Mercurial > repos > nilesh > rseqc
changeset 28:6e438a559a10
Deleted selected files
| author | nilesh |
|---|---|
| date | Thu, 11 Jul 2013 12:31:24 -0400 |
| parents | 5dbd20d3d623 |
| children | 907d4b021ff6 |
| files | rseqc/RPKM_count.xml rseqc/RPKM_saturation.xml rseqc/bam2wig.xml rseqc/bam_stat.xml rseqc/clipping_profile.xml rseqc/geneBody_coverage.xml rseqc/infer_experiment.xml rseqc/inner_distance.xml rseqc/junction_annotation.xml rseqc/junction_saturation.xml rseqc/read_GC.xml rseqc/read_NVC.xml rseqc/read_distribution.xml rseqc/read_duplication.xml rseqc/read_quality.xml rseqc/samtoolshelper.py |
| diffstat | 16 files changed, 0 insertions(+), 1125 deletions(-) [+] |
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--- a/rseqc/RPKM_count.xml Thu Jul 11 12:28:04 2013 -0400 +++ /dev/null Thu Jan 01 00:00:00 1970 +0000 @@ -1,143 +0,0 @@ -<tool id="RPKM_count" name="RPKM Count"> - <description>calculates raw count and RPKM values for transcript at exon, intron, and mRNA level</description> - <command interpreter="python"> samtoolshelper.py /home/nilesh/RSeQC-2.3.3/scripts/RPKM_count.py -i $input -o output -r $refgene - - #if $nx - -x - #end if - - #if str($strand_type.strand_specific) == "pair" - -d - #if str($strand_type.pair_type) == "sd" - '1++,1--,2+-,2-+' - #else - '1+-,1-+,2++,2--' - #end if - #end if - - #if str($strand_type.strand_specific) == "single" - -d - #if str($strand_type.single_type) == "s" - '++,--' - #else - '+-,-+' - #end if - #end if - - #if $skiphits - -u - #end if - - #if $onlyexonic - -e - #end if - - </command> - <inputs> - <param name="input" type="data" format="bam" label="input bam/sam file" /> - <param name="refgene" type="data" format="bed" label="Reference gene model" /> - <conditional name="strand_type"> - <param name="strand_specific" type="select" label="Strand-specific?" value="None"> - <option value="none">None</option> - <option value="pair">Pair-End RNA-seq</option> - <option value="single">Single-End RNA-seq</option> - </param> - <when value="pair"> - <param name="pair_type" type="select" display="radio" label="Pair-End Read Type (format: mapped --> parent)" value="sd"> - <option value="sd"> read1 (positive --> positive; negative --> negative), read2 (positive --> negative; negative --> positive)</option> - <option value="ds">read1 (positive --> negative; negative --> positive), read2 (positive --> positive; negative --> negative)</option> - </param> - </when> - <when value="single"> - <param name="single_type" type="select" display="radio" label="Single-End Read Type (format: mapped --> parent)" value="s"> - <option value="s">positive --> positive; negative --> negative</option> - <option value="d">positive --> negative; negative --> positive</option> - </param> - </when> - <when value="none"></when> - </conditional> - <param name="skiphits" type="boolean" value="false" label="Skip Multiple Hit Reads" /> - <param name="onlyexonic" type="boolean" value="false" label="Only use exonic (UTR exons and CDS exons) reads, otherwise use all reads" /> - </inputs> - <outputs> - <data format="xls" name="outputxls" from_work_dir="output_read_count.xls"/> - </outputs> - <help> -.. image:: https://code.google.com/p/rseqc/logo?cct=1336721062 - ------ - -About RSeQC -+++++++++++ - -The RSeQC package provides a number of useful modules that can comprehensively evaluate high throughput sequence data especially RNA-seq data. “Basic modules” quickly inspect sequence quality, nucleotide composition bias, PCR bias and GC bias, while “RNA-seq specific modules” investigate sequencing saturation status of both splicing junction detection and expression estimation, mapped reads clipping profile, mapped reads distribution, coverage uniformity over gene body, reproducibility, strand specificity and splice junction annotation. - -The RSeQC package is licensed under the GNU GPL v3 license. - -Inputs -++++++++++++++ - -Input BAM/SAM file - Alignment file in BAM/SAM format. - -Reference gene model - Gene model in BED format. - -Strand sequencing type (default=none) - See Infer Experiment tool if uncertain. - -Options -++++++++++++++ - -Skip Multiple Hit Reads - Use Multiple hit reads or use only uniquely mapped reads. - -Only use exonic reads - Renders program only used exonic (UTR exons and CDS exons) reads, otherwise use all reads. - -Sample Output -++++++++++++++ - -===== ===== === ========= ===== =========== ============= ============= ======== ======== -chrom start end accession score gene strand tag count (+) tag count (-) RPKM (+) RPKM (-) -===== ===== === ========= ===== =========== ============= ============= ======== ======== -chr1 29213722 29313959 NM_001166007_intron_1 0 + 431 4329 0.086 0.863 -chr1 29314417 29319841 NM_001166007_intron_2 0 + 31 1 0.114 0.004 -chr1 29320054 29323726 NM_001166007_intron_3 0 + 32 0 0.174 0 -chr1 29323831 29338376 NM_001166007_intron_4 0 + 33 2 0.045 0.003 -chr1 29338419 29342203 NM_001166007_intron_5 0 + 7 0 0.037 0 -chr1 29342279 29344735 NM_001166007_intron_6 0 + 35 4 0.285 0.033 -chr1 29344954 29356911 NM_001166007_intron_7 0 + 34 2 0.057 0.003 -chr1 29356999 29359604 NM_001166007_intron_8 0 + 19 1 0.146 0.008 -chr1 29359757 29362337 NM_001166007_intron_9 0 + 31 0 0.24 0 -chr1 29362435 29365765 NM_001166007_intron_10 0 + 11 1 0.066 0.006 -chr1 29365938 29379615 NM_001166007_intron_11 0 + 63 0 0.092 0 -chr1 29379824 29391493 NM_001166007_intron_12 0 + 383 8 0.656 0.014 -chr1 29391670 29424318 NM_001166007_intron_13 0 + 817 10 0.5 0.006 -chr1 29424447 29435847 NM_001166007_intron_14 0 + 28 0 0.049 0 -chr1 29435949 29438879 NM_001166007_intron_15 0 + 12 0 0.082 0 -chr1 29438960 29442210 NM_001166007_intron_16 0 + 22 2 0.135 0.012 -chr1 29442315 29443330 NM_001166007_intron_17 0 + 9 0 0.177 0 -chr1 29213602 29213722 NM_001166007_exon_1 0 + 164 0 27.321 0 -chr1 29313959 29314417 NM_001166007_exon_2 0 + 1699 4 74.158 0.175 -chr1 29319841 29320054 NM_001166007_exon_3 0 + 528 1 49.554 0.094 -chr1 29323726 29323831 NM_001166007_exon_4 0 + 168 0 31.985 0 -chr1 29338376 29338419 NM_001166007_exon_5 0 + 88 0 40.911 0 -chr1 29342203 29342279 NM_001166007_exon_6 0 + 114 3 29.986 0.789 -chr1 29344735 29344954 NM_001166007_exon_7 0 + 290 10 26.472 0.913 -chr1 29356911 29356999 NM_001166007_exon_8 0 + 146 1 33.166 0.227 -chr1 29359604 29359757 NM_001166007_exon_9 0 + 404 11 52.786 1.437 -chr1 29362337 29362435 NM_001166007_exon_10 0 + 85 7 17.339 1.428 -chr1 29365765 29365938 NM_001166007_exon_11 0 + 198 2 22.88 0.231 -chr1 29379615 29379824 NM_001166007_exon_12 0 + 306 5 29.269 0.478 -chr1 29391493 29391670 NM_001166007_exon_13 0 + 243 7 27.445 0.791 -chr1 29424318 29424447 NM_001166007_exon_14 0 + 298 7 46.18 1.085 -chr1 29435847 29435949 NM_001166007_exon_15 0 + 396 8 77.611 1.568 -chr1 29438879 29438960 NM_001166007_exon_16 0 + 307 0 75.767 0 -chr1 29442210 29442315 NM_001166007_exon_17 0 + 138 0 26.273 0 -chr1 29443330 29446558 NM_001166007_exon_18 0 + 2434 84 15.074 0.52 -chr1 29213602 29446558 NM_001166007_mRNA 0 + 8006 150 27.704 0.519 -===== ===== === ========= ===== =========== ============= ============= ======== ======== - - </help> -</tool>
--- a/rseqc/RPKM_saturation.xml Thu Jul 11 12:28:04 2013 -0400 +++ /dev/null Thu Jan 01 00:00:00 1970 +0000 @@ -1,114 +0,0 @@ -<tool id="RPKM_saturation" name="RPKM Saturation"> - <description>calculates raw count and RPKM values for transcript at exon, intron, and mRNA level</description> - <command interpreter="python"> bam2wig.py /home/nilesh/RSeQC-2.3.3/scripts/RPKM_saturation.py -i $input -o output -r $refgene - - #if str($strand_type.strand_specific) == "pair" - -d - #if str($strand_type.pair_type) == "sd" - '1++,1--,2+-,2-+' - #else - '1+-,1-+,2++,2--' - #end if - #end if - - #if str($strand_type.strand_specific) == "single" - -d - #if str($strand_type.single_type) == "s" - '++,--' - #else - '+-,-+' - #end if - #end if - - -l $percentileFloor -u $percentileCeiling -s $percentileStep -c $rpkmCutoff - - </command> - <inputs> - <param name="input" type="data" format="bam" label="input bam/sam file" /> - <param name="refgene" type="data" format="bed" label="Reference gene model" /> - <conditional name="strand_type"> - <param name="strand_specific" type="select" label="Strand-specific?" value="None"> - <option value="none">None</option> - <option value="pair">Pair-End RNA-seq</option> - <option value="single">Single-End RNA-seq</option> - </param> - <when value="pair"> - <param name="pair_type" type="select" display="radio" label="Pair-End Read Type (format: mapped --> parent)" value="sd"> - <option value="sd"> read1 (positive --> positive; negative --> negative), read2 (positive --> negative; negative --> positive)</option> - <option value="ds">read1 (positive --> negative; negative --> positive), read2 (positive --> positive; negative --> negative)</option> - </param> - </when> - <when value="single"> - <param name="single_type" type="select" display="radio" label="Single-End Read Type (format: mapped --> parent)" value="s"> - <option value="s">positive --> positive; negative --> negative</option> - <option value="d">positive --> negative; negative --> positive</option> - </param> - </when> - <when value="none"></when> - </conditional> - <param name="percentileFloor" type="integer" value="5" label="Begin sampling from this percentile (default=5)" /> - <param name="percentileCeiling" type="integer" value="100" label="End sampling at this percentile (default=100)" /> - <param name="percentileStep" type="integer" value="5" label="Sampling step size (default=5)" /> - <param name="rpkmCutoff" type="text" value="0.01" label="Ignore transcripts with RPKM smaller than this number (default=0.01)" /> - </inputs> - <outputs> - <data format="xls" name="outputxls" from_work_dir="output.eRPKM.xls"/> - <data format="xls" name="outputrawxls" from_work_dir="output.rawCount.xls"/> - <data format="r" name="outputr" from_work_dir="output.saturation.r"/> - <data format="pdf" name="outputpdf" from_work_dir="output.saturation.pdf"/> - </outputs> - <help> -.. image:: https://code.google.com/p/rseqc/logo?cct=1336721062 - ------ - -About RSeQC -+++++++++++ - -The RSeQC package provides a number of useful modules that can comprehensively evaluate high throughput sequence data especially RNA-seq data. “Basic modules” quickly inspect sequence quality, nucleotide composition bias, PCR bias and GC bias, while “RNA-seq specific modules” investigate sequencing saturation status of both splicing junction detection and expression estimation, mapped reads clipping profile, mapped reads distribution, coverage uniformity over gene body, reproducibility, strand specificity and splice junction annotation. - -The RSeQC package is licensed under the GNU GPL v3 license. - -Inputs -++++++++++++++ - -Input BAM/SAM file - Alignment file in BAM/SAM format. - -Reference gene model - Gene model in BED format. - -Strand sequencing type (default=none) - See Infer Experiment tool if uncertain. - -Options -++++++++++++++ - -Skip Multiple Hit Reads - Use Multiple hit reads or use only uniquely mapped reads. - -Only use exonic reads - Renders program only used exonic (UTR exons and CDS exons) reads, otherwise use all reads. - -Output -++++++++++++++ - -1. output..eRPKM.xls: RPKM values for each transcript -2. output.rawCount.xls: Raw count for each transcript -3. output.saturation.r: R script to generate plot -4. output.saturation.pdf: - -.. image:: http://dldcc-web.brc.bcm.edu/lilab/liguow/RSeQC/figure/saturation.png - -- All transcripts were sorted in ascending order according to expression level (RPKM). Then they are divided into 4 groups: - 1. Q1 (0-25%): Transcripts with expression level ranked below 25 percentile. - 2. Q2 (25-50%): Transcripts with expression level ranked between 25 percentile and 50 percentile. - 3. Q3 (50-75%): Transcripts with expression level ranked between 50 percentile and 75 percentile. - 4. Q4 (75-100%): Transcripts with expression level ranked above 75 percentile. -- BAM/SAM file containing more than 100 million alignments will make module very slow. -- Follow example below to visualize a particular transcript (using R console):: -- output example -.. image:: http://dldcc-web.brc.bcm.edu/lilab/liguow/RSeQC/figure/saturation_eg.png - - </help> -</tool>
--- a/rseqc/bam2wig.xml Thu Jul 11 12:28:04 2013 -0400 +++ /dev/null Thu Jan 01 00:00:00 1970 +0000 @@ -1,116 +0,0 @@ -<tool id="bam2wig" name="BAM to Wiggle"> - <description> - converts all types of RNA-seq data from .bam to .wig - </description> - <command interpreter="python"> - samtoolshelper.py /home/nilesh/RSeQC-2.3.3/scripts/bam2wig.py -i $input -s $chromsize -o outfile - - #if str($strand_type.strand_specific) == "pair" - -d - #if str($strand_type.pair_type) == "sd" - '1++,1--,2+-,2-+' - #else - '1+-,1-+,2++,2--' - #end if - #end if - - #if str($strand_type.strand_specific) == "single" - -d - #if str($strand_type.single_type) == "s" - '++,--' - #else - '+-,-+' - #end if - #end if - - #if $wigsum.wigsum_type - -t $wigsum.totalwig - #end if - - #if $skipmultihits - -u - #end if - </command> - <inputs> - <param name="input" type="data" label="Input .bam File" format="bam" /> - <param name="chromsize" type="data" label="Chromosome size file (tab or space separated)" format="txt,tabular" /> - <param name="skipmultihits" type="boolean" label="Skip Multiple Hit Reads/Only Use Uniquely Mapped Reads" value="false" /> - <conditional name="wigsum"> - <param name="wigsum_type" type="boolean" label="Specify wigsum?" value="false"> - </param> - <when value="true"> - <param name="totalwig" value="0" type="integer" label="specified wigsum" /> - </when> - <when value="false"></when> - </conditional> - <conditional name="strand_type"> - <param name="strand_specific" type="select" label="Strand-specific?" value="None"> - <option value="none">None</option> - <option value="pair">Pair-End RNA-seq</option> - <option value="single">Single-End RNA-seq</option> - </param> - <when value="pair"> - <param name="pair_type" type="select" display="radio" label="Pair-End Read Type (format: mapped --> parent)" value="sd"> - <option value="sd"> read1 (positive --> positive; negative --> negative), read2 (positive --> negative; negative --> positive)</option> - <option value="ds">read1 (positive --> negative; negative --> positive), read2 (positive --> positive; negative --> negative)</option> - </param> - </when> - <when value="single"> - <param name="single_type" type="select" display="radio" label="Single-End Read Type (format: mapped --> parent)" value="s"> - <option value="s">positive --> positive; negative --> negative</option> - <option value="d">positive --> negative; negative --> positive</option> - </param> - </when> - <when value="none"></when> - </conditional> - </inputs> - <outputs> - <data format="wig" name="output" from_work_dir="outfile.wig"> - <filter>strand_type['strand_specific'] == 'none'</filter> - </data> - <data format="wig" name="outputfwd" from_work_dir="outfile_Forward.wig"> - <filter>strand_type['strand_specific'] != 'none'</filter> - </data> - <data format="wig" name="outputrv" from_work_dir="outfile_Reverse.wig"> - <filter>strand_type['strand_specific'] != 'none'</filter> - </data> - </outputs> - <help> -.. image:: https://code.google.com/p/rseqc/logo?cct=1336721062 - ------ - -About RSeQC -+++++++++++ - -The RSeQC package provides a number of useful modules that can comprehensively evaluate high throughput sequence data especially RNA-seq data. “Basic modules” quickly inspect sequence quality, nucleotide composition bias, PCR bias and GC bias, while “RNA-seq specific modules” investigate sequencing saturation status of both splicing junction detection and expression estimation, mapped reads clipping profile, mapped reads distribution, coverage uniformity over gene body, reproducibility, strand specificity and splice junction annotation. - -The RSeQC package is licensed under the GNU GPL v3 license. - -Inputs -++++++++++++++ - -Input BAM file - Alignment file in BAM format (SAM is not supported). BAM file will be sorted and indexed using samTools. - -Chromosome size file - Tab or space separated text file with 2 columns: first column is chromosome name, second column is size of the chromosome. Chromosome names (such as "chr1") should be consistent between this file and BAM file. - -Specified wigsum (default=none) - Specified wigsum. Wigsum of 100000000 equals to coverage achieved by 1 million 100nt reads. Ignore this option to disable normalization. - -Skip multiple Hit reads - skips multiple hit reads or only use uniquely mapped reads - -Strand-specific (default=none) - How read(s) were stranded during sequencing. If you are not sure about the strand rule, run infer_experiment.py - -Outputs -++++++++++++++ - -If RNA-seq is not strand specific, one wig file will be generated, if RNA-seq -is strand specific, two wig files corresponding to Forward and Reverse will be generated. - - - </help> -</tool> \ No newline at end of file
--- a/rseqc/bam_stat.xml Thu Jul 11 12:28:04 2013 -0400 +++ /dev/null Thu Jan 01 00:00:00 1970 +0000 @@ -1,43 +0,0 @@ -<tool id="bam_stat" name="BAM/SAM Mapping Stats"> - <description> - reads mapping statistics for a provided BAM or SAM file. - </description> - <command interpreter="python"> - /home/nilesh/RSeQC-2.3.3/scripts/bam_stat.py -i $input > $output - </command> - <inputs> - <param name="input" type="data" label="Input .bam/.sam File" format="bam,sam" /> - </inputs> - <outputs> - <data format="txt" name="output" /> - </outputs> - <help> -.. image:: https://code.google.com/p/rseqc/logo?cct=1336721062 - ------ - -About RSeQC -+++++++++++ - -The RSeQC package provides a number of useful modules that can comprehensively evaluate high throughput sequence data especially RNA-seq data. “Basic modules” quickly inspect sequence quality, nucleotide composition bias, PCR bias and GC bias, while “RNA-seq specific modules” investigate sequencing saturation status of both splicing junction detection and expression estimation, mapped reads clipping profile, mapped reads distribution, coverage uniformity over gene body, reproducibility, strand specificity and splice junction annotation. - -The RSeQC package is licensed under the GNU GPL v3 license. - -Inputs -++++++++++++++ - -Input BAM/SAM file - Alignment file in BAM/SAM format. - - -Output -++++++++++++++ - -- Total Reads (Total records) = {Multiple mapped reads} + {Uniquely mapped} -- Uniquely mapped Reads = {read-1} + {read-2} (if paired end) -- Uniquely mapped Reads = {Reads map to '+'} + {Reads map to '-'} -- Uniquely mapped Reads = {Splice reads} + {Non-splice reads} - - - </help> -</tool> \ No newline at end of file
--- a/rseqc/clipping_profile.xml Thu Jul 11 12:28:04 2013 -0400 +++ /dev/null Thu Jan 01 00:00:00 1970 +0000 @@ -1,41 +0,0 @@ -<tool id="clipping_profile" name="Clipping Profile"> - <description> - estimates clipping profile of RNA-seq reads from BAM or SAM file - </description> - <command interpreter="python"> - /home/nilesh/RSeQC-2.3.3/scripts/clipping_profile.py -i $input -o output - </command> - <inputs> - <param name="input" type="data" label="Input .bam/.sam File" format="bam,sam" /> - </inputs> - <outputs> - <data format="xls" name="outputxls" from_work_dir="output.clipping_profile.xls" /> - <data format="r" name="outputr" from_work_dir="output.clipping_profile.r" /> - </outputs> - <help> -.. image:: https://code.google.com/p/rseqc/logo?cct=1336721062 - ------ - -About RSeQC -+++++++++++ - -The RSeQC package provides a number of useful modules that can comprehensively evaluate high throughput sequence data especially RNA-seq data. “Basic modules” quickly inspect sequence quality, nucleotide composition bias, PCR bias and GC bias, while “RNA-seq specific modules” investigate sequencing saturation status of both splicing junction detection and expression estimation, mapped reads clipping profile, mapped reads distribution, coverage uniformity over gene body, reproducibility, strand specificity and splice junction annotation. - -The RSeQC package is licensed under the GNU GPL v3 license. - -Inputs -++++++++++++++ - -Input BAM/SAM file - Alignment file in BAM/SAM format. - - -Sample Output -++++++++++++++ - -.. image:: http://dldcc-web.brc.bcm.edu/lilab/liguow/RSeQC/figure/clipping_good.png - - - </help> -</tool> \ No newline at end of file
--- a/rseqc/geneBody_coverage.xml Thu Jul 11 12:28:04 2013 -0400 +++ /dev/null Thu Jan 01 00:00:00 1970 +0000 @@ -1,50 +0,0 @@ -<tool id="geneBody_coverage" name="Gene Body Converage"> - <description> - Read coverage over gene body. - </description> - <command interpreter="python"> - /home/nilesh/RSeQC-2.3.3/scripts/inner_distance.py -i $input -r $refgene -o output - </command> - <inputs> - <param name="input" type="data" label="Input .bam file" format="bam" /> - <param name="refgene" type="data" label="Reference Genome" format="bed" /> - </inputs> - <outputs> - <data name="outputpdf" format="pdf" from_work_dir="output.geneBodyCoverage.pdf" /> - <data name="outputr" format="r" from_work_dir="output.geneBodyCoverage_plot.r" /> - <data name="outputtxt" format="txt" from_work_dir="output.geneBodyCoverage.txt" /> - </outputs> - <help> -.. image:: https://code.google.com/p/rseqc/logo?cct=1336721062 - ------ - -About RSeQC -+++++++++++ - -The RSeQC package provides a number of useful modules that can comprehensively evaluate high throughput sequence data especially RNA-seq data. “Basic modules” quickly inspect sequence quality, nucleotide composition bias, PCR bias and GC bias, while “RNA-seq specific modules” investigate sequencing saturation status of both splicing junction detection and expression estimation, mapped reads clipping profile, mapped reads distribution, coverage uniformity over gene body, reproducibility, strand specificity and splice junction annotation. - -The RSeQC package is licensed under the GNU GPL v3 license. - -Inputs -++++++++++++++ - -Input BAM/SAM file - Alignment file in BAM/SAM format. - -Reference gene model - Gene Model in BED format. - - -Outputs -++++++++++++++ - -Read coverage over gene body. This module is used to check if reads coverage is uniform and if there is any 5’/3’ bias. This module scales all transcripts to 100 nt and calculates the number of reads covering each nucleotide position. Finally, it generates a plot illustrating the coverage profile along the gene body. NOTE: this module requires lots of memory for large BAM files, because it load the entire BAM file into memory. We add another script "geneBody_coverage2.py" into v2.3.1 which takes bigwig (instead of BAM) as input. It only use 200M RAM, but users need to convert BAM into WIG, and then WIG into BigWig. - -Example output: - .. image:: http://dldcc-web.brc.bcm.edu/lilab/liguow/RSeQC/figure/geneBody_coverage.png - - - - </help> -</tool> \ No newline at end of file
--- a/rseqc/infer_experiment.xml Thu Jul 11 12:28:04 2013 -0400 +++ /dev/null Thu Jan 01 00:00:00 1970 +0000 @@ -1,114 +0,0 @@ -<tool id="infer_experiment" name="Infer Experiment"> - <description>speculates how RNA-seq were configured</description> - <command interpreter="python"> /home/nilesh/RSeQC-2.3.3/scripts/infer_experiment.py -i $input -r $refgene - - #if $sample_size.boolean - -s $sample_size.size - #end if - - > $output - </command> - <inputs> - <param name="input" type="data" format="bam,sam" label="Input BAM/SAM file" /> - <param name="refgene" type="data" format="bed" label="Reference gene model in bed format" /> - <conditional name="sample_size"> - <param name="boolean" type="boolean" label="Modify usable sampled reads" value="false" /> - <when value="true"> - <param name="size" type="integer" label="Number of usable sampled reads (default = 200000)" value="200000" /> - </when> - </conditional> - </inputs> - <outputs> - <data format="txt" name="output" /> - </outputs> - <help> -.. image:: https://code.google.com/p/rseqc/logo?cct=1336721062 - ------ - -About RSeQC -+++++++++++ - -The RSeQC package provides a number of useful modules that can comprehensively evaluate high throughput sequence data especially RNA-seq data. “Basic modules” quickly inspect sequence quality, nucleotide composition bias, PCR bias and GC bias, while “RNA-seq specific modules” investigate sequencing saturation status of both splicing junction detection and expression estimation, mapped reads clipping profile, mapped reads distribution, coverage uniformity over gene body, reproducibility, strand specificity and splice junction annotation. - -The RSeQC package is licensed under the GNU GPL v3 license. - -Inputs -++++++++++++++ - -Input BAM/SAM file - Alignment file in BAM/SAM format. - -Reference gene model - Gene model in BED format. - -Number of usable sampled reads (default=200000) - Number of usable reads sampled from SAM/BAM file. More reads will give more accurate estimation, but make program little slower. - - -Output -++++++++++++++ -This program is used to speculate how RNA-seq sequencing were configured, especially how reads were stranded for strand-specific RNA-seq data, through comparing reads' mapping information to the underneath gene model. Generally, strand specific RNA-seq data should be handled differently in both visualization and RPKM calculation. - -For pair-end RNA-seq, there are two different ways to strand reads: - -1) 1++,1--,2+-,2-+ - - read1 mapped to '+' strand indicates parental gene on '+' strand - - read1 mapped to '-' strand indicates parental gene on '-' strand - - read2 mapped to '+' strand indicates parental gene on '-' strand - - read2 mapped to '-' strand indicates parental gene on '+' strand -2) 1+-,1-+,2++,2-- - - read1 mapped to '+' strand indicates parental gene on '-' strand - - read1 mapped to '-' strand indicates parental gene on '+' strand - - read2 mapped to '+' strand indicates parental gene on '+' strand - - read2 mapped to '-' strand indicates parental gene on '-' strand - -For single-end RNA-seq, there are also two different ways to strand reads: - -1) ++,-- - -read mapped to '+' strand indicates parental gene on '+' strand - - read mapped to '-' strand indicates parental gene on '-' strand -2) +-,-+ - - read mapped to '+' strand indicates parental gene on '-' strand - - read mapped to '-' strand indicates parental gene on '+' strand - -Example Output -++++++++++++++ - -**Example1** :: - - ========================================================= - This is PairEnd Data :: - - Fraction of reads explained by "1++,1--,2+-,2-+": 0.4992 - Fraction of reads explained by "1+-,1-+,2++,2--": 0.5008 - Fraction of reads explained by other combinations: 0.0000 - ========================================================= - -*Conclusion*: We can infer that this is NOT a strand specific because 50% of reads can be explained by "1++,1--,2+-,2-+", while the other 50% can be explained by "1+-,1-+,2++,2--". - -**Example2** :: - - ============================================================ - This is PairEnd Data - - Fraction of reads explained by "1++,1--,2+-,2-+": 0.9644 :: - Fraction of reads explained by "1+-,1-+,2++,2--": 0.0356 - Fraction of reads explained by other combinations: 0.0000 - ============================================================ - -*Conclusion*: We can infer that this is a strand-specific RNA-seq data. strandness of read1 is consistent with that of gene model, while strandness of read2 is opposite to the strand of reference gene model. - -**Example3** :: - - ========================================================= - This is SingleEnd Data :: - - Fraction of reads explained by "++,--": 0.9840 :: - Fraction of reads explained by "+-,-+": 0.0160 - Fraction of reads explained by other combinations: 0.0000 - ========================================================= - -*Conclusion*: This is single-end, strand specific RNA-seq data. Strandness of reads are concordant with strandness of reference gene. - </help> -</tool> \ No newline at end of file
--- a/rseqc/inner_distance.xml Thu Jul 11 12:28:04 2013 -0400 +++ /dev/null Thu Jan 01 00:00:00 1970 +0000 @@ -1,91 +0,0 @@ -<tool id="inner_distance" name="Inner Distance"> - <description>calculate the inner distance (or insert size) between two paired RNA reads</description> - <command interpreter="python"> /home/nilesh/RSeQC-2.3.3/scripts/inner_distance.py -i $input -o output -r $refgene - - #if $bounds.hasLowerBound - -l $bounds.lowerBound - #end if - - #if $bounds2.hasUpperBound - -u $bounds2.upperBound - #end if - - #if $steps.step - -s $steps.stepSize - #end if - </command> - <inputs> - <param name="input" type="data" format="bam,sam" label="input bam/sam file" /> - <param name="refgene" type="data" format="bed" label="reference gene model" /> - <conditional name="bounds"> - <param name="hasLowerBound" type="boolean" label="Specify lower bound" value="false"/> - <when value="true"> - <param name="lowerBound" type="integer" value="-250" label="Estimated Lower Bound (bp, default=-250)" /> - </when> - </conditional> - <conditional name="bounds2"> - <param name="hasUpperBound" type="boolean" label="Specify upper bound" value="false" /> - <when value="true"> - <param name="upperBound" type="integer" value="250" label="Estimated Upper Bound (bp, default=250)" /> - </when> - </conditional> - <conditional name="steps"> - <param name="step" type="boolean" label="Specify step size" value="false" /> - <when value="true"> - <param name="stepSize" type="integer" value="5" label="Step size (bp, default=5)" /> - </when> - </conditional> - </inputs> - <outputs> - <data format="txt" name="outputtxt" from_work_dir="output.inner_distance.txt"/> - <data format="txt" name="outputfreqtxt" from_work_dir="output.inner_distance_freq.txt" /> - <data format="pdf" name="outputpdf" from_work_dir="output.inner_distance_plot.pdf" /> - <data format="r" name="outputr" from_work_dir="output.inner_distance_plot.r" /> - </outputs> - <help> -.. image:: https://code.google.com/p/rseqc/logo?cct=1336721062 - ------ - -About RSeQC -+++++++++++ - -The RSeQC package provides a number of useful modules that can comprehensively evaluate high throughput sequence data especially RNA-seq data. “Basic modules” quickly inspect sequence quality, nucleotide composition bias, PCR bias and GC bias, while “RNA-seq specific modules” investigate sequencing saturation status of both splicing junction detection and expression estimation, mapped reads clipping profile, mapped reads distribution, coverage uniformity over gene body, reproducibility, strand specificity and splice junction annotation. - -The RSeQC package is licensed under the GNU GPL v3 license. - -Inputs -++++++++++++++ - -Input BAM/SAM file - Alignment file in BAM/SAM format. - -Reference gene model - Gene model in BED format. - -Estimated Upper/Lower Bounds (defaults=250 and -250) - Estimated upper/lower bounds of inner distance (bp). - -Step size (default=5) - Step size of histogram - - -Output -++++++++++++++ - -1. output.inner_distance.txt: -- first column is read ID --second column is inner distance. Could be negative value if PE reads were overlapped or mapping error (e.g. Read1_start < Read2_start, while Read1_end >> Read2_end due to spliced mapping of read1) -- third column indicates how paired reads were mapped: PE_within_same_exon, PE_within_diff_exon,PE_reads_overlap -2. output..inner_distance_freq.txt: -- inner distance starts -- inner distance ends -- number of read pairs -- note the first 2 columns are left side half open interval -3. output.inner_distance_plot.r: R script to generate histogram -4. output.inner_distance_plot.pdf: histogram plot - -.. image:: http://dldcc-web.brc.bcm.edu/lilab/liguow/RSeQC/figure/inner_distance.png - - </help> -</tool>
--- a/rseqc/junction_annotation.xml Thu Jul 11 12:28:04 2013 -0400 +++ /dev/null Thu Jan 01 00:00:00 1970 +0000 @@ -1,69 +0,0 @@ -<tool id="junction_annotation" name="Junction Annotation"> - <description>compares detected splice junctions to reference gene model</description> - <command interpreter="python"> /home/nilesh/RSeQC-2.3.3/scripts/junction_annotation.py -i $input -o output -r $refgene - - #if $intron.hasIntron - -m $intron.min_Intron - #end if - - </command> - <inputs> - <param name="input" type="data" format="bam,sam" label="input bam/sam file" /> - <param name="refgene" type="data" format="bed" label="reference gene model" /> - <conditional name="intron"> - <param name="hasIntron" type="boolean" label="Specify minimum intron length" value="false"/> - <when value="true"> - <param name="min_Intron" type="integer" value="50" label="Minimum intron length (bp, default=50)" /> - </when> - </conditional> - </inputs> - <outputs> - <data format="xls" name="outputxls" from_work_dir="output.junction.xls"/> - <data format="r" name="outputr" from_work_dir="output.junction_plot.r" /> - <data format="pdf" name="outputpdf" from_work_dir="output.splice_events.pdf"/> - <data format="pdf" name="outputjpdf" from_work_dir="output.splice_junction.pdf" /> - </outputs> - <help> -.. image:: https://code.google.com/p/rseqc/logo?cct=1336721062 - ------ - -About RSeQC -+++++++++++ - -The RSeQC package provides a number of useful modules that can comprehensively evaluate high throughput sequence data especially RNA-seq data. “Basic modules” quickly inspect sequence quality, nucleotide composition bias, PCR bias and GC bias, while “RNA-seq specific modules” investigate sequencing saturation status of both splicing junction detection and expression estimation, mapped reads clipping profile, mapped reads distribution, coverage uniformity over gene body, reproducibility, strand specificity and splice junction annotation. - -The RSeQC package is licensed under the GNU GPL v3 license. - -Inputs -++++++++++++++ - -Input BAM/SAM file - Alignment file in BAM/SAM format. - -Reference gene model - Gene model in BED format. - -Minimum intron length (default=50) - Minimum intron length (bp). - - -Output -++++++++++++++ - -1. output.junc.anno.junction.xls: -- chrom ID -- start position of junction (coordinate is 0 based) -- end position of junction (coordinate is 1 based) -- number of splice events supporting this junction -- 'annotated', 'complete_novel' or 'partial_novel'. -2. output.anno.junction_plot.r: R script to generate pie chart -3. output.splice_junction.pdf: plot of splice junctions -4. output.splice_events.pdf: plot of splice events -.. image:: http://dldcc-web.brc.bcm.edu/lilab/liguow/RSeQC/figure/junction.png - - - - - </help> -</tool>
--- a/rseqc/junction_saturation.xml Thu Jul 11 12:28:04 2013 -0400 +++ /dev/null Thu Jan 01 00:00:00 1970 +0000 @@ -1,70 +0,0 @@ -<tool id="junction_saturation" name="Junction Saturation"> - <description>detects splice junctions from each subset and compares them to reference gene model</description> - <command interpreter="python"> /home/nilesh/RSeQC-2.3.3/scripts/junction_saturation.py -i $input -o output -r $refgene -m $intronSize -v $minSplice - - #if $percentiles.specifyPercentiles - -l $percentiles.lowBound -u $percentiles.upBound -s $percentiles.percentileStep - #end if - - </command> - <inputs> - <param name="input" type="data" format="bam,sam" label="input bam/sam file" /> - <param name="refgene" type="data" format="bed" label="reference gene model" /> - <param name="intronSize" type="integer" label="Minimum intron size (bp, default=50)" value="50"/> - <param name="minSplice" type="integer" label="Minimum coverage (default=1)" value="1" /> - <conditional name="percentiles"> - <param name="specifyPercentiles" type="boolean" label="Specify sampling bounds and frequency" value="false"/> - <when value="true"> - <param name="lowBound" type="integer" value="5" label="Lower Bound Sampling Frequency (bp, default=5)" /> - <param name="upBound" type="integer" value="100" label="Upper Bound Sampling Frequency (bp, default=100)" /> - <param name="percentileStep" type="integer" value="5" label="Sampling increment (default=5)" /> - </when> - </conditional> - </inputs> - <outputs> - <data format="r" name="outputr" from_work_dir="output.junctionSaturation_plot.r"/> - <data format="pdf" name="outputpdf" from_work_dir="output.junctionSaturation_plot.pdf"/> - </outputs> - <help> -.. image:: https://code.google.com/p/rseqc/logo?cct=1336721062 - ------ - -About RSeQC -+++++++++++ - -The RSeQC package provides a number of useful modules that can comprehensively evaluate high throughput sequence data especially RNA-seq data. “Basic modules” quickly inspect sequence quality, nucleotide composition bias, PCR bias and GC bias, while “RNA-seq specific modules” investigate sequencing saturation status of both splicing junction detection and expression estimation, mapped reads clipping profile, mapped reads distribution, coverage uniformity over gene body, reproducibility, strand specificity and splice junction annotation. - -The RSeQC package is licensed under the GNU GPL v3 license. - -Inputs -++++++++++++++ - -Input BAM/SAM file - Alignment file in BAM/SAM format. - -Reference gene model - Gene model in BED format. - -Sampling Percentiles - Upper Bound, Lower Bound, Sampling Increment (defaults= 100, 5, and 5) - Sampling starts from the Lower Bound and increments to the Upper Bound at the rate of the Sampling Increment. - -Minimum intron length (default=50) - Minimum intron length (bp). - -Minimum coverage (default=1) - Minimum number of supportting reads to call a junction. - -Output -++++++++++++++ - -1. output.junctionSaturation_plot.r: R script to generate plot -2. output.junctionSaturation_plot.pdf - -.. image:: http://dldcc-web.brc.bcm.edu/lilab/liguow/RSeQC/figure/junction_saturation.png - -In this example, current sequencing depth is almost saturated for "known junction" (red line) detection because the number of "known junction" reaches a plateau. In other words, nearly all "known junctions" (expressed in this particular tissue) have already been detected, and continue sequencing will not detect additional "known junction" and will only increase junction coverage (i.e. junction covered by more reads). While current sequencing depth is not saturated for novel junctions (green). - - - </help> -</tool> \ No newline at end of file
--- a/rseqc/read_GC.xml Thu Jul 11 12:28:04 2013 -0400 +++ /dev/null Thu Jan 01 00:00:00 1970 +0000 @@ -1,42 +0,0 @@ -<tool id="read_GC" name="Read GC"> - <description>determines GC% and read count</description> - <command interpreter="python"> /home/nilesh/RSeQC-2.3.3/scripts/read_GC.py -i $input -o output - </command> - <inputs> - <param name="input" type="data" format="bam,sam" label="input bam/sam file" /> - </inputs> - <outputs> - <data format="xls" name="outputxls" from_work_dir="output.dup.pos.DupRate.xls"/> - <data format="xls" name="outputseqxls" from_work_dir="output.dup.seq.DupRate.xls"/> - <data format="r" name="outputr" from_work_dir="output.DupRate_plot.r" /> - <data format="pdf" name="outputpdf" from_work_dir="output.DupRate_plot.pdf" /> - </outputs> - <help> - .. image:: https://code.google.com/p/rseqc/logo?cct=1336721062 - ------ - -About RSeQC -+++++++++++ - -The RSeQC package provides a number of useful modules that can comprehensively evaluate high throughput sequence data especially RNA-seq data. “Basic modules” quickly inspect sequence quality, nucleotide composition bias, PCR bias and GC bias, while “RNA-seq specific modules” investigate sequencing saturation status of both splicing junction detection and expression estimation, mapped reads clipping profile, mapped reads distribution, coverage uniformity over gene body, reproducibility, strand specificity and splice junction annotation. - -The RSeQC package is licensed under the GNU GPL v3 license. - -Inputs -++++++++++++++ - -Input BAM/SAM file - Alignment file in BAM/SAM format. - -Output -++++++++++++++ - -1. output.GC.xls: Two column, plain text file, first column is GC%, second column is read count -2. output.GC_plot.r: R script to generate pdf file. -3. output.GC_plot.pdf: graphical output generated from R script. - -.. image:: http://dldcc-web.brc.bcm.edu/lilab/liguow/RSeQC/figure/read_gc.png - - </help> -</tool>
--- a/rseqc/read_NVC.xml Thu Jul 11 12:28:04 2013 -0400 +++ /dev/null Thu Jan 01 00:00:00 1970 +0000 @@ -1,53 +0,0 @@ -<tool id="read_NVC" name="Read NVC"> - <description>to check the nucleotide composition bias</description> - <command interpreter="python"> /home/nilesh/RSeQC-2.3.3/scripts/read_NVC.py -i $input -o output - - #if $nx - -x - #end if - </command> - <inputs> - <param name="input" type="data" format="bam,sam" label="input bam/sam file" /> - <param name="nx" type="boolean" label="Include N,X in NVC plot" value="false" /> - </inputs> - <outputs> - <data format="xls" name="outputxls" from_work_dir="output.NVC.xls"/> - <data format="r" name="outputr" from_work_dir="output.NVC_plot.r" /> - <data format="pdf" name="outputpdf" from_work_dir="output.NVC_plot.pdf" /> - </outputs> - <help> -.. image:: https://code.google.com/p/rseqc/logo?cct=1336721062 - ------ - -About RSeQC -+++++++++++ - -The RSeQC package provides a number of useful modules that can comprehensively evaluate high throughput sequence data especially RNA-seq data. “Basic modules” quickly inspect sequence quality, nucleotide composition bias, PCR bias and GC bias, while “RNA-seq specific modules” investigate sequencing saturation status of both splicing junction detection and expression estimation, mapped reads clipping profile, mapped reads distribution, coverage uniformity over gene body, reproducibility, strand specificity and splice junction annotation. - -The RSeQC package is licensed under the GNU GPL v3 license. - -Inputs -++++++++++++++ - -Input BAM/SAM file - Alignment file in BAM/SAM format. - -Include N,X in NVC plot - Plots N and X alongside A, T, C, and G in plot. - -Output -++++++++++++++ - -This module is used to check the nucleotide composition bias. Due to random priming, certain patterns are over represented at the beginning (5'end) of reads. This bias could be easily examined by NVC (Nucleotide versus cycle) plot. NVC plot is generated by overlaying all reads together, then calculating nucleotide composition for each position of read (or each sequencing cycle). In ideal condition (genome is random and RNA-seq reads is randomly sampled from genome), we expect A%=C%=G%=T%=25% at each position of reads. - - -1. output.NVC.xls: plain text file, each row is position of read (or sequencing cycle), each column is nucleotide (A,C,G,T,N,X) -2. output.NVC_plot.r: R script to generate NVC plot. -3. output.NVC_plot.pdf: NVC plot. - - -.. image:: http://dldcc-web.brc.bcm.edu/lilab/liguow/RSeQC/figure/NVC_plot.png - - </help> -</tool>
--- a/rseqc/read_distribution.xml Thu Jul 11 12:28:04 2013 -0400 +++ /dev/null Thu Jan 01 00:00:00 1970 +0000 @@ -1,66 +0,0 @@ -<tool id="read_distribution" name="Read Distribution"> - <description>calculates how mapped reads were distributed over genome feature</description> - <command interpreter="python"> /home/nilesh/RSeQC-2.3.3/scripts/read_distribution.py -i $input -r $refgene > $output - </command> - <inputs> - <param name="input" type="data" format="bam,sam" label="input bam/sam file" /> - <param name="refgene" type="data" format="bed" label="reference gene model" /> - </inputs> - <outputs> - <data format="txt" name="output" /> - </outputs> - <help> -.. image:: https://code.google.com/p/rseqc/logo?cct=1336721062 - ------ - -About RSeQC -+++++++++++ - -The RSeQC package provides a number of useful modules that can comprehensively evaluate high throughput sequence data especially RNA-seq data. “Basic modules” quickly inspect sequence quality, nucleotide composition bias, PCR bias and GC bias, while “RNA-seq specific modules” investigate sequencing saturation status of both splicing junction detection and expression estimation, mapped reads clipping profile, mapped reads distribution, coverage uniformity over gene body, reproducibility, strand specificity and splice junction annotation. - -The RSeQC package is licensed under the GNU GPL v3 license. - -Inputs -++++++++++++++ - -Input BAM/SAM file - Alignment file in BAM/SAM format. - -Reference gene model - Gene model in BED format. - -Sample Output -++++++++++++++ - -:: - - Total Read: 44,826,454 :: - - Total Tags: 50,023,249 :: - - Total Assigned Tags: 36,057,402 :: - - Group Total_bases Tag_count Tags/Kb - CDS_Exons 33302033 20022538 601.24 - 5'UTR_Exons 21717577 4414913 203.29 - 3'UTR_Exons 15347845 3641689 237.28 - Introns 1132597354 6312099 5.57 - TSS_up_1kb 17957047 215220 11.99 - TSS_up_5kb 81621382 392192 4.81 - TSS_up_10kb 149730983 769210 5.14 - TES_down_1kb 18298543 266157 14.55 - TES_down_5kb 78900674 730072 9.25 - TES_down_10kb 140361190 896953 6.39 - -Note: -- "Total Reads": This does NOT include those QC fail,duplicate and non-primary hit reads -- "Total Tags": reads spliced once will be counted as 2 tags, reads spliced twice will be counted as 3 tags, etc. And because of this, "Total Fragments" >= "Total Reads" -- "Total Assigned Tags": number of tags that can be unambiguously assigned the 10 groups (above table). -- Tags assigned to "TSS_up_1kb" were also assigned to "TSS_up_5kb" and "TSS_up_10kb", tags assigned to "TSS_up_5kb" were also assigned to "TSS_up_10kb". Therefore, "Total Assigned Tags" = CDS_Exons + 5'UTR_Exons + 3'UTR_Exons + Introns + TSS_up_10kb + TES_down_10kb. -- When assigning tags to genome features, each tag is represented by its middle point. -- RSeQC cannot assign those reads that: 1) hit to intergenic regions that beyond region starting from TSS upstream 10Kb to TES downstream 10Kb. 2) hit to regions covered by both 5'UTR and 3' UTR. This is possible when two head-to-tail transcripts are overlapped in UTR regions. 3) hit to regions covered by both TSS upstream 10Kb and TES downstream 10Kb. - - - </help> -</tool>
--- a/rseqc/read_duplication.xml Thu Jul 11 12:28:04 2013 -0400 +++ /dev/null Thu Jan 01 00:00:00 1970 +0000 @@ -1,47 +0,0 @@ -<tool id="read_duplication" name="Read Duplication"> - <description>determines reads duplication rate with sequence-based and mapping-based strategies</description> - <command interpreter="python"> /home/nilesh/RSeQC-2.3.3/scripts/read_duplication.py -i $input -o output -u $upLimit - </command> - <inputs> - <param name="input" type="data" format="bam,sam" label="input bam/sam file" /> - <param name="upLimit" type="integer" label="Upper Limit of Plotted Duplicated Times (default=500)" value="500" /> - </inputs> - <outputs> - <data format="xls" name="outputxls" from_work_dir="output.dup.pos.DupRate.xls"/> - <data format="xls" name="outputseqxls" from_work_dir="output.dup.seq.DupRate.xls"/> - <data format="r" name="outputr" from_work_dir="output.DupRate_plot.r" /> - <data format="pdf" name="outputpdf" from_work_dir="output.DupRate_plot.pdf" /> - </outputs> - <help> -.. image:: https://code.google.com/p/rseqc/logo?cct=1336721062 - ------ - -About RSeQC -+++++++++++ - -The RSeQC package provides a number of useful modules that can comprehensively evaluate high throughput sequence data especially RNA-seq data. “Basic modules” quickly inspect sequence quality, nucleotide composition bias, PCR bias and GC bias, while “RNA-seq specific modules” investigate sequencing saturation status of both splicing junction detection and expression estimation, mapped reads clipping profile, mapped reads distribution, coverage uniformity over gene body, reproducibility, strand specificity and splice junction annotation. - -The RSeQC package is licensed under the GNU GPL v3 license. - -Inputs -++++++++++++++ - -Input BAM/SAM file - Alignment file in BAM/SAM format. - -Upper Limit of Plotted Duplicated Times (default=500) - Only used for plotting. - -Output -++++++++++++++ - -1. output.dup.pos.DupRate.xls: Read duplication rate determined from mapping position of read. First column is "occurrence" or duplication times, second column is number of uniquely mapped reads. -2. output.dup.seq.DupRate.xls: Read duplication rate determined from sequence of read. First column is "occurrence" or duplication times, second column is number of uniquely mapped reads. -3. output.DupRate_plot.r: R script to generate pdf file -4. output.DupRate_plot.pdf: graphical output generated from R script - -.. image:: http://dldcc-web.brc.bcm.edu/lilab/liguow/RSeQC/figure/duplicate.png - - </help> -</tool>
--- a/rseqc/read_quality.xml Thu Jul 11 12:28:04 2013 -0400 +++ /dev/null Thu Jan 01 00:00:00 1970 +0000 @@ -1,46 +0,0 @@ -<tool id="read_quality" name="Read Quality"> - <description>determines Phred quality score</description> - <command interpreter="python"> /home/nilesh/RSeQC-2.3.3/scripts/read_quality.py -i $input -o output -r $reduce - </command> - <inputs> - <param name="input" type="data" format="bam,sam" label="input bam/sam file" /> - <param name="reduce" type="integer" label="Ignore Phred scores less than this amount (only applies to 'boxplot', default=1000)" value="1000" /> - </inputs> - <outputs> - <data format="r" name="outputr" from_work_dir="output.qual.r" /> - <data format="pdf" name="outputpdf" from_work_dir="output.qual.heatmap.pdf" /> - <data format="pdf" name="outputpdf" from_work_dir="output.qual.boxplot.pdf" /> - </outputs> - <help> -.. image:: https://code.google.com/p/rseqc/logo?cct=1336721062 - ------ - -About RSeQC -+++++++++++ - -The RSeQC package provides a number of useful modules that can comprehensively evaluate high throughput sequence data especially RNA-seq data. “Basic modules” quickly inspect sequence quality, nucleotide composition bias, PCR bias and GC bias, while “RNA-seq specific modules” investigate sequencing saturation status of both splicing junction detection and expression estimation, mapped reads clipping profile, mapped reads distribution, coverage uniformity over gene body, reproducibility, strand specificity and splice junction annotation. - -The RSeQC package is licensed under the GNU GPL v3 license. - -Inputs -++++++++++++++ - -Input BAM/SAM file - Alignment file in BAM/SAM format. - -Ignore phred scores less than this number (default=1000) - To avoid making huge vector in R, nucleotide with certain phred score represented less than this number will be ignored. Increase this number save more memory while reduce precision. This option only applies to the 'boxplot'. - -Output -++++++++++++++ - -1. output.qual.r -2. output.qual.boxplot.pdf -.. image:: http://dldcc-web.brc.bcm.edu/lilab/liguow/RSeQC/figure/36mer.qual.plot.png -3. output.qual.heatmap.pdf -.. image:: http://dldcc-web.brc.bcm.edu/lilab/liguow/RSeQC/figure/36mer.qual.heatmap.png -use different color to represent nucleotide density ("blue"=low density,"orange"=median density,"red"=high density") - - </help> -</tool>
--- a/rseqc/samtoolshelper.py Thu Jul 11 12:28:04 2013 -0400 +++ /dev/null Thu Jan 01 00:00:00 1970 +0000 @@ -1,20 +0,0 @@ -import sys -import subprocess as sp -import os - -# Creates the sorted and indexed bam/bai files that are requried for both bam2wig and RSEQC_count -def samtools_sorted(bam): - sortedbam = bam + ".sorted" - indexedbam = ".".join([sortedbam,"bam.bai"]) - sp.call(['samtools', 'sort', '-m 1000000000', bam, sortedbam]) - sortedbam = sortedbam + '.bam' - sp.call(['samtools', 'index', sortedbam, indexedbam]) - return sortedbam - -def main(args): - args[2] = samtools_sorted(args[2]) - sp.call(args) - - -if __name__ == "__main__": - main(sys.argv[1:]) \ No newline at end of file