diff rgFastQC.xml @ 17:7b0207bd2183 draft

planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/fastqc commit 2f544e337886709995a93d53f394919ce8e4673a

--- a/rgFastQC.xml	Mon Nov 05 12:07:47 2018 -0500
+++ b/rgFastQC.xml	Fri May 10 14:23:28 2019 -0400
@@ -1,17 +1,9 @@
 <tool id="fastqc" name="FastQC" version="0.72">
     <description>Read Quality reports</description>
     <requirements>
-        <requirement type="package" version="0.11.8">fastqc</requirement>
+        <requirement type="package" version="0.11.7">fastqc</requirement>
     </requirements>
-    <stdio>
-        <exit_code range="1:" level="fatal" description="FastQC returned non zero exit code" />
-        <exit_code range=":-1" level="fatal" description="FastQC returned non zero exit code" />
-    <regex match="There is insufficient memory for the Java Runtime Environment"
-           source="stdout"
-           level="fatal_oom"
-           description="Out of memory error occurred" />
-    </stdio>
-    <command><![CDATA[
+    <command detect_errors="exit_code"><![CDATA[
         #import re
         #set input_name = re.sub('[^\w\-\s]', '_', str($input_file.element_identifier))
 
@@ -35,25 +27,17 @@
         mkdir -p '${html_file.files_path}' &&
         fastqc
             --outdir '${html_file.files_path}'
+
             #if $contaminants.dataset and str($contaminants) > ''
                 --contaminants '${contaminants}'
             #end if
 
-            #if $adapters.dataset and str($adapters) > ''
-                --adapters '${adapters}'
-            #end if
-
             #if $limits.dataset and str($limits) > ''
                 --limits '${limits}'
             #end if
 
             --quiet
             --extract
-            #if $min_length:
-                --min_length $min_length
-            #end if
-            $nogroup
-            --kmers $kmers
             -f '${format}'
             '${input_file_sl}'
 
@@ -66,17 +50,8 @@
                label="Short read data from your current history" />
         <param name="contaminants" type="data" format="tabular" optional="true" label="Contaminant list"
                help="tab delimited file with 2 columns: name and sequence.  For example: Illumina Small RNA RT Primer CAAGCAGAAGACGGCATACGA" />
-        <param argument="--adapters" type="data" format="tabular" optional="true" label="Adapter list"
-               help="list of adapters adapter sequences which will be explicity searched against the library. tab delimited file with 2 columns: name and sequence." />
         <param name="limits" type="data" format="txt" optional="true" label="Submodule and Limit specifing file"
                help="a file that specifies which submodules are to be executed (default=all) and also specifies the thresholds for the each submodules warning parameter" />
-        <param argument="--nogroup" type="boolean" truevalue="--nogroup" falsevalue="" checked="False"
-               label="Disable grouping of bases for reads >50bp" help="Using this option will cause fastqc to crash and burn if you use it on really long reads, and your plots may end up a ridiculous size. You have been warned!"/>
-        <param argument="--min_length" type="integer" value="" optional="true"
-               label="Lower limit on the length of the sequence to be shown in the report"
-               help=" As long as you set this to a value greater or equal to your longest read length then this will be the sequence length used to create your read groups.  This can be useful for making directly comaparable statistics from datasets with somewhat variable read lengths."/>
-        <param argument="--kmers" type="integer" value="7" min="2" max="10"
-               label="length of Kmer to look for" help="note: the Kmer test is disabled and needs to be enabled using a custom Submodule and limits file"/>
     </inputs>
     <outputs>
         <data format="html" name="html_file" from_work_dir="output.html" label="${tool.name} on ${on_string}: Webpage" />
@@ -84,67 +59,43 @@
     </outputs>
     <tests>
         <test>
-            <param name="input_file" value="1000trimmed.fastq" />
-            <output name="html_file" file="fastqc_report.html" ftype="html" compare="sim_size" delta="5000"/>
-            <output name="text_file" file="fastqc_data.txt" ftype="txt"/>
-        </test>
-        <test>
-            <param name="input_file" value="1000trimmed.fastq" />
+            <param name="input_file" value="1000gsample.fastq" />
             <param name="contaminants" value="fastqc_contaminants.txt" ftype="tabular" />
-            <output name="html_file" file="fastqc_report_contaminants.html" ftype="html" compare="sim_size" delta="5000"/>
-            <output name="text_file" file="fastqc_data_contaminants.txt" ftype="txt"/>
-        </test>
-        <test>
-            <param name="input_file" value="1000trimmed.fastq" />
-            <param name="adapters" value="fastqc_adapters.txt" ftype="tabular" />
-            <output name="html_file" file="fastqc_report_adapters.html" ftype="html" compare="sim_size" delta="5000"/>
-            <output name="text_file" file="fastqc_data_adapters.txt" ftype="txt"/>
-        </test>
-        <test>
-            <param name="input_file" value="1000trimmed.fastq" />
-            <param name="limits" value="fastqc_customlimits.txt" ftype="txt" />
-            <output name="html_file" file="fastqc_report_customlimits.html" ftype="html" compare="sim_size" delta="5000"/>
-            <output name="text_file" file="fastqc_data_customlimits.txt" ftype="txt"/>
+            <output name="html_file" file="fastqc_report.html" ftype="html" lines_diff="100"/>
+            <output name="text_file" file="fastqc_data.txt" ftype="txt" lines_diff="4"/>
         </test>
         <test>
-            <param name="input_file" value="1000trimmed.fastq" ftype="fastq" />
-            <param name="kmers" value="3" />
+            <param name="input_file" value="1000gsample.fastq" />
             <param name="limits" value="fastqc_customlimits.txt" ftype="txt" />
-            <output name="html_file" file="fastqc_report_kmer.html" ftype="html" compare="sim_size" delta="5000"/>
-            <output name="text_file" file="fastqc_data_kmer.txt" ftype="txt"/>
-            <assert_command>
-                <has_text text="--kmers 3"/>
-            </assert_command>
+            <output name="html_file" file="fastqc_report2.html" ftype="html" lines_diff="100"/>
+            <output name="text_file" file="fastqc_data2.txt" ftype="txt" lines_diff="4"/>
         </test>
         <test>
-            <param name="input_file" value="1000trimmed.fastq" />
-            <param name="min_length" value="108" />
-            <output name="html_file" file="fastqc_report_min_length.html" ftype="html" compare="sim_size" delta="5000"/>
-            <output name="text_file" file="fastqc_data_min_length.txt" ftype="txt"/>
+            <param name="input_file" value="1000gsample.fastq.gz" ftype="fastq.gz" />
+            <param name="contaminants" value="fastqc_contaminants.txt" ftype="tabular" />
+            <output name="html_file" file="fastqc_report.html" ftype="html" lines_diff="100"/>
+            <output name="text_file" file="fastqc_data.txt" ftype="txt" lines_diff="4"/>
         </test>
         <test>
-            <param name="input_file" value="1000trimmed.fastq" ftype="fastq" />
-            <param name="nogroup" value="--nogroup" />
-            <output name="html_file" file="fastqc_report_nogroup.html" ftype="html" compare="sim_size" delta="5000"/>
-            <output name="text_file" file="fastqc_data_nogroup.txt" ftype="txt"/>
-            <assert_command>
-                <has_text text="--nogroup"/>
-            </assert_command>
+            <param name="input_file" value="1000gsample.fastq.bz2" ftype="fastq.bz2" />
+            <param name="contaminants" value="fastqc_contaminants.txt" ftype="tabular" />
+            <output name="html_file" file="fastqc_report.html" ftype="html" lines_diff="100"/>
+            <output name="text_file" file="fastqc_data.txt" ftype="txt" lines_diff="4"/>
         </test>
         <test>
             <param name="input_file" value="hisat_output_1.bam" ftype="bam" />
-            <output name="html_file" file="fastqc_report_hisat.html" ftype="html" compare="sim_size" delta="5000"/>
-            <output name="text_file" file="fastqc_data_hisat.txt" ftype="txt"/>
+            <output name="html_file" file="fastqc_report_hisat.html" ftype="html" lines_diff="100"/>
+            <output name="text_file" file="fastqc_data_hisat.txt" ftype="txt" lines_diff="4"/>
         </test>
     </tests>
-    <help><![CDATA[
+    <help>
 .. class:: infomark
 
 **Purpose**
 
 FastQC aims to provide a simple way to do some quality control checks on raw
 sequence data coming from high throughput sequencing pipelines.
-It provides a set of analyses which you can use to get a quick
+It provides a modular set of analyses which you can use to give a quick
 impression of whether your data has any problems of
 which you should be aware before doing any further analysis.
 
@@ -202,7 +153,7 @@
 All except Basic Statistics and Overrepresented sequences are plots.
  .. _FastQC: http://www.bioinformatics.babraham.ac.uk/projects/fastqc/
  .. _Picard-tools: https://broadinstitute.github.io/picard/
-    ]]></help>
+    </help>
     <citations>
         <citation type="bibtex">
         @unpublished{andrews_s,