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author | devteam |
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date | Mon, 27 Jan 2014 09:27:10 -0500 |
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<tool id="express" name="eXpress" version="1.1.1"> <description>Quantify the abundances of a set of target sequences from sampled subsequences</description> <requirements> <requirement type="package" version="1.1.1">eXpress</requirement> </requirements> <command> express --no-update-check ## Additional parameters. #if $additional_params.use_additional == "yes": -B $additional_params.additional_batch -O $additional_params.additional_online #if str( $additional_params.calc_covar ) == 'yes': --calc-covar #end if -m $additional_params.mean_fragment_length -s $additional_params.fragment_length_deviation #end if ## Input files $multiFasta $bamOrSamFile </command> <inputs> <param format="fasta" name="multiFasta" type="data" label="A set of target references (annotation) in multi-FASTA format" help="The multi-FASTA file can also be a fasta file." /> <param format="sam,bam" name="bamOrSamFile" type="data" label="Alignments in the BAM or SAM format" help="The set of aligned reads." /> <conditional name="additional_params"> <param name="use_additional" type="select" label="Use Additional Parameters?"> <option value="no">No</option> <option value="yes">Yes</option> </param> <when value="no"> </when> <when value="yes"> <param name="additional_batch" type="integer" label="Additional batch EM rounds" value="0" help="0 is default. Can improve accuracy at the cost of time."/> <param name="additional_online" type="integer" label="Additional online EM rounds" value="0" help="0 is default. Can improve accuracy at the cost of time."/> <param name="calc_covar" type="select" label="Calculate the covariance between targets and outputs?" help="This calculation requires slightly more time and memory."> <option value="no">No</option> <option value="yes">Yes</option> </param> <param name="mean_fragment_length" type="integer" label="Specifies the mean fragment length" value="200" help="200 is default. While the empirical distribution is estimated from paired-end reads on-the-fly, this value paramaterizes the prior distribution."/> <param name="fragment_length_deviation" type="integer" label="Specified the fragment length standard deviation" value="60" help="60 is default. While the empirical distribution is estimated from paired-end reads on-the-fly, this value paramaterizes the prior distribution."/> </when> </conditional> </inputs> <outputs> <data format="txt" name="params" from_work_dir="params.xprs"/> <data format="txt" name="results" from_work_dir="results.xprs"/> <data format="txt" name="varcov" from_work_dir="varcov.xprs"> <filter>additional_params[ 'use_additional' ] == "yes" and additional_params[ 'calc_covar' ] == "yes"</filter> </data> </outputs> <tests> <!-- Test for the most simple case : Running eXpress with a .bam file and a .fasta file --> <test> <!-- TopHat commands: eXpress Trinity.fasta hits.bam --> <param name="bamOrSamFile" ftype="bam" value="eXpress_hits.bam"/> <param name="multiFasta" ftype="fasta" value="eXpress_Trinity.fasta"/> <param name="use_additional" value="no"/> <output name="params" file="eXpress_params.xprs" lines_diff="300"/> <output name="results" file="eXpress_results.xprs" lines_diff="10"/> </test> <!-- Test for an other simple case : Running eXpress with a .sam file and a .fasta file --> <test> <!-- TopHat commands: eXpress Trinity.fasta hits.sam --> <param name="bamOrSamFile" ftype="sam" value="eXpress_hits.sam"/> <param name="multiFasta" ftype="fasta" value="eXpress_Trinity.fasta"/> <param name="use_additional" value="no"/> <output name="params" file="eXpress_params_sam.xprs" lines_diff="300"/> <output name="results" file="eXpress_results_sam.xprs" lines_diff="10"/> </test> <!-- Test for a complex case : All the parameters has been activated and modified --> <test> <!-- TopHat commands: eXpress -B 1 -O 1 ++calc-covar -m 300 -s 85 Trinity.fasta hits.sam --> <param name="bamOrSamFile" ftype="sam" value="eXpress_hits_all_params.bam"/> <param name="multiFasta" ftype="fasta" value="eXpress_Trinity_all_params.fasta"/> <param name="use_additional" value="yes"/> <param name="additional_batch" value="1"/> <param name="additional_online" value="1" /> <param name="calc_covar" value="yes"/> <param name="mean_fragment_length" value="300"/> <param name="fragment_length_deviation" value="85"/> <output name="params" file="eXpress_params_all_params.xprs" lines_diff="300"/> <output name="results" file="eXpress_results_all_params.xprs" lines_diff="10"/> <output name="varcov" file="eXpress_varcov_all_params.xprs"/> </test> </tests> <help> **eXpress Overview** eXpress is a streaming tool for quantifying the abundances of a set of target sequences from sampled subsequences. Example applications include transcript-level RNA-Seq quantification, allele-specific/haplotype expression analysis (from RNA-Seq), transcription factor binding quantification in ChIP-Seq, and analysis of metagenomic data. .. _Ensembl: http://bio.math.berkeley.edu/eXpress/ ----- **Input format** eXpress requires two input files: - A multi-FASTA file containing the transcript sequences. - Read alignments to the multi-FASTA file in BAM or SAM format. ------ **Outputs** - The output for eXpress is saved in a file called results.xprs in an easy-to-parse tab-delimited format. - Also, params.xprs contains the values of the other parameters (besides abundances and counts) estimated by eXpress. - If you choose to use to calculate the covariance between targets and outputs, an other output would be : varcov.xprs. </help> </tool>