comparison fastq_to_fasta.xml @ 2:4844c1810c16 draft

planemo upload for repository https://github.com/galaxyproject/tools-devteam/tree/master/tool_collections/galaxy_sequence_utils/fastqtofasta commit f2582539542b33240234e8ea6093e25d0aee9b6a

1:723b5b38d88a

<tool id="fastq_to_fasta_python" name="FASTQ to FASTA" version="1.0.0">
  <description>converter</description>
  <requirements>
    <requirement type="package" version="1.0.0">galaxy_sequence_utils</requirement>
  </requirements>
  <command interpreter="python">fastq_to_fasta.py '$input_file' '$output_file' '${input_file.extension[len( 'fastq' ):]}'</command>
  <inputs>
    <param name="input_file" type="data" format="fastq" label="FASTQ file to convert" />
  </inputs>
  <outputs>
    <data name="output_file" format="fasta" />
  </outputs>
  <tests>
    <!-- basic test -->
    <test>
      <param name="input_file" value="sanger_full_range_original_sanger.fastqsanger" ftype="fastqsanger" />
      <output name="output_file" file="fastq_to_fasta_python_1.out" />
    </test>
    <!-- color space test -->
    <test>
      <param name="input_file" value="sanger_full_range_as_cssanger.fastqcssanger" ftype="fastqcssanger" />
      <output name="output_file" file="fastq_to_fasta_python_2.out" />
    </test>
    <!-- test of ignoring invalid score values: this input has ascii characters falling outside of illumina range, but they should not matter -->
    <test>
      <param name="input_file" value="sanger_full_range_original_sanger.fastqsanger" ftype="fastqillumina" />
      <output name="output_file" file="fastq_to_fasta_python_1.out" />
    </test>
  </tests>
  <help>
**What it does**

This tool converts FASTQ sequencing reads to FASTA sequences.


  </help>
  
  <citations>
    <citation type="doi">10.1093/bioinformatics/btq281</citation>
  </citations>
  
</tool>

2:4844c1810c16

<tool id="fastq_to_fasta_python" name="FASTQ to FASTA" version="1.1.1">
    <description>converter</description>
    <requirements>
        <requirement type="package" version="1.1.1">galaxy_sequence_utils</requirement>
    </requirements>
    <command><![CDATA[
gx-fastq-to-fasta '$input_file' '$output_file' '${input_file.extension[len('fastq'):]}'
    ]]></command>
    <inputs>
        <param name="input_file" type="data" format="fastq,fastq.gz,fastq.bz2" label="FASTQ file to convert" />
    </inputs>
    <outputs>
        <data name="output_file" format="fasta" />
    </outputs>
    <tests>
        <!-- basic test -->
        <test>
            <param name="input_file" value="sanger_full_range_original_sanger.fastqsanger" ftype="fastqsanger" />
            <output name="output_file" file="fastq_to_fasta_python_1.out" />
        </test>
        <!-- color space test -->
        <test>
            <param name="input_file" value="sanger_full_range_as_cssanger.fastqcssanger" ftype="fastqcssanger" />
            <output name="output_file" file="fastq_to_fasta_python_2.out" />
        </test>
        <!-- test of ignoring invalid score values: this input has ascii characters falling outside of illumina range, but they should not matter -->
        <test>
            <param name="input_file" value="sanger_full_range_original_sanger.fastqsanger" ftype="fastqillumina" />
            <output name="output_file" file="fastq_to_fasta_python_1.out" />
        </test>
    </tests>
    <help><![CDATA[
**What it does**

This tool converts FASTQ sequencing reads to FASTA sequences.
    ]]></help>
    <citations>
        <citation type="doi">10.1093/bioinformatics/btq281</citation>
    </citations>
</tool>