Mercurial > repos > mingchen0919 > rmarkdown_fastq_dump
view fastq_dump_se.xml @ 4:c9b56151f112 draft
planemo upload for repository https://github.com/statonlab/docker-GRReport/tree/master/my_tools/rmarkdown_fastq_dump commit c9517f0b061cdca3b79678d9a2620e1e43115d42-dirty
author | mingchen0919 |
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date | Wed, 27 Sep 2017 11:10:59 -0400 |
parents | dce9200ef1b7 |
children | a2ba5619f51b |
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<tool id="rmarkdown_fastqc_dump_se" name="fastqc-dump-se" 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 single end reads in fastq or fasta format from NCBI SRA. The output is a list of datasets collection. </description> <stdio> <regex match="Execution halted" source="both" level="fatal" description="Execution halted." /> <regex match="Error in" source="both" level="fatal" description="An undefined error occured, please check your intput carefully and contact your administrator." /> <regex match="Fatal error" source="both" level="fatal" description="An undefined error occured, please check your intput carefully and contact your administrator." /> </stdio> <command> <![CDATA[ Rscript '${__tool_directory__}/fastqc_dump_se_render.R' -i $sra_accession -e $echo -f $format -r $report -d $report.files_path -t '${__tool_directory__}/fastq_dump_se.Rmd' ]]> </command> <inputs> <param type="text" name="sra_accession" label="SRR/DRR/ERR accessions" 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="false" label="output files in fastq (true) or fasta (false)?"/> <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 (single end reads)" /> <collection type="list" name="list_collection"> <discover_datasets pattern="__name_and_ext__" directory="read_files_directory" /> </collection> </outputs> </tool>