| runMapping | R Documentation |
Mapping the output of "getSingleCellDeconv()"to the best matching cell from the reference dataset
runMapping(
object,
scDF,
ref.new,
cell_type_var = "annotation_level_4",
model = c("oGA", "BF"),
subset_ref = T,
only_var = T,
n_feature = 3000,
max_cells = 10000,
AE_norm = F,
dropout = 0,
bottleneck = 16,
activation = "relu",
layers = c(128, 64, 32),
epochs = 20,
multicore = T,
workers = 16,
iter = 200,
iter_GA = 20,
nr_mut = 2,
nr_offsprings = 7,
cross_over_point = 0.5,
ram = 60
)
object |
SPATA2 object |
scDF |
Data.frame; Output of the getSingleCellDeconv() |
ref.new |
Seurat Object; Reference dataset used for runRCTD() |
cell_type_var |
Character value; The col of the Seurat meta data indicating the cell type annotations |
model |
Character value; Model "BF" randomly select cell compositions and select the best match. Model "oGA" will perform a conditional genetic algorithm to find the best match. |
subset_ref |
Logical, if TRUE, Seurat object will we downsized to increase speed. |
only_var |
Logical, if TRUE only consider variable genes for mapping |
n_feature |
Integer value: Number of variable genes |
max_cells |
Integer value: Number of cells for downsampling |
AE_norm |
Logical, if TRUE use an autoencoder for data integration and normalization (recommended) |
multicore |
Logical, if TRUE use multicore |
workers |
Integer, Number of cors |
iter |
Integer: For model BF: Number of random spot compositions; For model oGA size of initial population |
iter_GA |
Integer: Number of iterations of the oGA model |
nr_mut |
Integer: Number of mutations |
nr_offsprings |
Integer: Number of offsprings |
cross_over_point |
Numeric value: Percentage of cross-over cutt-off |
ram |
Integer: GB of ram can be used for multicore session |
Dieter Henrik Heiland
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