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Get a named list of HVG data (gene IDs, fit, metadata).

Usage

hvg_int_list_fn(
  sce_int_multibatchnorm,
  hvg_selection_value,
  hvg_combination = c("hvg_metric", "intersection", "union", "all"),
  hvg_selection = c("top", "significance", "threshold")
)

Arguments

sce_int_multibatchnorm

(input target) A SingleCellExperiment object processed by batchelor::multiBatchNorm().

hvg_selection_value, hvg_combination, hvg_selection

See sce_int_combine_hvgs().

Value

A named list. Output target: hvg_int_list