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1 <tool id="FastqIlluminaToSanger" name="Convert Fastq qualities" version="1.0.0">
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2 <description>from Illumina to Sanger</description>
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3 <command interpreter="sh">galaxyToolRunner.sh converters.FastqIlluminaToSanger -i $input -o $output</command>
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4 <inputs>
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5 <param name="input" type="data" format="fastqillumina" label="FASTQ, Illumina qualities" />
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6 </inputs>
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7 <outputs>
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8 <data name="output" format="fastqsanger" metadata_source="input" />
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9 </outputs>
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10 <tests>
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11 <test>
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12 <param name="input" value="test.fastqillumina" ftype="fastqillumina"/>
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13 <output name="output" file="test.fastqsanger"/>
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14 </test>
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15 </tests>
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16 <help>
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17
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18 This tool will convert a FASTQ file with ASCII quality scores encoded in Illumina 1.3 format (Phred+64) to Sanger format (Phred+33). It is a simpler, faster version of the FASTQ Groomer.
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19
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20 .. class:: warningmark
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21
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22 This tool requires fastqillumina formatted data. If you have tabular data that was not correctly autodetected, change the metadata by clicking on the pencil icon for the dataset.
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23
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24 </help>
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25 </tool>
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