annotate bwa_0_7_5/bwa_0_7_5.xml @ 0:839e36b39c3f draft

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author yufei-luo
date Mon, 12 Aug 2013 08:44:05 -0400
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1 <tool id="bwa_0_7_5" name="Map with BWA (Version 0.7.5)" version="0.7.5">
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2 <requirements>
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3 <requirement type="package" version="0.7.5">bwa</requirement>
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4 </requirements>
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5 <description>This new version BWA (0.7.5) use 'mem' algorithm for mapping, dosen't need 'aln', 'samse', 'sampe' and picard AddOrReplace anymore.</description>
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6 <parallelism method="basic"></parallelism>
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7 <command interpreter="python">
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8 bwa_0_7_5.py
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9 --threads="1"
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10 --fileSource="${genomeSource.refGenomeSource}"
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11 #if $genomeSource.refGenomeSource == "history":
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12 ##build index on the fly
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13 --ref="${genomeSource.ownFile}"
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14 --dbkey="${dbkey}"
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15 #else:
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16 ##use precomputed indexes
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17 --ref="${genomeSource.indices.fields.path}"
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18 #end if
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19
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20 ## input file(s)
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21 --fastq="${paired.fastq}"
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22 #if $paired.sPaired == "paired":
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23 --rfastq="${paired.rfastq}"
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24 #end if
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25
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26 ## output file
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27 --output="${output}"
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28
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29 ## run parameters
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30 --genAlignType="${paired.sPaired}"
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31 --params="${params.source_select}"
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32 #if $params.source_select != "pre_set":
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33 --minEditDistSeed="${params.minEditDistSeed}"
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34 --bandWidth="${params.bandWidth}"
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35 --offDiagonal="${params.offDiagonal}"
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36 --internalSeeds="${params.internalSeeds}"
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37 --seedsOccurrence="${params.seedsOccurrence}"
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38 --mateRescue="${params.mateRescue}"
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39 --skipPairing="${params.skipPairing}"
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40 --seqMatch="${params.seqMatch}"
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41 --mismatch="${params.mismatch}"
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42 --gapOpen="${params.gapOpen}"
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43 --gapExtension="${params.gapExtension}"
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44 --clipping="${params.clipping}"
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45 --unpairedReadpair="${params.unpairedReadpair}"
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46 --interPairEnd="${params.interPairEnd}"
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47 --minScore="${params.minScore}"
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48 --mark="${params.mark}"
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49
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50 #if $params.readGroup.specReadGroup == "yes"
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51 --rgid="${params.readGroup.rgid}"
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52 --rgsm="${params.readGroup.rgsm}"
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53 --rgpl="${params.readGroup.rgpl}"
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54 --rglb="${params.readGroup.rglb}"
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55 --rgpu="${params.readGroup.rgpu}"
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56 --rgcn="${params.readGroup.rgcn}"
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57 --rgds="${params.readGroup.rgds}"
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58 --rgdt="${params.readGroup.rgdt}"
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59 --rgfo="${params.readGroup.rgfo}"
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60 --rgks="${params.readGroup.rgks}"
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61 --rgpg="${params.readGroup.rgpg}"
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62 --rgpi="${params.readGroup.rgpi}"
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63 #end if
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64 #end if
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65 </command>
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66
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67 <inputs>
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68 <conditional name="genomeSource">
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69 <param name="refGenomeSource" type="select" label="Will you select a reference genome from your history or use a built-in index?">
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70 <option value="indexed">Use a built-in index</option>
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71 <option value="history">Use one from the history</option>
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72 </param>
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73 <when value="indexed">
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74 <param name="indices" type="select" label="Select a reference genome">
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75 <options from_data_table="bwa_indexes">
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76 <filter type="sort_by" column="2" />
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77 <validator type="no_options" message="No indexes are available" />
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78 </options>
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79 </param>
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80 </when>
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81 <when value="history">
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82 <param name="ownFile" type="data" format="fasta" metadata_name="dbkey" label="Select a reference from history" />
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83 </when>
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84 </conditional>
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85 <conditional name="paired">
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86 <param name="sPaired" type="select" label="Is this library mate-paired?">
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87 <option value="single">Single-end</option>
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88 <option value="paired">Paired-end</option>
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89 </param>
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90 <when value="single">
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91 <param name="fastq" type="data" format="fastqsanger,fastqillumina" label="FASTQ file" help="FASTQ with either Sanger-scaled quality values (fastqsanger) or Illumina-scaled quality values (fastqillumina)" />
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92 </when>
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93 <when value="paired">
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94 <param name="fastq" type="data" format="fastqsanger,fastqillumina" label="Forward FASTQ file" help="FASTQ with either Sanger-scaled quality values (fastqsanger) or Illumina-scaled quality values (fastqillumina)" />
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95 <param name="rfastq" type="data" format="fastqsanger,fastqillumina" label="Reverse FASTQ file" help="FASTQ with either Sanger-scaled quality values (fastqsanger) or Illumina-scaled quality values (fastqillumina)" />
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96 </when>
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97 </conditional>
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98 <conditional name="params">
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99 <param name="source_select" type="select" label="BWA settings to use" help="For most mapping needs use Commonly Used settings. If you want full control use Full Parameter List">
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100 <option value="pre_set">Commonly Used</option>
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101 <option value="full">Full Parameter List</option>
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102 </param>
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103 <when value="pre_set" />
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104 <when value="full">
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105 <param name="minEditDistSeed" type="integer" value="19" label="Minimum seed length" />
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106 <param name="bandWidth" type="integer" value="100" label="Band width for banded alignment" />
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107 <param name="offDiagonal" type="integer" value="100" label="off-diagonal X-dropoff" />
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108 <param name="internalSeeds" type="float" value="1.5" label="look for internal seeds inside a seed longer than {-k} * FLOAT [1.5]" />
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109 <param name="seedsOccurrence" type="integer" value="10000" label="skip seeds with more than INT occurrences" />
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110 <param name="mateRescue" type="boolean" truevalue="True" falsevalue="False" checked="False" label="skip seeds with more than INT occurrences" />
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111 <param name="skipPairing" type="boolean" truevalue="True" falsevalue="False" checked="False" label="skpe pairing, mate rescue performed unless -S also in use" />
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112 <param name="seqMatch" type="integer" value="1" label="score of a sequence match" />
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113 <param name="mismatch" type="integer" value="4" label="penalty for a mismatch" />
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114 <param name="gapOpen" type="integer" value="6" label="gap open penalty" />
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115 <param name="gapExtension" type="text" value="None" label="gap extension penalty; a gap of size k cost {-O} + {-E}*k [1]" />
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116 <param name="clipping" type="integer" value="5" label="penalty for clipping" />
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117 <param name="unpairedReadpair" type="integer" value="17" label="penalty for an unpaired read pair" />
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118 <param name="interPairEnd" type="boolean" truevalue="True" falsevalue="False" checked="False" label="first query file consists of interleaved paired-end sequences" />
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119 <param name="minScore" type="integer" value="30" label="minimum score to output" />
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120 <param name="mark" type="boolean" truevalue="True" falsevalue="False" checked="False" label="mark shorter split hits as secondary (for Picard/GATK compatibility)" />
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121
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122 <conditional name="readGroup">
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123 <param name="specReadGroup" type="select" label="Specify the read group for this file? (samse/sampe -r)">
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124 <option value="yes">Yes</option>
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125 <option value="no" selected="True">No</option>
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126 </param>
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127 <when value="yes">
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128 <param name="rgid" type="text" size="25" label="[Essential]Read group identifier (ID). Each @RG line must have a unique ID. The value of ID is used in the RG
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129 tags of alignment records. Must be unique among all read groups in header section." help="Required if RG specified. Read group
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130 IDs may be modified when merging SAM files in order to handle collisions." />
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131 <param name="rgpl" type="text" size="25" label="[Essential]Platform/technology used to produce the reads (PL)" help="Required if RG specified. Valid values : CAPILLARY, LS454, ILLUMINA,
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132 SOLID, HELICOS, IONTORRENT and PACBIO" />
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133 <param name="rglb" type="text" size="25" label="[Essential]Library name (LB)" help="Required if RG specified" />
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134 <param name="rgsm" type="text" size="25" label="[Essential]Sample (SM)" help="Required if RG specified. Use pool name where a pool is being sequenced" />
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135 <param name="rgpu" type="text" size="25" label="Platform unit (PU)" help="Optional. Unique identifier (e.g. flowcell-barcode.lane for Illumina or slide for SOLiD)" />
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136 <param name="rgcn" type="text" size="25" label="Sequencing center that produced the read (CN)" help="Optional" />
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137 <param name="rgds" type="text" size="25" label="Description (DS)" help="Optional" />
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138 <param name="rgdt" type="text" size="25" label="Date that run was produced (DT)" help="Optional. ISO8601 format date or date/time, like YYYY-MM-DD" />
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139 <param name="rgfo" type="text" size="25" label="Flow order (FO). The array of nucleotide bases that correspond to the nucleotides used for each
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140 flow of each read." help="Optional. Multi-base flows are encoded in IUPAC format, and non-nucleotide flows by
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141 various other characters. Format : /\*|[ACMGRSVTWYHKDBN]+/" />
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142 <param name="rgks" type="text" size="25" label="The array of nucleotide bases that correspond to the key sequence of each read (KS)" help="Optional" />
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143 <param name="rgpg" type="text" size="25" label="Programs used for processing the read group (PG)" help="Optional" />
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144 <param name="rgpi" type="text" size="25" label="Predicted median insert size (PI)" help="Optional" />
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145 </when>
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146 <when value="no" />
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147 </conditional>
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148 </when>
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149 </conditional>
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150 </inputs>
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151
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152 <outputs>
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153 <data format="sam" name="output" label="${tool.name} on ${on_string}: mapped reads">
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154 <actions>
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155 <conditional name="genomeSource.refGenomeSource">
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156 <when value="indexed">
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157 <action type="metadata" name="dbkey">
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158 <option type="from_data_table" name="bwa_indexes" column="1">
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159 <filter type="param_value" column="0" value="#" compare="startswith" keep="False"/>
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160 <filter type="param_value" ref="genomeSource.indices" column="0"/>
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161 </option>
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162 </action>
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163 </when>
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164 <when value="history">
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165 <action type="metadata" name="dbkey">
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166 <option type="from_param" name="genomeSource.ownFile" param_attribute="dbkey" />
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167 </action>
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168 </when>
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169 </conditional>
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170 </actions>
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171 </data>
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172 </outputs>
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173
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174 <tests>
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175 <test>
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176 </test>
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177 <test>
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178 </test>
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179 <test>
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180 </test>
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181 </tests>
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182
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183
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184 </tool>
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185
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186