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"planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/art commit 7e2fa670ffad6bf9cd2411d7807c65db7c7e2f6b"
author | iuc |
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date | Wed, 04 Dec 2019 06:19:06 -0500 |
parents | ff8599e52a55 |
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<tool id="art_solid" name="ART SOLiD" version="2014.11.03.0"> <description>simulates SOLiD data</description> <macros> <import>macros.xml</import> </macros> <expand macro="requirements"/> <expand macro="stdio" /> <command><![CDATA[ art_SOLiD $sam #if $rndSeed and $rndSeed > -1: -r $rndSeed #end if #if $generate.amplicon.use_amplicon == "amplicon_true": -A #if $generate.choice == "single_end": s #else if $generate.choice == "paired_end": p #else: m #end if #end if '$input_seq_file' output #if $generate.choice == "single_end": $generate.LEN_READ $fold_coverage #else if $generate.choice == "paired_end": $generate.LEN_READ_F3 $generate.LEN_READ_F5 $fold_coverage $generate.fragment_size $generate.fragment_sd #else: $generate.LEN_READ $fold_coverage $generate.fragment_size $generate.fragment_sd #end if #if $generate.amplicon.use_amplicon == "amplicon_true": #if $generate.choice == "single_end": $generate.amplicon.reads_per_amplicon #else: $generate.amplicon.read_pairs_per_amplicon #end if #end if ]]></command> <inputs> <param label="DNA/RNA reference sequence" format="fasta" name="input_seq_file" type="data"/> <param label="the fold of read coverage over the reference sequences" name="fold_coverage" type="integer" value="20"/> <conditional name="generate"> <param name="choice" type="select" label="Type of data to generate"> <option value="single_end">Single-End</option> <option value="paired_end">Paired-End</option> <option value="mate_pair">Mate Pair</option> </param> <when value="single_end"> <param name="LEN_READ" type="integer" label="Length of F3/R3 reads" value="100" /> <expand macro="amplicon" /> </when> <when value="paired_end"> <param name="LEN_READ_F3" type="integer" label="Length of F3 reads" value="100" /> <param name="LEN_READ_F5" type="integer" label="Length of F5 reads" value="100" /> <expand macro="frag_len_sd" /> <expand macro="amplicon_pair" /> </when> <when value="mate_pair"> <param name="LEN_READ" type="integer" label="Length of F3/R3 reads" value="100" /> <expand macro="frag_len_sd" /> <expand macro="amplicon_pair" /> </when> </conditional> <expand macro="sam" /> <expand macro="rndSeed" /> </inputs> <outputs> <!-- Single End --> <data format="fastq" name="output_fq1_single" from_work_dir="output.fq" label="Simulated of SOLiD sequencing of $input_seq_file.name"> <filter>generate['choice'] == "single_end"</filter> </data> <!-- Paired End --> <data format="fastq" name="output_fq1_paired" from_work_dir="output_F3.fq" label="Simulated of SOLiD sequencing of $input_seq_file.name (F3)"> <filter>generate['choice'] == "paired_end"</filter> </data> <data format="fastq" name="output_fq2_paired" from_work_dir="output_F5.fq" label="Simulated of SOLiD sequencing of $input_seq_file.name (F5)"> <filter>generate['choice'] == "paired_end"</filter> </data> <!-- Mate Pair --> <data format="fastq" name="output_fq1_mate" from_work_dir="output_F3.fq" label="Simulated of SOLiD sequencing of $input_seq_file.name (Forward)"> <filter>generate['choice'] == "mate_pair"</filter> </data> <data format="fastq" name="output_fq2_mate" from_work_dir="output_R3.fq" label="Simulated of SOLiD sequencing of $input_seq_file.name (Reverse)"> <filter>generate['choice'] == "mate_pair"</filter> </data> <data format="sam" name="output_sam" from_work_dir="output.sam" label="Mapping of Simulated SOLiD data to $input_seq_file.name"> <filter>sam</filter> </data> <!-- todo? map file --> </outputs> <tests> <!-- Single End tests --> <test> <param name="rndSeed" value="42" /> <param name="input_seq_file" value="input.fa" /> <param name="LEN_READ" value="25" /> <param name="fold_coverage" value="10" /> <param name="choice" value="single_end" /> <param name="sam" value="False" /> <output name="output_fq1_single" file="art.solid.01.fq" compare="sim_size" delta="5000" /> </test> <test> <param name="rndSeed" value="42" /> <param name="input_seq_file" value="input.fa" /> <param name="fold_coverage" value="20" /> <param name="choice" value="paired_end" /> <param name="LEN_READ_F3" value="50" /> <param name="LEN_READ_F5" value="50" /> <param name="fragment_size" value="75" /> <param name="fragment_sd" value="10" /> <param name="sam" value="True" /> <output name="output_fq1_paired" file="art.solid.02_F3.fq" compare="sim_size" delta="5000" /> <output name="output_fq2_paired" file="art.solid.02_F5.fq" compare="sim_size" delta="5000" /> <output name="output_sam" file="art.solid.02.sam" compare="sim_size" delta="5000"/> </test> </tests> <help><![CDATA[ Art SOLiD Simulator =================== ART_SOLiD is a simulation program to generate sequence read data of SOLiD sequencing reads. ART generates reads according to a SOLiD read error profile. The built-in error profile is an empiricial error profile summarized from large SOLiD sequencing data. ART has been using for testing or benchmarking a variety of method or tools for next-generation sequencing data analysis, including read alignment, de novo assembly, detection of SNP, CNV, or other structure variation. art_SOLiD can generate both single-end, matepair, and paired-end of SOLiD sequencing platform. art_SOLiD also support amplicon sequencing simulation with RNA references. ]]></help> <expand macro="citation" /> </tool>