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annotate facets_analysis.xml @ 3:d1914f4d9daf draft

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planemo upload for repository https://github.com/ARTbio/tools-artbio/tree/main/tools/facets commit 64ac36125f04497dd51028f307e059fca9ec0503
author artbio
date Sun, 05 Oct 2025 00:55:34 +0000
parents 66a56502199d
children 3f62267c4be7
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66a56502199d planemo upload for repository https://github.com/ARTbio/tools-artbio/tree/main/tools/facets commit 0176d2cc4f1caf0ab948ef72efb25ccce735461e
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1 <tool id="facets_analysis" name="FACETS Analysis" version="@TOOL_VERSION@+galaxy@VERSION_SUFFIX@" profile="@PROFILE@">
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2 <description>Performs allele-specific copy number analysis from a pileup file</description>
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3 <macros>
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4 <import>macros.xml</import>
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5 </macros>
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6 <expand macro="requirements"/>
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7 <expand macro="stdio"/>
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8 <command detect_errors="exit_code"><![CDATA[
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9 Rscript '${__tool_directory__}/facets_analysis.R'
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10 --pileup '$pileup'
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11 --sample_id '$pileup.name'
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12 --output_seg '$output_seg'
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13 --output_summary '$output_summary'
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14 --output_spider '$output_spider'
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15 --output_plots '$output_plots'
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16 --cval $cval
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17 --min_nhet $min_nhet
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18 --snp_nbhd $snp_nbhd
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19 --gbuild '$gbuild'
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20 ]]></command>
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21 <inputs>
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22 <param name="pileup" type="data" format="tabular.gz" label="FACETS Pileup File" help="Output from the 'SNP Pileup for FACETS' tool."/>
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24 <param name="cval" type="float" value="150" label="Critical value for segmentation (cval)" help="Higher values lead to fewer segments (less sensitive). Lower values are more sensitive."/>
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25 <param name="min_nhet" type="integer" value="25" label="Minimum number of heterozygous SNPs per segment" help="Ensures that segments are supported by sufficient allelic information."/>
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27 <param name="gbuild" type="select" label="Genome Build">
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28 <option value="hg38" selected="true">Human (hg38)</option>
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29 <option value="hg19">Human (hg19)</option>
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30 <option value="hg18">Human (hg18)</option>
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31 <option value="mm10">Mouse (mm10)</option>
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32 <option value="mm9">Mouse (mm9)</option>
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33 </param>
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35 <param name="snp_nbhd" type="integer" value="300" label="SNP neighborhood size (snp.nbhd)" help="Should match the --pseudo-snps distance used to generate the pileup file. Default is 300."/>
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36 </inputs>
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37 <outputs>
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38 <data name="output_seg" format="tsv" label="FACETS Segmentation on ${on_string}"/>
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39 <data name="output_summary" format="tabular" label="FACETS Summary on ${on_string}"/>
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40 <data name="output_plots" format="png" label="FACETS Plots on ${on_string}"/>
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41 <data name="output_spider" format="png" label="FACETS Spider Plot on ${on_string}"/>
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42
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43 </outputs>
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44 <tests>
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45 <test>
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46 <param name="pileup" value="Pileup.input_test_facets.csv.gz" ftype="tabular.gz"/>
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47 <output name="output_seg" file="test_sample_01.seg.tsv" ftype="tsv"/>
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48 <output name="output_summary" file="test_sample_01.summary.txt" ftype="tabular"/>
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49 <output name="output_plots" file="test_sample_01.plots.png" ftype="png" compare="sim_size" delta="20000"/>
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50 <output name="output_spider" file="test_sample_01.spider.png" ftype="png" compare="sim_size" delta="10000"/>
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51 </test>
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52 </tests>
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53 <help><![CDATA[
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54 **What it does**
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56 This tool runs the `FACETS` R package to perform allele-specific copy number and clonal heterogeneity analysis. It takes the compressed pileup file generated by the "SNP Pileup for FACETS" tool as its primary input.
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58 The main outputs are:
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59 - A **Segmentation file (TSV)** with the genomic coordinates of each segment and their associated copy number (TCN, LCN), purity, and ploidy.
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60 - A **Summary file** containing the main estimated parameters for the sample (purity, ploidy, etc.).
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61 - A **Plots file (PDF)** with standard FACETS visualizations for quality control and interpretation.
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62 ]]></help>
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63 <expand macro="citations"/>
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64 </tool>