gcc.heatmap(x, cpus = 1, method = c("GCC", "PCC", "SCC", "KCC", "BiWt", "MI", "MINE", "ED"), distancemethod = c("Raw", "Abs", "Sqr"), clustermethod = c("complete", "average", "median", "centroid", "mcquitty", "single", "ward"), #hcdata output by gcc.tsheatmap function rowhcdata = NULL, colhcdata = NULL,
keynote = "FPKM",
## dendrogram control symm = FALSE, Rowv = TRUE, Colv = if (symm) "Rowv" else TRUE, dendrogram = c("both", "row", "column", "none"),
## data scaling scale = c("none", "row", "column"), na.rm = TRUE, revC = identical(Colv, "Rowv"), add.expr,
#break points for binning values in x breaks = 16, quanbreaks = TRUE, symbreaks = min(x < 0, na.rm = TRUE) || scale != "none",
#colors colrange = c("green", "black", "red"),
colsep, rowsep, sepcolor = "white", sepwidth = c(0.05, 0.05), cellnote, notecex = 1, notecol = "cyan", na.color = par("bg"), trace = c("none", "column", "row", "both"), tracecol = "cyan", hline = median(breaks), vline = median(breaks), linecol = tracecol, margins = c(5, 5), ColSideColors, RowSideColors, cexRow = 0.2 + 1/log10(dim(x)[1]), cexCol = 0.2 + 1/log10(dim(x)[2]), labRow = NULL, labCol = NULL,
#color key key = TRUE, keysize = 0.65, density.info = c("none", "histogram", "density"), denscol = tracecol, symkey = min(x < 0, na.rm = TRUE) || symbreaks, densadj = 0.25,
#image information main = NULL, xlab = NULL, ylab = NULL, lmat = NULL, lhei = NULL, lwid = NULL, ...)
gcc.dist
, cor.matrix
, gcc.hclust
, gcc.tsheatmap
.
## Not run:
# data(rsgcc)
# x <- rnaseq[1:50,]
# ghm <- gcc.heatmap(x, cpus = 1, method = "GCC",
# distancemethod = "Raw", clustermethod = "complete", labRow = "")
# ## End(Not run)
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