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genomeIntervals (version 1.28.0)

Genome_intervals-class: Class "Genome\_intervals"

Description

A set of genomic intervals without specified strand. Genomic intervals are intervals over the integers with two further annotations: seqnames (a chromosome or more generally a sequence of origin) and inter_base (logical) that states whether the interval is to be understood as an interval over bases (such as coding-sequence) or inter-bases (such as restriction sites or insertion positions).

Arguments

Slots

.Data:
See Intervals_full
annotation:
A "data.frame" with the same number of rows as .Data. It has a column named seq_name that is a factor and does not contain missing values. seq_name is used to represent the chromosome or more generally the sequence of origin of the intervals. annotation has a column named inter_base that is logical and does not contain missing values. inter_base is FALSE if the interval is to be understood as an interval over bases (such as coding-sequence) and TRUE if it is over inter-bases (such as restriction site or an insertion position). Like base intervals, inter-base interval are encoded over the integers. An inter-base at position n indicates the space between base n and n+1.
closed:
See Intervals_full
type:
See Intervals_full

Extends

Class "Intervals_full", directly. Class "Intervals_virtual", by class "Intervals\_full", distance 2. Class "matrix", by class "Intervals\_full", distance 3. Class "array", by class "Intervals\_full", distance 4. Class "structure", by class "Intervals\_full", distance 5. Class "vector", by class "Intervals\_full", distance 6, with explicit coerce.

Methods

[
signature(x = "Genome_intervals"): ...
[[
signature(x = "Genome_intervals"): ...
[[<-
signature(x = "Genome_intervals"): ...
\$
signature(x = "Genome_intervals"): ...
\$<-
signature(x = "Genome_intervals"): ...
annotation
signature(object = "Genome_intervals"): ...
annotation<-
signature(object = "Genome_intervals"): ...
coerce
signature(from = "Genome_intervals", to = "Intervals_full"): ...
coerce
signature(from = "Genome_intervals", to = "character"): ...
coerce
signature(from = "Genome_intervals", to = "data.frame"): ...
distance\_to\_nearest
signature(from = "Genome_intervals", to = "Genome_intervals"): ...
inter\_base
signature(x = "Genome_intervals"): ...
inter\_base<-
signature(x = "Genome_intervals"): ...
interval\_complement
signature(x = "Genome_intervals"): ...
interval\_intersection
signature(x = "Genome_intervals"): ...
interval\_overlap
signature(from = "Genome_intervals", to = "Genome_intervals"): ...
interval\_union
signature(x = "Genome_intervals"): ...
seqnames
signature(x = "Genome_intervals"): ...
seqnames<-
signature(x = "Genome_intervals"): ...
size
signature(x = "Genome_intervals"): ...
type<-
signature(x = "Genome_intervals"): ...
which\_nearest
For each interval in Set1, finds nearest (least distant) interval in Set2. Intervals on different chromsomes are never considered 'near' to each other. The returned value is a data.frame with the number of rows equal to the number of intervals in Set1. Each row specifies the distance to the nearest interval in Set2 (a 0 means that the interval overlaps one or more intervals in Set2), and the indices of near and overlapping intervals in Set2. See Intervals_full for further details.
width
Returns the interval length as the number of bp covered (base interval) or spanned(inter-base interval). Similar to the IRanges package width
function.

See Also

Genome_intervals_stranded for a derived class that allows stranded genomic intervals.

Examples

Run this code
# The "Genome_intervals" class

i <- new(
	 "Genome_intervals",
	 matrix(
	 	c(1,2,
	 	  3,5,
	 	  4,6,
	 	  8,9
	 	  ),
	 	byrow = TRUE,
                ncol = 2
	 ),
	 closed = matrix(
	 			c(
	 				TRUE, FALSE,
	 				TRUE, FALSE,
	 				TRUE, TRUE,
	 				TRUE, FALSE
	 			 ),
	 			byrow = TRUE,
     			ncol = 2
     			),
	 annotation = data.frame(
	 				seq_name = factor(c("chr01","chr01", "chr02","chr02")),
	 				inter_base = c(FALSE, FALSE, TRUE, TRUE)
	 				)
	 )

colnames(i) <- c( "start", "end" )

# print
print(i)

# size (number of bases per interval)
size(i)

## convert to a data.frame
as(i,"data.frame")

## simpler way to construct a Genome_intervals object:
G <- GenomeIntervals(start=c(1,3,4,5,10,8), end=c(5,5,6,8,11,9),
                     chromosome=rep(c("chr2","chrX","chr1"), each=2),
                     leftOpen=rep(c(FALSE, FALSE, TRUE), 2))
show(G)

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