Mercurial > repos > galaxyp > fragpipe
view macros.xml @ 3:da9ebef968bd draft default tip
planemo upload for repository https://github.com/galaxyproteomics/tools-galaxyp/tree/master/tools/fragpipe commit b1b03bb7cd31c1ec806b286d6c9444428b358e15
| author | galaxyp |
|---|---|
| date | Thu, 12 Sep 2024 08:06:44 +0000 |
| parents | ef46866326ef |
| children |
line wrap: on
line source
<macros> <import>msfragger_macros.xml</import> <token name="@TOOL_VERSION@">20.0</token> <token name="@VERSION_SUFFIX@">3</token> <xml name="requirements"> <requirements> <requirement type="package" version="@TOOL_VERSION@">fragpipe</requirement> </requirements> </xml> <!-- TMT-n uses the following n first labels from TMT-18 --> <token name="@TMT_LABELS@">['126', '127N', '127C', '128N', '128C', '129N', '129C', '130N', '130C', '131N', '131C', '132N', '132C', '133N', '133C', '134N', '134C', '135N']</token> <token name="@iTRAQ-4_LABELS@">['114', '115', '116', '117']</token> <token name="@iTRAQ-8_LABELS@">['113', '114', '115', '116', '117', '118', '119', '121']</token> <!-- User specifies input file format and selects sample files as are included by the scan_inputs macro User must also supply their own manifest file, a TSV file of the format: name, experiment, bioreplicate, data type --> <xml name="samples"> <param name="inputs" type="data" format="mzml,mzxml,thermo.raw" multiple="true" label="Proteomics Spectrum files" help="All input scan files must be named with one of the following extensions: .mzML, .mzXML, or .raw"/> <param name="input_prefix" type="text" value="" optional="true" label="File name prefix" help="Names inputs: prefix_rep#.mzXML Leave blank to use History names of inputs"> <validator type="regex" message="">[a-zA-Z][a-zA-Z0-9_-]*</validator> </param> <param name="manifest" type="data" format="tabular" label="Manifest file" help="TSV file with entries for each input scan file: Name (Name of input Galaxy history item. Extension in the name must be .mzML, .mzXML, or .raw.), Experiment (empty, alphanumeric, or _), Bioreplicate (empty or integer), Data type (DDA, DIA, GPF-DIA, DIA-Quant, or DIA-lib)"/> </xml> <!-- Prepares enviroment variables for FragPipe. --> <token name="@PREPARE_ENVIRONMENT@"><![CDATA[ env_location="\$(dirname \$(which philosopher))/.." && cp -r \${env_location}/share/fragpipe*/ fragpipe_local/ && mkdir .cache .config tmp && export XDG_CONFIG_HOME=\$(pwd)/.config && export XDG_CACHE_HOME=\$(pwd)/.cache && export JAVA_OPTS="\$JAVA_OPTS -Djava.io.tmpdir=\$(pwd)/tmp" && export LD_LIBRARY_PATH="\$LD_LIBRARY_PATH:/usr/local/lib" && ]]></token> <!-- Prepares input scan files. Scans and moved to a scan directory and linked. Annotation files are copied into the scan directory for TMT workflows. --> <token name="@LINK_SAMPLES@"><![CDATA[ CWD=\$(pwd | sed 's@/@\\/@g') && mkdir -p scans && #if $wf.workflow_name == "TMT10" or $wf.workflow_name == "TMT11" cp -p '$wf.annotation' 'scans/annotation.txt' && #end if sed "s@^@\$CWD/scans/@" $manifest > fp.manifest && #for $sf in $inputs #set $i_name = $ln_name($sf) ln -s '$sf' 'scans/${i_name}' && #end for ]]></token> <!-- Prepares input files, excluding database. --> <token name="@PREPARE_INPUTS@"><![CDATA[ mkdir -p outputs && @CMD_IMPORTS@ @LINK_SAMPLES@ ]]></token> <!-- Prepares database. First genericizes unknown sequence headers in the database. Then adds decoys, or decoys and contaminants depending on user selection. --> <token name="@PREPARE_DATABASE@"><![CDATA[ '$__tool_directory__/genericize_db.py' $database_name genericized_db.fas && #if str($database_options) != 'none' philosopher workspace --init && philosopher database --custom genericized_db.fas --prefix rev_ #if str($database_options) != 'decoy_and_contam' --contam #end if --contamprefix && ln -s *-decoys-*.fas final_db.fas && #else ln -s genericized_db.fas final_db.fas && #end if ]]></token> <!-- Prepares outputs. Creates log file symlink, makes a new directory for "combined" outputs and creates "concatenated" results. --> <token name="@PREPARE_OUTPUTS@"><![CDATA[ cd outputs && #if $output_options and 'combined_outputs' in $output_options mkdir combined_outputs && find . -name 'combined*tsv' | xargs -I {} mv {} combined_outputs && #end if ## For each category of results - psm, ion, peptide, protein - this loop concatenates results from each sample into a single result. ## For example, the entries sample1/psm.tsv and sample2/psm.tsv would be combined to concat_psm.tsv, a single psm.tsv header as its first line. for f in psm.tsv ion.tsv peptide.tsv protein.tsv; do n=0; for i in \$(find * -name \${f}); do d=\${i%/*}; if [[ \$n == 0 ]]; then awk 'NR==1{printf("Experiment\t%s\n",\$0);}' \$i > concat_\${f}; fi; awk 'NR>1{printf("'"\${d}"'\t%s\n",\$0);}' \$i >> concat_\${f}; t=\$(echo \${i} | tr '/' '.'); mv \${i} \${t}; n=\$((n+1)); done; done ]]></token> <!-- Input database for MSFragger --> <xml name="fragger_database"> <param name="database_name" type="data" format="fasta" label="Proteomics Search Database in FASTA format" help="Generic sequence headers in the input FASTA file that are not formatted according to the UniProt, NCBI, or ENSEMBL formats will be automatically prefixed with '>generic|' to avoid being misinterpreted by Philosopher."/> <!-- Whether to add decoys and contaminants to the database with Philosopher --> <param name="database_options" type="select" label="Decoys and contaminants" help="The default decoy prefix is "rev_"."> <option value="decoy_and_contam" selected="true">Add decoys and contaminants</option> <option value="decoy">Add decoys</option> <option value="none">Don't add decoys or contaminants</option> </param> <!-- Database may be split into chunks for performance benefits --> <param name="num_slices" type="integer" label="Split database" value="1" help="The number of chunks in which to split the database."/> </xml> <!-- The following macro allows users to select their FragPipe workfow. For a given workflow selection, the relevant parameter sections are expanded. Options specific to the selected workflow are passed to the parameter definitions in the expand element. The Galaxy parameters overwrite a workflow file provided by FragPipe for the selected workflow. As a result, any parameters that are not defined in the Galaxy tool will fall back on the FragPipe defaults for that workflow. This logic is defined in the <configfile> element. --> <xml name="workflow"> <conditional name="wf"> <param name="workflow_name" type="select" label="Workflow" help="Note: MSBooster is currently disabled in all Galaxy FragPipe workflows."> <option value="Default">Default</option> <option value="Open">Open</option> <option value="Nonspecific-HLA">Nonspecific-HLA</option> <option value="LFQ-MBR">LFQ-MBR</option> <option value="TMT10">TMT10</option> <option value="TMT11">TMT11</option> </param> <when value="Default"> <section name="msfragger" expanded="false" title="MSFragger Options"> <expand macro="msfragger_default"/> </section> <expand macro="validation" pep="false" perc="true" boost="false" no="false" masswidth="5" clevel="0" accmass="true" decoyprobs="true" nonparam="true" expectscore="true" ppm="true" combined_pepxml="false"/> <expand macro="label_free_quantification" yes="false" no="true"/> <expand macro="ptm_shepherd" yes="false" no="true" c="true" z="true"/> <expand macro="isobaric_quantification" yes="false" no="true"/> </when> <when value="Open"> <section name="msfragger" expanded="false" title="MSFragger Options"> <expand macro="msfragger_open"/> </section> <expand macro="validation" pep="true" perc="false" boost="false" no="false" masswidth="1000" clevel="-2" accmass="false" decoyprobs="true" nonparam="true" expectscore="true" ppm="false" combined_pepxml="true"> <expand macro="crystalc"/> </expand> <expand macro="label_free_quantification" yes="false" no="true"/> <expand macro="ptm_shepherd" yes="true" no="false"/> <expand macro="isobaric_quantification" yes="false" no="true" bridge="false" pool="true"/> </when> <when value="Nonspecific-HLA"> <section name="msfragger" expanded="false" title="MSFragger Options"> <expand macro="msfragger_nonspecific_HLA"/> </section> <expand macro="validation" pep="false" perc="true" boost="false" no="true" masswidth="5" clevel="0" accmass="true" decoyprobs="true" nonparam="true" expectscore="true" ppm="true" combined_pepxml="false"/> <expand macro="label_free_quantification" yes="false" no="true"/> <expand macro="ptm_shepherd" yes="false" no="true"/> <expand macro="isobaric_quantification" yes="false" no="true"/> </when> <when value="LFQ-MBR"> <section name="msfragger" expanded="false" title="MSFragger Options"> <expand macro="msfragger_LFQ_MBR"/> </section> <!-- MSBooster should be enabled once included in FragPipe Galaxy tool --> <expand macro="validation" pep="false" perc="true" boost="false" no="true" masswidth="5" clevel="0" accmass="true" decoyprobs="true" nonparam="true" expectscore="true" ppm="true" combined_pepxml="false"/> <expand macro="label_free_quantification" yes="true" no="false"/> <expand macro="ptm_shepherd" yes="false" no="true"/> <expand macro="isobaric_quantification" yes="false" no="true"/> </when> <when value="TMT10"> <expand macro="tmt_options" plex="TMT-10"/> </when> <!-- TMT11 is not in FragPipe GUI --> <when value="TMT11"> <expand macro="tmt_options" plex="TMT-11"/> </when> </conditional> </xml> <!-- Options for TMT workflows --> <xml name="tmt_options" token_plex=""> <param name="annotation" type="data" format="txt" optional="false" label="annotation file" help=""/> <section name="msfragger" expanded="false" title="MSFragger Options"> <expand macro="msfragger_TMT"/> </section> <expand macro="validation" pep="false" perc="true" boost="false" no="false" masswidth="5" clevel="0" accmass="true" decoyprobs="true" nonparam="true" expectscore="true" ppm="true" combined_pepxml="false" protp_minprob="0.5"/> <expand macro="isobaric_quantification" yes="true" no="false" plex="@PLEX@" level="2" ref_tag="Bridge" mod_tag="none"/> <expand macro="label_free_quantification" yes="false" no="true"/> <expand macro="ptm_shepherd" yes="false" no="true" token_unimod="false" token_common="true"/> </xml> <!-- Generates the FragPipe workflow--> <xml name="workflow_configfile"> <configfile name="workflow_configfile"><![CDATA[#slurp ## Create a fragpipe params dictionary from a file #set $comments = [] #set $wfdict = {} #set $wfpath = $__tool_directory__ + '/workflows/' + str($wf.workflow_name) + '.workflow' #set $fh = open($wfpath, 'r') #for $line in $fh: #if $line.startswith('#') #silent $comments.append($line) #elif $line.strip() != '' #set $kv = $line.strip().split('=') #if len($kv) < 2 #silent $kv.append('') #end if #set $wfdict[$kv[0]] = '='.join($kv[1:]) #end if #end for #set $wfdict['database.db-path'] = 'final_db.fas' #set $wfdict['msfragger.misc.slice-db'] = $num_slices ## Get the MSFragger Params (shared with the MSFragger tool) #set $prefix = $wf.msfragger @MSFRAGGER_PARAM_DICT@ #if len($vmods) > 0 #set $msfragger_dict['table.var-mods'] = '; '.join([$re.sub('^(.*,)(\d)$','\\1True,\\2',m) for m in $vmods]) #end if #for $k in $msfragger_dict.keys() #set $kv = $k + '=' + str($msfragger_dict[$k]) #set $wfk = 'msfragger.' + $k #set $wfdict[$wfk] = str($msfragger_dict[$k]) #end for @VALIDATION@ @PTM_SHEPHERD@ @LABEL_FREE_QUANTIFICATION@ @ISOBARIC_QUANTIFICATION@ ## Populate the workflow with configuration and comment dictionary entries populated by tool params. #for $comment in $comments $comment #end for #for $k in sorted($wfdict.keys()) #set $kv = $k + '=' + str($wfdict[$k]) $kv #end for #slurp]]></configfile> </xml> <!-- Percolator options --> <xml name="percolator"> <section name="percolator" expanded="true" title="Percolator"> <param name="keep_tsv_files" type="boolean" truevalue="true" falsevalue="false" checked="false" label="Keep intermediate files"/> <param name="min_prob" type="float" value="0.5" label="Minimum probability (default 0.5)"/> </section> </xml> <!-- Set Percolator workflow options --> <token name="@PERCOLATOR@"><![CDATA[ #set $prc = $wf.validation.validation_tab.psm_validation.percolator #set $wfdict['run-validation-tab'] = $wf.validation.validation_tab.run_validation #set $wfdict['peptide-prophet.run-peptide-prophet'] = 'false' #set $wfdict['percolator.run-percolator'] = 'true' #set $wfdict['percolator.keep-tsv-files'] = str($prc.keep_tsv_files) #set $wfdict['percolator.min-prob'] = str($prc.min_prob) ]]></token> <!-- Philosopher Report (phi-report) options --> <xml name="phi_report"> <conditional name="phi_report"> <param name="run_phi_report" type="select" label="Generate Philosopher Reports"> <option value="true" selected="true">Yes</option> <option value="false">No</option> </param> <when value="true"> <section name="phi_report_opts" expanded="false" title="FDR Filter and Report"> <param name="dont_use_prot_prophet_file" type="boolean" truevalue="true" falsevalue="false" checked="false"/> <param name="print_decoys" type="boolean" truevalue="true" falsevalue="false" checked="false"/> </section> </when> <when value="false"/> </conditional> </xml> <!-- Set Philosopher Report (phi-report) workflow options --> <token name="@PHIREPORT@"><![CDATA[ #set $prfx = $wf.validation.validation_tab.phi_report #if $prfx.run_phi_report == 'true' #set $wfdict['phi-report.run-report'] = 'true' #set $prfx = $wf.validation.validation_tab.phi_report.phi_report_opts #set $wfdict['phi-report.print-decoys'] = $prfx.print_decoys #else #set $wfdict['phi-report.run-report'] = 'false' #end if ]]></token> <!-- PeptideProphet options --> <xml name="peptide_prophet" token_masswidth="5" token_clevel="0" token_accmass="true" token_decoyprobs="true" token_nonparam="true" token_expectscore="true" token_ppm="true" token_combined_pepxml="false"> <section name="peptide_prophet" expanded="true" title="PeptideProphet"> <param name="combined_pepxml" type="boolean" truevalue="true" falsevalue="false" checked="@COMBINED_PEPXML@" label="Single combined pepxml per experiment or group"/> <param argument="--decoyprobs" type="boolean" truevalue="--decoyprobs" falsevalue="" checked="@DECOYPROBS@" label="compute possible non-zero probabilities for Decoy entries on the last iteration"/> <param argument="--ppm" type="boolean" truevalue="--ppm" falsevalue="" checked="@PPM@" label="use PPM mass error instead of Dalton for mass modeling"/> <param argument="--accmass" type="boolean" truevalue="--accmass" falsevalue="" checked="@ACCMASS@" label="use Accurate Mass model binning"/> <param argument="--nonparam" type="boolean" truevalue="--nonparam" falsevalue="" checked="@NONPARAM@" label="use semi-parametric modeling, must be used in conjunction with --decoy option"/> <param argument="--expectscore" type="boolean" truevalue="--expectscore" falsevalue="" checked="@EXPECTSCORE@" label="use expectation value as the only contributor to the f-value for modeling"/> <param argument="--masswidth" type="float" value="@MASSWIDTH@" label="model mass width (default 5)"/> <param argument="--clevel" type="integer" value="@CLEVEL@" label="set Conservative Level in neg_stdev from the neg_mean, low numbers are less conservative, high numbers are more conservative"/> <param argument="--glyc" type="boolean" truevalue="--glyc" falsevalue="" checked="false" label="enable peptide Glyco motif model"/> <param argument="--combine" type="boolean" truevalue="--combine" falsevalue="" checked="false" label="combine the results from PeptideProphet into a single result file" /> <param argument="--minpeplen" type="integer" value="7" label="minimum peptide length not rejected (default 7)" /> <param argument="--minprob" type="float" value="0.05" label="report results with minimum probability" /> <param argument="--nomass" type="boolean" truevalue="--nomass" falsevalue="" checked="false" label="disable mass model" /> <param argument="--nonmc" type="boolean" truevalue="--nonmc" falsevalue="" checked="false" label="disable NMC missed cleavage model" /> <param argument="--nontt" type="boolean" truevalue="--nontt" falsevalue="" checked="false" label="disable NTT enzymatic termini model" /> <param argument="--phospho" type="boolean" truevalue="--phospho" falsevalue="" checked="false" label="enable peptide phospho motif model" /> </section> </xml> <token name="@PEPTIDEPROPHET@"><![CDATA[ #set $prfx = $wf.validation.validation_tab.psm_validation.peptide_prophet #set $wfdict['peptide-prophet.run-peptide-prophet'] = 'true' #set $wfdict['peptide-prophet.combine-pepxml'] = str($prfx.combined_pepxml) #set $cmd_opts = [str($prfx.accmass),str($prfx.combine),str($prfx.decoyprobs),str($prfx.expectscore),str($prfx.glyc),str($prfx.nomass),str($prfx.nonmc),str($prfx.nonparam),str($prfx.nontt),str($prfx.phospho),str($prfx.ppm)] #silent $cmd_opts.append('--clevel ' + str($prfx.clevel)) #silent $cmd_opts.append('--masswidth ' + str($prfx.masswidth)) #silent $cmd_opts.append('--minpeplen ' + str($prfx.minpeplen)) #silent $cmd_opts.append('--minprob ' + str($prfx.minprob)) #set $wfdict['peptide-prophet.cmd-opts'] = ' '.join($cmd_opts).strip() ]]></token> <!-- CrystalC options --> <xml name="crystalc"> <param name="run_crystalc" type="boolean" truevalue="true" falsevalue="false" checked="true" label="Run Crystal-C" help="Recommend for open searches for additional resuts cleanup"/> </xml> <!-- MSBooster options. Disabled until DIA-NN integrated. <xml name="msbooster"> <section name="msbooster" expanded="false" title="MSBooster"> <param name="predict_rt" type="boolean" truevalue="true" falsevalue="false" checked="true" label="Predict RT"/> <param name="predict_spectra" type="boolean" truevalue="true" falsevalue="false" checked="true" label="Predict spectra"/> <param name="use_correlated_features" type="boolean" truevalue="true" falsevalue="false" checked="false" label="Use correlated features"/> </section> </xml> --> <!-- Protein Prophet options --> <xml name="protein_prophet" token_minprob="0.05"> <conditional name="protein_prophet"> <param name="run_protein_prophet" type="select" label="Run Protein Prophet"> <option value="true" selected="true">Yes</option> <option value="false">No</option> </param> <when value="true"> <section name="protein_prophet_opts" expanded="true" title="Protein Prophet"> <param argument="--iprophet" type="boolean" truevalue="--iprophet" falsevalue="" checked="false" label="input is from iProphet" /> <param argument="--maxppmdiff" type="integer" value="2000000" label="maximum peptide mass difference in ppm (default 2000000)" /> <param argument="--minprob" type="float" value="@MINPROB@" label="PeptideProphet probability threshold (default 0.05)" /> <param argument="--nonsp" type="boolean" truevalue="--nonsp" falsevalue="" checked="false" label="do not use NSP model" /> <param argument="--subgroups" type="boolean" truevalue="--subgroups" falsevalue="" checked="false" label="do not use NOGROUPS" /> <param argument="--unmapped" type="boolean" truevalue="--unmapped" falsevalue="" checked="false" label="report results for UNMAPPED proteins" /> </section> </when> <when value="false"/> </conditional> </xml> <!-- Set ProteinProphet workflow options --> <token name="@PROTEINPROPHET@"><![CDATA[ #set $prfx = $wf.validation.validation_tab.protein_prophet #if $prfx.run_protein_prophet == 'true' #set $prfx = $wf.validation.validation_tab.protein_prophet.protein_prophet_opts #set $wfdict['protein-prophet.run-protein-prophet'] = 'true' #set $cmd_opts = [str($prfx.iprophet),str($prfx.nonsp),str($prfx.subgroups),str($prfx.unmapped)] #silent $cmd_opts.append('--maxppmdiff ' + str($prfx.maxppmdiff)) #silent $cmd_opts.append('--minprob ' + str($prfx.minprob)) #set $wfdict['protein-prophet.cmd-opts'] = ' '.join($cmd_opts).strip() #else #set $wfdict[protein-prophet.run-protein-prophet] = 'false' #end if ]]></token> <!-- Validation options. Includes PeptideProphet, Percolator, MSBooster, ProteinProphet, and CrystalC --> <xml name="validation" token_expand="false" token_pep="false" token_perc="false" token_boost="false" token_no="true" token_masswidth="5" token_clevel="0" token_accmass="true" token_decoyprobs="true" token_nonparam="true" token_expectscore="true" token_ppm="true" token_combined_pepxml="false" token_protp_minprob="0.05"> <section name="validation" expanded="@EXPAND@" title="Validation"> <conditional name="validation_tab"> <param name="run_validation" type="select" label="Run Validation"> <option value="true" selected="true">Yes</option> <option value="false">No</option> </param> <when value="true"> <yield/> <!-- crystalc --> <conditional name="psm_validation"> <param name="run_psm_validation" type="select" label="PSM Validation"> <option value="peptide_prophet" selected="@PEP@">Run PeptideProphet</option> <option value="percolator" selected="@PERC@">Run Percolator</option> <!-- MSBooster disabled until DIA-NN integrated <option value="msbooster_percolator" selected="@BOOST@">Run MSBooster and Percolator</option> --> <option value="no" selected="@NO@">Use workflow values</option> </param> <when value="peptide_prophet"> <expand macro="peptide_prophet" masswidth="@MASSWIDTH@" clevel="@CLEVEL@" accmass="@ACCMASS@" decoyprobs="@DECOYPROBS@" nonparam="@NONPARAM@" expectscore="@EXPECTSCORE@" ppm="@PPM@" combined_pepxml="@COMBINED_PEPXML@"/> </when> <when value="percolator"> <expand macro="percolator"/> </when> <!-- MSBooster disabled until DIA-NN integrated <when value="msbooster_percolator"> <expand macro="msbooster"/> <expand macro="percolator"/> </when> --> <when value="no"> </when> </conditional> <expand macro="protein_prophet" minprob="@PROTP_MINPROB@"/> <expand macro="phi_report"/> </when> <when value="false"> </when> </conditional> </section> </xml> <!-- Set validation workflow options --> <token name="@VALIDATION@"><![CDATA[ #set $prfx = $wf.validation.validation_tab.psm_validation #if $prfx.run_psm_validation == 'peptide_prophet' #set $wfdict['run-psm-validation'] = 'true' #set $wfdict['msbooster.run-msbooster'] = 'false' #set $wfdict['percolator.run-percolator'] = 'false' @PEPTIDEPROPHET@ #elif $prfx.run_psm_validation == 'percolator' #set $wfdict['run-psm-validation'] = 'true' #set $wfdict['msbooster.run-msbooster'] = 'false' @PERCOLATOR@ ##elif $prfx.run_psm_validation == 'msbooster_percolator' # MSBooster disabled until DIA-NN integrated. #end if @PROTEINPROPHET@ @PHIREPORT@ ]]></token> <!-- PTM-Sheperd options --> <xml name="ptm_shepherd" token_expand="false" token_yes="true" token_no="false" token_a="false" token_b="true" token_c="false" token_x="false" token_y="true" token_z="false" token_unimod="true" token_common="false" token_glyco="false" token_custom="false"> <section name="ptms" expanded="false" title="PTMs"> <conditional name="ptm_shepherd"> <param name="run_ptm_shepherd" type="select" label="Run PTM Shepherd"> <option value="yes" selected="@YES@">yes</option> <option value="no" selected="@NO@">no</option> </param> <when value="yes"> <param name="output_extended" type="boolean" truevalue="true" falsevalue="false" checked="false" label="Extended output"/> <section name="ptm_profiling" expanded="false" title="PTM Profiling"> <param name="histo_smoothbins" type="integer" value="" min="0" optional="true" label="Smoothing factor" help="ptmshepherd.histo_smoothbins"/> <param name="precursor_mass_units" type="select" label="Precursor Mass tolerance units" help="ptmshepherd.precursor_mass_units"> <option value="1" selected="true">ppm</option> <option value="0" selected="false">Daltons</option> </param> <param name="precursor_tol" type="float" value="" min="0" optional="true" label="Precursor tolerance" help="ptmshepherd.precursor_tol"/> <param name="peakpicking_promRatio" type="float" value="" min="0" optional="true" label="Prominece ratio" help="ptmshepherd.peakpicking_promRatio"/> <param name="peakpicking_mass_units" type="select" label="Peakpicking Mass tolerance units" help="ptmshepherd.peakpicking_mass_units"> <option value="1" selected="true">ppm</option> <option value="0" selected="false">Daltons</option> </param> <param name="peakpicking_width" type="float" value="" min="0" optional="true" label="Peak picking width" help="ptmshepherd.peakpicking_width"/> <param name="peakpicking_minPsm" type="integer" value="" min="0" optional="true" label="Peak minimum PSMs" help="ptmshepherd.peakpicking_minPsm"/> <param name="spectra_ppmtol" type="float" value="" min="0" optional="true" label="Fragment Mass tolerance (PPM)" help="ptmshepherd.spectra_ppmtol"/> <param name="normalization" type="select" optional="true" label="Normalize data to" help="ptmshepherd.normalization-psms ptmshepherd.normalization-scans"> <option value="psms" selected="true">PSMs</option> <option value="scans" selected="false">MS2 scans</option> </param> <param name="varmod_masses" type="select" optional="true" label="Custom mass shifts" help="ptmshepherd.varmod_masses"> <option value="Failed_Carbamidomethylation\:-57.021464">Failed_Carbamidomethylation:-57.021464</option> </param> </section> <section name="ptm_annotation" expanded="true" title="PTM Annotation"> <param name="annotation_tol" type="float" value="" min="0" optional="true" label="Annotation tolerance (Da)" help="ptmshepherd.annotation_tol"/> <conditional name="annotation"> <param name="annotation_source" type="select" label="Annotation source" help="ptmshepherd.annotation"> <option value="unimod" selected="@UNIMOD@">Unimod</option> <option value="common" selected="@COMMON@">Common mass shifts</option> <option value="glyco" selected="@GLYCO@">Glyco mass shifts</option> <option value="custom" selected="@CUSTOM@">Custom annotation file</option> </param> <when value="unimod"/> <when value="common"/> <when value="glyco"/> <when value="custom"> <param name="annotation_file" type="data" format="txt" label="Custom annotation file"/> </when> </conditional> </section> <section name="ptm_localization" expanded="false" title="PTM Localization"> <param name="nions" type="select" multiple="true" optional="true" label="Use specified N-term ions" help="(default: a,b for CID, c for ETD)"> <option value="a" selected="@A@">a</option> <option value="b" selected="@B@">b</option> <option value="c" selected="@C@">c</option> </param> <param name="cions" type="select" multiple="true" optional="true" label="use specified C-term ions" help="(default: y for CID, z for ETD)"> <option value="x" selected="@X@">x</option> <option value="y" selected="@Y@">y</option> <option value="z" selected="@Z@">z</option> </param> <param name="spectra_maxfragcharge" type="integer" value="" min="0" optional="true" label="Max fragment charge" help="ptmshepherd.spectra_maxfragcharge"/> <param name="localization_background" type="integer" value="" min="0" optional="true" label="Localization background" help="ptmshepherd.localization_background"/> <param name="localization_allowed_res" type="select" label="Restrict localization to" help="ptmshepherd.localization_allowed_res"> <option value="" selected="true">none</option> <option value="all">all</option> <option value="N">N</option> <option value="ST">ST</option> </param> </section> <!-- Not yet implemented <section name="ion_discovery" expanded="false" title="Diagnostic Ion Discovery"> </section> <section name="glycan" expanded="false" title="Gyclan Assignment and FDR"> </section> --> </when> <when value="no"/> </conditional> </section> </xml> <!-- Set PTM-Sheperd workflow options --> <token name="@PTM_SHEPHERD@"><![CDATA[ #set $prfx = $wf.ptms.ptm_shepherd #if $prfx.run_ptm_shepherd == 'yes' #set $wfdict['ptmshepherd.run-shepherd'] = 'true' #set $cxt = $prfx.ptm_profiling #set $wfdict['ptmshepherd.output_extended'] = $prfx.output_extended #if $cxt.histo_smoothbins != '' #set $wfdict['ptmshepherd.histo_smoothbins'] = $cxt.histo_smoothbins #end if #if $cxt.precursor_tol != '' #set $wfdict['ptmshepherd.precursor_mass_units'] = $ctx.precursor_mass_units #set $wfdict['ptmshepherd.precursor_tol'] = $cxt.precursor_tol #end if #if $cxt.peakpicking_promRatio != '' #set $wfdict['ptmshepherd.peakpicking_promRatio'] = $cxt.peakpicking_promRatio #end if #if $cxt.peakpicking_width != '' #set $wfdict['ptmshepherd.peakpicking_mass_units'] = $ctx.peakpicking_mass_units #set $wfdict['ptmshepherd.peakpicking_width'] = $cxt.peakpicking_width #end if #if $cxt.peakpicking_minPsm != '' #set $wfdict['ptmshepherd.peakpicking_minPsm'] = $cxt.peakpicking_minPsm #end if #if $cxt.spectra_ppmtol != '' #set $wfdict['ptmshepherd.spectra_ppmtol'] = $cxt.spectra_ppmtol #end if #if $cxt.normalization != 'None' #if $cxt.normalization == "psms" #set $wfdict['ptmshepherd.normalization-psms'] = 'true' #set $wfdict['ptmshepherd.normalization-scans'] = 'false' #else #set $wfdict['ptmshepherd.normalization-psms'] = 'false' #set $wfdict['ptmshepherd.normalization-scans'] = 'true' #end if #end if #if $cxt.varmod_masses != 'None' #set $wfdict['ptmshepherd.varmod_masses'] = $cxt.varmod_masses #end if #set $cxt = $prfx.ptm_annotation #if $cxt.annotation_tol != '' #set $wfdict['ptmshepherd.annotation_tol'] = $cxt.annotation_tol #end if #if $cxt.annotation.annotation_source == 'unimod' #set $wfdict['ptmshepherd.annotation-unimod'] = 'true' #set $wfdict['ptmshepherd.annotation-common'] = 'false' #set $wfdict['ptmshepherd.annotation-glyco'] = 'false' #set $wfdict['ptmshepherd.annotation-custom'] = 'false' #elif $cxt.annotation.annotation_source == 'common' #set $wfdict['ptmshepherd.annotation-unimod'] = 'false' #set $wfdict['ptmshepherd.annotation-common'] = 'true' #set $wfdict['ptmshepherd.annotation-glyco'] = 'false' #set $wfdict['ptmshepherd.annotation-custom'] = 'false' #elif $cxt.annotation.annotation_source == 'glyco' #set $wfdict['ptmshepherd.annotation-unimod'] = 'false' #set $wfdict['ptmshepherd.annotation-common'] = 'false' #set $wfdict['ptmshepherd.annotation-glyco'] = 'true' #set $wfdict['ptmshepherd.annotation-custom'] = 'false' #elif $cxt.annotation.annotation_source == 'custom' #set $wfdict['ptmshepherd.annotation-unimod'] = 'false' #set $wfdict['ptmshepherd.annotation-common'] = 'false' #set $wfdict['ptmshepherd.annotation-glyco'] = 'false' #set $wfdict['ptmshepherd.annotation-custom'] = 'true' #set $wfdict['ptmshepherd.annotation_file'] = $cxt.annotation.annotation_file #end if #set $cxt = $prfx.ptm_localization #if $cxt.nions is not None #set $wfdict['ptmshepherd.iontype_a'] = str('a' in $cxt.nions).lower() #set $wfdict['ptmshepherd.iontype_b'] = str('b' in $cxt.nions).lower() #set $wfdict['ptmshepherd.iontype_c'] = str('c' in $cxt.nions).lower() #end if #if $cxt.cions is not None #set $wfdict['ptmshepherd.iontype_x'] = str('x' in $cxt.cions).lower() #set $wfdict['ptmshepherd.iontype_y'] = str('y' in $cxt.cions).lower() #set $wfdict['ptmshepherd.iontype_z'] = str('z' in $cxt.cions).lower() #end if #if $cxt.spectra_maxfragcharge != '' #set $wfdict['ptmshepherd.spectra_maxfragcharge'] = $cxt.spectra_maxfragcharge #end if #if $cxt.localization_background != '' #set $wfdict['ptmshepherd.localization_background'] = $cxt.localization_background #end if #set $wfdict['ptmshepherd.localization_allowed_res'] = $cxt.localization_allowed_res #else #set $wfdict['ptmshepherd.run-shepherd'] = 'false' #end if ]]></token> <token name="@RE_EXCLUDEMOD@">@RE_AA@,@RE_FLOAT@</token> <token name="@RE_EXCLUDEMODS@">@RE_EXCLUDEMOD@(;\s*@RE_EXCLUDEMOD@)*</token> <!-- Label-free quantification options --> <xml name="label_free_quantification" token_expand="false"> <section name="quant_ms1" expanded="@EXPAND@" title="Quant (MS1)"> <conditional name="label_free_quantification"> <param name="label_free_quantification_run" type="select" label="Perform Label-Free Quantification"> <option value="default" selected="true">Use workflow default</option> <option value="no">No Label-Free Quantification</option> <option value="ionquant">Run IonQuant</option> <option value="freequant">Run FreeQuant</option> </param> <when value="default"/> <when value="no"/> <when value="ionquant"> <section name="ionquant" expanded="false" title="IonQuant Label-Free Quantification"> <param name="mbr_select" type="select" optional="true" label="Match between runs (MBR)" help="ionquant.mbr"> <option value="0">No</option> <option value="1">Yes</option> </param> <param name="normalization" type="select" optional="true" label="Normalize" help="ionquant.normalization"> <option value="0">No</option> <option value="1">Yes</option> </param> <section name="feature_detection" expanded="false" title="Feature detection"> <param name="mztol" type="integer" value="" optional="true" label="m/z tolerance in ppm" help="ionquant.mztol (default 10)"/> <param name="rttol" type="float" value="" optional="true" label="RT tolerance (minutes)" help="ionquant.rttol (default 0.4)"/> <param name="imtol" type="float" value="" optional="true" label="IM tolerance (1/k0)" help="ionquant.imtol (default 0.05)"/> </section> <section name="mbr" expanded="false" title="Match between runs (MBR)"> <param name="mbrrttol" type="float" value="" optional="true" label="MBR RT tolerance (minutes)" help="ionquant.mbrrttol"/> <param name="mbrimtol" type="float" value="" optional="true" label="MBR IM tolerance (1/k0)" help="ionquant.mbrimtol"/> <param name="mbrmincorr" type="float" value="" optional="true" label="MBR min correlation" help="ionquant.mbrmincorr"/> <param name="mbrtoprun" type="integer" value="" optional="true" label="MBR top runs" help="ionquant.mbrtoprun"/> <param name="ionfdr" type="float" value="" min="0.00001" max="1.0" optional="true" label="MBR ion FDR" help="ionquant.ionfdr"/> <param name="peptidefdr" type="float" value="" min="0.00001" max="1.0" optional="true" label="MBR peptide FDR" help="ionquant.peptidefdr"/> <param name="proteinfdr" type="float" value="" min="0.00001" max="1.0" optional="true" label="MBR protein FDR" help="ionquant.proteinfdr"/> </section> <section name="topn" expanded="false" title="Top-N options"> <param name="tp" type="integer" value="" min="0" optional="true" label="Top N ions" help="ionquant.tp"/> <param name="minfreq" type="float" value="" min="0.0" max="1.0" optional="true" label="Min freq" help="ionquant.minfreq"/> <param name="minexps" type="integer" value="" optional="true" label="Min exps" help="ionquant.minexps"/> </section> <conditional name="labeling_conditional"> <param name="labeling_option" type="select" label="Labeling option"> <option value="lfq" selected="true">LFQ</option> <option value="labeling">Labeling</option> </param> <when value="lfq"> <section name="lfq" expanded="false" title="LFQ"> <param name="maxlfq" type="select" optional="true" label="MaxLFQ" help="ionquant.maxlfq"> <option value="0">No</option> <option value="1">Yes</option> </param> <param name="minions" type="integer" value="" optional="true" label="Min ions" help="ionquant.minions"/> </section> </when> <when value="labeling"> <section name="labeling" expanded="false" title="Labeling-based quant"> <param name="light" type="select" label="Light" help="ionquant.light"> <option value="" selected="true">none</option> <option value="C463.2366">C463.2366</option> <option value="C464.28596">C464.28596</option> <option value="C561.3387">C561.3387</option> <option value="K0;R0">K0;R0</option> </param> <param name="medium" type="select" label="Medium" help="ionquant.medium"> <option value="" selected="true">none</option> <option value="K4.025107;R6.020129">K4.025107;R6.020129</option> </param> <param name="heavy" type="select" label="Heavy" help="ionquant.heavy"> <option value="" selected="true">none</option> <option value="C467.2529">C467.2529</option> <option value="C470.29977">C470.29977</option> <option value="C567.3462">C567.3462</option> <option value="K8.014199;R10.008269">K8.014199;R10.008269</option> </param> <param name="requantify" type="select" label="Re-quantify" help="ionquant.requantify"> <option value="0">No</option> <option value="1" selected="true">Yes</option> </param> </section> </when> </conditional> <section name="advanced" expanded="false" title="Advanced options"> <param name="excludemods" type="text" optional="true" label="excludemods" help="ionquant.excludemods"> <validator type="regex">^\s*@RE_EXCLUDEMODS@\s*$</validator> </param> <param name="minscans" type="integer" value="" min="0" optional="true" label="Min scans" help="ionquant.minscans"/> <param name="minisotopes" type="integer" value="" min="1" max="3" optional="true" label="Min isotopes" help="ionquant.minisotopes"/> <param name="locprob" type="float" value="" min="0.0" max="1.0" optional="true" label="Min site probability" help="ionquant.locprob"/> <param name="writeindex" type="select" optional="true" label="Write index" help="ionquant.writeindex"> <option value="0">No</option> <option value="1">Yes</option> </param> </section> </section> </when> <when value="freequant"> <section name="freequant" expanded="false" title="IonQuant Label-Free Quantification"> <param name="rt_tol" type="float" value="" min="0" optional="true" label="RT Window (minutes)"/> <param name="mz_tol" type="integer" value="" min="1" optional="true" label="m/z Window (ppm)"/> </section> </when> </conditional> </section> </xml> <!-- Set label-free quantification workflow options --> <token name="@LABEL_FREE_QUANTIFICATION@"><![CDATA[ #set $prfx = $wf.quant_ms1.label_free_quantification #if $prfx.label_free_quantification_run == 'no' #set $wfdict['quantitation.run-label-free-quant'] = 'false' #elif $prfx.label_free_quantification_run == 'ionquant' #set $wfdict['quantitation.run-label-free-quant'] = 'false' #set $wfdict['ionquant.run-ionquant'] = 'true' #set $wfdict['freequant.run-freequant'] = 'false' #set $cxt = $prfx.ionquant #if $cxt.mbr_select != 'None' #set $wfdict['ionquant.mbr'] = $cxt.mbr_select #end if #if $cxt.normalization != 'None' #set $wfdict['ionquant.normalization'] = $cxt.normalization #end if #set $cxt = $prfx.ionquant.feature_detection #if $cxt.mztol != '' #set $wfdict['ionquant.mztol'] = $cxt.mztol #end if #if $cxt.rttol != '' #set $wfdict['ionquant.rttol'] = $cxt.rttol #end if #if $cxt.imtol != '' #set $wfdict['ionquant.imtol'] = $cxt.imtol #end if #set $cxt = $prfx.ionquant.mbr #if $cxt.mbrrttol != '' #set $wfdict['ionquant.mbrrttol'] = $cxt.mbrrttol #end if #if $cxt.mbrimtol != '' #set $wfdict['ionquant.mbrimtol'] = $cxt.mbrimtol #end if #if $cxt.mbrmincorr != '' #set $wfdict['ionquant.mbrmincorr'] = $cxt.mbrmincorr #end if #if $cxt.mbrtoprun != '' #set $wfdict['ionquant.mbrtoprun'] = $cxt.mbrtoprun #end if #if $cxt.ionfdr != '' #set $wfdict['ionquant.ionfdr'] = $cxt.ionfdr #end if #if $cxt.peptidefdr != '' #set $wfdict['ionquant.peptidefdr'] = $cxt.peptidefdr #end if #if $cxt.proteinfdr != '' #set $wfdict['ionquant.proteinfdr'] = $cxt.proteinfdr #end if #set $cxt = $prfx.ionquant.topn #if $cxt.tp != '' #set $wfdict['ionquant.tp'] = $cxt.tp #end if #if $cxt.minfreq != '' #set $wfdict['ionquant.minfreq'] = $cxt.minfreq #end if #if $cxt.minexps != '' #set $wfdict['ionquant.minexps'] = $cxt.minexps #end if #set $cxt = $prfx.ionquant.labeling_conditional #if $cxt.labeling_option == 'labeling' #set $cxt = $prfx.ionquant.labeling_conditional.labeling #set $wfdict['ionquant.use-labeling'] = 'true' #set $wfdict['ionquant.use-lfq'] = 'false' #set $wfdict['ionquant.light'] = $cxt.labeling.light #set $wfdict['ionquant.medium'] = $cxt.labeling.medium #set $wfdict['ionquant.heavy'] = $cxt.labeling.heavy #set $wfdict['ionquant.requantify'] = $cxt.labeling.requantify #else #set $cxt = $prfx.ionquant.labeling_conditional.lfq #set $wfdict['ionquant.use-labeling'] = 'false' #set $wfdict['ionquant.use-lfq'] = 'true' #if $cxt.maxlfq != 'None' #set $wfdict['ionquant.maxlfq'] = $cxt.maxlfq #end if #if $cxt.minions != '' #set $wfdict['ionquant.minions'] = $cxt.minions #end if #end if #set $cxt = $prfx.ionquant.advanced #if $cxt.excludemods != '' #set $wfdict['ionquant.excludemods'] = $cxt.excludemods #end if #if $cxt.minscans != '' #set $wfdict['ionquant.minscans'] = $cxt.minscans #end if #if $cxt.minisotopes != '' #set $wfdict['ionquant.minisotopes'] = $cxt.minisotopes #end if #if $cxt.locprob != '' #set $wfdict['ionquant.locprob'] = $cxt.locprob #end if #if $cxt.writeindex != 'None' #set $wfdict['ionquant.writeindex'] = $cxt.writeindex #end if #elif $prfx.label_free_quantification_run == 'freequant' #set $wfdict['quantitation.run-label-free-quant'] = 'false' #set $wfdict['ionquant.run-ionquant'] = 'false' #set $wfdict['freequant.run-freequant'] = 'true' #set $cxt = $prfx.freequant #if $cxt.rt_tol != '' #set $wfdict['freequant.rt-tol'] = $cxt.rt_tol #end if #if $cxt.mz_tol != '' #set $wfdict['freequant.mz-tol'] = $cxt.mz_tol #end if #end if ]]></token> <!-- Isobaric quantification options TMT-n uses the following n first labels from TMT-18 TMT-18 "126, 127N, 127C, 128N, 128C, 129N, 129C, 130N, 130C, 131N, 131C, 132N, 132C, 133N, 133C, 134N, 134C, 135N" iTRAQ-4 "114, 115, 116, 117" iTRAQ-8 "113, 114, 115, 116, 117, 118, 119, 121" --> <xml name="isobaric_quantification" token_expand="false" token_yes="true" token_no="false" token_plex="" token_level="2" token_virtual="false" token_pool="false" token_bridge="true"> <section name="quant_iso" expanded="@EXPAND@" title="Quant (Isobaric)"> <conditional name="isobaric_quantification"> <param name="isobaric_quantification_step" type="select" label="Perform Isobaric Quantification"> <option value="default">Use workflow defaults</option> <option value="yes" selected="@YES@">yes</option> <option value="no" selected="@NO@">no</option> </param> <when value="default"/> <when value="no"/> <when value="yes"> <section name="options" expanded="true" title="Isobaric Quantification"> <param name="quant_level" type="integer" value="@LEVEL@" min="1" max="3" label="MS level for the quantification"/> <param name="channel_num" type="text" value="@PLEX@" optional="true" label="Number of channels"> <validator type="regex" message="">^TMT-\d?</validator> </param> <param name="ref_tag" type="select" label="Set Unique tag to identify reference channels"> <help>Virtual or specify a Reference sample tag: pool or Bridge</help> <option value="Virtual" selected="@VIRTUAL@">Virtual - Add an artificial reference channel</option> <option value="pool" selected="@POOL@">pool</option> <option value="Bridge" selected="@BRIDGE@">Bridge</option> </param> <param name="groupby" type="select" optional="true" label="Group by level of summarization"> <option value="0">Gene level</option> <option value="1">Protein</option> <option value="2">Peptide sequence</option> <option value="3">Multiple PTM sites</option> <option value="4">Single PTM site</option> <option value="-1">All</option> </param> <param name="log2transformed" type="boolean" truevalue="true" falsevalue="false" checked="true" label="Log2 transform the intensity"/> <param name="prot_norm" type="select" optional="true" label="normalization"> <option value="0">None</option> <option value="1">MC (median centering)</option> <option value="2">GN (median centering + variance scaling)</option> <option value="-1">generate reports with all normalization options</option> </param> <conditional name="glycan_conditional"> <param name="use_glycan_composition" type="select" label="Perform Isobaric Quantification"> <option value="default">Use workflow defaults</option> <option value="yes">yes</option> </param> <when value="default"/> <when value="yes"> <param name="mod_tag" type="select" optional="true" label="PTM Mod tag"> <option value="none">none</option> <option value="N-glyco">N-glyco</option> <option value="C(239.1629)">C(239.1629)</option> <option value="K(-187.1524)">K(-187.1524)</option> <option value="K(-262.1966)">K(-262.1966)</option> <option value="K(114.0429),K(-115.12)">K(114.0429),K(-115.12)</option> <option value="S(79.9663),T(79.9663),Y(79.9663)">S(79.9663),T(79.9663),Y(79.9663)</option> </param> <param name="min_site_prob" type="float" min="-1.0" max="1.0" optional="true" label="Minimum site probability"> <help>site localization confidence thresholdr: -1 for global, 0 for search engine determined, above 0 for probability</help> </param> <param name="glyco_qval" type="integer" value="-1" optional="true" label="Glycan FDR filter"/> </when> </conditional> <param name="unique_gene" type="select" optional="true" label="Peptide-Gene uniqueness"> <option value="0">0: allow all PSMs</option> <option value="1">1: remove PSMs mapping to more than one GENE with evidence of expression in the dataset</option> <option value="2">2: remove all PSMs mapping to more than one GENE in the fasta file</option> </param> <param name="unique_pep" type="select" optional="true" label="Peptide-Protein uniqueness"> <option value="false">unique plus razor peptides</option> <option value="true">allow PSMs with unique peptides only</option> </param> <param name="min_pep_prob" type="float" min="0" max="1.0" optional="true" label="only use PSMs with a minimum probability score" help="minimum PSM probability threshold (in addition to FDR-based filtering by Philosopher)"/> <param name="min_purity" type="float" min="0" max="1.0" optional="true" label="ion purity threshold (default 0.5)"/> <param name="min_percent" type="float" min="0" max="1.0" optional="true" label="ignore the lower % PSMs based on their summed abundances" help="e.g. value of 0.05 indicates removal of PSMs with the summed TMT reporter ions intensity in the lowest 5% of all PSMs"/> <param name="max_pep_prob_thres" type="float" min="0" max="1.0" optional="true" label="threshold for maximum peptide probability"/> <param name="min_ntt" type="integer" min="0" max="2" optional="true" label="minimum allowed number of enzymatic termini"/> <param name="aggregation_method" type="select" optional="true" label="the aggregation method from the PSM level to the specified level"> <option value="0">0: median</option> <option value="1">1: weighted-ratio</option> </param> <param name="prot_exclude" type="text" optional="true" label="Exclude proteins with specified tags at the beginning of the accession number" help="e.g. none: no exclusion; sp|,tr| : exclude protein with sp| or tr|"> <validator type="regex">^(none|[a-zA-Z]+\|)$</validator> </param> <param name="best_psm" type="select" optional="true" label="keep the best PSM only (highest summed TMT intensity) among all redundant PSMs within the same LC-MS run"> <option value="true">Yes</option> <option value="false">No</option> </param> <param name="psm_norm" type="select" optional="true" label="perform additional retention time-based normalization at the PSM level"> <option value="false">No</option> <option value="true">Yes</option> </param> <param name="allow_overlabel" type="select" optional="true" label="allow PSMs with TMT on S (when overlabeling on S was allowed in the database search)"> <option value="true">Yes</option> <option value="false">No</option> </param> <param name="allow_unlabeled" type="select" optional="true" label="allow PSMs without TMT tag or acetylation on the peptide n-terminus"> <option value="true">Yes</option> <option value="false">No</option> </param> <param name="outlier_removal" type="select" optional="true" label="perform outlier removal"> <option value="true">Yes</option> <option value="false">No</option> </param> <param name="ms1_int" type="select" optional="true" label="MS1 precursor ion intensity for reference sample abundance estimation"> <option value="true">Yes - use MS1 precursor ion intensity</option> <option value="false">No - use MS2 reference intensity</option> </param> <param name="tolerance" type="integer" optional="true" label="Tolerance"/> <param name="top3_pep" type="select" optional="true" label="use top 3 most intense peptide ions as part of the reference sample abundance estimation"> <option value="true">Yes</option> <option value="false">No</option> </param> <param name="print_RefInt" type="select" optional="true" label="print individual reference sample abundance estimates for each multiplex in the final reports"> <option value="false">No</option> <option value="true">Yes</option> </param> </section> </when> </conditional> </section> </xml> <!-- Set isobaric quantification workflow options --> <token name="@ISOBARIC_QUANTIFICATION@"><![CDATA[ #set $prfx = $wf.quant_iso.isobaric_quantification #if $prfx.isobaric_quantification_step == 'no' #set $wfdict['tmtintegrator.run-tmtintegrator'] = 'false' #elif $prfx.isobaric_quantification_step == 'yes' #set $wfdict['tmtintegrator.run-tmtintegrator'] = 'true' #set $wfdict['tmtintegrator.dont-run-fq-lq'] = 'false' #set $cxt = $prfx.options #set $wfdict['tmtintegrator.quant_level'] = $cxt.quant_level #set $wfdict['tmtintegrator.channel_num'] = $cxt.channel_num #if $cxt.ref_tag == 'Virtual' #set $wfdict['tmtintegrator.add_Ref'] = -1 #else #set $wfdict['tmtintegrator.add_Ref'] = 1 #set $wfdict['tmtintegrator.ref_tag'] = $cxt.ref_tag #end if #if $cxt.groupby != '' #set $wfdict['tmtintegrator.groupby'] = $cxt.groupby #end if #set $wfdict['tmtintegrator.log2transformed'] = $cxt.log2transformed #if $cxt.prot_norm != 'None' #set $wfdict['tmtintegrator.prot_norm'] = $cxt.prot_norm #end if #if $cxt.glycan_conditional.use_glycan_composition == 'yes' #if $cxt.glycan_conditional.mod_tag != 'None' #set $wfdict['tmtintegrator.mod_tag'] = $cxt.glycan_conditional.mod_tag #end if #if $cxt.glycan_conditional.min_site_prob != '' #set $wfdict['tmtintegrator.min_site_prob'] = $cxt.glycan_conditional.min_site_prob #end if #if $cxt.glycan_conditional.glyco_qval != '' #set $wfdict['tmtintegrator.glyco_qval'] = $cxt.glycan_conditional.glyco_qval #end if #end if #if $cxt.unique_gene != 'None' #set $wfdict['tmtintegrator.unique_gene'] = $cxt.unique_gene #end if #if $cxt.unique_pep != 'None' #set $wfdict['tmtintegrator.unique_pep'] = $cxt.unique_pep #end if #if $cxt.min_pep_prob != '' #set $wfdict['tmtintegrator.min_pep_prob'] = $cxt.min_pep_prob #end if #if $cxt.min_purity != '' #set $wfdict['tmtintegrator.min_purity'] = $cxt.min_purity #end if #if $cxt.min_percent != '' #set $wfdict['tmtintegrator.min_percent'] = $cxt.min_percent #end if #if $cxt.max_pep_prob_thres != '' #set $wfdict['tmtintegrator.max_pep_prob_thres'] = $cxt.max_pep_prob_thres #end if #if $cxt.min_ntt != '' #set $wfdict['tmtintegrator.min_ntt'] = $cxt.min_ntt #end if #if $cxt.aggregation_method != 'None' #set $wfdict['tmtintegrator.aggregation_method'] = $cxt.aggregation_method #end if #if $cxt.prot_exclude != '' #set $wfdict['tmtintegrator.prot_exclude'] = $cxt.prot_exclude #end if #if $cxt.best_psm != 'None' #set $wfdict['tmtintegrator.best_psm'] = $cxt.best_psm #end if #if $cxt.psm_norm != 'None' #set $wfdict['tmtintegrator.psm_norm'] = $cxt.psm_norm #end if #if $cxt.allow_overlabel != 'None' #set $wfdict['tmtintegrator.allow_overlabel'] = $cxt.allow_overlabel #end if #if $cxt.allow_unlabeled != 'None' #set $wfdict['tmtintegrator.allow_unlabeled'] = $cxt.allow_unlabeled #end if #if $cxt.outlier_removal != 'None' #set $wfdict['tmtintegrator.outlier_removal'] = $cxt.outlier_removal #end if #if $cxt.ms1_int != 'None' #set $wfdict['tmtintegrator.ms1_int'] = $cxt.ms1_int #end if #if $cxt.tolerance != '' #set $wfdict['tmtintegrator.tolerance'] = $cxt.tolerance #end if #if $cxt.top3_pep != 'None' #set $wfdict['tmtintegrator.top3_pep'] = $cxt.top3_pep #end if #if $cxt.print_RefInt != 'None' #set $wfdict['tmtintegrator.print_RefInt'] = $cxt.print_RefInt #end if #end if ]]></token> <!-- License agreement texts. --> <token name="@MSFRAGGER_LICENSE_AGREEMENT@"> MSFragger is available freely for academic research and educational purposes only. I have read the ACADEMIC license for MSFragger software: http://msfragger-upgrader.nesvilab.org/upgrader/MSFragger-LICENSE.pdf. This license provides with non-exclusive, non-transferable right to use MSFragger solely for academic research, non-commercial or educational purposes. I agree to be subject to the terms and conditions of this license. I understand that to use MSFragger for other purposes requires a commercial license from the University of Michigan Office of Tech Transfer. </token> <token name="@IONQUANT_LICENSE_AGREEMENT@"> IonQuant is available freely for academic research and educational purposes only. I have read the ACADEMIC license for MSFragger software: https://msfragger.arsci.com/ionquant/IonQuant%20Academic%20Use%20License%2005162022.pdf </token> <token name="@THERMO_RAW_READER_LICENSE_AGREEMENT@"> I agree to the terms of Thermo (c) Raw File Reader License Agreement: http://msfragger-upgrader.nesvilab.org/upgrader/RawFileRdr_License_Agreement_RevA.pdf </token> <token name="@BRUKER_LICENSE_AGREEMENT@"> I agree to the terms of Bruker SDK library distribution conditions: http://msfragger-upgrader.nesvilab.org/upgrader/redist.txt </token> <token name="@LICENSE_AGREEMENTS@"> @MSFRAGGER_LICENSE_AGREEMENT@ @IONQUANT_LICENSE_AGREEMENT@ @THERMO_RAW_READER_LICENSE_AGREEMENT@ @BRUKER_LICENSE_AGREEMENT@ </token> <!-- User must check box agreeing to MSFragger license agreement. --> <xml name="license_agreements"> <param name="license_agreements" type="boolean" truevalue="true" falsevalue="false" checked="false" label="I understand that these tools, including MSFragger, IonQuant, Bruker, and Thermo Raw File Reader, are available freely for academic research and educational purposes only, and agree to the following terms."> <validator type="expression" message="You must agree to the MSFragger license!">value == True</validator> <help><![CDATA[ @MSFRAGGER_LICENSE_AGREEMENT@ <br/><br/> @IONQUANT_LICENSE_AGREEMENT@ <br/><br/> @THERMO_RAW_READER_LICENSE_AGREEMENT@ <br/><br/> @BRUKER_LICENSE_AGREEMENT@ ]]></help> </param> </xml> <xml name="citations"> <citations> <citation type="doi">10.1038/s41592-020-0912-y</citation> <citation type="doi">10.1038/nmeth.4256</citation> <citation type="doi">10.1038/s41467-020-17921-y</citation> <citation type="doi">10.1038/s41592-020-0967-9</citation> <citation type="doi">10.1021/acs.jproteome.0c00119</citation> <citation type="doi">10.1074/mcp.TIR120.002216</citation> <citation type="doi">10.1074/mcp.TIR120.002048</citation> <citation type="doi">10.1016/j.mcpro.2021.100077</citation> <citation type="doi">10.1021/acs.jproteome.0c00544</citation> <citation type="doi">10.1038/nmeth.3255</citation> <yield /> </citations> </xml> </macros>