CiteFuse | R Documentation |
A function to runSNF for CITE seq data
CiteFuse( sce, altExp_name = "ADT", W_list = NULL, gene_select = TRUE, dist_cal_RNA = "correlation", dist_cal_ADT = "propr", ADT_subset = NULL, K_knn = 20, K_knn_Aff = 30, sigma = 0.45, t = 10, metadata_names = NULL, verbose = TRUE, topN = 2000 )
sce |
a SingleCellExperiment |
altExp_name |
expression name of ADT matrix |
W_list |
affinity list, if it is NULL, the function will calculate it. |
gene_select |
whether highly variable genes will be selected for RNA-seq to calcualte simlarity matrix using 'scran' package |
dist_cal_RNA |
similarity metrics used for RNA matrix |
dist_cal_ADT |
similarity metrics used for ADT matrix |
ADT_subset |
A vector indicates the subset that will be used. |
K_knn |
Number of nearest neighbours |
K_knn_Aff |
Number of nearest neighbors for computing affinity matrix |
sigma |
Variance for local model for computing affinity matrix |
t |
Number of iterations for the diffusion process. |
metadata_names |
A vector indicates the names of metadata returned |
verbose |
whether print out the process |
topN |
top highly variable genes are used variable gene selection (see 'modelGeneVar' in 'scran' package for more details) |
A SingleCellExperiment object with fused matrix results stored
B Wang, A Mezlini, F Demir, M Fiume, T Zu, M Brudno, B Haibe-Kains, A Goldenberg (2014) Similarity Network Fusion: a fast and effective method to aggregate multiple data types on a genome wide scale. Nature Methods. Online. Jan 26, 2014
data("sce_ctcl_subset", package = "CiteFuse") sce_ctcl_subset <- CiteFuse(sce_ctcl_subset)
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