diff hicup_macros.xml @ 0:396bdc215399 draft

planemo upload for repository https://github.com/bgruening/galaxytools/tree/master/tools/hicup commit 50173a1994a72d9774fd46777de94dd02d35bd42

--- /dev/null	Thu Jan 01 00:00:00 1970 +0000
+++ b/hicup_macros.xml	Mon Oct 24 15:58:52 2022 +0000
@@ -0,0 +1,99 @@
+<macros>
+    <token name="@VERSION@">0.8.3</token>
+    <xml name="requirements_hicup">
+        <requirements>
+            <requirement type="package" version="@VERSION@">hicup</requirement>
+            <requirement type="package" version="2.4.5">bowtie2</requirement>
+            <requirement type="package" version="1.16.1">samtools</requirement>
+            <yield/>
+        </requirements>
+        <version_command>hicup --version</version_command>
+    </xml>
+    <xml name="citation_hicup">
+        <citations>
+            <citation type="doi">10.12688/f1000research.7334.1</citation>
+        </citations>
+    </xml>
+    <xml name="reference_genome_macro">
+        <conditional name="reference_genome">
+            <param name="source" type="select" label="Will you select a reference genome from your history or use a built-in index?" help="Built-ins were indexed using default options. See `Indexes` section of help below">
+                <option value="indexed">Use a built-in genome index</option>
+                <option value="history">Use a genome from the history and build index</option>
+            </param>
+            <when value="indexed">
+                <param name="index" type="select" label="Select reference genome" help="If your genome of interest is not listed, contact the Galaxy team">
+                <options from_data_table="bowtie2_indexes">
+                    <filter type="sort_by" column="2"/>
+                    <validator type="no_options" message="No indexes are available for the selected input dataset"/>
+                </options>
+                </param>
+            </when>
+            <when value="history">
+                <param name="own_file" type="data" format="fasta" label="Select reference genome" />
+                <!--<param name="own_file" type="data" format="fasta" metadata_name="dbkey" label="Select reference genome" />-->
+            </when>
+        </conditional>
+    </xml>
+    <xml name="re1">
+        <param argument="--re1" type="text" value="" label="Restriction enzyme recognition sequence" help="Restriction enzyme used e.g. A^GATCT,BglII. Some Hi-C protocols may use several enzymes. To specify several enzymes, use the ':' to separate them e.g. A^GATCT,BglII:A^AGCTT,HindIII:^GATC,DpnII. HiCUP accomodates N in restriction enzyme: e.g. :A^ANCTT"/>
+    </xml>
+    <xml name="re2">
+        <param argument="--re2" type="text" value="" label="Restriction enzyme instead of sonication to shorten di-tags."
+            help="To specify a restriction enzyme instead of sonication to shorten di-tags. This restriction site does NOT form a Hi-C ligation junction. 2 .g. AG^CT,AluI. Typically the sonication protocol is followed."/>
+    </xml>
+    <xml name="filter_longest_shortest">
+        <param argument="--longest" type="text" value="" label="Max insert size" help="Maximum allowable insert size (bps)"/>
+        <param argument="--shortest" type="text" value="" label="Min insert size" help="Minimum allowable insert size (bps)"/>
+    </xml>
+    <xml name="no_fill">
+        <param argument="--nofill" type="boolean" value="false" truevalue="--nofill" falsevalue="" label="No fill"
+            help="Hi-C protocol did NOT include a fill-in of sticky ends prior to re-ligation and therefore reads shall be truncated at the restriction site sequence"/>
+    </xml>
+    <token name="@PAIRED-END_INPUT@"><![CDATA[
+    ## Taken from cutadapt except that I don't accept space in name
+    #import re
+    #set library_type = str($library.type)
+    #if $library_type == 'paired':
+        #set input_1 = $library.input_1
+        #set input_2 = $library.input_2
+    #else if $library_type == 'paired_collection'
+        #set input_1 = $library.input_1.forward
+        #set input_2 = $library.input_1.reverse
+    #end if
+    
+    #if $input_1.is_of_type("fastq.gz", "fastqsanger.gz"):
+        #set ext = ".fq.gz"
+    #else:
+        #set ext = ".fq"
+    #end if
+    #set read1 = "dataset1" + $ext
+    ln -f -s '${input_1}' '$read1' &&
+
+    #if $input_2.is_of_type("fastq.gz", "fastqsanger.gz"):
+        #set ext2 = ".fq.gz"
+    #else:
+        #set ext2 = ".fq"
+    #end if
+    #set read2 = "dataset2" + $ext2
+    ln -f -s '${input_2}' '$read2' &&
+    ]]>
+    </token>
+    <xml name="input_paired">
+        <conditional name="library">
+            <param name="type" type="select" label="How Paired-end reads are organized">
+                <option value="paired">Separately</option>
+                <option value="paired_collection">Paired-end Collection</option>
+            </param>
+
+            <when value="paired">
+                <param name="input_1" format="fastq,fastq.gz" type="data" label="FASTQ/A file #1" help="Should be of datatype &quot;fastq.gz&quot;or &quot;fasta&quot;" />
+                <param name="input_2" format="fastq,fastq.gz" type="data" label="FASTQ/A file #2" help="Should be of datatype &quot;fastq.gz&quot;or &quot;fasta&quot;" />
+            </when>
+
+            <when value="paired_collection">
+                <param name="input_1" format="fastq,fastq.gz" type="data_collection" collection_type="paired" label="Paired Collection" help="Should be of datatype &quot;fastq.gz&quot; or &quot;fastq&quot;" />
+            </when>
+
+        </conditional>
+    </xml>
+</macros>