View source: R/AllCloseByRegions.R
| AllCloseByRegions | R Documentation |
A wrapper function to extract clusters of RNA editing sites that are located closely in genomic regions.
AllCloseByRegions( regions_gr, rnaEditMatrix, maxGap = 50, minSites = 3, progressBar = "time" )
regions_gr |
A GRanges object of input genomic regions. |
rnaEditMatrix |
A matrix (or data frame) of RNA editing level values on
individual sites, with row names as site IDs in the form of
"chrAA:XXXXXXXX", and column names as sample IDs. Please make sure to
follow the format of example dataset ( |
maxGap |
An integer, genomic locations within |
minSites |
An integer, minimum number of RNA editing sites within each resulting cluster. Defaults to 3. |
progressBar |
Name of the progress bar to use. There are currently five
types of progress bars: |
The algorithm of this function is based on the
clusterMaker function in the bumphunter
R package. Each cluster is essentially a group of site locations such that
two consecutive locations in the cluster are separated by less than
maxGap.
A GRanges object containing genomic regions of RNA editing sites located closely within each input pre-defined genomic region.
TransformToGR, AllCoeditedRegions,
CreateEditingTable, SummarizeAllRegions,
TestAssociations, AnnotateResults
data(rnaedit_df)
exm_regions <- TransformToGR(
genes_char = c("PHACTR4", "CCR5", "METTL7A"),
type = "symbol",
genome = "hg19"
)
AllCloseByRegions(
regions_gr = exm_regions,
rnaEditMatrix = rnaedit_df,
maxGap = 50,
minSites = 3,
progressBar = "time"
)
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