[prev in list] [next in list] [prev in thread] [next in thread]
List: bioconductor
Subject: [BioC] htSeqTools - filtered reads > BED?
From: Ian Donaldson <Ian.Donaldson () manchester ! ac ! uk>
Date: 2012-01-27 11:56:23
Message-ID: 7E756F18289AF64B967C333AC3BF7021C6728B70 () MBXP02 ! ds ! man ! ac ! uk
[Download RAW message or body]
I have found the htSeqTools methods useful for creating PCA plots of samples. The \
filtering of reads to remove those that are deemed to be over amplified looks very \
interesting.
The function is called like this:
# BAM to IRanges object:
reads01 <- readAligned(dirPath , "reads01.bam", type='BAM')
ranges01 <- RangedData(ranges=IRanges(position(reads01),position(reads01)+width(reads01)), \
space=chromosome(reads01), strand=strand(reads01))
ranges01Fil <- filterDuplReads(ranges01, fdrOverAmp=0.01)
However, how can i get the filtered reads (ranges01Fil) out as BED formatted files?
Thank you!
Ian
[[alternative HTML version deleted]]
_______________________________________________
Bioconductor mailing list
Bioconductor@r-project.org
https://stat.ethz.ch/mailman/listinfo/bioconductor
Search the archives: \
http://news.gmane.org/gmane.science.biology.informatics.conductor
[prev in list] [next in list] [prev in thread] [next in thread]
Configure |
About |
News |
Add a list |
Sponsored by KoreLogic