Description Usage Arguments Details Value Examples
Calculate pvalues using wilcoxon test
| 1 2 3 4 5 6 7 8 9 10 | 
| data | SummarizedExperiment obtained from the TCGAPrepare | 
| groupCol | Columns with the groups inside the SummarizedExperiment object. (This will be obtained by the function colData(data)) | 
| group1 | In case our object has more than 2 groups, you should set the groups | 
| group2 | In case our object has more than 2 groups, you should set the groups | 
| paired | Do a paired wilcoxon test? Default: True | 
| adj.method | P-value adjustment method. Default:"BH" Benjamini-Hochberg | 
| alternative | wilcoxon test alternative | 
| cores | Number of cores to be used | 
Verify if the data is significant between two groups. For the methylation we search for probes that have a difference in the mean methylation and also a significant value. Input: A SummarizedExperiment object that will be used to compared two groups with wilcoxon test, a boolean value to do a paired or non-paired test Output: p-values (non-adj/adj) histograms, p-values (non-adj/adj)
Data frame with cols p values/p values adjusted
Data frame with two cols p-values/p-values adjusted
| 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 | nrows <- 200; ncols <- 20
 counts <- matrix(runif(nrows * ncols, 1, 1e4), nrows,
           dimnames = list(paste0("cg",1:200),LETTERS[1:20]))
rowRanges <- GenomicRanges::GRanges(rep(c("chr1", "chr2"), c(50, 150)),
                   IRanges::IRanges(floor(runif(200, 1e5, 1e6)), width=100),
                    strand=sample(c("+", "-"), 200, TRUE),
                    feature_id=sprintf("ID%03d", 1:200))
colData <- S4Vectors::DataFrame(Treatment=rep(c("ChIP", "Input"), 10),
                    row.names=LETTERS[1:20],
                    group=rep(c("group1","group2"),c(10,10)))
data <- SummarizedExperiment::SummarizedExperiment(
         assays=S4Vectors::SimpleList(counts=counts),
         rowRanges=rowRanges,
         colData=colData)
results <- TCGAbiolinks:::dmc.non.parametric.se(data,"group")
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