Mercurial > repos > iuc > vardict_java

annotate vardict.xml @ 2:d262577e04b0 draft

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"planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/vardict commit c247c47e1bc869c9094997f5052ce31367e10b1e"
author iuc
date Tue, 16 Nov 2021 19:05:56 +0000
parents 5f756651a1bc
children e0734e88a104
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1 <tool id="vardict_java" name="VarDict" version="@TOOL_VERSION@+galaxy@VERSION_SUFFIX@">
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2 <description>calls SNVs and indels for tumor-normal pairs</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 <requirements>
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7 <requirement type="package" version="@TOOL_VERSION@">vardict-java</requirement>
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8 <requirement type="package" version="5.1.0">gawk</requirement>
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9 <requirement type="package" version="1.14">samtools</requirement>
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10 </requirements>
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11 <expand macro="stdio" />
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12 <command detect_errors="exit_code"><![CDATA[
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13 #if $select_mode.mode == "paired"
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14 ln -s '$select_mode.normal' ./normal.bam &&
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15 ln -s '$select_mode.normal.metadata.bam_index' ./normal.bam.bai &&
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16 #end if
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17 ln -s '$select_mode.tumor' ./tumor.bam &&
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18 ln -s '$select_mode.tumor.metadata.bam_index' ./tumor.bam.bai &&
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19
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20 ## INDEX REFERENCE FASTA FILE IF FROM HISTORY
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21 #if $reference_source.reference_source_selector == "history":
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22 ln -s '$reference_source.ref_file' ./ref.fa &&
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23 samtools faidx ./ref.fa 2>&1 || echo 'Error running samtools faidx for indexing fasta reference for vardict' >&2 &&
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24 #else if $reference_source.reference_source_selector == "cached"
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25 ln -s '$reference_source.ref_file.fields.path' ./ref.fa &&
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26 ln -s '${reference_source.ref_file.fields.path}.fai' ./ref.fa.fai &&
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27 #end if
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28
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29 ## build BED file from chromosome list
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30 #if $interval_file:
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31 grep -w -f '$interval_file' ./ref.fa.fai > ./chromosomes.fa.fai &&
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32 #else
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33 ln -s ./ref.fa.fai ./chromosomes.fa.fai &&
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34 #end if
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35 awk 'BEGIN {FS=OFS="\t"} {print $1, "1", $2}' ./chromosomes.fa.fai > ./regions.bed &&
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36
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37 vardict-java
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38 #if $select_mode.mode == "paired"
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39 -b "./tumor.bam|./normal.bam"
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40 -N 'Tumor'
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41 #else
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42 -b "./tumor.bam"
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43 -N 'Sample'
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44 #end if
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45 -G ./ref.fa
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46 -z
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47 -th \${GALAXY_SLOTS:-1}
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48
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49 -f '$advancedsettings.f'
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50 -k '$advancedsettings.k'
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51 -r '$advancedsettings.r'
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52 -B '$advancedsettings.B'
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53 -Q '$advancedsettings.Q'
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54 -q '$advancedsettings.q'
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55 -m '$advancedsettings.m'
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56 -T '$advancedsettings.T'
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57 -X '$advancedsettings.X'
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58 -P '$advancedsettings.P'
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59 -o '$advancedsettings.o'
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60 -O '$advancedsettings.O'
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61 -V '$advancedsettings.V'
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62
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63 ## construct VFC table
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64 -c 1 -S 2 -E 3 -g 4
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65 ./regions.bed
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66
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67 ## postprocessing
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68 #if $select_mode.mode == "paired"
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69 | testsomatic.R
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70 | var2vcf_paired.pl
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71 -N 'Tumor|Normal'
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72 #else
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73 | teststrandbias.R
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74 | var2vcf_valid.pl
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75 -N 'Sample'
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76 -E
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77 #end if
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78 -f '$advancedsettings.f'
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79
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80 > '$all_variants' &&
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81
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82 ## Filter for PASS variants
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83 awk 'BEGIN {FS=OFS="\t"} substr(\$0, 1, 1) == "#" {print \$0; next} \$7 == "PASS" {print \$0}' '$all_variants' > '$passed_variants'
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84 ]]></command>
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85 <inputs>
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86 <conditional name="select_mode">
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87 <param name="mode" type="select" label="Choose run mode">
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88 <option value="single">Single sample mode</option>
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89 <option value="paired" selected="true">Paired variant calling</option>
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90 </param>
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91 <when value="single">
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92 <expand macro="input_default" />
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93 </when>
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94 <when value="paired">
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95 <param name="normal" type="data" format="bam" label="Normal file" />
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96 <expand macro="input_default" />
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97 </when>
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98 </conditional>
2
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99 <section name="advancedsettings" title="Advanced Settings" expanded="false">
0
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100 <param argument="-f" type="float" min="0.0" max="1.0" value="0.01" label="Minimum variant allele fraction" />
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101 <param argument="-k" type="boolean" truevalue="1" falsevalue="0" checked="true" label="Indicate whether to perform local realignment" />
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102 <param argument="-r" type="integer" min="0" value="2" label="Minimum number of reads supporting the variant" />
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103 <param argument="-B" type="integer" min="0" value="2" label="Minimum number of reads for determining strand bias" />
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104 <param argument="-Q" type="integer" min="0" value="1" label="Minimum mapping quality for reads to be considered" />
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105 <param argument="-m" type="integer" value="8" label="Maximum number of mismatches before a read is no longer considered (gaps are not counted as mismatches)" />
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106 <param argument="-T" type="integer" value="0" label="Maximum number of bases considered from 5' end (default: 0, no trimming)" />
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107 <param argument="-X" type="integer" value="3" label="Maximum number of extended based after indel to look for mismatches" />
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108 <param argument="-P" type="integer" value="5" label="Maximum average read position for a variant to be considered." />
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109 <param argument="-q" type="integer" value="25" label="Minimum phred score for a base to be considered a good call" />
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110 <param argument="-o" type="float" value="1.5" label="Minimum quality ratio [(good_quality_reads)/(bad_quality_reads+0.5)] (based on definition of a good call; see previous option)" />
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111 <param argument="-O" type="float" min="0" value="0" label="Minimum average mapping quality" />
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112 <param argument="-V" type="float" min="0.0" max="1.0" value="0.05" label="Maximum allowed variant allele fraction in the normal sample" />
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113 </section>
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114 <expand macro="ref_select" />
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115 </inputs>
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116 <outputs>
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117 <data name="all_variants" format="vcf" label="VarDict SNVs and Indels (All)" />
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118 <data name="passed_variants" format="vcf" label="VarDict SNVs and Indels (Passed)" />
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119 </outputs>
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120 <tests>
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121 <test expect_num_outputs="2">
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122 <conditional name="select_mode">
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123 <param name="mode" value="paired" />
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124 <param name="normal" ftype="bam" value="normal.bam" />
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125 <param name="tumor" ftype="bam" value="tumor.bam" />
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126 </conditional>
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127 <conditional name="reference_source">
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128 <param name="reference_source_selector" value="history"/>
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129 <param name="ref_file" ftype="fasta" value="genome.fasta" />
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130 </conditional>
2
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131 <output name="all_variants" compare="re_match_multiline" file="all_variants_paired.vcf" />
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132 <output name="passed_variants" compare="re_match_multiline" file="passed_variants_paired.vcf" />
0
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133 </test>
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134 <test expect_num_outputs="2">
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135 <conditional name="select_mode">
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136 <param name="mode" value="paired" />
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137 <param name="normal" ftype="bam" value="normal.bam" />
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138 <param name="tumor" ftype="bam" value="tumor.bam" />
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139 </conditional>
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140 <conditional name="reference_source">
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141 <param name="reference_source_selector" value="cached"/>
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142 <param name="ref_file" value="test_buildid"/>
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143 </conditional>
2
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144 <output name="all_variants" compare="re_match_multiline" file="all_variants_paired.vcf" />
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145 <output name="passed_variants" compare="re_match_multiline" file="passed_variants_paired.vcf" />
0
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146 </test>
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147 <test expect_num_outputs="2">
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148 <conditional name="select_mode">
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149 <param name="mode" value="single" />
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150 <param name="tumor" ftype="bam" value="tumor.bam" />
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151 </conditional>
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152 <conditional name="reference_source">
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153 <param name="reference_source_selector" value="cached"/>
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154 <param name="ref_file" value="test_buildid"/>
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155 </conditional>
2
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156 <output name="all_variants" compare="re_match_multiline" file="all_variants_single.vcf" />
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157 <output name="passed_variants" compare="re_match_multiline" file="passed_variants_single.vcf" />
0
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158 </test>
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159 </tests>
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160 <help>
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161 <![CDATA[
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162 VarDict
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163 =======
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164
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165 VarDict is a sensitive variant caller for both single and paired sample variant calling from BAM files.
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166 VarDict implements several novel features such as amplicon bias aware variant calling from targeted sequencing experiments,
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167 rescue of long indels by realigning bwa soft clipped reads and better scalability than many other Java based variant callers.
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168
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169 For more information see the VarDict documentation_.
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170
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171 .. _documentation: https://github.com/AstraZeneca-NGS/VarDictJava
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172 ]]>
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173 </help>
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174 <citations>
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175 <citation type="doi">10.1093/nar/gkw227</citation>
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176 </citations>
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177 </tool>