view fastx_barcode_splitter.xml @ 0:a12850d0559b

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<tool id="cshl_fastx_barcode_splitter" version="1.0.0" name="Barcode Splitter">
	<description></description>
    <requirements>
        <requirement type="package" version="0.0.13">fastx_toolkit</requirement>
    </requirements>
	<command interpreter="bash">fastx_barcode_splitter_galaxy_wrapper.sh $BARCODE $input "$input.name" "$output.files_path" --mismatches $mismatches --partial $partial $EOL > $output </command>

	<inputs>
		<param format="txt" version="1.0.0" name="BARCODE" type="data" label="Barcodes to use" />
		<param format="fasta,fastqsanger,fastqsolexa,fastqillumina" version="1.0.0" name="input" type="data" label="Library to split" />

		<param version="1.0.0" name="EOL" type="select" label="Barcodes found at">
			<option value="--bol">Start of sequence (5' end)</option>
			<option value="--eol">End of sequence (3' end)</option>
		</param>

		<param version="1.0.0" name="mismatches" type="integer" size="3" value="2" label="Number of allowed mismatches" />
		
		<param version="1.0.0" name="partial" type="integer" size="3" value="0" label="Number of allowed barcodes nucleotide deletions" />
	
	</inputs>
	
	<tests>
		<test>
			<!-- Split a FASTQ file -->
			<param version="1.0.0" name="BARCODE" value="fastx_barcode_splitter1.txt" />
			<param version="1.0.0" name="input" value="fastx_barcode_splitter1.fastq" ftype="fastqsolexa" />
			<param version="1.0.0" name="EOL" value="Start of sequence (5' end)" />
			<param version="1.0.0" name="mismatches" value="2" />
			<param version="1.0.0" name="partial" value="0" />
			<output version="1.0.0" name="output" file="fastx_barcode_splitter1.out" />
		</test>
	</tests>

	<outputs>
		<data format="html" version="1.0.0" name="output" />
	</outputs>
<help>

**What it does**

This tool splits a Solexa library (FASTQ file) or a regular FASTA file into several files, using barcodes as the split criteria.

--------

**Barcode file Format**

Barcode files are simple text files.
Each line should contain an identifier (descriptive name for the barcode), and the barcode itself (A/C/G/T), separated by a TAB character.
Example::

    #This line is a comment (starts with a 'number' sign)
    BC1	GATCT
    BC2	ATCGT
    BC3	GTGAT
    BC4 TGTCT
    
For each barcode, a new FASTQ file will be created (with the barcode's identifier as part of the file name).
Sequences matching the barcode will be stored in the appropriate file.

One additional FASTQ file will be created (the 'unmatched' file), where sequences not matching any barcode will be stored.

The output of this tool is an HTML file, displaying the split counts and the file locations.

**Output Example**

.. image:: ${static_path}/fastx_icons/barcode_splitter_output_example.png


------

This tool is based on `FASTX-toolkit`__ by Assaf Gordon.

 .. __: http://hannonlab.cshl.edu/fastx_toolkit/
 
</help>
<!-- FASTX-barcode-splitter is part of the FASTX-toolkit, by A.Gordon ([e-mail]) -->
</tool>