simplify_history: Simplify the mutational history based on likelihood evidence
In numbat: Haplotype-Aware CNV Analysis from scRNA-Seq
simplify_history R Documentation
Simplify the mutational history based on likelihood evidence
Description
Simplify the mutational history based on likelihood evidence
Usage
simplify_history(G, l_matrix, max_cost = 150, n_cut = 0, verbose = TRUE)
Arguments
G
igraph Mutation graph
l_matrix
matrix Mutation placement likelihood matrix (node by mutation)
Value
igraph Mutation graph
numbat documentation built on May 29, 2024, 1:29 a.m.
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| simplify_history | R Documentation |
Simplify the mutational history based on likelihood evidence
Description
Simplify the mutational history based on likelihood evidence
Usage
simplify_history(G, l_matrix, max_cost = 150, n_cut = 0, verbose = TRUE)
Arguments
G |
igraph Mutation graph |
l_matrix |
matrix Mutation placement likelihood matrix (node by mutation) |
Value
igraph Mutation graph
R Package Documentation
Browse R Packages
We want your feedback!
Note that we can't provide technical support on individual packages. You should contact the package authors for that.
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