# HG changeset patch
# User iuc
# Date 1639508688 0
# Node ID 15a02df32c2b5ae05a57d470c6c25e3c620b701c
# Parent  148b595025b3488331740de1b02a853aa7d70233
"planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/delly commit d76130cdcb21f0390b4e68e733d38575fd5cc6c7"

diff -r 148b595025b3 -r 15a02df32c2b classify.xml
--- a/classify.xml	Tue Aug 31 08:00:10 2021 +0000
+++ b/classify.xml	Tue Dec 14 19:04:48 2021 +0000
@@ -105,7 +105,7 @@
             </output>
             <output name="out_vcf">
                 <assert_contents>
-                    <has_size value="7762"/>
+                    <has_size value="7758"/>
                 </assert_contents>
             </output>
         </test>
@@ -140,7 +140,7 @@
             </output>
             <output name="out_vcf">
                 <assert_contents>
-                    <has_size value="7762"/>
+                    <has_size value="7758"/>
                 </assert_contents>
             </output>
         </test>
@@ -167,7 +167,7 @@
             </output>
             <output name="out_vcf">
                 <assert_contents>
-                    <has_size value="7665"/>
+                    <has_size value="7661"/>
                 </assert_contents>
             </output>
         </test>
@@ -197,7 +197,7 @@
             </output>
             <output name="out_vcf">
                 <assert_contents>
-                    <has_size value="7665"/>
+                    <has_size value="7661"/>
                 </assert_contents>
             </output>
         </test>
diff -r 148b595025b3 -r 15a02df32c2b cnv.xml.orig
--- a/cnv.xml.orig	Tue Aug 31 08:00:10 2021 +0000
+++ /dev/null	Thu Jan 01 00:00:00 1970 +0000
@@ -1,207 +0,0 @@
-<?xml version="1.0"?>
-<<<<<<< HEAD:tools/delly/cnv.xml
-<tool id="delly_cnv" name="Delly cnv" version="@TOOL_VERSION@+galaxy@VERSION_SUFFIX@" profile="18.01">
-    <description>discover and genotype copy-number variants</description>
-=======
-<tool id="delly_rd" name="Delly read-depth (rd)" version="@TOOL_VERSION@+galaxy@VERSION_SUFFIX@" profile="18.01">
-    <description>normalization on read-depth profiles</description>
-    <expand macro="bio_tools"/>
->>>>>>> 20ed9dd6f (add bio.tools ID):tools/delly/rd.xml
-    <macros>
-        <import>macros.xml</import>
-    </macros>
-    <expand macro="requirements"/>
-    <expand macro="version_command"/>
-    <command detect_errors="exit_code"><![CDATA[
-## run
-delly cnv
-## generic options
---genome '$generic.genome'
---quality '$generic.quality'
---mappability '$generic.mappability'
---ploidy $generic.ploidy
---outfile 'result.bcf'
---covfile 'result.gz'
-## cnv calling options
---sdrd $cnv.sdrd
---cn-offset $cnv.cnoffset
---cnv-size $cnv.cnvsize
-#if $cnv.svfile
-    --svfile $cnv.svfile
-#end if
-#if $cnv.vcffile
-    --vcffile '$cnv.vcffile'
-#end if
-$cnv.segmentation
-## read-depth window options
---window-size $read.windowsize
---window-offset $read.windowoffset
-#if $read.bedintervals
-    --bed-intervals '$read.bedintervals'
-#end if
---fraction-window $read.fractionwindow
-$read.adaptivewindowing
-## gc fragment normalization options
---scan-window $gc.scanwindow
---fraction-unique $gc.fractionunique
-#if $gc.scanregions
-    --scan-regions '$gc.scanregions'
-#end if
---mad-cutoff $gc.madcutoff
---percentile $gc.percentile
-$gc.nowindowselection
-## input
-'$input'
-
-## postprocessing
-@LOG@
-    ]]></command>
-    <inputs>
-        <expand macro="input" format="bam" label="Select input file"/>
-        <section name="generic" title="Generic options" expanded="true">
-            <expand macro="genome"/>
-            <param argument="--quality" type="integer" value="10" label="Set minimum mapping quality"/>
-            <param argument="--mappability" type="data" format="fasta" label="Select mappability map file"/>
-            <param argument="--ploidy" type="integer" value="2" label="Set baseline ploidy"/>
-        </section>
-        <section name="cnv" title="CNV calling options" expanded="true">
-            <param argument="--sdrd" type="integer" value="2" label="Set minimum SD read-depth shift"/>
-            <expand macro="cnoffset" default="0.1"/>
-            <param name="cnvsize" type="integer" value="1000" label="Set minimum CNV size" help="(--cnv-size)"/>
-            <param argument="--svfile" type="data" format="bcf" optional="true" label="Select delly SV file for breakpoint refinement"/> <!-- filetype sv.bcf not supported by galaxy -->
-            <expand macro="vcffile"/>
-            <param argument="--segmentation" type="boolean" truevalue="--segmentation" falsevalue="" label="Use copy-number segmentation?"/>
-        </section>
-        <section name="read" title="Read-depth window options" expanded="true">
-            <param name="windowsize" type="integer" value="10000" label="Set window size" help="(--window-size)"/>
-            <param name="windowoffset" type="integer" value="10000" label="Set window offset" help="(--window-offset)"/>
-            <param name="bedintervals" type="data" format="bed" optional="true" label="Select input BED file" help="(--bed-intervals)"/>
-            <param name="fractionwindow" type="float" min="0.0" max="1.0" value="0.25" label="Set minimum callable window fraction" help="(--fraction-window)"/>
-            <param name="adaptivewindowing" type="boolean" truevalue="-a" falsevalue="" label="Use mappable bases for window size?" help="(--adaptive-windowing)"/>
-        </section>
-        <section name="gc" title="GC fragment normalization options" expanded="true">
-            <param name="scanwindow" type="integer" value="10000" label="Set scan window size" help="(--scan-window)"/>
-            <param name="fractionunique" type="float" min="0.0" max="1.0" value="0.8" label="Set uniqueness filter for scan windows" help="(--fraction-unique)"/>
-            <param name="scanregions" type="data" format="bed" optional="true" label="Select file with scanning regions" help="(--scan-regions)"/>
-            <param name="madcutoff" type="integer" value="3" label="Set count cutoff" help="(median + 3 * mad) (--mad-cutoff)"/>
-            <param argument="--percentile" type="float" min="0.0" max="1.0" value="0.0005" label="Set threshold for excluding extreme GC fraction"/>
-            <param name="nowindowselection" type="boolean" truevalue="-n" falsevalue="" label="Skip scan window selection?" help="(--no-window-selection)"/>
-        </section>
-        <section name="oo" title="Output options" expanded="true">
-            <param name="out" type="select" multiple="true" optional="false" label="Select output file(s)">
-                <option value="cnv" selected="true">CNV</option>
-                <option value="coverage">Coverage</option>
-                <option value="log">Log</option>
-            </param>
-        </section>
-    </inputs>
-    <outputs>
-        <data name="out_cnv" format="bcf" from_work_dir="result.bcf" label="${tool.name} on ${on_string}: CNV">
-            <filter>'cnv' in oo['out']</filter>
-        </data>
-        <data name="out_coverage" format="tabular.gz" from_work_dir="result.gz" label="${tool.name} on ${on_string}: Coverage">
-            <filter>'coverage' in oo['out']</filter>
-        </data>
-        <expand macro="log"/>
-    </outputs>
-    <tests>
-        <!-- no test implemented for vcffile, svfile, bed-intervals, scanregions -->
-
-        <!-- #1 default; test data to small, results are empty -->
-        <test expect_num_outputs="3">
-            <param name="input" value="normal.bam"/>
-            <section name="generic">
-                <param name="genome" value="genome.fasta"/>
-                <param name="mappability" value="map.fasta"/>
-            </section>
-            <section name="oo">
-                <param name="out" value="cnv,coverage,log"/>
-            </section>
-            <output name="out_cnv">
-                <assert_contents>
-                    <has_size value="0"/>
-                </assert_contents>
-            </output>
-            <output name="out_coverage">
-                <assert_contents>
-                    <has_size value="0"/>
-                </assert_contents>
-            </output>
-            <output name="out_log">
-                <assert_contents>
-                    <has_text_matching expression=".+Scanning Windows"/>
-                    <has_line line="***************************************************"/>
-                </assert_contents>
-            </output>
-        </test>
-        <!-- #2 -->
-        <test expect_num_outputs="3">
-            <param name="input" value="normal.bam"/>
-            <section name="generic">
-                <param name="genome" value="genome.fasta"/>
-                <param name="quality" value="11"/>
-                <param name="mappability" value="map.fasta"/>
-                <param name="ploidy" value="3"/>
-            </section>
-            <section name="cnv">
-                <param name="sdrd" value="3"/>
-                <param name="cnoffset" value="0.2"/>
-                <param name="cnvsize" value="1001"/>
-                <param name="segmentation" value="true"/>
-            </section>
-            <section name="read">
-                <param name="windowsize" value="10001"/>
-                <param name="windowoffset" value="9999"/>
-                <param name="fractionwindow" value="0.24"/>
-                <param name="adaptivewindowing" value="true"/>
-            </section>
-            <section name="gc">
-                <param name="scanwindow" value="10001"/>
-                <param name="fractionunique" value="0.79"/>
-                <param name="madcutoff" value="2"/>
-                <param name="percentile" value="0.0006"/>
-                <param name="nowindowselection" value="true"/>
-            </section>
-            <section name="oo">
-                <param name="out" value="cnv,coverage,log"/>
-            </section>
-            <output name="out_cnv">
-                <assert_contents>
-                    <has_size value="700" delta="10"/>
-                </assert_contents>
-            </output>
-            <output name="out_coverage">
-                <assert_contents>
-                    <has_size value="61"/>
-                </assert_contents>
-            </output>
-            <output name="out_log">
-                <assert_contents>
-                    <has_text_matching expression=".+Done.+"/>
-                </assert_contents>
-            </output>
-        </test>
-    </tests>
-    <help><![CDATA[
-.. class:: infomark
-
-**What it does**
-
-@WID@
-
-**Input**
-
-Delly *cnv* requires are a sample (BAM), a genome (FASTA) and a mappability map (FASTA), which is available `here <https://gear.embl.de/data/delly/>`_. Intervals (BED), scanning regions (BED) and a delly SV file for breakpoint refinement (BCF) can be provided optionally.
-
-**Output**
-
-CNV (BCF) and coverage (compressed tabular) files are created.
-
-.. class:: infomark
-
-**References**
-
-@REFERENCES@
-    ]]></help>
-    <expand macro="citations"/>
-</tool>
\ No newline at end of file
diff -r 148b595025b3 -r 15a02df32c2b macros.xml
--- a/macros.xml	Tue Aug 31 08:00:10 2021 +0000
+++ b/macros.xml	Tue Dec 14 19:04:48 2021 +0000
@@ -1,11 +1,11 @@
 <?xml version="1.0"?>
 <macros>
-    <token name="@TOOL_VERSION@">0.8.7</token>
+    <token name="@TOOL_VERSION@">0.9.1</token>
     <token name="@VERSION_SUFFIX@">0</token>
     <xml name="requirements">
         <requirements>
             <requirement type="package" version="@TOOL_VERSION@">delly</requirement>
-            <requirement type="package" version="1.10.2">bcftools</requirement>
+            <requirement type="package" version="1.12">bcftools</requirement>
         </requirements>
     </xml>
     <xml name="version_command">
diff -r 148b595025b3 -r 15a02df32c2b macros.xml.orig
--- a/macros.xml.orig	Tue Aug 31 08:00:10 2021 +0000
+++ /dev/null	Thu Jan 01 00:00:00 1970 +0000
@@ -1,162 +0,0 @@
-<?xml version="1.0"?>
-<macros>
-    <token name="@TOOL_VERSION@">0.8.7</token>
-    <token name="@VERSION_SUFFIX@">0</token>
-    <xml name="requirements">
-        <requirements>
-            <requirement type="package" version="@TOOL_VERSION@">delly</requirement>
-            <requirement type="package" version="1.10.2">bcftools</requirement>
-        </requirements>
-    </xml>
-    <xml name="version_command">
-        <version_command><![CDATA[delly -v 2>&1 | grep 'Delly version' | cut -f 3 -d ' ']]></version_command>
-    </xml>
-	<xml name="citations">
-        <citations>
-            <citation type="doi">10.1093/bioinformatics/bts378</citation>
-        </citations>
-    </xml>
-<<<<<<< HEAD
-	
-    <!-- command -->
-=======
-    <xml name="bio_tools">
-        <xrefs>
-            <xref type='bio.tools'>delly2</xref>
-        </xrefs>
-    </xml>
-    <!--
-        command 
-    -->
->>>>>>> 20ed9dd6f (add bio.tools ID)
-
-    <token name="@BAM@"><![CDATA[
-#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[
-#if 'dump' in $oo.out
-    && test -f 'dump.tsv.gz' && bgzip -d 'dump.tsv.gz' || echo 'No dump file.'
-#end if
-    ]]></token>
-    <token name="@LOG@"><![CDATA[
-#if 'log' in $oo.out
-    |& tee '$out_log'
-#end if
-    ]]></token>
-    <token name="@VCF@"><![CDATA[
-#if 'vcf' in $oo.out
-    && test -f 'result.bcf' && bcftools view 'result.bcf' > 'result.vcf' || echo 'No results.'
-#end if
-    ]]></token>
-
-    <!-- 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 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="mincliquesize">
-        <param name="mincliquesize" type="integer" value="2" label="Set minimum paired-end/single-read clique size" help="(--min-clique-size)"/>
-    </xml>
-    <xml name="minrefsep" token_default="">
-        <param argument="--minrefsep" type="integer" value="@DEFAULT@" label="Set minimum reference separation"/>
-    </xml>
-    <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="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="INV">Inversion (INV)</option>
-            <option value="BND">Translocation (BND)</option>
-        </param>
-    </xml>
-    <xml name="vcffile">
-        <param argument="--vcffile" type="data" format="bcf,vcf" optional="true" label="Select genotyping file"/>
-    </xml>
-
-    <!-- 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 ${on_string}: Result (VCF)">
-            <filter>'vcf' in oo['out']</filter>
-        </data>
-    </xml>
-    <xml name="dump">
-        <data name="out_dump" format="tabular" from_work_dir="dump.tsv" label="${tool.name} on ${on_string}: SV-reads">
-            <filter>'dump' in oo['out']</filter>
-        </data>
-    </xml>
-    <xml name="log">
-        <data name="out_log" format="txt" label="${tool.name} on ${on_string}: Log">
-            <filter>'log' in oo['out']</filter>
-        </data>
-    </xml>
-
-    <!-- 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>`_.
-    ]]></token>
-</macros>
\ No newline at end of file
diff -r 148b595025b3 -r 15a02df32c2b merge.xml.orig
--- a/merge.xml.orig	Tue Aug 31 08:00:10 2021 +0000
+++ /dev/null	Thu Jan 01 00:00:00 1970 +0000
@@ -1,179 +0,0 @@
-<?xml version="1.0"?>
-<tool id="delly_merge" name="Delly merge" version="@TOOL_VERSION@+galaxy@VERSION_SUFFIX@" profile="18.01">
-<<<<<<< HEAD
-    <description>structural variants across/within BCF/VCF file(s)</description>
-=======
-    <description>structural variants across/within VCF/BCF file(s)</description>
-    <expand macro="bio_tools"/>
->>>>>>> 20ed9dd6f (add bio.tools ID)
-    <macros>
-        <import>macros.xml</import>
-    </macros>
-    <expand macro="requirements"/>
-    <expand macro="version_command"/>
-    <command detect_errors="exit_code"><![CDATA[
-## initialize
-#for $i, $current in enumerate($input)
-    #if $current.is_of_type('vcf')
-        bcftools view -Ob '$current' > 'input_${i}.bcf.gz' &&
-        bcftools index 'input_${i}.bcf.gz' &&
-    #else
-        ln -s '${current}' 'input_${i}.bcf.gz' &&
-        ln -s '${current.metadata.bcf_index}' 'input_${i}.bcf.gz.csi' &&
-    #end if
-#end for
-
-## run
-delly merge
-## generic options
---outfile 'result.bcf'
---chunks $generic.chunks
---vaf $generic.vaf
---coverage $generic.coverage
---minsize $generic.minsize
---maxsize $generic.maxsize
-$generic.cnvmode
-$generic.precise
-$generic.pass
-## overlap options
---bp-offset $overlap.bpoffset
---rec-overlap $overlap.recoverlap
-## input
-#for $i, $current in enumerate($input)
-    'input_${i}.bcf.gz'
-#end for
-
-## postprocessing
-@LOG@
-@VCF@
-    ]]></command>
-    <inputs>
-        <expand macro="input" format="bcf,vcf" multiple="true" label="Select input files"/>
-        <section name="generic" title="Generic options" expanded="true">
-            <param argument="--chunks" type="integer" value="500" label="Set maximum chunk size to merge groups of BCF files"/>
-            <param argument="--vaf" type="float" value="0.15" min="0.0" max="1.0" label="Set minimum fractional ALT support"/>
-            <expand macro="coverage" label="Set minimum coverage"/>
-            <expand macro="minsize" default="0" label="Set minimum SV size"/>
-            <expand macro="maxsize" default="1000000" label="Set maximum SV size"/>
-            <param argument="--cnvmode" type="boolean" truevalue="--cnvmode" falsevalue="" label="Merge Delly CNV files?"/>
-            <param argument="--precise" type="boolean" truevalue="--precise" falsevalue="" label="Filter sites for PRECISE?"/>
-            <expand macro="pass"/>
-        </section>
-        <section name="overlap" title="Overlap options" expanded="true">
-            <param name="bpoffset" type="integer" value="1000" label="Set maximum breakpoint offset" help="(--bp-offset)"/>
-            <param name="recoverlap" type="float" value="0.8" label="Set minimum reciprocal overlap" help="(--rec-overlap)"/>
-        </section>
-        <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>
-            </param>
-        </section>
-    </inputs>
-    <outputs>
-        <expand macro="bcf"/>
-        <expand macro="log"/>
-        <expand macro="vcf"/>
-    </outputs>
-    <tests>
-        <!-- #1 bcf, default -->
-        <test expect_num_outputs="2">
-            <param name="input" value="call_1.bcf.gz,call_2.bcf.gz"/>
-            <section name="oo">
-                <param name="out" value="vcf,bcf"/>
-            </section>
-            <output name="out_bcf">
-                <assert_contents>
-                    <has_size value="1851" delta="10"/>
-                </assert_contents>
-            </output>
-            <output name="out_vcf">
-                <assert_contents>
-                    <has_n_lines n="128"/>
-                    <has_line line="##fileformat=VCFv4.2"/>
-                    <has_line line="#CHROM&#009;POS&#009;ID&#009;REF&#009;ALT&#009;QUAL&#009;FILTER&#009;INFO"/>
-                </assert_contents>
-            </output>
-        </test>
-        <!-- #2 bcf -->
-        <test expect_num_outputs="3">
-            <param name="input" value="call_1.bcf.gz,call_2.bcf.gz"/>
-            <section name="generic">
-                <param name="chunks" value="500"/>
-                <param name="vaf" value="0.16"/>
-                <param name="coverage" value="10"/>
-                <param name="minsize" value="0"/>
-                <param name="maxsize" value="1000000"/>
-                <param name="cnvmode" value="true"/>
-                <param name="precise" value="true"/>
-                <param name="pass" value="true"/>
-            </section>
-            <section name="overlap">
-                <param name="bp-offset" value="1000"/>
-                <param name="rec-overlap" value="0.79"/>
-            </section>
-            <section name="oo">
-                <param name="out" value="vcf,bcf,log"/>
-            </section>
-            <output name="out_bcf">
-                <assert_contents>
-                    <has_size value="1021" 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="108"/>
-                    <has_line line="##fileformat=VCFv4.2"/>
-                    <has_line line="#CHROM&#009;POS&#009;ID&#009;REF&#009;ALT&#009;QUAL&#009;FILTER&#009;INFO"/>
-                </assert_contents>
-            </output>
-        </test>
-        <!-- #3 vcf, default -->
-        <test expect_num_outputs="2">
-            <param name="input" value="call_1.vcf.gz,call_2.vcf.gz"/>
-            <section name="oo">
-                <param name="out" value="vcf,bcf"/>
-            </section>
-            <output name="out_bcf">
-                <assert_contents>
-                    <has_size value="1851" delta="10"/>
-                </assert_contents>
-            </output>
-            <output name="out_vcf">
-                <assert_contents>
-                    <has_n_lines n="128"/>
-                    <has_line line="##fileformat=VCFv4.2"/>
-                    <has_line line="#CHROM&#009;POS&#009;ID&#009;REF&#009;ALT&#009;QUAL&#009;FILTER&#009;INFO"/>
-                </assert_contents>
-            </output>
-        </test>
-    </tests>
-    <help><![CDATA[
-.. class:: infomark
-
-**What it does**
-
-@WID@
-
-**Input**
-
-Delly *merge* requires BCF or VCF files.
-
-**Output**
-
-A single file in BCF/VCF format.  Additionally a log file is provided.
-
-.. class:: infomark
-
-**References**
-
-@REFERENCES@
-    ]]></help>
-    <expand macro="citations"/>
-</tool>
\ No newline at end of file