comparison MetaProSIP.xml @ 7:8febc104e78c draft

planemo upload for repository https://github.com/galaxyproteomics/tools-galaxyp/tree/master/tools/openms commit f608f41d45664d04d3124c6ebc791bf8a566b3c5

6:96cc79adfadb

<?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

#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:

    "$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

  -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_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 &lt;= -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) "/>

    </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>

7:8febc104e78c

<?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="2.3.2">
  <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 detect_errors="aggressive"><![CDATA[
MetaProSIP

#if $param_in_mzML:
  -in_mzML $param_in_mzML
#end if

#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:

    "$param_plot_extension"
  #else
    $param_plot_extension
  #end if
#end if
-qc_output_directory images
#if $param_labeling_element:
  -labeling_element
  #if " " in str($param_labeling_element):
    "$param_labeling_element"
  #else

  -force
#end if
#end if
-threads "\${GALAXY_SLOTS:-1}"

## - add comment char to first line, 
## - remove leading/trailing spaces in fields
## - remove empty line(s) 
## - remove 'file://' and get basename of filenames in the table
## - add empty fields as '0' (MetaproSIP output has varying number of output columns, ie it omits the last columns if there are no values)
&& cat param_out_peptide_centric_csv | 
	sed '1 s/^/#/' | 
	sed 's/\t /\t/g; s/ \t/\t/g; s/ /_/g' | 
	grep -v "^$" | 
	sed "s/\tfile:\/\//\t/g; s/\t\/[^\t]\+\//\t/g; s/\.$param_plot_extension//g" | 
	awk -v FS='\t' 'BEGIN{line=0}{if(line==0){ncol=NF; print $0}else{printf("%s",$0); for(i=0; i<ncol-NF; i++){printf("\t0")}printf("\n")}line+=1}' > "$param_out_peptide_centric_csv"

## get html file (should be only one [?])

#if $param_collection or $param_plot_extension == 'pdf'
	&& rm -f images/*\.html
#else
	&& mv images/*\.html '${html_file}'
	&& mv images/ '${html_file.files_path}'
#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_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) "/>
    <param name="param_collection" type="boolean" checked="true" label="output images as collection" help="if enabled images are written to a collection amd to a webpage otherwise (pdf is always written to a collection)"/>
    <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 &lt;= -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) "/>

    </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 ${on_string}: peptide centric tabular"/>
    <data format="html" name="html_file" label="${tool.name} on ${on_string}: Webpage">
      <filter>not param_collection and (param_plot_extension == 'png' or param_plot_extension == 'svg')</filter>
    </data>
    <collection name="images" type="list" label="${tool.name} on ${on_string}: images">
      <filter>param_collection or 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" ftype="mzml"/>
      <param name="param_in_fasta" value="MetaProSIP_1_input.fasta" ftype="fasta"/>
      <param name="param_in_featureXML" value="MetaProSIP_1_input.featureXML" ftype="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"  compare="sim_size" lines_diff="2"/>
    </test>
  </tests>
  <help>Performs proteinSIP on peptide features for elemental flux analysis.

	  ** Galaxy specific notes **

	  The peptide centric tabular data set generated by the tool is not rendered properly by Galaxy, because it has more than 50 columns. You might extract columns of interst. 
  </help>
<expand macro="references"/>
</tool>