The function counts DMPs overlapping with gene-body. In fact, this function also can be used to count DMPs overlapping with any set of regions given in a GRanges object.
getDIMPatGenes(
GR,
GENES,
type = "within",
ignore.strand = TRUE,
only.hypo = FALSE,
only.hyper = FALSE,
output = c("list", "GRanges"),
by.coord = FALSE,
gene_id_col = NULL,
gene_name_col = NULL,
...
)
# S3 method for default
getDIMPatGenes(
GR,
GENES,
type = "within",
ignore.strand = TRUE,
only.hypo = FALSE,
only.hyper = FALSE,
output = NULL,
by.coord = FALSE,
gene_id_col = NULL,
gene_name_col = NULL,
...
)
# S3 method for GRanges
getDIMPatGenes(
GR,
GENES,
type = "within",
ignore.strand = TRUE,
only.hypo = FALSE,
only.hyper = FALSE,
output = NULL,
by.coord = FALSE,
gene_id_col = NULL,
gene_name_col = NULL,
...
)
# S3 method for pDMP
getDIMPatGenes(
GR,
GENES,
type = "within",
ignore.strand = TRUE,
only.hypo = FALSE,
only.hyper = FALSE,
output = c("list", "GRanges"),
by.coord = FALSE,
gene_id_col = NULL,
gene_name_col = NULL,
...
)
# S3 method for InfDiv
getDIMPatGenes(
GR,
GENES,
type = "within",
ignore.strand = TRUE,
only.hypo = FALSE,
only.hyper = FALSE,
output = c("list", "GRanges"),
by.coord = FALSE,
gene_id_col = NULL,
gene_name_col = NULL,
...
)
# S3 method for list
getDIMPatGenes(
GR,
GENES,
type = "within",
ignore.strand = TRUE,
only.hypo = FALSE,
only.hyper = FALSE,
output = c("list", "GRanges"),
by.coord = FALSE,
gene_id_col = NULL,
gene_name_col = NULL,
...
)
An objects object from the any of the classes: 'pDMP', 'InfDiv', GRangesList, GRanges or a list of GRanges.
A GRanges object with gene coordinates and gene IDs. A column named 'gene_id' carrying the gene ids should be included in the metacolumns. If the meta-column named 'gene_id' is not provided, then gene (region) ids will be created using the gene (region) coordinates.
Same as for
findOverlaps-methods
.
logical(1). Whether to select only hypo-methylated or hyper-methylated cytosine sites.
Class of the object to be returned, a "list", or a "GRanges" object.
logical(1). If TRUE, then the DMP are count per coordinate and not per gene id.
Optional. An integer denoting the column from the GENES metacolumn where the gene ids are given.
Optional. An integer denoting the column from the GENES metacolumn where the gene 'name' are given.
optional arguments for
findOverlaps-methods
. Users must evaluate
whether specific setting makes sense on each particular context.
A a list GRanges object.
If by.coord == FALSE and "gene_id" is provided in GENES argument, then DMP counts are made per gene-id. Hence, DMPs from different regions with the same gene-id, say e.g. exons, will be pooled in the count as they bear the same id.
## Gene annotation
genes <- GRanges(seqnames = '1',
ranges = IRanges(start = c(3631, 6788, 11649), end = c(5899, 9130, 13714)),
strand = c('+', '-', '-'))
mcols(genes) <- data.frame(gene_id = c('AT1G01010', 'AT1G01020',
'AT1G01030'))
## Get a dataset of potential signals and the estimated cutpoint from the
## package
data(PS, cutpoint)
## The estimated cutpoints are used to discriminate signals from the noise.
## That is, DMPs are selected using the cupoints
DIMPs <- selectDIMP(PS, div.col = 9L, cutpoint = cutpoint$cutpoint)
## Finally DMPs found on genes
DIMR <- getDIMPatGenes(GR = DIMPs$T1, GENES = genes)