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planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tool_collections/galaxy_sequence_utils/fastqtofasta commit bb5df9e62585e12f08dfc0a9f86eec8e205b4845
author | iuc |
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date | Fri, 04 Oct 2024 10:35:33 +0000 |
parents | 297962e79f39 |
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<tool id="fastq_to_fasta_python" name="FASTQ to FASTA" version="@TOOL_VERSION@+galaxy@VERSION_SUFFIX@" profile="@PROFILE@"> <description>converter</description> <macros> <import>macros.xml</import> </macros> <edam_topics> <edam_topic>topic_0622</edam_topic> </edam_topics> <edam_operations> <edam_operation>operation_3434</edam_operation> </edam_operations> <expand macro="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>