Mercurial > repos > devteam > picard

annotate picard_CollectAlignmentSummaryMetrics.xml @ 11:3d8d70436d02 draft

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planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/picard commit 2bfbb5ae6b801e43355fdc3f964a5111fe3fe3a1
author iuc
date Wed, 08 Feb 2017 12:41:25 -0500
parents 41b8d087a2d2
children 486d7500da69
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1 <tool name="Collect Alignment Summary Metrics" id="picard_CASM" version="@TOOL_VERSION@.1">
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2 <description>writes a file containing summary alignment metrics</description>
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3 <macros>
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4 <import>picard_macros.xml</import>
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5 </macros>
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6 <expand macro="requirements" />
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7 <command detect_errors="exit_code"><![CDATA[
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8 @java_options@
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9 @symlink_element_identifier@
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10 ##set up input files
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12 #set $reference_fasta_filename = "localref.fa"
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14 #if str( $reference_source.reference_source_selector ) == "history":
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15 ln -s "${reference_source.ref_file}" "${reference_fasta_filename}" &&
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16 #else:
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17 #set $reference_fasta_filename = str( $reference_source.ref_file.fields.path )
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18 #end if
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20 picard
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21 CollectAlignmentSummaryMetrics
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22 INPUT='$escaped_element_identifier'
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23 OUTPUT="${outFile}"
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24 MAX_INSERT_SIZE=${maxinsert}
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25 #for $sequence in $adapters:
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26 ADAPTER_SEQUENCE="${sequence.adapter}"
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27 #end for
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28 #for $level in str($metric_accumulation_level).split(','):
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29 METRIC_ACCUMULATION_LEVEL="${level}"
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30 #end for
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31 IS_BISULFITE_SEQUENCED="${bisulphite}"
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32
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33 REFERENCE_SEQUENCE="${reference_fasta_filename}"
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34
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35 ASSUME_SORTED="${assume_sorted}"
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37 VALIDATION_STRINGENCY="${validation_stringency}"
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38 QUIET=true
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39 VERBOSITY=ERROR
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40
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41 ]]></command>
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42 <inputs>
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43 <param format="sam,bam" name="inputFile" type="data" label="Select SAM/BAM dataset or dataset collection" help="If empty, upload or import a SAM/BAM dataset."/>
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44 <conditional name="reference_source">
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45 <param name="reference_source_selector" type="select" label="Load reference genome from">
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46 <option value="cached">Local cache</option>
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47 <option value="history">History</option>
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48 </param>
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49 <when value="cached">
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50 <param name="ref_file" type="select" label="Using reference genome" help="REFERENCE_SEQUENCE">
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51 <options from_data_table="all_fasta">
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52 </options>
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53 <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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54 </param>
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55 </when>
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56 <when value="history">
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57 <param name="ref_file" type="data" format="fasta" label="Use the following dataset as the reference sequence" help="REFERENCE_SEQUENCE; You can upload a FASTA sequence to the history and use it as reference" />
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58 </when>
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59 </conditional>
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60 <param name="metric_accumulation_level" type="select" label="The level(s) at which to accumulate metrics" multiple="true" help="METRIC_ACCUMULATION_LEVEL">
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61 <option value="ALL_READS" selected="True">All reads</option>
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62 <option value="SAMPLE">Sample</option>
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63 <option value="LIBRARY">Library</option>
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64 <option value="READ_GROUP">Read group</option>
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65 </param>
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66 <param name="assume_sorted" type="boolean" label="Assume the input file is already sorted" checked="true" truevalue="true" falsevalue="false" help="ASSUME_SORTED"/>
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67 <param name="bisulphite" type="boolean" label="Input file contains Bisulphite sequenced reads" checked="false" falsevalue="false" truevalue="true" help="IS_BISULFITE_SEQUENCED"/>
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68 <repeat name="adapters" title="Adapter" min="0" help="You can provide multiple adaptor sequences">
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69 <param name="adapter" type="text" label="Use this adaptor sequence" help="ADAPTER_SEQUENCE"/>
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70 </repeat>
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71 <param name="maxinsert" value="100000" type="integer" label="Larger paired end reads and inter-chromosomal pairs considered chimeric" help="MAX_INSERT_SIZE"/>
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72 <expand macro="VS" />
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73
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74 </inputs>
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75 <outputs>
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76 <data format="tabular" name="outFile" label="${tool.name} on ${on_string}: Summary stats"/>
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77 </outputs>
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78 <tests>
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79 <test>
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80 <param name="bisulphite" value="false" />
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81 <param name="sorted" value="true" />
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82 <param name="adaptors" value="" />
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83 <param name="maxinsert" value="100000" />
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84 <param name="reference_source_selector" value="history" />
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85 <param name="ref_file" value="picard_CASM_ref.fa" />
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86 <param name="inputFile" value="picard_CASM.bam" ftype="bam" />
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87 <output name="outFile" file="picard_CASM_test1.tab" ftype="tabular" lines_diff="4"/>
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88 </test>
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89 </tests>
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90 <help>
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91
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92 .. class:: infomark
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93
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94 **Purpose**
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95
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96 Reads a SAM or BAM file and writes a file containing summary alignment metrics.
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97
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98 @dataset_collections@
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99
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100 @description@
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101
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102 MAX_INSERT_SIZE=Integer Paired end reads above this insert size will be considered chimeric along with
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103 inter-chromosomal pairs. Default value: 100000.
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104
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105 ADAPTER_SEQUENCE=String List of adapter sequences to use when processing the alignment metrics This option may
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106 be specified 0 or more times.
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107
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108 METRIC_ACCUMULATION_LEVEL=MetricAccumulationLevel
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109 LEVEL=MetricAccumulationLevel The level(s) at which to accumulate metrics. Possible values: {ALL_READS, SAMPLE,
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110 LIBRARY, READ_GROUP} This option may be specified 0 or more times.
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111
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112 IS_BISULFITE_SEQUENCED=Boolean
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113 BS=Boolean Whether the SAM or BAM file consists of bisulfite sequenced reads.
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114
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115
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116 REFERENCE_SEQUENCE=File
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117 R=File Reference sequence fasta Default value: null.
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118
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119 ASSUME_SORTED=Boolean
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120 AS=Boolean If true (default), then the sort order in the header file will be ignored.
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121
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122 @more_info@
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123
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124 </help>
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125 </tool>
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126
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127