diff fastq_dump_pe.xml @ 0:1a11c4fd13d0 draft

planemo upload for repository https://github.com/statonlab/docker-GRReport/tree/master/my_tools/rmarkdown_fastq_dump commit 65063d5b207a70df38a0bcb6fb57a8f9170d9e9b
author mingchen0919
date Wed, 27 Sep 2017 21:41:29 -0400
parents
children cd86400bbaed
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+++ b/fastq_dump_pe.xml	Wed Sep 27 21:41:29 2017 -0400
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+<tool id="rmarkdown_fastqc_dump_pe" name="fastqc-dump-pe" version="1.0.0">
+    <requirements>
+        <requirement type="package" version="1.15.0.6-0">pandoc</requirement>
+        <requirement type="package" version="1.20.0">r-getopt</requirement>
+        <requirement type="package" version="1.2">r-rmarkdown</requirement>
+        <requirement type="package" version="0.3.5">r-htmltools</requirement>
+        <requirement type="package" version="0.5.0">r-dplyr</requirement>
+        <requirement type="package" version="0.5.4">parallel-fastq-dump</requirement>
+    </requirements>
+    <description>
+        Download and extract paired end reads in fastq or fasta format from NCBI SRA. The output is a list of paired datasets
+        collection.
+    </description>
+    <stdio>
+        <!--All stderr are redirected to a file. "XXX" is used to match with nothing-->
+        <regex match="XXX"
+               source="stderr"
+               level="warning"
+               description="Check the warnings_and_errors.txt file for more details."/>
+    </stdio>
+    <command>
+        <![CDATA[
+            Rscript '${__tool_directory__}/fastq_dump_pe_render.R'
+                -i '$sra_accession'
+                -e $echo
+                -f $format
+
+                -r $report
+                -d $report.files_path
+                -s $sink_message
+
+                -t '${__tool_directory__}/fastq_dump_pe.Rmd'
+        ]]>
+    </command>
+    <inputs>
+        <param type="text" name="sra_accession" label="SRR/DRR/ERR accessions" optional="false"
+               help="A list of SRR/DRR/ERR accessions separated by comma or space. e.g. SRR6077558,ERR343809"/>
+        <param type="boolean" name="format" truevalue="fastq" falsevalue="fasta" checked="true"
+               label="output files in fastq (Yes) or fasta (No)?"/>
+        <param type="boolean" name="echo" truevalue="TRUE" falsevalue="FALSE" checked="false"
+               label="Display analysis code in report?"/>
+    </inputs>
+    <outputs>
+        <data format="html" name="report" label="Fastq-dump report" />
+        <collection type="list:paired" name="list_collection" label="Fastq-dump (paired end reads)">
+            <discover_datasets pattern="(?P&lt;identifier_0&gt;[^_]+)_(?P&lt;identifier_1&gt;[^_]+)\.(?P&lt;ext&gt;[^\._]+)?" directory="read_files_directory"/>
+        </collection>
+        <data format="txt" name="sink_message" label="Warnings and Errors" from_work_dir="warnings_and_errors.txt" />
+    </outputs>
+</tool>
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