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planemo upload for repository https://github.com/galaxyproject/tools-devteam/tree/master/tool_collections/galaxy_sequence_utils/fastq_paired_end_joiner commit 28c441e8aa66a55d276b0f6325d34086eb715872
author | devteam |
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date | Sat, 07 Oct 2017 09:58:38 -0400 |
parents | bce792b8e239 |
children | 8a372f389ced |
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<tool id="fastq_paired_end_joiner" name="FASTQ joiner" version="2.0.1.1"> <description>on paired end reads</description> <requirements> <requirement type="package" version="1.1.2">galaxy_sequence_utils</requirement> </requirements> <command><![CDATA[ gx-fastq-paired-end-joiner '$input1_file' '${input1_file.extension[len('fastq'):]}' '$input2_file' '${input2_file.extension[len('fastq'):]}' '$output_file' $style '${paste_sequence}' ]]></command> <inputs> <param name="input1_file" type="data" format="fastqsanger,fastqcssanger,fastqsanger.gz,fastqcssanger.gz,fastqsanger.bz2,fastqcssanger.bz2" label="Left-hand Reads" /> <param name="input2_file" type="data" format="fastqsanger,fastqcssanger,fastqsanger.gz,fastqcssanger.gz,fastqsanger.bz2,fastqcssanger.bz2" label="Right-hand Reads" /> <param name="style" type="select" label="FASTQ Header Style"> <option value="old" selected="true">old</option> <option value="new">new</option> </param> <param name="paste_sequence" type="text" value="" label="Bases to insert between joined reads" help="Values are in Base-space and quality scores of maximal value will be used"/> </inputs> <outputs> <data name="output_file" format_source="input1_file" /> </outputs> <tests> <test> <param name="input1_file" value="split_pair_reads_1.fastqsanger" ftype="fastqsanger" /> <param name="input2_file" value="split_pair_reads_2.fastqsanger" ftype="fastqsanger" /> <output name="output_file" file="3.fastqsanger" ftype="fastqsanger" /> </test> <test> <param name="input1_file" value="split_pair_reads_1.fastqsanger.gz" ftype="fastqsanger.gz" /> <param name="input2_file" value="split_pair_reads_2.fastqsanger.gz" ftype="fastqsanger.gz" /> <output name="output_file" file="3.fastqsanger" ftype="fastqsanger.gz" decompress="true" /> </test> <test> <param name="input1_file" value="split_pair_reads_1.fastqsanger.bz2" ftype="fastqsanger.bz2" /> <param name="input2_file" value="split_pair_reads_2.fastqsanger.bz2" ftype="fastqsanger.bz2" /> <output name="output_file" file="3.fastqsanger" ftype="fastqsanger.bz2" decompress="true" /> </test> </tests> <help><![CDATA[ **What it does** This tool joins paired end FASTQ reads from two separate files into a single read in one file. The join is performed using sequence identifiers, allowing the two files to contain differing ordering. If a sequence identifier does not appear in both files, it is excluded from the output. ----- **Input formats** Both old and new (from recent Illumina software) style FASTQ headers are supported. The following example uses the "old" style. Left-hand Read:: @HWI-EAS91_1_30788AAXX:7:21:1542:1758/1 GTCAATTGTACTGGTCAATACTAAAAGAATAGGATC +HWI-EAS91_1_30788AAXX:7:21:1542:1758/1 hhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhh Right-hand Read:: @HWI-EAS91_1_30788AAXX:7:21:1542:1758/2 GCTCCTAGCATCTGGAGTCTCTATCACCTGAGCCCA +HWI-EAS91_1_30788AAXX:7:21:1542:1758/2 hhhhhhhhhhhhhhhhhhhhhhhh`hfhhVZSWehR ----- **Output** A multiple-fastq file, for example:: @HWI-EAS91_1_30788AAXX:7:21:1542:1758 GTCAATTGTACTGGTCAATACTAAAAGAATAGGATCGCTCCTAGCATCTGGAGTCTCTATCACCTGAGCCCA +HWI-EAS91_1_30788AAXX:7:21:1542:1758 hhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhh`hfhhVZSWehR ------ **The "new" style** Recent Illumina FASTQ headers are structured as follows:: @COORDS FLAGS COORDS = INSTRUMENT:RUN_#:FLOWCELL_ID:LANE:TILE:X:Y FLAGS = READ:IS_FILTERED:CONTROL_NUMBER:INDEX_SEQUENCE where the whitespace character between COORDS and FLAGS can be either a space or a tab. ------ **Credits** New style header support added by Simone Leo <simone.leo@crs4.it> . ]]></help> <citations> <citation type="doi">10.1093/bioinformatics/btq281</citation> </citations> </tool>