Mercurial > repos > lparsons > rseqc

annotate junction_annotation.xml @ 1:cd2daa987b69 draft default tip

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planemo upload for repository https://github.com/lparsons/galaxy_tools/tree/master/tools/rseqc commit 2400cce6e3918648fda8f2a8d8485ab251a58827
author lparsons
date Tue, 07 Jul 2015 14:14:04 -0400
parents 306127635959
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306127635959 planemo upload for repository https://github.com/lparsons/galaxy_tools/tree/master/tools/rseqc commit aeb25d807817746dd6957f30ce2070662cc10e91
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1 <tool id="rseqc_junction_annotation" name="Junction Annotation" version="2.4galaxy1">
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2 <description>compares detected splice junctions to reference gene model</description>
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4 <macros>
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5 <import>rseqc_macros.xml</import>
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6 </macros>
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8 <requirements>
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9 <expand macro="requirement_package_r" />
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10 <expand macro="requirement_package_numpy" />
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11 <expand macro="requirement_package_rseqc" />
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12 </requirements>
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14 <expand macro="stdio" />
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16 <version_command><![CDATA[junction_annotation.py --version]]></version_command>
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18 <command><![CDATA[
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19 junction_annotation.py
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20 --input-file $input
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21 --refgene $refgene
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22 --out-prefix output
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23 --min-intron $min_intron
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24 --mapq $mapq
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25 ]]>
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26 </command>
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28 <inputs>
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29 <param name="input" type="data" format="bam,sam" label="input bam/sam file" help="(--input-file)"/>
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30 <param name="refgene" type="data" format="bed" label="reference gene model" help="(--refgene)"/>
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31 <param name="min_intron" type="integer" value="50" label="Minimum intron length (bp, default=50)" help="(--min-intron)" />
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32 <param name="mapq" type="integer" label="Minimum mapping quality (default=30)" help="Minimum phred scale mapping quality to consider a read 'uniquely mapped' (--mapq)" value="30" />
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33 </inputs>
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35 <outputs>
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36 <data format="xls" name="outputxls" from_work_dir="output.junction.xls" label="${tool.name} on ${on_string} (XLS)"/>
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37 <data format="txt" name="outputr" from_work_dir="output.junction_plot.r" label="${tool.name} on ${on_string} (R Script)" />
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38 <data format="pdf" name="outputpdf" from_work_dir="output.splice_events.pdf" label="${tool.name} on ${on_string} (Splice Events PDF)"/>
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39 <data format="pdf" name="outputjpdf" from_work_dir="output.splice_junction.pdf" label="${tool.name} on ${on_string} (Splice Junction PDF)" />
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40 </outputs>
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42 <tests>
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43 <test>
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44 <param name="input" value="pairend_strandspecific_51mer_hg19_chr1_1-100000.bam"/>
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45 <param name="refgene" value="hg19_RefSeq_chr1_1-100000.bed"/>
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46 <output name="outputxls" file="output.junction.xls"/>
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47 <output name="outputr" file="output.junction_plot.r"/>
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48 <output name="outputpdf" file="output.splice_events.pdf"/>
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49 <output name="outputjpdf" file="output.splice_junction.pdf"/>
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50 </test>
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51 </tests>
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53 <help><![CDATA[
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54 junction_annotation.py
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55 ++++++++++++++++++++++
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57 For a given alignment file (-i) in BAM or SAM format and a reference gene model (-r) in BED
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58 format, this program will compare detected splice junctions to reference gene model. splicing
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59 annotation is performed in two levels: splice event level and splice junction level.
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61 * splice event: An RNA read, especially long read, can be spliced 2 or more times, each time is called a splicing event; In this sense, 100 spliced reads can produce >= 100 splicing events.
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62 * splice junction: multiple splicing events spanning the same intron can be consolidated into one splicing junction.
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64 All detected junctions can be grouped to 3 exclusive categories:
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65
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66 1. Annotated: The junction is part of the gene model. Both splice sites, 5' splice site
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67 (5'SS) and 3'splice site (3'SS) can be annotated by reference gene model.
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68 2. complete_novel: Complete new junction. Neither of the two splice sites cannot be annotated by gene model
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69 3. partial_novel: One of the splice site (5'SS or 3'SS) is new, while the other splice site is annotated (known)
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70
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71 Inputs
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72 ++++++++++++++
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73
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74 Input BAM/SAM file
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75 Alignment file in BAM/SAM format.
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76
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77 Reference gene model
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78 Gene model in BED format.
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80 Minimum intron length (default=50)
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81 Minimum intron length (bp).
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82
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83
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84 Output
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85 ++++++++++++++
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86
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87 1. output.junc.anno.junction.xls:
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88 - chrom ID
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89 - start position of junction (coordinate is 0 based)
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90 - end position of junction (coordinate is 1 based)
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91 - number of splice events supporting this junction
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92 - 'annotated', 'complete_novel' or 'partial_novel'.
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93 2. output.anno.junction_plot.r: R script to generate pie chart
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94 3. output.splice_junction.pdf: plot of splice junctions
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95 4. output.splice_events.pdf: plot of splice events
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96
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97 .. image:: http://rseqc.sourceforge.net/_images/junction.png
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98 :height: 400 px
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99 :width: 850 px
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100 :scale: 80 %
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101
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102 -----
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103
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104 About RSeQC
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105 +++++++++++
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106
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107 The RSeQC_ package provides a number of useful modules that can comprehensively evaluate high throughput sequence data especially RNA-seq data. "Basic modules" quickly inspect sequence quality, nucleotide composition bias, PCR bias and GC bias, while "RNA-seq specific modules" investigate sequencing saturation status of both splicing junction detection and expression estimation, mapped reads clipping profile, mapped reads distribution, coverage uniformity over gene body, reproducibility, strand specificity and splice junction annotation.
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108
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109 The RSeQC package is licensed under the GNU GPL v3 license.
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110
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111 .. image:: http://rseqc.sourceforge.net/_static/logo.png
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112
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113 .. _RSeQC: http://rseqc.sourceforge.net/
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114 ]]>
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115 </help>
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116
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117 <expand macro="citations" />
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118
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119 </tool>