View source: R/geneADTnetwork.R
geneADTnetwork | R Documentation |
A function to visualise the features distribtuion
geneADTnetwork( sce, RNA_exprs_value = "logcounts", altExp_name = "ADT", altExp_exprs_value = "logcounts", RNA_feature_subset = NULL, ADT_feature_subset = NULL, cell_subset = NULL, cor_threshold = 0.5, cor_method = c("pearson", "kendall", "spearman"), RNA_exprs_pct = 0.1, ADT_exprs_pct = 0.1, RNA_exprs_threshold = 0, ADT_exprs_threshold = 0, network_layout = NULL, return_igraph = FALSE )
sce |
A singlecellexperiment object |
RNA_exprs_value |
A character indicates which expression value for RNA in assayNames is used. |
altExp_name |
A character indicates which expression matrix is used. by default is none (i.e. RNA). |
altExp_exprs_value |
A character indicates which expression value in assayNames is used. |
RNA_feature_subset |
A vector of characters indicates the subset of features of RNA that are used for visualisation |
ADT_feature_subset |
A vector of characters indicates the subset of features of ADT that are used for visualisation |
cell_subset |
A vector of characters indicates the subset of cells that are used for visualisation |
cor_threshold |
Thresholds of correlation. |
cor_method |
a character string indicating which correlation coefficient (or covariance) is to be computed. One of "pearson" (default), "kendall", or "spearman": can be abbreviated. |
RNA_exprs_pct |
A numeric indicates the threshold expression percentage of a gene to be considered in correlation analysis |
ADT_exprs_pct |
A numeric indicates the threshold expression percentage of a gene to be considered in correlation analysis |
RNA_exprs_threshold |
A numeric indicates the threshold of RNA expression. By default is 0. |
ADT_exprs_threshold |
A numeric indicates the threshold of ADT expression. By default is 0. |
network_layout |
layout of the network |
return_igraph |
indicates whether return the igraph object |
A igraph object of gene-ADT network
library(SingleCellExperiment) set.seed(2020) data(sce_control_subset, package = "CiteFuse") RNA_feature_subset <- sample(rownames(sce_control_subset), 50) ADT_feature_subset <- rownames(altExp(sce_control_subset, "ADT")) geneADTnetwork(sce_control_subset, RNA_feature_subset = RNA_feature_subset, ADT_feature_subset = ADT_feature_subset, cor_method = "pearson", network_layout = igraph::layout_with_fr)
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