Entering edit mode
Hi All,
I appreciate if anyone can provide an example to use DeepSNV where the
reference genome is used.
I have used BSgenpme and tried
sq<-as(seqinfo(Hsapiens), "GRanges")
counts<- loadAllData(files, sq, q = 10) but I got memory allocation
error
Warning messages:
1: In structure(y, class = class(x), levels = levels(x)) :
Reached total allocation of 3958Mb: see help(memory.size)
2: In structure(y, class = class(x), levels = levels(x)) :
Reached total allocation of 3958Mb: see help(memory.size)
3: In structure(y, class = class(x), levels = levels(x)) :
Reached total allocation of 3958Mb: see help(memory.size)
4: In structure(y, class = class(x), levels = levels(x)) :
Reached total allocation of 3958Mb: see help(memory.size)
Error in unlist(sapply(1:nrow(regions), function(i)
rep(regions$chr[i], :
error in evaluating the argument 'x' in selecting a method for
function
'unlist': Error: cannot allocate vector of size 927.7 Mb
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Shall i use the exome sequence only ??
Any help is highly appreciated
----------------------------------
In deepSNV example
library(deepSNV)
regions <- data.frame(chr="B.FR.83.HXB2_LAI_IIIB_BRU_K034", start =
2074,
stop=3585)
## -------------------------------------------------------------------
-----
# HIVmix <- deepSNV(test = "
http://www.bsse.ethz.ch/cbg/software/deepSNV/data/test.bam",
# control = "
http://www.bsse.ethz.ch/cbg/software/deepSNV/data/control.bam",
# regions=regions, q=10)
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