Mercurial > repos > rnateam > segemehl
diff segemehl.xml @ 5:9c0d4ec99ba9 draft default tip
planemo upload for repository https://github.com/bgruening/galaxytools/tree/master/tools/segemehl commit 2f6d48e1d2161d03411d9fbb4fc3d16f0fa3d2e1
author | rnateam |
---|---|
date | Thu, 27 Sep 2018 06:31:11 -0400 |
parents | db367d012fa3 |
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--- a/segemehl.xml Wed Jul 26 15:32:09 2017 -0400 +++ b/segemehl.xml Thu Sep 27 06:31:11 2018 -0400 @@ -1,4 +1,4 @@ -<tool id="segemehl" name="segemehl" version="0.2.0.3"> +<tool id="segemehl" name="segemehl" version="0.2.0.4"> <description>short read mapping with gaps</description> <requirements> <requirement type="package" version="0.2.0">segemehl</requirement> @@ -10,8 +10,39 @@ description="Execution halted." /> </stdio> <command> +<!-- + ## check for single/pair-end + #if str( $library.type ) == "single": + #set $query_list = list() + ## prepare inputs + #for $fastq in $library.input_query: + $query_list.append('%s' % $fastq ) + #end for + -q "#echo ' '.join( $query_list )#" + #else + ## prepare inputs + #set $mate1 = list() + #set $mate2 = list() + #for $mate_pair in $library.mate_list: + $mate1.append( str($mate_pair.first_strand_query) ) + $mate2.append( str($mate_pair.second_strand_query) ) + #end for + + -q #echo ','.join($mate1) + -p #echo ','.join($mate2) + + -I $library.maxinsertsize + #end if +--> <![CDATA[ - ## prepare segemehl index if no reference genome is supplied +## UNIMPLEMENTED +## [SEEDEXTENSIONPARAMS] +## -e, --extensionscore <n> score of a match during extension (default:2) +## -n, --extensionpenalty <n> penalty for a mismatch during extension (default:4) +## -X, --dropoff <n> dropoff parameter for extension (default:8) +## --showalign + +## prepare segemehl index if no reference genome is supplied #if $refGenomeSource.genomeSource == "history": mkdir ./temp_index/ && #set $temp_index = './temp_index/temp.idx' @@ -36,25 +67,15 @@ ## check for single/pair-end #if str( $library.type ) == "single": - #set $query_list = list() - ## prepare inputs - #for $fastq in $library.input_query: - $query_list.append('%s' % $fastq ) - #end for - -q "#echo ' '.join( $query_list )#" - #else - ## prepare inputs - #set $mate1 = list() - #set $mate2 = list() - #for $mate_pair in $library.mate_list: - $mate1.append( str($mate_pair.first_strand_query) ) - $mate2.append( str($mate_pair.second_strand_query) ) - #end for - - -q #echo ','.join($mate1) - -p #echo ','.join($mate2) - - -I $library.maxinsertsize + ## prepare inputs + -q ${library.input_query} + #else + -q ${mate_pair.first_strand_query} + -p ${mate_pair.second_strand_query} + -I ${library.maxinsertsize} + #end if + #if str( $bisulfite ) != "0": + -F $bisulfite #end if -m $minsize -A $accuracy @@ -65,10 +86,11 @@ #if str( $prime3 ).strip(): -Q "$prime3" #end if - $polyA - $autoclip - $hardclip - $order + -R $clipacc + $polyA + $autoclip + $hardclip + $order #if $maxout: --maxout $maxout #end if @@ -77,13 +99,18 @@ --minsplicecover $splitreads.minsplicecover --minfragscore $splitreads.minfragscore --minfraglen $splitreads.minfraglen - --splicescorescale $splitreads.splicescorescale + --splicescorescale $splitreads.splicescorescale + --maxsplitevalue $splitreads.maxsplitevalue #end if -M $maxinterval -E $evalue -D $differences + -J $jump -s -o '$segemehl_out' + #if str( $nomatchfilename ) == 'yes': + -u '$segemehl_outunmatched' + #end if ]]> </command> <inputs> @@ -116,7 +143,8 @@ <option value="paired">Paired-end</option> </param> <when value="single"> - <param name="input_query" type="data" multiple="True" format="fastqsanger,fastqillumina,fastq,fasta" label="Reads in FASTQ/FASTA files" /> + <!-- <param name="input_query" type="data" multiple="True" format="fastqsanger,fastqillumina,fastq,fasta" label="Reads in FASTQ/FASTA files" /> --> + <param name="input_query" type="data" format="fastqsanger,fastqillumina,fastq,fasta" label="Reads in FASTQ/FASTA files" /> </when> <when value="paired"> <!-- ToDo paired coolections --> @@ -124,47 +152,57 @@ <param name="first_strand_query" type="data" format="fastqsanger,fastqillumina,fastq,fasta" label="Reads from first strand" /> <param name="second_strand_query" type="data" format="fastqsanger,fastqillumina,fastq,fasta" label="Reads from second strand" /> </repeat> - <param name="maxinsertsize" type="integer" value="5000" label="Maximum size of the inserts (paired end)" help="default: 5000 (-I)" /> + <param argument="--maxinsertsize" type="integer" value="5000" label="Maximum size of the inserts (paired end)" help="default: 5000" /> </when> </conditional> <conditional name="splitreads"> - <param name="splits" type="select" label="Detect split/spliced reads" help="(--splits)"> + <param argument="splits" type="select" label="Detect split/spliced reads"> <option value="nosplit">No splits</option> <option value="splits">Split reads</option> </param> <when value="splits"> - <param name="minsplicecover" type="integer" value="80" label="Min coverage for spliced transcripts" help="(--minsplicecover)" /> - <param name="minfragscore" type="integer" value="18" label="Min coverage for spliced transcripts" help="(--minfragscore)" /> - <param name="minfraglen" type="integer" value="20" label="Min length of a spliced fragment" help="(--minfraglen)" /> - <param name="splicescorescale" type="float" value="1.0" label="Report spliced alignment with score greater than this scale times the score" - help="Report only if this value x score is larger than next best spliced alignment (--splicescorescale)" /> - <param name="sevalue" type="float" min="0" value="50.000000" label="max split evalue" help="(--maxsplitevalue)"/> + <param argument="--minsplicecover" type="integer" value="80" label="Min coverage for spliced transcripts" /> + <param argument="--minfragscore" type="integer" value="18" label="Min coverage for spliced transcripts" /> + <param argument="--minfraglen" type="integer" value="20" label="Min length of a spliced fragment" /> + <param argument="--splicescorescale" type="float" value="1.0" label="Report spliced alignment with score greater than this scale times the score" + help="Report only if this value x score is larger than next best spliced alignment" /> + <param argument="--maxsplitevalue" type="float" min="0" value="50.000000" label="max evalue for splits"/> </when> <when value="nosplit"> </when> </conditional> - - <param name="minsize" type="integer" value="12" min="1" label="Minimum size of queries" help="(-m)" /> - <param name="maxout" type="integer" min="0" value="0" optional="True" - label="Maximum number of alignments that will be reported" help="(--maxout)" /> - <param name="accuracy" type="integer" value="85" min="1" max="100" label="Min percentage of matches per read in semi-global alignment" help="(-A)" /> - <param name="hitstrategy" type="select" label="Hits to report?" help="(-H)"> + <param argument="--bisulfite" type="select" label="Bisulfite mapping"> + <option value="0">No bisulfite mapping</option> + <option value="1">bisulfite mapping with methylC-seq/Lister et al.</option> + <option value="2">bs-seq/Cokus et al. protocol</option> + </param> + <param argument="--minsize" type="integer" value="12" min="1" label="Minimum size of queries" /> + <param argument="--maxout" type="integer" min="0" value="0" optional="True" + label="Maximum number of alignments that will be reported"/> + <param argument="--accuracy" type="integer" value="85" min="1" max="100" label="Min percentage of matches per read in semi-global alignment" /> + <param argument="--hitstrategy" type="select" label="Hits to report?"> <option value="1">report only best scoring hits</option> <option value="0">report all scoring hits</option> </param> - <param name="prime5" type="text" label="add 5' adapter" help="default: none (-Q)" /> - <param name="prime3" type="text" label="add 3' adapter" help="default: none (-P)"/> - <param name="polyA" type="boolean" truevalue="--polyA" falsevalue="" checked="false" label="Clip polyA tail" help="(-T)"/> - <param name="autoclip" type="boolean" truevalue="--autoclip" falsevalue="" checked="false" label="Autoclip unknown 3prime adapter" help="(-Y)"/> - <param name="hardclip" type="boolean" truevalue="--hardclip" falsevalue="" checked="false" label="Enable hard clipping" help="(-C)"/> - <param name="order" type="boolean" truevalue="--order" falsevalue="" checked="false" label="Sorts the output by chromsome and position" help="(-O)"/> - <param name="differences" type="integer" min="0" value="1" label="search seeds initially with n differences" help="(--differences)"/> - <param name="evalue" type="float" min="0" value="5.000000" label="max evalue" help="(--evalue)"/> - <param name="maxinterval" type="integer" min="1" value="100" label="maximum width of a suffix array interval, i.e. a query seed will be omitted if it matches more than n times" help="(--maxinterval)"/> + <param argument="--prime5" type="text" label="add 5' adapter" help="default: none" /> + <param argument="--prime3" type="text" label="add 3' adapter" help="default: none"/> + <param argument="--clipacc" value="70" type="integer" label="clipping accuracy" /> + <param argument="--polyA" type="boolean" truevalue="--polyA" falsevalue="" checked="false" label="Clip polyA tail" /> + <param argument="--autoclip" type="boolean" truevalue="--autoclip" falsevalue="" checked="false" label="Autoclip unknown 3prime adapter"/> + <param argument="--hardclip" type="boolean" truevalue="--hardclip" falsevalue="" checked="false" label="Enable hard clipping"/> + <param argument="--order" type="boolean" truevalue="--order" falsevalue="" checked="false" label="Sorts the output by chromsome and position" /> + <param argument="--differences" type="integer" min="0" value="1" label="search seeds initially with n differences"/> + <param argument="--jump" type="integer" value="0" min="0" label="search seeds with jump size" help="(0=automatic) (default:0)?"/> + <param argument="--evalue" type="float" min="0" value="5.000000" label="max evalue"/> + <param argument="--maxinterval" type="integer" min="1" value="100" label="maximum width of a suffix array interval, i.e. a query seed will be omitted if it matches more than n times"/> + <param argument="--nomatchfilename" type="boolean" truevalue="yes" falsevalue="no" checked="false" label="Output unmatched reads"/> </inputs> <outputs> - <data format="sam" name="segemehl_out" label="Read alignments on ${on_string}"/> + <data format="sam" name="segemehl_out" label="${tool.name} on ${on_string}"/> + <data format="fastq" name="segemehl_outunmatched" label="${tool.name} unaligned reads ${on_string}"> + <filter>output_unmatched</filter> + </data> </outputs> <tests> <test> @@ -181,8 +219,10 @@ <param name="library" value="single" /> <param name="input_query" value="test.fastq" /> <param name="splits" value="splits" /> - <param name="minsplicecover" value="40" /> + <param name="minsplicecover" value="40" /> + <param name="nomatchfilename" value="yes" /> <output name="segemehl_out" file="testmap2.sam" lines_diff="2" /> + <output name="segemehl_outunmatched" file="testmap2.fastq" /> </test> </tests> <help>