ti_scuba | R Documentation |
Will generate a trajectory using SCUBA.
This method was wrapped inside a container. The original code of this method is available here.
ti_scuba(
rigorous_gap_stats = TRUE,
N_dim = 2L,
low_gene_threshold = 1L,
low_gene_fraction_max = 0.7,
min_split = 15L,
min_percentage_split = 0.25
)
rigorous_gap_stats |
Whether to use rigorous gap statistics to determine number of clusters. Default: TRUE. Format: logical. |
N_dim |
Number of TSNE dimensions. Domain: U(2, 3). Default: 2. Format: integer. |
low_gene_threshold |
Threshold value for genes of low expression levels. Domain: U(0, 5). Default: 1. Format: numeric. |
low_gene_fraction_max |
Maximum fraction of lowly-expressed cells allowed for each gene. Domain: U(0, 1). Default: 0.7. Format: numeric. |
min_split |
Lower threshold on the number of cells in a cluster for this cluster to be split. Domain: U(1, 100). Default: 15. Format: integer. |
min_percentage_split |
Minimum fraction of cells in the smaller cluster during a bifurcation. Domain: U(0, 1). Default: 0.25. Format: numeric. |
A TI method wrapper to be used together with
infer_trajectory
Marco, E., Karp, R.L., Guo, G., Robson, P., Hart, A.H., Trippa, L., Yuan, G.-C., 2014. Bifurcation analysis of single-cell gene expression data reveals epigenetic landscape. Proceedings of the National Academy of Sciences 111, E5643–E5650.
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