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date | Tue, 09 Aug 2016 10:52:40 -0400 |
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1 <tool id="rnaspades" name="rnaspades" version="1.0"> |
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2 <description>pipeline for de novo transcriptome assembly from RNA-Seq</description> |
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3 <requirements> |
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4 <requirement type="package" version="3.9.0">spades</requirement> |
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5 </requirements> |
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6 <command interpreter="perl">spades.pl |
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7 $out_contigs |
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8 $out_paths |
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9 $out_log |
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10 |
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11 ## if the first fileset is a paired-collection, use the key as the name |
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12 #if $files[0].file_type.type == "paired-collection": |
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13 $files[0].file_type.fastq_collection.name |
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14 #else: |
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15 NODE |
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16 #end if |
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17 ## A real command looks like: spades.py -k 21,33,55,77,99,127 -1 Y.fastq.gz -2 X.fastq.gz -t 24 -o output |
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18 spades.py |
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19 ## Forces unzipped output, faster |
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20 --disable-gzip-output |
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21 --rna |
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22 $onlyassembler |
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23 |
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24 -t \${GALAXY_SLOTS:-16} |
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25 |
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26 -k "$kmers" |
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27 |
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28 |
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29 ## Sequence files |
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30 #set num=1 |
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31 #if str( $lib_type ) == "paired_end": |
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32 #set prefix = 'pe' |
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33 #end if |
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34 --$prefix$num-$orientation |
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35 #for $file in $files |
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36 #if $file.file_type.type == "separate" |
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37 --$prefix$num-1 fastq:$file.file_type.fwd_reads |
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38 --$prefix$num-2 fastq:$file.file_type.rev_reads |
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39 #elif $file.file_type.type == "interleaved" |
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40 --$prefix$num-12 fastq:$file.file_type.interleaved_reads |
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41 #elif $file.file_type.type == "paired-collection" |
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42 --$prefix$num-1 fastq:$file.file_type.fastq_collection.forward |
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43 --$prefix$num-2 fastq:$file.file_type.fastq_collection.reverse |
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44 #end if |
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45 #end for |
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46 |
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47 |
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48 </command> |
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49 <inputs> |
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50 <param name="onlyassembler" type="boolean" truevalue="--only-assembler" falsevalue="" checked="False" label="Run only assembly? (without read error correction)" /> |
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51 |
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52 <param name="kmers" type="text" label="K-mers to use, separated by commas" value="55" help="Recommended to use default of k-mer size of 55. In case your RNA-Seq data set contains long Illumina reads (150 bp and longer) you may try to use longer k-mer size (approximately half of the read length)" /> |
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53 <!-- Reads --> |
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54 |
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55 <param name="lib_type" type="select" label="Library type"> |
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56 <option value="paired_end">Paired-end</option> |
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57 </param> |
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58 <param name="orientation" type="select" label="Orientation"> |
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59 <option value="fr" selected="true">-> <- (fr)</option> |
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60 <option value="rf"><- -> (rf)</option> |
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61 <option value="ff">-> -> (ff)</option> |
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62 </param> |
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63 <repeat name="files" title="Files" min="1"> |
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64 <conditional name="file_type"> |
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65 <param name="type" type="select" label="Select file format"> |
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66 <option value="separate">Separate input files</option> |
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67 <option value="interleaved">Interleaved files</option> |
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68 <option value="paired-collection">Paired List Collection</option> |
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69 </param> |
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70 <when value="separate"> |
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71 <param name="fwd_reads" type="data" format="fastq" label="Forward reads" help="FASTQ format" /> |
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72 <param name="rev_reads" type="data" format="fastq" label="Reverse reads" help="FASTQ format" /> |
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73 </when> |
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74 <when value="interleaved"> |
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75 <param name="interleaved_reads" type="data" format="fastq" label="Interleaved paired reads" help="FASTQ format" /> |
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76 </when> |
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77 <when value="paired-collection"> |
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78 <param name="fastq_collection" type="data_collection" label="Paired-end reads collection" optional="false" format="fastq" collection_type="paired" help="FASTQ format" /> |
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79 </when> |
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80 </conditional> |
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81 </repeat> |
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82 |
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83 |
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84 </inputs> |
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85 <outputs> |
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86 <data name="out_contigs" format="fasta" label="rnaSPAdes fasta" /> |
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87 <data name="out_paths" format="txt" label="rnaSPAdes fastg" /> |
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88 <data name="out_log" format="txt" label="SPAdes log" /> |
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89 </outputs> |
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90 <tests> |
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91 <test> |
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92 <param name="kmers" value="55" /> |
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93 <param name="lib_type" value="paired_end" /> |
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94 <param name="fwd_reads" value="ecoli_1K_1.fq" ftype="fastq" /> |
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95 <param name="rev_reads" value="ecoli_1K_2.fq" ftype="fastq" /> |
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96 <output name="out_contigs" file="transcripts.fasta" ftype="fasta" compare="re_match" lines_diff="1" /> |
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97 <output name="out_paths" file="transcripts.paths" ftype="txt" compare="re_match" lines_diff="1" /> |
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98 </test> |
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99 </tests> |
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100 <help> |
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101 **What it does** |
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102 |
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103 SPAdes – St. Petersburg genome assembler – is intended for both standard isolates and single-cell MDA bacteria assemblies. See http://bioinf.spbau.ru/en/spades for more details on SPAdes. |
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104 |
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105 This wrapper runs SPAdes 3.9, collects the output, and throws away all the temporary files. It also produces a single Fasta file with a corresponding file assembly_graph.fastg. |
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106 |
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107 **License** |
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108 |
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109 SPAdes is developed by and copyrighted to Saint-Petersburg Academic University, and is released under GPLv2. |
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110 |
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111 This wrapper is copyrighted by Philip Mabon and is free software: you can redistribute it and/or modify it under the terms of the GNU General Public License as published by the Free Software Foundation, either version 3 of the License, or (at your option) any later version. |
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112 |
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113 This program is distributed in the hope that it will be useful, but WITHOUT ANY WARRANTY; without even the implied warranty of MERCHANTABILITY or FITNESS FOR A PARTICULAR PURPOSE. See the GNU General Public License for more details. |
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114 |
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115 You should have received a copy of the GNU General Public License along with this program. If not, see http://www.gnu.org/licenses/. |
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116 |
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117 ** Acknowledgments ** |
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118 |
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119 Original wrapper developed by Lionel Guy. |
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120 |
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121 Anton Korobeynikov greatlty helped understanding how SPAdes work, and integrated handy features into SPAdes. |
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122 |
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123 Nicola Soranzo fixed various bugs. |
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124 </help> |
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125 <citations> |
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126 <citation type="doi">10.1089/cmb.2012.0021</citation> |
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127 </citations> |
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128 </tool> |