annotate trinity.xml @ 10:831abd20e690 draft

planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/trinity commit e23a8ad798830209db722d5496d19ec7a5e06214
author iuc
date Mon, 01 Aug 2016 14:42:55 -0400
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1 <tool id="trinity" name="Trinity" version="@WRAPPER_VERSION@.0">
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2 <description>de novo assembly of RNA-Seq data</description>
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3 <macros>
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4 <import>macros.xml</import>
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5 </macros>
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6 <expand macro="requirements">
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7 <requirement type="package" version="1.1.2">bowtie</requirement>
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8 <requirement type="package" version="1.2">samtools</requirement>
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9 <requirement type="set_environment">TRINITY_MEM_OPTIONS</requirement>
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10 </expand>
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11 <expand macro="stdio"/>
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12 <command><![CDATA[
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13 Trinity
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15 ## Inputs.
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16 #if $inputs.paired_or_single == "paired":
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18 --left ${ ','.join(['"%s"' % x for x in $inputs.left_input]) }
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20 --right ${ ','.join(['"%s"' % x for x in $inputs.right_input]) }
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22 #if $inputs.left_input[0].is_of_type('fasta'):
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23 --seqType fa
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24 #else:
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25 --seqType fq
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26 #end if
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27
0
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28 #if $inputs.strand.is_strand_specific:
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29 --SS_lib_type $inputs.strand.library_type
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30 #end if
3
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31
0
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32 $inputs.jaccard_clip
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34 #else:
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35 --single ${ ','.join(['"%s"' % x for x in $inputs.input]) }
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36
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37 #if $inputs.input[0].is_of_type('fasta'):
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38 --seqType fa
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39 #else:
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40 --seqType fq
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41 #end if
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42
0
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43 #if $inputs.strand.is_strand_specific:
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44 --SS_lib_type $inputs.strand.library_type
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45 #end if
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46 #end if
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0
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48 $norm
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49
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50 ## Additional parameters.
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51 #if $additional_params.min_contig_length:
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52 --min_contig_length $additional_params.min_contig_length
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53 #end if
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54 #if $additional_params.long_reads:
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55 --long_reads $additional_params.long_reads
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56 #end if
1
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57 #if $additional_params.guided.is_guided == "yes":
0
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58 --genome_guided_bam $additional_params.guided.genome_guided_bam
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59
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60 #if $additional_params.guided.genome_guided_min_coverage:
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61 --genome_guided_min_coverage $additional_params.guided.genome_guided_min_coverage
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62 #end if
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63
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64 #if $additional_params.guided.genome_guided_min_reads_per_partition:
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65 --genome_guided_min_reads_per_partition $additional_params.guided.genome_guided_min_reads_per_partition
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66 #end if
3
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67
0
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68 #end if
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69
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70 #if $additional_params.min_kmer_cov:
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71 --min_kmer_cov $additional_params.min_kmer_cov
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72 #end if
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73
0
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74 ## CPU and butterfly options.
2
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75 --CPU \${GALAXY_SLOTS:-4} \${TRINITY_MEM_OPTIONS:---max_memory 1G} --bfly_opts "-V 10 --stderr"
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76
2
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77 ## > $trinity_log 2>&1
0
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78
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79 ]]></command>
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80 <inputs>
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81 <conditional name="inputs">
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82 <param name="paired_or_single" type="select" label="Paired or Single-end data?">
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83 <option value="paired">Paired</option>
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84 <option value="single">Single</option>
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85 </param>
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86 <when value="paired">
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87 <param format="fasta,fastqsanger" argument="--left" name="left_input" multiple="true" type="data" label="Left/Forward strand reads" help=""/>
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88 <param format="fasta,fastqsanger" argument="--right" name="right_input" multiple="true" type="data" label="Right/Reverse strand reads" help=""/>
0
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89 <conditional name="strand">
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90 <param name="is_strand_specific" type="boolean" checked="false" label="Strand specific data"/>
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91 <when value="false">
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92 </when>
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93 <when value="true">
10
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94 <param name="library_type" argument="--SS_lib_type" type="select" label="Strand-specific Library Type">
0
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95 <option value="FR">Forward-Reverse</option>
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96 <option value="RF">Reverse-Forward</option>
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97 </param>
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98 </when>
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99 </conditional>
10
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100 <param name="jaccard_clip" argument="--jaccard_clip" type="boolean" truevalue="--jaccard_clip" falsevalue="" checked="false" label="Jaccard Clip options" help="set if you expect high gene density with UTR overlap"/>
0
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101 </when>
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102 <when value="single">
10
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103 <param format="fasta,fastqsanger" name="input" argument="--single" multiple="true" type="data" label="Single-end reads" help=""/>
0
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104 <conditional name="strand">
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105 <param name="is_strand_specific" type="boolean" checked="false" label="Strand specific data"/>
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106 <when value="false">
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107 </when>
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108 <when value="true">
10
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109 <param name="library_type" argument="--SS_lib_type" type="select" label="Strand-specific Library Type">
0
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110 <option value="F">F</option>
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111 <option value="R">R</option>
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112 </param>
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113 </when>
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114 </conditional>
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115 </when>
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116 </conditional>
3
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117
10
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118 <param name="norm" type="boolean" argument="--normalize_reads" truevalue="--normalize_reads" falsevalue="" checked="true" label="Run in silico normalization of reads" help="Defaults to max. read coverage of 50."/>
0
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119
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120 <section name="additional_params" title="Additional Options" expanded="False">
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121 <param name="min_contig_length" argument="--min_contig_length" type="integer" optional="true" value="200" min="1" label="Minimum Contig Length" help="All contigs shorter than this will be discarded"/>
3
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122
0
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123 <conditional name="guided">
1
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124 <param name="is_guided" type="select" label="Use the genome guided mode?" help="If you already mapped the reads to the genome, Trinity can use this information">
0
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125 <option value="no">No</option>
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126 <option value="yes">Yes</option>
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127 </param>
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128 <when value="no">
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129 </when>
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130 <when value="yes">
10
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131 <param format="bam" name="genome_guided_bam" argument="--genome_guided_bam" type="data" label="Coordinate-sorted BAM file" />
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132 <param name="genome_guided_min_coverage" argument="--genome_guided_min_coverage" type="integer" optional="true" value="1" min="1" label="Minimum read coverage for identifying an expressed region of the genome"/>
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133 <param name="genome_guided_min_reads_per_partition" argument="--genome_guided_min_reads_per_partition" type="integer" optional="true" value="10" min="1" label="Minimum number of reads per partition"/>
0
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134 </when>
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135 </conditional>
3
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136
10
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137 <param format="fasta" name="long_reads" argument="--long_reads" type="data" optional="true" label="Error-corrected or circular consensus (CCS) pac bio reads" help="Experimental feature! Long reads must be in the same orientation as short reads if they are strand specific"/>
3
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138
10
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139 <param name="min_kmer_cov" argument="--min_kmer_cov" type="integer" optional="true" value="1" min="1" label="Minimum count for K-mers to be assembled"/>
0
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140 </section>
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141 </inputs>
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142 <outputs>
2
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143 <!--data format="txt" name="trinity_log" label="${tool.name} on ${on_string}: log" /-->
0
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144 <data format="fasta" name="assembled_transcripts" label="${tool.name} on ${on_string}: Assembled Transcripts" from_work_dir="trinity_out_dir/Trinity.fasta"/>
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145 </outputs>
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146 <tests>
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147 <test>
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148 <param name="paired_or_single" value="paired"/>
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149 <param name="left_input" value="reads.left.fq" ftype="fastqsanger"/>
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150 <param name="right_input" value="reads.right.fq" ftype="fastqsanger"/>
0
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151 <param name="is_strand_specific" value="true"/>
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152 <param name="norm" value="false"/>
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153 <param name="library_type" value="RF"/>
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154 <output name="assembled_transcripts" file="raw/Trinity.fasta" compare="sim_size" delta="500" />
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155 </test>
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156 <test>
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157 <param name="paired_or_single" value="paired"/>
3
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158 <param name="left_input" value="reads.left.fq" ftype="fastqsanger"/>
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159 <param name="right_input" value="reads.right.fq" ftype="fastqsanger"/>
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160 <param name="is_strand_specific" value="true"/>
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161 <param name="norm" value="true"/>
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162 <param name="library_type" value="RF"/>
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163 <output name="assembled_transcripts" file="norm/Trinity.fasta" compare="sim_size" delta="500" />
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164 </test>
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165 </tests>
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166 <help>
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167 Trinity_ assembles transcript sequences from Illumina RNA-Seq data.
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168
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169 .. _Trinity: http://trinityrnaseq.github.io
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170 </help>
3
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171
10
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172 <expand macro="citation" />
0
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173 </tool>
PKE~E<.}4 caddsuite_linux_x86_64-026f5a483650/.hg_archival.txtUTzTPKk