This 2D-TPP analysis was executed on r format(Sys.time(), "%a %b %d %X %Y")
on machine r Sys.info()["nodename"]
with the following parameters:
str_break <- function(x, width = 80L) { n <- nchar(x) if (n <= width) { return(x) } n1 <- seq(1L, n, by = width) n2 <- seq(width, n, by = width) if (n %% width != 0) { n2 = c(n2, n) } substring(x, n1, n2) }
if ("Path" %in% colnames(configTable)){ tab1 <- configTable %>% select(Compound, Experiment, Temperature, Path) kable(tab1) }else { tab1 <- configTable %>% select(Compound, Experiment, Temperature) kable(tab1) } tab2 <- melt(extractConc(configTable)) # find respective reference columns tab2$ref <- sapply(rownames(tab2), function(rn){ ref <- unique(configTable$RefCol[which(configTable[[rn]]!="-")]) return(ref) }) colnames(tab2) <- c("Concentration [uM]", "Reference label") kable(tab2, row.names=TRUE)
print(configFile)
if (is.null(fcStr)){ fcStr <- "none" } if (is.null(fcStrUpdated)){ fcStrUpdated <- "none" } if (is.null(addCol)){ addCol <- "none" } param <- c("Protein identifier", "Fold change suffix", "Updated Fold change suffix (after normalization)", "Intensity value suffix", "Median normalization", "Added columns", "R2 cutoff", "Fold change cutoff", "Slope bounds", "Chosen methods for analysis", "TR reference data set") variab <- c(idVar, fcStr, fcStrUpdated, intensityStr, normalize, addCol, r2Cutoff, fcCutoff, paste(as.character(slopeBounds), collapse=","), paste(methods, sep=" "), trRef) tab <- data.frame(param, variab) colnames(tab) <- c("Parameter", "Setting") kable(tab)
rver <- sessionInfo()[["R.version"]][["version.string"]] print(rver)
pnames <- loadedNamespaces() pvers <- unlist(lapply(pnames, function(pn) as.character(packageVersion(pn)))) ptab <- data.frame(pnames, pvers) colnames(ptab) <- c("Package", "Version") kable(ptab)
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