view SMART/galaxy/coordinatesToSequence.xml @ 29:c78966712a57

Deleted selected files
author m-zytnicki
date Mon, 29 Apr 2013 03:44:49 -0400
parents 94ab73e8a190
children 0ab839023fe4
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<tool id="coordinatesToSequence" name="coordinates to sequence">
	<description>Coordinates to Sequences: Extract the sequences from a list of coordinates.</description>
	<requirements>
		<requirement type="set_environment">PYTHONPATH</requirement>
	</requirements>
	<command interpreter="python">
		../Java/Python/coordinatesToSequence.py -i $formatType.inputFileName1
		#if $formatType.FormatInputFileName1 == 'bed':
			-f bed
		#elif $formatType.FormatInputFileName1 == 'gff':
			-f gff	
		#elif $formatType.FormatInputFileName1 == 'gff2':
			-f gff2
		#elif $formatType.FormatInputFileName1 == 'gff3':
			-f gff3
		#elif $formatType.FormatInputFileName1 == 'sam':
			-f sam
		#elif $formatType.FormatInputFileName1 == 'gtf':
			-f gtf
		#end if
			
		-s $sequence
		-o $outputFileFasta
		
	</command>

	<inputs>
		<conditional name="formatType">
			<param name="FormatInputFileName1" type="select" label="Input File Format">
				<option value="bed">bed</option>
				<option value="gff">gff</option>
				<option value="gff2">gff2</option>
				<option value="gff3">gff3</option>
				<option value="sam">sam</option>
				<option value="gtf">gtf</option>
			</param>
			<when value="bed">
				<param name="inputFileName1" format="bed" type="data" label="Input File"/>
			</when>
			<when value="gff">
				<param name="inputFileName1" format="gff" type="data" label="Input File"/>
			</when>
			<when value="gff2">
				<param name="inputFileName1" format="gff2" type="data" label="Input File"/>
			</when>
			<when value="gff3">
				<param name="inputFileName1" format="gff3" type="data" label="Input File"/>
			</when>
			<when value="sam">
				<param name="inputFileName1" format="sam" type="data" label="Input File"/>
			</when>
			<when value="gtf">
				<param name="inputFileName1" format="gtf" type="data" label="Input File"/>
			</when>
		</conditional>

 	    <param name="sequence" type="data" label="Reference fasta File" format="fasta"/>

	</inputs>

	<outputs>
		<data name="outputFileFasta" format="fasta" label="coordinates to sequences output"/>
	</outputs> 
	
	<help>
You can use this tool, if you just want to convert your mapping data to genomic coordinates, without any filtering. It requires a genomic coordinates file together with its format, an output format (GFF3, BED, etc...), the genome, and prints you the corresponding file.
	</help>
</tool>