<tool id="cutadapt" name="Remove adapter sequences" version="0.9.4">
	<description>from high-throughput sequence data</description>
	<requirements>
		<requirement type="python-module">cutadapt</requirement>
	</requirements>

	<command>cutadapt 
		#if $input.extension.startswith( "fastq"):
		--format=fastq
		#else
		--format=$input.extension
		#end if 
		#for $a in $adapters
		-a '${a.adapter_source.adapter}'
		#end for
		#for $aa in $anywhere_adapters
		-b '${aa.anywhere_adapter_source.anywhere_adapter}'
		#end for
		-e $error_rate
		-n $count
		-O $overlap
		#if str($min) != '0':
		-m $min
		#end if
		#if str($max) != '0':
		-M $max
		#end if
		#if $discard:
		--discard
		#end if
		'$input'
		--output='$output' 
		2> $report
	</command>
	<inputs>
		<param format="fastqsanger, fasta" name="input" type="data" optional="false" label="Fastq file to trim" length="100"/>

		<repeat name="adapters" title="3' Adapters">
			<conditional name="adapter_source">
				<param name="adapter_source_list" type="select" label="Source" >
					<option value="prebuilt" selected="true">Standard (select from the list below)</option>
					<option value="user">Enter custom sequence</option>
				</param>

				<when value="user">
					<param name="adapter" size="30" label="Enter custom 3' adapter sequence" type="text" value="AATTGGCC" help="Sequence of an adapter that was ligated to the 3' end. The adapter itself and anything that follows is trimmed. If multiple adapters are specified, only the best matching adapter is trimmed."/>
				</when>

				<when value="prebuilt">
					<param name="adapter" type="select" label="Choose 3' adapter" help="Sequence of an adapter that was ligated to the 3' end. The adapter itself and anything that follows is trimmed. If multiple adapters are specified, only the best matching adapter is trimmed.">
						<options from_file="fastx_clipper_sequences.txt">
							<column name="name" index="1"/>
							<column name="value" index="0"/>
						</options>
					</param> 
				</when>
			</conditional>
		</repeat>

		<repeat name="anywhere_adapters" title="5' or 3' (Anywhere) Adapters" help="Sequence of an adapter that was ligated to the 5' or 3' end.  If the adapter is found within the read or overlapping the 3' end of the read, the behavior is the same as for the -a option. If the adapter overlaps the 5' end (beginning of the read), the initial portion of the read matching the adapter is trimmed, but anything that follows is kept. If multiple -a or -b options are given, only the best matching adapter is trimmed.">
			<conditional name="anywhere_adapter_source">
				<param name="anywhere_adapter_source_list" type="select" label="Source">
					<option value="prebuilt" selected="true">Standard (select from the list below)</option>
					<option value="user">Enter custom sequence</option>
				</param>

				<when value="user">
					<param name="anywhere_adapter" size="30" label="Enter custom 5' or 3' adapter sequence" type="text" value="AATTGGCC" help="Sequence of an adapter that was ligated to the 5' or 3' end.  If the adapter is found within the read or overlapping the 3' end of the read, the behavior is the same as for the -a option. If the adapter overlaps the 5' end (beginning of the read), the initial portion of the read matching the adapter is trimmed, but anything that follows is kept. If multiple -a or -b options are given, only the best matching adapter is trimmed."/>
				</when>
				<when value="prebuilt">
					<param name="anywhere_adapter" type="select" label="Choose 5' or 3' adapter" help="Sequence of an adapter that was ligated to the 5' or 3' end.  If the adapter is found within the read or overlapping the 3' end of the read, the behavior is the same as for the -a option. If the adapter overlaps the 5' end (beginning of the read), the initial portion of the read matching the adapter is trimmed, but anything that follows is kept. If multiple -a or -b options are given, only the best matching adapter is trimmed.">
						<options from_file="fastx_clipper_sequences.txt">
							<column name="name" index="1"/>
							<column name="value" index="0"/>
						</options>
					</param> 
				</when>
			</conditional>
		</repeat>

		<param name="error_rate" type="float" min="0" max="1" value="0.1" label="Maximum error rate" help="Maximum allowed error rate (no. of errors divided by the length of the matching region)." />
		<param name="count" type="integer" min="1" value="1" label="Match times" help="Try to remove adapters at most COUNT times. Useful when an adapter gets appended multiple times." />
		<param name="overlap" type="integer" min="1" value="3" label="Minimum overlap length" help="Minimum overlap length. If the overlap between the adapter and the sequence is shorter than LENGTH, the read is not modified." />
		<param name="discard" type="boolean" checked="False" default="False" label="Discard Trimmed Reads" help="Discard reads that contain the adapter instead of trimming them. Use the 'Minimum overlap length' option in order to avoid throwing away too many randomly matching reads!" />
		<param name="min" type="integer" min="0" optional="true" value="0" label="Minimum length" help="Discard trimmed reads that are shorter than LENGTH.  Reads that are too short even before adapter removal are also discarded. In colorspace, an initial primer is not counted. Value of 0 means no minimum length." />
		<param name="max" type="integer" min="0" optional="true" value="0" label="Maximum length" help="Discard trimmed reads that are longer than LENGTH.  Reads that are too long even before adapter removal are also discarded. In colorspace, an initial primer is not counted. Value of 0 means no maximum length." />
	</inputs>
	<outputs>
		<data format="txt" name="report" label="${tool.name} on ${on_string} (Report)" />
		<data format="input" name="output" metadata_source="input"/>
	</outputs>

	<tests>
		<test>
			<param name="input" value="fa_gc_content_input.fa"/>
			<output name="out_file1" file="fa_gc_content_output.txt"/>
		</test>
	</tests>

	<help>
This tool removes adapter sequences from DNA high-throughput
sequencing data. This is usually necessary when the read length of the
machine is longer than the molecule that is sequenced, such as in
microRNA data.

The tool is based on the opensource cutadapt_ tool.

-----

**Algorithm**

cutadapt uses a simple semi-global alignment algorithm, without any special optimizations.
For speed, the algorithm is implemented as a Python extension module in calignmodule.c.


**Partial adapter matches**

Cutadapt correctly deals with partial adapter matches. As an example, suppose
your adapter sequence is "ADAPTER" (specified via 3' Adapters parameter).
If you have these input sequences:

::

	MYSEQUENCEADAPTER
	MYSEQUENCEADAP
	MYSEQUENCEADAPTERSOMETHINGELSE

All of them will be trimmed to "MYSEQUENCE". If the sequence starts with an
adapter, like this:

::

	ADAPTERSOMETHING

It will be empty after trimming.

When the allowed error rate is sufficiently high, errors in
the adapter sequence are allowed. For example, ADABTER (1 mismatch), ADAPTR (1 deletion),
and ADAPPTER (1 insertion) will all be recognized if the error rate is set to 0.15.


**Allowing adapters anywhere**

Cutadapt assumes that any adapter specified via the *3` Adapters* parameter
was ligated to the 3' end of the sequence. This is the correct assumption for
at least the SOLiD and Illumina small RNA protocols and probably others.

If, on the other hand, your adapter can also be ligated to the 5' end (on
purpose or by accident), you should tell cutadapt so by using the *5' or 3' (Anywhere)
Adapters* parameter. It will then use a different alignment algorithm and
correctly trim adapters that appear in the beginning of a read. An adapter
specified this way will also be found if it appears only partially in the
beginning of a read. For example, these sequences

::

	ADAPTERMYSEQUENCE
	PTERMYSEQUENCE

will be trimmed to "MYSEQUENCE". Note that the regular algorithm would trim
the first read to an empty sequence.

This parameter currently does not work with color space data.


.. _cutadapt: http://code.google.com/p/cutadapt/
	</help>

</tool>