diff bam_bed_gff_to_bigwig.xml @ 0:65a296d558e7 draft default tip

planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/main/tools/bbgbigwig commit decf6daa4769664f779bc088b83b0f89ac1df147

--- /dev/null	Thu Jan 01 00:00:00 1970 +0000
+++ b/bam_bed_gff_to_bigwig.xml	Fri Dec 12 21:28:28 2025 +0000
@@ -0,0 +1,109 @@
+<tool id="bbgtobigwig" name="BAM BED GFF coverage bigWigs" version="0.1" profile="22.05"> 
+    <xrefs>
+        <xref type="bio.tools">UCSC_Genome_Browser_Utilities</xref>
+    </xrefs>
+    <requirements>
+        <requirement type="package" version="455">ucsc-bedgraphtobigwig</requirement>
+        <requirement type="package" version="2.31.1">bedtools</requirement>
+        <requirement type="package" version="9.5">coreutils</requirement> 
+        <requirement type="package" version="3.12.3">python</requirement>
+    </requirements>
+    <required_files>
+        <include path="gff_to_bed_converter.py"/>
+    </required_files>
+    <command detect_errors="aggressive"><![CDATA[
+#if $hist_or_builtin.genosrc == "indexed":
+    ln -s '$hist_or_builtin.chromfile.fields.len_path' ./CHROMFILE &&
+#else:
+    ln -s '$chromfile' ./CHROMFILE &&
+#end if
+#if $input1.ext in ['gff', 'gff3']:
+    python '$__tool_directory__/gff_to_bed_converter.py' < '$input1' > input2 && 
+#else:
+    ln -s '$input1' input2 &&
+#end if
+#if $input1.ext == "bam":
+    bedtools genomecov -bg -split -ibam input2 | 
+#else
+    bedtools genomecov -bg -i input2 -g ./CHROMFILE |
+#end if
+LC_COLLATE=C sort -k1,1 -k2,2n > temp.bg &&
+bedGraphToBigWig temp.bg ./CHROMFILE '$output'
+    ]]></command>
+    <inputs>
+        <conditional name="hist_or_builtin">
+            <param name="genosrc" type="select" label="Is the input assigned to a built-in or custom reference genome?" 
+                help="If the input has no dbkey, supply a chromosome lengths file">
+                <option selected="True" value="indexed">Input data was made with a built-in genome or already has a custom genome dbkey</option>
+                <option value="history">Input data mapped on a genome from the current history. The chromosome lengths file is also in the history</option>
+            </param>
+            <when value="indexed">
+                <param name="input1" type="data" format="bam,unsorted.bam,bed,gff,gff3" label="bam/bed/gff to convert">
+                    <validator type="unspecified_build" />
+                </param>
+                <param name="chromfile" type="select" label="Source Genome Build">
+                    <options from_data_table="__dbkeys__">
+                        <filter type="data_meta" column="0" key="dbkey" ref="input1"/>
+                    </options>
+                    <validator type="no_options" message="The chosen genome build is not available."/>
+                </param>
+            </when>
+            <when value="history">
+                <param name="input1" type="data" format="bam,unsorted.bam,bed,gff,gff3" label="bam/bed/gff to convert"/>
+                <param name="chromfile" type="data" format="len,txt,tabular" label="Chromosome length file" 
+                   help="Sequence lengths for the history reference are required to make a bigwig. Compute sequence length tool makes these from fasta files"/>
+            </when>
+        </conditional>
+    </inputs>
+    <outputs>
+        <data name="output" format="bigwig"/>
+    </outputs>
+    <tests>
+        <test expect_num_outputs="1">
+            <conditional name="hist_or_builtin">
+                <param name="genosrc" value="indexed"/>
+                <param name="input1" value="featureCounts_input1.bam" dbkey="hg38"/>
+                <param name="chromfile" value="hg38"/>
+            </conditional>
+            <output name="output" value="featureCounts_input1.bigwig" compare="sim_size"/>
+        </test>
+        <test expect_num_outputs="1">
+            <conditional name="hist_or_builtin">
+                <param name="genosrc" value="history"/>
+                <param name="input1" value="srma_out2.bam"/>
+                <param name="chromfile" value="testing.len"/>
+            </conditional>
+            <output name="output" value="srma_out2.bigwig" compare="sim_size"/>
+        </test>
+        <test expect_num_outputs="1">
+            <conditional name="hist_or_builtin">
+                <param name="genosrc" value="history"/>
+                <param name="input1" value="test5.gff3"/>
+                <param name="chromfile" value="testing.len"/>
+            </conditional>
+            <output name="output" value="test5.gff.bigwig" compare="sim_size"/>
+        </test>
+        <test expect_num_outputs="1">
+            <conditional name="hist_or_builtin">
+                <param name="genosrc" value="history"/>
+                <param name="input1" value="test5.bed"/>
+                <param name="chromfile" value="testing.len"/>
+            </conditional>
+            <output name="output" value="test5.bed.bigwig" compare="sim_size"/>
+        </test>
+    </tests>
+    <help>
+
+   Estimates coverage of a reference genome for bam, bed or gff as a bigwig, suitable for viewing in JBrowse2 or other browser.
+ 
+   A chromosome lengths file must be provided if the input has a missing dbkey (='?') on the pencil (edit attributes) form. 
+   
+   The actual reference is not needed. The Compute sequence length tool can generate the lengths file.
+ 
+   This can be useful in workflows with assemblies in progress before a stable reference is available for a custom or built in reference dbkey.
+
+    </help>    
+    <citations>
+        <citation type="doi">10.1093/bioinformatics/btq351</citation>
+    </citations>
+</tool>