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

Changeset 1:383bb5ad32e2 (2021-02-13)
Previous changeset 0:85658cabbbed (2021-02-11) Next changeset 2:cb4768eeca3b (2021-10-04)
Commit message:
"planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/trycycler commit e88166111fa3b6c57c870ea4cff6e012a1b1a912"
modified:
trycycler_subsample.xml
b
diff -r 85658cabbbed -r 383bb5ad32e2 trycycler_subsample.xml
--- a/trycycler_subsample.xml Thu Feb 11 19:25:20 2021 +0000
+++ b/trycycler_subsample.xml Sat Feb 13 17:30:32 2021 +0000
[
b"@@ -1,10 +1,10 @@\n-<tool id='trycycler_subsample' name='Trycycler subsample' version='@TOOL_VERSION@' profile='21.01'>\n+<tool id='trycycler_subsample' name='Trycycler subsample' version='@TOOL_VERSION@' profile='20.01'>\n     <description>make a maximally-independent read subsets of an appropiate depth for your genome</description>\n     <macros>\n         <import>macros.xml</import>\n     </macros>\n-    <expand macro='edam_ontology'/>\n-    <expand macro='requirements'/>\n+    <expand macro='edam_ontology' />\n+    <expand macro='requirements' />\n     <version_command>trycycler --version</version_command>\n     <command detect_errors='exit_code'><![CDATA[\n         mkdir -p output_subsamples &&\n@@ -17,34 +17,21 @@\n             --min_read_depth $min_read_depth\n             --threads \\${GALAXY_SLOTS:-2}\n             --out_dir output_subsamples\n-    ]]></command>\n+    ]]>    </command>\n     <inputs>\n-        <param name='reads' type='data' \n-            format='fastq,fastq.gz'  \n-            label='Long-read dataset' help='--reads' />\n-        <param argument='--count' type='integer' \n-            min='2' max='20' \n-            value='12' label='Number of subsampled reads set to output' \n-            help='The number of subsamples reads to make maximally-independent read subsets. The default is 12, a good number for most cases.' />\n+        <param name='reads' type='data' format='fastq,fastq.gz' label='Long-read dataset' help='--reads' />\n+        <param argument='--count' type='integer' min='2' max='20' value='12' label='Number of subsampled reads set to output' help='The number of subsamples reads to make maximally-independent read subsets. The default is 12, a good number for most cases.' />\n         <conditional name='option'>\n-            <param name='genome' type='select' \n-                label='Provide an estimated genomoe size'\n-                help='If you do not provide this, Trycycler subsample will run miniasm to quickly assemble your read set to get a size. This value is used to calculate read depths and does not need to be exact, e.g. 10% error is fine.' >\n-                    <option value='true'>Provide estimeted genome size</option>\n-                    <option value='false'>Run miniasm for estimating genome size</option>\n+            <param name='genome' type='select' label='Provide an estimated genomoe size' help='If you do not provide this, Trycycler subsample will run miniasm to quickly assemble your read set to get a size. This value is used to calculate read depths and does not need to be exact, e.g. 10% error is fine.' >\n+                <option value='true'>Provide estimeted genome size</option>\n+                <option value='false'>Run miniasm for estimating genome size</option>\n             </param>\n-            <when value='false'/>\n+            <when value='false' />\n             <when value='true'>\n-                <param argument='--genome_size' type='integer' \n-                    min='10000' max='15000000' \n-                    value='30000' label='Estimated total genome size' \n-                    help='An estimate of the isolate total genome size.' />\n+                <param argument='--genome_size' type='integer' min='10000' max='15000000' value='30000' label='Estimated total genome size' help='An estimate of the isolate total genome size.' />\n             </when>\n         </conditional>\n-        <param argument='--min_read_depth' type='integer' min='15' max='120' \n-            value='25' \n-            label='Minimum subset read depth' \n-            help='This is the minimum allowed read depth and also controls the subsampled depths. If is not provided, Trycycle decides what read depth each subset will be.' />\n+        <param argument='--min_read_depth' type='integer' min='15' max='120' value='25' label='Minimum subset read depth' help='This is the minimum allowed read depth and also controls the subsampled depths. If is not provided, Trycycle decides what read depth each subset will be.' />\n     </"..b"amples_fastq' type='list' count='5'>\n-                <element name='sample_01' file='sample_01_03.fastq' ftype='fastq'/>\n-                <element name='sample_02' file='sample_02_03.fastq' ftype='fastq'/>\n-                <element name='sample_03' file='sample_03_03.fastq' ftype='fastq'/>\n-                <element name='sample_04' file='sample_04_03.fastq' ftype='fastq'/>\n-                <element name='sample_05' file='sample_05_03.fastq' ftype='fastq'/>\n+                <element name='sample_01' file='sample_01_03.fastq' ftype='fastq' />\n+                <element name='sample_02' file='sample_02_03.fastq' ftype='fastq' />\n+                <element name='sample_03' file='sample_03_03.fastq' ftype='fastq' />\n+                <element name='sample_04' file='sample_04_03.fastq' ftype='fastq' />\n+                <element name='sample_05' file='sample_05_03.fastq' ftype='fastq' />\n             </output_collection>\n         </test>\n         <test>\n-            <param name='reads' value='reads.fastq.gz'/>\n+            <param name='reads' value='reads.fastq.gz' />\n             <conditional name='option'>\n-                <param name='genome' value='true'/>\n-                <param name='genome_size' value='10000'/>\n+                <param name='genome' value='true' />\n+                <param name='genome_size' value='10000' />\n             </conditional>\n-            <param name='min_read_depth' value='30'/>\n-            <param name='count' value='12'/>\n+            <param name='min_read_depth' value='30' />\n+            <param name='count' value='12' />\n             <output_collection name='subsamples_fastq' type='list' count='12'>\n-                <element name='sample_01' file='sample_01_04.fastq' ftype='fastq'/>\n-                <element name='sample_02' file='sample_02_04.fastq' ftype='fastq'/>\n-                <element name='sample_03' file='sample_03_04.fastq' ftype='fastq'/>\n-                <element name='sample_04' file='sample_04_04.fastq' ftype='fastq'/>\n-                <element name='sample_05' file='sample_05_04.fastq' ftype='fastq'/>\n-                <element name='sample_06' file='sample_06_04.fastq' ftype='fastq'/>\n-                <element name='sample_07' file='sample_07_04.fastq' ftype='fastq'/>\n-                <element name='sample_08' file='sample_08_04.fastq' ftype='fastq'/>\n-                <element name='sample_09' file='sample_09_04.fastq' ftype='fastq'/>\n-                <element name='sample_10' file='sample_10_04.fastq' ftype='fastq'/>\n-                <element name='sample_11' file='sample_11_04.fastq' ftype='fastq'/>\n-                <element name='sample_12' file='sample_12_04.fastq' ftype='fastq'/>\n+                <element name='sample_01' file='sample_01_04.fastq' ftype='fastq' />\n+                <element name='sample_02' file='sample_02_04.fastq' ftype='fastq' />\n+                <element name='sample_03' file='sample_03_04.fastq' ftype='fastq' />\n+                <element name='sample_04' file='sample_04_04.fastq' ftype='fastq' />\n+                <element name='sample_05' file='sample_05_04.fastq' ftype='fastq' />\n+                <element name='sample_06' file='sample_06_04.fastq' ftype='fastq' />\n+                <element name='sample_07' file='sample_07_04.fastq' ftype='fastq' />\n+                <element name='sample_08' file='sample_08_04.fastq' ftype='fastq' />\n+                <element name='sample_09' file='sample_09_04.fastq' ftype='fastq' />\n+                <element name='sample_10' file='sample_10_04.fastq' ftype='fastq' />\n+                <element name='sample_11' file='sample_11_04.fastq' ftype='fastq' />\n+                <element name='sample_12' file='sample_12_04.fastq' ftype='fastq' />\n             </output_collection>\n-        </test> \n+        </test>\n     </tests>\n     <help><![CDATA[\n .. class:: infomark\n@@ -153,6 +140,6 @@\n .. class:: infomark\n \n @PIPELINE@\n-    ]]></help>\n-    <expand macro='citations'/>\n+    ]]>    </help>\n+    <expand macro='citations' />\n </tool>\n"