annotate vcfvcfintersect.xml @ 1:ab5790197e8a draft

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author devteam
date Mon, 09 Nov 2015 15:18:58 -0500
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children 64d95a7df265
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1 <tool id="vcfvcfintersect" name="VCF-VCFintersect:" version="0.0.3">
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2 <description>Intersect two VCF datasets</description>
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3 <macros>
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4 <import>macros.xml</import>
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5 </macros>
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6 <expand macro="requirements"></expand>
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7 <expand macro="stdio"></expand>
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8 <command>
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9
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10 #set $reference_fasta_filename = "localref.fa"
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11 #if str( $reference_source.reference_source_selector ) == "history":
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12 ln -s "${reference_source.ref_file}" "${reference_fasta_filename}" &amp;&amp;
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13 #else:
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14 #set $reference_fasta_filename = str( $reference_source.ref_file.fields.path )
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15 #end if
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16
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17 #if $adv_options.adv_options_selector == True:
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19 vcfintersect "${adv_options.adv_options_input}" ${loci} ${invert} -r "${reference_fasta_filename}" -w "${window_size}" ${isect_union} "${vcf_input1}" "${vcf_input2}" > "${out_file1}"
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21 #else:
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22
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23 vcfintersect ${loci} ${invert} -r "${reference_fasta_filename}" -w "${window_size}" ${isect_union} "${vcf_input1}" "${vcf_input2}" > "${out_file1}"
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24
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25 #end if
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26
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27 </command>
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28 <inputs>
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29 <!-- selecting refernce source -->
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30 <param name="vcf_input1" type="data" format="vcf" label="The first VCF dataset" />
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31 <param name="vcf_input2" type="data" format="vcf" label="The second VCF dataset" help="The second dataset will be instersected with the first"/>
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32 <conditional name="reference_source">
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33 <param name="reference_source_selector" type="select" label="Choose the source for the reference genome" help="This tools needs to access reference genomes sequence specified by this option.">
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34 <option value="cached">Locally cached</option>
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35 <option value="history">History</option>
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36 </param>
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37 <when value="cached">
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38 <param name="ref_file" type="select" label="Select reference genome">
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39 <options from_data_table="fasta_indexes">
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40 <!--<filter type="data_meta" key="dbkey" ref="input_bam" column="value"/>-->
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41 </options>
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42 <validator type="no_options" message="A built-in reference genome is not available for the build associated with the selected input file"/>
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43 </param>
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44 </when>
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45 <when value="history"> <!-- FIX ME!!!! -->
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46 <param name="ref_file" type="data" format="fasta" label="Using reference file" />
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47 </when>
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48 </conditional>
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49 <param name="isect_union" type="select" label="Union or intersection" help="-i or -u">
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50 <option value="-i">Intersect</option>
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51 <option value="-u">Union</option>
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52 </param>
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53 <param name="invert" type="boolean" truevalue="-v" falsevalue="" label="Invert selection?" help="-v, --invert" />
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54 <param name="window_size" type="integer" value="30" label="compare records up to this many bp away (window size)" help="-w, --window-size" />
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55 <param name="loci" type="boolean" truevalue="-l" falsevalue="" label="output whole loci when one alternate allele matches" help="-l, --loci" />
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56 <conditional name="adv_options">
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57 <param name="adv_options_selector" type="boolean" truevalue="use_adv_controls" label="Advanced controls" help="Allows you to specify options that are not listed above"/>
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58 <when value="use_adv_controls">
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59 <param name="adv_options_input" type="text" value="-t &quot;vcfvcf-intersect-result&quot;" label="Enter additional command line options described in the help section below" help="such as -m, -t, -V, -M, and -T" />
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60 <sanitizer>
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61 <valid initial="string.printable">
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62 <remove value="&apos;"/>
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63 </valid>
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64 <mapping initial="none">
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65 <add source="&apos;" target="__sq__"/>
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66 </mapping>
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67 </sanitizer>
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68 </when>
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69 </conditional>
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70 </inputs>
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71 <outputs>
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72 <data format="vcf" name="out_file1" />
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73 </outputs>
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74 <tests>
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75 <test>
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76 <param name="reference_source_selector" value="history" />
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77 <param name="vcf_input1" value="vcfvcfintersect-input1.vcf" />
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78 <param name="vcf_input2" value="vcfvcfintersect-input2.vcf" />
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79 <param name="isect_union" value="-i" />
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80 <param name="invert" value="False" />
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81 <param name="loci" value="False" />
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82 <patam name="adv_options" value="False" />
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83 <param name="window_size" value="30" />
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84 <param name="ref_file" value="vcflib-test-genome-phix.fa" />
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85 <output name="out_file1" file="vcfvcfintersect-test1.vcf"/>
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86 </test>
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87 <test>
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88 <param name="reference_source_selector" value="history" />
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89 <param name="vcf_input1" value="vcfvcfintersect-input1.vcf" />
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90 <param name="vcf_input2" value="vcfvcfintersect-input2.vcf" />
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91 <param name="isect_union" value="-u" />
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92 <param name="invert" value="False" />
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93 <param name="loci" value="False" />
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94 <patam name="adv_options" value="False" />
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95 <param name="window_size" value="30" />
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96 <param name="ref_file" value="vcflib-test-genome-phix.fa" />
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97 <output name="out_file1" file="vcfvcfintersect-test2.vcf"/>
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98 </test>
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99 </tests>
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100 <help>
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101
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102 Computes intersections and unions for two VCF datasets. Unifies equivalent alleles within window-size bp.
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103
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104 The options are::
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105
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106 -v, --invert invert the selection, printing only records which would
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107 -i, --intersect-vcf FILE use this VCF for set intersection generation
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108 -u, --union-vcf FILE use this VCF for set union generation
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109 -w, --window-size N compare records up to this many bp away (default 30)
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110 -l, --loci output whole loci when one alternate allele matches
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111 -m, --ref-match intersect on the basis of record REF string
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112 -t, --tag TAG attach TAG to each record's info field if it would intersect
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113 -V, --tag-value VAL use this value to indicate that the allele is passing
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114 '.' will be used otherwise. default: 'PASS'
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115 -M, --merge-from FROM-TAG
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116 -T, --merge-to TO-TAG merge from FROM-TAG used in the -i file, setting TO-TAG
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117 in the current file.
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118
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119 ----
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120
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121 VCFVCFintersect is based on vcfintersect utility of VCFlib toolkit developed by Erik Garrison (https://github.com/ekg/vcflib).
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122 </help>
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123 <expand macro="citations" />
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124 </tool>