diff mqppep_preproc.xml @ 5:b889e05ce77d draft default tip

planemo upload for repository https://github.com/galaxyproteomics/tools-galaxyp/tree/master/tools/mqppep commit aa5f4a19e76ec636812865293b8ee9b196122121
author galaxyp
date Fri, 17 Feb 2023 22:38:40 +0000
parents b76c75521d91
children
line wrap: on
line diff
--- a/mqppep_preproc.xml	Tue Feb 14 17:37:36 2023 +0000
+++ b/mqppep_preproc.xml	Fri Feb 17 22:38:40 2023 +0000
@@ -35,7 +35,7 @@
         --startCol '$startcol_script'
         --intervalCol $intervalCol
         --localProbCutoff $localProbCutoff
-        --collapse_func $collapse_func
+        --collapse_func $merge_function
         -o '$phosphoPepIntensities'
         --locProbCutoffGraph $locProbCutoffGraph
         --enrichGraph $enrichGraph
@@ -121,22 +121,17 @@
             <option value="st" selected="true">pST</option>
             <option value="y">pY</option>
         </param>
-        <param name="collapse_func" type="select"
+        <param name="merge_function" type="select"
                label="Intensity merge function"
                help="When a peptide is multiply phosphorylated, how should intensities be merged? [default: sum]"
                >
             <option value="sum" selected="true">sum</option>
-            <option value="mean">average</option>
+            <option value="average">average</option>
         </param>
         <param name="localProbCutoff" type="float" value="0.75" min="0" max="1.0"
                label="Localization Probability Cutoff"
                help="See help below for an explanation."
                />
-        <param name="merge_function" type="select" label="intensity merge-function"
-               help="Specifies how intensities for identical phosphosites should be merged">
-            <option value="sum" selected="true">sum</option>
-            <option value="average">average</option>
-        </param>
         <param name="protein_fasta" type="data" format="fasta" label="UniProtKB/SwissProt FASTA database"
                help="Sequence database; supply the same FASTA file as you supplied to by MaxQuant"
                />
@@ -187,7 +182,6 @@
             <param name="phosphoCol" value="^Number of Phospho [(][STY][STY]*[)]$"/>
             <param name="startCol" value="^Intensity[^_]"/>
             <param name="intervalCol" value="1"/>
-            <param name="collapse_func" value="sum"/>
             <param name="localProbCutoff" value="0.75"/>
             <param name="species" value="human"/>
 
@@ -252,7 +246,6 @@
             <param name="phosphoCol" value="^Number of Phospho [(][STY][STY]*[)]$"/>
             <param name="startCol" value="^Intensity[^_]"/>
             <param name="intervalCol" value="1"/>
-            <param name="collapse_func" value="sum"/>
             <param name="localProbCutoff" value="0.75"/>
             <param name="species" value="human"/>
 
@@ -355,7 +348,7 @@
   Minimum localization probability; see above.
 
 Intensity merge-function
-  Specifies how intensities for identical phosphosites should be merged; see above.
+  Specifies how intensities for identical phosphosites should be merged. Choosing "sum" means that relative intensities reflect number of phospho-*residues*; choosing "average" means that relative intensities reflect number of phospho-*peptides*.
 
 Output datasets
 ===============