| sce_to_scmet | R Documentation |
Helper function that converts SCE objects to scmet objects
that can be used as input to the scmet function. The structure of the
SCE object to store single cell methylation data is the following. We
create two sparse assays, met storing methylated CpGs and total storing
total number of CpGs. Rows correspond to features and columns to cells,
similar to scRNA-seq convention.To distinguish between a feature (in a cell)
having zero methylated CpGs vs not having CpG coverage at all (missing value),
we check if the corresponding entry in total is zero as well.
The rownames and colnames slots should store the feature and cell names,
respectively. Covariates X that might explain variability in mean
(methylation) should be stored in metadata(rowData(sce)X.
sce_to_scmet(sce)
sce |
SummarizedExperiment object |
A named list containing the matrix Y (methylation data in format
required by the scmet function) and the covariates X.
C.A.Kapourani C.A.Kapourani@ed.ac.uk
scmet, scmet_differential,
scmet_hvf_lvf
# Extract
sce <- scmet_to_sce(Y = scmet_dt$Y, X = scmet_dt$X)
df <- sce_to_scmet(sce)
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