Mercurial > repos > yhoogstrate > flaimapper
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author | yhoogstrate |
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date | Fri, 07 Nov 2014 10:21:45 -0500 |
parents | 83bf9e65cc10 |
children | c5df479c423b |
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<?xml version="1.0" encoding="UTF-8"?> <tool id="flaimapper" name="FlaiMapper" version="1.1.0"> <description>Detect small ncRNA derived fragments using Fragment Location Annotation Identification Mapper.</description> <requirements> <requirement type="package" version="1.1.0">flaimapper</requirement> <requirement type="package" version="0.7.7">pysam</requirement> </requirements> <command> ##rm $mask".tbi" ##rm $fasta".fai" flaimapper -v -f $output_format -o $output -m $mask -r $fasta #for $alignment in $alignments $alignment #end for </command> <version_command>flaimapper --version</version_command> <inputs> <param name="alignments" type="data" format="bam,sam" label="Alignment file(s)" help="The input alignment file(s) where the gene expression has to be counted. The file can have a SAM or BAM format; but ALL files in the series must be in THE SAME format." multiple="true" /> <param name="mask" type="data" format="gtf,gff,gtf3" label="small ncRNA Annotation (gtf)" help="" /> <param name="fasta" type="data" format="fasta" label="Fasta sequence corresponding to reference genome" help="" /> <param name="output_format" type="select" label="Output format"> <option value="1">Tabular (1 fragment per column)</option> <option value="2">Tabular (1 precursor per column)</option> <option value="3">GenBank</option> <!-- option value="gtf">GTF/GFF</option --> </param> </inputs> <outputs> <data format="tabular" name="output" label="${tool.name} on ${', '.join([ str(a.hid)+': '+a.name for a in $alignments ])}" /> </outputs> <help> FlaiMapper: computational annotation of small ncRNA derived fragments using RNA-seq high throughput data doi:10.1093/bioinformatics/btu696 </help> </tool>