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annotate gffread.xml @ 4:0232f19d300f draft

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planemo upload for repository https://github.com/galaxyproject/tools-devteam/tree/master/tool_collections/cufflinks/gffread commit 82ee6fc860c52c531b7a57bbb346ab1a67a434a5
author devteam
date Sun, 19 Feb 2017 12:09:52 -0500
parents 9f243677c4c6
children 69e0806b63a4
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1 <tool id="gffread" name="gffread" version="@VERSION@.1">
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2 <description>Filters and/or converts GFF3/GTF2 records</description>
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3 <macros>
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4 <import>cuff_macros.xml</import>
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5 <xml name="fasta_output_select">
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6 <param name="fa_outputs" type="select" display="checkboxes" multiple="true" label="Select fasta outputs">
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7 <option value="-w exons.fa">fasta file with spliced exons for each GFF transcript (-w exons.fa)</option>
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8 <option value="-x cds.fa">fasta file with spliced CDS for each GFF transcript (-x cds.fa)</option>
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9 <option value="-y pep.fa">protein fasta file with the translation of CDS for each record (-y pep.fa)</option>
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10 <option value="-W">for each fasta: record the exon coordinates projected onto the spliced sequence (-W)</option>
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11 </param>
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12 </xml>
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13 <xml name="ref_filtering_select">
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14 <param name="ref_filtering" type="select" display="checkboxes" multiple="true" label="reference based filters">
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15 <option value="-N">discard multi-exon mRNAs that have any intron with a non-canonical splice site consensus, i.e. not GT-AG, GC-AG or AT-AC (-N)</option>
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16 <option value="-J">discard any mRNAs that either lack initial START codon or the terminal STOP codon, or have an in-frame stop codon (-J)</option>
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17 <option value="-V">discard any mRNAs with CDS having in-frame stop codons (-V)</option>
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18 <option value="-H">check and adjust the starting CDS phase if the original phase leads to a translation with an in-frame stop codon (-H with -V)</option>
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19 <!-- gffread bug: B not in missing from param to the arg parser
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20 <option value="-B">single-exon transcripts are also checked on the opposite strand (-B with -V)</option>
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21 -->
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22 </param>
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23 </xml>
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24 <xml name="trackname">
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25 <param name="tname" type="text" value="" optional="true" label="Trackname to use in the second column of each GFF output line" help="(-t track_name}">
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26 <validator type="regex">\w+</validator>
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27 </param>
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28 </xml>
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29 <xml name="merge_opts">
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30 <option value="-K">also collapse shorter, fully contained transcripts with fewer introns than the container (-K)</option>
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31 <option value="-Q">remove the containment restriction: multi-exon transcripts will be collapsed if just their introns match, while single-exon transcripts can partially overlap 80% (-Q)</option>
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32 <option value="-d dupinfo">output collapsing info (-d dupinfo)</option>
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33 </xml>
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34 <xml name="cluster_opts">
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35 <option value="--force-exons"> make sure that the lowest level GFF features are printed as 'exon' features (--force-exons)</option>
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36 <option value="-Z">merge close exons into a single exon (for intron size &lt; 4) (-Z)</option>
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37 </xml>
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38 <xml name="merge_opt_sel">
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39 <param name="merge_options" type="select" display="checkboxes" multiple="true" label="Merge options">
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40 <expand macro="cluster_opts" />
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41 <expand macro="merge_opts" />
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42 </param>
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43 </xml>
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44 <xml name="cluster_opt_sel">
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45 <param name="merge_options" type="select" display="checkboxes" multiple="true" label="Cluster options">
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46 <expand macro="cluster_opts" />
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47 </param>
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48 </xml>
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49 </macros>
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50 <expand macro="requirements" />
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51 <command detect_errors="aggressive">
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52 <![CDATA[
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53 #if $reference_genome.source == 'history':
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54 ln -s '$reference_genome.genome_fasta' genomeref.fa &&
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55 #end if
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56 gffread '$input'
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57 #if $reference_genome.source == 'cached':
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58 -g '${reference_genome.fasta_indexes.fields.path}'
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59 #if $reference_genome.ref_filtering and str($reference_genome.ref_filtering) != '':
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60 #echo ' '.join(str($reference_genome.ref_filtering).split(','))
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61 #end if
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62 #elif $reference_genome.source == 'history':
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63 -g genomeref.fa
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64 #if $reference_genome.ref_filtering and str($reference_genome.ref_filtering) != '':
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65 #echo ' '.join(str($reference_genome.ref_filtering).split(','))
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66 #end if
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67 #end if
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68 #if $filtering and str($filtering) != '':
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69 #echo " "
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70 #echo ' '.join(str($filtering).split(','))
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71 #end if
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72 #if $maxintron and $maxintron > 0:
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73 -i $maxintron
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74 #end if
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75 #if $region.region_filter == 'filter':
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76 -r '$region.range' $region.discard_partial
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77 #end if
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78 #if $merging.merge_sel != 'none':
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79 $merging.merge_cmd
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80 #if $merging.merge_options:
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81 #echo ' '.join(str($merging.merge_options).split(','))
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82 #end if
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83 #end if
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84 #if $chr_replace:
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85 -m '$chr_replace'
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86 #end if
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87 ##
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88 ## Although documented, does not appear to be used in the gffread code
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89 ## #if $seq_info:
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90 ## -A -s "$seq_info"
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91 ## #end if
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92 ##
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93 ## outputs
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94 #if $reference_genome.source != 'none':
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95 #if $reference_genome.fa_outputs and str($reference_genome.fa_outputs) != '':
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96 #echo ' ' + ' '.join(str($reference_genome.fa_outputs).split(','))
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97 #end if
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98 #end if
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99 #if $gffs.gff_fmt != 'none':
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100 #if $gffs.tname:
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101 -t '$gffs.tname'
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102 #end if
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103 #if $gffs.gff_fmt == 'gff':
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104 #if $input.datatype.file_ext == 'gft':
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105 $gffs.ensembl
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106 #end if
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107 $gffs.output_cmd
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108 #elif $gffs.gff_fmt == 'gtf':
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109 $gffs.output_cmd
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110 #end if
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111 #end if
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112 ]]>
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113 </command>
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114 <inputs>
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115 <param name="input" type="data" format="gff3,gtf" label="Input GFF3 or GTF feature file"/>
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116 <!-- filtering -->
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117 <param name="filtering" type="select" display="checkboxes" multiple="true" label="filters">
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118 <option value="-U">discard single-exon transcripts (-U)</option>
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119 <option value="-C">coding only: discard mRNAs that have no CDS feature (-C)</option>
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120 <option value="-G">only parse additional exon attributes from the first exon and move them to the mRNA level (useful for GTF input) (-G)</option>
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121 <option value="-O">process also non-transcript GFF records (by default non-transcript records are ignored) (-O)</option>
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122 <option value="--no-pseudo">filter out records matching the 'pseudo' keyword (--no-pseudo)</option>
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123 </param>
0
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124 <conditional name="region">
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125 <param name="region_filter" type="select" label="Filter by genome region">
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126 <option value="none">No</option>
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127 <option value="filter">Yes</option>
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128 </param>
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129 <when value="none"/>
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130 <when value="filter">
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131 <param name="range" type="text" value="" label="Only show transcripts overlapping coordinate range">
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132 <help><![CDATA[
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133 (-r [['strand']'chr':]'start'..'end') <br>
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134 examples: <br>
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135 1000..500000 <br>
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136 chr1:1000..500000 <br>
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137 +chr1:1000..500000 <br>
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138 -chr1:1000..500000
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139 ]]>
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140 </help>
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141 <validator type="regex">(([+-])?(\w+:))?\d+\.\.\d+</validator>
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142 </param>
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143 <param name="discard_partial" type="boolean" truevalue="-R" falsevalue="" checked="false"
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144 label="Discard all transcripts that are not fully contained within the given range" help="(-R)"/>
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145 </when>
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146 </conditional>
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147 <param name="maxintron" type="integer" value="" optional="true" min="0" label="Filter out transcipts with large introns"
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148 help="If set, discard transcripts having an intron larger (-i max_intron)"/>
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149 <param name="chr_replace" type="data" format="tabular" optional="true" label="Replace reference sequence names" >
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150 <help><![CDATA[(-m chr_replace) <br>
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151 chr_replace is a reference sequence replacement table consisting of 2 columns: "original_ref_ID" "new_ref_ID"<br>
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152 It is useful for switching between Ensembl and UCSC naming conventions <br>
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153 NOTE: GFF records on reference sequences that are not found among the "original_ref_ID" entries in this file will be filtered out
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154 ]]>
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155 </help>
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156 </param>
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157
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158 <!-- Although documented, does not appear to be used in the gffread code
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159 <param name="seq_info" type="data" format="tabular" optional="true" label="Use the description field as the value for a 'descr' attribute to the GFF record">
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160 <help>
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161 (-s seq_info.fsize -A) useful with mRNA/EST/protein mappings &lt;br&gt;
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162 seq_info input file is a 3 column tab-delimited file providing this info for each of the mapped sequences: &lt;br&gt;
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163 "seq-name" "seq-length" "seq-description" &lt;br&gt;
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164 </help>
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165 </param>
0
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166 -->
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167
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168 <!-- merging -->
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169 <conditional name="merging">
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170 <param name="merge_sel" type="select" label="Transcript merging" help="(-M/--merge or --cluster-only)">
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171 <option value="none">none</option>
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172 <option value="merge">merge: cluster the input transcripts into loci, collapsing matching transcripts</option>
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173 <option value="cluster">cluster-only: merge but without collapsing matching transcripts</option>
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174 </param>
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175 <when value="none"/>
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176 <when value="merge">
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177 <param name="merge_cmd" type="hidden" value="--merge"/>
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178 <expand macro="merge_opt_sel" />
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179 </when>
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180 <when value="cluster">
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181 <param name="merge_cmd" type="hidden" value="--cluster-only"/>
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182 <expand macro="cluster_opt_sel" />
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183 </when>
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184 </conditional>
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185 <!-- reference sequence file -->
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186 <!-- Error: -g option is required for options -w, -x, -y, -V, -N, -M -->
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187 <conditional name="reference_genome">
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188 <param name="source" type="select" label="Reference Genome" help="(-g genome.fasta) NOTE: Required for fasta outputs">
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189 <option value="none">none</option>
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190 <option value="cached"></option>
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191 <option value="history">From your history</option>
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192 </param>
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193 <when value="none">
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194 </when>
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195 <when value="cached">
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196 <param name="fasta_indexes" type="select" label="Source FASTA Sequence">
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197 <options from_data_table="all_fasta"/>
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198 </param>
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199 <expand macro="ref_filtering_select" />
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200 <expand macro="fasta_output_select" />
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201 </when>
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202 <when value="history">
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203 <param name="genome_fasta" type="data" format="fasta" label="Genome Reference Fasta"/>
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204 <expand macro="ref_filtering_select" />
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205 <expand macro="fasta_output_select" />
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206 </when>
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207 </conditional>
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208
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209 <!-- outputs -->
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210 <conditional name="gffs">
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211 <param name="gff_fmt" type="select" label="Feature File Output" help="(-o output.gff3|output.gtf)">
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212 <option value="none">none</option>
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213 <option value="gff">GFF</option>
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214 <option value="gtf">GTF</option>
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215 </param>
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216 <when value="none">
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217 </when>
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218 <when value="gff">
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219 <param name="output_cmd" type="hidden" value="-o output.gff3"/>
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220 <param name="ensembl" type="boolean" truevalue="-L" falsevalue="" checked="false" label="Ensembl GTF to GFF3 conversion" help="(-L)"/>
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221 <expand macro="trackname" />
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222 </when>
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223 <when value="gtf">
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224 <param name="output_cmd" type="hidden" value="-T -o output.gtf"/>
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225 <expand macro="trackname" />
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226 </when>
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227 </conditional>
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228
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229 <param name="full_gff_attribute_preservation" type="boolean" truevalue="-F" falsevalue="" checked="false"
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230 label="full GFF attribute preservation (all attributes are shown)" help="(-F)"/>
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231 <param name="decode_url" type="boolean" truevalue="-D" falsevalue="" checked="false"
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232 label="decode url encoded characters within attributes" help="(-D)"/>
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233 <param name="expose" type="boolean" truevalue="-E" falsevalue="" checked="false"
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234 label="warn about duplicate transcript IDs and other potential problems with the given GFF/GTF records" help="(-E)"/>
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235
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236 </inputs>
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237 <outputs>
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238 <data name="output_gff" format="gff3" metadata_source="input" label="${tool.name} on ${on_string}: gff3" from_work_dir="output.gff3">
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239 <filter>gffs['gff_fmt'] == 'gff'</filter>
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240 </data>
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241 <data name="output_gtf" format="gtf" metadata_source="input" label="${tool.name} on ${on_string}: gtf" from_work_dir="output.gtf">
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242 <filter>gffs['gff_fmt'] == 'gtf'</filter>
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243 </data>
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244 <data name="output_exons" format="fasta" label="${tool.name} on ${on_string}: exons.fa" from_work_dir="exons.fa">
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245 <filter>'fa_outputs' in reference_genome and str(reference_genome['fa_outputs']).find('exons.fa') > 0 </filter>
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246 </data>
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247 <data name="output_cds" format="fasta" label="${tool.name} on ${on_string}: cds.fa" from_work_dir="cds.fa">
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248 <filter>'fa_outputs' in reference_genome and str(reference_genome['fa_outputs']).find('cds.fa') > 0</filter>
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249 </data>
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250 <data name="output_pep" format="fasta" label="${tool.name} on ${on_string}: pep.fa" from_work_dir="pep.fa">
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251 <filter>'fa_outputs' in reference_genome and str(reference_genome['fa_outputs']).find('pep.fa') > 0</filter>
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252 </data>
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253 <data name="output_dupinfo" format="txt" label="${tool.name} on ${on_string}: dupinfo" from_work_dir="dupinfo">
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254 <filter>'merge_options' in merging and merging['merge_options'].find('dupinfo') > 0</filter>
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255 </data>
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256 </outputs>
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257 <tests>
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258 <test>
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259 <param name="input" ftype="gtf" value="Homo_sapiens.GRCh37_19.71.gtf"/>
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260 <param name="gff_fmt" value="gff"/>
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261 <output name="output_gff" file="Homo_sapiens.GRCh37_19.71.gff3" ftype="gff3" lines_diff="2" />
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262 </test>
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263
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264 <test>
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265 <param name="input" ftype="gtf" value="Homo_sapiens.GRCh37_19.71.gtf"/>
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266 <param name="filtering" value="--no-pseudo"/>
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267 <param name="gff_fmt" value="gtf"/>
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268 <output name="output_gtf">
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269 <assert_contents>
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270 <not_has_text text="pseudo" />
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271 </assert_contents>
0
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272 </output>
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273 </test>
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274
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275 <test>
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276 <param name="input" ftype="gtf" value="Homo_sapiens.GRCh37_19.71.gtf"/>
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277 <param name="region_filter" value="filter"/>
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278 <param name="range" value="19:496500..504965"/>
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279 <param name="gff_fmt" value="gtf"/>
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280 <output name="output_gtf">
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281 <assert_contents>
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282 <has_text text="ENST00000587541" />
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283 <has_text text="ENST00000382683" />
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284 </assert_contents>
0
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285 </output>
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286 </test>
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287
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288 <test>
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289 <param name="input" ftype="gtf" value="Homo_sapiens.GRCh37_19.71.gtf"/>
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290 <param name="region_filter" value="filter"/>
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291 <param name="range" value="19:496500..504965"/>
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292 <param name="discard_partial" value="true"/>
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293 <param name="gff_fmt" value="gtf"/>
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294 <output name="output_gtf">
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295 <assert_contents>
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296 <not_has_text text="ENST00000587541" />
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297 <has_text text="ENST00000382683" />
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298 </assert_contents>
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299 </output>
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300 </test>
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301
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302 <test>
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303 <param name="input" ftype="gtf" value="Homo_sapiens.GRCh37_19.71.gtf"/>
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304 <param name="filtering" value="-C"/>
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305 <param name="region_filter" value="filter"/>
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306 <param name="range" value="19:496500..504965"/>
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307 <param name="gff_fmt" value="gtf"/>
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308 <output name="output_gtf">
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309 <assert_contents>
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310 <not_has_text text="ENST00000587541" />
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311 <has_text text="ENST00000382683" />
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312 </assert_contents>
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313 </output>
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314 </test>
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315
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316 <test>
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317 <param name="input" ftype="gtf" value="Homo_sapiens.GRCh37_19.71.gtf"/>
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318 <param name="source" value="history"/>
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319 <param name="genome_fasta" ftype="fasta" value="Homo_sapiens.GRCh37.71.dna.chromosome.19.fa"/>
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320 <param name="fa_outputs" value="-w exons.fa,-x cds.fa,-y pep.fa"/>
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321 <param name="region_filter" value="filter"/>
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322 <param name="range" value="19:496500..504965"/>
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323 <param name="gff_fmt" value="gtf"/>
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324 <output name="output_gtf">
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325 <assert_contents>
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326 <not_has_text text="ENST00000587541" />
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327 <has_text text="ENST00000382683" />
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328 </assert_contents>
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329 </output>
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330 <output name="output_exons">
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331 <assert_contents>
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332 <has_text text="ENST00000346144 gene=MADCAM1 CDS=47-932" />
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333 <has_text text="CTATTTAAGCGGCTTCCCCGCGGCCTCGGGACAGAGGGGACTGAGCATGGATTTCGGACTGGCCCTCCTG" />
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334 </assert_contents>
0
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335 </output>
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336 <output name="output_cds">
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337 <assert_contents>
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338 <has_text text="ENST00000346144 gene=MADCAM1" />
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339 <has_text text="ATGGATTTCGGACTGGCCCTCCTGCTGGCGGGGCTTCTGGGGCTCCTCCTCGGCCAGTCCCTCCAGGTGA" />
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340 </assert_contents>
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341 </output>
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342 <output name="output_pep">
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343 <assert_contents>
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344 <has_text text="ENST00000346144 gene=MADCAM1" />
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345 <has_text text="MDFGLALLLAGLLGLLLGQSLQVKPLQVEPPEPVVAVALGASRQLTCRLACADRGASVQWRGLDTSLGAV" />
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346 </assert_contents>
0
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347 </output>
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348 </test>
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349
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350 </tests>
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351 <help>
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352 <![CDATA[
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353 **gffread Filters and/or converts GFF3/GTF2 records**
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354
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355 The gffread command is distributed with the cufflinks_ package.
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356
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357 .. _cufflinks: http://cole-trapnell-lab.github.io/cufflinks/
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358
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359 Usage: ::
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360
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361 gffread "input_gff" [-g "genomic_seqs_fasta" | "dir"][-s "seq_info.fsize"]
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362 [-o "outfile.gff"] [-t "tname"] [-r [["strand"]"chr":]"start".."end" [-R]]
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363 [-CTVNJMKQAFGUBHZWTOLE] [-w "exons.fa"] [-x "cds.fa"] [-y "tr_cds.fa"]
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364 [-i "maxintron"]
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365
0
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366 Options: ::
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367
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368 -g full path to a multi-fasta file with the genomic sequences
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369 for all input mappings, OR a directory with single-fasta files
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370 (one per genomic sequence, with file names matching sequence names)
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371 -s <seq_info.fsize> is a tab-delimited file providing this info
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372 for each of the mapped sequences:
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373 <seq-name> <seq-length> <seq-description>
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374 (useful for -A option with mRNA/EST/protein mappings)
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375 -i discard transcripts having an intron larger than <maxintron>
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376 -r only show transcripts overlapping coordinate range <start>..<end>
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377 (on chromosome/contig <chr>, strand <strand> if provided)
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378 -R for -r option, discard all transcripts that are not fully
0
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379 contained within the given range
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380 -U discard single-exon transcripts
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381 -C coding only: discard mRNAs that have no CDS feature
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382 -F full GFF attribute preservation (all attributes are shown)
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383 -G only parse additional exon attributes from the first exon
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384 and move them to the mRNA level (useful for GTF input)
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385 -A use the description field from <seq_info.fsize> and add it
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386 as the value for a 'descr' attribute to the GFF record
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387
0
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388 -O process also non-transcript GFF records (by default non-transcript
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389 records are ignored)
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390 -V discard any mRNAs with CDS having in-frame stop codons
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391 -H for -V option, check and adjust the starting CDS phase
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392 if the original phase leads to a translation with an
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393 in-frame stop codon
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394 -B for -V option, single-exon transcripts are also checked on the
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395 opposite strand
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396 -N discard multi-exon mRNAs that have any intron with a non-canonical
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397 splice site consensus (i.e. not GT-AG, GC-AG or AT-AC)
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398 -J discard any mRNAs that either lack initial START codon
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399 or the terminal STOP codon, or have an in-frame stop codon
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400 (only print mRNAs with a fulll, valid CDS)
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401 --no-pseudo: filter out records matching the 'pseudo' keyword
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402
0
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403 -M/--merge : cluster the input transcripts into loci, collapsing matching
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404 transcripts (those with the same exact introns and fully contained)
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405 -d <dupinfo> : for -M option, write collapsing info to file <dupinfo>
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406 --cluster-only: same as --merge but without collapsing matching transcripts
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407 -K for -M option: also collapse shorter, fully contained transcripts
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408 with fewer introns than the container
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409 -Q for -M option, remove the containment restriction:
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410 (multi-exon transcripts will be collapsed if just their introns match,
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411 while single-exon transcripts can partially overlap (80%))
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412
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413 --force-exons: make sure that the lowest level GFF features are printed as
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414 "exon" features
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415 -E expose (warn about) duplicate transcript IDs and other potential
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416 problems with the given GFF/GTF records
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417 -D decode url encoded characters within attributes
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418 -Z merge close exons into a single exon (for intron size<4)
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419 -w write a fasta file with spliced exons for each GFF transcript
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420 -x write a fasta file with spliced CDS for each GFF transcript
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421 -W for -w and -x options, also write for each fasta record the exon
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422 coordinates projected onto the spliced sequence
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423 -y write a protein fasta file with the translation of CDS for each record
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424 -L Ensembl GTF to GFF3 conversion (implies -F; should be used with -m)
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425 -m <chr_replace> is a reference (genomic) sequence replacement table with
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426 this format:
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427 <original_ref_ID> <new_ref_ID>
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428 For example from UCSC naming to Ensembl naming:
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429 chr1 1
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430 chr2 2
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431 GFF records on reference sequences that are not found among the
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432 <original_ref_ID> entries in this file will be filtered out
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433 -o the "filtered" GFF records will be written to <outfile.gff>
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434 (use -o- for printing to stdout)
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435 -t use <trackname> in the second column of each GFF output line
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436 -T -o option will output GTF format instead of GFF3
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437
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438 ]]>
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439 </help>
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440 <citations>
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441 <citation type="doi">10.1038/nbt.1621</citation>
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442 </citations>
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443 </tool>