# HG changeset patch # User nilesh # Date 1373559928 14400 # Node ID 80f857718ca02ff1c1f01f10df54e36465885072 # Parent 6a354a3248b6793390628e9c2e9d3a0f1057356f Uploaded diff -r 6a354a3248b6 -r 80f857718ca0 read_duplication.xml --- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/read_duplication.xml Thu Jul 11 12:25:28 2013 -0400 @@ -0,0 +1,51 @@ + + determines reads duplication rate with sequence-based and mapping-based strategies + + R + rseqc + + read_duplication.py -i $input -o output -u $upLimit + + + + + + + + + + + + +.. 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 + + +