# * Creating `data-raw`.
# * Adding `data-raw` to `.Rbuildignore`.
# Next:
# * Add data creation scripts in data-raw
# * Use devtools::use_data() to add data to package
library(forcats)
#### Pasilla ####
library(DESeq2)
library(pasilla)
data("pasillaGenes")
pEM <- counts(pasillaGenes)
pGR <- data.frame(geneName=rownames(pEM),
row.names=rownames(pEM))
pDM <- pData(pasillaGenes)
pDM <- subset(pDM, select=c(condition, type))
pasilla <- list(Expression=pEM, Design=pDM, Annotation=pGR)
devtools::use_data(pasilla, overwrite=TRUE)
#### Zebrafish ####
library(zebrafishRNASeq)
data(zfGenes)
zEM <- zfGenes
zDM <- data.frame(gallein=factor(x=c("control", "control", "control",
"treated", "treated", "treated"),
levels=c("control", "treated")),
row.names=colnames(zEM))
zGR <- data.frame(id=rownames(zEM), row.names=rownames(zEM))
zebrafish <- list(Expression=zEM, Design=zDM, Annotation=zGR)
devtools::use_data(zebrafish, overwrite=TRUE)
#### Fission yeast ####
library(fission)
data(fission)
fEM <- assay(fission, "counts")
fGR <- as.data.frame(rowRanges(fission))
fDM <- as.data.frame(colData(fission))
fDM$minute <- fct_drop(fDM$minute)
yeast <- list(Expression=fEM, Design=fDM, Annotation=fGR)
devtools::use_data(yeast, overwrite=TRUE)
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