Mercurial > repos > iuc > cnvkit_scatter
diff scatter.xml @ 0:ec9731970f8b draft
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/cnvkit commit c35b83e4b65b211377c9f616c77d7306da48a984
author | iuc |
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date | Sun, 14 May 2023 20:10:25 +0000 |
parents | |
children | 3323a7867128 |
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--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/scatter.xml Sun May 14 20:10:25 2023 +0000 @@ -0,0 +1,103 @@ +<tool id="cnvkit_scatter" name="CNVkit Scatter" version="@TOOL_VERSION@+galaxy@VERSION_SUFFIX@" profile="21.05"> + <description>Plot bin-level log2 coverages and segmentation calls together</description> + <macros> + <import>macros.xml</import> + </macros> + <expand macro="xrefs"/> + <expand macro="requirements"/> + <command detect_errors="exit_code"><![CDATA[ + ln -s '$input_cnr_file' ./tumor.cnr && + #if $advanced_settings.segment + ln -s '$advanced_settings.segment' ./segment.cns && + #end if + #if $advanced_settings.range_list + ln -s '$advanced_settings.range_list' ./list.bed && + #end if + #if $advanced_settings.additional_SNP_allelic_process.vcf + ln -s '$advanced_settings.additional_SNP_allelic_process.vcf' ./vcf_file.vcf && + #end if + cnvkit.py scatter + ./tumor.cnr + --output sample-scatter.png + #if $advanced_settings.segment + --segment ./segment.cns + #end if + #if $advanced_settings.chromosome + --chromosome '$advanced_settings.chromosome' + #end if + #if $advanced_settings.gene + --gene '$advanced_settings.gene' + #end if + #if $advanced_settings.range_list + --range-list ./list.bed + #end if + #if str($advanced_settings.width) + --width $advanced_settings.width + #end if + #if $advanced_settings.plot_aesthetics.antitarget_marker + --antitarget-marker '$advanced_settings.plot_aesthetics.antitarget_marker' + #end if + $advanced_settings.plot_aesthetics.by_bin + #if $advanced_settings.plot_aesthetics.segment_color + --segment-color '$advanced_settings.plot_aesthetics.segment_color' + #end if + #if $advanced_settings.plot_aesthetics.title + --title '$advanced_settings.plot_aesthetics.title' + #end if + $advanced_settings.plot_aesthetics.trend + #if str($advanced_settings.plot_aesthetics.y_max) + --y-max $advanced_settings.plot_aesthetics.y_max + #end if + #if str($advanced_settings.plot_aesthetics.y_min) + --y-min $advanced_settings.plot_aesthetics.y_min + #end if + #if str($advanced_settings.plot_aesthetics.fig_size) + --fig-size $advanced_settings.plot_aesthetics.fig_size + #end if + #if $advanced_settings.additional_SNP_allelic_process.vcf + --vcf ./vcf_file.vcf + #end if + #if $advanced_settings.additional_SNP_allelic_process.sample_id + --sample-id '$advanced_settings.additional_SNP_allelic_process.sample_id' + #end if + #if $advanced_settings.additional_SNP_allelic_process.normal_id + --normal-id '$advanced_settings.additional_SNP_allelic_process.normal_id' + #end if + #if str($advanced_settings.additional_SNP_allelic_process.min_variant_depth) + --min-variant-depth $advanced_settings.additional_SNP_allelic_process.min_variant_depth + #end if + #if str($advanced_settings.additional_SNP_allelic_process.zygosity_freq) + --zygosity-freq $advanced_settings.additional_SNP_allelic_process.zygosity_freq + #end if + ]]></command> + <inputs> + <param name="input_cnr_file" type="data" format="tabular" label="cnn file" help="" /> + <section name="advanced_settings" title="Advanced settings" expanded="false"> + <expand macro="scatter_optional" /> + <section name="plot_aesthetics" title="Plot aesthetics" expanded="false"> + <expand macro="scatter_plot" /> + </section> + <section name="additional_SNP_allelic_process" title="Plot aesthetics" expanded="false"> + <expand macro="additionally_SNP_process" /> + </section> + </section> + </inputs> + <outputs> + <data name="out_scatter_file" format="png" label="${tool.name} on ${on_string}: diagram pdf file" from_work_dir="sample-scatter.png" /> + </outputs> + <tests> + <test expect_num_outputs="1"> + <param name="input_cnr_file" ftype="tabular" value="tumor.cnr" /> + <param name="zygosity_freq" value="0.25" /> + <param name="by_bin" value="1" /> + <output name="out_scatter_file" file="sample-scatter.png" ftype="png" compare="sim_size"> + <assert_contents><has_size value="12000" delta="5000" /></assert_contents> + </output> + </test> + </tests> + <help><![CDATA[ + Plot bin-level log2 coverages and segmentation calls together. Without any further arguments, + this plots the genome-wide copy number in a form familiar to those who have used array CGH. + ]]></help> + <expand macro="citations" /> +</tool>