View source: R/find_mutations.R
find_mutations | R Documentation |
Searching for mutations related to signature score
find_mutations(
mutation_matrix,
signature_matrix,
id_signature_matrix = "ID",
signature,
min_mut_freq = 0.05,
plot = TRUE,
method = "multi",
point.alpha = 0.1,
save_path = NULL,
palette = "jco",
show_plot = TRUE,
show_col = FALSE,
width = 8,
height = 4,
oncoprint_group_by = "mean",
oncoprint_col = "#224444",
gene_counts = 10,
jitter = FALSE,
genes = NULL,
point_size = 4.5
)
mutation_matrix |
mutation matrix with sample name in the row and genes in the column |
signature_matrix |
signature data frame with identifier and target signatures |
id_signature_matrix |
column name of identifier |
signature |
name of target signature |
min_mut_freq |
minimum frequency of mutations |
plot |
logical variable, if TRUE, plot will be save in the 'save_path' |
method |
multi or Wilcoxon test only, if 'multi' is applied, both 'cuzick test' and 'wilcoxon' will be performed |
point.alpha |
point.alpha of boxplot |
save_path |
path to save plot and statistical analyses |
palette |
palette of box plot |
show_plot |
logical variable, if TRUE, plot will be printed. |
show_col |
show code of palette |
width |
width of oncoprint |
height |
height of oncoprint |
oncoprint_group_by |
signature must be group by mean or quantile |
oncoprint_col |
color of mutation |
gene_counts |
define the number of genes which will be shown in the oncoprint |
jitter |
if true, each point will be drawn in the box plot with jitter |
genes |
genes for drawing |
point_size |
default is 4.5 |
Dongqiang Zeng
# MAF data download from UCSC Xena hub
maf_file<-"E:/18-Github/Organization/TCGA.STAD.mutect.c06465a3-50e7-46f7-b2dd-7bd654ca206b.DR-10.0.somatic.maf"
mut_list<-make_mut_matrix(maf = maf_file, isTCGA = T, category = "multi")
mut<-mut_list$snp
res<-find_mutations(mutation_matrix = mut, signature_matrix = tcga_stad_sig, id_signature_matrix = "ID",signature = "CD_8_T_effector",min_mut_freq = 0.01, plot = TRUE, jitter = TRUE, point.alpha = 0.25
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