Mercurial > repos > nilesh > rseqc
view junction_annotation.xml @ 54:5873cd7afb67 draft
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/rseqc commit 62a9135bf04aec398d3172d17ccd60f5242d8e82
author | iuc |
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date | Wed, 13 Jun 2018 18:02:25 -0400 |
parents | 34e4c586e3c0 |
children | dbedfc5f5a3c |
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<tool id="rseqc_junction_annotation" name="Junction Annotation" version="@WRAPPER_VERSION@.1"> <description>compares detected splice junctions to reference gene model</description> <macros> <import>rseqc_macros.xml</import> </macros> <expand macro="requirements"> <!-- Required due to conda solver bug: https://github.com/conda/conda/issues/6269 See: https://github.com/galaxyproject/tools-iuc/pull/1578 for more info --> <requirement type="package" version="3.4.1">r-base</requirement> </expand> <expand macro="stdio" /> <version_command><![CDATA[junction_annotation.py --version]]></version_command> <command><![CDATA[ junction_annotation.py --input-file '${input}' --refgene '${refgene}' --out-prefix output --min-intron ${min_intron} --mapq ${mapq} ]]> </command> <inputs> <expand macro="bam_sam_param" /> <expand macro="refgene_param" /> <expand macro="min_intron_param" /> <expand macro="mapq_param" /> <expand macro="rscript_output_param" /> </inputs> <outputs> <data format="pdf" name="outputpdf" from_work_dir="output.splice_events.pdf" label="${tool.name} on ${on_string} (Splice Events pdf)"/> <data format="pdf" name="outputjpdf" from_work_dir="output.splice_junction.pdf" label="${tool.name} on ${on_string} (Splice Junction pdf)" /> <expand macro="xls_output_data" filename="output.junction.xls" /> <expand macro="rscript_output_data" filename="output.junction_plot.r" /> </outputs> <tests> <test> <param name="input" value="pairend_strandspecific_51mer_hg19_chr1_1-100000.bam" /> <param name="refgene" value="hg19_RefSeq_chr1_1-100000.bed" /> <param name="rscript_output" value="true" /> <output name="outputxls" file="output.junction.xls" /> <output name="outputr" file="output.junction_plot.r" /> <output name="outputpdf" file="output.splice_events.pdf" compare="sim_size" /> <output name="outputjpdf" file="output.splice_junction.pdf" compare="sim_size" /> </test> </tests> <help><![CDATA[ junction_annotation.py ++++++++++++++++++++++ For a given alignment file (-i) in BAM or SAM format and a reference gene model (-r) in BED format, this program will compare detected splice junctions to reference gene model. splicing annotation is performed in two levels: splice event level and splice junction level. * 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. * splice junction: multiple splicing events spanning the same intron can be consolidated into one splicing junction. All detected junctions can be grouped to 3 exclusive categories: 1. Annotated: The junction is part of the gene model. Both splice sites, 5' splice site (5'SS) and 3'splice site (3'SS) can be annotated by reference gene model. 2. complete_novel: Complete new junction. Neither of the two splice sites cannot be annotated by gene model 3. partial_novel: One of the splice site (5'SS or 3'SS) is new, while the other splice site is annotated (known) Inputs ++++++++++++++ Input BAM/SAM file Alignment file in BAM/SAM format. Reference gene model Gene model in BED format. Minimum intron length (default=50) Minimum intron length (bp). Output ++++++++++++++ 1. output.junc.anno.junction.xls: - chrom ID - start position of junction (coordinate is 0 based) - end position of junction (coordinate is 1 based) - number of splice events supporting this junction - 'annotated', 'complete_novel' or 'partial_novel'. 2. output.anno.junction_plot.r: R script to generate pie chart 3. output.splice_junction.pdf: plot of splice junctions 4. output.splice_events.pdf: plot of splice events .. image:: $PATH_TO_IMAGES/junction.png :height: 400 px :width: 850 px :scale: 80 % @ABOUT@ ]]> </help> <expand macro="citations" /> </tool>