Repository 'quast'
hg clone https://toolshed.g2.bx.psu.edu/repos/iuc/quast

Changeset 15:72472698a2df (2023-03-02)
Previous changeset 14:3061c8b029e5 (2022-08-05) Next changeset 16:a3b35edea53a (2024-11-12)
Commit message:
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/quast commit 617a2c388e73d6c93a2a1db9a58b914510052b69
modified:
macros.xml
quast.xml
b
diff -r 3061c8b029e5 -r 72472698a2df macros.xml
--- a/macros.xml Fri Aug 05 15:21:27 2022 +0000
+++ b/macros.xml Thu Mar 02 10:38:54 2023 +0000
b
@@ -1,6 +1,6 @@
 <macros>
     <token name="@TOOL_VERSION@">5.2.0</token>
-    <token name="@VERSION_SUFFIX@">0</token>
+    <token name="@VERSION_SUFFIX@">1</token>
     <token name="@PROFILE@">21.01</token>
     <xml name="requirements">
         <requirements>
@@ -15,7 +15,7 @@
         </xrefs>
     </xml>
     <xml name="gene_thresholds">
-        <param name="gene_thresholds" argument="--gene-thresholds" type="text" value="0,300,1500,3000" label="Comma-separated list of thresholds (in bp) for gene lengths to find with a finding tool"/>
+        <param argument="--gene-thresholds" type="text" value="0,300,1500,3000" label="Comma-separated list of thresholds (in bp) for gene lengths to find with a finding tool"/>
     </xml>
     <xml name="citations">
         <citations>
@@ -26,7 +26,28 @@
         </citations>
     </xml>
     <xml name="min_identity_macros" token_value="">
-        <param argument="--min-identity" type="float" value="@VALUE@" min="80" max="100" label="Minimum IDY% considered as proper alignment" help="Alignments with IDY% worse than this value will be filtered. Note that all alignments
-            with IDY% less than 80.0% will be filtered regardless of this threshold. "/>
+        <param argument="--min-identity" type="float" value="@VALUE@" min="80" max="100" label="Minimum IDY% considered as proper alignment" help="Alignments with IDY% worse than this value will be filtered. Note that all alignments with IDY% less than 80.0% will be filtered regardless of this threshold. "/>
+    </xml>
+    <xml name="custom">
+        <param name="custom" type="select" label="Use customized names for the input files?" help="They will be used in reports, plots and logs">
+            <option value="true">Yes, specify custom names</option>
+            <option value="false" selected="true">No, use dataset names</option>
+        </param>
+    </xml>
+    <xml name="labelled_input">
+        <param name="input" type="data" format="fasta" label="Contigs/scaffolds file"/>
+        <param argument="--labels" type="text" value="" label="Name"/>
+    </xml>
+    <xml name="reads_option">
+        <param name="reads_option" type="select" label="Reads options" help="Currently, the supported read types are Illumina unpaired, paired-end and mate-pair reads, PacBio SMRT, and Oxford Nanopore long reads.">
+            <option value="disabled">Disabled</option>
+            <option value="single">Illumina single-end reads</option>
+            <option value="paired">Illumina paired-end reads</option>
+            <option value="paired_collection">Illumina paired-end reads in paired collection</option>
+            <option value="paired_interlaced">Illumina interlaced paired-end reads</option>
+            <option value="mate_paired">Illumina mate-pair reads</option>
+            <option value="pacbio">Pacbio SMRT reads</option>
+            <option value="nanopore">Nanopore reads</option>
+        </param>
     </xml>
 </macros>
b
diff -r 3061c8b029e5 -r 72472698a2df quast.xml
--- a/quast.xml Fri Aug 05 15:21:27 2022 +0000
+++ b/quast.xml Thu Mar 02 10:38:54 2023 +0000
[
b"@@ -10,19 +10,31 @@\n #import re\n #import os\n \n-#if str($in.custom) == 'false'\n-    #set $labels = ','.join( [re.sub('[^\\w\\-_]', '_', str($x.element_identifier)) for $x in $in.inputs])\n+#if str($mode.in.custom) == 'false'\n+    #if $mode.mode == 'individual'\n+        #set $labels = re.sub('[^\\w\\-_]', '_', str($mode.in.inputs.element_identifier))\n+    #else\n+        #set $labels = ','.join( [re.sub('[^\\w\\-_]', '_', str($x.element_identifier)) for $x in $mode.in.inputs])\n+    #end if\n echo $labels &&\n #else\n-    #set $labels = []\n-    #for $x in $in.inputs\n-        #if str($x.labels) != ''\n-            #silent $labels.append(re.sub('[^\\w\\-_]', '_', str($x.labels)))\n+    #if $mode.mode == 'individual'\n+        #if str($mode.in.labels) != ''\n+            #set $labels = re.sub('[^\\w\\-_]', '_', str($mode.in.labels))\n         #else\n-            #silent $labels.append(re.sub('[^\\w\\-_]', '_', str($x.input.element_identifier)))\n+            #set $labels = re.sub('[^\\w\\-_]', '_', str($mode.in.input.element_identifier))\n         #end if\n-    #end for\n-    #set $labels = ','.join($labels)\n+    #else\n+        #set $labels = []\n+        #for $x in $mode.in.inputs\n+            #if str($x.labels) != ''\n+                #silent $labels.append(re.sub('[^\\w\\-_]', '_', str($x.labels)))\n+            #else\n+                #silent $labels.append(re.sub('[^\\w\\-_]', '_', str($x.input.element_identifier)))\n+            #end if\n+        #end for\n+        #set $labels = ','.join($labels)\n+    #end if\n #end if\n \n #if $assembly.type == 'metagenome' and $assembly.ref.origin == 'list'\n@@ -32,19 +44,34 @@\n     #end for\n #end if\n \n-#if $reads.reads_option == 'paired'\n-    #for $read in $reads.input_1\n-        #set $identifier = re.sub('[^\\s\\w\\-\\\\.]', '_', str($read.element_identifier))\n+#if $mode.reads.reads_option == 'paired'\n+    #if $mode.mode == 'individual'\n+        #set $identifier = re.sub('[^\\s\\w\\-\\\\.]', '_', str($mode.reads.input_1.element_identifier))\n+ln -s '$mode.reads.input_1' 'pe1-${identifier}.${mode.reads.input_1.ext}' &&\n+        #set $identifier = re.sub('[^\\s\\w\\-\\\\.]', '_', str($mode.reads.input_2.element_identifier))\n+ln -s '$mode.reads.input_2' 'pe2-${identifier}.${mode.reads.input_2.ext}' &&\n+    #else\n+        #for $read in $mode.reads.input_1\n+            #set $identifier = re.sub('[^\\s\\w\\-\\\\.]', '_', str($read.element_identifier))\n ln -s '$read' 'pe1-${identifier}.${read.ext}' &&\n-    #end for\n-    #for $read in $reads.input_2\n-        #set $identifier = re.sub('[^\\s\\w\\-\\\\.]', '_', str($read.element_identifier))\n+        #end for\n+        #for $read in $mode.reads.input_2\n+            #set $identifier = re.sub('[^\\s\\w\\-\\\\.]', '_', str($read.element_identifier))\n ln -s '$read' 'pe2-${identifier}.${read.ext}' &&\n-    #end for\n-#else if $reads.reads_option == 'paired_collection'\n-    #set $identifier = re.sub('[^\\s\\w\\-\\\\.]', '_', str($reads.input_1.element_identifier))\n-ln -s '$reads.input_1.forward' 'pe1-${identifier}.${reads.input_1.forward.ext}' &&\n-ln -s '$reads.input_1.reverse' 'pe2-${identifier}.${reads.input_1.reverse.ext}' &&\n+        #end for\n+    #end if\n+#else if $mode.reads.reads_option == 'paired_collection'\n+    #if $mode.mode == 'individual'\n+        #set $identifier = re.sub('[^\\s\\w\\-\\\\.]', '_', str($mode.reads.input_1.element_identifier))\n+ln -s '$mode.reads.input_1.forward' 'pe1-${identifier}.${mode.reads.input_1.forward.ext}' &&\n+ln -s '$mode.reads.input_1.reverse' 'pe2-${identifier}.${mode.reads.input_1.reverse.ext}' &&\n+    #else\n+        #for $read in $mode.reads.input_1\n+            #set $identifier = re.sub('[^\\s\\w\\-\\\\.]', '_', str($read.element_identifier))\n+ln -s '$read.forward' 'pe1-${identifier}.${read.forward.ext}' &&\n+ln -s '$read.reverse' 'pe2-${identifier}.${read.reverse.ext}' &&\n+        #end for\n+    #end if\n #end if\n \n #if $assembly.type == 'genome'\n@@ -53,44 +80,79 @@\n metaquast\n #end if\n \n-#if $reads.reads_option == 'single'\n-    #for $read in $reads.input_1\n+#if $mode.reads.reads_option == 'single'\n+  "..b'tom" value="true"/>\n-                <repeat name="inputs">\n+            <conditional name="mode">\n+                <param name="mode" value="individual"/>\n+                <conditional name="in">\n+                    <param name="custom" value="true"/>\n                     <param name="input" value="contigs1.fna"/>\n                     <param name="labels" value="contig1"/>\n-                </repeat>\n-            </conditional>\n-            <conditional name="reads">\n-                <param name="reads_option" value="paired_collection"/>\n-                <param name="input_1">\n-                    <collection type="paired">\n-                        <element name="forward" value="reads1.fastq.gz" ftype="fastqsanger.gz"/>\n-                        <element name="reverse" value="reads2.fastq.gz" ftype="fastqsanger.gz"/>\n-                    </collection>\n-                </param>\n+                </conditional>\n+                <conditional name="reads">\n+                    <param name="reads_option" value="paired_collection"/>\n+                    <param name="input_1">\n+                        <collection type="paired">\n+                            <element name="forward" value="reads1.fastq.gz" ftype="fastqsanger.gz"/>\n+                            <element name="reverse" value="reads2.fastq.gz" ftype="fastqsanger.gz"/>\n+                        </collection>\n+                    </param>\n+                </conditional>\n             </conditional>\n             <conditional name="assembly">\n                 <param name="type" value="genome"/>\n@@ -909,6 +1040,50 @@\n                 </assert_contents>\n             </output>\n         </test>\n+        <!-- Test 13: Test co-assembly with paired-collection fastq.gz inputs -->\n+        <test expect_num_outputs="1">\n+            <conditional name="mode">\n+                <param name="mode" value="co"/>\n+                <conditional name="in">\n+                    <param name="custom" value="false"/>\n+                    <param name="inputs" value="contigs1.fna,contigs2.fna"/>\n+                </conditional>\n+                <conditional name="reads">\n+                    <param name="reads_option" value="paired_collection"/>\n+                    <param name="input_1">\n+                        <collection type="list:paired">\n+                            <element name="s1">\n+                                <collection type="paired">\n+                                    <element name="forward" value="reads1.fastq.gz" ftype="fastqsanger.gz"/>\n+                                    <element name="reverse" value="reads2.fastq.gz" ftype="fastqsanger.gz"/>\n+                                </collection>\n+                            </element>\n+                            <element name="s2">\n+                                <collection type="paired">\n+                                    <element name="forward" value="reads1.fastq.gz" ftype="fastqsanger.gz"/>\n+                                    <element name="reverse" value="reads2.fastq.gz" ftype="fastqsanger.gz"/>\n+                                </collection>\n+                            </element>\n+                        </collection>\n+                    </param>\n+                </conditional>\n+            </conditional>\n+            <conditional name="assembly">\n+                <param name="type" value="genome"/>\n+                <conditional name="ref">\n+                    <param name="use_ref" value="false"/>\n+                </conditional>\n+            </conditional>\n+            <param name="output_files" value="tabular"/>\n+            <output name="report_tabular" ftype="tabular">\n+                <assert_contents>\n+                    <has_text text="# contigs (>= 0 bp)"/>\n+                    <has_text text="contigs1"/>\n+                    <has_text text="# N\'s per 100 kbp"/>\n+                    <has_n_lines n="22"/>\n+                </assert_contents>\n+            </output>\n+        </test>\n     </tests>\n     <help>\n <![CDATA[\n'