callPatterns | R Documentation |
Given results from epigraHMM's differential peak caller, this function will output either posterior probabilities or combinatorial patterns associated with the mixture components of the embedded mixture model.
callPatterns(
object,
peaks,
hdf5 = metadata(object)$output,
type = "all",
fdr = NULL,
pattern = NULL,
ranges = NULL
)
object |
an epigraHMMDataSet |
peaks |
a GRanges object with differential peaks from 'callPeaks' |
hdf5 |
a character with the location of the epigraHMM HDF5 output file |
type |
a character string that defines which output will be givem (see details; default is 'all') |
fdr |
the desired fdr thresholding level to define combinatorial patterns |
pattern |
a string that explicitly specifies the combinatorial pattern to be output |
ranges |
a GRanges object with the genomic ranges to subset the output |
The output of 'callPatterns' is always restricted to genomic windows intersecting peaks.
If ‘type = ’all'‘, all windows’ posterior probabilities associated with all differential combinatorial patterns are returned. If ‘type = ’fdr'', users must also specify the input argument 'pattern' and this function will output windows wich are associated with the given 'pattern' that pass a particular fdr threshold level. If ‘type = ’max'', this function will output the combinatorial pattern which has the maximal posterior probability for each window. If ‘type = ’ranges'', the windows that are output are restricted to those that intersect the 'ranges' input argument.
A GRanges object with metadata
Pedro L. Baldoni, pedrobaldoni@gmail.com
https://github.com/plbaldoni/epigraHMM
# Creating dummy object
countData <- cbind(rbind(matrix(rnbinom(1e2, mu = 1, size = 10), ncol = 1),
matrix(rnbinom(1e2, mu = 10, size = 5), ncol = 1),
matrix(rnbinom(1e2, mu = 1, size = 10), ncol = 1),
matrix(rnbinom(1e2, mu = 10, size = 5), ncol = 1),
matrix(rnbinom(1e2, mu = 1, size = 10), ncol = 1),
matrix(rnbinom(1e2, mu = 1, size = 10), ncol = 1),
matrix(rnbinom(1e2, mu = 1, size = 10), ncol = 1)),
rbind(matrix(rnbinom(1e2, mu = 1, size = 10), ncol = 1),
matrix(rnbinom(1e2, mu = 1, size = 10), ncol = 1),
matrix(rnbinom(1e2, mu = 1, size = 10), ncol = 1),
matrix(rnbinom(1e2, mu = 10, size = 5), ncol = 1),
matrix(rnbinom(1e2, mu = 1, size = 10), ncol = 1),
matrix(rnbinom(1e2, mu = 10, size = 5), ncol = 1),
matrix(rnbinom(1e2, mu = 1, size = 10), ncol = 1)))
colData <- data.frame(condition = c('A','B'), replicate = c(1,1))
rowRanges <- GenomicRanges::GRanges('chrA',
IRanges::IRanges(start = seq(1,by = 500,
length.out = nrow(countData)),width = 500))
object <- epigraHMMDataSetFromMatrix(countData,colData,rowRanges = rowRanges)
# Initializing
object <- initializer(object,controlEM())
# Running epigraHMM
object <- epigraHMM(object,controlEM(),type = 'differential',dist = 'nb')
# Calling peaks
peaks <- callPeaks(object = object,
hdf5 = S4Vectors::metadata(object)$output,
method = 'viterbi')
# Extracting posterior probabilities
patterns <- callPatterns(object = object,peaks = peaks,type = 'max')
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