Mercurial > repos > devteam > cuffquant
diff cuffquant_wrapper.xml @ 0:5d8b9dcaf17d draft
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author | devteam |
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date | Fri, 19 Dec 2014 12:01:59 -0500 |
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children | 986b63735a5e |
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--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/cuffquant_wrapper.xml Fri Dec 19 12:01:59 2014 -0500 @@ -0,0 +1,218 @@ +<tool id="cuffquant" name="Cuffquant" version="@VERSION@.0"> + <!-- Wrapper supports Cuffdiff versions 2.2.1 --> + <description>Precompute gene expression levels</description> + <expand macro="requirements" /> + <expand macro="stdio" /> + <macros> + <import>cuff_macros.xml</import> + </macros> + <version_command>cuffquant 2>&1 | head -n 1</version_command> + <command> + cuffquant + --no-update-check + --num-threads=\${GALAXY_SLOTS:-4} + ## Set advanced SE data parameters? + #if $additional.sAdditional == "Yes": + -m $additional.frag_mean_len + -s $additional.frag_len_std_dev + #end if + + ## Multi-read correct? + #if $multiread_correct : + -u + #end if + + ## Bias correction? + #if $bias_correction.do_bias_correction == "Yes": + -b + #if $bias_correction.seq_source.index_source == "history": + ## Custom genome from history. + $bias_correction.seq_source.ref_file + #else: + ## Built-in genome. + "${ bias_correction.seq_source.index.fields.path }" + #end if + #end if + + $length_correction + + ## Set advanced parameters for cufflinks + #if $advanced_settings.sAdvanced == "Yes": + #if str($advanced_settings.library_type) != 'auto': + --library-type=$advanced_settings.library_type + #end if + #if $advanced_settings.mask_file: + --mask-file=$advanced_settings.mask_file + #end if + --max-mle-iterations=$advanced_settings.max_mle_iterations + --max-bundle-frags=$advanced_settings.max_bundle_frags + #end if + ## Inputs. + $gtf_input + #set samplestring = ','.join( [ str( $sample.sample ) for $sample in $samples ] ) + $samplestring + </command> + <inputs> + <param format="gtf,gff3" name="gtf_input" type="data" label="Transcripts" + help="A transcript annotation (GFF3 or GTF) file produced by cufflinks, cuffcompare, or other source."/> + + <repeat name="samples" title="Replicate" min="1"> + <param name="sample" label="Add replicate" type="data" format="sam,bam"/> + </repeat> + + <param name="multiread_correct" type="boolean" label="Use multi-read correct" + help="Tells Cufflinks to do an initial estimation procedure to more accurately weight reads mapping to multiple locations in the genome." /> + + <conditional name="bias_correction"> + <param name="do_bias_correction" type="select" label="Perform Bias Correction" + help="Bias detection and correction can significantly improve accuracy of transcript abundance estimates."> + <option value="No">No</option> + <option value="Yes">Yes</option> + </param> + <when value="Yes"> + <conditional name="seq_source"> + <param name="index_source" type="select" label="Reference sequence data"> + <option value="cached">Locally cached</option> + <option value="history">History</option> + </param> + <when value="cached"> + <param name="index" type="select" label="Using reference genome"> + <options from_data_table="fasta_indexes"> + <filter type="data_meta" ref="gtf_input" key="dbkey" column="1" /> + <validator type="no_options" message="No reference genome is available for the build associated with the selected input dataset" /> + </options> + </param> + </when> + <when value="history"> + <param name="ref_file" type="data" format="fasta" label="Using reference file" /> + </when> + </conditional> + </when> + <when value="No"></when> + </conditional> + + <param name="length_correction" type="select" label="apply length correction" help="mode of length normalization to transcript fpkm."> + <option value="" selected="true">cufflinks effective length correction</option> + <option value="--no-effective-length-correction">standard length correction</option> + <option value="--no-length-correction">no length correction at all (use raw counts)</option> + </param> + + <conditional name="additional"> + <param name="sAdditional" type="select" label="Set Additional Parameters for single end reads? (not recommended for paired-end reads)"> + <option value="No" selected="True">No</option> + <option value="Yes">Yes</option> + </param> + <when value="No"></when> + <when value="Yes"> + <param name="frag_mean_len" type="integer" value="200" label="Average Fragment Length"/> + <param name="frag_len_std_dev" type="integer" value="80" label="Fragment Length Standard Deviation"/> + </when> + </conditional> + + <conditional name="advanced_settings"> + <param name="sAdvanced" type="select" label="Set Advanced Cuffquant parameters? "> + <option value="No" selected="True">No</option> + <option value="Yes">Yes</option> + </param> + <when value="No"></when> + <when value="Yes"> + <param type="select" name="library_type" label="Library prep used for input reads" help=""> + <option value="auto" selected="True">Auto Detect</option> + <option value="ff-firststrand">ff-firststrand</option> + <option value="ff-secondstrand">ff-secondstrand</option> + <option value="ff-unstranded">ff-unstranded</option> + <option value="fr-firststrand">fr-firststrand</option> + <option value="fr-secondstrand">fr-secondstrand</option> + <option value="fr-unstranded" >fr-unstranded</option> + <option value="transfrags">transfrags</option> + </param> + <param name="mask_file" type="data" format="gtf,gff3" label="Mask File" help="Ignore all alignment within transcripts in this file" optional="True" /> + <param name="max_mle_iterations" value="5000" type="integer" label="Max MLE iterations" help="Maximum iterations allowed for Maximal Likelyhood Estimation calculations" /> + <param name="max_bundle_frags" type="integer" value="500000" label="Maximum number of fragments per locus" + help="Sets the maximum number of fragments a locus may have before being skipped. Default: 500,000" /> + </when> + </conditional> + </inputs> + <outputs> + <!-- Standard datasets. --> + <data format="cxb" name="out_file" label="${tool.name} on ${on_string}: Abundances.cxb" from_work_dir="abundances.cxb" /> + </outputs> + <tests> + <test> + <!-- + cuffquant cuffcompare_out5.gtf cuffdiff_in1.sam,cuffdiff_in2.sam + --> + <param name="gtf_input" value="cuffquant_in.gtf" ftype="gtf" /> + <repeat name="samples"> + <param name="sample" value="cuffquant_in1.sam" ftype="sam" /> + </repeat> + <repeat name="samples"> + <param name="sample" value="cuffquant_in2.sam" ftype="sam" /> + </repeat> + <param name="length_correction" value="" /> + <param name="do_bias_correction" value="No" /> + <param name="multiread_correct" value="No"/> + <param name="sAdditional" value="No"/> + <param name="sAdvanced" value="No" /> + <output name="out_file" file="cuffquant_out1.cxb" compare="sim_size" /> + </test> + </tests> + + <help> +**Cuffquant Overview** + +Cuffquant is part of Cufflinks_. Cuffquant provides pre-calculation of gene expression levels. The resulting file can be provided to cuffdiff or cuffnorm for further processing. Please cite: Trapnell C, Williams BA, Pertea G, Mortazavi AM, Kwan G, van Baren MJ, Salzberg SL, Wold B, Pachter L. Transcript assembly and abundance estimation from RNA-Seq reveals thousands of new transcripts and switching among isoforms. Nature Biotechnology doi:10.1038/nbt.1621 + +.. _Cufflinks: http://cole-trapnell-lab.github.io/cufflinks/ + +------ + +**Know what you are doing** + +.. class:: warningmark + +There is no such thing (yet) as an automated gearshift in expression analysis. It is all like stick-shift driving in San Francisco. In other words, running this tool with default parameters will probably not give you meaningful results. A way to deal with this is to **understand** the parameters by carefully reading the `documentation`__ and experimenting. Fortunately, Galaxy makes experimenting easy. + +.. __: http://cole-trapnell-lab.github.io/cufflinks/cuffquant/ + +------ + +**Input format** + +Cuffquant takes Cufflinks or Cuffcompare GTF files as input along with two or more SAM files containing the fragment alignments for two or more samples. + +------ + +**Outputs** + +Cuffquant produces one output file: + +1. Transcript expression values in binary format. + +------- + +**Settings** + +All of the options have a default value. You can change any of them. Most of the options in Cuffdiff have been implemented here. + +------ + +**Cuffdiff parameter list** + +This is a list of implemented Cuffdiff options:: + + -m INT Average fragment length (SE reads); default 200 + -s INT Fragment legnth standard deviation (SE reads); default 80 + --max-mle-iterations INT Sets the number of iterations allowed during maximum likelihood estimation of abundances. Default: 5000 + -u Multi read correction tells Cufflinks to do an initial estimation procedure to more accurately weight reads mapping to multiple locations in the genome. + -b ref.fasta bias correction. Bias detection and correction can significantly improve accuracy of transcript abundance estimates. + --no-effective-length-correction Use standard length correction + --no-length-correction Disable all length correction. + --library-type ff-firststrand,ff-secondstrand,ff-unstranded,fr-firstrand,fr-secondstrand,fr-unstranded,transfrags + --mask-file (gff3/gtf) Ignore all alignment within transcripts in this file + --max-bundle-frags Sets the maximum number of fragments a locus may have before being skipped. Skipped loci are listed in skipped.gtf. + </help> + <citations> + <citation type="doi">10.1038/nbt.1621</citation> + </citations> +</tool>