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1 <?xml version="1.0"?>
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2 <tool id="shear_sv" name="SHEAR-SV" version="0.0.11">
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3 <description>find SVs and estimate the heterogeneity levels from a BAM</description>
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4 <requirements>
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3
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5 <requirement type="package" version="0.2.11">shear</requirement>
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6 <requirement type="package" version="0.1.19">samtools</requirement>
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7 <requirement type="package" version="0.6.2">bwa</requirement>
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8 <requirement type="package" version="1.0.1">crest</requirement>
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9 <requirement type="package" version="latest">blat_server</requirement>
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10 <requirement type="package" version="3">cap3</requirement>
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11 </requirements>
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12 <!--
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13 <version_command></version_command>
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14 -->
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15 <command interpreter="python">
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16 shear_wrapper.py -j \$SHEAR_JAR_PATH/SHEAR.jar --command sv
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17 -p $prefix ## used in gerenating ouput file names
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18 -b $bamfile
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19 #if $genomeSource.refGenomeSource == 'indexed':
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20 -f $genomeSource.ref_fastas.fields.path
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21 -i $genomeSource.bwa_indices.fields.path
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22 -t $genomeSource.twobit_indices.fields.path
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23 #elif $genomeSource.refGenomeSource == 'svidx':
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24 -f $genomeSource.svidx.extra_files_path/${genomeSource.svidx.metadata.base_name}.fa
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25 -i $genomeSource.svidx.extra_files_path/${genomeSource.svidx.metadata.base_name}.fa
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26 -t $genomeSource.svidx.extra_files_path/${genomeSource.svidx.metadata.base_name}.2bit
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27 #else:
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28 -f $genomeSource.ref_fasta
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29 #if $genomeSource.save_svidx:
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30 -D $sv_idx.extra_files_path
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31 #end if
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32 #end if
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33 #if $region and $region.__str__.strip() != '':
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34 -r $region
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35 #end if
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36 $sv_only
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37 </command>
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38 <inputs>
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39 <param name="bamfile" type="data" format="bam" label="BAM alignment file containing the input sequences to the assembly."/>
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40 <param name="prefix" type="hidden" value="shear_sv" label="Prefix for all generated files"/>
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41 <!--
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42 <param name="prefix" type="text" value="shear_sv" label="Prefix for all generated files">
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43 <validator type="regex" message="Prefix should start with a letter and contain only letter, digit, and '_' or '-' characters">[a-zA-Z0-9][_a-zA-Z0-9-]*</validator>
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44 </param>
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45 -->
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46 <!-- reference data -->
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47 <conditional name="genomeSource">
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48 <param name="refGenomeSource" type="select" label="Will you select a reference genome from your history or use a cached file?">
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49 <option value="indexed" selected="true">Use a cached reference genome</option>
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50 <option value="history">Use fasta from the history</option>
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51 <option value="svidx">Use SHEAR sv index from the history</option>
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52 </param>
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53 <when value="indexed">
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54 <param name="ref_fastas" type="select" label="Select a reference genome fasta">
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55 <options from_data_table="all_fasta">
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56 <filter type="sort_by" column="2" />
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57 <validator type="no_options" message="No reference fasta files are available" />
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58 </options>
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59 </param>
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60 <param name="twobit_indices" type="select" label="Select the reference genome 2bit">
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61 <options from_data_table="twobit">
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62 <filter type="sort_by" column="0" />
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63 <!--
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64 <filter type="data_meta" ref="ref_fastas" key="dbkey" column="0" />
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65 -->
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66 <validator type="no_options" message="No indexes are available" />
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67 </options>
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68 </param>
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69 <param name="bwa_indices" type="select" label="Select the reference genome bwa indices">
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70 <options from_data_table="bwa_indexes">
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71 <filter type="sort_by" column="2" />
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72 <!--
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73 <filter type="data_meta" ref="ref_fastas" key="dbkey" column="0" />
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74 -->
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75 <validator type="no_options" message="No indexes are available" />
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76 </options>
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77 </param>
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78 </when>
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79 <when value="history">
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80 <param name="ref_fasta" type="data" format="fasta" label="Select a reference from history" />
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81 <param name="save_svidx" type="boolean" truevalue="yes" falsevalue="no" label="Save sv generated reference indexes"/>
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82 </when>
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83 <when value="svidx">
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84 <param name="svidx" type="data" format="shear.svidx" label="Select a reference from history" />
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85 </when>
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86 </conditional>
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87 <param name="region" type="text" value="" optional="true" label="Region of the input alignment to analyze">
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88 <help>"chr1" for full chromosome or "chr1:10000-15000" for a particular region, including endpoints).
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89 Coordinates are 1-based.
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90 </help>
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91 <validator type="regex" message="format: chr1:100-200">^\w+(:\d+-\d+)?$</validator>
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92 </param>
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93 <param name="sv_only" type="boolean" truevalue="--sv-only" falsevalue="" checked="false" label="SV Only prediction mode."
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94 help="Will skip SNP/INDEL prediction and only return *.sdi and *.report results for SVs."/>
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95 </inputs>
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96 <stdio>
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97 <exit_code range="1:" level="fatal" description="Error" />
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98 </stdio>
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99 <outputs>
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100 <data format="txt" name="report_snpindel" label="${tool.name} on ${on_string}: ${prefix}.snpindel.report" from_work_dir="shear_sv.snpindel.report">
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101 <filter>sv_only == False</filter>
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102 </data>
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103 <data format="txt" name="report_sv" label="${tool.name} on ${on_string}: ${prefix}.sv.report" from_work_dir="shear_sv.sv.report"/>
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104 <data format="txt" name="report_all" label="${tool.name} on ${on_string}: ${prefix}.all.report" from_work_dir="shear_sv.all.report">
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105 <filter>sv_only == False</filter>
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106 </data>
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107 <data format="shear.sdi" name="sdi_snpindel" label="${tool.name} on ${on_string}: ${prefix}.snpindel.sdi" from_work_dir="shear_sv.snpindel.sdi">
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108 <filter>sv_only == False</filter>
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109 </data>
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110 <data format="shear.sdi" name="sdi_sv" label="${tool.name} on ${on_string}: ${prefix}.sv.sdi" from_work_dir="shear_sv.sv.sdi"/>
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111 <data format="shear.sdi" name="sdi_all" label="${tool.name} on ${on_string}: ${prefix}.all.sdi" from_work_dir="shear_sv.all.sdi">
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112 <filter>sv_only == False</filter>
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113 </data>
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114 <data format="shear.svidx" name="sv_idx" label="${tool.name} on ${on_string}: ${prefix}.svidx">
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115 <filter>genomeSource['refGenomeSource'] == 'history' and genomeSource['save_svidx'] == True</filter>
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116 </data>
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117 </outputs>
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118 <tests>
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119 <test>
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120 <param name="prefix" value="shear_test" />
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121 <param name="bamfile" value="simulated-data.bam" ftype="bam" />
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122 <param name="refGenomeSource" value="history"/>
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123 <param name="ref_fasta" value="syn.fa" ftype="fasta" />
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124 <param name="save_svidx" value="false"/>
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125 <param name="sv_only" value="true"/>
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126 <output name="sdi_sv" file="shear_sv.sdi"/>
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127 <output name="report_sv" file="shear_sv.report"/>
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128 </test>
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129 </tests>
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130 <help>
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131 SHEAR-SV will process a BAM alignment file to find SVs and estimate the
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132 heterogeneity level of those SVs. It will output a *.report file reporing the
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133 SVs and their heterogeneity levels, and it will output a *.sdi file that can be
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134 used for SHEAR-Assemble to reconstruct the new genome.
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135
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136 Please cite the following article:
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137
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138 Landman SR, Hwang TH, Silverstein KAT, Li Y, Dehm SM, Steinbach M, and Kumar V. SHEAR: sample heterogeneity estimation and assembly by reference. BMC Genomics 2014, 15:84.
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139
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140 </help>
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141 </tool>
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