ti_fateid.Rd
Will generate a trajectory using FateID.
This method was wrapped inside a container. The original code of this method is available here.
ti_fateid(reclassify = TRUE, clthr = 0.9, nbfactor = 5L, q = 0.75, k = 3L, m = "tsne", minnr = 5L, minnrh = 10L, trthr = 0.4, force = FALSE)
reclassify | Whether to reclassify the cell grouping. Default: TRUE. Format: logical. |
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clthr | Real number between zero and one. This is the threshold for the fraction of random forest votes required to assign a cell not contained within the target clusters to one of these clusters. The value of this parameter should be sufficiently high to only reclassify cells with a high-confidence assignment. Default value is 0.9. Domain: U(0.1, 1). Default: 0.9. Format: numeric. |
nbfactor | Positive integer number. Determines the number of trees grown
for each random forest. The number of trees is given by the number of columns
of th training set multiplied by |
q | Q real value between zero and one. This number specifies a threshold used for feature selection based on importance sampling. A reduced expression table is generated containing only features with an importance larger than the q-quantile for at least one of the classes (i. e. target clusters). Default value is 0.75. Domain: U(0, 1). Default: 0.75. Format: numeric. |
k | Number of dimensions. Domain: U(2, 100). Default: 3. Format: integer. |
m | Dimensionality reduction method to use. Can be tsne, cmd, dm or lle. Domain: tsne, cmd, dm, lle. Default: tsne. Format: character. |
minnr | Integer number of cells per target cluster to be selected for
classification (test set) in each round of training. For each target cluster,
the |
minnrh | Integer number of cells from the training set used for
classification. From each training set, the |
trthr | Real value representing the threshold of the fraction of random
forest votes required for the inclusion of a given cell for the computation of
the principal curve. If |
force | Do not use! This is a parameter to force FateID to run on benchmark datasets where not enough end groups are present. Default: FALSE. Format: logical. |
A TI method wrapper to be used together with
infer_trajectory
Herman, J.S., Sagar, Grün, D., 2018. FateID infers cell fate bias in multipotent progenitors from single-cell RNA-seq data. Nature Methods 15, 379–386.