| asMethBlocks | R Documentation | 
By default, data(methBlocks) is used for summarization, singleton probes are included, methylation block rownames are returned against hg19, and neither singletons (!proper) nor unstable mappings (!stable) are filtered out.
asMethBlocks(x, g = c("hg19", "hg38"), proper = FALSE, stable = FALSE)
x | 
 a GenomicRatioSet or something like it  | 
g | 
 genome to use for methylation block coordinates (hg19)  | 
proper | 
 restrict to methylation blocks defined in Kaplan? (FALSE)  | 
stable | 
 restrict to sites/blocks shared across hg19 & hg38? (FALSE)  | 
stable is a weird flag and you probably should not use it. If and only if
a probe maps to the same region in hg19 and hg38, it is deemed stable. That
region can be one base pair wide, or it can be a thousand base pairs wide.
The point is that this set of mappings is very small (about 4000 probes).
an object with same colData but with new rowRanges & assays
switchMethBlocksGenome
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