Mercurial > repos > jpayne > snp_pipeline
view 1_map_reads.xml @ 54:2939020396a4
"planemo upload"
author | jpayne |
---|---|
date | Thu, 05 Nov 2020 15:50:11 -0500 |
parents | e90a783a4e8b |
children | d53281e6edae |
line wrap: on
line source
<tool id="map_reads" name="1. Map Reads" version="1.0.1" profile="16.10"> <description>to index, or lookup cached alignment</description> <requirements> <requirement type="package" version="1.0.6">bzip2</requirement> <requirement type="package" version="2.3.5">bowtie2</requirement> <requirement type="package" version="1.9.134">boto3</requirement> <requirement type="package" version="3.6.8">python</requirement> </requirements> <command detect_errors="exit_code"><![CDATA[ export LD_LIBRARY_PATH="\$CONDA_DEFAULT_ENV/lib" && #if $reads.reads_select == 'collection' #set forward=$reads.coll.forward #set reverse=$reads.coll.reverse #end if python ${__tool_directory__}/snp-cache.py snp_mapped_reads "\$(md5sum $reference $forward $reverse | cut -c -32 | md5sum | cut -c -32)" -c " cp $reference ./reference.fasta #if $forward.is_of_type("fastq.gz","fastqsanger.gz") && cp $forward ./forward.gz #set $forward="./forward.gz" #else if $forward.is_of_type("fastq.bz2", "fastqsanger.bz2") && cp $forward ./forward.bz2 #set $forward="./forward.bz2" #end if #if $reverse.is_of_type("fastq.gz","fastqsanger.gz") && cp $reverse ./reverse.gz #set $reverse="./reverse.gz" #else if $reverse.is_of_type("fastq.bz2", "fastqsanger.bz2") && cp $reverse ./reverse.bz2 #set $reverse="./reverse.bz2" #end if && bowtie2-build ./reference.fasta --quiet --threads \${GALAXY_SLOTS:-4} ./reference && bowtie2 -q -x ./reference -1 $forward -2 $reverse -p \${GALAXY_SLOTS:-4} --reorder -X 1000 " #if $reads.reads_select == 'collection' -o ${align_from_collection} #else -o ${align_from_history} #end if -l $cache_log && cat $cache_log #if $source.source_select == 'curated' && cp $reference $ref_out #end if ]]></command> <inputs> <!-- <conditional name="source"> <param name="source_select" type="select" label="Use the reference associated with a provided BioProject, a curated GalaxyTrakr reference, or a reference from your history"> <option value="bioproject">Provide a BioProject</option> <option value="curated">Use a GalaxyTrakr reference</option> <option value="history">Use a reference from your history</option> </param> <when value="bioproject"> <param type="data" name="bioproject" format="text" /> </when> <when value="curated"> <param name="input" type="select" label="Select reference fasta"> <options from_data_table="all_fasta"> <filter type="sort_by" column="2"/> <validator type="no_options" message="No assemblies are available for the selected input dataset"/> </options> </param> </when> <when value="history"> <param type="data" name="input" format="fasta" label="Select reference FASTA"/> </when> </conditional> --> <conditional name="source"> <param name="source_select" type="select" label="Use a curated GalaxyTrakr reference or a reference from your history"> <option value="curated">Use a GalaxyTrakr reference</option> <option value="history">Use a reference from your history</option> </param> <when value="curated"> <param name="reference" type="select" label="Select reference fasta"> <options from_data_table="all_fasta"> <filter type="sort_by" column="2"/> <validator type="no_options" message="No assemblies are available for the selected input dataset"/> </options> </param> </when> <when value="history"> <param type="data" name="reference" format="fasta" label="Select reference FASTA"/> </when> </conditional> <conditional name="reads"> <param name="reads_select" type="select" label="Paired-end collection, or two datasets from your history"> <option value="collection">Paired collection from your history</option> <option value="history">Two FASTQ datasets from your history</option> </param> <when value="collection"> <param label="Paired reads" name="coll" type="data_collection" format="fastq,fastqsanger,fastq.gz,fastqsanger.gz,fastq.bz2,fastqsanger.bz2" collection_type="paired" /> </when> <when value="history"> <param label="Forward reads" type="data" name="forward" format="fastq,fastqsanger,fastq.gz,fastqsanger.gz,fastq.bz2,fastqsanger.bz2" /> <param label="Reverse reads" type="data" name="reverse" format="fastq,fastqsanger,fastq.gz,fastqsanger.gz,fastq.bz2,fastqsanger.bz2" /> </when> </conditional> </inputs> <outputs> <data label="${reads.coll.name} alignment" name="align_from_collection" format="sam"> <filter>reads['reads_select'] == 'collection'</filter> </data> <data label="${reads.forward.name.split('_')[0]} alignment" name="align_from_history" format="sam"> <filter>reads['reads_select'] == 'history'</filter> </data> <data label="S3 Cache log" name="cache_log" format="txt" hidden="true" /> <data label="Reference" name="ref_out" format="fasta" hidden="true"> <filter>source['source_select'] == curated</filter> </data> </outputs> <tests> <test> <param name="source_select" value="history" /> <param name="reference" value="reference/lambda_virus.fasta" ftype="fasta" /> <param name="reads_select" value="history" /> <param name="forward" value="samples/sample1/sample1_1.fastq" ftype="fastqsanger" /> <param name="reverse" value="samples/sample1/sample1_2.fastq" ftype="fastqsanger" /> <output name="align_from_history" value="samples/sample1/reads.sam" lines_diff="3" /> </test> <test> <param name="source_select" value="history" /> <param name="reference" value="reference/lambda_virus.fasta" ftype="fasta" /> <param name="reads_select" value="collection" /> <param name="coll"> <collection type="paired"> <element name="forward" value="samples/sample1/sample1_1.fastq" ftype="fastqsanger" /> <element name="reverse" value="samples/sample1/sample1_2.fastq" ftype="fastqsanger" /> </collection> </param> <output name="align_from_collection" value="samples/sample1/reads.sam" lines_diff="3" /> </test> <test> <param name="source_select" value="history" /> <param name="reference" value="reference/lambda_virus.fasta" ftype="fasta" /> <param name="reads_select" value="history" /> <param name="forward" value="samples/sample1/sample1_1.fastq.gz" ftype="fastqsanger.gz" /> <param name="reverse" value="samples/sample1/sample1_2.fastq.gz" ftype="fastqsanger.gz" /> <output name="align_from_history" value="samples/sample1/reads.sam" lines_diff="3" /> </test> </tests> <help><![CDATA[ <a href="http://snp-pipeline.readthedocs.io/en/latest/index.html">http://snp-pipeline.readthedocs.io/en/latest/index.html</a> ]]></help> <citations> <citation type="doi">10.7717/peerj-cs.20</citation> <!-- <citation type="bibtex"> @misc{cfsan-snp-pipeline, author = {Steve Davis and James Pettengill and Yan Luo and Justin Payne and Albert Shpuntoff and Rugh Rand and Errol Strain}, year = {2015}, title = {CFSAN SNP Pipeline: an automated method for constructing SNP matrices from next-generation sequence data}, url = {https://doi.org/10.7717/peerj-cs.20}, journal = {PeerJ Computer Science}, }</citation> --> </citations> </tool>