Mercurial > repos > bgruening > hicup_mapper
diff hicup_mapper.xml @ 4:99dd0efa992b draft
planemo upload for repository https://github.com/joachimwolff/galaxytools/tree/hicup/tools/hicup commit 22eec1b3b20b788e762837c02488f332f831fab3
author | bgruening |
---|---|
date | Fri, 25 May 2018 17:48:10 -0400 |
parents | 320a2d826a00 |
children | 396e8c4ebfee |
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--- a/hicup_mapper.xml Thu Nov 09 11:16:29 2017 -0500 +++ b/hicup_mapper.xml Fri May 25 17:48:10 2018 -0400 @@ -4,55 +4,66 @@ <import>hicup_macros.xml</import> </macros> <expand macro="requirements_hicup" /> - <expand macro="stdio" /> - - <command><![CDATA[ + <command detect_errors="exit_code"><![CDATA[ BOWTIE_PATH_BASH="\$(which bowtie2)" && #set index_path = '' #if str($reference_genome.source) == "history": - bowtie2-build "$reference_genome.own_file" genome && - ln -s "$reference_genome.own_file" genome.fa && + bowtie2-build '$reference_genome.own_file' genome && + ln -s '$reference_genome.own_file' genome.fa && #set index_path = 'genome' #else: #set index_path = $reference_genome.index.fields.path #end if - hicup_mapper - --index '$index_path' - --bowtie2 \$BOWTIE_PATH_BASH - $input_first_sequence $input_second_sequence + ##Dealing with fastq and fastq.gz + #if $input_first_sequence.is_of_type("fastq.gz", "fastqsanger.gz"): + ln -s $input_first_sequence dataset1.gz && + #set input1='dataset1.gz' + #else + ln -s $input_first_sequence dataset1 && + #set input1='dataset1' + #end if - ## output handling - && mv hicup_mapper_summary* hicup_mapper_summary.txt - && mv *.pair.sam result.pair.sam - && trunc_result_1=\$(echo '$input_first_sequence' | rev | cut -d'/' -f1 | rev) - && trunc_result_2=\$(echo '$input_second_sequence' | rev | cut -d'/' -f1 | rev) - && mv \$trunc_result_1*.mapper_barchart.svg dataset1.mapper_barchart.svg - && mv \$trunc_result_2*.mapper_barchart.svg dataset2.mapper_barchart.svg - && echo \$trunc_result_1.mapper_barchart.svg - && echo \$trunc_result_2.mapper_barchart.svg + #if $input_second_sequence.is_of_type("fastq.gz", "fastqsanger.gz"): + ln -s $input_second_sequence dataset2.gz && + #set input2='dataset2.gz' + #else + ln -s $input_second_sequence dataset2 && + #set input2='dataset2' + #end if + + + hicup_mapper + --zip + --threads \${GALAXY_SLOTS:-1} + --index '$index_path' + --bowtie2 \$BOWTIE_PATH_BASH + $input1 + $input2 + ]]></command> <inputs> <expand macro="input_files" /> <expand macro="reference_genome_macro" /> </inputs> <outputs> - <expand macro="mapper_output" /> + <data name="hicup_mapper_summary" format="txt" from_work_dir="hicup_mapper_summary*" label="hicup_mapper_summary.txt"/> + <data name="result_pair" format="qname_sorted.bam" from_work_dir="*pair.bam" label="pair.bam"/> + <data name="dataset1_mapper_barchart" format="svg" from_work_dir="dataset1*.mapper_barchart.svg" label="Mapper Dataset1 Barchart.svg" /> + <data name="dataset2_mapper_barchart" format="svg" from_work_dir="dataset2*.mapper_barchart.svg" label="Mapper Dataset2 Barchart.svg" /> </outputs> <tests> <test> - <param name="input_first_sequence" value="dataset1.trunc.fastq" ftype="fastq"/> - <param name="input_second_sequence" value="dataset2.trunc.fastq" ftype="fastq"/> - + <param name="input_first_sequence" value="dataset1.trunc.fastq.gz" ftype="fastq.gz"/> + <param name="input_second_sequence" value="dataset2.trunc.fastq.gz" ftype="fastq.gz"/> <conditional name="reference_genome"> <param name="source" value="history" /> - <param name="own_file" value="chr1.fa"/> + <param name="own_file" value="chr21And22FromHg38.fasta"/> </conditional> <output name="hicup_mapper_summary" file="hicup_mapper_summary.txt" lines_diff="4"/> - <output name="result_pair" file="result.pair.sam" lines_diff="8"/> + <output name="result_pair" file="dataset1_2.pair.bam" lines_diff="8" ftype="qname_sorted.bam" /> <output name="dataset1_mapper_barchart" file="dataset1.mapper_barchart.svg" ftype="svg" lines_diff="1000"/> <output name="dataset2_mapper_barchart" file="dataset2.mapper_barchart.svg" ftype="svg" lines_diff="1000"/> - </test> </tests> <help><![CDATA[