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date | Wed, 12 Apr 2017 17:50:21 -0400 |
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<?xml version="1.0"?> <tool id="ucsc_pslcdnafilter" name="UCSC pslCDnaFilter" version="1.0"> <description>Filter cDNA alignments in psl format</description> <requirements> <requirement type="package" version="1.0">ucsc_tools_340_for_BLAT</requirement> </requirements> <command detect_errors="exit_code"><![CDATA[ pslReps -minAli=0.25 '${alignment}' output.reps.psl output.reps.psr && faPolyASizes '${query}' query.polyA && pslCDnaFilter #if $assembly_type == "native" -localNearBest=0.001 #if $assembly_category == "finished" -minId=0.95 -minCover=0.25 #elif $assembly_category == "well-ordered" -minId=0.95 -minCover=0.15 #else -minId=0.94 -minAlnSize=80 #end if #else -localNearBest=0.010 #if $assembly_category == "finished" -minId=0.35 -minCover=0.25 #elif $assembly_category == "well-ordered" -minId=0.35 -minCover=0.15 #else -minId=0.33 -minAlnSize=80 #end if #end if -minQSize=20 -ignoreIntrons -repsAsMatch -ignoreNs -bestOverlap -polyASizes=query.polyA output.reps.psl '${output_filtered}' ]]></command> <inputs> <param type="data" name="alignment" format="psl" /> <param type="data" name="query" format="fasta" /> <param name="assembly_type" type="select" label="Choose your type of cDNA sequence"> <option value="native">Same species</option> <option value="xeno">Across species</option> </param> <param name="assembly_category" type="select" label="Choose your genome assembly category"> <option value="finished">finished assemblies (high quality)</option> <option value="well-ordered">well-ordered assemblies (well ordered, whole genome shotgun)</option> <option value="low-coverage">low-coverage assemblies (low coverage (< 4x"), lots of contigs, N50 scaffold size < 1mb) </option> </param> </inputs> <outputs> <data format="psl" name="output_filtered" label="${tool.name} on ${on_string}:filtered BLAT results"></data> </outputs> <tests> <test> <param name="alignment" value="amaVit1_Gallus/amaVit1_Gallus_gallus.psl" /> <param name="query" value="amaVit1_Gallus/Gallus_gallus_RefSeq.fa" /> <param name="assembly_type" value="xeno" /> <param name="assembly_category" value="well-ordered" /> <output name="output_filtered" value="amaVit1_Gallus/amaVit1_Gallus_gallus_filtered.psl" /> </test> <test> <param name="alignment" value="dbia3/dbia3.sorted.psl" /> <param name="query" value="dbia3/dmel-all-transcript-r6.13.fasta" /> <param name="assembly_type" value="xeno" /> <param name="assembly_category" value="well-ordered" /> <output name="output_filtered" value="dbia3/dbia3_dmel_filtered.psl" /> </test> </tests> <help> <![CDATA[ pslCDnaFilter (version: v340) ============================== Filter cDNA alignments in psl format. Filtering criteria are comparative, selecting near best in genome alignments for each given cDNA and non-comparative, based only on the quality of an individual alignment. usage: ------- $ pslCDnaFilter [options] inPsl outPsl Source code: ------------- http://hgdownload.cse.ucsc.edu/admin/exe/ Licence ======== Please note that commercial download and installation of the Blat and In-Silico PCR software may be licensed through Kent Informatics (http://www.kentinformatics.com). ]]> </help> <citations> <citation type="bibtex">@article{kent2002blat, title={BLAT—the BLAST-like alignment tool}, author={Kent, W James}, journal={Genome research}, volume={12}, number={4}, pages={656--664}, year={2002}, publisher={Cold Spring Harbor Lab} }</citation> </citations> </tool>