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#' Calculate the presence of your gene set within each brain region
#'
#' Calculates the presence of gene set within each region
#'
#' @param genes query gene set
#' @param background background gene list, default = NULL (uses all ABA genes)
#' @param reps replicates for bootstrap, default = 10
#' @param refset reference brain map. developing (default) or adult
#' @return "Comp" object
#'
#' @examples
#' #brainImageR:::loadworkspace()
#' ##First load in a gene set
#' data(vth)
#' ##Then calculate the spatial enrichment
#' #composite <- SpatialEnrichment(vth,20,"developing")
#' @importFrom methods new
#'@export
SpatialEnrichment <- function(genes,
background = NULL,
reps = 10,
refset = c("developing", "adult")){
refset <- match.arg(refset)
rowmeta <- .cache[["EH1449"]]
if(is.null(rowmeta)){
warning(paste(c("workspace not loaded: ",
"Run brainImageR:::loadworkspace()",
" with Bioconductor >= v3.8 installed")))
}
stopifnot(exprs = !is.null(rowmeta))
refset <- tolower(refset)
refset <- tolower(refset)
gene_match <- match(genes,rowmeta$gene_symbol)
probes <- rowmeta[gene_match,"probeset_id"]
probe_match <- match(probes[!is.na(probes)],rowmeta$probeset_id)
samplesize <- length(unique(rowmeta[probe_match,"gene_symbol"]))
surviving <- samplesize
starting <- length(genes)
probe_match <- match(probes[!is.na(probes)],rowmeta$probeset_id)
genes <- unique(as.character(rowmeta[probe_match,"gene_symbol"]))
message(paste(surviving,"of",starting,"genes are present in ref dataset"))
tissueExp1 <- TissueSummary(genes, refset)
message(paste(surviving,"genes are expressed using",reps , "iterations"))
if(!is.null(background)){
message("Using user-provided set of background genes")
starting.b <- length(background)
probes.b <- rowmeta[match(background,rowmeta$gene_symbol),"probeset_id"]
probe_match <- match(probes.b[!is.na(probes.b)],rowmeta$probeset_id)
background <- unique(as.character(rowmeta[probe_match,"gene_symbol"]))
surviving.b <- length(background)
message(paste(surviving.b,
"of",
starting.b,
"background genes are in ref dataset"))
}else{
message("Using all genes in ABA microarray as background")
background <- unique(as.character(rowmeta$gene_symbol))
}
#random.matrix <- as.data.frame(sapply(X=c(1:reps),
# FUN=RandomTissueSummary,
# genes= background,
# samplesize = surviving,
# refset = refset))
template <- c(brainrange(1,length((names(tissueExp1)))))
names(template) <- (names(tissueExp1))
random.matrix <- as.data.frame(vapply(X=brainrange(1,reps),
FUN.VALUE = template,
FUN=RandomTissueSummary,
genes= background,
samplesize = surviving,
refset = refset))
tissueExp2 <- apply(X=random.matrix,MARGIN=1,FUN=mean)
# tissueExp1b <- vector()
# for(i in unique(names(tissueExp1))){
# tissueExp1b[i] <- mean(tissueExp1[names(tissueExp1) == i])
# }
# tissueExp1 <- tissueExp1b
tissueExp1b <- vapply(unique(names(tissueExp1)), function(i) {
mean(tissueExp1[names(tissueExp1) == i])
}, numeric(1))
# tissueExp2b <- vector()
# for(i in unique(names(tissueExp1))){
# tissueExp2b[i] <- mean(tissueExp2[names(tissueExp1) == i])
# }
# tissueExp2 <- tissueExp2b
tissueExp2b <- vapply(unique(names(tissueExp2)), function(i) {
mean(tissueExp2[names(tissueExp2) == i])
}, numeric(1))
rm2 <- matrix(data = NA,
nrow = length(unique(names(tissueExp1))),
ncol = ncol(random.matrix),
dimnames = list(unique(names(tissueExp1)),
colnames(random.matrix))
)
for(i in unique(names(tissueExp1))){
rm2[i,] <- apply(random.matrix[names(tissueExp1) == i,], 2, mean)
}
random.matrix <- data.frame(rm2)
comp <- new(Class="Comp",
genes = genes,
tissueExp1 = tissueExp1,
tissueExp2 = tissueExp2,
composite = matrix(NA,1,1),
random.matrix = random.matrix,
refset = refset
)
return(comp)
}
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