Mercurial > repos > xuebing > sharplabtool
diff tools/fastq/fastq_to_fasta.xml @ 0:9071e359b9a3
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author | xuebing |
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date | Fri, 09 Mar 2012 19:37:19 -0500 |
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--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/tools/fastq/fastq_to_fasta.xml Fri Mar 09 19:37:19 2012 -0500 @@ -0,0 +1,40 @@ +<tool id="fastq_to_fasta_python" name="FASTQ to FASTA" version="1.0.0"> + <description>converter</description> + <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. + +------ + +**Citation** + +If you use this tool, please cite `Blankenberg D, Gordon A, Von Kuster G, Coraor N, Taylor J, Nekrutenko A; Galaxy Team. Manipulation of FASTQ data with Galaxy. Bioinformatics. 2010 Jul 15;26(14):1783-5. <http://www.ncbi.nlm.nih.gov/pubmed/20562416>`_ + + + </help> +</tool>