DeepSNV,Granges and BSgenome question
1
0
Entering edit mode
Asma rabe ▴ 290
@asma-rabe-4697
Last seen 6.9 years ago
Japan
Dear All, I am trying to run Shearwater and deep SNV to analyze exome-seq data. In the deepSNV vignette #========== ## Load data from deepSNV example regions <- GRanges("B.FR.83.HXB2_LAI_IIIB_BRU_K034", IRanges(start = 3120, end = 3140)) files <- c(system.file("extdata", "test.bam", package = "deepSNV"), system.file("extdata", "control.bam", package = "deepSNV")) counts <- loadAllData(files, regions, q = 10) dim(counts) ## [1] 2 21 10 ## Run (bbb) computes the Bayes factor bf <- bbb(counts, model = "OR", rho = 1e-04) #========== I have two questions: 1-How to create GRnages object for human reference genome, I have used BSgenome package as follows library(BSgenome.Hsapiens.UCSC.hg19) but i do not know how to proceed further for obtaining reference genome as Granges object.. 2-I would like to know how can i specify rho value in Bayes factor calculation. Any help is appreciated. [[alternative HTML version deleted]]
deepSNV deepSNV • 1.3k views
ADD COMMENT
0
Entering edit mode
@michael-lawrence-3846
Last seen 3.0 years ago
United States
On Thu, Jul 10, 2014 at 10:29 PM, Asma rabe <asma.rabe@gmail.com> wrote: > Dear All, > > > I am trying to run Shearwater and deep SNV to analyze exome-seq data. > > > In the deepSNV vignette > > #========== > > ## Load data from deepSNV example > > regions <- GRanges("B.FR.83.HXB2_LAI_IIIB_BRU_K034", IRanges(start = 3120, > end > = 3140)) > > files <- c(system.file("extdata", "test.bam", package = "deepSNV"), > system.file("extdata", > > "control.bam", package = "deepSNV")) > > counts <- loadAllData(files, regions, q = 10) > > dim(counts) > > ## [1] 2 21 10 > > > ## Run (bbb) computes the Bayes factor > > bf <- bbb(counts, model = "OR", rho = 1e-04) > > > #========== > > I have two questions: > > > 1-How to create GRnages object for human reference genome, I have used > BSgenome package as follows > > library(BSgenome.Hsapiens.UCSC.hg19) but i do not know how to proceed > further for obtaining reference genome as Granges object.. > > If you mean that you need a GRanges that spans the entire genome, use: as(seqinfo(Hsapiens), "GRanges") > > 2-I would like to know how can i specify rho value in Bayes factor > calculation. > > Any help is appreciated. > > [[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 > [[alternative HTML version deleted]]
ADD COMMENT

Login before adding your answer.

Traffic: 753 users visited in the last hour
Help About
FAQ
Access RSS
API
Stats

Use of this site constitutes acceptance of our User Agreement and Privacy Policy.

Powered by the version 2.3.6