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annotate fastq_to_fasta.xml @ 2:19543b836ff5 draft

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planemo upload for repository https://github.com/galaxyproject/tools-devteam/tree/master/tool_collections/galaxy_sequence_utils/fastqtofasta commit de7140295cce07e1bc1697e51dab4271c8d7a8a6
author devteam
date Fri, 18 Dec 2015 19:31:24 -0500
parents 2ebd6fcee4c4
children 74831e85c49b
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1 <tool id="fastq_to_fasta_python" name="FASTQ to FASTA" version="1.0.0">
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2 <description>converter</description>
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3 <requirements>
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4 <requirement type="package" version="1.0.0">galaxy_sequence_utils</requirement>
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5 </requirements>
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6 <command interpreter="python">fastq_to_fasta.py '$input_file' '$output_file' '${input_file.extension[len( 'fastq' ):]}'</command>
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7 <inputs>
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8 <param name="input_file" type="data" format="fastq" label="FASTQ file to convert" />
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9 </inputs>
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10 <outputs>
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11 <data name="output_file" format="fasta" />
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12 </outputs>
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13 <tests>
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14 <!-- basic test -->
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15 <test>
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16 <param name="input_file" value="sanger_full_range_original_sanger.fastqsanger" ftype="fastqsanger" />
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17 <output name="output_file" file="fastq_to_fasta_python_1.out" />
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18 </test>
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19 <!-- color space test -->
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20 <test>
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21 <param name="input_file" value="sanger_full_range_as_cssanger.fastqcssanger" ftype="fastqcssanger" />
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22 <output name="output_file" file="fastq_to_fasta_python_2.out" />
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23 </test>
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24 <!-- test of ignoring invalid score values: this input has ascii characters falling outside of illumina range, but they should not matter -->
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25 <test>
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26 <param name="input_file" value="sanger_full_range_original_sanger.fastqsanger" ftype="fastqillumina" />
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27 <output name="output_file" file="fastq_to_fasta_python_1.out" />
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28 </test>
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29 </tests>
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30 <help>
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31 **What it does**
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32
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33 This tool converts FASTQ sequencing reads to FASTA sequences.
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34
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35
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36 </help>
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38 <citations>
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39 <citation type="doi">10.1093/bioinformatics/btq281</citation>
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40 </citations>
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41
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42 </tool>