Mercurial > repos > pjbriggs > trimmomatic
annotate trimmomatic.xml @ 7:6eeacf19a38e draft
Version 0.36.3: fix the naming of output collections to differentiate btwn paired/unpaired; document the _JAVA_OPTIONS env var (thanks Marius van den Beek).
author | pjbriggs |
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date | Tue, 21 Mar 2017 08:42:05 -0400 |
parents | 141bba0e9a77 |
children | 415a165d92bb |
rev | line source |
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7
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1 <tool id="trimmomatic" name="Trimmomatic" version="0.36.3"> |
0 | 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> |
4 | 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.'$r2_ext' |
0 | 31 #else |
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32 SE -threads \${GALAXY_SLOTS:-6} -phred33 fastq_in.'$fastq_in.extension' fastq_out.'$fastq_in.extension' |
0 | 33 #end if |
34 ## ILLUMINACLIP option | |
35 #if $illuminaclip.do_illuminaclip | |
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36 ILLUMINACLIP:\$TRIMMOMATIC_ADAPTERS_PATH/$illuminaclip.adapter_fasta:$illuminaclip.seed_mismatches:$illuminaclip.palindrome_clip_threshold:$illuminaclip.simple_clip_threshold |
0 | 37 #end if |
38 ## Other operations | |
39 #for $op in $operations | |
40 ## SLIDINGWINDOW | |
41 #if str( $op.operation.name ) == "SLIDINGWINDOW" | |
42 SLIDINGWINDOW:$op.operation.window_size:$op.operation.required_quality | |
43 #end if | |
44 ## MINLEN:36 | |
45 #if str( $op.operation.name ) == "MINLEN" | |
46 MINLEN:$op.operation.minlen | |
47 #end if | |
48 #if str( $op.operation.name ) == "LEADING" | |
49 LEADING:$op.operation.leading | |
50 #end if | |
51 #if str( $op.operation.name ) == "TRAILING" | |
52 TRAILING:$op.operation.trailing | |
53 #end if | |
54 #if str( $op.operation.name ) == "CROP" | |
55 CROP:$op.operation.crop | |
56 #end if | |
57 #if str( $op.operation.name ) == "HEADCROP" | |
58 HEADCROP:$op.operation.headcrop | |
59 #end if | |
4 | 60 #if str( $op.operation.name ) == "AVGQUAL" |
61 AVGQUAL:$op.operation.avgqual | |
62 #end if | |
63 #if str( $op.operation.name ) == "MAXINFO" | |
64 MAXINFO:$op.operation.target_length:$op.operation.strictness | |
65 #end if | |
0 | 66 #end for |
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67 2>&1 | tee trimmomatic.log && |
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68 if [ -z "\$(tail -1 trimmomatic.log | grep "Completed successfully")" ]; then echo "Trimmomatic did not finish successfully" >&2 ; exit 1 ; fi |
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69 && |
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70 #if $readtype.single_or_paired == "pair_of_files" |
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71 mv fastq_out_r1_paired.'$r1_ext' '${fastq_out_r1_paired}' && |
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72 mv fastq_out_r1_unpaired.'$r1_ext' '${fastq_out_r1_unpaired}' && |
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73 mv fastq_out_r2_paired.'$r2_ext' '${fastq_out_r2_paired}' && |
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74 mv fastq_out_r2_unpaired.'$r2_ext' '${fastq_out_r2_unpaired}' |
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75 #elif $readtype.single_or_paired == "collection" |
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76 mv fastq_out_r1_paired.'$r1_ext' '${fastq_out_paired.forward}' && |
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77 mv fastq_out_r1_unpaired.'$r1_ext' '${fastq_out_unpaired.forward}' && |
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78 mv fastq_out_r2_paired.'$r2_ext' '${fastq_out_paired.reverse}' && |
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79 mv fastq_out_r2_unpaired.'$r2_ext' '${fastq_out_unpaired.reverse}' |
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80 #else |
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81 mv fastq_out.'$fastq_in.extension' '${fastq_out}' |
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82 #end if |
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83 ]]></command> |
0 | 84 <inputs> |
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85 <conditional name="readtype"> |
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86 <param name="single_or_paired" type="select" label="Single-end or paired-end reads?"> |
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87 <option value="se" selected="true">Single-end</option> |
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88 <option value="pair_of_files">Paired-end (two separate input files)</option> |
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89 <option value="collection">Paired-end (as collection)</option> |
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90 </param> |
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91 <when value="se"> |
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92 <param name="fastq_in" type="data" format="fastqsanger,fastqsanger.gz" label="Input FASTQ file" /> |
0 | 93 </when> |
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94 <when value="pair_of_files"> |
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95 <param name="fastq_r1_in" type="data" format="fastqsanger,fastqsanger.gz" |
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96 label="Input FASTQ file (R1/first of pair)" /> |
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97 <param name="fastq_r2_in" type="data" format="fastqsanger,fastqgsanger.gz" |
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98 label="Input FASTQ file (R2/second of pair)" /> |
0 | 99 </when> |
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100 <when value="collection"> |
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101 <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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102 </when> |
0 | 103 </conditional> |
104 <conditional name="illuminaclip"> | |
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105 <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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106 <when value="yes"> |
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107 <param name="adapter_fasta" type="select" label="Adapter sequences to use"> |
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108 <option value="TruSeq2-SE.fa">TruSeq2 (single-ended, for Illumina GAII)</option> |
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109 <option value="TruSeq3-SE.fa">TruSeq3 (single-ended, for MiSeq and HiSeq)</option> |
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110 <option value="TruSeq2-PE.fa">TruSeq2 (paired-ended, for Illumina GAII)</option> |
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111 <option value="TruSeq3-PE.fa">TruSeq3 (paired-ended, for MiSeq and HiSeq)</option> |
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112 <option value="TruSeq3-PE-2.fa">TruSeq3 (additional seqs) (paired-ended, for MiSeq and HiSeq)</option> |
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113 <option value="NexteraPE-PE.fa">Nextera (paired-ended)</option> |
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114 </param> |
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115 <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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116 <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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117 <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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118 </when> |
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119 <when value="no" /> <!-- empty clause to satisfy planemo lint --> |
0 | 120 </conditional> |
121 <repeat name="operations" title="Trimmomatic Operation" min="1"> | |
122 <conditional name="operation"> | |
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123 <param name="name" type="select" label="Select Trimmomatic operation to perform"> |
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124 <option selected="true" value="SLIDINGWINDOW">Sliding window trimming (SLIDINGWINDOW)</option> |
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125 <option value="MINLEN">Drop reads below a specified length (MINLEN)</option> |
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126 <option value="LEADING">Cut bases off the start of a read, if below a threshold quality (LEADING)</option> |
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127 <option value="TRAILING">Cut bases off the end of a read, if below a threshold quality (TRAILING)</option> |
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128 <option value="CROP">Cut the read to a specified length (CROP)</option> |
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129 <option value="HEADCROP">Cut the specified number of bases from the start of the read (HEADCROP)</option> |
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130 <option value="AVGQUAL">Drop reads with average quality lower than a specified level (AVGQUAL)</option> |
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131 <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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132 </param> |
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133 <when value="SLIDINGWINDOW"> |
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134 <param name="window_size" type="integer" label="Number of bases to average across" value="4" /> |
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135 <param name="required_quality" type="integer" label="Average quality required" value="20" /> |
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136 </when> |
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137 <when value="MINLEN"> |
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138 <param name="minlen" type="integer" label="Minimum length of reads to be kept" value="20" /> |
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139 </when> |
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140 <when value="LEADING"> |
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141 <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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142 </when> |
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143 <when value="TRAILING"> |
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144 <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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145 </when> |
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146 <when value="CROP"> |
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147 <param name="crop" type="integer" label="Number of bases to keep from the start of the read" value="" /> |
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148 </when> |
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149 <when value="HEADCROP"> |
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150 <param name="headcrop" type="integer" label="Number of bases to remove from the start of the read" value="" /> |
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151 </when> |
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152 <when value="AVGQUAL"> |
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153 <param name="avgqual" type="integer" label="Minimum average quality required to keep a read" value="" /> |
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154 </when> |
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155 <when value="MAXINFO"> |
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156 <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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157 <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 (<0.2) favours longer reads, high values (>0.8) favours read correctness." /> |
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158 </when> |
0 | 159 </conditional> |
160 </repeat> | |
161 </inputs> | |
162 <outputs> | |
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163 <data name="fastq_out_r1_paired" label="${tool.name} on ${readtype.fastq_r1_in.name} (R1 paired)" format_source="fastq_r1_in"> |
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164 <filter>readtype['single_or_paired'] == "pair_of_files"</filter> |
0 | 165 </data> |
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166 <data name="fastq_out_r2_paired" label="${tool.name} on ${readtype.fastq_r2_in.name} (R2 paired)" format_source="fastq_r2_in"> |
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167 <filter>readtype['single_or_paired'] == "pair_of_files"</filter> |
0 | 168 </data> |
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169 <data name="fastq_out_r1_unpaired" label="${tool.name} on ${readtype.fastq_r1_in.name} (R1 unpaired)" format_source="fastq_r1_in"> |
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170 <filter>readtype['single_or_paired'] == "pair_of_files"</filter> |
0 | 171 </data> |
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172 <data name="fastq_out_r2_unpaired" label="${tool.name} on ${readtype.fastq_r2_in.name} (R2 unpaired)" format_source="fastq_r2_in"> |
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173 <filter>readtype['single_or_paired'] == "pair_of_files"</filter> |
0 | 174 </data> |
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175 <data name="fastq_out" label="${tool.name} on ${readtype.fastq_in.name}" format_source="fastq_in"> |
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176 <filter>readtype['single_or_paired'] == 'se'</filter> |
0 | 177 </data> |
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178 <collection name="fastq_out_paired" type="paired" label="${tool.name} on ${on_string}: paired"> |
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179 <filter>readtype['single_or_paired'] == "collection"</filter> |
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180 <data name="forward" label="${tool.name} on ${readtype.fastq_pair.forward.name} (R1 paired)" format_source="fastq_pair['forward']"/> |
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181 <data name="reverse" label="${tool.name} on ${readtype.fastq_pair.reverse.name} (R2 paired)" format_source="fastq_pair['reverse']"/> |
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182 </collection> |
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183 <collection name="fastq_out_unpaired" type="paired" label="${tool.name} on ${on_string}: unpaired"> |
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184 <filter>readtype['single_or_paired'] == "collection"</filter> |
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185 <data name="forward" label="${tool.name} on ${readtype.fastq_pair.forward.name} (R1 unpaired)" format_source="fastq_pair['forward']"/> |
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186 <data name="reverse" label="${tool.name} on ${readtype.fastq_pair.reverse.name} (R2 unpaired)" format_source="fastq_pair['reverse']"/> |
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187 </collection> |
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188 |
0 | 189 </outputs> |
190 <tests> | |
191 <test> | |
192 <!-- Single-end example --> | |
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193 <param name="single_or_paired" value="se" /> |
0 | 194 <param name="fastq_in" value="Illumina_SG_R1.fastq" ftype="fastqsanger" /> |
195 <param name="operations_0|operation|name" value="SLIDINGWINDOW" /> | |
196 <output name="fastq_out" file="trimmomatic_se_out1.fastq" /> | |
197 </test> | |
198 <test> | |
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199 <!-- Single-end example - gzipped --> |
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200 <param name="single_or_paired" value="se" /> |
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201 <param name="fastq_in" value="Illumina_SG_R1.fastq.gz" ftype="fastqsanger.gz" /> |
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202 <param name="operations_0|operation|name" value="SLIDINGWINDOW" /> |
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203 <output name="fastq_out" file="trimmomatic_se_out1.fastq.gz" /> |
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204 </test> |
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205 <test> |
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206 <!-- Paired-end example - gzipped --> |
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207 <param name="single_or_paired" value="pair_of_files" /> |
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208 <param name="fastq_r1_in" value="Illumina_SG_R1.fastq.gz" ftype="fastqsanger.gz" /> |
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209 <param name="fastq_r2_in" value="Illumina_SG_R2.fastq.gz" ftype="fastqsanger.gz" /> |
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210 <param name="operations_0|operation|name" value="SLIDINGWINDOW" /> |
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211 <output name="fastq_out_r1_paired" file="trimmomatic_pe_r1_paired_out1.fastq.gz" /> |
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212 <output name="fastq_out_r1_unpaired" file="trimmomatic_pe_r1_unpaired_out1.fastq.gz" /> |
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213 <output name="fastq_out_r2_paired" file="trimmomatic_pe_r2_paired_out1.fastq.gz" /> |
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214 <output name="fastq_out_r2_unpaired" file="trimmomatic_pe_r2_unpaired_out1.fastq.gz" /> |
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215 </test> |
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216 <test> |
0 | 217 <!-- Paired-end example --> |
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218 <param name="single_or_paired" value="pair_of_files" /> |
0 | 219 <param name="fastq_r1_in" value="Illumina_SG_R1.fastq" ftype="fastqsanger" /> |
220 <param name="fastq_r2_in" value="Illumina_SG_R2.fastq" ftype="fastqsanger" /> | |
221 <param name="operations_0|operation|name" value="SLIDINGWINDOW" /> | |
222 <output name="fastq_out_r1_paired" file="trimmomatic_pe_r1_paired_out1.fastq" /> | |
223 <output name="fastq_out_r1_unpaired" file="trimmomatic_pe_r1_unpaired_out1.fastq" /> | |
224 <output name="fastq_out_r2_paired" file="trimmomatic_pe_r2_paired_out1.fastq" /> | |
225 <output name="fastq_out_r2_unpaired" file="trimmomatic_pe_r2_unpaired_out1.fastq" /> | |
226 </test> | |
227 <test> | |
228 <!-- Single-end example (cropping) --> | |
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229 <param name="single_or_paired" value="se" /> |
0 | 230 <param name="fastq_in" value="Illumina_SG_R1.fastq" ftype="fastqsanger" /> |
231 <param name="operations_0|operation|name" value="CROP" /> | |
232 <param name="operations_0|operation|crop" value="10" /> | |
233 <output name="fastq_out" file="trimmomatic_se_out2.fastq" /> | |
234 </test> | |
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235 <test> |
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236 <!-- Paired-end with dataset collection --> |
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237 <param name="single_or_paired" value="collection" /> |
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238 <param name="fastq_pair"> |
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239 <collection type="paired"> |
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240 <element name="forward" value="Illumina_SG_R1.fastq" ftype="fastqsanger" /> |
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241 <element name="reverse" value="Illumina_SG_R2.fastq" ftype="fastqsanger"/> |
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242 </collection> |
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243 </param> |
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244 <param name="operations_0|operation|name" value="SLIDINGWINDOW" /> |
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245 <output_collection name="fastq_out_paired" type="paired"> |
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246 <element name="forward" file="trimmomatic_pe_r1_paired_out1.fastq" /> |
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247 <element name="reverse" file="trimmomatic_pe_r2_paired_out1.fastq" /> |
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248 </output_collection> |
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249 <output_collection name="fastq_out_unpaired" type="paired"> |
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250 <element name="forward" file="trimmomatic_pe_r1_unpaired_out1.fastq" /> |
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251 <element name="reverse" file="trimmomatic_pe_r2_unpaired_out1.fastq" /> |
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252 </output_collection> |
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253 </test> |
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254 <test> |
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255 <!-- Paired-end with dataset collection - gzipped --> |
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256 <param name="single_or_paired" value="collection" /> |
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257 <param name="fastq_pair"> |
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258 <collection type="paired"> |
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259 <element name="forward" value="Illumina_SG_R1.fastq.gz" ftype="fastqsanger.gz" /> |
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260 <element name="reverse" value="Illumina_SG_R2.fastq.gz" ftype="fastqsanger.gz"/> |
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261 </collection> |
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262 </param> |
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263 <param name="operations_0|operation|name" value="SLIDINGWINDOW" /> |
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264 <output_collection name="fastq_out_paired" type="paired"> |
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265 <element name="forward" file="trimmomatic_pe_r1_paired_out1.fastq.gz" /> |
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266 <element name="reverse" file="trimmomatic_pe_r2_paired_out1.fastq.gz" /> |
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267 </output_collection> |
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268 <output_collection name="fastq_out_unpaired" type="paired"> |
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269 <element name="forward" file="trimmomatic_pe_r1_unpaired_out1.fastq.gz" /> |
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270 <element name="reverse" file="trimmomatic_pe_r2_unpaired_out1.fastq.gz" /> |
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271 </output_collection> |
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272 </test> |
4 | 273 <test> |
274 <!-- Single-end using AVGQUAL --> | |
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275 <param name="single_or_paired" value="se" /> |
4 | 276 <param name="fastq_in" value="Illumina_SG_R1.fastq" ftype="fastqsanger" /> |
277 <param name="operations_0|operation|name" value="AVGQUAL" /> | |
278 <param name="operations_0|operation|avgqual" value="30" /> | |
279 <output name="fastq_out" file="trimmomatic_avgqual.fastq" /> | |
280 </test> | |
281 <test> | |
282 <!-- Single-end using MAXINFO --> | |
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283 <param name="single_or_paired" value="se" /> |
4 | 284 <param name="fastq_in" value="Illumina_SG_R1.fastq" ftype="fastqsanger" /> |
285 <param name="operations_0|operation|name" value="MAXINFO" /> | |
286 <param name="operations_0|operation|target_length" value="75" /> | |
287 <param name="operations_0|operation|strictness" value="0.8" /> | |
288 <output name="fastq_out" file="trimmomatic_maxinfo.fastq" /> | |
289 </test> | |
0 | 290 </tests> |
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291 <help><![CDATA[ |
0 | 292 .. class:: infomark |
293 | |
294 **What it does** | |
295 | |
296 Trimmomatic performs a variety of useful trimming tasks for illumina paired-end and | |
297 single ended data. | |
298 | |
299 This tool allows the following trimming steps to be performed: | |
300 | |
301 * **ILLUMINACLIP:** Cut adapter and other illumina-specific sequences from the read | |
302 * **SLIDINGWINDOW:** Perform a sliding window trimming, cutting once the average | |
303 quality within the window falls below a threshold | |
304 * **MINLEN:** Drop the read if it is below a specified length | |
305 * **LEADING:** Cut bases off the start of a read, if below a threshold quality | |
306 * **TRAILING:** Cut bases off the end of a read, if below a threshold quality | |
307 * **CROP:** Cut the read to a specified length | |
308 * **HEADCROP:** Cut the specified number of bases from the start of the read | |
4 | 309 * **AVGQUAL:** Drop the read if the average quality is below a specified value |
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310 * **MAXINFO:** Trim reads adaptively, balancing read length and error rate to |
4 | 311 maximise the value of each read |
0 | 312 |
313 If ILLUMINACLIP is requested then it is always performed first; subsequent options | |
314 can be mixed and matched and will be performed in the order that they have been | |
315 specified. | |
316 | |
317 .. class:: warningmark | |
318 | |
319 Note that trimming operation order is important. | |
320 | |
321 ------------- | |
322 | |
323 .. class:: infomark | |
324 | |
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325 **Inputs** |
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326 |
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327 For single-end data this Trimmomatic tool accepts a single FASTQ file; for |
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328 paired-end data it will accept either two FASTQ files (R1 and R2), or a |
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329 dataset collection containing the R1/R2 FASTQ pair. |
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330 |
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331 .. class:: infomark |
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332 |
0 | 333 **Outputs** |
334 | |
335 For paired-end data a particular strength of Trimmomatic is that it retains the | |
336 pairing of reads (from R1 and R2) in the filtered output files: | |
337 | |
338 * Two FASTQ files (R1-paired and R2-paired) contain one read from each pair where | |
339 both have survived filtering. | |
340 * Additionally two FASTQ files (R1-unpaired and R2-unpaired) contain reads where | |
341 one of the pair failed the filtering steps. | |
342 | |
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343 .. class:: warningmark |
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344 |
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345 If the input consists of a dataset collection with the R1/R2 FASTQ pair then |
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346 the outputs will also inclue two dataset collections: one for the 'paired' |
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347 outputs and one for the 'unpaired' (as described above) |
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348 |
0 | 349 Retaining the same order and number of reads in the filtered output fastq files is |
350 essential for many downstream analysis tools. | |
351 | |
352 For single-end data the output is a single FASTQ file containing just the filtered | |
353 reads. | |
354 | |
355 ------------- | |
356 | |
357 .. class:: infomark | |
358 | |
359 **Credits** | |
360 | |
361 This Galaxy tool has been developed within the Bioinformatics Core Facility at the | |
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362 University of Manchester, with contributions from Peter van Heusden and Marius |
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363 van den Beek. |
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364 |
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365 It runs the Trimmomatic program which has been developed |
0 | 366 within Bjorn Usadel's group at RWTH Aachen university. |
367 | |
368 Trimmomatic website (including documentation): | |
369 | |
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370 * http://www.usadellab.org/cms/index.php?page=trimmomatic |
0 | 371 |
372 The reference for Trimmomatic is: | |
373 | |
1 | 374 * Bolger, A.M., Lohse, M., & Usadel, B. (2014). Trimmomatic: A flexible trimmer |
375 for Illumina Sequence Data. Bioinformatics, btu170. | |
0 | 376 |
377 Please kindly acknowledge both this Galaxy tool and the Trimmomatic program if you | |
378 use it. | |
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379 ]]></help> |
1 | 380 <citations> |
381 <!-- | |
382 See https://wiki.galaxyproject.org/Admin/Tools/ToolConfigSyntax#A.3Ccitations.3E_tag_set | |
383 Can be either DOI or Bibtex | |
384 Use http://www.bioinformatics.org/texmed/ to convert PubMed to Bibtex | |
385 --> | |
386 <citation type="doi">10.1093/bioinformatics/btu170</citation> | |
387 </citations> | |
0 | 388 </tool> |