Mercurial > repos > geert-vandeweyer > varscan_wrapper
annotate varscan/varscan_somatic.xml @ 4:572397bbe057 draft default tip
Added Xmx10G setting to both varscan_somatic wrappers
author | geert-vandeweyer |
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date | Wed, 26 Mar 2014 05:24:22 -0400 |
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1 <tool id="varscan_somatic_vcf" name="VarScan Somatic (VCF Output)" version="2.3.5"> |
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2 <description> |
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3 somatic mutation caller for cancer genomics |
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4 </description> |
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5 <requirements> |
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6 <requirement type="package" version="2.3.5">VarScan</requirement> |
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7 </requirements> |
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8 <command interpreter="perl"> |
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9 |
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10 varscan_somatic.pl |
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11 "COMMAND::java -Xmx10G -jar \$JAVA_JAR_PATH/VarScan.v2.3.5.jar somatic" |
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12 "NORMAL::$normal" |
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13 "TUMOR::$tumor" |
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14 "TUMORBAM::$tumorbam" |
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15 "OUTPUT::$output" |
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16 "LOG::$log" |
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17 |
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18 "OPTION::--min-coverage $min_coverage" |
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19 "OPTION::--min-coverage-normal $min_coverage_normal" |
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20 "OPTION::--min-coverage-tumor $min_coverage_tumor" |
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21 |
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22 "OPTION::--min-var-freq $min_var_freq" |
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23 "OPTION::--min-freq-for-hom $min_freq_for_hom" |
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24 |
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25 "OPTION::--normal-purity $normal_purity" |
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26 "OPTION::--tumor-purity $tumor_purity" |
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27 |
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28 "OPTION::--p-value $p_value" |
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29 "OPTION::--somatic-p-value $somatic_p_value" |
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30 |
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31 "OPTION::--strand-filter $strand_filter" |
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32 "OPTION::--validation $validation" |
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33 "OPTION::--output-vcf 1" |
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34 |
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35 |
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36 |
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37 </command> |
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38 |
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39 <inputs> |
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40 |
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41 <param name="normal" type="data" format="pileup" label="normal mpileup file" help="The SAMtools mpileup file for normal sample" /> |
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42 <param name="tumor" type="data" format="pileup" label="tumor mpileup file" help="The SAMtools mpileup file for tumor sample" /> |
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43 <param name="tumorbam" type="data" format="bam" label="tumor BAM file" help="The BAM file of the tumor sample used in mpileup step" /> |
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44 |
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45 <param name="min_coverage" type="integer" label="min-coverage" help="" optional="true" value="8"/> |
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46 <param name="min_coverage_normal" type="integer" label="min-coverage-normal" help="" optional="true" value="8"/> |
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47 <param name="min_coverage_tumor" type="integer" label="min-coverage-tumor" help="" optional="true" value="6"/> |
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48 |
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49 <param name="min_var_freq" type="float" label="min-var-freq" help="" optional="true" value="0.10"/> |
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50 <param name="min_freq_for_hom" type="float" label="min-freq-for-hom" help="" optional="true" value="0.75"/> |
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51 |
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52 <param name="normal_purity" type="float" label="normal-purity" help="" optional="true" value="1.00"/> |
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53 <param name="tumor_purity" type="float" label="tumor-purity" help="" optional="true" value="1.00"/> |
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54 |
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55 |
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56 <param name="p_value" type="text" label="p-value" help="" optional="true" value="0.99"/> |
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57 <param name="somatic_p_value" type="text" label="somatic-p-value" help="" optional="true" value="0.05"/> |
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58 |
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59 <param name="strand_filter" type="integer" label="strand-filter" help="" optional="true" value="1"/> |
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60 <param name="validation" type="integer" label="validation" help="" optional="true" value="0"/> |
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61 |
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62 </inputs> |
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63 <outputs> |
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64 <data type="data" format="vcf" name="output" label="${tool.name} result on ${on_string}"/> |
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65 <data type="data" format="txt" name="log" label="${tool.name} result on ${on_string} (log) "/> |
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66 <!--<data type="data" format="txt" name="snp" label="${tool.name} result on ${on_string} (SNP file)" /> |
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67 <data type="data" format="txt" name="indel" label="${tool.name} result on ${on_string} (INDEL file)" />--> |
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68 |
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69 |
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70 </outputs> |
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71 |
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72 <help> |
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73 |
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74 .. class:: infomark |
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75 |
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76 **What it does** |
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77 |
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78 :: |
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79 |
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80 VarScan is a platform-independent mutation caller for targeted, exome, and whole-genome resequencing data generated on Illumina, SOLiD, Life/PGM, Roche/454, and similar instruments. The newest version, VarScan 2, is written in Java, so it runs on most operating systems. It can be used to detect different types of variation: |
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81 |
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82 Germline variants (SNPs an dindels) in individual samples or pools of samples. |
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83 Multi-sample variants (shared or private) in multi-sample datasets (with mpileup). |
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84 Somatic mutations, LOH events, and germline variants in tumor-normal pairs. |
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85 Somatic copy number alterations (CNAs) in tumor-normal exome data. |
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86 |
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87 |
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88 **Input** |
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89 |
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90 :: |
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91 |
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92 mpileup normal file - The SAMtools mpileup file for normal |
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93 mpileup tumor file - The SAMtools mpileup file for tumor |
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94 |
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95 |
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96 **Parameters** |
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97 |
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98 :: |
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99 |
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100 min-coverage |
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101 Minimum read depth at a position to make a call [8] |
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102 |
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103 min-coverage-normal |
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104 Minimum coverage in normal to call somatic [8] |
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105 |
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106 min-coverage-tumor |
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107 Minimum coverage in tumor to call somatic [6] |
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108 |
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109 min-var-freq |
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110 Minimum variant frequency to call a heterozygote [0.10] |
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111 |
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112 min-freq-for-hom |
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113 Minimum frequency to call homozygote [0.75] |
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114 |
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115 normal-purity |
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116 Estimated purity (non-tumor content) of normal sample [1.00] |
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117 |
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118 tumor-purity |
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119 Estimated purity (tumor content) of tumor sample [1.00] |
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120 |
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121 p-value |
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122 Default p-value threshold for calling variants [0.99] |
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123 |
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124 somatic-p-value |
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125 P-value threshold to call a somatic site [0.05] |
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126 |
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127 strand-filter |
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128 If set to 1, removes variants with >90% strand bias |
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129 |
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130 validation |
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131 If set to 1, outputs all compared positions even if non-variant |
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132 |
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133 output-vcf |
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134 If set to 1, outputs in VCF format [Default] |
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135 |
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136 |
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137 |
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138 </help> |
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139 </tool> |
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140 |