Mercurial > repos > artbio > mutational_patterns
view mutational_patterns.xml @ 21:8a5aaa97dbd6 draft
"planemo upload for repository https://github.com/ARTbio/tools-artbio/tree/master/tools/mutational_patterns commit 91415d0273efacfc605199a8fbebaf421da9df7e"
author | artbio |
---|---|
date | Wed, 20 Oct 2021 17:38:25 +0000 |
parents | a2cb7dc9250a |
children | 00be8f0b2c89 |
line wrap: on
line source
<tool id="mutational_patterns" name="Analyse Mutational Patterns/Signatures" version="3.2.0+galaxy6"> <description>from genomic variations in vcf files</description> <requirements> <requirement type="package" version="3.2.0=r41hdfd78af_0">bioconductor-mutationalpatterns</requirement> <requirement type="package" version="1.1.1l=h7f98852_0">openssl</requirement> <requirement type="package" version="3.3.5=r41hc72bb7e_0">r-ggplot2</requirement> <requirement type="package" version="1.6.6=r41hc72bb7e_1">r-optparse</requirement> <requirement type="package" version="0.2.20=r41h03ef668_1002">r-rjson</requirement> <requirement type="package" version="0.21.0=r41h03ef668_1004">r-nmf</requirement> <requirement type="package" version="2.3=r41hc72bb7e_1003">r-gridextra</requirement> <requirement type="package" version="1.4.3=r41hdfd78af_3">bioconductor-bsgenome.hsapiens.ucsc.hg19</requirement> <requirement type="package" version="1.4.3=r41hdfd78af_3">bioconductor-bsgenome.hsapiens.ucsc.hg38</requirement> <!-- install more bioconda genomes bioconductor-bsgenome.mmusculus.ucsc.mm9 bioconductor-bsgenome.mmusculus.ucsc.mm10 --> </requirements> <stdio> <exit_code range="1:" level="fatal" description="Tool exception" /> </stdio> <command detect_errors="exit_code"><![CDATA[ #import json #import os Rscript $__tool_directory__/mutational_patterns.R --inputs #set $filename_to_element_identifiers = {} #for $sample in $vcfs: $filename_to_element_identifiers.__setitem__(str($sample), $sample.element_identifier) #end for '#echo json.dumps(filename_to_element_identifiers)#' --genome '$genome' #if $set_levels.choices == 'yes': --levels '$set_levels.levels' #end if #if $set_spectrum.choices == 'yes': --output_spectrum '$spectrum' #end if #if $set_denovo.choices == 'yes': --nrun '$set_denovo.nrun' --rank '$set_denovo.rank' --newsignum '$set_denovo.newsignum' --output_denovo '$denovo' --sigmatrix '$sigmatrix' #end if #if $set_preset.choices == 'yes': #if $set_preset.set_signature_input.input_signature_choices == 'cosmic' --cosmic_version '$set_preset.set_signature_input.cosmic_version' #end if #if $set_preset.set_signature_input.input_signature_choices == 'user_signatures' --own_signatures '$set_preset.set_signature_input.own_matrix' #end if --signum '$set_preset.signum' --colors '$set_preset.colors' --output_sigpattern '$sig_contrib' #if $set_preset.contrib_matrix_out == 'yes' --sig_contrib_matrix '$sig_contrib_matrix' #end if #end if #if $rdata_out --rdata '$rdata' #end if --tooldir '$__tool_directory__/' ]]></command> <inputs> <param name="vcfs" type="data_collection" format="vcf" label="VCF file(s) collection" multiple="true"/> <param name="genome" type="select" label="Reference Genome"> <option value="BSgenome.Hsapiens.UCSC.hg19">BSgenome.Hsapiens.UCSC.hg19</option> <option value="BSgenome.Hsapiens.UCSC.hg38" selected="true">BSgenome.Hsapiens.UCSC.hg38</option> </param> <conditional name="set_levels"> <param name="choices" type="select" label="samples have levels/labels for grouping them in the analysis" display="radio" help="for instance, female/male or genotype-1/genotype-2/genotype-3, etc."> <option value="no" selected="true">No</option> <option value="yes">Yes</option> </param> <when value="yes"> <param name="levels" type="data" format="tabular" label="A two-column tab-separated file describing levels attributed to each sample name" help="Tip: the sample name list in the vcf collection can be obtained using the IUC Galaxy tool 'Extract element identifiers of a list collection' <br> example:<br> sample1 female<br> sample2 female<br> sample3 male<br> sample4 female<br> sample5 male<br> sample5 male" /> </when> <when value="no" /> </conditional> <conditional name="set_spectrum"> <param name="choices" type="select" label="Analyse Mutational Spectrum" display="radio"> <option value="yes" selected="true">Yes</option> <option value="no">No</option> </param> <when value="yes" /> <when value="no" /> </conditional> <conditional name="set_denovo"> <param name="choices" type="select" label="Extract de novo signatures with MutationalPatterns" display="radio"> <option value="yes">Yes</option> <option value="no" selected="true">No</option> </param> <when value="yes"> <param name="nrun" type="integer" value="10" min="10" max="200" label="Number of cycles to find best fitting of signatures" help="High values extend the computational time"/> <param name="rank" type="integer" value="4" min="3" max="30" label="Number of ranks to be displayed for control of optimal number of signature" help="High values extend the computational time. In addition the number of ranks cannot be greater than the number of available samples in the study"/> <param name="newsignum" type="integer" value="4" min="2" max="30" label="Number of de novo signatures to capture" help="High values extend the computational time. Note also that you cannot extract more signature than the number of available samples in the study"/> </when> <when value="no" /> </conditional> <conditional name="set_preset"> <param name="choices" type="select" label="Decompose with preset signatures" display="radio"> <option value="yes" selected="true">Yes</option> <option value="no">No</option> </param> <when value="yes"> <conditional name="set_signature_input"> <param name="input_signature_choices" type="select" label="type of signatures" display="radio"> <option value="cosmic" selected="true">COSMIC signatures</option> <option value="user_signatures">Use your own signature matrix</option> </param> <when value="cosmic"> <param name="cosmic_version" type="select" label="Version of the Cosmic signature set"> <option value="v2" selected="true">Cosmic v2, March 2015</option> <option value="v3">Cosmic v3, May 2019</option> <option value="v3.1">Cosmic v3.1, June 2020</option> <option value="v3.2">Cosmic v3.2, March 2021</option> </param> </when> <when value="user_signatures"> <param name="own_matrix" type="data" format="tabular" label="A tab-separated matrix describing elementary signatures" help="see https://cancer.sanger.ac.uk/signatures/documents/453/COSMIC_v3.2_SBS_GRCh38.txt for the required format" /> </when> </conditional> <param name="signum" type="integer" value="3" min="2" max="30" label="selects the N most significant signatures in samples to express mutational patterns" help="an integer between 2 and the number of elementary signatures in your signature matrix"/> <param name="contrib_matrix_out" type="select" label="Output Signature Contribution table ?" help="Output the normalized signatures contributions for further visualization" > <option value="no" selected="true">No</option> <option value="yes">Yes</option> </param> <param name="colors" type="select" label="Color set" display="radio"> <option value="brewer">RColorBrewer</option> <option value="intense" selected="true">Intense</option> </param> </when> <when value="no" /> </conditional> <param name="rdata_out" type="boolean" checked="false" label="Output RData file?" help="Output all the data used by R to construct the tables and plots, can be loaded into R" /> </inputs> <outputs> <data name="spectrum" format="pdf" label="Mutational Spectrum"> <filter>set_spectrum['choices'] == "yes"</filter> </data> <data name="denovo" format="pdf" label="De novo signatures"> <filter>set_denovo['choices'] == "yes"</filter> </data> <data name="sigmatrix" format="tabular" label="De novo signatures probability matrix"> <filter>set_denovo['choices'] == "yes"</filter> </data> <data name="sig_contrib" format="pdf" label="Signature contributions"> <filter>set_preset['choices'] == "yes"</filter> </data> <data name="sig_contrib_matrix" format="tabular" label="${tool.name}: Signature contribution table"> <filter>set_preset['choices'] == "yes" and set_preset['contrib_matrix_out'] == "yes"</filter> </data> <data name="rdata" format="rdata" label="${tool.name}: RData file"> <filter>rdata_out</filter> </data> </outputs> <tests> <!-- user defined (v3.2 restricted 30 minus 27) --> <test> <param name="vcfs"> <collection type="list"> <element name="6" value="F.vcf"/> <element name="7" value="G.vcf"/> <element name="8" value="H.vcf"/> <element name="9" value="I.vcf"/> </collection> </param> <param name="genome" value="BSgenome.Hsapiens.UCSC.hg38"/> <param name="levels" value="FGHI_levels.tab" ftype="tabular"/> <conditional name="set_spectrum"> <param name="choices" value="no"/> </conditional> <conditional name="set_denovo"> <param name="choices" value="no"/> </conditional> <conditional name="set_preset"> <param name="choices" value="yes"/> <conditional name="set_signature_input"> <param name="input_signature_choices" value="user_signatures" /> <param name="own_matrix" value="user_defined_signature.tsv" ftype="tabular"/> </conditional> <param name="contrib_matrix_out" value="yes" /> </conditional> <param name="signum" value="4" /> <output name="sig_contrib" file="user_output.pdf" compare="sim_size"/> <output name="sig_contrib_matrix" file="sig_contrib_table_user_defined.tsv" compare="sim_size"/> </test> <!-- cosmic v3.2 --> <test> <param name="vcfs"> <collection type="list"> <element name="6" value="F.vcf"/> <element name="7" value="G.vcf"/> <element name="8" value="H.vcf"/> <element name="9" value="I.vcf"/> </collection> </param> <param name="genome" value="BSgenome.Hsapiens.UCSC.hg38"/> <param name="levels" value="FGHI_levels.tab" ftype="tabular"/> <conditional name="set_spectrum"> <param name="choices" value="no"/> </conditional> <conditional name="set_denovo"> <param name="choices" value="no"/> </conditional> <conditional name="set_preset"> <param name="choices" value="yes"/> <conditional name="set_signature_input"> <param name="input_signature_choices" value="cosmic" /> <param name="cosmic_version" value="v3.2"/> </conditional> <param name="contrib_matrix_out" value="yes" /> </conditional> <param name="signum" value="3" /> <output name="sig_contrib" file="cosmic_output_v3.pdf" compare="sim_size"/> <output name="sig_contrib_matrix" file="sig_contrib_table_v3.tsv" compare="sim_size"/> </test> <!-- cosmic v2 --> <test> <param name="vcfs"> <collection type="list"> <element name="6" value="F.vcf"/> <element name="7" value="G.vcf"/> <element name="8" value="H.vcf"/> <element name="9" value="I.vcf"/> </collection> </param> <param name="genome" value="BSgenome.Hsapiens.UCSC.hg38"/> <param name="levels" value="FGHI_levels.tab" ftype="tabular"/> <conditional name="set_spectrum"> <param name="choices" value="no"/> </conditional> <conditional name="set_denovo"> <param name="choices" value="no"/> </conditional> <conditional name="set_preset"> <param name="choices" value="yes"/> <conditional name="set_signature_input"> <param name="input_signature_choices" value="cosmic" /> <param name="cosmic_version" value="v2"/> </conditional> <param name="contrib_matrix_out" value="yes" /> </conditional> <param name="signum" value="3" /> <output name="sig_contrib" file="cosmic_output1.pdf" compare="sim_size"/> <output name="sig_contrib_matrix" file="sig_contrib_table.tsv" compare="sim_size"/> </test> <!-- simple spectrum --> <test> <param name="vcfs"> <collection type="list"> <element name="1" ftype="vcf" value="G.vcf"/> <element name="2" ftype="vcf" value="H.vcf"/> </collection> </param> <param name="genome" value="BSgenome.Hsapiens.UCSC.hg38"/> <conditional name="set_levels"> <param name="choices" value="yes"/> </conditional> <param name="levels" value="GH_levels.tab" ftype="tabular"/> <conditional name="set_spectrum"> <param name="choices" value="yes"/> </conditional> <conditional name="set_denovo"> <param name="choices" value="no"/> </conditional> <conditional name="set_preset"> <param name="choices" value="no"/> </conditional> <output name="spectrum" file="spectrum_output1.pdf" compare="sim_size"/> </test> <!-- de novo signatures --> <test> <param name="vcfs"> <collection type="list"> <element name="6" value="F.vcf"/> <element name="7" value="G.vcf"/> <element name="8" value="H.vcf"/> <element name="9" value="I.vcf"/> </collection> </param> <param name="genome" value="BSgenome.Hsapiens.UCSC.hg38"/> <conditional name="set_spectrum"> <param name="choices" value="no"/> </conditional> <conditional name="set_denovo"> <param name="choices" value="yes"/> </conditional> <conditional name="set_preset"> <param name="choices" value="no"/> </conditional> <param name="nrun" value="10" /> <param name="rank" value="4" /> <param name="newsignum" value="4" /> <param name="rdata_out" value="true" /> <output name="denovo" file="denovo_output1.pdf" compare="sim_size"/> <output name="sigmatrix" file="sigmatrix.tab" compare="sim_size"/> <output name="rdata" file="denovo_1.RData" compare="sim_size" delta="400000"/> <!-- delta="170000" --> </test> </tests> <help> **What it does** This tool implement the R package MutationalPatterns to decompose mutations found in cancers in a linear combination of elementary mutational signatures, as first described by Alexandrov_ et al (2013) and recently improved in an update_ published in 2020. .. _Alexandrov: https://www.nature.com/articles/nature12477 .. _update: https://www.nature.com/articles/s41586-020-1943-3 Sets of elementary signatures found by analyzing large cohortes of patients are published in the COSMIC databases v2_ to v3.2_. You can choose among these COSMIC signature sets to analyse your own VCFs. In addition, you can use your own signature sets (or filtered COSMIC signature sets) since MutationalPatterns implements a method to extract elementary signatures from user-provided VCFs. **Inputs** * a collection of VCF files with somatic mutations calls from analysis of samples. * a tabular table describing the correspondance of sample names to levels of a factor (tissues, ages, sexes, etc.) **Outputs** This tool returns pdf files with various visualisations of : * the spectrum of single nucleotide mutation types * the absolute contribution of the elementary signatures in the samples * the relative contribution of the elementary signatures in the samples * an unrooted hierarchical clustering of the reconstructed samples with respect to the relative contribution of elementary signatures * the Cosine similarity between true samples and samples reconstructed with elementary signatures * pie charts displaying the relative contribution of the n most contributing elementary signatures in the reconstructed sample profiles .. _v2: https://cancer.sanger.ac.uk/signatures/signatures_v2/ .. _v3.2: https://cancer.sanger.ac.uk/signatures/sbs/ </help> <citations> <citation type="doi">10.18129/B9.bioc.MutationalPatterns</citation> <citation type="doi">10.1186/s13073-018-0539-0</citation> <citation type="doi">10.1038/nature12477</citation> <citation type="doi">10.1038/s41586-020-1943-3</citation> </citations> </tool>