
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275 <option value="paired_collection">Paired-end Dataset Collection</option>
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276 </param>
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277
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278 <when value="single">
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279 <param name="input_1" format="fastqsanger,fastqsanger.gz,fastqsanger.bz2" type="data" label="FASTQ file" help="Must be of datatype &quot;fastqsanger&quot;" />
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280 <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 (possibly with -gz or -bz2); This triggers --un parameter for single reads and --un-conc for paired reads" />
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281 <param name="aligned_file" type="boolean" truevalue="true" falsevalue="false" checked="False" label="Write aligned reads (in fastq format) to separate file(s)" help="--al/--al-conc (possibly with -gz or -bz2); This triggers --al parameter for single reads and --al-conc for paired reads" />
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282 </when>
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283 <when value="paired">
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284 <param name="input_1" format="fastqsanger,fastqsanger.gz,fastqsanger.bz2" type="data" label="FASTQ file #1" help="Must be of datatype &quot;fastqsanger&quot;" />
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285 <param name="input_2" format="fastqsanger,fastqsanger.gz,fastqsanger.bz2" type="data" label="FASTQ file #2" help="Must be of datatype &quot;fastqsanger&quot;" />
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286 <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 (possibly with -gz or -bz2); This triggers --un parameter for single reads and --un-conc for paired reads" />
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287 <param name="aligned_file" type="boolean" truevalue="true" falsevalue="false" checked="False" label="Write aligned reads (in fastq format) to separate file(s)" help="--al/--al-conc (possibly with -gz or -bz2); This triggers --al parameter for single reads and --al-conc for paired reads" />
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288 <conditional name="paired_options">
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289 <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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290 <option value="no" selected="True">No</option>
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291 <option value="yes">Yes</option>
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292 </param>
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293 <when value="yes">
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294 <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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295 <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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296 <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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297 <option value="--fr" selected="True">--fr</option>
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298 <option value="--rf">--rf</option>
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299 <option value="--ff">--ff</option>
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300 </param>
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301 <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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302 <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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303 <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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304 <param name="no_contain" type="boolean" truevalue="--no-contain" falsevalue="" checked="False" label="Disallow 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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305 <param name="no_overlap" type="boolean" truevalue="--no-overlap" falsevalue="" checked="False" label="Disallow 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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306 </when>
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307 <when value="no">
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308 <!-- do nothing -->
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309 </when>
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310 </conditional>
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311 </when>
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312 <when value="paired_collection">
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313 <param name="input_1" format="fastqsanger,fastqsanger.gz,fastqsanger.bz2" type="data_collection" collection_type="paired" label="FASTQ Paired Dataset" help="Must be of datatype &quot;fastqsanger&quot;" />
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314 <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 (possibly with -gz or -bz2); This triggers --un parameter for single reads and --un-conc for paired reads" />
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315 <param name="aligned_file" type="boolean" truevalue="true" falsevalue="false" checked="False" label="Write aligned reads (in fastq format) to separate file(s)" help="--al/--al-conc (possibly with -gz or -bz2); This triggers --al parameter for single reads and --al-conc for paired reads" />
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316 <conditional name="paired_options">
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317 <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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318 <option value="no" selected="True">No</option>
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319 <option value="yes">Yes</option>
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320 </param>
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321 <when value="yes">
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322 <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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323 <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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324 <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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325 <option value="--fr" selected="True">--fr</option>
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326 <option value="--rf">--rf</option>
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327 <option value="--ff">--ff</option>
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328 </param>
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329 <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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330 <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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331 <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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332 <param name="no_contain" type="boolean" truevalue="--no-contain" falsevalue="" checked="False" label="Disallow 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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333 <param name="no_overlap" type="boolean" truevalue="--no-overlap" falsevalue="" checked="False" label="Disallow 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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334 </when>
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335 <when value="no">
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336 <!-- do nothing -->
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337 </when>
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338 </conditional>
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339 </when>
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340 </conditional>
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341
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342 <!-- reference genome -->
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343 <conditional name="reference_genome">
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344 <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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345 <option value="indexed">Use a built-in genome index</option>
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346 <option value="history">Use a genome from the history and build index</option>
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347 </param>
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348 <when value="indexed">
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349 <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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350 <options from_data_table="bowtie2_indexes">
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351 <filter type="sort_by" column="2"/>
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352 <validator type="no_options" message="No indexes are available for the selected input dataset"/>
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353 </options>
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354 </param>
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355 </when>
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356 <when value="history">
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357 <param name="own_file" type="data" format="fasta" label="Select reference genome" />
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358 </when>
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359 </conditional>
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360
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361 <!-- read group settings -->
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362 <expand macro="read_group_conditional" />
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363 <conditional name="analysis_type">
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364 <param name="analysis_type_selector" type="select" label="Select analysis mode">
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365 <option value="simple">1: Default setting only</option>
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366 <option value="full">2: Full parameter list</option>
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367 </param>
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368 <when value="simple">
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369 <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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370 <option value="no_presets" selected="True">No, just use defaults</option>
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371 <option value="--very-fast">Very fast end-to-end (--very-fast)</option>
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372 <option value="--fast">Fast end-to-end (--fast)</option>
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373 <option value="--sensitive">Sensitive end-to-end (--sensitive)</option>
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374 <option value="--very-sensitive">Very sensitive end-to-end (--very-sensitive)</option>
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375 <option value="--very-fast-local">Very fast local (--very-fast-local)</option>
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376 <option value="--fast-local">Fast local (--fast-local)</option>
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377 <option value="--sensitive-local">Sensitive local (--sensitive-local)</option>
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378 <option value="--very-sensitive-local">Very sensitive local (--very-sensitive-local)</option>
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379 </param>
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380 </when>
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381 <when value="full">
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382 <conditional name="input_options">
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383 <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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384 <option value="yes">Yes</option>
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385 <option value="no" selected="true">No</option>
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386 </param>
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387 <when value="yes">
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388 <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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389 <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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390 <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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391 <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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392 <param name="qv_encoding" type="select" display="radio" label="Select quality score encoding" help="See help below for more details">
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393 <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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394 <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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395 </param>
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396 <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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397 <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"/>
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398 </when>
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399 <when value="no">
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400 <!-- do nothing -->
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401 </when>
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402 </conditional>
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403 <conditional name="alignment_options">
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404 <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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405 <option value="yes">Yes</option>
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406 <option value="no" selected="true">No</option>
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407 </param>
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408 <when value="yes">
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409 <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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410 <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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411 <param name="i" type="text" value="S,1,1.15" 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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412 <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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413 <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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414 <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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415 <param name="ignore_quals" type="boolean" truevalue="--ignore-quals" falsevalue="" 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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416 <param name="nofw" type="boolean" truevalue="--nofw" falsevalue="" 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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417 <param name="norc" type="boolean" truevalue="--norc" falsevalue="" 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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418 <param name="no_1mm_upfront" type="boolean" truevalue="--no-1mm-upfront" falsevalue="" 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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419 <conditional name="align_mode">
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420 <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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421 <option value="end-to-end" selected="True">End to End (--end-to-end)</option>
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422 <option value="local">Local (--local)</option>
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423 </param>
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424 <when value="end-to-end">
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425 <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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426 </when>
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427 <when value="local">
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428 <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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429 </when>
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430 </conditional>
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431 </when>
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432 <when value="no">
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433 <!-- do nothing -->
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434 </when>
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435 </conditional>
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436 <conditional name="scoring_options">
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437 <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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438 <option value="yes">Yes</option>
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439 <option value="no" selected="true">No</option>
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440 </param>
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441 <when value="yes">
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442 <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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443 <param name="mp" type="text" 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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444 <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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445 <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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446 <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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447 <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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448 <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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449 </when>
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450 <when value="no">
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451 <!-- do nothing -->
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452 </when>
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453 </conditional>
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454 <conditional name="reporting_options">
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455 <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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456 <option value="no" selected="true">No, do not set</option>
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457 <option value="k">Set -k option and enter -k value</option>
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458 <option value="a">Set -a option</option>
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459 </param>
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460 <when value="no">
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461 <!-- do nothing -->
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462 </when>
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463 <when value="k">
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464 <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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465 </when>
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466 <when value="a">
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467 <!-- do nothing here; set -a flag on the command line-->
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468 </when>
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469 </conditional>
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470 <conditional name="effort_options">
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471 <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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472 <option value="yes">Yes</option>
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473 <option value="no" selected="true">No</option>
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474 </param>
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475 <when value="yes">
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476 <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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477 <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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478 </when>
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479 <when value="no">
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480 <!-- do nothing -->
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481 </when>
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482 </conditional>
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483
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484 <conditional name="sam_options">
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485 <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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486 <option value="yes">Yes</option>
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487 <option value="no" selected="true">No</option>
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488 </param>
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489 <when value="yes">
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490 <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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491 <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"/>
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492 </when>
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493 <when value="no">
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494 <!-- do nothing -->
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495 </when>
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496 </conditional>
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497 <conditional name="other_options">
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498 <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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499 <option value="yes">Yes</option>
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500 <option value="no" selected="true">No</option>
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501 </param>
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502 <when value="yes">
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503 <param name="reorder" type="boolean" truevalue="--reorder" falsevalue="" label="Guarantee that output SAM records are printed in an order corresponding to the order of the reads in the original input file" help="--reorder; Default=False"/>
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504 <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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505 <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"/>
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506 </when>
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507 <when value="no">
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508 <!-- do nothing -->
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509 </when>
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510 </conditional>
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511 <param name="sam_opt" type="boolean" truevalue="true" falsevalue="false" label="Would you like the output to be a SAM file" help="By default, the output from this Bowtie2 wrapper is a sorted BAM file."/>
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512 </when>
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513 </conditional>
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514 <param name="save_mapping_stats" type="boolean" checked="False" label="Save the bowtie2 mapping statistics to the history" />
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515 </inputs>
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516
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517 <!-- define outputs -->
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518
0
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519 <outputs>
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520
0
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521 <data format="fastqsanger" name="output_unaligned_reads_l" label="${tool.name} on ${on_string}: unaligned reads (L)" >
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522 <filter>library['unaligned_file'] is True</filter>
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523 <actions>
5
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524 <conditional name="library.type">
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525 <when value="single">
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526 <action type="format">
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527 <option type="from_param" name="library.input_1" param_attribute="ext" />
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528 </action>
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529 </when>
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530 <when value="paired">
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531 <action type="format">
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532 <option type="from_param" name="library.input_1" param_attribute="ext" />
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533 </action>
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534 </when>
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535 <when value="paired_collection">
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536 <action type="format">
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537 <option type="from_param" name="library.input_1" param_attribute="forward.ext" />
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538 </action>
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539 </when>
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540 </conditional>
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541 </actions>
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542 </data>
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543 <data format="fastqsanger" name="output_aligned_reads_l" label="${tool.name} on ${on_string}: aligned reads (L)" >
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544 <filter>library['aligned_file'] is True</filter>
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545 <actions>
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546 <conditional name="library.type">
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547 <when value="single">
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548 <action type="format">
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549 <option type="from_param" name="library.input_1" param_attribute="ext" />
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550 </action>
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551 </when>
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552 <when value="paired">
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553 <action type="format">
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554 <option type="from_param" name="library.input_1" param_attribute="ext" />
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555 </action>
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556 </when>
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557 <when value="paired_collection">
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558 <action type="format">
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559 <option type="from_param" name="library.input_1" param_attribute="forward.ext" />
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560 </action>
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561 </when>
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562 </conditional>
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563 </actions>
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564 </data>
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565 <data format="fastqsanger" name="output_aligned_reads_r" label="${tool.name} on ${on_string}: aligned reads (R)">
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566 <filter>( library['type'] == "paired" or library['type'] == "paired_collection" ) and library['aligned_file'] is True</filter>
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567 <actions>
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568 <conditional name="library.type">
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569 <when value="paired">
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570 <action type="format">
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571 <option type="from_param" name="library.input_2" param_attribute="ext" />
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572 </action>
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573 </when>
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574 <when value="paired_collection">
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575 <action type="format">
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576 <option type="from_param" name="library.input_1" param_attribute="reverse.ext" />
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577 </action>
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578 </when>
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579 </conditional>
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580 </actions>
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581 </data>
0
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582 <data format="fastqsanger" name="output_unaligned_reads_r" label="${tool.name} on ${on_string}: unaligned reads (R)">
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parents: 1
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583 <filter>( library['type'] == "paired" or library['type'] == "paired_collection" ) and library['unaligned_file'] is True</filter>
0
a03a7ee6cdff Imported from capsule None
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584 <actions>
5
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585 <conditional name="library.type">
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586 <when value="paired">
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587 <action type="format">
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588 <option type="from_param" name="library.input_2" param_attribute="ext" />
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589 </action>
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590 </when>
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591 <when value="paired_collection">
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diff changeset
592 <action type="format">
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593 <option type="from_param" name="library.input_1" param_attribute="reverse.ext" />
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594 </action>
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595 </when>
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596 </conditional>
0
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597 </actions>
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598 </data>
11
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599
5
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600 <data format="bam" name="output" label="${tool.name} on ${on_string}: aligned reads (sorted BAM)">
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601 <filter>analysis_type['analysis_type_selector'] == "simple" or analysis_type['sam_opt'] is False</filter>
0
a03a7ee6cdff Imported from capsule None
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602 <actions>
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603 <conditional name="reference_genome.source">
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604 <when value="indexed">
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605 <action type="metadata" name="dbkey">
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606 <option type="from_data_table" name="bowtie2_indexes" column="1" offset="0">
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607 <filter type="param_value" column="0" value="#" compare="startswith" keep="False"/>
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608 <filter type="param_value" ref="reference_genome.index" column="0"/>
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609 </option>
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610 </action>
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611 </when>
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612 <when value="history">
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613 <action type="metadata" name="dbkey">
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614 <option type="from_param" name="reference_genome.own_file" param_attribute="dbkey" />
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615 </action>
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616 </when>
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617 </conditional>
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618 </actions>
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619 </data>
5
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620
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621 <data format="sam" name="output_sam" label="${tool.name} on ${on_string}: aligned reads (SAM)">
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622 <filter>analysis_type['analysis_type_selector'] == "full" and analysis_type['sam_opt'] is True</filter>
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623 <actions>
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624 <conditional name="reference_genome.source">
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625 <when value="indexed">
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626 <action type="metadata" name="dbkey">
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627 <option type="from_data_table" name="bowtie2_indexes" column="1" offset="0">
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628 <filter type="param_value" column="0" value="#" compare="startswith" keep="False"/>
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629 <filter type="param_value" ref="reference_genome.index" column="0"/>
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630 </option>
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631 </action>
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632 </when>
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633 <when value="history">
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634 <action type="metadata" name="dbkey">
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635 <option type="from_param" name="reference_genome.own_file" param_attribute="dbkey" />
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636 </action>
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637 </when>
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638 </conditional>
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639 </actions>
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640 </data>
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641 <data format="txt" name="mapping_stats" label="${tool.name} on ${on_string}: mapping stats">
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642 <filter>save_mapping_stats is True</filter>
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643 </data>
5
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644
0
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645 </outputs>
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646
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647 <tests>
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648 <test>
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649 <!-- basic test on single paired default run -->
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650 <param name="type" value="paired"/>
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651 <param name="selection" value="no"/>
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652 <param name="paired_options_selector" value="no"/>
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653 <param name="unaligned_file" value="false"/>
2
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654 <param name="analysis_type_selector" value="simple"/>
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a03a7ee6cdff Imported from capsule None
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655 <param name="source" value="history" />
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656 <param name="input_1" value="bowtie2-fq1.fq" ftype="fastqsanger"/>
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657 <param name="input_2" value="bowtie2-fq2.fq" ftype="fastqsanger"/>
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658 <param name="own_file" value="bowtie2-ref.fasta" />
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659 <output name="output" file="bowtie2-test1.bam" ftype="bam" lines_diff="2"/>
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660 </test>
5
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661 <test>
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662 <!-- basic test on single paired default run -->
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663 <param name="type" value="paired"/>
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664 <param name="selection" value="no"/>
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665 <param name="paired_options_selector" value="no"/>
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666 <param name="unaligned_file" value="false"/>
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667 <param name="analysis_type_selector" value="simple"/>
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668 <param name="rg_selector" value="set"/>
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669 <param name="ID" value="rg1"/>
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670 <param name="PL" value="CAPILLARY"/>
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671 <param name="source" value="history" />
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672 <param name="input_1" value="bowtie2-fq1.fq" ftype="fastqsanger"/>
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673 <param name="input_2" value="bowtie2-fq2.fq" ftype="fastqsanger"/>
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674 <param name="own_file" value="bowtie2-ref.fasta" />
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675 <output name="output" file="bowtie2-test2.bam" ftype="bam" lines_diff="2"/>
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676 </test>
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677 <test>
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678 <!-- basic test on single paired default run with stats-->
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679 <param name="type" value="paired"/>
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680 <param name="selection" value="no"/>
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681 <param name="paired_options_selector" value="no"/>
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diff changeset
682 <param name="unaligned_file" value="false"/>
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diff changeset
683 <param name="analysis_type_selector" value="simple"/>
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diff changeset
684 <param name="source" value="history" />
fed480fea9f0 planemo upload for repository https://github.com/galaxyproject/tools-devteam/tree/master/tools/bowtie2 commit de7140295cce07e1bc1697e51dab4271c8d7a8a6
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diff changeset
685 <param name="input_1" value="bowtie2-fq1.fq" ftype="fastqsanger"/>
fed480fea9f0 planemo upload for repository https://github.com/galaxyproject/tools-devteam/tree/master/tools/bowtie2 commit de7140295cce07e1bc1697e51dab4271c8d7a8a6
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diff changeset
686 <param name="input_2" value="bowtie2-fq2.fq" ftype="fastqsanger"/>
fed480fea9f0 planemo upload for repository https://github.com/galaxyproject/tools-devteam/tree/master/tools/bowtie2 commit de7140295cce07e1bc1697e51dab4271c8d7a8a6
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diff changeset
687 <param name="own_file" value="bowtie2-ref.fasta" />
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diff changeset
688 <param name="save_mapping_stats" value="true" />
fed480fea9f0 planemo upload for repository https://github.com/galaxyproject/tools-devteam/tree/master/tools/bowtie2 commit de7140295cce07e1bc1697e51dab4271c8d7a8a6
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diff changeset
689 <output name="output" file="bowtie2-test1.bam" ftype="bam" lines_diff="2"/>
fed480fea9f0 planemo upload for repository https://github.com/galaxyproject/tools-devteam/tree/master/tools/bowtie2 commit de7140295cce07e1bc1697e51dab4271c8d7a8a6
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diff changeset
690 <output name="mapping_stats" file="bowtie2-stats.out" ftype="txt"/>
fed480fea9f0 planemo upload for repository https://github.com/galaxyproject/tools-devteam/tree/master/tools/bowtie2 commit de7140295cce07e1bc1697e51dab4271c8d7a8a6
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diff changeset
691 </test>
14
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diff changeset
692 <test>
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diff changeset
693 <!-- test fastqsanger.gz input -->
85f0e9edb32d planemo upload for repository https://github.com/galaxyproject/tools-devteam/tree/master/tools/bowtie2 commit 954b2052cb74a0bc88f65df37f429ff27c45ea8f
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diff changeset
694 <param name="type" value="paired"/>
85f0e9edb32d planemo upload for repository https://github.com/galaxyproject/tools-devteam/tree/master/tools/bowtie2 commit 954b2052cb74a0bc88f65df37f429ff27c45ea8f
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diff changeset
695 <param name="selection" value="no"/>
85f0e9edb32d planemo upload for repository https://github.com/galaxyproject/tools-devteam/tree/master/tools/bowtie2 commit 954b2052cb74a0bc88f65df37f429ff27c45ea8f
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diff changeset
696 <param name="paired_options_selector" value="no"/>
85f0e9edb32d planemo upload for repository https://github.com/galaxyproject/tools-devteam/tree/master/tools/bowtie2 commit 954b2052cb74a0bc88f65df37f429ff27c45ea8f
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diff changeset
697 <param name="unaligned_file" value="false"/>
85f0e9edb32d planemo upload for repository https://github.com/galaxyproject/tools-devteam/tree/master/tools/bowtie2 commit 954b2052cb74a0bc88f65df37f429ff27c45ea8f
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diff changeset
698 <param name="analysis_type_selector" value="simple"/>
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diff changeset
699 <param name="source" value="history" />
85f0e9edb32d planemo upload for repository https://github.com/galaxyproject/tools-devteam/tree/master/tools/bowtie2 commit 954b2052cb74a0bc88f65df37f429ff27c45ea8f
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diff changeset
700 <param name="input_1" value="bowtie2-fq1.fq.gz" ftype="fastqsanger.gz"/>
85f0e9edb32d planemo upload for repository https://github.com/galaxyproject/tools-devteam/tree/master/tools/bowtie2 commit 954b2052cb74a0bc88f65df37f429ff27c45ea8f
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diff changeset
701 <param name="input_2" value="bowtie2-fq2.fq.gz" ftype="fastqsanger.gz"/>
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diff changeset
702 <param name="own_file" value="bowtie2-ref.fasta" />
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diff changeset
703 <output name="output" file="bowtie2-test1.bam" ftype="bam" lines_diff="2"/>
85f0e9edb32d planemo upload for repository https://github.com/galaxyproject/tools-devteam/tree/master/tools/bowtie2 commit 954b2052cb74a0bc88f65df37f429ff27c45ea8f
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diff changeset
704 </test>
85f0e9edb32d planemo upload for repository https://github.com/galaxyproject/tools-devteam/tree/master/tools/bowtie2 commit 954b2052cb74a0bc88f65df37f429ff27c45ea8f
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diff changeset
705 <test>
85f0e9edb32d planemo upload for repository https://github.com/galaxyproject/tools-devteam/tree/master/tools/bowtie2 commit 954b2052cb74a0bc88f65df37f429ff27c45ea8f
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diff changeset
706 <!-- test fastqsanger.bz2 input -->
85f0e9edb32d planemo upload for repository https://github.com/galaxyproject/tools-devteam/tree/master/tools/bowtie2 commit 954b2052cb74a0bc88f65df37f429ff27c45ea8f
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diff changeset
707 <param name="type" value="paired"/>
85f0e9edb32d planemo upload for repository https://github.com/galaxyproject/tools-devteam/tree/master/tools/bowtie2 commit 954b2052cb74a0bc88f65df37f429ff27c45ea8f
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diff changeset
708 <param name="selection" value="no"/>
85f0e9edb32d planemo upload for repository https://github.com/galaxyproject/tools-devteam/tree/master/tools/bowtie2 commit 954b2052cb74a0bc88f65df37f429ff27c45ea8f
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parents: 13
diff changeset
709 <param name="paired_options_selector" value="no"/>
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diff changeset
710 <param name="unaligned_file" value="false"/>
85f0e9edb32d planemo upload for repository https://github.com/galaxyproject/tools-devteam/tree/master/tools/bowtie2 commit 954b2052cb74a0bc88f65df37f429ff27c45ea8f
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diff changeset
711 <param name="analysis_type_selector" value="simple"/>
85f0e9edb32d planemo upload for repository https://github.com/galaxyproject/tools-devteam/tree/master/tools/bowtie2 commit 954b2052cb74a0bc88f65df37f429ff27c45ea8f
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diff changeset
712 <param name="source" value="history" />
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parents: 13
diff changeset
713 <param name="input_1" value="bowtie2-fq1.fq.bz2" ftype="fastqsanger.bz2"/>
85f0e9edb32d planemo upload for repository https://github.com/galaxyproject/tools-devteam/tree/master/tools/bowtie2 commit 954b2052cb74a0bc88f65df37f429ff27c45ea8f
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diff changeset
714 <param name="input_2" value="bowtie2-fq2.fq.bz2" ftype="fastqsanger.bz2"/>
85f0e9edb32d planemo upload for repository https://github.com/galaxyproject/tools-devteam/tree/master/tools/bowtie2 commit 954b2052cb74a0bc88f65df37f429ff27c45ea8f
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diff changeset
715 <param name="own_file" value="bowtie2-ref.fasta" />
85f0e9edb32d planemo upload for repository https://github.com/galaxyproject/tools-devteam/tree/master/tools/bowtie2 commit 954b2052cb74a0bc88f65df37f429ff27c45ea8f
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diff changeset
716 <output name="output" file="bowtie2-test1.bam" ftype="bam" lines_diff="2"/>
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diff changeset
717 </test>
0
a03a7ee6cdff Imported from capsule None
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718 </tests>
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719
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diff changeset
720 <help><![CDATA[
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721
0
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722 **Bowtie2 Overview**
11
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723
2
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724 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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725 Majority of information in this page is derived from an excellent `Bowtie2 manual`_ written by Ben Langmead.
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726
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727 .. _Bowtie2: http://bowtie-bio.sourceforge.net/bowtie2/
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728 .. _`Bowtie2 manual`: http://bowtie-bio.sourceforge.net/bowtie2/manual.shtml
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729 .. _`BAM format`: http://samtools.github.io/hts-specs/SAMv1.pdf
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730
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731 -----
0
a03a7ee6cdff Imported from capsule None
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732
2
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733 **Selecting reference genomes for Bowtie2**
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734
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735 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
a03a7ee6cdff Imported from capsule None
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736
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diff changeset
737 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.
2
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parents: 1
diff changeset
738 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.
11
fa69d5a7b8c8 planemo upload for repository https://github.com/galaxyproject/tools-devteam/tree/master/tools/bowtie2 commit d0e857ba2691ca15b6239890baf98dbe7bc3ccbd
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diff changeset
739
2
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diff changeset
740 If your genome of interest is not listed here you have two choices:
2a6cfe8997aa Uploaded from GH
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diff changeset
741
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diff changeset
742 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
2a6cfe8997aa Uploaded from GH
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parents: 1
diff changeset
743 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
a03a7ee6cdff Imported from capsule None
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744
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diff changeset
745 ------
a03a7ee6cdff Imported from capsule None
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diff changeset
746
2
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diff changeset
747 .. class:: infomark
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diff changeset
748
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diff changeset
749 **Bowtie2 options**
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750
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751 Galaxy wrapper for Bowtie2 implements most but not all options available through the command line. Supported options are described below.
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752
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753 -----
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754
0
a03a7ee6cdff Imported from capsule None
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755 **Inputs**
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756
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757 Bowtie 2 accepts files in Sanger FASTQ format (single or pair-end). Use the FASTQ Groomer to prepare your files.
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758
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759 ------
a03a7ee6cdff Imported from capsule None
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760
2
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761 **Input options**::
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762
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diff changeset
763 -s/--skip <int>
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diff changeset
764 Skip (i.e. do not align) the first `<int>` reads or pairs in the input.
2
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765
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diff changeset
766 -u/--qupto <int>
fa69d5a7b8c8 planemo upload for repository https://github.com/galaxyproject/tools-devteam/tree/master/tools/bowtie2 commit d0e857ba2691ca15b6239890baf98dbe7bc3ccbd
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diff changeset
767 Align the first `<int>` reads or read pairs from the input (after the
2
2a6cfe8997aa Uploaded from GH
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768 `-s`/`--skip` reads or pairs have been skipped), then stop. Default: no limit.
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diff changeset
769
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diff changeset
770 -5/--trim5 <int>
fa69d5a7b8c8 planemo upload for repository https://github.com/galaxyproject/tools-devteam/tree/master/tools/bowtie2 commit d0e857ba2691ca15b6239890baf98dbe7bc3ccbd
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771 Trim `<int>` bases from 5' (left) end of each read before alignment (default: 0).
0
a03a7ee6cdff Imported from capsule None
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772
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773 -3/--trim3 <int>
fa69d5a7b8c8 planemo upload for repository https://github.com/galaxyproject/tools-devteam/tree/master/tools/bowtie2 commit d0e857ba2691ca15b6239890baf98dbe7bc3ccbd
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diff changeset
774 Trim `<int>` bases from 3' (right) end of each read before alignment (default: 0).
2
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diff changeset
775
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diff changeset
776 --phred33
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777 Input qualities are ASCII chars equal to the Phred quality plus 33. This is
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diff changeset
778 also called the "Phred+33" encoding, which is used by the very latest Illumina
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diff changeset
779 pipelines.
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diff changeset
780
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diff changeset
781 --phred64
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diff changeset
782 Input qualities are ASCII chars equal to the Phred quality plus 64. This is
2
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783 also called the "Phred+64" encoding.
0
a03a7ee6cdff Imported from capsule None
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diff changeset
784
2
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785 --solexa-quals
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786 Convert input qualities from Solexa Phred quality (which can be negative) to
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diff changeset
787 Phred Phred quality (which can't). This scheme was used in older Illumina GA
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788 Pipeline versions (prior to 1.3). Default: off.
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789
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diff changeset
790 --int-quals
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791 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`....
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diff changeset
792 Integers are treated as being on the Phred quality scale unless
2
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793 `--solexa-quals` is also specified. Default: off.
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794
2
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795 ------
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796
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797 **Presets in `--end-to-end` mode**::
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798
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diff changeset
799 --very-fast
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diff changeset
800 Same as: `-D 5 -R 1 -N 0 -L 22 -i S,0,2.50`
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801
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diff changeset
802 --fast
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parents: 1
diff changeset
803 Same as: `-D 10 -R 2 -N 0 -L 22 -i S,0,2.50`
11
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diff changeset
804
2
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diff changeset
805 --sensitive
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diff changeset
806 Same as: `-D 15 -R 2 -L 22 -i S,1,1.15` (default in `--end-to-end` mode)
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parents: 1
diff changeset
807
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diff changeset
808 --very-sensitive
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diff changeset
809 Same as: `-D 20 -R 3 -N 0 -L 20 -i S,1,0.50`
0
a03a7ee6cdff Imported from capsule None
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parents:
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810
a03a7ee6cdff Imported from capsule None
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parents:
diff changeset
811 ------
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parents:
diff changeset
812
2
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diff changeset
813 **Presets options in `--local` mode**::
0
a03a7ee6cdff Imported from capsule None
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parents:
diff changeset
814
2
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diff changeset
815 --very-fast-local
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diff changeset
816 Same as: `-D 5 -R 1 -N 0 -L 25 -i S,1,2.00`
0
a03a7ee6cdff Imported from capsule None
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parents:
diff changeset
817
2
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diff changeset
818 --fast-local
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diff changeset
819 Same as: `-D 10 -R 2 -N 0 -L 22 -i S,1,1.75`
0
a03a7ee6cdff Imported from capsule None
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parents:
diff changeset
820
2
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diff changeset
821 --sensitive-local
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diff changeset
822 Same as: `-D 15 -R 2 -N 0 -L 20 -i S,1,0.75` (default in `--local` mode)
0
a03a7ee6cdff Imported from capsule None
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parents:
diff changeset
823
2
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diff changeset
824 --very-sensitive-local
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parents: 1
diff changeset
825 Same as: `-D 20 -R 3 -N 0 -L 20 -i S,1,0.50`
11
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diff changeset
826
0
a03a7ee6cdff Imported from capsule None
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parents:
diff changeset
827 ------
a03a7ee6cdff Imported from capsule None
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parents:
diff changeset
828
2
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diff changeset
829 **Alignment options**::
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parents: 1
diff changeset
830
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diff changeset
831 -N <int>
5
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parents: 2
diff changeset
832 Sets the number of mismatches to allowed in a seed alignment during multiseed
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parents: 2
diff changeset
833 alignment. Can be set to 0 or 1. Setting this higher makes alignment slower
2
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diff changeset
834 (often much slower) but increases sensitivity. Default: 0.
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diff changeset
835
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fa69d5a7b8c8 planemo upload for repository https://github.com/galaxyproject/tools-devteam/tree/master/tools/bowtie2 commit d0e857ba2691ca15b6239890baf98dbe7bc3ccbd
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diff changeset
836 -L <int>
5
5cfa4b6db588 planemo upload commit 33927a87ba2eee9bf0ecdd376a66241b17b3d734
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diff changeset
837 Sets the length of the seed substrings to align during multiseed alignment.
5cfa4b6db588 planemo upload commit 33927a87ba2eee9bf0ecdd376a66241b17b3d734
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parents: 2
diff changeset
838 Smaller values make alignment slower but more sensitive. Default: the
5cfa4b6db588 planemo upload commit 33927a87ba2eee9bf0ecdd376a66241b17b3d734
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parents: 2
diff changeset
839 `--sensitive` preset is used by default, which sets `-L` to 22 in
5cfa4b6db588 planemo upload commit 33927a87ba2eee9bf0ecdd376a66241b17b3d734
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diff changeset
840 `--end-to-end` mode and to 20 in `--local` mode.
2
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parents: 1
diff changeset
841
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diff changeset
842 -i <func>
2
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diff changeset
843 Sets a function governing the interval between seed substrings to use during
5
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diff changeset
844 multiseed alignment. For instance, if the read has 30 characers, and seed
2
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845 length is 10, and the seed interval is 6, the seeds extracted will be:
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846
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847 Read: TAGCTACGCTCTACGCTATCATGCATAAAC
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848 Seed 1 fw: TAGCTACGCT
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parents: 1
diff changeset
849 Seed 1 rc: AGCGTAGCTA
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diff changeset
850 Seed 2 fw: CGCTCTACGC
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851 Seed 2 rc: GCGTAGAGCG
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diff changeset
852 Seed 3 fw: ACGCTATCAT
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parents: 1
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853 Seed 3 rc: ATGATAGCGT
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854 Seed 4 fw: TCATGCATAA
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855 Seed 4 rc: TTATGCATGA
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856
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diff changeset
857 Since it's best to use longer intervals for longer reads, this parameter sets
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858 the interval as a function of the read length, rather than a single
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diff changeset
859 one-size-fits-all number. For instance, specifying `-i S,1,2.5` sets the
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diff changeset
860 interval function `f` to `f(x) = 1 + 2.5 * sqrt(x)`, where x is the read length.
5
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diff changeset
861 If the function returns a result less than
2
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diff changeset
862 1, it is rounded up to 1. Default: the `--sensitive` preset is used by
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diff changeset
863 default, which sets `-i` to `S,1,1.15` in `--end-to-end` mode to `-i S,1,0.75`
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864 in `--local` mode.
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865
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diff changeset
866 --n-ceil <func>
2
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diff changeset
867 Sets a function governing the maximum number of ambiguous characters (usually
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diff changeset
868 `N`s and/or `.`s) allowed in a read as a function of read length. For instance,
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diff changeset
869 specifying `-L,0,0.15` sets the N-ceiling function `f` to `f(x) = 0 + 0.15 * x`,
5
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870 where x is the read length. Reads exceeding this ceiling are filtered out.
5cfa4b6db588 planemo upload commit 33927a87ba2eee9bf0ecdd376a66241b17b3d734
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diff changeset
871 Default: `L,0,0.15`.
2
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872
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diff changeset
873 --dpad <int>
fa69d5a7b8c8 planemo upload for repository https://github.com/galaxyproject/tools-devteam/tree/master/tools/bowtie2 commit d0e857ba2691ca15b6239890baf98dbe7bc3ccbd
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diff changeset
874 "Pads" dynamic programming problems by `<int>` columns on either side to allow
2
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875 gaps. Default: 15.
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diff changeset
876
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diff changeset
877 --gbar <int>
fa69d5a7b8c8 planemo upload for repository https://github.com/galaxyproject/tools-devteam/tree/master/tools/bowtie2 commit d0e857ba2691ca15b6239890baf98dbe7bc3ccbd
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diff changeset
878 Disallow gaps within `<int>` positions of the beginning or end of the read.
2
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879 Default: 4.
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880
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881 --ignore-quals
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diff changeset
882 When calculating a mismatch penalty, always consider the quality value at the
11
fa69d5a7b8c8 planemo upload for repository https://github.com/galaxyproject/tools-devteam/tree/master/tools/bowtie2 commit d0e857ba2691ca15b6239890baf98dbe7bc3ccbd
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diff changeset
883 mismatched position to be the highest possible, regardless of the actual value.
2
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884 I.e. input is treated as though all quality values are high. This is also the
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885 default behavior when the input doesn't specify quality values (e.g. in `-f`,
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886 `-r`, or `-c` modes).
0
a03a7ee6cdff Imported from capsule None
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parents:
diff changeset
887
2
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diff changeset
888 --nofw/--norc
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diff changeset
889 If `--nofw` is specified, `bowtie2` will not attempt to align unpaired reads to
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diff changeset
890 the forward (Watson) reference strand. If `--norc` is specified, `bowtie2` will
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diff changeset
891 not attempt to align unpaired reads against the reverse-complement (Crick)
2a6cfe8997aa Uploaded from GH
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diff changeset
892 reference strand. In paired-end mode, `--nofw` and `--norc` pertain to the
2a6cfe8997aa Uploaded from GH
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diff changeset
893 fragments; i.e. specifying `--nofw` causes `bowtie2` to explore only those
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894 paired-end configurations corresponding to fragments from the reverse-complement
11
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diff changeset
895 (Crick) strand. Default: both strands enabled.
2
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diff changeset
896
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diff changeset
897 --no-1mm-upfront
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diff changeset
898 By default, Bowtie 2 will attempt to find either an exact or a 1-mismatch
5
5cfa4b6db588 planemo upload commit 33927a87ba2eee9bf0ecdd376a66241b17b3d734
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diff changeset
899 end-to-end alignment for the read *before* trying the multiseed heuristic. Such
2
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900 alignments can be found very quickly, and many short read alignments have exact or
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diff changeset
901 near-exact end-to-end alignments. However, this can lead to unexpected
5
5cfa4b6db588 planemo upload commit 33927a87ba2eee9bf0ecdd376a66241b17b3d734
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diff changeset
902 alignments when the user also sets options governing the multiseed heuristic,
2
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diff changeset
903 like `-L` and `-N`. For instance, if the user specifies `-N 0` and `-L` equal
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diff changeset
904 to the length of the read, the user will be surprised to find 1-mismatch alignments
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905 reported. This option prevents Bowtie 2 from searching for 1-mismatch end-to-end
5
5cfa4b6db588 planemo upload commit 33927a87ba2eee9bf0ecdd376a66241b17b3d734
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diff changeset
906 alignments before using the multiseed heuristic, which leads to the expected
2
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diff changeset
907 behavior when combined with options such as `-L` and `-N`. This comes at the
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908 expense of speed.
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diff changeset
909
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910 --end-to-end
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911 In this mode, Bowtie 2 requires that the entire read align from one end to the
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912 other, without any trimming (or "soft clipping") of characters from either end.
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913 The match bonus `--ma` always equals 0 in this mode, so all alignment scores
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914 are less than or equal to 0, and the greatest possible alignment score is 0.
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915 This is mutually exclusive with `--local`. `--end-to-end` is the default mode.
0
a03a7ee6cdff Imported from capsule None
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diff changeset
916
2
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917 --local
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918 In this mode, Bowtie 2 does not require that the entire read align from one end
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919 to the other. Rather, some characters may be omitted ("soft clipped") from the
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920 ends in order to achieve the greatest possible alignment score. The match bonus
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921 `--ma` is used in this mode, and the best possible alignment score is equal to
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922 the match bonus (`--ma`) times the length of the read. Specifying `--local`
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923 and one of the presets (e.g. `--local --very-fast`) is equivalent to specifying
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924 the local version of the preset (`--very-fast-local`). This is mutually
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925 exclusive with `--end-to-end`. `--end-to-end` is the default mode.
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926
2
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927 -----
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928
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929 **Scoring options**::
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930
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diff changeset
931 --ma <int>
fa69d5a7b8c8 planemo upload for repository https://github.com/galaxyproject/tools-devteam/tree/master/tools/bowtie2 commit d0e857ba2691ca15b6239890baf98dbe7bc3ccbd
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diff changeset
932 Sets the match bonus. In `--local` mode `<int>` is added to the alignment
2
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933 score for each position where a read character aligns to a reference character
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934 and the characters match. Not used in `--end-to-end` mode. Default: 2.
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935
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936 --mp MX,MN
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937 Sets the maximum (`MX`) and minimum (`MN`) mismatch penalties, both integers. A
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938 number less than or equal to `MX` and greater than or equal to `MN` is
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939 subtracted from the alignment score for each position where a read character
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940 aligns to a reference character, the characters do not match, and neither is an
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diff changeset
941 `N`. If `--ignore-quals` is specified, the number subtracted quals `MX`.
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942 Otherwise, the number subtracted is `MN + floor( (MX-MN)(MIN(Q, 40.0)/40.0) )`
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943 where Q is the Phred quality value. Default: `MX` = 6, `MN` = 2.
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944
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diff changeset
945 --np <int>
2
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946 Sets penalty for positions where the read, reference, or both, contain an
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diff changeset
947 ambiguous character such as `N`. Default: 1.
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diff changeset
948
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fa69d5a7b8c8 planemo upload for repository https://github.com/galaxyproject/tools-devteam/tree/master/tools/bowtie2 commit d0e857ba2691ca15b6239890baf98dbe7bc3ccbd
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diff changeset
949 --rdg <int1>,<int2>
fa69d5a7b8c8 planemo upload for repository https://github.com/galaxyproject/tools-devteam/tree/master/tools/bowtie2 commit d0e857ba2691ca15b6239890baf98dbe7bc3ccbd
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950 Sets the read gap open (`<int1>`) and extend (`<int2>`) penalties. A read gap of
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951 length N gets a penalty of `<int1>` + N * `<int2>`. Default: 5, 3.
2
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952
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diff changeset
953 --rfg <int1>,<int2>
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diff changeset
954 Sets the reference gap open (`<int1>`) and extend (`<int2>`) penalties. A
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diff changeset
955 reference gap of length N gets a penalty of `<int1>` + N * `<int2>`. Default:
2
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diff changeset
956 5, 3.
0
a03a7ee6cdff Imported from capsule None
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diff changeset
957
11
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diff changeset
958 --score-min <func>
2
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diff changeset
959 Sets a function governing the minimum alignment score needed for an alignment to
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diff changeset
960 be considered "valid" (i.e. good enough to report). This is a function of read
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diff changeset
961 length. For instance, specifying `L,0,-0.6` sets the minimum-score function `f`
5
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diff changeset
962 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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diff changeset
963 the default in `--local` mode is `G,20,8`.
11
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diff changeset
964
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diff changeset
965 -----
2
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966
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diff changeset
967 **Reporting options**::
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968
11
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diff changeset
969 -k <int>
2
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970 By default, `bowtie2` searches for distinct, valid alignments for each read.
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971 When it finds a valid alignment, it continues looking for alignments that are
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diff changeset
972 nearly as good or better. The best alignment found is reported (randomly
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973 selected from among best if tied). Information about the best alignments is
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974 used to estimate mapping quality and to set SAM optional fields, such as
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diff changeset
975 `AS:i` and `XS:i`.
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976
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977 When `-k` is specified, however, `bowtie2` behaves differently. Instead, it
11
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diff changeset
978 searches for at most `<int>` distinct, valid alignments for each read. The
2
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979 search terminates when it can't find more distinct valid alignments, or when it
11
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diff changeset
980 finds `<int>`, whichever happens first. All alignments found are reported in
2
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981 descending order by alignment score. The alignment score for a paired-end
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982 alignment equals the sum of the alignment scores of the individual mates. Each
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983 reported read or pair alignment beyond the first has the SAM 'secondary' bit
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984 (which equals 256) set in its FLAGS field. For reads that have more than
11
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diff changeset
985 `<int>` distinct, valid alignments, `bowtie2` does not guarantee that the
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diff changeset
986 `<int>` alignments reported are the best possible in terms of alignment score.
2
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987 `-k` is mutually exclusive with `-a`.
0
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988
2
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989 Note: Bowtie 2 is not designed with large values for `-k` in mind, and when
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990 aligning reads to long, repetitive genomes large `-k` can be very, very slow.
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991
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992 -a
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diff changeset
993 Like `-k` but with no upper limit on number of alignments to search for. `-a`
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994 is mutually exclusive with `-k`.
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995
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996 Note: Bowtie 2 is not designed with `-a` mode in mind, and when
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diff changeset
997 aligning reads to long, repetitive genomes this mode can be very, very slow.
11
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diff changeset
998
2
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999 -----
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1000
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1001 **Effort options**::
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1002
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diff changeset
1003 -D <int>
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diff changeset
1004 Up to `<int>` consecutive seed extension attempts can "fail" before Bowtie 2
2
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1005 moves on, using the alignments found so far. A seed extension "fails" if it
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1006 does not yield a new best or a new second-best alignment. This limit is
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1007 automatically adjusted up when -k or -a are specified. Default: 15.
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1008
11
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diff changeset
1009 -R <int>
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diff changeset
1010 `<int>` is the maximum number of times Bowtie 2 will "re-seed" reads with
2
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1011 repetitive seeds. When "re-seeding," Bowtie 2 simply chooses a new set of reads
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1012 (same length, same number of mismatches allowed) at different offsets and
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1013 searches for more alignments. A read is considered to have repetitive seeds if
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1014 the total number of seed hits divided by the number of seeds that aligned at
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1015 least once is greater than 300. Default: 2.
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diff changeset
1016
2
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1017 -----
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1018
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1019 **Paired-end options**::
0
a03a7ee6cdff Imported from capsule None
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1020
11
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diff changeset
1021 -I/--minins <int>
2
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1022 The minimum fragment length for valid paired-end alignments. E.g. if `-I 60` is
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1023 specified and a paired-end alignment consists of two 20-bp alignments in the
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1024 appropriate orientation with a 20-bp gap between them, that alignment is
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1025 considered valid (as long as `-X` is also satisfied). A 19-bp gap would not
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1026 be valid in that case. If trimming options `-3` or `-5` are also used, the
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1027 `-I` constraint is applied with respect to the untrimmed mates.
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1028
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1029 The larger the difference between `-I` and `-X`, the slower Bowtie 2 will
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1030 run. This is because larger differences bewteen `-I` and `-X` require that
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diff changeset
1031 Bowtie 2 scan a larger window to determine if a concordant alignment exists.
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1032 For typical fragment length ranges (200 to 400 nucleotides), Bowtie 2 is very
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diff changeset
1033 efficient.
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1034
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1035 Default: 0 (essentially imposing no minimum)
2
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1036
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diff changeset
1037 -X/--maxins <int>
2
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1038 The maximum fragment length for valid paired-end alignments. E.g. if `-X 100`
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1039 is specified and a paired-end alignment consists of two 20-bp alignments in the
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diff changeset
1040 proper orientation with a 60-bp gap between them, that alignment is considered
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diff changeset
1041 valid (as long as `-I` is also satisfied). A 61-bp gap would not be valid in
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diff changeset
1042 that case. If trimming options `-3` or `-5` are also used, the `-X`
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1043 constraint is applied with respect to the untrimmed mates, not the trimmed
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1044 mates.
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1045
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1046 The larger the difference between `-I` and `-X`, the slower Bowtie 2 will
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1047 run. This is because larger differences bewteen `-I` and `-X` require that
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diff changeset
1048 Bowtie 2 scan a larger window to determine if a concordant alignment exists.
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1049 For typical fragment length ranges (200 to 400 nucleotides), Bowtie 2 is very
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1050 efficient.
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1051
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1052 Default: 500.
0
a03a7ee6cdff Imported from capsule None
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1053
2
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1054 --fr/--rf/--ff
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1055 The upstream/downstream mate orientations for a valid paired-end alignment
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1056 against the forward reference strand. E.g., if `--fr` is specified and there is
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1057 a candidate paired-end alignment where mate 1 appears upstream of the reverse
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1058 complement of mate 2 and the fragment length constraints (`-I` and `-X`) are
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1059 met, that alignment is valid. Also, if mate 2 appears upstream of the reverse
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1060 complement of mate 1 and all other constraints are met, that too is valid.
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1061 `--rf` likewise requires that an upstream mate1 be reverse-complemented and a
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1062 downstream mate2 be forward-oriented. ` --ff` requires both an upstream mate 1
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1063 and a downstream mate 2 to be forward-oriented. Default: `--fr` (appropriate
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1064 for Illumina's Paired-end Sequencing Assay).
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1065
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1066 --no-mixed
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1067 By default, when `bowtie2` cannot find a concordant or discordant alignment for
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1068 a pair, it then tries to find alignments for the individual mates. This option
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1069 disables that behavior.
0
a03a7ee6cdff Imported from capsule None
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1070
2
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1071 --no-discordant
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1072 By default, `bowtie2` looks for discordant alignments if it cannot find any
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1073 concordant alignments. A discordant alignment is an alignment where both mates
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1074 align uniquely, but that does not satisfy the paired-end constraints
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1075 (`--fr`/`--rf`/`--ff`, `-I`, `-X`). This option disables that behavior.
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1076
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1077 --dovetail
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1078 If the mates "dovetail", that is if one mate alignment extends past the
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1079 beginning of the other such that the wrong mate begins upstream, consider that
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1080 to be concordant. Default: mates cannot dovetail in a concordant alignment.
2
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1081
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1082 --no-contain
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1083 If one mate alignment contains the other, consider that to be non-concordant.
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1084 Default: a mate can contain the other in a concordant alignment.
2
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1085
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1086 --no-overlap
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1087 If one mate alignment overlaps the other at all, consider that to be
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diff changeset
1088 non-concordant. Default: mates can overlap in a concordant alignment.
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1089
0
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1090 ------
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1091
2
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1092 **SAM options**::
0
a03a7ee6cdff Imported from capsule None
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1093
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diff changeset
1094 --rg-id <text>
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1095 Set the read group ID to `<text>`. This causes the SAM `@RG` header line to be
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diff changeset
1096 printed, with `<text>` as the value associated with the `ID:` tag. It also
2
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1097 causes the `RG:Z:` extra field to be attached to each SAM output record, with
11
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diff changeset
1098 value set to `<text>`.
0
a03a7ee6cdff Imported from capsule None
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parents:
diff changeset
1099
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diff changeset
1100 --rg <text>
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1101 Add `<text>` (usually of the form `TAG:VAL`, e.g. `SM:Pool1`) as a field on the
2
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1102 `@RG` header line. Note: in order for the `@RG` line to appear, `--rg-id`
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1103 must also be specified. This is because the `ID` tag is required by the SAM
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1104 Specification. Specify `--rg` multiple times to set multiple fields. See the
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1105 SAM Specification for details about what fields are legal.
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1106
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1107 --omit-sec-seq
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1108 When printing secondary alignments, Bowtie 2 by default will write out the `SEQ`
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1109 and `QUAL` strings. Specifying this option causes Bowtie 2 to print an asterix
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1110 in those fields instead.
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1111
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1112 -----
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1113
2
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1114 **Other options**::
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1115
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1116 --reorder
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1117 Guarantees that output SAM records are printed in an order corresponding to the
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1118 order of the reads in the original input file, even when `-p` is set greater
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1119 than 1. Specifying `--reorder` and setting `-p` greater than 1 causes Bowtie
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1120 2 to run somewhat slower and use somewhat more memory then if `--reorder` were
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1121 not specified. Has no effect if `-p` is set to 1, since output order will
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1122 naturally correspond to input order in that case.
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1123
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1124 --seed <int>
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1125 Use `<int>` as the seed for pseudo-random number generator. Default: 0.
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1126
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1127 --non-deterministic
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1128 Normally, Bowtie 2 re-initializes its pseudo-random generator for each read. It
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1129 seeds the generator with a number derived from (a) the read name, (b) the
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1130 nucleotide sequence, (c) the quality sequence, (d) the value of the `--seed`
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1131 option. This means that if two reads are identical (same name, same
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1132 nucleotides, same qualities) Bowtie 2 will find and report the same alignment(s)
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1133 for both, even if there was ambiguity. When `--non-deterministic` is specified,
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1134 Bowtie 2 re-initializes its pseudo-random generator for each read using the
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1135 current time. This means that Bowtie 2 will not necessarily report the same
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1136 alignment for two identical reads. This is counter-intuitive for some users,
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1137 but might be more appropriate in situations where the input consists of many
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1138 identical reads.
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1139
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1140 ]]></help>
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1141 <citations>
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1142 <citation type="doi">10.1186/gb-2009-10-3-r25</citation>
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1143 <citation type="doi">10.1038/nmeth.1923</citation>
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1144 </citations>
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1145 </tool>