annotate trimmomatic.xml @ 10:dfa082f84068 draft

Uploaded version 0.36.5 (use conda to resolve tool dependencies)
author pjbriggs
date Mon, 05 Mar 2018 10:13:48 -0500
parents 53af7b5b1b56
children 59054f086eca
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1 <tool id="trimmomatic" name="Trimmomatic" version="0.36.5">
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2 <description>flexible read trimming tool for Illumina NGS data</description>
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3 <macros>
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4 <import>trimmomatic_macros.xml</import>
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5 </macros>
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6 <requirements>
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7 <requirement type="package" version="0.36">trimmomatic</requirement>
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8 </requirements>
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9 <command detect_errors="aggressive"><![CDATA[
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10 @CONDA_TRIMMOMATIC_JAR_PATH@ &&
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11 @CONDA_TRIMMOMATIC_ADAPTERS_PATH@ &&
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12 #if $readtype.single_or_paired == "pair_of_files"
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13 #set r1_ext = $readtype.fastq_r1_in.extension
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14 #set r2_ext = $readtype.fastq_r2_in.extension
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15 ln -s '$readtype.fastq_r1_in' fastq_r1.'$r1_ext' &&
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16 ln -s '$readtype.fastq_r2_in' fastq_r2.'$r2_ext' &&
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17 #elif $readtype.single_or_paired == "collection"
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18 #set r1_ext = $readtype.fastq_pair.forward.extension
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19 #set r2_ext = $readtype.fastq_pair.reverse.extension
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20 ln -s '$readtype.fastq_pair.forward' fastq_r1.'$r1_ext' &&
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21 ln -s '$readtype.fastq_pair.reverse' fastq_r2.'$r2_ext' &&
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22 #else
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23 ln -s '$fastq_in' fastq_in.'$fastq_in.extension' &&
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24 #end if
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25 java \${_JAVA_OPTIONS:--Xmx8G} -jar \$TRIMMOMATIC_JAR_PATH/trimmomatic.jar
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26 #if $readtype.single_or_paired in ["pair_of_files","collection"]
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27 PE -threads \${GALAXY_SLOTS:-6} -phred33
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28 fastq_r1.'$r1_ext' fastq_r2.'$r2_ext'
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29 fastq_out_r1_paired.'$r1_ext' fastq_out_r1_unpaired.'$r1_ext'
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30 fastq_out_r2_paired.'$r2_ext' fastq_out_r2_unpaired.'$r2_ext'
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31 #else
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32 SE -threads \${GALAXY_SLOTS:-6} -phred33 fastq_in.'$fastq_in.extension' fastq_out.'$fastq_in.extension'
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33 #end if
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34 ## ILLUMINACLIP option
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35 #if $illuminaclip.do_illuminaclip
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36 #if $illuminaclip.adapter_type.standard_or_custom == "custom"
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37 #if $readtype.single_or_paired in ["pair_of_files","collection"]
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38 ILLUMINACLIP:$adapter_file_from_text:$illuminaclip.seed_mismatches:$illuminaclip.palindrome_clip_threshold:$illuminaclip.simple_clip_threshold:$illuminaclip.min_adapter_len:$illuminaclip.keep_both_reads
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39 #else
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40 ILLUMINACLIP:$adapter_file_from_text:$illuminaclip.seed_mismatches:$illuminaclip.palindrome_clip_threshold:$illuminaclip.simple_clip_threshold
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41 #end if
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42 #else
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43 #if $readtype.single_or_paired in ["pair_of_files","collection"]
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44 ILLUMINACLIP:\$TRIMMOMATIC_ADAPTERS_PATH/$illuminaclip.adapter_type.adapter_fasta:$illuminaclip.seed_mismatches:$illuminaclip.palindrome_clip_threshold:$illuminaclip.simple_clip_threshold:$illuminaclip.min_adapter_len:$illuminaclip.keep_both_reads
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45 #else
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46 ILLUMINACLIP:\$TRIMMOMATIC_ADAPTERS_PATH/$illuminaclip.adapter_type.adapter_fasta:$illuminaclip.seed_mismatches:$illuminaclip.palindrome_clip_threshold:$illuminaclip.simple_clip_threshold
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47 #end if
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48 #end if
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49 #end if
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50 ## Other operations
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51 #for $op in $operations
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52 ## SLIDINGWINDOW
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53 #if str( $op.operation.name ) == "SLIDINGWINDOW"
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54 SLIDINGWINDOW:$op.operation.window_size:$op.operation.required_quality
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55 #end if
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56 ## MINLEN:36
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57 #if str( $op.operation.name ) == "MINLEN"
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58 MINLEN:$op.operation.minlen
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59 #end if
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60 #if str( $op.operation.name ) == "LEADING"
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61 LEADING:$op.operation.leading
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62 #end if
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63 #if str( $op.operation.name ) == "TRAILING"
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64 TRAILING:$op.operation.trailing
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65 #end if
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66 #if str( $op.operation.name ) == "CROP"
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67 CROP:$op.operation.crop
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68 #end if
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69 #if str( $op.operation.name ) == "HEADCROP"
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70 HEADCROP:$op.operation.headcrop
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71 #end if
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72 #if str( $op.operation.name ) == "AVGQUAL"
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73 AVGQUAL:$op.operation.avgqual
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74 #end if
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75 #if str( $op.operation.name ) == "MAXINFO"
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76 MAXINFO:$op.operation.target_length:$op.operation.strictness
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77 #end if
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78 #end for
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79 2>&1 | tee trimmomatic.log &&
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80 if [ -z "\$(tail -1 trimmomatic.log | grep "Completed successfully")" ]; then echo "Trimmomatic did not finish successfully" >&2 ; exit 1 ; fi
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81 &&
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82 #if $readtype.single_or_paired == "pair_of_files"
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83 mv fastq_out_r1_paired.'$r1_ext' '${fastq_out_r1_paired}' &&
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84 mv fastq_out_r1_unpaired.'$r1_ext' '${fastq_out_r1_unpaired}' &&
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85 mv fastq_out_r2_paired.'$r2_ext' '${fastq_out_r2_paired}' &&
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86 mv fastq_out_r2_unpaired.'$r2_ext' '${fastq_out_r2_unpaired}'
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87 #elif $readtype.single_or_paired == "collection"
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88 mv fastq_out_r1_paired.'$r1_ext' '${fastq_out_paired.forward}' &&
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89 mv fastq_out_r1_unpaired.'$r1_ext' '${fastq_out_unpaired.forward}' &&
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90 mv fastq_out_r2_paired.'$r2_ext' '${fastq_out_paired.reverse}' &&
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91 mv fastq_out_r2_unpaired.'$r2_ext' '${fastq_out_unpaired.reverse}'
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92 #else
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93 mv fastq_out.'$fastq_in.extension' '${fastq_out}'
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94 #end if
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95 ]]></command>
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96 <configfiles>
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97 <configfile name="adapter_file_from_text">#set from_text_area = ''
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98 #if str( $illuminaclip.do_illuminaclip ) == "yes" and str( $illuminaclip.adapter_type.standard_or_custom ) == "custom":
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99 #set from_text_area = $illuminaclip.adapter_type.adapter_text
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100 #end if
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101 ${from_text_area}</configfile>
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102 </configfiles>
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103
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104 <inputs>
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105 <conditional name="readtype">
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106 <param name="single_or_paired" type="select" label="Single-end or paired-end reads?">
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107 <option value="se" selected="true">Single-end</option>
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108 <option value="pair_of_files">Paired-end (two separate input files)</option>
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109 <option value="collection">Paired-end (as collection)</option>
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110 </param>
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111 <when value="se">
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112 <param name="fastq_in" type="data" format="fastqsanger,fastqsanger.gz" label="Input FASTQ file" />
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113 </when>
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114 <when value="pair_of_files">
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115 <param name="fastq_r1_in" type="data" format="fastqsanger,fastqsanger.gz"
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116 label="Input FASTQ file (R1/first of pair)" />
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117 <param name="fastq_r2_in" type="data" format="fastqsanger,fastqsanger.gz"
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118 label="Input FASTQ file (R2/second of pair)" />
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119 </when>
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120 <when value="collection">
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121 <param name="fastq_pair" format="fastqsanger,fastqsanger.gz" type="data_collection" collection_type="paired" label="Select FASTQ dataset collection with R1/R2 pair" />
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122 </when>
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123 </conditional>
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124 <conditional name="illuminaclip">
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125 <param name="do_illuminaclip" type="boolean" label="Perform initial ILLUMINACLIP step?" help="Cut adapter and other illumina-specific sequences from the read" truevalue="yes" falsevalue="no" checked="False" />
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126 <when value="yes">
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127 <conditional name="adapter_type">
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128 <param name="standard_or_custom" type="select" label="Select standard adapter sequences or provide custom?">
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129 <option value="standard" selected="true">Standard</option>
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130 <option value="custom">Custom</option>
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131 </param>
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132 <when value="standard">
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133 <param name="adapter_fasta" type="select" label="Adapter sequences to use">
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134 <option value="TruSeq2-SE.fa">TruSeq2 (single-ended, for Illumina GAII)</option>
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135 <option value="TruSeq3-SE.fa">TruSeq3 (single-ended, for MiSeq and HiSeq)</option>
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136 <option value="TruSeq2-PE.fa">TruSeq2 (paired-ended, for Illumina GAII)</option>
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137 <option value="TruSeq3-PE.fa">TruSeq3 (paired-ended, for MiSeq and HiSeq)</option>
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138 <option value="TruSeq3-PE-2.fa">TruSeq3 (additional seqs) (paired-ended, for MiSeq and HiSeq)</option>
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139 <option value="NexteraPE-PE.fa">Nextera (paired-ended)</option>
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140 </param>
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141 </when>
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142 <when value="custom">
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143 <param name="adapter_text" type="text" area="True" size="10x30" value=""
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144 label="Custom adapter sequences in fasta format" help="Write sequences in the fasta format.">
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145 <sanitizer>
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146 <valid initial="string.printable"></valid>
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147 <mapping initial="none"/>
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148 </sanitizer>
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149 </param>
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150 </when>
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151 </conditional>
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152 <param name="seed_mismatches" type="integer" label="Maximum mismatch count which will still allow a full match to be performed" value="2" />
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153 <param name="palindrome_clip_threshold" type="integer" label="How accurate the match between the two 'adapter ligated' reads must be for PE palindrome read alignment" value="30" />
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154 <param name="simple_clip_threshold" type="integer" label="How accurate the match between any adapter etc. sequence must be against a read" value="10" />
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155 <param name="min_adapter_len" type="integer" label="Minimum length of adapter that needs to be detected (PE specific/palindrome mode)" value="8" />
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156 <param name="keep_both_reads" type="boolean" label="Always keep both reads (PE specific/palindrome mode)?" truevalue="true" falsevalue="false" checked="true"
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157 help="See help below"/>
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158 </when>
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159 <when value="no" /> <!-- empty clause to satisfy planemo lint -->
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160 </conditional>
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161 <repeat name="operations" title="Trimmomatic Operation" min="1">
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162 <conditional name="operation">
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163 <param name="name" type="select" label="Select Trimmomatic operation to perform">
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164 <option selected="true" value="SLIDINGWINDOW">Sliding window trimming (SLIDINGWINDOW)</option>
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165 <option value="MINLEN">Drop reads below a specified length (MINLEN)</option>
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166 <option value="LEADING">Cut bases off the start of a read, if below a threshold quality (LEADING)</option>
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167 <option value="TRAILING">Cut bases off the end of a read, if below a threshold quality (TRAILING)</option>
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168 <option value="CROP">Cut the read to a specified length (CROP)</option>
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169 <option value="HEADCROP">Cut the specified number of bases from the start of the read (HEADCROP)</option>
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170 <option value="AVGQUAL">Drop reads with average quality lower than a specified level (AVGQUAL)</option>
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171 <option value="MAXINFO">Trim reads adaptively, balancing read length and error rate to maximise the value of each read (MAXINFO)</option>
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172 </param>
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173 <when value="SLIDINGWINDOW">
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174 <param name="window_size" type="integer" label="Number of bases to average across" value="4" />
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175 <param name="required_quality" type="integer" label="Average quality required" value="20" />
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176 </when>
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177 <when value="MINLEN">
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178 <param name="minlen" type="integer" label="Minimum length of reads to be kept" value="20" />
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179 </when>
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180 <when value="LEADING">
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181 <param name="leading" type="integer" label="Minimum quality required to keep a base" value="3" help="Bases at the start of the read with quality below the threshold will be removed" />
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182 </when>
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183 <when value="TRAILING">
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184 <param name="trailing" type="integer" label="Minimum quality required to keep a base" value="3" help="Bases at the end of the read with quality below the threshold will be removed" />
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185 </when>
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186 <when value="CROP">
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187 <param name="crop" type="integer" label="Number of bases to keep from the start of the read" value="" />
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188 </when>
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189 <when value="HEADCROP">
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190 <param name="headcrop" type="integer" label="Number of bases to remove from the start of the read" value="" />
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191 </when>
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192 <when value="AVGQUAL">
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193 <param name="avgqual" type="integer" label="Minimum average quality required to keep a read" value="" />
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194 </when>
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195 <when value="MAXINFO">
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196 <param name="target_length" type="integer" label="Target read length" value="" help="The read length which is likely to allow the location of the read within the target sequence to be determined." />
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197 <param name="strictness" type="float" label="Strictness" value="" help="Set between zero and one - specifies the balance between preserving read length versus removal of incorrect bases; low values (&lt;0.2) favours longer reads, high values (&gt;0.8) favours read correctness." />
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198 </when>
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199 </conditional>
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200 </repeat>
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201 </inputs>
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202 <outputs>
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203 <data name="fastq_out_r1_paired" label="${tool.name} on ${readtype.fastq_r1_in.name} (R1 paired)" format_source="fastq_r1_in">
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204 <filter>readtype['single_or_paired'] == "pair_of_files"</filter>
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205 </data>
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206 <data name="fastq_out_r2_paired" label="${tool.name} on ${readtype.fastq_r2_in.name} (R2 paired)" format_source="fastq_r2_in">
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207 <filter>readtype['single_or_paired'] == "pair_of_files"</filter>
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208 </data>
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209 <data name="fastq_out_r1_unpaired" label="${tool.name} on ${readtype.fastq_r1_in.name} (R1 unpaired)" format_source="fastq_r1_in">
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210 <filter>readtype['single_or_paired'] == "pair_of_files"</filter>
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211 </data>
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212 <data name="fastq_out_r2_unpaired" label="${tool.name} on ${readtype.fastq_r2_in.name} (R2 unpaired)" format_source="fastq_r2_in">
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213 <filter>readtype['single_or_paired'] == "pair_of_files"</filter>
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214 </data>
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215 <data name="fastq_out" label="${tool.name} on ${readtype.fastq_in.name}" format_source="fastq_in">
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216 <filter>readtype['single_or_paired'] == 'se'</filter>
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217 </data>
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218 <collection name="fastq_out_paired" type="paired" label="${tool.name} on ${on_string}: paired">
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219 <filter>readtype['single_or_paired'] == "collection"</filter>
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220 <data name="forward" label="${tool.name} on ${readtype.fastq_pair.forward.name} (R1 paired)" format_source="fastq_pair['forward']"/>
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221 <data name="reverse" label="${tool.name} on ${readtype.fastq_pair.reverse.name} (R2 paired)" format_source="fastq_pair['reverse']"/>
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222 </collection>
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223 <collection name="fastq_out_unpaired" type="paired" label="${tool.name} on ${on_string}: unpaired">
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224 <filter>readtype['single_or_paired'] == "collection"</filter>
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225 <data name="forward" label="${tool.name} on ${readtype.fastq_pair.forward.name} (R1 unpaired)" format_source="fastq_pair['forward']"/>
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226 <data name="reverse" label="${tool.name} on ${readtype.fastq_pair.reverse.name} (R2 unpaired)" format_source="fastq_pair['reverse']"/>
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227 </collection>
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228
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229 </outputs>
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230 <tests>
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231 <test>
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232 <!-- Single-end example -->
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233 <param name="single_or_paired" value="se" />
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234 <param name="fastq_in" value="Illumina_SG_R1.fastq" ftype="fastqsanger" />
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235 <param name="operations_0|operation|name" value="SLIDINGWINDOW" />
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236 <output name="fastq_out" file="trimmomatic_se_out1.fastq" />
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237 </test>
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238 <test>
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239 <!-- Single-end example - gzipped -->
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240 <param name="single_or_paired" value="se" />
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241 <param name="fastq_in" value="Illumina_SG_R1.fastq.gz" ftype="fastqsanger.gz" />
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242 <param name="operations_0|operation|name" value="SLIDINGWINDOW" />
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243 <output name="fastq_out" file="trimmomatic_se_out1.fastq.gz" />
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244 </test>
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245 <test>
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246 <!-- Paired-end example - gzipped -->
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247 <param name="single_or_paired" value="pair_of_files" />
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248 <param name="fastq_r1_in" value="Illumina_SG_R1.fastq.gz" ftype="fastqsanger.gz" />
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249 <param name="fastq_r2_in" value="Illumina_SG_R2.fastq.gz" ftype="fastqsanger.gz" />
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250 <param name="operations_0|operation|name" value="SLIDINGWINDOW" />
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251 <output name="fastq_out_r1_paired" file="trimmomatic_pe_r1_paired_out1.fastq.gz" />
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252 <output name="fastq_out_r1_unpaired" file="trimmomatic_pe_r1_unpaired_out1.fastq.gz" />
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253 <output name="fastq_out_r2_paired" file="trimmomatic_pe_r2_paired_out1.fastq.gz" />
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254 <output name="fastq_out_r2_unpaired" file="trimmomatic_pe_r2_unpaired_out1.fastq.gz" />
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255 </test>
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256 <test>
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257 <!-- Paired-end example -->
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258 <param name="single_or_paired" value="pair_of_files" />
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259 <param name="fastq_r1_in" value="Illumina_SG_R1.fastq" ftype="fastqsanger" />
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260 <param name="fastq_r2_in" value="Illumina_SG_R2.fastq" ftype="fastqsanger" />
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261 <param name="operations_0|operation|name" value="SLIDINGWINDOW" />
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262 <output name="fastq_out_r1_paired" file="trimmomatic_pe_r1_paired_out1.fastq" />
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263 <output name="fastq_out_r1_unpaired" file="trimmomatic_pe_r1_unpaired_out1.fastq" />
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264 <output name="fastq_out_r2_paired" file="trimmomatic_pe_r2_paired_out1.fastq" />
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265 <output name="fastq_out_r2_unpaired" file="trimmomatic_pe_r2_unpaired_out1.fastq" />
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266 </test>
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267 <test>
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268 <!-- Single-end example (cropping) -->
6
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269 <param name="single_or_paired" value="se" />
0
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270 <param name="fastq_in" value="Illumina_SG_R1.fastq" ftype="fastqsanger" />
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271 <param name="operations_0|operation|name" value="CROP" />
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272 <param name="operations_0|operation|crop" value="10" />
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pjbriggs
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273 <output name="fastq_out" file="trimmomatic_se_out2.fastq" />
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pjbriggs
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274 </test>
3
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275 <test>
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276 <!-- Paired-end with dataset collection -->
6
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277 <param name="single_or_paired" value="collection" />
3
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278 <param name="fastq_pair">
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279 <collection type="paired">
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280 <element name="forward" value="Illumina_SG_R1.fastq" ftype="fastqsanger" />
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281 <element name="reverse" value="Illumina_SG_R2.fastq" ftype="fastqsanger"/>
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282 </collection>
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283 </param>
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284 <param name="operations_0|operation|name" value="SLIDINGWINDOW" />
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285 <output_collection name="fastq_out_paired" type="paired">
6
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286 <element name="forward" file="trimmomatic_pe_r1_paired_out1.fastq" />
141bba0e9a77 Uploaded v0.36.2 (adds support for compressed fastq inputs)
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287 <element name="reverse" file="trimmomatic_pe_r2_paired_out1.fastq" />
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288 </output_collection>
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289 <output_collection name="fastq_out_unpaired" type="paired">
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290 <element name="forward" file="trimmomatic_pe_r1_unpaired_out1.fastq" />
141bba0e9a77 Uploaded v0.36.2 (adds support for compressed fastq inputs)
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291 <element name="reverse" file="trimmomatic_pe_r2_unpaired_out1.fastq" />
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292 </output_collection>
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293 </test>
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294 <test>
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295 <!-- Paired-end with dataset collection - gzipped -->
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296 <param name="single_or_paired" value="collection" />
141bba0e9a77 Uploaded v0.36.2 (adds support for compressed fastq inputs)
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297 <param name="fastq_pair">
141bba0e9a77 Uploaded v0.36.2 (adds support for compressed fastq inputs)
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298 <collection type="paired">
141bba0e9a77 Uploaded v0.36.2 (adds support for compressed fastq inputs)
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299 <element name="forward" value="Illumina_SG_R1.fastq.gz" ftype="fastqsanger.gz" />
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300 <element name="reverse" value="Illumina_SG_R2.fastq.gz" ftype="fastqsanger.gz"/>
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301 </collection>
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302 </param>
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303 <param name="operations_0|operation|name" value="SLIDINGWINDOW" />
141bba0e9a77 Uploaded v0.36.2 (adds support for compressed fastq inputs)
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304 <output_collection name="fastq_out_paired" type="paired">
141bba0e9a77 Uploaded v0.36.2 (adds support for compressed fastq inputs)
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305 <element name="forward" file="trimmomatic_pe_r1_paired_out1.fastq.gz" />
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306 <element name="reverse" file="trimmomatic_pe_r2_paired_out1.fastq.gz" />
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pjbriggs
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307 </output_collection>
141bba0e9a77 Uploaded v0.36.2 (adds support for compressed fastq inputs)
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308 <output_collection name="fastq_out_unpaired" type="paired">
141bba0e9a77 Uploaded v0.36.2 (adds support for compressed fastq inputs)
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309 <element name="forward" file="trimmomatic_pe_r1_unpaired_out1.fastq.gz" />
141bba0e9a77 Uploaded v0.36.2 (adds support for compressed fastq inputs)
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310 <element name="reverse" file="trimmomatic_pe_r2_unpaired_out1.fastq.gz" />
3
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311 </output_collection>
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312 </test>
4
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313 <test>
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314 <!-- Single-end using AVGQUAL -->
6
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315 <param name="single_or_paired" value="se" />
4
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316 <param name="fastq_in" value="Illumina_SG_R1.fastq" ftype="fastqsanger" />
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317 <param name="operations_0|operation|name" value="AVGQUAL" />
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318 <param name="operations_0|operation|avgqual" value="30" />
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319 <output name="fastq_out" file="trimmomatic_avgqual.fastq" />
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320 </test>
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321 <test>
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322 <!-- Single-end using MAXINFO -->
6
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323 <param name="single_or_paired" value="se" />
4
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324 <param name="fastq_in" value="Illumina_SG_R1.fastq" ftype="fastqsanger" />
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pjbriggs
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325 <param name="operations_0|operation|name" value="MAXINFO" />
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326 <param name="operations_0|operation|target_length" value="75" />
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pjbriggs
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327 <param name="operations_0|operation|strictness" value="0.8" />
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pjbriggs
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328 <output name="fastq_out" file="trimmomatic_maxinfo.fastq" />
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329 </test>
8
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330 <test>
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331 <!-- Paired-end ILLUMINACLIP - this does not check valid clipping -->
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pjbriggs
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332 <param name="single_or_paired" value="pair_of_files" />
415a165d92bb Uploaded v0.36.4.
pjbriggs
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333 <param name="fastq_r1_in" value="Illumina_SG_R1.fastq" ftype="fastqsanger" />
415a165d92bb Uploaded v0.36.4.
pjbriggs
parents: 7
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334 <param name="fastq_r2_in" value="Illumina_SG_R2.fastq" ftype="fastqsanger" />
415a165d92bb Uploaded v0.36.4.
pjbriggs
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335 <param name="do_illuminaclip" value="true"/>
415a165d92bb Uploaded v0.36.4.
pjbriggs
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336 <param name="adapter_fasta" value="TruSeq2-PE.fa"/>
415a165d92bb Uploaded v0.36.4.
pjbriggs
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337 <param name="operations_0|operation|name" value="SLIDINGWINDOW" />
415a165d92bb Uploaded v0.36.4.
pjbriggs
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338 <output name="fastq_out_r1_paired" file="trimmomatic_pe_r1_paired_out1_clip.fastq" />
415a165d92bb Uploaded v0.36.4.
pjbriggs
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339 <output name="fastq_out_r1_unpaired" file="trimmomatic_pe_r1_unpaired_out1.fastq" />
415a165d92bb Uploaded v0.36.4.
pjbriggs
parents: 7
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340 <output name="fastq_out_r2_paired" file="trimmomatic_pe_r2_paired_out1.fastq" />
415a165d92bb Uploaded v0.36.4.
pjbriggs
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341 <output name="fastq_out_r2_unpaired" file="trimmomatic_pe_r2_unpaired_out1_clip.fastq" />
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342 </test>
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343 <test>
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344 <!-- Paired-end ILLUMINACLIP providing 'custom' adapters - this does not check valid clipping -->
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345 <param name="single_or_paired" value="pair_of_files" />
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346 <param name="fastq_r1_in" value="Illumina_SG_R1.fastq" ftype="fastqsanger" />
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347 <param name="fastq_r2_in" value="Illumina_SG_R2.fastq" ftype="fastqsanger" />
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pjbriggs
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348 <param name="do_illuminaclip" value="true"/>
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349 <param name="standard_or_custom" value="custom"/>
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350 <param name="adapter_text"
415a165d92bb Uploaded v0.36.4.
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351 value=">PrefixPE/1&#10;AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT&#10;>PrefixPE/2&#10;CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT&#10;>PCR_Primer1&#10;AATGATACGGCGACCACCGAGATCTACACTCTTTCCCTACACGACGCTCTTCCGATCT&#10;>PCR_Primer1_rc&#10;AGATCGGAAGAGCGTCGTGTAGGGAAAGAGTGTAGATCTCGGTGGTCGCCGTATCATT&#10;>PCR_Primer2&#10;CAAGCAGAAGACGGCATACGAGATCGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCT&#10;>PCR_Primer2_rc&#10;AGATCGGAAGAGCGGTTCAGCAGGAATGCCGAGACCGATCTCGTATGCCGTCTTCTGCTTG&#10;>FlowCell1&#10;TTTTTTTTTTAATGATACGGCGACCACCGAGATCTACAC&#10;>FlowCell2&#10;TTTTTTTTTTCAAGCAGAAGACGGCATACGA&#10;"/>
415a165d92bb Uploaded v0.36.4.
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352 <param name="adapter_fasta" value="TruSeq2-PE.fa"/>
415a165d92bb Uploaded v0.36.4.
pjbriggs
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353 <param name="operations_0|operation|name" value="SLIDINGWINDOW" />
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pjbriggs
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354 <output name="fastq_out_r1_paired" file="trimmomatic_pe_r1_paired_out1_clip.fastq" />
415a165d92bb Uploaded v0.36.4.
pjbriggs
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355 <output name="fastq_out_r1_unpaired" file="trimmomatic_pe_r1_unpaired_out1.fastq" />
415a165d92bb Uploaded v0.36.4.
pjbriggs
parents: 7
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356 <output name="fastq_out_r2_paired" file="trimmomatic_pe_r2_paired_out1.fastq" />
415a165d92bb Uploaded v0.36.4.
pjbriggs
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357 <output name="fastq_out_r2_unpaired" file="trimmomatic_pe_r2_unpaired_out1_clip.fastq" />
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358 </test>
0
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359 </tests>
3
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360 <help><![CDATA[
0
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361 .. class:: infomark
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pjbriggs
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362
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pjbriggs
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363 **What it does**
3358c3d30143 Uploaded initial version.
pjbriggs
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364
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365 Trimmomatic performs a variety of useful trimming tasks for illumina paired-end and
3358c3d30143 Uploaded initial version.
pjbriggs
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366 single ended data.
3358c3d30143 Uploaded initial version.
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367
3358c3d30143 Uploaded initial version.
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368 This tool allows the following trimming steps to be performed:
3358c3d30143 Uploaded initial version.
pjbriggs
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369
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370 * **ILLUMINACLIP:** Cut adapter and other illumina-specific sequences from the read
8
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371
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372 * If **Always keep both reads (PE specific/palindrome mode)** is True, the reverse read will also be retained in palindrome mode.
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373 After read-though has been detected by palindrome mode, and the adapter sequence removed,
415a165d92bb Uploaded v0.36.4.
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374 the reverse read contains the same sequence information as the forward read, albeit in reverse complement.
415a165d92bb Uploaded v0.36.4.
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375 For this reason, the default behaviour is to entirely drop the reverse read.
415a165d92bb Uploaded v0.36.4.
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376 Retaining the reverse read may be useful e.g. if the downstream tools cannot handle a combination of paired and unpaired reads.
0
3358c3d30143 Uploaded initial version.
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377 * **SLIDINGWINDOW:** Perform a sliding window trimming, cutting once the average
3358c3d30143 Uploaded initial version.
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378 quality within the window falls below a threshold
3358c3d30143 Uploaded initial version.
pjbriggs
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379 * **MINLEN:** Drop the read if it is below a specified length
3358c3d30143 Uploaded initial version.
pjbriggs
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380 * **LEADING:** Cut bases off the start of a read, if below a threshold quality
3358c3d30143 Uploaded initial version.
pjbriggs
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381 * **TRAILING:** Cut bases off the end of a read, if below a threshold quality
3358c3d30143 Uploaded initial version.
pjbriggs
parents:
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382 * **CROP:** Cut the read to a specified length
3358c3d30143 Uploaded initial version.
pjbriggs
parents:
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383 * **HEADCROP:** Cut the specified number of bases from the start of the read
4
14d05f2d511d Version that supports Trimmomatic 0.36.
pjbriggs
parents: 3
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384 * **AVGQUAL:** Drop the read if the average quality is below a specified value
6
141bba0e9a77 Uploaded v0.36.2 (adds support for compressed fastq inputs)
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385 * **MAXINFO:** Trim reads adaptively, balancing read length and error rate to
4
14d05f2d511d Version that supports Trimmomatic 0.36.
pjbriggs
parents: 3
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386 maximise the value of each read
0
3358c3d30143 Uploaded initial version.
pjbriggs
parents:
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387
3358c3d30143 Uploaded initial version.
pjbriggs
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388 If ILLUMINACLIP is requested then it is always performed first; subsequent options
3358c3d30143 Uploaded initial version.
pjbriggs
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389 can be mixed and matched and will be performed in the order that they have been
3358c3d30143 Uploaded initial version.
pjbriggs
parents:
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390 specified.
3358c3d30143 Uploaded initial version.
pjbriggs
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391
3358c3d30143 Uploaded initial version.
pjbriggs
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392 .. class:: warningmark
3358c3d30143 Uploaded initial version.
pjbriggs
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393
3358c3d30143 Uploaded initial version.
pjbriggs
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394 Note that trimming operation order is important.
3358c3d30143 Uploaded initial version.
pjbriggs
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395
3358c3d30143 Uploaded initial version.
pjbriggs
parents:
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396 -------------
3358c3d30143 Uploaded initial version.
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397
3358c3d30143 Uploaded initial version.
pjbriggs
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398 .. class:: infomark
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399
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400 **Inputs**
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401
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402 For single-end data this Trimmomatic tool accepts a single FASTQ file; for
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403 paired-end data it will accept either two FASTQ files (R1 and R2), or a
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404 dataset collection containing the R1/R2 FASTQ pair.
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405
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406 .. class:: infomark
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407
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408 **Outputs**
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409
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410 For paired-end data a particular strength of Trimmomatic is that it retains the
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411 pairing of reads (from R1 and R2) in the filtered output files:
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412
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413 * Two FASTQ files (R1-paired and R2-paired) contain one read from each pair where
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414 both have survived filtering.
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415 * Additionally two FASTQ files (R1-unpaired and R2-unpaired) contain reads where
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416 one of the pair failed the filtering steps.
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417
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418 .. class:: warningmark
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419
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420 If the input consists of a dataset collection with the R1/R2 FASTQ pair then
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421 the outputs will also inclue two dataset collections: one for the 'paired'
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422 outputs and one for the 'unpaired' (as described above)
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423
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424 Retaining the same order and number of reads in the filtered output fastq files is
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425 essential for many downstream analysis tools.
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426
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427 For single-end data the output is a single FASTQ file containing just the filtered
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428 reads.
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429
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430 -------------
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431
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432 .. class:: infomark
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433
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434 **Credits**
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435
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436 This Galaxy tool has been developed within the Bioinformatics Core Facility at the
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437 University of Manchester, with contributions from Peter van Heusden, Marius
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438 van den Beek, Jelle Scholtalbers and Charles Girardot.
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439
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440 It runs the Trimmomatic program which has been developed
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441 within Bjorn Usadel's group at RWTH Aachen university.
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442
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443 Trimmomatic website (including documentation):
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444
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445 * http://www.usadellab.org/cms/index.php?page=trimmomatic
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446
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447 The reference for Trimmomatic is:
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448
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449 * Bolger, A.M., Lohse, M., &amp; Usadel, B. (2014). Trimmomatic: A flexible trimmer
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450 for Illumina Sequence Data. Bioinformatics, btu170.
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451
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452 Please kindly acknowledge both this Galaxy tool and the Trimmomatic program if you
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453 use it.
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454 ]]></help>
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455 <citations>
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456 <!--
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457 See https://wiki.galaxyproject.org/Admin/Tools/ToolConfigSyntax#A.3Ccitations.3E_tag_set
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458 Can be either DOI or Bibtex
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459 Use http://www.bioinformatics.org/texmed/ to convert PubMed to Bibtex
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460 -->
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461 <citation type="doi">10.1093/bioinformatics/btu170</citation>
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462 </citations>
0
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463 </tool>