Mercurial > repos > galaxyp > fasta_merge_files_and_filter_unique_sequences

changeset 3:1c12ec822e1b draft

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planemo upload for repository https://github.com/galaxyproteomics/tools-galaxyp/tree/master/tools/fasta_merge_files_and_filter_unique_sequences commit b4c90f4b5d7e9b233f1150dbc9e5dcbe156809e8
author galaxyp
date Mon, 24 Jul 2017 17:12:56 -0400
parents 7892a1fd1648
children c94c2b84221e
files fasta_merge_files_and_filter_unique_sequences.xml
diffstat 1 files changed, 23 insertions(+), 4 deletions(-) [+]
line wrap: on
line diff
--- a/fasta_merge_files_and_filter_unique_sequences.xml	Fri Feb 03 14:27:44 2017 -0500
+++ b/fasta_merge_files_and_filter_unique_sequences.xml	Mon Jul 24 17:12:56 2017 -0400
@@ -1,4 +1,4 @@
-<tool id="fasta_merge_files_and_filter_unique_sequences" name="FASTA Merge Files and Filter Unique Sequences" version="1.1">
+<tool id="fasta_merge_files_and_filter_unique_sequences" name="FASTA Merge Files and Filter Unique Sequences" version="1.2.0">
     <description>Concatenate FASTA database files together</description>
     <requirements>
         <requirement type="package" version="2.7.12">python</requirement>
@@ -6,12 +6,29 @@
     <command>
         python '$__tool_directory__/fasta_merge_files_and_filter_unique_sequences.py'
         '$output' $uniqueness_criterion '$accession_parser'
+
+        #if $batchmode.processmode == 'merge':
+          #set $inputs = $batchmode.input_fastas
+        #else:
+          #set $inputs = [ $batchmode.input_fastas ]
+        #end if
         #for $input in $inputs:
             '$input'
         #end for
     </command>
     <inputs>
-        <param name="inputs" format="fasta" multiple="True" type="data" label="Input FASTA files"/>
+        <conditional name="batchmode">
+            <param name="processmode" type="select" label="Run in batch mode?" help="The 'merge all' mode produces one output FASTA for all input FASTA files. The individual mode generates one FASTA file for each set of input FASTAs. For example, if the tool is given 2 collections of 10 FASTAs, it will merge the collections pairwise to create an output collection of 10 FASTAs." display="radio">
+                <option value="individual" selected="True">Merge individual FASTAs (output collection if input is collection)</option>
+                <option value="merge">Merge all FASTAs (always output a single FASTA)</option>
+            </param>
+            <when value="individual">
+                <param name="input_fastas" type="data" format="fasta" label="FASTA file" />
+            </when>
+            <when value="merge">
+                <param name="input_fastas" type="data" format="fasta" multiple="True" label="FASTA file" />
+            </when>
+        </conditional>
         <param name="uniqueness_criterion" type="select" label="How are sequences judged to be unique?">
             <option value="sequence" selected="true">Accession and Sequence</option>
             <option value="accession">Accession Only</option>
@@ -35,7 +52,8 @@
     </outputs>
     <tests>
         <test>
-          <param name="inputs" value="1.fa,2.fa" ftype="fasta" />
+          <param name="input_fastas" value="1.fa,2.fa" ftype="fasta" />
+          <param name="processmode" value="merge" />
           <param name="uniqueness_criterion" value="sequence" />
           <param name="accession_parser" value="^&gt;([^ |]+).*$" />
           <output name="output" file="res-sequence.fa" ftype="fasta" />
@@ -47,7 +65,8 @@
           </assert_stdout>
         </test>
         <test>
-          <param name="inputs" value="1.fa,2.fa" ftype="fasta" />
+          <param name="input_fastas" value="1.fa,2.fa" ftype="fasta" />
+          <param name="processmode" value="merge" />
           <param name="uniqueness_criterion" value="accession" />
           <param name="accession_parser" value="^&gt;([^ |]+).*$" />
           <output name="output" file="res-accession.fa" ftype="fasta" />