R/ti_raceid_stemid.R
ti_raceid_stemid.Rd
Will generate a trajectory using RaceID / StemID.
This method was wrapped inside a container. The original code of this method is available here.
ti_raceid_stemid(knn = 10L, ccor = 0.4, metric = "pearson", sat = TRUE, samp = 1000L, cln = 30L, clustnr = 30L, bootnr = 50L, FUNcluster = "kmedoids", probthr = 0.001, outminc = 5L, outlg = 2L, outdistquant = 0.95, initial_cmd = TRUE, perplexity = 30L, cthr = 5L, nmode = TRUE, projcells_knn = 3L, fr = FALSE, pdishuf = 500L, fast = FALSE, pthr = 0.01, scthr = 0.2, run_environment = NULL)
knn | integer; Number of nearest neighbors used to infer corresponding
cell types in different batches. (default: |
---|---|
ccor | numeric; Correlation coefficient used as a treshhold for
determining genes correlated to eachother. (default: |
metric | discrete; Distances are computed from the filtered expression
matrix after optional feature selection, dimensional reduction, and/or
transformation (batch correction). (default: |
sat | logical; If |
samp | integer; Number of booststrapping runs for clusterboot. Default is
50 (default: |
cln | integer; Number of clusters to be used. If |
clustnr | integer; Maximum number of clusters for the derivation of the
cluster number by the saturation of mean within-cluster-dispersion. (default:
|
bootnr | integer; Number of booststrapping runs for clusterboot. (default:
|
FUNcluster | discrete; Clustering method used by RaceID3. (default:
|
probthr | numeric; Outlier probability threshold for a minimum of outlg
genes to be an outlier cell. This probability is computed from a negative
binomial background model of expression in a cluster. (default: |
outminc | integer; Minimal transcript count of a gene in a clusters to be
tested for being an outlier gene. (default: |
outlg | integer; Minimum number of outlier genes required for being an
outlier cell. (default: |
outdistquant | numeric; Real number between zero and one. Outlier cells
are merged to outlier clusters if their distance smaller than the
outdistquant-quantile of the distance distribution of pairs of cells in the
orginal clusters after outlier removal. (default: |
initial_cmd | logical; If TRUE, then the t-SNE map computation is initialized with a configuration obtained by classical multidimensional scaling. |
perplexity | integer; Perplexity of the t-SNE map. (default: |
cthr | integer; Clusters to be included into the StemID2 analysis must
contain more than cthr cells. D (default: |
nmode | logical; If |
projcells_knn | integer; See |
fr | logical; Use Fruchterman-Rheingold layout instead of t-SNE for dimensional-reduction representation of the lineage tree. |
pdishuf | integer; Number of randomizations of cell positions for which to
compute projections of cells on inter-cluster links. (default: |
fast | logical; If |
pthr | numeric; P-value cutoff for link significance. This threshold is
applied for the calculation of link scores reflecting how uniformly a link is
occupied by cells. (default: |
scthr | numeric; Score threshold for links to be shown in the graph.
(default: |
run_environment | In which environment to run the method, can be |
A TI method wrapper to be used together with
infer_trajectory
Grün, D., Muraro, M.J., Boisset, J.-C., Wiebrands, K., Lyubimova, A., Dharmadhikari, G., van den Born, M., van Es, J., Jansen, E., Clevers, H., de Koning, E.J.P., van Oudenaarden, A., 2016. De Novo Prediction of Stem Cell Identity using Single-Cell Transcriptome Data. Cell Stem Cell 19, 266–277.