Mercurial > repos > jjohnson > snpeff
annotate snpEff.xml @ 21:c780e3f75b3d
Filter genome history snpeffdb by snpeff_version
| author | Jim Johnson <jj@umn.edu> |
|---|---|
| date | Wed, 14 Jan 2015 12:03:21 -0600 |
| parents | 2e37b58fc24d |
| children | bb0797deab78 |
| rev | line source |
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1 <tool id="snpEff" name="SnpEff" version="@WRAPPER_VERSION@.3"> |
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2 <description>Variant effect and annotation</description> |
| 7 | 3 <expand macro="requirements" /> |
| 4 <macros> | |
| 5 <import>snpEff_macros.xml</import> | |
| 6 </macros> | |
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7 <command> |
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8 <![CDATA[ |
| 7 | 9 java -Xmx6G -jar \$SNPEFF_JAR_PATH/snpEff.jar eff |
| 10 -c \$SNPEFF_JAR_PATH/snpEff.config | |
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11 -i $inputFormat -o ${outputConditional.outputFormat} -upDownStreamLen $udLength |
| 7 | 12 #if $spliceSiteSize and $spliceSiteSize.__str__ != '': |
| 13 -spliceSiteSize $spliceSiteSize | |
| 14 #end if | |
| 15 #if $filterIn and $filterIn.__str__ != 'no_filter': | |
| 16 $filterIn | |
| 17 #end if | |
| 18 #if $filterHomHet and $filterHomHet.__str__ != 'no_filter': | |
| 19 $filterHomHet | |
| 20 #end if | |
| 21 #if $annotations and $annotations.__str__ != '': | |
| 22 #echo " " | |
| 23 #echo ' '.join($annotations.__str__.split(',')) | |
| 24 #end if | |
| 25 #if $filterOut and $filterOut.__str__ != '': | |
| 26 #echo " " | |
| 27 #echo ' '.join($filterOut.__str__.split(',')) | |
| 28 #end if | |
| 29 #if str( $transcripts ) != 'None': | |
| 30 -onlyTr $transcripts | |
| 31 #end if | |
| 32 #if str( $intervals ) != 'None': ### fix this for multiple dataset input | |
| 33 -interval $intervals | |
| 34 #end if | |
| 35 #if $statsFile: | |
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36 -stats $statsFile |
| 7 | 37 #end if |
| 16 | 38 #if $offset.__str__ != 'default': |
| 7 | 39 ${offset} |
| 40 #end if | |
| 41 #if $chr.__str__.strip() != '': | |
| 42 -chr "$chr" | |
| 43 #end if | |
| 16 | 44 $noLog |
| 7 | 45 #if $snpDb.genomeSrc == 'cached': |
| 46 -dataDir ${snpDb.genomeVersion.fields.path} | |
| 47 #if $snpDb.extra_annotations and $snpDb.extra_annotations.__str__ != '': | |
| 48 #echo " " | |
| 49 #echo ' '.join($snpDb.extra_annotations.__str__.split(',')) | |
| 50 #end if | |
| 51 #if $snpDb.regulation and $snpDb.regulation.__str__ != '': | |
| 52 -reg #echo ' -reg '.join($snpDb.regulation.__str__.split(','))# | |
| 53 #end if | |
| 54 $snpDb.genomeVersion | |
| 55 #elif $snpDb.genomeSrc == 'history': | |
| 56 -dataDir ${snpDb.snpeff_db.extra_files_path} | |
| 57 #if $snpDb.extra_annotations and $snpDb.extra_annotations.__str__ != '': | |
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58 #set xannotations = [' '] + $snpDb.extra_annotations.__str__.split(',') |
| 7 | 59 #echo " " |
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60 #echo ' -'.join($xannotations) |
| 7 | 61 #end if |
| 62 #if $snpDb.regulation and $snpDb.regulation.__str__ != '': | |
| 63 -reg #echo ' -reg '.join($snpDb.regulation.__str__.split(','))# | |
| 64 #end if | |
| 65 ${snpDb.snpeff_db.metadata.genome_version} | |
| 66 #else | |
| 67 -download | |
| 68 $snpDb.genome_version | |
| 69 #end if | |
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70 $input > $snpeff_output ; |
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71 #if $statsFile: |
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72 #import os |
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73 #set $genes_file = str($statsFile) + '.genes.txt' |
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74 #set $genes_file_name = os.path.split($genes_file)[-1] |
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75 mkdir $statsFile.files_path; |
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76 mv $genes_file #echo os.path.join($statsFile.files_path, $genes_file_name)#; |
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77 #end if |
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78 #if $outputConditional.outputFormat == 'gatk' and $outputConditional.gatk_v1 |
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79 ## Replace real SnpEff version with 2.0.5 to prevent this GATK 1.x error: "The version of SnpEff used to generate the SnpEff input file (x.x) is not currently supported by the GATK. Supported versions are: [2.0.5]" |
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80 sed -i 's/^\#\#SnpEffVersion="\(\S*\s\)/\#\#SnpEffVersion="2.0.5 - real is \1/' $snpeff_output |
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81 #end if |
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82 ]]> |
| 7 | 83 </command> |
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84 <inputs> |
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85 <param format="vcf,tabular,pileup,bed" name="input" type="data" label="Sequence changes (SNPs, MNPs, InDels)"/> |
| 0 | 86 |
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87 <param name="inputFormat" type="select" label="Input format"> |
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88 <option value="vcf" selected="true">VCF</option> |
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89 <option value="txt">Tabular (Deprecated)</option> |
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90 <option value="pileup">Pileup (Deprecated)</option> |
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91 <option value="bed">BED (Deprecated)</option> |
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92 </param> |
| 0 | 93 |
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94 <conditional name="outputConditional"> |
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95 <param name="outputFormat" type="select" label="Output format"> |
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96 <option value="vcf" selected="true">VCF (only if input is VCF)</option> |
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97 <option value="gatk">GATK-compatible VCF (only if input is VCF)</option> |
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98 <option value="txt">Tabular</option> |
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99 <option value="bed">BED</option> |
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100 <option value="bedAnn">BED annotations</option> |
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101 </param> |
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102 <when value="vcf" /> |
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103 <when value="gatk"> |
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104 <param name="gatk_v1" type="boolean" checked="true" label="Compatible with GATK 1.x" /> |
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105 </when> |
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106 <when value="txt" /> |
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107 <when value="bed" /> |
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108 <when value="bedAnn" /> |
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109 </conditional> |
| 0 | 110 |
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111 <conditional name="snpDb"> |
| 7 | 112 <param name="genomeSrc" type="select" label="Genome source"> |
| 113 <option value="cached">Locally installed reference genome</option> | |
| 114 <option value="history">Reference genome from your history</option> | |
| 115 <option value="named">Named on demand</option> | |
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116 </param> |
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117 <when value="cached"> |
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118 <param name="genomeVersion" type="select" label="Genome"> |
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119 <!--GENOME DESCRIPTION--> |
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120 <options from_data_table="snpeffv_genomedb"> |
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121 <filter type="static_value" name="snpeff_version" value="@SNPEFF_VERSION@" column="1"/> |
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122 <filter type="unique_value" column="2" /> |
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123 </options> |
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124 </param> |
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125 <param name="extra_annotations" type="select" display="checkboxes" multiple="true" label="Additional annotations"> |
| 2 | 126 <help>These are available for only a few genomes</help> |
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127 <options from_data_table="snpeffv_annotations"> |
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128 <filter type="param_value" ref="genomeVersion" key="genome" column="2" /> |
| 19 | 129 <filter type="unique_value" column="3" /> |
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130 </options> |
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131 </param> |
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132 <param name="regulation" type="select" display="checkboxes" multiple="true" label="Non-coding and regulatory annotation"> |
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133 <help>These are available for only a few genomes</help> |
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134 <options from_data_table="snpeffv_regulationdb"> |
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135 <filter type="param_value" ref="genomeVersion" key="genome" column="2" /> |
| 19 | 136 <filter type="unique_value" column="3" /> |
| 2 | 137 </options> |
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138 </param> |
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139 </when> |
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140 <when value="history"> |
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141 <param format="snpeffdb" name="snpeff_db" type="data" label="@SNPEFF_VERSION@ Genome Data"> |
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142 <options options_filter_attribute="metadata.snpeff_version" > |
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143 <filter type="add_value" value="@SNPEFF_VERSION@" /> |
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144 </options> |
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145 <validator type="expression" message="This version of SnpEff will only work with @SNPEFF_VERSION@ Genome databases.">value is not None and value.metadata.snpeff_version == "@SNPEFF_VERSION@"</validator> |
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146 </param> |
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147 <!-- From metadata --> |
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148 <param name="extra_annotations" type="select" display="checkboxes" multiple="true" label="Additional annotations"> |
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149 <help>These are available for only a few genomes</help> |
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150 <options> |
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151 <filter type="data_meta" ref="snpeff_db" key="annotation" /> |
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152 </options> |
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153 </param> |
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154 <param name="regulation" type="select" display="checkboxes" multiple="true" label="Non-coding and regulatory annotation"> |
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155 <help>These are available for only a few genomes</help> |
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156 <options> |
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157 <filter type="data_meta" ref="snpeff_db" key="regulation" /> |
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158 </options> |
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159 </param> |
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160 </when> |
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161 <when value="named"> |
| 16 | 162 <param name="genome_version" type="text" size="40" value="" label="Snpff Genome Version Name (e.g. GRCh38.76)"> |
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163 <help>@SNPEFF_DATABASE_URL@</help> |
| 16 | 164 <validator type="regex" message="A genome version name is required">\S+</validator> |
| 165 </param> | |
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166 </when> |
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167 </conditional> |
| 0 | 168 |
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169 <param name="udLength" type="select" label="Upstream / Downstream length"> |
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170 <option value="0">No upstream / downstream intervals (0 bases)</option> |
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171 <option value="200">200 bases</option> |
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172 <option value="500">500 bases</option> |
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173 <option value="1000">1000 bases</option> |
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174 <option value="2000">2000 bases</option> |
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175 <option value="5000" selected="true">5000 bases</option> |
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176 <option value="10000">10000 bases</option> |
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177 <option value="20000">20000 bases</option> |
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178 </param> |
| 0 | 179 |
| 7 | 180 <param name="spliceSiteSize" type="select" optional="true" label="Set size for splice sites (donor and acceptor) in bases" help="Default: 2"> |
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181 <option value="1">1 base</option> |
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182 <option value="2" selected="true">2 bases</option> |
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183 <option value="3">3 bases</option> |
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184 <option value="4">4 bases</option> |
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185 <option value="5">5 bases</option> |
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186 <option value="6">6 bases</option> |
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187 <option value="7">7 bases</option> |
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188 <option value="8">8 bases</option> |
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189 <option value="9">9 bases</option> |
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190 </param> |
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191 |
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192 <param name="filterHomHet" type="select" display="radio" label="Filter homozygous / heterozygous changes"> |
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193 <option value="no_filter" selected="true">No filter (analyze everything)</option> |
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194 <option value="-hom">Analyze homozygous sequence changes only</option> |
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195 <option value="-het">Analyze heterozygous sequence changes only</option> |
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196 </param> |
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197 |
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198 <!-- The tool testing code can not handle select,radio,check boxes values that start with '-', so the '-' is added in the command generation --> |
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199 <param name="filterIn" type="select" display="radio" label="Filter sequence changes"> |
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200 <option value="no_filter" selected="true">No filter (analyze everything)</option> |
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201 <option value="-del">Analyze deletions only</option> |
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202 <option value="-ins">Analyze insertions only</option> |
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203 <option value="-mnp">Only MNPs (multiple nucleotide polymorphisms)</option> |
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204 <option value="-snp">Only SNPs (single nucleotide polymorphisms)</option> |
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205 </param> |
| 2 | 206 |
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207 <param name="annotations" type="select" display="checkboxes" multiple="true" label="Annotation options"> |
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208 <option value="-cancer">Perform 'cancer' comparisons (somatic vs. germline)</option> |
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209 <option value="-canon">Only use canonical transcripts</option> |
| 7 | 210 <option value="-geneId">Use gene ID instead of gene name (VCF output)</option> |
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211 <option value="-lof">Add loss of function (LOF) and nonsense mediated decay (NMD) tags</option> |
| 7 | 212 <option value="-oicr">Add OICR tag in VCF file</option> |
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213 <option value="-onlyReg">Only use regulation tracks</option> |
| 12 | 214 <option value="-classic">Use Classic Effect names and amino acid variant annotations (NON_SYNONYMOUS_CODING vs missense_variant and G180R vs p.Gly180Arg/c.538G>C)</option> |
| 215 <option value="-hgvs">Override classic and use HGVS annotations for amino acid annotations (p.Gly180Arg/c.538G>C vs G180R)</option> | |
| 216 <option value="-sequenceOntology">Override classic and use Sequence Ontolgy terms for effects (missense_variant vs NON_SYNONYMOUS_CODING)</option> | |
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217 </param> |
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218 <param name="intervals" format="bed" type="data" optional="true" label="Use custom interval file for annotation"/> |
| 7 | 219 <param name="transcripts" format="tabular" type="data" optional="true" label="Only use the transcripts in this file." help="Format is one transcript ID per line."/> |
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220 <param name="filterOut" type="select" display="checkboxes" multiple="true" label="Filter output"> |
| 7 | 221 <option value="-no-downstream">Do not show DOWNSTREAM changes</option> |
| 222 <option value="-no-intergenic">Do not show INTERGENIC changes</option> | |
| 223 <option value="-no-intron">Do not show INTRON changes</option> | |
| 224 <option value="-no-upstream">Do not show UPSTREAM changes</option> | |
| 225 <option value="-no-utr">Do not show 5_PRIME_UTR or 3_PRIME_UTR changes</option> | |
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226 </param> |
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227 |
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228 <param name="offset" type="select" display="radio" optional="true" label="Chromosomal position"> |
| 16 | 229 <option value="default" selected="true">Use default (based on input type)</option> |
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230 <option value="-0">Force zero-based positions (both input and output)</option> |
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231 <option value="-1">Force one-based positions (both input and output)</option> |
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232 </param> |
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233 <param name="chr" type="text" optionl="true" label="Text to prepend to chromosome name"> |
| 7 | 234 <help> |
| 235 By default SnpEff simplifies all chromosome names. For instance 'chr1' is just '1'. | |
| 236 You can prepend any string you want to the chromosome name. | |
| 237 </help> | |
| 238 <validator type="regex" message="No whitespace allowed">^\S*$</validator> | |
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239 </param> |
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240 <param name="generate_stats" type="boolean" truevalue="" falsevalue="-noStats" checked="true" label="Produce Summary Stats"/> |
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241 <param name="noLog" type="boolean" truevalue="-noLog" falsevalue="" checked="true" label="Do not report usage statistics to server"/> |
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242 </inputs> |
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243 <outputs> |
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244 <data format="vcf" name="snpeff_output" > |
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245 <change_format> |
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246 <when input="outputConditional.outputFormat" value="txt" format="tabular" /> |
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247 <when input="outputConditional.outputFormat" value="bed" format="bed" /> |
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248 <when input="outputConditional.outputFormat" value="bedAnn" format="bed" /> |
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249 </change_format> |
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250 </data> |
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251 <data format="html" name="statsFile" label="${tool.name} on ${on_string} - stats"> |
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252 <filter>generate_stats == True</filter> |
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253 </data> |
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254 </outputs> |
| 7 | 255 <expand macro="stdio" /> |
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256 <tests> |
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257 <!-- Check that an effect was added in out VCF --> |
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258 <!-- Check for a HTML header indicating that this was successful --> |
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259 <!-- |
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260 <output name="statsFile"> |
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261 <assert_contents> |
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262 <has_text text="SnpEff: Variant analysis" /> |
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263 </assert_contents> |
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264 </output> |
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265 --> |
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266 <!-- Setting filterOut throws exception in twilltestcase.py |
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267 <test> |
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268 <param name="input" ftype="vcf" value="vcf_homhet.vcf"/> |
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269 <param name="inputFormat" value="vcf"/> |
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270 <param name="outputFormat" value="vcf"/> |
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271 <param name="genomeSrc" value="named"/> |
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272 <param name="genome_version" value="testCase"/> |
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273 <param name="udLength" value="0"/> |
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274 <param name="filterHomHet" value="no_filter"/> |
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275 <param name="filterIn" value="no_filter"/> |
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276 <param name="generate_stats" value="False"/> |
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277 <param name="filterOut" value="+-no-upstream"/> |
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278 <output name="snpeff_output"> |
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279 <assert_contents> |
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280 <has_text text="EFF=" /> |
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281 </assert_contents> |
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282 </output> |
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283 </test> |
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284 --> |
| 0 | 285 |
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286 <test> |
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287 <param name="input" ftype="vcf" value="vcf_homhet.vcf"/> |
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288 <param name="inputFormat" value="vcf"/> |
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289 <param name="outputFormat" value="vcf"/> |
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290 <param name="genomeSrc" value="named"/> |
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291 <param name="genome_version" value="testCase"/> |
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292 <param name="udLength" value="0"/> |
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293 <param name="filterHomHet" value="+-het"/> |
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294 <param name="filterIn" value="no_filter"/> |
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295 <!-- |
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296 <param name="filterOut" value=""/> |
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297 --> |
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298 <param name="generate_stats" value="False"/> |
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299 <output name="snpeff_output"> |
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300 <assert_contents> |
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301 <!-- Check that NO effects were added since -het is set --> |
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302 <not_has_text text="EFF=NON_SYNONYMOUS_CODING" /> |
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303 </assert_contents> |
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304 </output> |
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305 </test> |
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306 |
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307 <test> |
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308 <param name="input" ftype="vcf" value="vcf_homhet.vcf"/> |
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309 <param name="inputFormat" value="vcf"/> |
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310 <param name="outputFormat" value="vcf"/> |
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311 <param name="genomeSrc" value="named"/> |
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312 <param name="genome_version" value="testCase"/> |
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313 <param name="udLength" value="0"/> |
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314 <param name="filterHomHet" value="no_filter"/> |
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315 <param name="filterIn" value="+-del"/> |
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316 <!-- |
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317 <param name="filterOut" value=""/> |
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318 --> |
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319 <param name="generate_stats" value="False"/> |
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320 <output name="snpeff_output"> |
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321 <assert_contents> |
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322 <!-- Check that deleletions were evaluated --> |
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323 <has_text_matching expression="Y\t59030478\t.*EFF=INTERGENIC" /> |
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324 <!-- Check that insertion on last line was NOT evaluated --> |
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325 <has_text_matching expression="Y\t59032947\t.*SF=5\tGT" /> |
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326 </assert_contents> |
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327 </output> |
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328 </test> |
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329 |
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330 <!-- Check that NO UPSTREAM effect was added --> |
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331 <!-- Setting filterOut throws exception in twilltestcase.py |
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332 <test> |
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333 <param name="input" ftype="vcf" value="vcf_homhet.vcf"/> |
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334 <param name="inputFormat" value="vcf"/> |
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335 <param name="outputFormat" value="vcf"/> |
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336 <param name="genomeSrc" value="named"/> |
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337 <param name="genome_version" value="testCase"/> |
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338 <param name="udLength" value="0"/> |
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339 <param name="filterHomHet" value="no_filter"/> |
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340 <param name="filterIn" value="no_filter"/> |
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341 <param name="filterOut" value="+-no-upstream"/> |
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342 <param name="generate_stats" value="False"/> |
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343 <output name="snpeff_output"> |
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344 <assert_contents> |
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345 <not_has_text text="UPSTREAM" /> |
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346 </assert_contents> |
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347 </output> |
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348 </test> |
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349 --> |
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350 |
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351 </tests> |
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352 <help> |
| 0 | 353 |
| 354 This tool calculate the effect of variants (SNPs/MNPs/Insertions) and deletions. | |
| 355 | |
| 7 | 356 @EXTERNAL_DOCUMENTATION@ |
| 0 | 357 |
| 7 | 358 @CITATION_SECTION@ |
|
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359 |
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360 </help> |
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361 <expand macro="citations" /> |
| 0 | 362 </tool> |
| 363 |
