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1 <tool id="trinity_psc" name="Trinity" version="0.0.1">
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3 <!-- Written by Jeremy Goecks, now maintained here by bhaas and additional
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4 modifications by Nate Coraor -->
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5 <description>(Beta) De novo assembly of RNA-Seq data Using Trinity on PSC's Bridges</description>
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6 <requirements>
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7 <!-- These are versions available as modules on Bridges -->
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8 <requirement type="package" version="1.1.2">bowtie</requirement>
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9 <requirement type="package" version="1.3">samtools</requirement>
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10 <requirement type="package" version="jre7">java</requirement>
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11 <requirement type="package" version="5.18.4">perl</requirement>
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12 <requirement type="package" version="2.2.0">trinity</requirement>
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13 </requirements>
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14 <command>
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15 MEM=`expr "\${GALAXY_SLOTS:-16}" \* 48 - 16` ;
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16
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17 workdir=`pwd`;
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18 echo "workdir is \$workdir";
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19 cd \$LOCAL;
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20 echo "Running Trinity from `pwd`";
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21
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22 Trinity --max_memory "\${MEM}G"
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23 --CPU "\${GALAXY_SLOTS:-16}"
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24 --bflyHeapSpaceMax "32G"
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25 --bflyHeapSpaceInit "2G"
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26 --bflyGCThreads "6"
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27
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28 ## Inputs.
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29 #if str($inputs.paired_or_single) == "paired":
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30 --left $inputs.left_input --right $inputs.right_input
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31 #if $inputs.left_input.ext == 'fa':
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32 --seqType fa
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33 #else:
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34 --seqType fq
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35 #end if
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36 #if str($inputs.library_type) != "undefined":
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37 --SS_lib_type $inputs.library_type
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38 #end if
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39 --group_pairs_distance $inputs.group_pairs_distance
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40 #else:
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41 --single $inputs.input
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42 #if str($inputs.input.ext) == 'fa':
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43 --seqType fa
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44 #else:
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45 --seqType fq
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46 #end if
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47 #if str($inputs.library_type) != "undefined":
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48 --SS_lib_type $inputs.library_type
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49 #end if
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50 #end if
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51
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52 ## Additional parameters.
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53 #if str($additional_params.use_additional) == "yes":
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54 --min_kmer_cov $additional_params.min_kmer_cov --max_reads_per_graph $additional_params.max_reads_per_graph
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55 #if $additional_params.bfly_opts != 'None':
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56 --bfly_opts " $additional_params.bfly_opts "
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57 #end if
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58 #end if
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59
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60 ## direct to output
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61 > $trinity_log 2>&1
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62
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63 ## if Trinity fails, output the end of the log to stderr for Galaxy, and touch the output file for Pulsar
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64 || (ec=\$? ; cp -pr . \$workdir; cd \$workdir; cat $trinity_log >&2 ; mkdir -p trinity_out_dir ; touch trinity_out_dir/Trinity.fasta ; exit \$ec);
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65
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66 cp -pr . \$workdir;
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67 cd \$workdir;
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68
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69 </command>
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70 <stdio>
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71 <exit_code range="1:" level="fatal" description="Program failed" />
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72 <exit_code range=":-1" level="fatal" description="DRM killed job" />
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73 </stdio>
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74 <inputs>
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75 <conditional name="inputs">
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76 <param name="paired_or_single" type="select" label="Paired or Single-end data?">
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77 <option value="paired">Paired</option>
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78 <option value="single">Single</option>
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79 </param>
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80 <when value="paired">
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81 <param format="fasta,fastq" name="left_input" type="data" label="Left/Forward strand reads" help=""/>
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82 <param format="fasta,fastq" name="right_input" type="data" label="Right/Reverse strand reads" help=""/>
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83 <param name="library_type" type="select" label="Strand-specific Library Type">
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84 <option value="undefined">Not set</option>
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85 <option value="FR">FR</option>
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86 <option value="RF">RF</option>
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87 </param>
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88 <param name="group_pairs_distance" type="integer" value="500" min="1" label="Group pairs distance" help="Maximum length expected between fragment pairs"/>
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89 <param name="path_reinforcement_distance" type="integer" value="75" min="1" label="Path reinforcement distance" help="Minimum read overlap required for path extension in the graph" />
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90 </when>
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91 <when value="single">
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92 <param format="fasta,fastq" name="input" type="data" label="Single-end reads" help=""/>
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93 <param name="library_type" type="select" label="Strand-specific Library Type">
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94 <option value="undefined">Not set</option>
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95 <option value="F">F</option>
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96 <option value="R">R</option>
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97 </param>
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98 <param name="path_reinforcement_distance" type="integer" value="40" min="1" label="Path reinforcement distance" help="Minimum read overlap required for path extension in the graph" />
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99 </when>
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100 </conditional>
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101
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102 <conditional name="additional_params">
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103 <param name="use_additional" type="select" label="Use Additional Params?">
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104 <option value="no">No</option>
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105 <option value="yes">Yes</option>
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106 </param>
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107 <when value="no">
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108 </when>
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109 <when value="yes">
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110 <param name="min_kmer_cov" type="integer" value="1" min="1" label="inchworm_min_kmer_cov" help="Minimum kmer coverage required by Inchworm for initial contig construction" />
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111 <param name="max_reads_per_graph" type="integer" value="20000000" min="10000" label="chrysalis_max_reads_per_graph" help="Maximum number of reads to be anchored within each transcript graph by Chrysalis" />
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112 <param name="bfly_opts" type="text" value="None" label="bfly_opts" help="Options to pass on to Butterfly" />
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113 <param name="min_contig_length" type="integer" value="200" min="1" label="Minimum Contig Length" help=""/>
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114 </when>
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115 </conditional>
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116 </inputs>
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117 <outputs>
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118 <data format="txt" name="trinity_log" label="${tool.name} on ${on_string}: log" />
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119 <data format="fasta" name="assembled_transcripts" label="${tool.name} on ${on_string}: Assembled Transcripts" from_work_dir="trinity_out_dir/Trinity.fasta"/>
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120 </outputs>
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121 <tests>
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122 </tests>
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123 <help>
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124 .. warning:: This version of Trinity, which runs on Bridges_ at the `Pittsburgh Supercomputing Center`_, is a **beta** version. It may not be possible to rerun the same version of this tool, Trinity itself, or its other dependencies (Bowtie, SAMtools) in the future. **When rerunning this tool on the same data, it should, but cannot be guaranteed to reproduce the exact same results to the level of certainty as other Galaxy tools.**
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125
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126 Trinity is a de novo transcript assembler that uses RNA-seq data as input. This tool runs all Trinity_ commands--Inchworm, Chrysalis, and Butterfly--in a single pass.
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127
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128 .. _Trinity: http://trinityrnaseq.github.io
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129 .. _Pittsburgh Supercomputing Center: http://www.psc.edu
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130 .. _Bridges: http://www.psc.edu/bridges
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131 </help>
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132 </tool>
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