Mercurial > repos > tyty > structurefold
view Iterative_mapping/iterative_map.xml @ 53:52538ebd3c4b draft
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author | tyty |
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date | Mon, 17 Nov 2014 15:14:21 -0500 |
parents | 6c8f3149dc41 |
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<tool id="iterative_map_pipeline" name="Iterative Mapping" version="1.0"> <description></description> <command interpreter="python"> #if $mapping_file.type == "user" iterative_map.py $file_format.type $file_format.seq_file $reference_file $shift $length $mapping_file.type $output $mapping_file.param_v $mapping_file.param_five $mapping_file.param_three $mapping_file.param_k $mapping_file.param_a $mapping_file.param_m $mapping_file.param_best #else iterative_map.py $file_format.type $file_format.seq_file $reference_file $shift $length $mapping_file.type $output #end if </command> <requirements> <requirement type="package" version="1.61">biopython</requirement> <requirement type="package" version="1.7.1">numpy</requirement> <requirement type="package" version="0.1.18">samtools</requirement> <requirement type="package" version="0.12.7">bowtie</requirement> </requirements> <inputs> <conditional name="file_format"> <param name="type" type="select" label="File format of the reads (Default FASTQ)"> <option value="fastq">FASTQ</option> <option value="fasta">FASTA</option> </param> <when value="fastq"> <param name="seq_file" type="data" format="fastq" label="Fastq file"/> </when> <when value="fasta"> <param name="seq_file" type="data" format="fasta" label="Fasta file"/> </when> </conditional> <param name="reference_file" type="data" format="fasta" label="Reference genome/transcriptome"/> <param name="shift" type="integer" value="1" label="Number of nucleotides trimmed each round"/> <param name="length" type="integer" value="21" label="Minimum requirement of read length for mapping"/> <conditional name="mapping_file"> <param name="type" type="select" label="Bowtie mapping flags (Default -v 0 -a --best --strata)"> <option value="default">Default</option> <option value="user">User specified</option> </param> <when value="default"/> <when value="user"> <param name="param_v" type="integer" value="0" label="Number of mismatches for SOAP-like alignment policy (-v)"/> <param name="param_five" type="integer" value="0" label="Trim n bases from high-quality (left) end of each read before alignment (-5)"/> <param name="param_three" type="integer" value="0" label="Trim n bases from high-quality (right) end of each read before alignment (-3)"/> <param name="param_k" type="integer" value="1" label="Report up to n valid alignments per read (-k)"/> <param name="param_a" type="boolean" checked="False" truevalue = "1" falsevalue = "0" label="Whether or not to report all valid alignments per read (-a)"/> <param name="param_m" type="integer" value="-1" label="Suppress all alignments for a read if more than n reportable alignments exist (-m), -1 for unlimited"/> <param name="param_best" type="boolean" checked="False" truevalue = "1" falsevalue = "0" label="Whether or not to make Bowtie guarantee that reported singleton alignments are 'best' in terms of stratum and in terms of the quality values at the mismatched positions (--best --strata)"/> </when> </conditional> </inputs> <outputs> <data name="output" type="data" format="bam"/> </outputs> <tests> <test> <param name="file_format.type" value="fasta" /> <param name="file_format.seq_file" value="sample.fasta" /> <param name="reference_file" value="rRNA.txt" /> <param name="shift" value="1" /> <param name="length" value="21" /> <param name="mapping_file.type" value="default" /> <output name="output" file="mapped.out" /> </test> </tests> <help> **TIPS**: ----- **Input**: * 1. Sequence file type (FASTA/FASTQ) * 2. Sequence file (fasta/fastq format) * 3. Reference file (fasta) used to map the reads to * 4. “Shift” (The length of the sequence that will be trimmed at the 3’end of the reads before each round of mapping) * 5. “Length” (The minimum length of the reads for mapping after trimming) * [Optional] * 1. Bowtie mapping flags (options) [Default: -v 0 -a --best --strata] (-v flag indicates the number of allowed mismatches. Use -5/-3 flag to trim the nucleotides from 5'/3' end of the reads) ----- **Output**: A bam file with all of the reads that are mapped </help> </tool>