comparison demultiplex.xml.v1 @ 0:da4101033e10 draft default tip

planemo upload

0:da4101033e10

<?xml version="1.0"?>
<!--
# Copyright (C) 2015 INRA
#
# This program is free software: you can redistribute it and/or modify
# it under the terms of the GNU General Public License as published by
# the Free Software Foundation, either version 3 of the License, or
# (at your option) any later version.
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# This program is distributed in the hope that it will be useful,
# but WITHOUT ANY WARRANTY; without even the implied warranty of
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# GNU General Public License for more details.
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# along with this program.  If not, see <http://www.gnu.org/licenses/>.
-->
<tool id="FROGS_demultiplex" name="FROGS Demultiplex reads" version="2.0.0">
	<description>Attribute reads to samples in function of inner barcode.</description>
 	<requirements>
        	<requirement type="package" version="0.20">perl-io-gzip</requirement>
    	</requirements>
	<command interpreter="python2.7">
		demultiplex.py
		#if str( $fastq_input.fastq_input_selector ) == "paired":
		    --input-R1 "${fastq_input.fastq_input1}"               
		    --input-R2 "${fastq_input.fastq_input2}"
		#else:
		    --input-R1 "${fastq_input.fastq_input1}"
		#end if              
		    --input-barcode $barcode_file
		    --mismatches $mismatches
		    --end $end
		    --summary $summary
		    --output-demultiplexed $demultiplexed_archive
		    --output-excluded $undemultiplexed_archive
	</command>
	<inputs>
		<!-- Input file -->
		<param format="tabular" name="barcode_file" type="data" label="Barcode file" help="This file describes barcodes and samples (one line by sample tabulated separated from barcode sequence(s)). See Help section" optional="false" />
		
		<conditional name="fastq_input">
	      	<param name="fastq_input_selector" type="select" label="Single or Paired-end reads" help="Select between paired and single-end data">
	      		<option value="single">Single</option>
	        	<option value="paired">Paired</option>
	        </param>
	      	<when value="paired">
	        	<param name="fastq_input1" type="data" format="fastq" label="Select first set of reads" help="Specify dataset of your forward reads"/>
	        	<param name="fastq_input2" type="data" format="fastq" label="Select second set of reads" help="Specify dataset of your reverse reads"/>
	        </when>
	        <when value="single">
	        	<param name="fastq_input1" type="data" format="fastq" label="Select fastq dataset" help="Specify dataset of your single end reads"/>
	      	</when>
      	</conditional>

		<!-- Option -->
		<param name="mismatches" type="integer" label="Barcode mismatches" help="Number of mismatches allowed in barcode" value="0" optional="false" />
		<param name="end" type="select" label="Barcode on which end ?" help="The barcode is placed either at the beginning of the forward end or of the reverse end or both?">
			<option value="bol" selected="true">Forward</option>
			<option value="eol">Reverse</option>
			<option value="both">Both ends</option>
		</param>
	</inputs>
	<outputs>
		<data format="tar.gz" name="demultiplexed_archive" label="${tool.name}: demultiplexed.tar.gz" from_work_dir="demultiplexed.tar.gz"/>
		<data format="tar.gz" name="undemultiplexed_archive" label="${tool.name}: undemultiplexed.tar.gz" from_work_dir="undemultiplexed.tar.gz"/>
		<data format="tabular" name="summary" label="${tool.name}: report" from_work_dir="report.tsv"/>
	</outputs>
 	<tests>
        	<test>
            		<param name="fastq_input1" value="multiplex.fastq"/>
			<param name="barcode_file" value="barcode.tabular"/>
			<output name="demultiplexed_archive" file="FROGS_Demultiplex_reads__demultiplexed.tar.gz"/>
			<output name="undemultiplexed_archive" file="FROGS_Demultiplex_reads__undemultiplexed.tar.gz"/>
			<output name="summary" file="FROGS_Demultiplex_reads__report.tabular"/>
        	</test>
    	</tests>
	<help>
.. class:: infomark page-header h2

What it does

This tool classifies single or paired-end reads in function of barcode forward or reverse in the first or both reads.

**Command line**::

  demultiplex.py --input-R1 *FQ_INPUT1* [--input-R2 *FQ_INPUT2*] --input-barcode *TXT_BARCODE* --mismatches *MISMATCH* --end *END* --summary *TXT_SUMMARY_OUTPUT* --output-demultiplexed *TARGZ_DEMULT_ARCHIVE_OUTPUT* --output-excluded *TARGZ_UNDEMULT_ARCHIVE_OUTPUT*

.. csv-table:: Inputs
   :header: "Input name", "Meaning"
   :widths: 20, 80
   :class: table table-striped

   "FQ_INPUT1", "Fastq input file for the first read (single-end or forward read of paired-end sequences)"
   "FQ_INPUT2", "Fastq input file for the second read (only for paired-end sequences)"
   "TXT_BARCODE", "Tabulated text file that describes barcode sequences used to multiplexe samples: SAMPLE_NAME	BARCODE1	[BARCODE2]"

.. csv-table:: Options
   :header: "Option name", "Meaning"
   :widths: 20, 80
   :class: table table-striped

   "-m/--mismatches MISMATCH", "Number of allowed mismatch in each barcode"
   "-e/--end END", "To which end must the barcode be found : forward (begin of the (first) read), reverse (end of the (second) read) or both"

.. csv-table:: Outputs
   :header: "Output name", "Meaning"
   :widths: 20, 80
   :class: table table-striped

   "TXT_SUMMARY_OUTPUT", "A tabulated text file which summarises the number of sequences (single or paired) for each sample"
   "TARGZ_DEMULT_ARCHIVE_OUTPUT", "A TAR.GZ archive that contains all fastq files for each sample"
   "TARGZ_UNDEMULT_ARCHIVE_OUTPUT", "A TAR.GZ archive that contains all fastq files for undemultiplexed reads"

.. class:: h3

Format

BARCODE_FILE :
 This file is expected to be tabulated
		
 -first column corresponds to the sample name
 
 -second column corresponds to the sequence barcode used
 
 -third column (optional) corresponds to the reverse sequence barcode
 
.. class:: warningmark

Take care to indicate sequence barcode in the strand of the read, so you may need to reverse complement the reverse barcode sequence

.. class:: warningmark

All barcode sequences must have the same length
 
Example of barcode file: Here the sample is multiplexed by both fragment ends.

.. image:: ${static_path}/images/tools/frogs/demultiplex_barcode.png
   :height: 18
   :width: 286

FASTQ : 
 Text file describing biological sequences in a 4 line format: 
		
 -first line starts by "@" corresponds to the sequence identifier and optionally the sequence description
 
 -second line is the sequence itself
 
 -third line is a "+" following by the sequence identifier or not depending on the version
 
 -fourth line is the quality sequence, one code per base. The code depends on its version and the sequencer
 
`Click here for more details on the fastq format &lt;https://en.wikipedia.org/wiki/FASTQ_format&gt;`_

Example of fastq read corresponding to the previous barcode file  

.. image:: ${static_path}/images/tools/frogs/demultiplex_fastq_ex.png
   :height: 57
   :width: 420


.. class:: infomark page-header h2

How it works

For each sequence or sequence pair, the sequence fragment at the beginning (forward multiplexing) of the (first) read or at the end (reverse multiplexing) of the (second) read will be compared to all barcodes of the barecode file.

If this fragment is found once and only once (regarding the mismatch threshold), the fragment is trimmed and the sequence will be attributed to the corresponding sample.

Finally fastq files (or pair of fastq files) for each sample are included in an archive and a report, describing how many sequences are attributed for each sample, is created.


.. class:: infomark page-header h2

Advices

Do not forget to indicate barcode sequence as they really are in the fastq sequence file, especially if you have multiplexed data via the reverse strand.

For the mismatch threshold, we advised to let the threshold to 0. Then if you are not satisfied by the result try with 1. The number of mismatches depends on the length of the barcode, but frequently this sequences are very short so 1 mismatch is already more than the sequencing error rate.

If you have different barcode lengths, you must demultiplex your data in several steps,  beginning by the longest barcode set. Then to trim the barcodes with smaller lengths, you use the "unmatched" or "ambiguous" sequence file with smaller barcodes and so on.

If you have Roche 454 sequences in sff format, you must convert them with some programs like `sff2fastq &lt;https://github.com/indraniel/sff2fastq&gt;`_ or sff_to_fastq (installable in Galaxy)


----

**Contact**

Contacts: [e-mail]

Repository: https://github.com/geraldinepascal/FROGS

Please cite the FROGS Publication: *Escudie F., Auer L., Bernard M., Cauquil L., Vidal K., Maman S., Mariadassou M., Combes S., Hernandez-Raquet G., Pascal G., 2016. FROGS: Find Rapidly OTU with Galaxy Solution. In: ISME-2016 Montreal, CANADA ,* http://bioinfo.genotoul.fr/wp-content/uploads/FROGS_ISME2016_poster.pdf

Depending on the help provided you can cite us in acknowledgements, references or both.
	</help>
</tool>