Mercurial > repos > fubar > rgrnastar_203e
changeset 15:9d72d0221c7f draft
Changed over to a separate STAR package dependency
| author | fubar |
|---|---|
| date | Tue, 04 Mar 2014 18:40:08 -0500 |
| parents | 1e40b977aa58 |
| children | bab81f19eeea |
| files | prepStar.sh rg_rnaStar.xml rgrnastar/prepStar.sh rgrnastar/rg_rnaStar.xml rgrnastar/tool-data/rnastar_indices.loc.sample rgrnastar/tool_data_table_conf.xml.sample rgrnastar/tool_dependencies.xml tool-data/rnastar_indices.loc.sample tool_data_table_conf.xml.sample tool_dependencies.xml |
| diffstat | 10 files changed, 341 insertions(+), 350 deletions(-) [+] |
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--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/prepStar.sh Tue Mar 04 18:40:08 2014 -0500 @@ -0,0 +1,21 @@ +# automate rnastar index generation +# from existing fasta genomes using limited ram - cut genomeChrbinNbits down to 13, genomeSAindexNbases 12 genomeSAsparseD 1 + +INDEXROOT=/mnt/galaxyIndices/genomes +# fix that, the list of genomes below and SOURCE below to suit your needs. This is for GVL august 2013 +for genome in Arabidopsis_thaliana_TAIR9 ce10 danRer7 dm3 hg19 hg_g1k_v37 mm9 phiX rn5 sacCer2 sacCer3 xenTro2 +do + SOURCE=${INDEXROOT}/${genome}/seq/ + TARGET=${INDEXROOT}/${genome}/rnastar + mkdir -p $TARGET + cd $TARGET +/mnt/galaxy/tools/rnastar/2.3.0e/fubar/rgrnastar_203e/9425706f4e97/bin/STAR --runMode genomeGenerate --genomeDir $TARGET --genomeFastaFiles ${SOURCE}/${genome}.fa --runThreadN 2 genomeLoad=NoSharedMemory --genomeChrBinNbits 13 genomeSAindexNbases 12 genomeSAsparseD 1 +done + +echo "#add these lines TABS not spaces please to rnastar_indexes.loc in tool-data" > rnastar_indexes.loc +for genome in Arabidopsis_thaliana_TAIR9 ce10 danRer7 dm3 hg19 hg_g1k_v37 mm9 phiX rn5 sacCer2 sacCer3 xenTro2 +do + SOURCE=${INDEXROOT}/${genome}/seq/ + TARGET=${INDEXROOT}/${genome}/rnastar + echo ${genome}'\t'${genome}'\t'${genome}'\t'/mnt/galaxyIndices/genomes/${genome}/rnastar >> rnastar_indexes.loc +done
--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/rg_rnaStar.xml Tue Mar 04 18:40:08 2014 -0500 @@ -0,0 +1,287 @@ +<tool id="rna_star" name="RNA-STAR" version="0.23"> + <description>Gapped-read mapper for RNA-seq data</description> + <requirements> + <requirement type="package" version="2.3.0e">rnastar</requirement> + <requirement type="package" version="0.1.19">samtools</requirement> + </requirements> + <command> + ## + ## Run STAR. + ## + + STAR + ## Can adjust this as appropriate for the system. + --genomeLoad NoSharedMemory + + --genomeDir ${refGenomeSource.index.fields.path} + --readFilesIn $input1 + #if $singlePaired.sPaired == "paired" + $singlePaired.input2 + #end if + --runThreadN 4 + #if $params.settingsType == "full": + --chimSegmentMin $params.chim_segment_min + --chimScoreMin $params.chim_score_min + #end if + + ## may or may not need to generate SAM tags and handle non-canonicals for Cufflinks tools. + ${outSAMstrandField} ${outFilterIntronMotifs} ${outSAMattributes} + + ; + + ## + ## BAM conversion. + ## + + ## Convert aligned reads. + samtools view -Shb Aligned.out.sam | samtools sort - Aligned.out + + ## Convert chimeric reads. + #if $params.settingsType == "full" and $params.chim_segment_min > 0: + ; samtools view -Shb Chimeric.out.sam | samtools sort - Chimeric.out + #end if + </command> + + <stdio> + <regex match=".*" source="both" level="warning" description="generic stdout/err chatter"/> + </stdio> + + <inputs> + <param name="jobName" type="text" size="120" value="rna-star run" label="Job narrative (added to output names)" + help="Only letters, numbers and underscores (_) will be retained in this field"> + <sanitizer invalid_char=""> + <valid initial="string.letters,string.digits"><add value="_" /> </valid> + </sanitizer> + </param> + <!-- FASTQ input(s) and options specifically for paired-end data. --> + <conditional name="singlePaired"> + <param name="sPaired" type="select" label="Single ended or mate-pair ended reads in this library?"> + <option value="single" selected="true">Single-end</option> + <option value="paired">Paired-end</option> + </param> + <when value="single"> + <param format="fastqsanger,fastq,fasta" name="input1" type="data" label="RNA-Seq FASTQ file" help="Nucleotide-space: Must have Sanger-scaled quality values with ASCII offset 33"/> + </when> + <when value="paired"> + <param format="fastqsanger,fastq,fasta" name="input1" type="data" label="RNA-Seq FASTQ file, forward reads" help="Nucleotide-space: Must have Sanger-scaled quality values with ASCII offset 33" /> + <param format="fastqsanger,fastq,fasta" name="input2" type="data" label="RNA-Seq FASTQ file, reverse reads" help="Nucleotide-space: Must have Sanger-scaled quality values with ASCII offset 33" /> + </when> + </conditional> + + <!-- Genome source. --> + <conditional name="refGenomeSource"> + <param name="genomeSource" type="select" label="Will you select a reference genome from your history or use a built-in index?" help="Built-ins were indexed using default options"> + <option value="indexed">Use a built-in index</option> + <option value="history">Use one from the history</option> + </param> + <when value="indexed"> + <param name="index" type="select" label="Select a reference genome"> + <options from_data_table="rnastar_indexes"> + <filter type="sort_by" column="2"/> + <validator type="no_options" message="No indexes are available for the selected input dataset"/> + </options> + </param> + </when> + <when value="history"> + <param name="ownFile" type="data" format="fasta" metadata_name="dbkey" label="Select the reference genome" /> + </when> + </conditional> + <param name="outSAMattributes" type="select" label="Include extra sam attributes for downstream processing"> + <option value="--outSAMattributes Standard">Standard - eg for old Samtools downstream</option> + <option value="--outSAMattributes All" selected="true">All modern Samtools attributes - see below</option> + </param> + <param name="outSAMstrandField" type="select" label="Include extra sam attributes for downstream processing"> + <option value="--outSAMstrandField intronMotif" selected="true">Add XS for cufflinks</option> + <option value="">No XS added to sam output</option> + </param> + <param name="outFilterIntronMotifs" type="select" label="Canonical junction preparation for unstranded data"> + <option value="">No special handling - all non-canonical junctions passed through</option> + <option value="--outFilterIntronMotifs RemoveNoncanonical" selected="true">Remove all non-canonical junctions for eg cufflinks</option> + <option value="--outFilterIntronMotifs RemoveNoncanonicalUnannotated">Remove only unannotated non-canonical junctions for eg cufflinks</option> + </param> + <!-- Parameter settings. --> + <conditional name="params"> + <param name="settingsType" type="select" label="Settings to use" help="You can use the default settings or set custom values for any STAR parameter."> + <option value="preSet" selected="true">Use Defaults</option> + <option value="full">Full parameter list</option> + </param> + <when value="preSet" /> + <!-- Full/advanced params. --> + <when value="full"> + <param name="chim_segment_min" type="integer" min="0" value="0" label="Minimum chimeric segment length" /> + <param name="chim_score_min" type="integer" min="0" value="0" label="Minimum total (summed) score of the chimeric segments" /> + + </when> + </conditional> + </inputs> + + <outputs> + <data format="txt" name="output_log" label="${on_string}_{jobName}.log" from_work_dir="Log.final.out"/> + <data format="interval" name="chimeric_junctions" label="${on_string}_{jobName}_starchimjunc.bed" from_work_dir="Chimeric.out.junction"> + <filter>(params['settingsType'] == 'full' and params['chim_segment_min'] > 0)</filter> + <actions> + <conditional name="refGenomeSource.genomeSource"> + <when value="indexed"> + <action type="metadata" name="dbkey"> + <option type="from_data_table" name="star_indexes" column="1" offset="0"> + <filter type="param_value" column="0" value="#" compare="startswith" keep="False"/> + <filter type="param_value" ref="refGenomeSource.index" column="0"/> + </option> + </action> + </when> + <when value="history"> + <action type="metadata" name="dbkey"> + <option type="from_param" name="refGenomeSource.ownFile" param_attribute="dbkey" /> + </action> + </when> + </conditional> + </actions> + </data> + <data format="bam" name="chimeric_reads" label="${on_string}_${jobName}_starmappedchim.bam" + from_work_dir="Chimeric.out.bam"> + <filter>(params['settingsType'] == 'full' and params['chim_segment_min'] > 0)</filter> + <actions> + <conditional name="refGenomeSource.genomeSource"> + <when value="indexed"> + <action type="metadata" name="dbkey"> + <option type="from_data_table" name="star_indexes" column="1" offset="0"> + <filter type="param_value" column="0" value="#" compare="startswith" keep="False"/> + <filter type="param_value" ref="refGenomeSource.index" column="0"/> + </option> + </action> + </when> + <when value="history"> + <action type="metadata" name="dbkey"> + <option type="from_param" name="refGenomeSource.ownFile" param_attribute="dbkey" /> + </action> + </when> + </conditional> + </actions> + </data> + <data format="interval" name="splice_junctions" label="${on_string}_${jobName}_starsplicejunct.bed" + from_work_dir="SJ.out.tab"> + <actions> + <conditional name="refGenomeSource.genomeSource"> + <when value="indexed"> + <action type="metadata" name="dbkey"> + <option type="from_data_table" name="star_indexes" column="1" offset="0"> + <filter type="param_value" column="0" value="#" compare="startswith" keep="False"/> + <filter type="param_value" ref="refGenomeSource.index" column="0"/> + </option> + </action> + </when> + <when value="history"> + <action type="metadata" name="dbkey"> + <option type="from_param" name="refGenomeSource.ownFile" param_attribute="dbkey" /> + </action> + </when> + </conditional> + </actions> + </data> + <data format="bam" name="mapped_reads" label="${on_string}_${jobName}_starmapped.bam" + from_work_dir="Aligned.out.bam"> + <actions> + <conditional name="refGenomeSource.genomeSource"> + <when value="indexed"> + <action type="metadata" name="dbkey"> + <option type="from_data_table" name="star_indexes" column="1" offset="0"> + <filter type="param_value" column="0" value="#" compare="startswith" keep="False"/> + <filter type="param_value" ref="refGenomeSource.index" column="0"/> + </option> + </action> + </when> + <when value="history"> + <action type="metadata" name="dbkey"> + <option type="from_param" name="refGenomeSource.ownFile" param_attribute="dbkey" /> + </action> + </when> + </conditional> + </actions> + </data> + </outputs> +<help> + +**What it does** +Runs the rna star gapped aligner. Suited to paired or single end rna-seq. + +8.2: SAM alignments + +The number of loci Nmap a read maps to (multi-mapping) is given by NH:i: field. +The mapping quality MAPQ (column 5) is 255 for uniquely mapping reads, and int(-10*log10(1-1/Nmap)) for +multi-mapping reads. This scheme is same as the one used by Tophat and is compatible with Cufflinks. + +For multi-mappers, all alignments except one are marked with 0x100 (secondary alignment) in the FLAG +column 2. The un-marked alignment is either the best one (i.e. highest scoring), or is randomly selected from +the alignments of equal quality. + +8.2.1: Standard SAM attributes +With default --outSAMattributes Standard option the following SAM attributes will be generated: + +Column 12: NH: number of loci a read (pair) maps to +Column 13: IH: alignment index for all alignments of a read +Column 14: aS: alignment score +Column 15: nM: number of mismatches (does not include indels) + +8.2.2: Extra SAM attrbiutes +If --outSAMattributes All option is used, the following additional attributes will be output: + +Column 16: jM:B:c,M1,M2,... Intron motifs for all junctions (i.e. N in CIGAR): +0: non-canonical; 1:GT/AG, 2: CT/AC, 3: GC/AG, 4: CT/GC, 5: AT/AC, 6: GT/AT. + +If splice junctions database is used, and a junction is annotated, 20 is added to its motif value. +Column 17: jI:B:I,Start1,End1,Start2,End2,... Start and End of introns for all junctions (1-based) + +Note, that samtools 0.1.18 or later have to be used with these extra attributes. + + +8.2.3: XS SAM strand attribute for Cufflinks/Cuffdiff + +If you have un-stranded RNA-seq data, and wish to run Cufflinks/Cuffdiff on STAR alignments, you will +need to run STAR with --outSAMstrandField intronMotif option, which will generate the XS +strand attribute for all alignments that contain splice junctions. The spliced alignments that have undefined +strand (i.e. containing only non-canonical junctions) will be suppressed. + +If you have stranded RNA-seq data, you do not need to use any specific STAR options. Instead, you need +to run Cufflinks with the library option --library-type options. For example, cufflinks with +library-type fr-firststrand should be used for the “standard” dUTP protocol. +This option has to be used only for Cufflinks runs and not for STAR runs. + +It is recommended to remove the non-canonical junctions for Cufflinks runs using – + +--outFilterIntronMotifs RemoveNoncanonical +filter out alignments that contain non-canonical junctions + +OR + +--outFilterIntronMotifs RemoveNoncanonicalUnannotated +filter out alignments that contain non-canonical unannotated junctions +when using annotated splice junctions database. The annotated non- +canonical junctions will be kept. + + +**Attributions** + +Note that each component has its own license. Good luck with figuring out your obligations. + +rna_star - see the web site at rna_star_ + +For details, please see the rna_starMS_ +"STAR: ultrafast universal RNA-seq aligner" +A. Dobin et al, Bioinformatics 2012; doi: 10.1093/bioinformatics/bts635 + +Galaxy_ (that's what you are using right now!) for gluing everything together + +Most of the work for this wrapper XML is Jeremy Goecks' original STAR_ wrapper + +Minor tweaks to output names to suit our downstream purposes, toolshed automated dependencies +and odds and ends of other code and documentation comprising this tool was +written by Ross Lazarus and that part is licensed_ the same way as other rgenetics artefacts + +.. _STAR: https://bitbucket.org/jgoecks/jeremys-code/raw/fa1930a689b8e2f6b59cc1706e5ba0ed8ad357be/galaxy/tool-wrappers/star.xml +.. _licensed: http://creativecommons.org/licenses/by-nc-nd/3.0/ +.. _rna_star: http://code.google.com/p/rna-star/ +.. _rna_starMS: http://bioinformatics.oxfordjournals.org/content/29/1/15.full +.. _Galaxy: http://getgalaxy.org + +</help> +</tool>
--- a/rgrnastar/prepStar.sh Sat Aug 31 03:06:03 2013 -0400 +++ /dev/null Thu Jan 01 00:00:00 1970 +0000 @@ -1,21 +0,0 @@ -# automate rnastar index generation -# from existing fasta genomes using limited ram - cut genomeChrbinNbits down to 13, genomeSAindexNbases 12 genomeSAsparseD 1 - -INDEXROOT=/mnt/galaxyIndices/genomes -# fix that, the list of genomes below and SOURCE below to suit your needs. This is for GVL august 2013 -for genome in Arabidopsis_thaliana_TAIR9 ce10 danRer7 dm3 hg19 hg_g1k_v37 mm9 phiX rn5 sacCer2 sacCer3 xenTro2 -do - SOURCE=${INDEXROOT}/${genome}/seq/ - TARGET=${INDEXROOT}/${genome}/rnastar - mkdir -p $TARGET - cd $TARGET - /mnt/galaxy/tools/rnastar/2.3.0e/fubar/rgrnastar_203e/9425706f4e97/bin/STAR --runMode genomeGenerate --genomeDir $TARGET --genomeFastaFiles ${SOURCE}/${genome}.fa --runThreadN 2 genomeLoad=NoSharedMemory -done - -echo "#add these lines TABS not spaces please to rnastar_indexes.loc in tool-data" > rnastar_indexes.loc -for genome in Arabidopsis_thaliana_TAIR9 ce10 danRer7 dm3 hg19 hg_g1k_v37 mm9 phiX rn5 sacCer2 sacCer3 xenTro2 -do - SOURCE=${INDEXROOT}/${genome}/seq/ - TARGET=${INDEXROOT}/${genome}/rnastar - echo ${genome}'\t'${genome}'\t'${genome}'\t'/mnt/galaxyIndices/genomes/${genome}/rnastar >> rnastar_indexes.loc -done
--- a/rgrnastar/rg_rnaStar.xml Sat Aug 31 03:06:03 2013 -0400 +++ /dev/null Thu Jan 01 00:00:00 1970 +0000 @@ -1,287 +0,0 @@ -<tool id="rna_star" name="RNA-STAR" version="0.23"> - <description>Gapped-read mapper for RNA-seq data</description> - <requirements> - <requirement type="package" version="2.3.0e">rnastar</requirement> - <requirement type="package">samtools</requirement> - </requirements> - <command> - ## - ## Run STAR. - ## - - STAR - ## Can adjust this as appropriate for the system. - --genomeLoad NoSharedMemory - - --genomeDir ${refGenomeSource.index.fields.path} - --readFilesIn $input1 - #if $singlePaired.sPaired == "paired" - $singlePaired.input2 - #end if - --runThreadN 4 - #if $params.settingsType == "full": - --chimSegmentMin $params.chim_segment_min - --chimScoreMin $params.chim_score_min - #end if - - ## may or may not need to generate SAM tags and handle non-canonicals for Cufflinks tools. - ${outSAMstrandField} ${outFilterIntronMotifs} ${outSAMattributes} - - ; - - ## - ## BAM conversion. - ## - - ## Convert aligned reads. - samtools view -Shb Aligned.out.sam | samtools sort - Aligned.out - - ## Convert chimeric reads. - #if $params.settingsType == "full" and $params.chim_segment_min > 0: - ; samtools view -Shb Chimeric.out.sam | samtools sort - Chimeric.out - #end if - </command> - - <stdio> - <regex match=".*" source="both" level="warning" description="generic stdout/err chatter"/> - </stdio> - - <inputs> - <param name="jobName" type="text" size="120" value="rna-star run" label="Job narrative (added to output names)" - help="Only letters, numbers and underscores (_) will be retained in this field"> - <sanitizer invalid_char=""> - <valid initial="string.letters,string.digits"><add value="_" /> </valid> - </sanitizer> - </param> - <!-- FASTQ input(s) and options specifically for paired-end data. --> - <conditional name="singlePaired"> - <param name="sPaired" type="select" label="Single ended or mate-pair ended reads in this library?"> - <option value="single" selected="true">Single-end</option> - <option value="paired">Paired-end</option> - </param> - <when value="single"> - <param format="fastqsanger,fastq,fasta" name="input1" type="data" label="RNA-Seq FASTQ file" help="Nucleotide-space: Must have Sanger-scaled quality values with ASCII offset 33"/> - </when> - <when value="paired"> - <param format="fastqsanger,fastq,fasta" name="input1" type="data" label="RNA-Seq FASTQ file, forward reads" help="Nucleotide-space: Must have Sanger-scaled quality values with ASCII offset 33" /> - <param format="fastqsanger,fastq,fasta" name="input2" type="data" label="RNA-Seq FASTQ file, reverse reads" help="Nucleotide-space: Must have Sanger-scaled quality values with ASCII offset 33" /> - </when> - </conditional> - - <!-- Genome source. --> - <conditional name="refGenomeSource"> - <param name="genomeSource" type="select" label="Will you select a reference genome from your history or use a built-in index?" help="Built-ins were indexed using default options"> - <option value="indexed">Use a built-in index</option> - <option value="history">Use one from the history</option> - </param> - <when value="indexed"> - <param name="index" type="select" label="Select a reference genome"> - <options from_data_table="rnastar_indexes"> - <filter type="sort_by" column="2"/> - <validator type="no_options" message="No indexes are available for the selected input dataset"/> - </options> - </param> - </when> - <when value="history"> - <param name="ownFile" type="data" format="fasta" metadata_name="dbkey" label="Select the reference genome" /> - </when> - </conditional> - <param name="outSAMattributes" type="select" label="Include extra sam attributes for downstream processing"> - <option value="--outSAMattributes Standard">Standard - eg for old Samtools downstream</option> - <option value="--outSAMattributes All" selected="true">All modern Samtools attributes - see below</option> - </param> - <param name="outSAMstrandField" type="select" label="Include extra sam attributes for downstream processing"> - <option value="--outSAMstrandField intronMotif" selected="true">Add XS for cufflinks</option> - <option value="">No XS added to sam output</option> - </param> - <param name="outFilterIntronMotifs" type="select" label="Canonical junction preparation for unstranded data"> - <option value="">No special handling - all non-canonical junctions passed through</option> - <option value="--outFilterIntronMotifs RemoveNoncanonical" selected="true">Remove all non-canonical junctions for eg cufflinks</option> - <option value="--outFilterIntronMotifs RemoveNoncanonicalUnannotated">Remove only unannotated non-canonical junctions for eg cufflinks</option> - </param> - <!-- Parameter settings. --> - <conditional name="params"> - <param name="settingsType" type="select" label="Settings to use" help="You can use the default settings or set custom values for any STAR parameter."> - <option value="preSet" selected="true">Use Defaults</option> - <option value="full">Full parameter list</option> - </param> - <when value="preSet" /> - <!-- Full/advanced params. --> - <when value="full"> - <param name="chim_segment_min" type="integer" min="0" value="0" label="Minimum chimeric segment length" /> - <param name="chim_score_min" type="integer" min="0" value="0" label="Minimum total (summed) score of the chimeric segments" /> - - </when> - </conditional> - </inputs> - - <outputs> - <data format="txt" name="output_log" label="${on_string}_${jobName}.log" from_work_dir="Log.final.out"/> - <data format="interval" name="chimeric_junctions" label="${on_string}_${jobName}_starchimjunc.bed" from_work_dir="Chimeric.out.junction"> - <filter>(params['settingsType'] == 'full' and params['chim_segment_min'] > 0)</filter> - <actions> - <conditional name="refGenomeSource.genomeSource"> - <when value="indexed"> - <action type="metadata" name="dbkey"> - <option type="from_data_table" name="star_indexes" column="1" offset="0"> - <filter type="param_value" column="0" value="#" compare="startswith" keep="False"/> - <filter type="param_value" ref="refGenomeSource.index" column="0"/> - </option> - </action> - </when> - <when value="history"> - <action type="metadata" name="dbkey"> - <option type="from_param" name="refGenomeSource.ownFile" param_attribute="dbkey" /> - </action> - </when> - </conditional> - </actions> - </data> - <data format="bam" name="chimeric_reads" label="${on_string}_${jobName}_starmappedchim.bam" - from_work_dir="Chimeric.out.bam"> - <filter>(params['settingsType'] == 'full' and params['chim_segment_min'] > 0)</filter> - <actions> - <conditional name="refGenomeSource.genomeSource"> - <when value="indexed"> - <action type="metadata" name="dbkey"> - <option type="from_data_table" name="star_indexes" column="1" offset="0"> - <filter type="param_value" column="0" value="#" compare="startswith" keep="False"/> - <filter type="param_value" ref="refGenomeSource.index" column="0"/> - </option> - </action> - </when> - <when value="history"> - <action type="metadata" name="dbkey"> - <option type="from_param" name="refGenomeSource.ownFile" param_attribute="dbkey" /> - </action> - </when> - </conditional> - </actions> - </data> - <data format="interval" name="splice_junctions" label="${on_string}_${jobName}_starsplicejunct.bed" - from_work_dir="SJ.out.tab"> - <actions> - <conditional name="refGenomeSource.genomeSource"> - <when value="indexed"> - <action type="metadata" name="dbkey"> - <option type="from_data_table" name="star_indexes" column="1" offset="0"> - <filter type="param_value" column="0" value="#" compare="startswith" keep="False"/> - <filter type="param_value" ref="refGenomeSource.index" column="0"/> - </option> - </action> - </when> - <when value="history"> - <action type="metadata" name="dbkey"> - <option type="from_param" name="refGenomeSource.ownFile" param_attribute="dbkey" /> - </action> - </when> - </conditional> - </actions> - </data> - <data format="bam" name="mapped_reads" label="${on_string}_${jobName}_starmapped.bam" - from_work_dir="Aligned.out.bam"> - <actions> - <conditional name="refGenomeSource.genomeSource"> - <when value="indexed"> - <action type="metadata" name="dbkey"> - <option type="from_data_table" name="star_indexes" column="1" offset="0"> - <filter type="param_value" column="0" value="#" compare="startswith" keep="False"/> - <filter type="param_value" ref="refGenomeSource.index" column="0"/> - </option> - </action> - </when> - <when value="history"> - <action type="metadata" name="dbkey"> - <option type="from_param" name="refGenomeSource.ownFile" param_attribute="dbkey" /> - </action> - </when> - </conditional> - </actions> - </data> - </outputs> -<help> - -**What it does** -Runs the rna star gapped aligner. Suited to paired or single end rna-seq. - -8.2: SAM alignments - -The number of loci Nmap a read maps to (multi-mapping) is given by NH:i: field. -The mapping quality MAPQ (column 5) is 255 for uniquely mapping reads, and int(-10*log10(1-1/Nmap)) for -multi-mapping reads. This scheme is same as the one used by Tophat and is compatible with Cufflinks. - -For multi-mappers, all alignments except one are marked with 0x100 (secondary alignment) in the FLAG -column 2. The un-marked alignment is either the best one (i.e. highest scoring), or is randomly selected from -the alignments of equal quality. - -8.2.1: Standard SAM attributes -With default --outSAMattributes Standard option the following SAM attributes will be generated: - -Column 12: NH: number of loci a read (pair) maps to -Column 13: IH: alignment index for all alignments of a read -Column 14: aS: alignment score -Column 15: nM: number of mismatches (does not include indels) - -8.2.2: Extra SAM attrbiutes -If --outSAMattributes All option is used, the following additional attributes will be output: - -Column 16: jM:B:c,M1,M2,... Intron motifs for all junctions (i.e. N in CIGAR): -0: non-canonical; 1:GT/AG, 2: CT/AC, 3: GC/AG, 4: CT/GC, 5: AT/AC, 6: GT/AT. - -If splice junctions database is used, and a junction is annotated, 20 is added to its motif value. -Column 17: jI:B:I,Start1,End1,Start2,End2,... Start and End of introns for all junctions (1-based) - -Note, that samtools 0.1.18 or later have to be used with these extra attributes. - - -8.2.3: XS SAM strand attribute for Cufflinks/Cuffdiff - -If you have un-stranded RNA-seq data, and wish to run Cufflinks/Cuffdiff on STAR alignments, you will -need to run STAR with --outSAMstrandField intronMotif option, which will generate the XS -strand attribute for all alignments that contain splice junctions. The spliced alignments that have undefined -strand (i.e. containing only non-canonical junctions) will be suppressed. - -If you have stranded RNA-seq data, you do not need to use any specific STAR options. Instead, you need -to run Cufflinks with the library option --library-type options. For example, cufflinks with -library-type fr-firststrand should be used for the “standard” dUTP protocol. -This option has to be used only for Cufflinks runs and not for STAR runs. - -It is recommended to remove the non-canonical junctions for Cufflinks runs using – - ---outFilterIntronMotifs RemoveNoncanonical -filter out alignments that contain non-canonical junctions - -OR - ---outFilterIntronMotifs RemoveNoncanonicalUnannotated -filter out alignments that contain non-canonical unannotated junctions -when using annotated splice junctions database. The annotated non- -canonical junctions will be kept. - - -**Attributions** - -Note that each component has its own license. Good luck with figuring out your obligations. - -rna_star - see the web site at rna_star_ - -For details, please see the rna_starMS_ -"STAR: ultrafast universal RNA-seq aligner" -A. Dobin et al, Bioinformatics 2012; doi: 10.1093/bioinformatics/bts635 - -Galaxy_ (that's what you are using right now!) for gluing everything together - -Most of the work for this wrapper XML is Jeremy Goecks' original STAR_ wrapper - -Minor tweaks to output names to suit our downstream purposes, toolshed automated dependencies -and odds and ends of other code and documentation comprising this tool was -written by Ross Lazarus and that part is licensed_ the same way as other rgenetics artefacts - -.. _STAR: https://bitbucket.org/jgoecks/jeremys-code/raw/fa1930a689b8e2f6b59cc1706e5ba0ed8ad357be/galaxy/tool-wrappers/star.xml -.. _licensed: http://creativecommons.org/licenses/by-nc-nd/3.0/ -.. _rna_star: http://code.google.com/p/rna-star/ -.. _rna_starMS: http://bioinformatics.oxfordjournals.org/content/29/1/15.full -.. _Galaxy: http://getgalaxy.org - -</help> -</tool>
--- a/rgrnastar/tool-data/rnastar_indices.loc.sample Sat Aug 31 03:06:03 2013 -0400 +++ /dev/null Thu Jan 01 00:00:00 1970 +0000 @@ -1,11 +0,0 @@ -#This is a sample file distributed with Galaxy that enables tools -#to use a directory of rna-star indexed sequences data files. You will -#need to create these data files and then create a bowtie_indices.loc -#file similar to this one (store it in this directory) that points to -#the directories in which those files are stored. The bowtie2_indices.loc -#file has this format (longer white space characters are TAB characters): -# -#<unique_build_id> <dbkey> <display_name> <file_base_path> -# -#hg19 hg19 hg19 full /mnt/galaxyIndices/genomes/hg19/rnastar -
--- a/rgrnastar/tool_data_table_conf.xml.sample Sat Aug 31 03:06:03 2013 -0400 +++ /dev/null Thu Jan 01 00:00:00 1970 +0000 @@ -1,7 +0,0 @@ -<!-- Use the file tool_data_table_conf.xml.oldlocstyle if you don't want to update your loc files as changed in revision 4550:535d276c92bc--> -<tables> - <table name="rnastar_indexes" comment_char="#"> - <columns>value, dbkey, name, path</columns> - <file path="tool-data/rnastar_indices.loc" /> - </table> -</tables>
--- a/rgrnastar/tool_dependencies.xml Sat Aug 31 03:06:03 2013 -0400 +++ /dev/null Thu Jan 01 00:00:00 1970 +0000 @@ -1,24 +0,0 @@ -<?xml version="1.0"?> -<tool_dependency> - <package name="rnastar" version="2.3.0e"> - <install version="1.0"> - <actions> - <action type="download_by_url">https://rna-star.googlecode.com/files/STAR_2.3.0e.tgz</action> - <action type="shell_command">make</action> - <action type="make_directory">$INSTALL_DIR</action> - <action type="make_directory">$INSTALL_DIR/bin</action> - <action type="move_file"> - <source>STAR</source> - <destination>$INSTALL_DIR/bin</destination> - </action> - <action type="set_environment"> - <environment_variable name="PATH" action="prepend_to">$INSTALL_DIR/bin</environment_variable> - </action> - </actions> - </install> - <readme> -Installs the STAR binary for rnastar - see https://code.google.com/p/rna-star/ - </readme> - </package> -</tool_dependency> -
--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/tool-data/rnastar_indices.loc.sample Tue Mar 04 18:40:08 2014 -0500 @@ -0,0 +1,11 @@ +#This is a sample file distributed with Galaxy that enables tools +#to use a directory of rna-star indexed sequences data files. You will +#need to create these data files and then create a bowtie_indices.loc +#file similar to this one (store it in this directory) that points to +#the directories in which those files are stored. The bowtie2_indices.loc +#file has this format (longer white space characters are TAB characters): +# +#<unique_build_id> <dbkey> <display_name> <file_base_path> +# +#hg19 hg19 hg19 full /mnt/galaxyIndices/genomes/hg19/rnastar +
--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/tool_data_table_conf.xml.sample Tue Mar 04 18:40:08 2014 -0500 @@ -0,0 +1,7 @@ +<!-- Use the file tool_data_table_conf.xml.oldlocstyle if you don't want to update your loc files as changed in revision 4550:535d276c92bc--> +<tables> + <table name="rnastar_indexes" comment_char="#"> + <columns>value, dbkey, name, path</columns> + <file path="tool-data/rnastar_indices.loc" /> + </table> +</tables>
--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/tool_dependencies.xml Tue Mar 04 18:40:08 2014 -0500 @@ -0,0 +1,15 @@ +<?xml version="1.0"?> +<tool_dependency> + <package name="rnastar" version="2.3.0e"> + <repository changeset_revision="6dcdb10d0d8b" name="package_rnastar_230e" owner="fubar" prior_installation_required="True" toolshed="http://testtoolshed.g2.bx.psu.edu/" /> + </package> + <package name="samtools" version="0.1.19"> + <repository changeset_revision="54195f1d4b0f" name="package_samtools_0_1_19" owner="iuc" prior_installation_required="True" toolshed="http://testtoolshed.g2.bx.psu.edu/" /> + </package> + <package name="star_230e" version="2.3.0e"> + <readme> +Installs the STAR wrapper and dependency packages samtools and star - see https://code.google.com/p/rna-star/ +STAR is a very fast mapper for rna-seq giving junctions if the indexes are constructed with a junction library + </readme> + </package> +</tool_dependency>