# HG changeset patch
# User iuc
# Date 1611325923 0
# Node ID 6184cfc70e28aa71cf7816f9f6b5bf8d472297f0
# Parent  9919057a466c1d2408f163ffcde903e7fc8fec3d
"planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/delly commit d18d984264f54b45e94d97b5b97ed499a32a334a"

diff -r 9919057a466c -r 6184cfc70e28 filter.xml
--- a/filter.xml	Thu Oct 29 20:50:57 2020 +0000
+++ b/filter.xml	Fri Jan 22 14:32:03 2021 +0000
@@ -8,12 +8,12 @@
     <expand macro="version_command"/>
     <command detect_errors="exit_code"><![CDATA[
 ## initialize
-#if $samples.is_of_type('vcf')
-    bcftools view -Ob '$samples' > 'sample.bcf.gz' &&
-    bcftools index 'sample.bcf.gz' &&
+#if $input.is_of_type('vcf')
+    bcftools view -Ob '$input' > 'input.bcf.gz' &&
+    bcftools index 'input.bcf.gz' &&
 #else
-    ln -s '${samples}' 'sample.bcf.gz' &&
-    ln -s '${samples.metadata.bcf_index}' 'sample.bcf.gz.csi' &&
+    ln -s '${input}' 'input.bcf.gz' &&
+    ln -s '${input.metadata.bcf_index}' 'input.bcf.gz.csi' &&
 #end if
 
 ## run
@@ -31,38 +31,37 @@
     --samples '$sv.mode_cond.samples'
     --coverage $sv.mode_cond.coverage
     --controlcontamination $sv.mode_cond.controlcontamination
-#end if
 ## germline options
-#if $sv.mode_cond.mode_sel == 'germline'
+#else if $sv.mode_cond.mode_sel == 'germline'
     --gq $sv.mode_cond.gq
     --rddel $sv.mode_cond.rddel
     --rddup $sv.mode_cond.rddup
 #end if
-## samples
-'sample.bcf.gz' ## input
+## input
+'input.bcf.gz'
 
 ## postprocessing
 @LOG@
 @VCF@
     ]]></command>
     <inputs>
-        <expand macro="samples" format="bcf,vcf" multiple="false" label="Select file"/>
+        <expand macro="input" format="bcf,vcf" label="Select input file"/>
         <section name="generic" title="Generic options" expanded="true">
             <param argument="--altaf" type="float" value="0.2" min="0.0" max="1.0" label="Set minimum fractional ALT support"/>
-            <expand macro="minsize"/>
-            <expand macro="maxsize" default="500000000"/>
+            <expand macro="minsize" default="0" label="Set minimum SV size"/>
+            <expand macro="maxsize" default="500000000" label="Set maximum SV size"/>
             <param argument="--ratiogeno" type="float" value="0.75" min="0.0" max="1.0" label="Set minimum fraction of genotyped samples"/>
             <param argument="--pass" type="boolean" truevalue="--pass" falsevalue="" label="Filter sites for PASS?"/>
         </section>
         <section name="sv" title="SV calling options" expanded="true">
             <conditional name="mode_cond">
-                <param argument="mode_sel" type="select" label="Select filter mode">
+                <param name="mode_sel" type="select" label="Select filter mode" help="(--filter)">
                     <option value="somatic" selected="true">Somatic</option>
                     <option value="germline">Germline</option>
                 </param>
                 <when value="somatic">
-                    <param argument="--samples" type="data" format="tabular" label="Select sample file" help="Two-column sample file listing sample name and tumor or control."/>
-                    <param argument="--coverage" type="integer" value="10" label="Set minimum coverage in tumor."/>
+                    <expand macro="samples"/>
+                    <expand macro="coverage" label="Set minimum coverage in tumor"/>
                     <param argument="--controlcontamination" type="float" value="0.0" min="0.0" max="1.0" label="Set maximum fractional ALT support in control"/>
                 </when>
                 <when value="germline">
@@ -72,23 +71,23 @@
                 </when>
             </conditional>
         </section>
-        <section name="oo" title="Output options">
+        <section name="oo" title="Output options" expanded="true">
             <param name="out" type="select" multiple="true" optional="false" label="Select output file(s)">
                 <option value="bcf" selected="true">BCF</option>
+                <option value="log">Log</option>
                 <option value="vcf">VCF</option>
-                <option value="log">Log</option>
             </param>
         </section>
     </inputs>
     <outputs>
-        <expand macro="vcf"/>
         <expand macro="bcf"/>
         <expand macro="log"/>
+        <expand macro="vcf"/>
     </outputs>
     <tests>
         <!-- #1 default, somatic, bcf -->
         <test expect_num_outputs="2">
-            <param name="samples" value="call_1.bcf.gz"/>
+            <param name="input" value="call_1.bcf.gz"/>
             <section name="sv">
                 <conditional name="mode_cond">
                     <param name="mode_sel" value="somatic"/>
@@ -113,7 +112,7 @@
         </test>
         <!-- #2 somatic, bcf -->
         <test expect_num_outputs="3">
-            <param name="samples" value="call_1.bcf.gz"/>
+            <param name="input" value="call_1.bcf.gz"/>
             <section name="generic">
                 <param name="altaf" value="0.3"/>
                 <param name="minsize" value="1"/>
@@ -137,6 +136,11 @@
                     <has_size value="2281" delta="10"/>
                 </assert_contents>
             </output>
+            <output name="out_log">
+                <assert_contents>
+                    <has_text_matching expression=".+Done\."/>
+                </assert_contents>
+            </output>
             <output name="out_vcf">
                 <assert_contents>
                     <has_n_lines n="140"/>
@@ -144,15 +148,10 @@
                     <has_line line="#CHROM&#009;POS&#009;ID&#009;REF&#009;ALT&#009;QUAL&#009;FILTER&#009;INFO&#009;FORMAT&#009;NORMAL&#009;TUMOR"/>
                 </assert_contents>
             </output>
-            <output name="out_log">
-                <assert_contents>
-                    <has_text_matching expression=".+Done\."/>
-                </assert_contents>
-            </output>
         </test>
        <!-- #3 default, germline, bcf -->
         <test expect_num_outputs="2">
-            <param name="samples" value="call_1.bcf.gz"/>
+            <param name="input" value="call_1.bcf.gz"/>
             <section name="sv">
                 <conditional name="mode_cond">
                     <param name="mode_sel" value="germline"/>
@@ -176,7 +175,7 @@
         </test>
         <!-- #4 germline, bcf -->
         <test expect_num_outputs="3">
-            <param name="samples" value="call_1.bcf.gz"/>
+            <param name="input" value="call_1.bcf.gz"/>
             <section name="generic">
                 <param name="altaf" value="0.1"/>
                 <param name="minsize" value="1"/>
@@ -200,6 +199,11 @@
                     <has_size value="2264" delta="10"/>
                 </assert_contents>
             </output>
+            <output name="out_log">
+                <assert_contents>
+                    <has_text_matching expression=".+Done\."/>
+                </assert_contents>
+            </output>
             <output name="out_vcf">
                 <assert_contents>
                     <has_n_lines n="139"/>
@@ -207,15 +211,10 @@
                     <has_line line="#CHROM&#009;POS&#009;ID&#009;REF&#009;ALT&#009;QUAL&#009;FILTER&#009;INFO&#009;FORMAT&#009;NORMAL&#009;TUMOR"/>
                 </assert_contents>
             </output>
-            <output name="out_log">
-                <assert_contents>
-                    <has_text_matching expression=".+Done\."/>
-                </assert_contents>
-            </output>
         </test>
         <!-- #5 default, somatic, vcf -->
         <test expect_num_outputs="2">
-            <param name="samples" value="call_1.vcf.gz"/>
+            <param name="input" value="call_1.vcf.gz"/>
             <section name="sv">
                 <conditional name="mode_cond">
                     <param name="mode_sel" value="somatic"/>
@@ -227,7 +226,7 @@
             </section>
             <output name="out_bcf">
                 <assert_contents>
-                    <has_size value="2440" delta="10"/>
+                    <has_size value="2451" delta="10"/>
                 </assert_contents>
             </output>
             <output name="out_vcf">
@@ -246,8 +245,6 @@
 
 @WID@
 
-Delly *filter* contains workflows for germline and somatic SV calling.
-
 **Input**
 
 *Somatic* filtering requires a called SV input with at least one tumor sample and a matched control sample. In addition, a tab-delimited sample description needs to be provided, in which the first column holds the sample ids (as found in the VCF/BCF input) and the second column specifies either tumor or control.
@@ -256,7 +253,7 @@
 
 **Output**
 
-The output is available in BCF and VCF format.
+The output is available in BCF and VCF format. Additionally a log file is provided.
 
 .. class:: infomark
 
diff -r 9919057a466c -r 6184cfc70e28 macros.xml
--- a/macros.xml	Thu Oct 29 20:50:57 2020 +0000
+++ b/macros.xml	Fri Jan 22 14:32:03 2021 +0000
@@ -1,6 +1,6 @@
 <?xml version="1.0"?>
 <macros>
-    <token name="@TOOL_VERSION@">0.8.5</token>
+    <token name="@TOOL_VERSION@">0.8.7</token>
     <token name="@VERSION_SUFFIX@">0</token>
     <xml name="requirements">
         <requirements>
@@ -17,14 +17,12 @@
         </citations>
     </xml>
 	
-    <!--
-        command 
-    -->
+    <!-- command -->
 
     <token name="@BAM@"><![CDATA[
-#for $i, $current in enumerate($samples)
-    ln -s '${current}' 'sample_${i}.bam' &&
-    ln -s '${current.metadata.bam_index}' 'sample_${i}.bam.bai' &&
+#for $i, $current in enumerate($input)
+    ln -s '${current}' 'input_${i}.bam' &&
+    ln -s '${current.metadata.bam_index}' 'input_${i}.bam.bai' &&
 #end for
     ]]></token>
     <token name="@DUMP@"><![CDATA[
@@ -43,68 +41,79 @@
 #end if
     ]]></token>
 
-    <!--
-        input 
-    -->
+    <!-- input -->
 
+    <xml name="cnoffset" token_default="">
+        <param name="cnoffset" type="float" min="0.0" max="1.0" value="@DEFAULT@" label="Set minimum CN offset" help="(--cn-offset)"/>
+    </xml>
+    <xml name="coverage" token_label="">
+        <param argument="--coverage" type="integer" value="10" label="@LABEL@"/>
+    </xml>
     <xml name="exclude">
         <param argument="--exclude" type="data" format="tabular" optional="true" label="Select file with regions to exclude"/>
     </xml>
     <xml name="genome">
-        <param argument="--genome" type="data" format="fasta" label="Select genome"/>
+        <param argument="--genome" type="data" format="fasta" label="Select genome file"/>
     </xml>
     <xml name="genoqual">
         <param name="genoqual" type="integer" value="5" label="Set minimum mapping quality for genotyping" help="(--geno-qual)"/>
     </xml>
+    <xml name="input" token_format="" token_multiple="false" token_label="">
+        <param name="input" type="data" format="@FORMAT@" multiple="@MULTIPLE@" label="@LABEL@"/>
+    </xml>
+    <xml name="maxreadsep" token_default="">
+        <param argument="--maxreadsep" type="integer" value="@DEFAULT@" label="Set maximum read separation"/>
+    </xml>
+    <xml name="maxsize" token_default="" token_label="">
+        <param argument="--maxsize" type="integer" value="@DEFAULT@" label="@LABEL@"/>
+    </xml>
     <xml name="minclip">
         <param argument="--minclip" type="integer" value="25" label="Set minimum clipping length"/>
     </xml>
-    <xml name="maxreadsep" token_default="40">
-        <param argument="--maxreadsep" type="integer" value="@DEFAULT@" label="Set maximum read separation"/>
+    <xml name="mincliquesize">
+        <param name="mincliquesize" type="integer" value="2" label="Set minimum paired-end/single-read clique size" help="(--min-clique-size)"/>
     </xml>
-    <xml name="maxsize" token_default="1000000">
-        <param argument="--maxsize" type="integer" value="@DEFAULT@" label="Set maximum SV size"/>
-    </xml>
-    <xml name="mincliquesize">
-        <param name="mincliquesize" type="integer" value="2" label="Set minimum min. PE/SR clique size" help="(--min-clique-size)"/>
-    </xml>
-    <xml name="minrefsep" token_default="25">
+    <xml name="minrefsep" token_default="">
         <param argument="--minrefsep" type="integer" value="@DEFAULT@" label="Set minimum reference separation"/>
     </xml>
-    <xml name="minsize">
-        <param argument="--minsize" type="integer" value="0" label="Set minimum SV size"/>
+    <xml name="minsize" token_default="" token_label="">
+        <param argument="--minsize" type="integer" value="@DEFAULT@" label="@LABEL@"/>
+    </xml>
+    <xml name="pass">
+        <param argument="--pass" type="boolean" truevalue="--pass" falsevalue="" label="Filter sites for PASS?"/>
     </xml>
-    <xml name="samples" token_format="bam" token_multiple="true" token_label="Select sample file(s)">
-        <param name="samples" type="data" format="@FORMAT@" multiple="@MULTIPLE@" label="@LABEL@"/>
+    <xml name="ploidy">
+        <param argument="--ploidy" type="integer" value="2" label="Set baseline ploidy"/>
+    </xml>
+    <xml name="samples">
+        <param argument="--samples" type="data" format="tabular" label="Select sample file" help="Two-column sample file listing sample name and tumor or control."/>
     </xml>
     <xml name="svtype">
         <param argument="--svtype" type="select" label="Select type(s) of structural variants to detect">
             <option value="ALL" selected="true">All types (ALL)</option>
             <option value="DEL">Deletion (DEL)</option>
+            <option value="DUP">Duplication (DUP)</option>
             <option value="INS">Insertion (INS)</option>
-            <option value="DUP">Duplication (DUP)</option>
             <option value="INV">Inversion (INV)</option>
             <option value="BND">Translocation (BND)</option>
         </param>
     </xml>
     <xml name="vcffile">
-        <param argument="--vcffile" type="data" format="vcf,bcf" optional="true" label="Select genotyping file"/>
+        <param argument="--vcffile" type="data" format="bcf,vcf" optional="true" label="Select genotyping file"/>
     </xml>
 
-    <!--
-        output 
-    -->
+    <!-- output -->
 
+    <xml name="bcf">
+        <data name="out_bcf" format="bcf" from_work_dir="result.bcf" label="${tool.name} on ${on_string}: Result (BCF)">
+            <filter>'bcf' in oo['out']</filter>
+        </data>
+    </xml>
     <xml name="vcf">
         <data name="out_vcf" format="vcf" from_work_dir="result.vcf" label="${tool.name} on ${on_string}: Result (VCF)">
             <filter>'vcf' in oo['out']</filter>
         </data>
     </xml>
-     <xml name="bcf">
-        <data name="out_bcf" format="bcf" from_work_dir="result.bcf" label="${tool.name} on ${on_string}: Result (BCF)">
-            <filter>'bcf' in oo['out']</filter>
-        </data>
-    </xml>
     <xml name="dump">
         <data name="out_dump" format="tabular" from_work_dir="dump.tsv" label="${tool.name} on ${on_string}: SV-reads">
             <filter>'dump' in oo['out']</filter>
@@ -116,12 +125,25 @@
         </data>
     </xml>
 
-    <!--
-        Help
-    -->
+    <!-- help -->
 
     <token name="@WID@"><![CDATA[
 Delly is an integrated structural variant (SV) prediction method that can discover, genotype and visualize deletions, tandem duplications, inversions and translocations at single-nucleotide resolution in short-read massively parallel sequencing data. It uses paired-ends, split-reads and read-depth to sensitively and accurately delineate genomic rearrangements throughout the genome.
+
+Short-read SV calling
+
+- *call* to discover and genotype structural variants
+- *merge* structural variants across VCF/BCF files and within a single VCF/BCF file
+- *filter* somatic or germline structural variants
+
+Long-read SV calling
+
+- *lr* for long-read SV discovery
+
+Copy-number variant calling
+
+- *cnv* to discover and genotype copy-number variants
+- *classify* somatic or germline copy-number variants
     ]]></token>
     <token name="@REFERENCES@"><![CDATA[
 More information are available on `GitHub <https://github.com/dellytools/delly>`_.