| diff_SNP_tcga | R Documentation |
Do difference analysis of SNP data downloaded from TCGAbiolinks
diff_SNP_tcga(snpData, sampleType)
snpData |
data.frame of SNP data downloaded from TCGAbiolinks |
sampleType |
vector of sample group |
## Not run:
library(TCGAbiolinks)
query <- GDCquery(
project = "TCGA-CHOL",
data.category = "Simple Nucleotide Variation",
access = "open",
legacy = FALSE,
data.type = "Masked Somatic Mutation",
workflow.type = "Aliquot Ensemble Somatic Variant Merging and Masking"
)
GDCdownload(query)
data_snp <- GDCprepare(query)
samples <- unique(data_snp$Tumor_Sample_Barcode)
sampleType <- sample(c("A","B"), length(samples), replace = TRUE)
names(sampleType) <- samples
pvalue <- diff_SNP_tcga(snpData = data_snp, sampleType = sampleType)
## End(Not run)
Add the following code to your website.
For more information on customizing the embed code, read Embedding Snippets.