Mercurial > repos > galaxyp > openms_metaprosip
view MetaProSIP.xml @ 6:96cc79adfadb draft
planemo upload for repository https://github.com/galaxyproteomics/tools-galaxyp/tree/master/tools/openms commit 981be1bde91d6d565693cd691553f77465e653bb
author | galaxyp |
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date | Tue, 20 Mar 2018 14:37:53 -0400 |
parents | fdb3fbfef4cc |
children | 8febc104e78c |
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<?xml version='1.0' encoding='UTF-8'?> <!--This is a configuration file for the integration of a tools into Galaxy (https://galaxyproject.org/). This file was automatically generated using CTDConverter.--> <!--Proposed Tool Section: [Utilities]--> <tool id="MetaProSIP" name="MetaProSIP" version="2.3.1"> <description>Performs proteinSIP on peptide features for elemental flux analysis.</description> <macros> <token name="@EXECUTABLE@">MetaProSIP</token> <import>macros.xml</import> </macros> <expand macro="requirements"> <requirement type="package" version="3.4.1">r-base</requirement> <requirement type="package" version="3.0.1">r-gplots</requirement> </expand> <expand macro="stdio"/> <command><![CDATA[ MetaProSIP #if $param_in_mzML: -in_mzML $param_in_mzML #end if #if $param_in_fasta: -in_fasta $param_in_fasta #end if #if $param_out_csv: -out_csv $param_out_csv #end if #if $param_out_peptide_centric_csv: -out_peptide_centric_csv $param_out_peptide_centric_csv #end if #if $param_in_featureXML: -in_featureXML $param_in_featureXML #end if #if $param_mz_tolerance_ppm: -mz_tolerance_ppm $param_mz_tolerance_ppm #end if #if $param_rt_tolerance_s: -rt_tolerance_s $param_rt_tolerance_s #end if #if $param_intensity_threshold: -intensity_threshold $param_intensity_threshold #end if #if $param_correlation_threshold: -correlation_threshold $param_correlation_threshold #end if #if $param_xic_threshold: -xic_threshold $param_xic_threshold #end if #if $param_decomposition_threshold: -decomposition_threshold $param_decomposition_threshold #end if #if $param_weight_merge_window: -weight_merge_window $param_weight_merge_window #end if #if $param_plot_extension: -plot_extension #if " " in str($param_plot_extension): "$param_plot_extension" #else $param_plot_extension #end if #end if #if $param_plot_extension == 'pdf': -qc_output_directory images #else -qc_output_directory '${html_file.files_path}' #end if #if $param_labeling_element: -labeling_element #if " " in str($param_labeling_element): "$param_labeling_element" #else $param_labeling_element #end if #end if #if $param_use_unassigned_ids: -use_unassigned_ids #end if #if $param_use_averagine_ids: -use_averagine_ids #end if #if $param_report_natural_peptides: -report_natural_peptides #end if #if $param_filter_monoisotopic: -filter_monoisotopic #end if #if $param_cluster: -cluster #end if #if $adv_opts.adv_opts_selector=='advanced': #if $adv_opts.param_min_correlation_distance_to_averagine: -min_correlation_distance_to_averagine $adv_opts.param_min_correlation_distance_to_averagine #end if #if $adv_opts.param_pattern_15N_TIC_threshold: -pattern_15N_TIC_threshold $adv_opts.param_pattern_15N_TIC_threshold #end if #if $adv_opts.param_pattern_13C_TIC_threshold: -pattern_13C_TIC_threshold $adv_opts.param_pattern_13C_TIC_threshold #end if #if $adv_opts.param_pattern_2H_TIC_threshold: -pattern_2H_TIC_threshold $adv_opts.param_pattern_2H_TIC_threshold #end if #if $adv_opts.param_pattern_18O_TIC_threshold: -pattern_18O_TIC_threshold $adv_opts.param_pattern_18O_TIC_threshold #end if #if $adv_opts.param_heatmap_bins: -heatmap_bins $adv_opts.param_heatmap_bins #end if #if $adv_opts.param_observed_peak_fraction: -observed_peak_fraction $adv_opts.param_observed_peak_fraction #end if #if $adv_opts.param_min_consecutive_isotopes: -min_consecutive_isotopes $adv_opts.param_min_consecutive_isotopes #end if #if $adv_opts.param_score_plot_yaxis_min: -score_plot_yaxis_min $adv_opts.param_score_plot_yaxis_min #end if #if $adv_opts.param_collect_method: -collect_method #if " " in str($adv_opts.param_collect_method): "$adv_opts.param_collect_method" #else $adv_opts.param_collect_method #end if #end if #if $adv_opts.param_lowRIA_correlation_threshold: -lowRIA_correlation_threshold $adv_opts.param_lowRIA_correlation_threshold #end if #if $adv_opts.param_force: -force #end if #end if -threads "\${GALAXY_SLOTS:-1}" ## remove urls and paths (keeping the file name basename) && sed -i -e 's/file:\/\/[^[:space:]]\+\///g; s/\/[^[:space:]]\+\///g' $param_out_csv ## get html file (should be only one [?]) #if $param_plot_extension != 'pdf': && cp '${html_file.files_path}'/*\.html output.html #end if ]]></command> <inputs> <param name="param_in_mzML" type="data" format="mzml" optional="False" label="Centroided MS1 data" help="(-in_mzML) "/> <param name="param_in_fasta" type="data" format="fasta" optional="False" label="Protein sequence database" help="(-in_fasta) "/> <param name="param_in_featureXML" type="data" format="featurexml" optional="False" label="Feature data annotated with identifications (IDMapper)" help="(-in_featureXML) "/> <param name="param_mz_tolerance_ppm" type="float" value="10.0" label="Tolerance in ppm" help="(-mz_tolerance_ppm) "/> <param name="param_rt_tolerance_s" type="float" value="30.0" label="Rolerance window around feature rt for XIC extraction" help="(-rt_tolerance_s) "/> <param name="param_intensity_threshold" type="float" value="10.0" label="Intensity threshold to collect peaks in the MS1 spectrum" help="(-intensity_threshold) "/> <param name="param_correlation_threshold" type="float" value="0.7" label="Correlation threshold for reporting a RIA" help="(-correlation_threshold) "/> <param name="param_xic_threshold" type="float" value="0.7" label="Minimum correlation to mono-isotopic peak for retaining a higher isotopic peak" help="(-xic_threshold) If featureXML from reference file is used it should be disabled (set to -1) as no mono-isotopic peak is expected to be present"/> <param name="param_decomposition_threshold" type="float" value="0.7" label="Minimum R² of decomposition that must be achieved for a peptide to be reported" help="(-decomposition_threshold) "/> <param name="param_weight_merge_window" type="float" value="5.0" label="Decomposition coefficients within +- this rate window will be combined" help="(-weight_merge_window) "/> <param name="param_plot_extension" display="radio" type="select" optional="False" value="png" label="Extension used for plots (png|svg|pdf)" help="(-plot_extension) "> <option value="png" selected="true">png</option> <option value="svg">svg</option> <option value="pdf">pdf</option> </param> <param name="param_labeling_element" display="radio" type="select" optional="False" value="C" label="Which element (single letter code) is labeled" help="(-labeling_element) "> <option value="C" selected="true">C</option> <option value="N">N</option> <option value="H">H</option> <option value="O">O</option> </param> <param name="param_use_unassigned_ids" display="radio" type="boolean" truevalue="-use_unassigned_ids" falsevalue="" checked="false" optional="True" label="Include identifications not assigned to a feature in pattern detection" help="(-use_unassigned_ids) "/> <param name="param_use_averagine_ids" display="radio" type="boolean" truevalue="-use_averagine_ids" falsevalue="" checked="false" optional="True" label="Use averagine peptides as model to perform pattern detection on unidentified peptides" help="(-use_averagine_ids) "/> <param name="param_report_natural_peptides" display="radio" type="boolean" truevalue="-report_natural_peptides" falsevalue="" checked="false" optional="True" label="Whether purely natural peptides are reported in the quality report" help="(-report_natural_peptides) "/> <param name="param_filter_monoisotopic" display="radio" type="boolean" truevalue="-filter_monoisotopic" falsevalue="" checked="false" optional="True" label="Try to filter out mono-isotopic patterns to improve detection of low RIA patterns" help="(-filter_monoisotopic) "/> <param name="param_cluster" display="radio" type="boolean" truevalue="-cluster" falsevalue="" checked="false" optional="True" label="Perform grouping" help="(-cluster) "/> <expand macro="advanced_options"> <param name="param_min_correlation_distance_to_averagine" type="float" value="-1.0" label="Minimum difference in correlation between incorporation pattern and averagine pattern" help="(-min_correlation_distance_to_averagine) Positive values filter all RIAs passing the correlation threshold but that also show a better correlation to an averagine peptide. Disabled for values <= -1"/> <param name="param_pattern_15N_TIC_threshold" type="float" value="0.95" label="The most intense peaks of the theoretical pattern contributing to at least this TIC fraction are taken into account" help="(-pattern_15N_TIC_threshold) "/> <param name="param_pattern_13C_TIC_threshold" type="float" value="0.95" label="The most intense peaks of the theoretical pattern contributing to at least this TIC fraction are taken into account" help="(-pattern_13C_TIC_threshold) "/> <param name="param_pattern_2H_TIC_threshold" type="float" value="0.95" label="The most intense peaks of the theoretical pattern contributing to at least this TIC fraction are taken into account" help="(-pattern_2H_TIC_threshold) "/> <param name="param_pattern_18O_TIC_threshold" type="float" value="0.95" label="The most intense peaks of the theoretical pattern contributing to at least this TIC fraction are taken into account" help="(-pattern_18O_TIC_threshold) "/> <param name="param_heatmap_bins" type="integer" value="20" label="Number of RIA bins for heat map generation" help="(-heatmap_bins) "/> <param name="param_observed_peak_fraction" type="float" value="0.5" label="Fraction of observed/expected peaks" help="(-observed_peak_fraction) "/> <param name="param_min_consecutive_isotopes" type="integer" value="2" label="Minimum number of consecutive isotopic intensities needed" help="(-min_consecutive_isotopes) "/> <param name="param_score_plot_yaxis_min" type="float" value="0.0" label="The minimum value of the score axis" help="(-score_plot_yaxis_min) Values smaller than zero usually only make sense if the observed peak fraction is set to 0"/> <param name="param_collect_method" display="radio" type="select" optional="False" value="correlation_maximum" label="How RIAs are collected" help="(-collect_method) "> <option value="correlation_maximum" selected="true">correlation_maximum</option> <option value="decomposition_maximum">decomposition_maximum</option> </param> <param name="param_lowRIA_correlation_threshold" type="float" value="-1.0" label="Correlation threshold for reporting low RIA patterns" help="(-lowRIA_correlation_threshold) Disable and take correlation_threshold value for negative values"/> <param name="param_force" display="radio" type="boolean" truevalue="-force" falsevalue="" checked="false" optional="True" label="Overwrite tool specific checks" help="(-force) "/> </expand> </inputs> <outputs> <data name="param_out_csv" format="tabular" label="${tool.name} on ${on_string}: tabular"/> <data name="param_out_peptide_centric_csv" format="tabular" label="${tool.name} on ${on_string}: peptide centric tabular"/> <data format="html" name="html_file" from_work_dir="output.html" label="${tool.name} on ${on_string}: Webpage"> <filter>param_plot_extension == 'png' or param_plot_extension == 'svg'</filter> </data> <collection name="images" type="list" label="${tool.name} on ${on_string}: images"> <filter>param_plot_extension == 'pdf'</filter> <discover_datasets pattern="__name_and_ext__" directory="images" /> </collection> </outputs> <tests> <test> <param name="param_in_mzML" value="MetaProSIP_1_input.mzML"/> <param name="param_in_fasta" value="MetaProSIP_1_input.fasta"/> <param name="param_in_featureXML" value="MetaProSIP_1_input.featureXML"/> <output name="param_out_csv" file="MetaProSIP_1_output_1.csv" /> <output name="param_out_peptide_centric_csv" file="MetaProSIP_1_output_2.csv" /> </test> </tests> <help>Performs proteinSIP on peptide features for elemental flux analysis. For more information, visit http://ftp.mi.fu-berlin.de/OpenMS/release-documentation/html/UTILS_MetaProSIP.html</help> <expand macro="references"/> </tool>