| SpliceSitesGenomic-class {splicegear} | R Documentation |
A class to store alternative splicing information on a genomic point of view.
Objects can be created by calls of the form new("SpliceSitesGenomic", seq, seq.length, spsiteIpos, spsiteIIpos, spsiteIIIpos, spsiteIpos.pData, spsiteIIpos.pData, spsiteIIIpos.pData, ...).
variants:Object of class "list". There is one
element per splice variant. Each element in the list should be a
vector of integers. Each integer refers to an exon. The sequence
of integers determines the sequence of exons in the splice variant.
seq:Object of class "character", from class "SpliceSites".
seq.length:Object of class "integer", from class "SpliceSites".
spsiteIpos:Object of class "matrix", from class "SpliceSites".
spsiteIIpos:Object of class "integer", from
class "SpliceSites". This should not have any practical use in this class.
spsiteIIIpos:Object of class "matrix", from
class "SpliceSites". This should not have any practical use in this class.
spsiteIpos.pData:Object of class "AnnotatedDataFrame", from class "SpliceSites".
spsiteIIpos.pData:Object of class "AnnotatedDataFrame",
from class "SpliceSites". This should not have any practical use in this class.
spsiteIIIpos.pData:Object of class "AnnotatedDataFrame",
from class "SpliceSites". This should not have any practical use in this class.
Class "SpliceSites", directly.
signature(x = "SpliceSitesGenomic", y =
"missing"): a plotting method for demonstration purposes.
SpliceSites-class and plot.SpliceSitesGenomic.
## a 10 bp window
seq.length <- as.integer(10)
## positions of the exons
spsiteIpos <- matrix(c(1, 3.5, 5, 9, 3, 4, 8, 10), nc=2)
## known variants
variants <- list(a=c(1,2,3,4), b=c(1,2,3), c=c(1,3,4))
spvar <- new("SpliceSitesGenomic", spsiteIpos=spsiteIpos,
variants=variants, seq.length=seq.length)
plot(spvar)