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planemo upload commit 2e9511a184a1ca667c7be0c6321a36dc4e3d116d
author | jpayne |
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date | Thu, 20 Mar 2025 00:01:12 -0400 |
parents | 33d812a61356 |
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<tool id="csp2-screen" name="CSP2 (Screening Mode)" version="0.9.7_Dev21"> <description>Screen query assemblies against reference assemblies</description> <requirements> <!-- <requirement type="package" version="24.10.1">nextflow</requirement> <requirement type="package" version="1.5.8">micromamba</requirement> --> <container type="docker">cfsanbiostatistics/csp2:v.0.9.7.4</container> </requirements> <version_command>nextflow -version</version_command> <command detect_errors="exit_code"><![CDATA[ mkdir -p queries references #set readext="" #for $reads in $query.coll #if $hasattr($reads, "is_of_type") and $reads.is_of_type("fasta") && ln -sf ${reads} 'queries/${reads.element_identifier}.fasta' #else if $reads.forward.is_of_type("fastq.gz","fastqsanger.gz") #set readext="fastq.gz" && ln -sf '${reads.forward}' 'queries/${reads.forward.element_identifier}_1.fastq.gz' && ln -sf '${reads.reverse}' 'queries/${reads.reverse.element_identifier}_2.fastq.gz' #else if $reads.forward.is_of_type("fastq.bz2", "fastqsanger.bz2") #set readext="fastq.bz2" && ln -sf '${reads.forward}' 'queries/${reads.forward.element_identifier}_1.fastq.bz2' && ln -sf '${reads.reverse}' 'queries/${reads.reverse.element_identifier}_2.fastq.bz2' #else #set readext="fastq" && ln -sf '${reads.forward}' 'queries/${reads.forward.element_identifier}_1.fastq' && ln -sf '${reads.reverse}' 'queries/${reads.reverse.element_identifier}_2.fastq' #end if #end for && echo "*** Files in queries directory: ***" && ls -lah queries/ && ln -sf '$source.reference' 'references/${source.reference.element_identifier}.fasta' && nextflow run ${__tool_directory__}/CSP2/CSP2.nf -profile csp2_galaxy --runmode screen #if $query.query_select == 'reads' --reads queries --readext $readext --forward "_1.${readext}" --reverse "_2.${readext}" #else --fasta queries #end if --ref_fasta 'references/${source.reference.element_identifier}.fasta' --min_cov $opt.min_cov --min_iden $opt.min_iden --min_len $opt.min_len --ref_edge $opt.ref_edge --query_edge $opt.query_edge --dwin $opt.dwin --wsnps $opt.wsnps --out CSP2_Screen_Output && echo "*** Files in output directory: ***" && ls -lah CSP2_Screen_Output && echo "*** Nextflow log follows: ***" && cat .nextflow.log ]]> </command> <inputs> <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="query"> <param name="query_select" type="select" label="Screen a list of paired-end reads or a list of assemblies"> <option value="reads">Screen a list of paired reads</option> <option value="assemblies">Screen a list of assemblies</option> </param> <when value="reads"> <param label="Paired reads" name="coll" type="data_collection" format="fastq,fastqsanger,fastq.gz,fastqsanger.gz,fastq.bz2,fastqsanger.bz2" collection_type="list:paired" /> </when> <when value="assemblies"> <param label="Assemblies" name="coll" type="data_collection" format="fasta" collection_type="list" /> </when> </conditional> <section name="opt" title="Advanced options..."> <param argument="--min_cov" name="min_cov" type="float" value="85" label="Minimum reference genome coverage to proceed with distance estimation" /> <param argument="--min_eden" name="min_iden" type="float" value="99" label="Minimum alignment percent identity to detect SNPs" /> <param argument="--min_len" name="min_len" type="integer" value="500" label="Minimum alignment length to detect SNPs" /> <param argument="--ref_edge" name="ref_edge" type="integer" value="150" label="Prune SNPs within this many bases of reference contig edge" /> <param argument="--query_edge" name="query_edge" type="integer" value="150" label="Prune SNPs within this many bases of query contig edge" /> <param argument="--dwin" name="dwin" type="text" value="1000,125,15" label="Comma-separated set of window sizes for SNP density filtration (Set to 0 to disable density filtration)" /> <param argument="--wsnips" name="wsnps" type="text" value="3,2,1" label="Comma-separated list of maximum SNP counts per density window" /> </section> </inputs> <outputs> <data name="raw_mummer" format="tabular" label="Raw MUMmer Output" from_work_dir="CSP2_Screen_Output/Raw_MUMmer_Summary.tsv" /> <data name="isolate_data" format="tabular" label="Isolate Data" from_work_dir="CSP2_Screen_Output/Isolate_Data.tsv" /> <data name="screening_results" format="tabular" label="Screening Results" from_work_dir="CSP2_Screen_Output/Screening_Results.tsv" /> <!-- <data name="nextflow_log" format="txt" label="Nextflow Log" from_work_dir="Nextflow_Log.txt" /> --> </outputs> <tests> <test> <param name="source_select" value="history" /> <param name="reference" value="assemblies/Sample_A.fasta" ftype="fasta" /> <param name="query_select" value="assemblies" /> <param name="coll"> <collection type="list"> <!-- <element name="Sample_A" value="assemblies/Sample_A.fasta" /> --> <element name="Sample_B" value="assemblies/Sample_B.fasta" /> <element name="Sample_C" value="assemblies/Sample_C.fasta" /> <element name="Sample_D" value="assemblies/Sample_D.fasta" /> <element name="Sample_E" value="assemblies/Sample_E.fasta" /> <element name="Sample_F" value="assemblies/Sample_F.fasta" /> <element name="Sample_G" value="assemblies/Sample_G.fasta" /> <element name="Sample_H" value="assemblies/Sample_H.fasta" /> <element name="Sample_I" value="assemblies/Sample_I.fasta" /> <element name="Sample_J" value="assemblies/Sample_J.fasta" /> <element name="Sample_K" value="assemblies/Sample_K.fasta" /> <element name="Sample_L" value="assemblies/Sample_L.fasta" /> <element name="Sample_M" value="assemblies/Sample_M.fasta" /> <element name="Sample_N" value="assemblies/Sample_N.fasta" /> <element name="Sample_O" value="assemblies/Sample_O.fasta" /> </collection> </param> <output name="screening_results" value="Screening_Results.tsv" /> <output name="isolate_data" value="Isolate_Data.tsv" /> </test> <test> <param name="source_select" value="history" /> <param name="reference" value="assemblies/Sample_A.fasta" ftype="fasta" /> <param name="query_select" value="reads" /> <param name="coll"> <collection type="list:paired"> <element name="Sample_A" > <collection type="paired"> <element name="forward" value="reads/Week_42_Reads_1.fq.gz" ftype="fastqsanger.gz" /> <element name="reverse" value="reads/Week_42_Reads_2.fq.gz" ftype="fastqsanger.gz" /> </collection> </element> </collection> </param> <output name="screening_results" value="Screening_Results.tsv" /> <output name="isolate_data" value="Isolate_Data.tsv" /> </test> </tests> <help> This tool takes query assemblies and reference assemblies and calculates the pairwise distance between each query/reference combination. If no reference is provided, all queries are compared to all other queries. </help> <citations> <citation type="doi">10.XXXX/placeholder.doi</citation> <citation type="bibtex">@article{example2024,title={CFSAN SNP Pipeline 2 (CSP2): a pipeline for fast and accurate SNP distance estimation from bacterial genome assemblies.},author={Doe, John and Smith, Jane},journal={Submitted},year={2024}} </citation> </citations> </tool>