ovcYoshihara | R Documentation |
This function computes subtype scores and risk classifications from gene expression values following the algorithm developed by Yoshihara et al, for prognosis in ovarian cancer.
ovcYoshihara(data, annot, hgs, gmap = c("entrezgene", "ensembl_gene_id", "hgnc_symbol", "unigene", "refseq_mrna"), do.mapping = FALSE, verbose = FALSE)
data |
Matrix of gene expressions with samples in rows and probes in columns, dimnames being properly defined. |
annot |
Matrix of annotations with one column named as gmap, dimnames being properly defined. |
hgs |
vector of booleans with TRUE represents the ovarian cancer patients who have a high grade, late stage, serous tumor, FALSE otherwise. This is particularly important for properly rescaling the data. If hgs is missing, all the patients will be used to rescale the subtype score. |
gmap |
character string containing the biomaRt attribute to use for mapping if do.mapping=TRUE |
do.mapping |
TRUE if the mapping through Entrez Gene ids must be performed (in case of ambiguities, the most variant probe is kept for each gene), FALSE otherwise. |
verbose |
TRUE to print informative messages, FALSE otherwise. |
A list with items:
score: Continuous signature scores.
risk: Binary risk classification, 1 being high risk and 0 being low risk.
mapping: Mapping used if necessary.
probe: If mapping is performed, this matrix contains the correspondence between the gene list (aka signature) and gene expression data.
Yoshihara K, Tajima A, Yahata T, Kodama S, Fujiwara H, Suzuki M, Onishi Y, Hatae M, Sueyoshi K, Fujiwara H, Kudo, Yoshiki, Kotera K, Masuzaki H, Tashiro H, Katabuchi H, Inoue I, Tanaka K (2010) "Gene expression profile for predicting survival in advanced-stage serous ovarian cancer across two independent datasets", PloS one, 5(3):e9615.
sigOvcYoshihara
# load the ovcYoshihara signature data(sigOvcYoshihara) # load NKI dataset data(nkis) colnames(annot.nkis)[is.element(colnames(annot.nkis), "EntrezGene.ID")] <- "entrezgene" # compute relapse score ovcYoshihara.nkis <- ovcYoshihara(data=data.nkis, annot=annot.nkis, gmap="entrezgene", do.mapping=TRUE) table(ovcYoshihara.nkis$risk)
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