annotate bowtie2_wrapper.xml @ 15:7e0b333f39e1 draft

planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/bowtie2 commit cf554b9b69c32acb484c34fdc60384fa49c7c482
author iuc
date Thu, 01 Jun 2017 06:46:49 -0400
parents 85f0e9edb32d
children def46fdb3909
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1 <tool id="bowtie2" name="Bowtie2" version="2.3.2.1" 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>bowtie2_macros.xml</import>
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5 </macros>
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6 <requirements>
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7 <requirement type="package" version="2.3.2">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}' ${read2} &&
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69
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70 #else if str($library.type) == 'paired_interleaved':
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71 #if $library.input_1.is_of_type("fastq.gz", "fastqsanger.gz"):
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72 #set read1 = "input_il.fastq.gz"
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73 #set compressed = "GZ"
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74 #else if $library.input_1.is_of_type("fastq.bz2", "fastqsanger.bz2"):
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75 #set read1 = "input_il.fastq.bz2"
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76 #set compressed = "BZ2"
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77 #else:
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78 #set read1 = "input_il.fastq"
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79 #end if
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80 ln -s '${library.input_1}' ${read1} &&
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81 #else:
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82 #if $library.input_1.is_of_type("fastq.gz", "fastqsanger.gz"):
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83 #set read1 = "input_f.fastq.gz"
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84 #set compressed = "GZ"
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85 #else if $library.input_1.is_of_type("fastq.bz2", "fastqsanger.bz2"):
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86 #set read1 = "input_f.fastq.bz2"
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87 #set compressed = "BZ2"
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88 #else:
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89 #set read1 = "input_f.fastq"
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90 #end if
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91 ln -s '${library.input_1}' ${read1} &&
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92 #end if
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93
0
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94 ## execute bowtie2
5
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95
0
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96 bowtie2
5
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97
0
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98 ## number of threads
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99 -p \${GALAXY_SLOTS:-4}
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100
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101 ## index file path
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102 -x '$index_path'
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103
2
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104 ## Fastq inputs
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105 #if str( $library.type ) == "single":
14
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106 -U '${read1}'
2
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107 #if str( $library.unaligned_file ) == "true":
14
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108 #if $compressed == "GZ":
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109 --un-gz '${output_unaligned_reads_l}'
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110 #else if $compressed == "BZ2":
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111 --un-bz2 '${output_unaligned_reads_l}'
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112 #else:
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113 --un '${output_unaligned_reads_l}'
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114 #end if
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115 #end if
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116 #if str( $library.aligned_file ) == "true":
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117 #if $compressed == "GZ":
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118 --al-gz '${output_aligned_reads_l}'
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119 #else if $compressed == "BZ2":
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120 --al-bz2 '${output_aligned_reads_l}'
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121 #else:
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122 --al '${output_aligned_reads_l}'
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123 #end if
0
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124 #end if
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125
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126 #elif str( $library.type ) == "paired_interleaved":
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127 --interleaved '${read1}'
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128 #if str( $library.unaligned_file ) == "true":
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129 #if $compressed == "GZ":
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130 --un-gz '${output_unaligned_reads_l}'
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131 #else if $compressed == "BZ2":
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132 --un-bz2 '${output_unaligned_reads_l}'
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133 #else:
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134 --un '${output_unaligned_reads_l}'
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135 #end if
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136 #end if
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137 #if str( $library.aligned_file ) == "true":
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138 #if $compressed == "GZ":
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139 --al-gz '${output_aligned_reads_l}'
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140 #else if $compressed == "BZ2":
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141 --al-bz2 '${output_aligned_reads_l}'
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142 #else:
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143 --al '${output_aligned_reads_l}'
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144 #end if
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145 #end if
14
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146 #else:
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147 -1 '${read1}'
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148 -2 '${read2}'
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149 #if str( $library.unaligned_file ) == "true":
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150 #if $compressed == "GZ":
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151 --un-conc-gz '${output_unaligned_reads_l}'
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152 #else if $compressed == "BZ2":
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153 --un-conc-bz2 '${output_unaligned_reads_l}'
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154 #else:
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155 --un-conc '${output_unaligned_reads_l}'
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156 #end if
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157 #end if
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158 #if str( $library.aligned_file ) == "true":
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159 #if $compressed == "GZ":
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160 --al-conc-gz '${output_aligned_reads_l}'
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161 #else if $compressed == "BZ2":
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162 --al-conc-bz2 '${output_aligned_reads_l}'
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163 #else:
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164 --al-conc '${output_aligned_reads_l}'
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165 #end if
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166 #end if
2
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167 #if str( $library.paired_options.paired_options_selector ) == "yes":
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168 -I "${library.paired_options.I}"
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169 -X "${library.paired_options.X}"
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170 ${library.paired_options.fr_rf_ff}
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171 ${library.paired_options.no_mixed}
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172 ${library.paired_options.no_discordant}
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173 ${library.paired_options.dovetail}
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174 ${library.paired_options.no_contain}
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175 ${library.paired_options.no_overlap}
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176 #end if
0
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177 #end if
5
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178
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179 ## Read group information.
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180 @define_read_group_helpers@
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181 #if str( $library.type ) == "single":
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182 #set $rg_auto_name = $read_group_name_default($library.input_1)
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183 #elif str( $library.type ) == "paired":
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184 #set $rg_auto_name = $read_group_name_default($library.input_1, $library.input_2)
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185 #else
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186 #set $rg_auto_name = $read_group_name_default($library.input_1)
2
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187 #end if
5
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188 @set_use_rg_var@
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189 @set_read_group_vars@
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190 #if $use_rg
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191 $format_read_group("", $rg_id, '"', arg='--rg-id ')
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192 $format_read_group("SM:", $rg_sm, '"', arg='--rg ')
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193 $format_read_group("PL:", $rg_pl, '"', arg='--rg ')
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194 $format_read_group("LB:", $rg_lb, '"', arg='--rg ')
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195 $format_read_group("CN:", $rg_cn, '"', arg='--rg ')
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196 $format_read_group("DS:", $rg_ds, '"', arg='--rg ')
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197 $format_read_group("DT:", $rg_dt, '"', arg='--rg ')
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198 $format_read_group("FO:", $rg_fo, '"', arg='--rg ')
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199 $format_read_group("KS:", $rg_ks, '"', arg='--rg ')
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200 $format_read_group("PG:", $rg_pg, '"', arg='--rg ')
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201 $format_read_group("PI:", $rg_pi, '"', arg='--rg ')
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202 $format_read_group("PU:", $rg_pu, '"', arg='--rg ')
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203 #end if
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204
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205 ## Analysis type
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206 #if ( str( $analysis_type.analysis_type_selector ) == "simple" and str( $analysis_type.presets ) != "no_presets" ):
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207 $analysis_type.presets
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208 #elif str( $analysis_type.analysis_type_selector ) == "full":
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209 #if str( $analysis_type.input_options.input_options_selector ) == "yes":
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210 --skip "${analysis_type.input_options.skip}"
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211 --qupto "${analysis_type.input_options.qupto}"
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212 --trim5 "${analysis_type.input_options.trim5}"
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213 --trim3 "${analysis_type.input_options.trim3}"
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214 ${analysis_type.input_options.qv_encoding}
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215 ${analysis_type.input_options.solexa_quals}
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216 ${analysis_type.input_options.int_quals}
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217 #end if
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218
2
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219 #if str( $analysis_type.alignment_options.alignment_options_selector ) == "yes":
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220 -N "${analysis_type.alignment_options.N}"
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221 -L "${analysis_type.alignment_options.L}"
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222 -i "${analysis_type.alignment_options.i}"
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223 --n-ceil "${analysis_type.alignment_options.n_ceil}"
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224 --dpad "${analysis_type.alignment_options.dpad}"
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225 --gbar "${analysis_type.alignment_options.gbar}"
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226 ${analysis_type.alignment_options.ignore_quals}
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227 ${analysis_type.alignment_options.nofw}
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228 ${analysis_type.alignment_options.norc}
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229 ${analysis_type.alignment_options.no_1mm_upfront}
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230 #if str( $analysis_type.alignment_options.align_mode.align_mode_selector ) == "end-to-end":
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231 --end-to-end
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232 --score-min "${analysis_type.alignment_options.align_mode.score_min_ete}"
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233 #elif str( $analysis_type.alignment_options.align_mode.align_mode_selector ) == "local":
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234 --local
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235 --score-min "${analysis_type.alignment_options.align_mode.score_min_loc}"
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236 #end if
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237 #end if
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238
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239 #if str( $analysis_type.scoring_options.scoring_options_selector ) == "yes":
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240 #if ( str( $analysis_type.alignment_options.alignment_options_selector ) == "yes" and str( $analysis_type.alignment_options.align_mode.align_mode_selector ) == "local" ):
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241 --ma "${analysis_type.scoring_options.ma}"
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242 #end if
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243 --mp "${analysis_type.scoring_options.mp}"
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244 --np "${analysis_type.scoring_options.np}"
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245 --rdg "${analysis_type.scoring_options.rdg_read_open},${analysis_type.scoring_options.rdg_read_extend}"
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246 --rfg "${analysis_type.scoring_options.rfg_ref_open},${analysis_type.scoring_options.rfg_ref_extend}"
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247 #end if
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248
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249 #if str( $analysis_type.reporting_options.reporting_options_selector ) == "k":
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250 -k "${analysis_type.reporting_options.k}"
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251 #elif str( $analysis_type.reporting_options.reporting_options_selector ) == "a":
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252 -a
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253 #end if
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254
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255 #if str( $analysis_type.effort_options.effort_options_selector ) == "yes":
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256 -D "${analysis_type.effort_options.D}"
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257 -R "${analysis_type.effort_options.R}"
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258 #end if
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259
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260 #if str( $analysis_type.sam_options.sam_options_selector ) == "yes":
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261 ${analysis_type.sam_options.no_unal}
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262 ${analysis_type.sam_options.omit_sec_seq}
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263 #end if
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264
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265 #if str( $analysis_type.other_options.other_options_selector ) == "yes":
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266 ${analysis_type.other_options.reorder}
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267 ${analysis_type.other_options.non_deterministic}
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268 --seed "${analysis_type.other_options.seed}"
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269 #end if
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270
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271 #elif str( $analysis_type.analysis_type_selector ) == "cline":
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272 ${analysis_type.cline}
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273 #end if
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274
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275 ## mapping stats (i.e. stderr from bowtie2)
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276 #if $save_mapping_stats
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277 2> '$mapping_stats'
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278 #end if
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279
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280 ## output file
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281 #if ( str( $analysis_type.analysis_type_selector ) != "full" or str( $analysis_type.sam_opt ) != "true" ):
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282 | samtools sort -O bam -o '$output'
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283 #else
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284 > '$output_sam'
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285 #end if
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286
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287 ## rename unaligned sequence files
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288 #if $library.type == "paired" and $output_unaligned_reads_l and $output_unaligned_reads_r:
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289 #from os.path import splitext
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290 #set _unaligned_root, _unaligned_ext = splitext( str( $output_unaligned_reads_l ) )
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291 && mv "${ _unaligned_root }.1${_unaligned_ext}" '$output_unaligned_reads_l'
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292 && mv "${ _unaligned_root }.2${_unaligned_ext}" '$output_unaligned_reads_r'
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293 #end if
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294 #if $library.type == "paired" and $output_aligned_reads_l and $output_aligned_reads_r:
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295 #from os.path import splitext
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296 #set _aligned_root, _aligned_ext = splitext( str( $output_aligned_reads_l ) )
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297 && mv "${ _aligned_root }.1${_aligned_ext}" '$output_aligned_reads_l'
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298 && mv "${ _aligned_root }.2${_aligned_ext}" '$output_aligned_reads_r'
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299 #end if
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300
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301 ]]></command>
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302 <inputs>
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303 <!-- single/paired -->
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304 <conditional name="library">
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305 <param name="type" type="select" label="Is this single or paired library">
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306 <option value="single">Single-end</option>
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307 <option value="paired">Paired-end</option>
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308 <option value="paired_collection">Paired-end Dataset Collection</option>
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309 <option value="paired_interleaved">Paired-end data from single interleaved dataset</option>
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310 </param>
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311
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312 <when value="single">
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313 <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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314
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315 <expand macro="align_unalign" />
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316
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317 </when>
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318 <when value="paired">
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319 <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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320 <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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321
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322 <expand macro="align_unalign" />
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323 <expand macro="paired_end_options" />
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324
2
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325 </when>
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326 <when value="paired_collection">
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327 <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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328
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329 <expand macro="align_unalign" />
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330 <expand macro="paired_end_options" />
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331
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332 </when>
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333 <when value="paired_interleaved">
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334 <param name="input_1" format="fastqsanger,fastqsanger.gz,fastqsanger.bz2" type="data" label="Interleaved FASTQ file" help="Must be of datatype &quot;fastqsanger&quot;. --interleaved"/>
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335
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336 <expand macro="align_unalign" />
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337 <expand macro="paired_end_options" />
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338
0
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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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parents:
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605 <action type="metadata" name="dbkey">
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parents:
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606 <option type="from_data_table" name="bowtie2_indexes" column="1" offset="0">
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parents:
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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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parents:
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611 </when>
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612 <when value="history">
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parents:
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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 ${on_string}: aligned reads (SAM)">
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622 <filter>analysis_type['analysis_type_selector'] == "full" and analysis_type['sam_opt'] is True</filter>
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623 <actions>
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624 <conditional name="reference_genome.source">
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625 <when value="indexed">
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626 <action type="metadata" name="dbkey">
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627 <option type="from_data_table" name="bowtie2_indexes" column="1" offset="0">
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628 <filter type="param_value" column="0" value="#" compare="startswith" keep="False"/>
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629 <filter type="param_value" ref="reference_genome.index" column="0"/>
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630 </option>
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631 </action>
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632 </when>
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633 <when value="history">
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634 <action type="metadata" name="dbkey">
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635 <option type="from_param" name="reference_genome.own_file" param_attribute="dbkey" />
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636 </action>
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637 </when>
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638 </conditional>
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639 </actions>
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640 </data>
10
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641 <data format="txt" name="mapping_stats" label="${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="paired_options_selector" value="no"/>
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652 <param name="unaligned_file" value="false"/>
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653 <param name="analysis_type_selector" value="simple"/>
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a03a7ee6cdff Imported from capsule None
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654 <param name="source" value="history" />
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655 <param name="input_1" value="bowtie2-fq1.fq" ftype="fastqsanger"/>
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parents: 1
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656 <param name="input_2" value="bowtie2-fq2.fq" ftype="fastqsanger"/>
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657 <param name="own_file" value="bowtie2-ref.fasta" />
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658 <output name="output" file="bowtie2-test1.bam" ftype="bam" lines_diff="2"/>
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659 </test>
5
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660 <test>
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661 <!-- basic test on single paired default run -->
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662 <param name="type" value="paired"/>
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663 <param name="paired_options_selector" value="no"/>
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664 <param name="unaligned_file" value="false"/>
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665 <param name="analysis_type_selector" value="simple"/>
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666 <param name="rg_selector" value="set"/>
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667 <param name="ID" value="rg1"/>
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668 <param name="PL" value="CAPILLARY"/>
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669 <param name="source" value="history" />
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670 <param name="input_1" value="bowtie2-fq1.fq" ftype="fastqsanger"/>
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671 <param name="input_2" value="bowtie2-fq2.fq" ftype="fastqsanger"/>
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672 <param name="own_file" value="bowtie2-ref.fasta" />
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673 <output name="output" file="bowtie2-test2.bam" ftype="bam" lines_diff="2"/>
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674 </test>
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675 <test>
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676 <!-- basic test on single paired default run with stats-->
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677 <param name="type" value="paired"/>
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678 <param name="paired_options_selector" value="no"/>
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679 <param name="unaligned_file" value="false"/>
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680 <param name="analysis_type_selector" value="simple"/>
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681 <param name="source" value="history" />
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682 <param name="input_1" value="bowtie2-fq1.fq" ftype="fastqsanger"/>
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683 <param name="input_2" value="bowtie2-fq2.fq" ftype="fastqsanger"/>
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diff changeset
684 <param name="own_file" value="bowtie2-ref.fasta" />
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diff changeset
685 <param name="save_mapping_stats" value="true" />
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diff changeset
686 <output name="output" file="bowtie2-test1.bam" ftype="bam" lines_diff="2"/>
15
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diff changeset
687 <output name="mapping_stats">
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diff changeset
688 <assert_contents>
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diff changeset
689 <has_text text="of these" />
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diff changeset
690 </assert_contents>
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diff changeset
691 </output>
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diff changeset
692 </test>
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iuc
parents: 14
diff changeset
693 <test>
7e0b333f39e1 planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/bowtie2 commit cf554b9b69c32acb484c34fdc60384fa49c7c482
iuc
parents: 14
diff changeset
694 <!-- basic test on interleaved paired default run -->
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iuc
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diff changeset
695 <param name="type" value="paired_interleaved"/>
7e0b333f39e1 planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/bowtie2 commit cf554b9b69c32acb484c34fdc60384fa49c7c482
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diff changeset
696 <!-- <param name="paired_options_selector" value="no"/> -->
7e0b333f39e1 planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/bowtie2 commit cf554b9b69c32acb484c34fdc60384fa49c7c482
iuc
parents: 14
diff changeset
697 <param name="unaligned_file" value="false"/>
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diff changeset
698 <param name="analysis_type_selector" value="simple"/>
7e0b333f39e1 planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/bowtie2 commit cf554b9b69c32acb484c34fdc60384fa49c7c482
iuc
parents: 14
diff changeset
699 <param name="rg_selector" value="set"/>
7e0b333f39e1 planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/bowtie2 commit cf554b9b69c32acb484c34fdc60384fa49c7c482
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diff changeset
700 <param name="ID" value="rg1"/>
7e0b333f39e1 planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/bowtie2 commit cf554b9b69c32acb484c34fdc60384fa49c7c482
iuc
parents: 14
diff changeset
701 <param name="PL" value="CAPILLARY"/>
7e0b333f39e1 planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/bowtie2 commit cf554b9b69c32acb484c34fdc60384fa49c7c482
iuc
parents: 14
diff changeset
702 <param name="source" value="history" />
7e0b333f39e1 planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/bowtie2 commit cf554b9b69c32acb484c34fdc60384fa49c7c482
iuc
parents: 14
diff changeset
703 <param name="input_1" value="bowtie2-fq_il.fq" ftype="fastqsanger"/>
7e0b333f39e1 planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/bowtie2 commit cf554b9b69c32acb484c34fdc60384fa49c7c482
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parents: 14
diff changeset
704 <param name="own_file" value="bowtie2-ref.fasta" />
7e0b333f39e1 planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/bowtie2 commit cf554b9b69c32acb484c34fdc60384fa49c7c482
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diff changeset
705 <output name="output" file="bowtie2-test_il.bam" ftype="bam" lines_diff="2"/>
10
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diff changeset
706 </test>
14
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diff changeset
707 <test>
85f0e9edb32d planemo upload for repository https://github.com/galaxyproject/tools-devteam/tree/master/tools/bowtie2 commit 954b2052cb74a0bc88f65df37f429ff27c45ea8f
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diff changeset
708 <!-- 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
709 <param name="type" value="paired"/>
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diff changeset
710 <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
711 <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
712 <param name="analysis_type_selector" value="simple"/>
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diff changeset
713 <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
714 <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
715 <param name="input_2" value="bowtie2-fq2.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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parents: 13
diff changeset
716 <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
717 <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
718 </test>
85f0e9edb32d planemo upload for repository https://github.com/galaxyproject/tools-devteam/tree/master/tools/bowtie2 commit 954b2052cb74a0bc88f65df37f429ff27c45ea8f
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diff changeset
719 <test>
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diff changeset
720 <!-- 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
721 <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
722 <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
723 <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
724 <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
725 <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
726 <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
727 <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
728 <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
729 <output name="output" file="bowtie2-test1.bam" ftype="bam" lines_diff="2"/>
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diff changeset
730 </test>
0
a03a7ee6cdff Imported from capsule None
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diff changeset
731 </tests>
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diff changeset
732
11
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diff changeset
733 <help><![CDATA[
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734
0
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735 **Bowtie2 Overview**
11
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736
2
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737 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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738 Majority of information in this page is derived from an excellent `Bowtie2 manual`_ written by Ben Langmead.
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739
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740 .. _Bowtie2: http://bowtie-bio.sourceforge.net/bowtie2/
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741 .. _`Bowtie2 manual`: http://bowtie-bio.sourceforge.net/bowtie2/manual.shtml
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742 .. _`BAM format`: http://samtools.github.io/hts-specs/SAMv1.pdf
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743
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744 -----
0
a03a7ee6cdff Imported from capsule None
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745
2
2a6cfe8997aa Uploaded from GH
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746 **Selecting reference genomes for Bowtie2**
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747
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diff changeset
748 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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749
11
fa69d5a7b8c8 planemo upload for repository https://github.com/galaxyproject/tools-devteam/tree/master/tools/bowtie2 commit d0e857ba2691ca15b6239890baf98dbe7bc3ccbd
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diff changeset
750 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
2a6cfe8997aa Uploaded from GH
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parents: 1
diff changeset
751 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
752
2
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diff changeset
753 If your genome of interest is not listed here you have two choices:
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754
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755 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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756 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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757
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758 ------
a03a7ee6cdff Imported from capsule None
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759
2
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diff changeset
760 .. class:: infomark
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761
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diff changeset
762 **Bowtie2 options**
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763
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diff changeset
764 Galaxy wrapper for Bowtie2 implements most but not all options available through the command line. Supported options are described below.
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765
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766 -----
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767
0
a03a7ee6cdff Imported from capsule None
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768 **Inputs**
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769
15
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diff changeset
770 Bowtie 2 accepts files in Sanger FASTQ format (single or paired-end). Paired-end data can represented as two individual (forward and reverse) datasets, as well as a single interleaved dataset (see an example at the end of the help section).
0
a03a7ee6cdff Imported from capsule None
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771
a03a7ee6cdff Imported from capsule None
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772 ------
a03a7ee6cdff Imported from capsule None
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773
2
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diff changeset
774 **Input options**::
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diff changeset
775
15
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diff changeset
776 --interleaved
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diff changeset
777 Reads interleaved FASTQ files where the first two records (8 lines) represent a mate pair.
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778
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779 -s/--skip <int>
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780 Skip (i.e. do not align) the first `<int>` reads or pairs in the input.
2
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781
11
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diff changeset
782 -u/--qupto <int>
fa69d5a7b8c8 planemo upload for repository https://github.com/galaxyproject/tools-devteam/tree/master/tools/bowtie2 commit d0e857ba2691ca15b6239890baf98dbe7bc3ccbd
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783 Align the first `<int>` reads or read pairs from the input (after the
2
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784 `-s`/`--skip` reads or pairs have been skipped), then stop. Default: no limit.
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785
11
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786 -5/--trim5 <int>
fa69d5a7b8c8 planemo upload for repository https://github.com/galaxyproject/tools-devteam/tree/master/tools/bowtie2 commit d0e857ba2691ca15b6239890baf98dbe7bc3ccbd
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787 Trim `<int>` bases from 5' (left) end of each read before alignment (default: 0).
0
a03a7ee6cdff Imported from capsule None
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788
11
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diff changeset
789 -3/--trim3 <int>
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diff changeset
790 Trim `<int>` bases from 3' (right) end of each read before alignment (default: 0).
2
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diff changeset
791
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diff changeset
792 --phred33
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793 Input qualities are ASCII chars equal to the Phred quality plus 33. This is
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diff changeset
794 also called the "Phred+33" encoding, which is used by the very latest Illumina
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diff changeset
795 pipelines.
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796
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diff changeset
797 --phred64
5
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798 Input qualities are ASCII chars equal to the Phred quality plus 64. This is
2
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diff changeset
799 also called the "Phred+64" encoding.
0
a03a7ee6cdff Imported from capsule None
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diff changeset
800
2
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diff changeset
801 --solexa-quals
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diff changeset
802 Convert input qualities from Solexa Phred quality (which can be negative) to
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diff changeset
803 Phred Phred quality (which can't). This scheme was used in older Illumina GA
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804 Pipeline versions (prior to 1.3). Default: off.
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diff changeset
805
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diff changeset
806 --int-quals
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807 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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808 Integers are treated as being on the Phred quality scale unless
2
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809 `--solexa-quals` is also specified. Default: off.
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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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810
2
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diff changeset
811 ------
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812
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813 **Presets in `--end-to-end` mode**::
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814
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815 --very-fast
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diff changeset
816 Same as: `-D 5 -R 1 -N 0 -L 22 -i S,0,2.50`
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817
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818 --fast
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819 Same as: `-D 10 -R 2 -N 0 -L 22 -i S,0,2.50`
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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
820
2
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821 --sensitive
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822 Same as: `-D 15 -R 2 -L 22 -i S,1,1.15` (default in `--end-to-end` mode)
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823
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824 --very-sensitive
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825 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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826
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827 ------
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828
2
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829 **Presets options in `--local` mode**::
0
a03a7ee6cdff Imported from capsule None
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830
2
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831 --very-fast-local
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832 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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833
2
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834 --fast-local
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835 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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836
2
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837 --sensitive-local
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838 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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839
2
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840 --very-sensitive-local
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841 Same as: `-D 20 -R 3 -N 0 -L 20 -i S,1,0.50`
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842
0
a03a7ee6cdff Imported from capsule None
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843 ------
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844
2
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845 **Alignment options**::
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846
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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
847 -N <int>
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848 Sets the number of mismatches to allowed in a seed alignment during multiseed
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849 alignment. Can be set to 0 or 1. Setting this higher makes alignment slower
2
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850 (often much slower) but increases sensitivity. Default: 0.
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851
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diff changeset
852 -L <int>
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853 Sets the length of the seed substrings to align during multiseed alignment.
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854 Smaller values make alignment slower but more sensitive. Default: the
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855 `--sensitive` preset is used by default, which sets `-L` to 22 in
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856 `--end-to-end` mode and to 20 in `--local` mode.
2
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857
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858 -i <func>
2
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859 Sets a function governing the interval between seed substrings to use during
5
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860 multiseed alignment. For instance, if the read has 30 characers, and seed
2
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861 length is 10, and the seed interval is 6, the seeds extracted will be:
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862
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863 Read: TAGCTACGCTCTACGCTATCATGCATAAAC
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864 Seed 1 fw: TAGCTACGCT
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865 Seed 1 rc: AGCGTAGCTA
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866 Seed 2 fw: CGCTCTACGC
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867 Seed 2 rc: GCGTAGAGCG
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868 Seed 3 fw: ACGCTATCAT
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869 Seed 3 rc: ATGATAGCGT
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870 Seed 4 fw: TCATGCATAA
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871 Seed 4 rc: TTATGCATGA
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872
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873 Since it's best to use longer intervals for longer reads, this parameter sets
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874 the interval as a function of the read length, rather than a single
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875 one-size-fits-all number. For instance, specifying `-i S,1,2.5` sets the
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876 interval function `f` to `f(x) = 1 + 2.5 * sqrt(x)`, where x is the read length.
5
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diff changeset
877 If the function returns a result less than
2
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878 1, it is rounded up to 1. Default: the `--sensitive` preset is used by
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879 default, which sets `-i` to `S,1,1.15` in `--end-to-end` mode to `-i S,1,0.75`
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880 in `--local` mode.
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881
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diff changeset
882 --n-ceil <func>
2
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883 Sets a function governing the maximum number of ambiguous characters (usually
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884 `N`s and/or `.`s) allowed in a read as a function of read length. For instance,
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diff changeset
885 specifying `-L,0,0.15` sets the N-ceiling function `f` to `f(x) = 0 + 0.15 * x`,
5
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886 where x is the read length. Reads exceeding this ceiling are filtered out.
5cfa4b6db588 planemo upload commit 33927a87ba2eee9bf0ecdd376a66241b17b3d734
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diff changeset
887 Default: `L,0,0.15`.
2
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888
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diff changeset
889 --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
890 "Pads" dynamic programming problems by `<int>` columns on either side to allow
2
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891 gaps. Default: 15.
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892
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diff changeset
893 --gbar <int>
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diff changeset
894 Disallow gaps within `<int>` positions of the beginning or end of the read.
2
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895 Default: 4.
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896
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897 --ignore-quals
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898 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
899 mismatched position to be the highest possible, regardless of the actual value.
2
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900 I.e. input is treated as though all quality values are high. This is also the
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901 default behavior when the input doesn't specify quality values (e.g. in `-f`,
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902 `-r`, or `-c` modes).
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a03a7ee6cdff Imported from capsule None
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903
2
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904 --nofw/--norc
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905 If `--nofw` is specified, `bowtie2` will not attempt to align unpaired reads to
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906 the forward (Watson) reference strand. If `--norc` is specified, `bowtie2` will
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907 not attempt to align unpaired reads against the reverse-complement (Crick)
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908 reference strand. In paired-end mode, `--nofw` and `--norc` pertain to the
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909 fragments; i.e. specifying `--nofw` causes `bowtie2` to explore only those
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910 paired-end configurations corresponding to fragments from the reverse-complement
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diff changeset
911 (Crick) strand. Default: both strands enabled.
2
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912
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913 --no-1mm-upfront
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914 By default, Bowtie 2 will attempt to find either an exact or a 1-mismatch
5
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diff changeset
915 end-to-end alignment for the read *before* trying the multiseed heuristic. Such
2
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916 alignments can be found very quickly, and many short read alignments have exact or
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917 near-exact end-to-end alignments. However, this can lead to unexpected
5
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diff changeset
918 alignments when the user also sets options governing the multiseed heuristic,
2
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919 like `-L` and `-N`. For instance, if the user specifies `-N 0` and `-L` equal
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920 to the length of the read, the user will be surprised to find 1-mismatch alignments
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921 reported. This option prevents Bowtie 2 from searching for 1-mismatch end-to-end
5
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diff changeset
922 alignments before using the multiseed heuristic, which leads to the expected
2
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923 behavior when combined with options such as `-L` and `-N`. This comes at the
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924 expense of speed.
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925
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926 --end-to-end
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927 In this mode, Bowtie 2 requires that the entire read align from one end to the
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928 other, without any trimming (or "soft clipping") of characters from either end.
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929 The match bonus `--ma` always equals 0 in this mode, so all alignment scores
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930 are less than or equal to 0, and the greatest possible alignment score is 0.
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931 This is mutually exclusive with `--local`. `--end-to-end` is the default mode.
0
a03a7ee6cdff Imported from capsule None
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932
2
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933 --local
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934 In this mode, Bowtie 2 does not require that the entire read align from one end
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935 to the other. Rather, some characters may be omitted ("soft clipped") from the
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936 ends in order to achieve the greatest possible alignment score. The match bonus
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937 `--ma` is used in this mode, and the best possible alignment score is equal to
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938 the match bonus (`--ma`) times the length of the read. Specifying `--local`
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939 and one of the presets (e.g. `--local --very-fast`) is equivalent to specifying
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940 the local version of the preset (`--very-fast-local`). This is mutually
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941 exclusive with `--end-to-end`. `--end-to-end` is the default mode.
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942
2
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943 -----
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944
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945 **Scoring options**::
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946
11
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diff changeset
947 --ma <int>
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diff changeset
948 Sets the match bonus. In `--local` mode `<int>` is added to the alignment
2
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949 score for each position where a read character aligns to a reference character
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950 and the characters match. Not used in `--end-to-end` mode. Default: 2.
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951
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diff changeset
952 --mp MX,MN
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diff changeset
953 Sets the maximum (`MX`) and minimum (`MN`) mismatch penalties, both integers. A
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diff changeset
954 number less than or equal to `MX` and greater than or equal to `MN` is
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955 subtracted from the alignment score for each position where a read character
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956 aligns to a reference character, the characters do not match, and neither is an
2a6cfe8997aa Uploaded from GH
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diff changeset
957 `N`. If `--ignore-quals` is specified, the number subtracted quals `MX`.
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958 Otherwise, the number subtracted is `MN + floor( (MX-MN)(MIN(Q, 40.0)/40.0) )`
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959 where Q is the Phred quality value. Default: `MX` = 6, `MN` = 2.
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960
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diff changeset
961 --np <int>
2
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962 Sets penalty for positions where the read, reference, or both, contain an
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963 ambiguous character such as `N`. Default: 1.
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964
11
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diff changeset
965 --rdg <int1>,<int2>
fa69d5a7b8c8 planemo upload for repository https://github.com/galaxyproject/tools-devteam/tree/master/tools/bowtie2 commit d0e857ba2691ca15b6239890baf98dbe7bc3ccbd
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diff changeset
966 Sets the read gap open (`<int1>`) and extend (`<int2>`) penalties. A read gap of
fa69d5a7b8c8 planemo upload for repository https://github.com/galaxyproject/tools-devteam/tree/master/tools/bowtie2 commit d0e857ba2691ca15b6239890baf98dbe7bc3ccbd
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diff changeset
967 length N gets a penalty of `<int1>` + N * `<int2>`. Default: 5, 3.
2
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968
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diff changeset
969 --rfg <int1>,<int2>
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diff changeset
970 Sets the reference gap open (`<int1>`) and extend (`<int2>`) penalties. A
fa69d5a7b8c8 planemo upload for repository https://github.com/galaxyproject/tools-devteam/tree/master/tools/bowtie2 commit d0e857ba2691ca15b6239890baf98dbe7bc3ccbd
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diff changeset
971 reference gap of length N gets a penalty of `<int1>` + N * `<int2>`. Default:
2
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972 5, 3.
0
a03a7ee6cdff Imported from capsule None
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973
11
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974 --score-min <func>
2
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975 Sets a function governing the minimum alignment score needed for an alignment to
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976 be considered "valid" (i.e. good enough to report). This is a function of read
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977 length. For instance, specifying `L,0,-0.6` sets the minimum-score function `f`
5
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diff changeset
978 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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979 the default in `--local` mode is `G,20,8`.
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diff changeset
980
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981 -----
2
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982
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diff changeset
983 **Reporting options**::
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984
11
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diff changeset
985 -k <int>
2
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986 By default, `bowtie2` searches for distinct, valid alignments for each read.
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987 When it finds a valid alignment, it continues looking for alignments that are
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988 nearly as good or better. The best alignment found is reported (randomly
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989 selected from among best if tied). Information about the best alignments is
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990 used to estimate mapping quality and to set SAM optional fields, such as
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diff changeset
991 `AS:i` and `XS:i`.
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992
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993 When `-k` is specified, however, `bowtie2` behaves differently. Instead, it
11
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diff changeset
994 searches for at most `<int>` distinct, valid alignments for each read. The
2
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995 search terminates when it can't find more distinct valid alignments, or when it
11
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diff changeset
996 finds `<int>`, whichever happens first. All alignments found are reported in
2
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997 descending order by alignment score. The alignment score for a paired-end
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998 alignment equals the sum of the alignment scores of the individual mates. Each
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diff changeset
999 reported read or pair alignment beyond the first has the SAM 'secondary' bit
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diff changeset
1000 (which equals 256) set in its FLAGS field. For reads that have more than
11
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diff changeset
1001 `<int>` distinct, valid alignments, `bowtie2` does not guarantee that the
fa69d5a7b8c8 planemo upload for repository https://github.com/galaxyproject/tools-devteam/tree/master/tools/bowtie2 commit d0e857ba2691ca15b6239890baf98dbe7bc3ccbd
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diff changeset
1002 `<int>` alignments reported are the best possible in terms of alignment score.
2
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1003 `-k` is mutually exclusive with `-a`.
0
a03a7ee6cdff Imported from capsule None
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1004
2
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1005 Note: Bowtie 2 is not designed with large values for `-k` in mind, and when
2a6cfe8997aa Uploaded from GH
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1006 aligning reads to long, repetitive genomes large `-k` can be very, very slow.
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1007
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1008 -a
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1009 Like `-k` but with no upper limit on number of alignments to search for. `-a`
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1010 is mutually exclusive with `-k`.
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1011
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1012 Note: Bowtie 2 is not designed with `-a` mode in mind, and when
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diff changeset
1013 aligning reads to long, repetitive genomes this mode can be very, very slow.
11
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diff changeset
1014
2
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1015 -----
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1016
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1017 **Effort options**::
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1018
11
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diff changeset
1019 -D <int>
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diff changeset
1020 Up to `<int>` consecutive seed extension attempts can "fail" before Bowtie 2
2
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1021 moves on, using the alignments found so far. A seed extension "fails" if it
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1022 does not yield a new best or a new second-best alignment. This limit is
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1023 automatically adjusted up when -k or -a are specified. Default: 15.
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1024
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1025 -R <int>
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diff changeset
1026 `<int>` is the maximum number of times Bowtie 2 will "re-seed" reads with
2
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1027 repetitive seeds. When "re-seeding," Bowtie 2 simply chooses a new set of reads
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1028 (same length, same number of mismatches allowed) at different offsets and
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1029 searches for more alignments. A read is considered to have repetitive seeds if
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1030 the total number of seed hits divided by the number of seeds that aligned at
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1031 least once is greater than 300. Default: 2.
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1032
2
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1033 -----
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1034
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1035 **Paired-end options**::
0
a03a7ee6cdff Imported from capsule None
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1036
11
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diff changeset
1037 -I/--minins <int>
2
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1038 The minimum fragment length for valid paired-end alignments. E.g. if `-I 60` is
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1039 specified and a paired-end alignment consists of two 20-bp alignments in the
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diff changeset
1040 appropriate orientation with a 20-bp gap between them, that alignment is
2a6cfe8997aa Uploaded from GH
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1041 considered valid (as long as `-X` is also satisfied). A 19-bp gap would not
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1042 be valid in that case. If trimming options `-3` or `-5` are also used, the
2a6cfe8997aa Uploaded from GH
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1043 `-I` constraint is applied with respect to the untrimmed mates.
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1044
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1045 The larger the difference between `-I` and `-X`, the slower Bowtie 2 will
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1046 run. This is because larger differences bewteen `-I` and `-X` require that
2a6cfe8997aa Uploaded from GH
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diff changeset
1047 Bowtie 2 scan a larger window to determine if a concordant alignment exists.
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1048 For typical fragment length ranges (200 to 400 nucleotides), Bowtie 2 is very
2a6cfe8997aa Uploaded from GH
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diff changeset
1049 efficient.
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1050
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1051 Default: 0 (essentially imposing no minimum)
2
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1052
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diff changeset
1053 -X/--maxins <int>
2
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1054 The maximum fragment length for valid paired-end alignments. E.g. if `-X 100`
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1055 is specified and a paired-end alignment consists of two 20-bp alignments in the
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1056 proper orientation with a 60-bp gap between them, that alignment is considered
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1057 valid (as long as `-I` is also satisfied). A 61-bp gap would not be valid in
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1058 that case. If trimming options `-3` or `-5` are also used, the `-X`
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1059 constraint is applied with respect to the untrimmed mates, not the trimmed
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1060 mates.
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1061
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1062 The larger the difference between `-I` and `-X`, the slower Bowtie 2 will
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1063 run. This is because larger differences bewteen `-I` and `-X` require that
2a6cfe8997aa Uploaded from GH
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1064 Bowtie 2 scan a larger window to determine if a concordant alignment exists.
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1065 For typical fragment length ranges (200 to 400 nucleotides), Bowtie 2 is very
2a6cfe8997aa Uploaded from GH
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1066 efficient.
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1067
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1068 Default: 500.
0
a03a7ee6cdff Imported from capsule None
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1069
2
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1070 --fr/--rf/--ff
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1071 The upstream/downstream mate orientations for a valid paired-end alignment
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1072 against the forward reference strand. E.g., if `--fr` is specified and there is
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1073 a candidate paired-end alignment where mate 1 appears upstream of the reverse
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1074 complement of mate 2 and the fragment length constraints (`-I` and `-X`) are
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1075 met, that alignment is valid. Also, if mate 2 appears upstream of the reverse
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1076 complement of mate 1 and all other constraints are met, that too is valid.
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1077 `--rf` likewise requires that an upstream mate1 be reverse-complemented and a
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1078 downstream mate2 be forward-oriented. ` --ff` requires both an upstream mate 1
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1079 and a downstream mate 2 to be forward-oriented. Default: `--fr` (appropriate
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1080 for Illumina's Paired-end Sequencing Assay).
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1081
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1082 --no-mixed
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1083 By default, when `bowtie2` cannot find a concordant or discordant alignment for
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1084 a pair, it then tries to find alignments for the individual mates. This option
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1085 disables that behavior.
0
a03a7ee6cdff Imported from capsule None
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1086
2
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1087 --no-discordant
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1088 By default, `bowtie2` looks for discordant alignments if it cannot find any
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1089 concordant alignments. A discordant alignment is an alignment where both mates
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1090 align uniquely, but that does not satisfy the paired-end constraints
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1091 (`--fr`/`--rf`/`--ff`, `-I`, `-X`). This option disables that behavior.
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1092
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1093 --dovetail
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1094 If the mates "dovetail", that is if one mate alignment extends past the
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1095 beginning of the other such that the wrong mate begins upstream, consider that
5
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1096 to be concordant. Default: mates cannot dovetail in a concordant alignment.
2
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1097
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diff changeset
1098 --no-contain
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diff changeset
1099 If one mate alignment contains the other, consider that to be non-concordant.
5
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diff changeset
1100 Default: a mate can contain the other in a concordant alignment.
2
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1101
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diff changeset
1102 --no-overlap
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1103 If one mate alignment overlaps the other at all, consider that to be
5
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diff changeset
1104 non-concordant. Default: mates can overlap in a concordant alignment.
11
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diff changeset
1105
0
a03a7ee6cdff Imported from capsule None
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diff changeset
1106 ------
a03a7ee6cdff Imported from capsule None
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diff changeset
1107
2
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diff changeset
1108 **SAM options**::
0
a03a7ee6cdff Imported from capsule None
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diff changeset
1109
11
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diff changeset
1110 --rg-id <text>
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diff changeset
1111 Set the read group ID to `<text>`. This causes the SAM `@RG` header line to be
fa69d5a7b8c8 planemo upload for repository https://github.com/galaxyproject/tools-devteam/tree/master/tools/bowtie2 commit d0e857ba2691ca15b6239890baf98dbe7bc3ccbd
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diff changeset
1112 printed, with `<text>` as the value associated with the `ID:` tag. It also
2
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1113 causes the `RG:Z:` extra field to be attached to each SAM output record, with
11
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diff changeset
1114 value set to `<text>`.
0
a03a7ee6cdff Imported from capsule None
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diff changeset
1115
11
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diff changeset
1116 --rg <text>
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diff changeset
1117 Add `<text>` (usually of the form `TAG:VAL`, e.g. `SM:Pool1`) as a field on the
2
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1118 `@RG` header line. Note: in order for the `@RG` line to appear, `--rg-id`
5
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diff changeset
1119 must also be specified. This is because the `ID` tag is required by the SAM
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diff changeset
1120 Specification. Specify `--rg` multiple times to set multiple fields. See the
5cfa4b6db588 planemo upload commit 33927a87ba2eee9bf0ecdd376a66241b17b3d734
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diff changeset
1121 SAM Specification for details about what fields are legal.
0
a03a7ee6cdff Imported from capsule None
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1122
2
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diff changeset
1123 --omit-sec-seq
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1124 When printing secondary alignments, Bowtie 2 by default will write out the `SEQ`
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1125 and `QUAL` strings. Specifying this option causes Bowtie 2 to print an asterix
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1126 in those fields instead.
11
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1127
2
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1128 -----
0
a03a7ee6cdff Imported from capsule None
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1129
2
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1130 **Other options**::
0
a03a7ee6cdff Imported from capsule None
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1131
2
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1132 --reorder
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1133 Guarantees that output SAM records are printed in an order corresponding to the
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1134 order of the reads in the original input file, even when `-p` is set greater
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1135 than 1. Specifying `--reorder` and setting `-p` greater than 1 causes Bowtie
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1136 2 to run somewhat slower and use somewhat more memory then if `--reorder` were
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1137 not specified. Has no effect if `-p` is set to 1, since output order will
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diff changeset
1138 naturally correspond to input order in that case.
0
a03a7ee6cdff Imported from capsule None
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diff changeset
1139
11
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diff changeset
1140 --seed <int>
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diff changeset
1141 Use `<int>` as the seed for pseudo-random number generator. Default: 0.
0
a03a7ee6cdff Imported from capsule None
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1142
2
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1143 --non-deterministic
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1144 Normally, Bowtie 2 re-initializes its pseudo-random generator for each read. It
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1145 seeds the generator with a number derived from (a) the read name, (b) the
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1146 nucleotide sequence, (c) the quality sequence, (d) the value of the `--seed`
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1147 option. This means that if two reads are identical (same name, same
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1148 nucleotides, same qualities) Bowtie 2 will find and report the same alignment(s)
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1149 for both, even if there was ambiguity. When `--non-deterministic` is specified,
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1150 Bowtie 2 re-initializes its pseudo-random generator for each read using the
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diff changeset
1151 current time. This means that Bowtie 2 will not necessarily report the same
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diff changeset
1152 alignment for two identical reads. This is counter-intuitive for some users,
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1153 but might be more appropriate in situations where the input consists of many
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diff changeset
1154 identical reads.
0
a03a7ee6cdff Imported from capsule None
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diff changeset
1155
15
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1156 -----
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diff changeset
1157
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diff changeset
1158
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diff changeset
1159 **Paired-end (and mate-pair) data in fastq format**
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diff changeset
1160
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diff changeset
1161 Paired end datasets can be represented as two individual datasets:
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diff changeset
1162
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diff changeset
1163 First dataset::
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diff changeset
1164
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diff changeset
1165 @1/1
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1166 AGGGATGTGTTAGGGTTAGGGTTAGGGTTAGGGTTAGGGTTAGGGTTA
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diff changeset
1167 +
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1168 EGGEGGGDFGEEEAEECGDEGGFEEGEFGBEEDDECFEFDD@CDD<ED
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diff changeset
1169 @2/1
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1170 AGGGATGTGTTAGGGTTAGGGTTAGGGTTAGGGTTAGGGTTAGGGTTA
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diff changeset
1171 +
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1172 HHHHHHEGFHEEFEEHEEHHGGEGGGGEFGFGGGGHHHHFBEEEEEFG
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diff changeset
1173
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diff changeset
1174 Second dataset::
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1175
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diff changeset
1176 @1/2
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1177 CCTAACCCTAACCCTAACCCTAACCCTAACCCTAACCCTAACCCTAAC
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1178 +
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1179 GHHHDFDFGFGEGFBGEGGEGEGGGHGFGHFHFHHHHHHHEF?EFEFF
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diff changeset
1180 @2/2
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diff changeset
1181 CCTAACCCTAACCCTAACCCTAACCCTAACCCTAACCCTAACCCTAAC
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1182 +
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1183 HHHHHHHHHHHHHGHHHHHHGHHHHHHHHHHHFHHHFHHHHHHHHHHH
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1184
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1185 Or a single *interleaved* dataset::
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1186
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1187 @1/1
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1188 AGGGATGTGTTAGGGTTAGGGTTAGGGTTAGGGTTAGGGTTAGGGTTA
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1189 +
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1190 EGGEGGGDFGEEEAEECGDEGGFEEGEFGBEEDDECFEFDD@CDD<ED
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1191 @1/2
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1192 CCTAACCCTAACCCTAACCCTAACCCTAACCCTAACCCTAACCCTAAC
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1193 +
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1194 GHHHDFDFGFGEGFBGEGGEGEGGGHGFGHFHFHHHHHHHEF?EFEFF
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1195 @2/1
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1196 AGGGATGTGTTAGGGTTAGGGTTAGGGTTAGGGTTAGGGTTAGGGTTA
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1197 +
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1198 HHHHHHEGFHEEFEEHEEHHGGEGGGGEFGFGGGGHHHHFBEEEEEFG
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1199 @2/2
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1200 CCTAACCCTAACCCTAACCCTAACCCTAACCCTAACCCTAACCCTAAC
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1201 +
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1202 HHHHHHHHHHHHHGHHHHHHGHHHHHHHHHHHFHHHFHHHHHHHHHHH
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1203
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1204
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1205
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1206
11
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1207 ]]></help>
2
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1208 <citations>
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1209 <citation type="doi">10.1186/gb-2009-10-3-r25</citation>
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1210 <citation type="doi">10.1038/nmeth.1923</citation>
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1211 </citations>
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1212 </tool>