pipelineCNA | R Documentation |
pipelineCNA Executes the entire SCEVAN pipeline that classifies tumour and normal cells from the raw count matrix, infer the clonal profile of cancer cells and looks for possible sub-clones in the tumour cell matrix automatically analysing the specific and shared alterations of each subclone and a differential analysis of pathways and genes expressed in each subclone.
pipelineCNA(
count_mtx,
sample = "",
par_cores = 20,
norm_cell = NULL,
SUBCLONES = TRUE,
beta_vega = 0.5,
ClonalCN = TRUE,
plotTree = TRUE,
AdditionalGeneSets = NULL,
SCEVANsignatures = TRUE,
organism = "human",
ngenes_chr = 5,
perc_genes = 10,
FIXED_NORMAL_CELLS = FALSE
)
count_mtx |
Raw count matrix with genes on rows (both Gene Symbol or Ensembl ID are allowed) and cells on columns. |
sample |
Sample name to save results (optional) |
par_cores |
Number of cores to run the pipeline (optional - default 20) |
norm_cell |
Vector of possible known normal cells to be used as confident normal cells (optional) |
SUBCLONES |
Boolean value TRUE if you are interested in analysing the clonal structure and FALSE if you are only interested in the classification of malignant and non-malignant cells (optional - default TRUE) |
beta_vega |
Specifies beta parameter for segmentation, higher beta for more coarse-grained segmentation. (optional - default 0.5) |
ClonalCN |
Get clonal CN profile inference from all tumour cells (optional) |
plotTree |
Plot Phylogenetic tree (optional - default FALSE) |
AdditionalGeneSets |
list of additional signatures of normal cell types (optional) |
SCEVANsignatures |
FALSE if you only want to use only the signatures specified in AdditionalGeneSets (default TRUE) |
organism |
Organism to be analysed (optional - "mouse" or "human" - default "human") |
ngenes_chr |
Minimum number of genes expressed on chromosome (optional - default 5) |
perc_genes |
Minimum percentage gene expressed in each cell (optional - default 10) |
FIXED_NORMAL_CELLS |
TRUE if norm_cell vector to be used as fixed reference, if you are only interested in clonal structure and not normal/tumor classification (default FALSE) |
res_pip <- pipelineCNA(count_mtx)
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