Description Usage Arguments Slots See Also Examples
The maximum a posteriori estimate of the trio copy number state for
each genomic range is represented in a
GRanges
-derived class. Ultimately, these ranges will
be filtered based on the trio copy number state (e.g., denovo
deletions), size, number of features (SNPs), or chromosome.
FilterParam
is a container for the parameters commmonly used
to filter the genomic ranges.
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 | FilterParam(
probability = 0.99,
numberFeatures = 10,
seqnames = paste0("chr", c(1:22, "X", "Y")),
state = as.character(1:6),
width = 1L
)
## S4 method for signature 'FilterParam'
probability(object)
## S4 method for signature 'FilterParam'
state(object)
## S4 method for signature 'FilterParam'
show(object)
|
probability |
minumum probability for the call |
numberFeatures |
minumum number of SNPs/nonpolymorphic features in a region |
seqnames |
the seqnames (character string or |
state |
character: the HMM states to keep |
width |
the minimum widht of a region |
object |
a |
probability
a length-one numeric vector indicating the
minimum posterior probability for the called state. Genomic
intervals with posterior probabilities below probability
will be filtered.
numberFeatures
a positive integer indicating the minimum number of features in a segment
seqnames
a character vector of seqnames
to select
(i.e., 'chr1' for only those intervals on chromosome 1)
width
positive integer indicating the minimal width of genomic intervals
state
character string indicating which hidden Markov model states to select
1 2 3 4 5 6 7 8 9 | fp <- FilterParam()
width(fp)
numberFeatures(fp)
seqnames(fp)
## To select CNV segments for which
## - the CNV call has a 'posterior' probability of at least 0.95
## - the number of features is at least 10
## - the HMM states are 1 (homozygous deletion) or 2 (hemizygous deletion)
FilterParam(probability=0.95, numberFeatures=10, state=c("1", "2"))
|
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