R/Cell_markers.ident.R
In CostaLab/sc2marker: Detect marker panel from scRNA-seq profile
Defines functions
get_split_neg
get_split_pos
get_gene_score_neg
get_gene_score_pos
plot_filter_combination_first2
plot_filter_stepbystep_first2
get_PRAUC_matrix_combine_markers
get_PRAUC_matrix_combine_markers_neg
get_PRAUC_matrix_combine_markers_neg_pos
get_split_neg_tp
get_split_pos_tp
plot_combine_PRAUC
get_split_neg_neg
get_split_pos_neg
get_split_pos_pos
Detect_combine_markers
generate_report_rmd
generate_report
intersect.ignorecase
get_gene_score_neg.fbeta
get_gene_score_pos.fbeta
plot_ridge
get_antibody
Detect_single_marker
normalize
makeid
firstup
get_original_alpha
Documented in
Detect_single_marker
firstup
generate_report
generate_report_rmd
get_antibody
get_gene_score_neg
get_gene_score_neg.fbeta
get_gene_score_pos
get_gene_score_pos.fbeta
get_original_alpha
get_split_pos_pos
intersect.ignorecase
makeid
normalize
plot_filter_stepbystep_first2
plot_ridge
#' Calculate gene negative specific score
#'
#' Calculate gene specific score in negative direction
#' @param scrna obj to use
#' @param gene gene to use
#' @param assay which assay to use in obj, default RNA
#' @param slot which slot to use, default data
#' @export
#' @examples
#' @return alpha before normalization
#'
get_original_alpha <- function(scrna, gene, x.alpha, assay = "RNA", slot = "data"){
Seurat::DefaultAssay(scrna) <- assay
g.exprs <- FetchData(scrna, gene, slot = slot)
g.max <- max(g.exprs[,1])
g.min <- min(g.exprs[,1])
alpha.ori <- x.alpha*g.max + g.min
return(alpha.ori)
}
#' Firstup character
#'
#' @param x character
#' @return up case first letter
#' @export
#'
firstup <- function(x) {
x <- tolower(x)
substr(x, 1, 1) <- toupper(substr(x, 1, 1))
x
}
#' make id for plotting
#'
#' Reset active.ident of obj for plotting.
#' @param scrna obj to use
#' @param id interested cell id
#' @param panel ID panel in metadata of obj
#' @export
#' @examples
#' @return seurat obj with re-set Idents
#'
makeid <- function(scrna, id, panel = "seurat_clusters"){
levels(Seurat::Idents(scrna)) <- c(levels(Seurat::Idents(scrna)), "other")
Seurat::Idents(scrna)[Seurat::Idents(scrna) != id] <- 'other'
return(scrna)
}
#' Min-Max Normalization
#'
#' Normalize scRNA sequencing data.
#' @param x Gene expression
#' @export
#' @examples
#' @return Normalized expression data
#'
normalize <- function(x, ...) {
return((x - min(x, ...)) /(max(x, ...) - min(x, ...)))
}
#' Detect single markers of specific cell groups
#' @param scrna seurat obj to be used
#' @param geneset custom genes to test, all genes in obj to use if NULL
#' @param id interested cell group
#' @param category Denotes which experiment to use. Available options are:
#' \itemize{
#' \item{"IHC"} : use genes with valid antibody for IHC in human protein atlas
#' \item{"ICC"} : use genes with valid antibody for ICC in human protein atlas
#' \item{"ICC.IHC"} : use genes with valid antibody for ICC or IHC in human protein atlas
#' \item{"Flow"} : Only use cell surface genes with at least one valid antibody(ICC or IHC)
#' }
#' @param assay indicate the assay to compute
#' @param slot indicate the slot of data to compute
#' @param step quantile steps
#' @param min.pct only test genes that are detected in a minimum fraction of cells in interested cell types. Default is 0.15
#' @param use.all Don't do any filter on input geneset
#' @param geneset custom genes to test
#' @param self.db self defined antibody database
#' @param self.db.only Bolean. Only use the self deifned antibody database or not
#' @return list of markers performance
#' @export
#'
#'
Detect_single_marker <- function(scrna, id, step = 0.1, slot = "data", category = NULL,
geneset = NULL, assay = "RNA", do.fast = F, min.pct = 0.15, min.fc = 0.25,
use.all = F, do.f1score = F, pseudo.count = 0.01, min.tnr = 0.65, org = "human",
self.db = NULL, self.db.only = F,...){
genes.to.use <- NULL
SeuratObject::DefaultAssay(scrna) <- assay
## get application and org
if (org == "human") {
if (!is.null(category)) {
if (!(category %in% c("ICC.IHC", "ICC", "IHC", "Flow", "FlowComet"))) {
print("category not found, it should be one of ICC, IHC, ICC.IHC, FlowComet or Flow.")
return(NULL)
}
if (category == "ICC.IHC") {
genes.to.use <- unique(union(ICC$Gene, IHC$Gene))
}else if(category == "ICC"){
genes.to.use <- ICC$Gene
}else if(category == "IHC"){
genes.to.use <- IHC$Gene
}else if(category == "Flow"){
genes.to.use <- surface.genes
}
}
if (!is.null(category)){
if(category == "FlowComet"){
genes.to.use <- intersect(firstup(comet_human), rownames(scrna[[assay]]))
}
}
}
if (org == "mouse") {
if (!is.null(category)) {
if (!(category %in% c("ICC.IHC", "ICC", "IHC", "Flow", "FlowComet"))) {
print("category not found, it should be one of ICC, IHC, ICC.IHC, FlowComet or Flow.")
return(NULL)
}
if (category == "ICC.IHC") {
genes.to.use <- unique(union(ICC_mouse$Gene, IHC_mouse$Gene))
genes.to.use <- c(genes.to.use, flow_mouse$Gene)
}else if(category == "ICC"){
genes.to.use <- ICC_mouse$Gene
genes.to.use <- c(genes.to.use, flow_mouse$Gene)
}else if(category == "IHC"){
genes.to.use <- IHC_mouse$Gene
genes.to.use <- c(genes.to.use, flow_mouse$Gene)
}else if(category == "Flow"){
genes.to.use <- flow_mouse$Gene
}
}
genes.to.use <- unique(genes.to.use)
if (!is.null(category)){
if(category == "FlowComet"){
genes.to.use <- intersect(firstup(comet_genes), rownames(scrna[[assay]]))
}
}
}
if (!is.null(self.db)){
self.db.table <- utils::read.csv(self.db)
if(self.db.only){
genes.to.use <- self.db.table[,1]
}else{
genes.to.use <- c(genes.to.use, self.db.table[,1])
}
}
genes.to.use <- c(genes.to.use, geneset)
if (!is.null(genes.to.use)) {
genes.to.use <- intersect.ignorecase(rownames(scrna[[assay]]), genes.to.use)
geneset.in <- intersect.ignorecase(geneset, rownames(scrna[[assay]]))
geneset.out <- setdiff(geneset, geneset.in)
if (length(geneset.out) > 0) {
cat(paste("\nThese genes are not in the obj. Please check! \n"))
cat(geneset.out)
cat(paste("\n"))
}
}else{
cat(paste("\n Using all genes as input."))
cat(paste("\n"))
genes.to.use <- rownames(scrna[[assay]])
}
if (use.all) {
de <- Seurat::FoldChange(scrna, ident.1 = id, features = genes.to.use)
}
if (!use.all) {
de <- Seurat::FoldChange(scrna, ident.1 = id, features = genes.to.use)
de <- de[de$pct.1 > min.pct, ]
de$avg_log2FC <- abs(de$avg_log2FC)
de <- de[de$avg_log2FC > min.fc, ]
}
de <- na.omit(de)
markers <- de
gene.rank.list <- data.frame()
Seurat::DefaultAssay(scrna) <- assay
exprs.matrix <- Seurat::FetchData(scrna, vars = c(rownames(markers), "ident"), slot = slot)
# Ids.totest <- Idents(scrna)
gene.list <- rownames(markers)
gene.list <- intersect.ignorecase(rownames(scrna[[assay]]), gene.list)
pb <- utils::txtProgressBar(min = 0, max = length(gene.list), style = 3, file = stderr())
i = 1
for (genes in gene.list) {
tryCatch({
# exprs.matrix <- Seurat::FetchData(scrna, vars = c(genes, "ident"), slot = slot)
df.input <- exprs.matrix[, c(genes, "ident")]
de <- data.frame(get_gene_score(df.input, gene = genes, celltype = id,
step = step, pseudo.count = pseudo.count, min.tnr = min.tnr))
names(de)<-c("gene", "split.value","x.margin", "x.margin.adj", "TP", "FP", "TN", "FN", "direction", "FP details")
gene.rank.list <- rbind(gene.rank.list, de)
}, error=function(e){cat("Warning :",conditionMessage(e), "\n")})
setTxtProgressBar(pb = pb, value = i)
i = i + 1
}
close(con = pb)
gene.rank.list <- gene.rank.list[order(gene.rank.list$x.margin.adj, decreasing = T),]
rownames(gene.rank.list) <- seq(nrow(gene.rank.list))
gene.rank.list <- dplyr::distinct(gene.rank.list, gene, .keep_all = TRUE)
return(gene.rank.list)
}
#' Calculate gene specific score in both direction
#' @param exprs.matrix exprs matrix with ident panel
#' @param id interested cell id
#' @param gene gene to use
#' @param step quantile step
#' @export
#' @examples
#' @return gene score in both direction
#'
#'
get_gene_score <- function (exprs.matrix, celltype, gene, step = 0.01, pseudo.count = 0.01,
min.tnr = 0.65)
{
colnames(exprs.matrix) <- c("exp", "id")
exprs.matrix <- data.table::as.data.table(exprs.matrix)
exprs.max <- max(exprs.matrix$exp)
exprs.min <- min(exprs.matrix$exp)
# Min-max normalization
exprs.matrix$exp <- normalize(exprs.matrix$exp)
exprs.matrix$exp <- round(exprs.matrix$exp, 3)
exprs.matrix$exp.n <- 0 - exprs.matrix$exp
gene.prauc.p <- data.frame(x.val <- c(), margin <- c())
gene.prauc.n <- data.frame(x.val <- c(), margin <- c())
celltype.in <- celltype
data.id <- subset(exprs.matrix, id == celltype.in)
data.other <- subset(exprs.matrix, id != celltype.in)
data.id.l <- nrow(data.id)
data.o.l <- nrow(data.other)
data.all.l <- nrow(exprs.matrix)
# grid search for optimal cutoff
for (x.val in seq(0.001, 0.99, step)) {
# Positive direction
# get subset for TP, FP, TN, FN
data.i.a <- subset(data.id, exp > x.val)
data.o.a <- subset(data.other, exp > x.val)
data.i.b <- subset(data.id, exp <= x.val)
data.o.b <- subset(data.other, exp <= x.val)
# get the margin
x.margin.p <- sum((data.i.a$exp - x.val)) * nrow(data.o.b) +
sum((x.val - data.o.b$exp)) * nrow(data.i.a) - sum((data.o.a$exp -
x.val)) * nrow(data.i.b)
x.margin.p <- x.margin.p/data.all.l
de.p <- data.frame(x.val, x.margin.p)
gene.prauc.p <- rbind(gene.prauc.p, de.p)
# Negative direction
# get subset for TP, FP, TN, FN
x.val.n <- 0 - x.val
data.i.a <- subset(data.id, exp.n > x.val.n)
data.o.a <- subset(data.other, exp.n > x.val.n)
data.i.b <- subset(data.id, exp.n <= x.val.n)
data.o.b <- subset(data.other, exp.n <= x.val.n)
# get the margin
x.margin.n <- sum((data.i.a$exp.n - x.val.n)) * nrow(data.o.b) +
sum((x.val.n - data.o.b$exp.n)) * nrow(data.i.a) -
sum((data.o.a$exp.n - x.val.n)) * nrow(data.i.b)
x.margin.n <- x.margin.n/data.all.l
de.n <- data.frame(x.val, x.margin.n)
gene.prauc.n <- rbind(gene.prauc.n, de.n)
}
# get the max margin
gene.prauc.p <- gene.prauc.p[order(gene.prauc.p$x.margin,
decreasing = T), ]
gene.prauc.n <- gene.prauc.n[order(gene.prauc.n$x.margin,
decreasing = T), ]
# Positive direction final score calculation
x.split <- gene.prauc.p[1, ]
x.val <- x.split[, 1]
x.margin <- x.split[, 2]
tp <- sum(data.id$exp > x.val)
fp <- sum(data.other$exp > x.val)
fn <- sum(data.id$exp <= x.val)
tn <- sum(data.other$exp <= x.val)
# get top 5 false positive resources
fp.pro <- subset(data.other, exp > x.val)
fp.pro <- as.data.frame(table(fp.pro$id))
fp.pro <- fp.pro[order(fp.pro$Freq, decreasing = T), ]
if (nrow(fp.pro) >= 5) {
fp.pro <- fp.pro[1:5, ]
}
fp.string <- paste(fp.pro$Var1, fp.pro$Freq)
fp.string <- toString(fp.string)
x.factor.p <- (mean(data.id$exp) + pseudo.count)/(mean(data.other$exp) +
pseudo.count)
# get the score
x.margin.adj <- x.margin * (tp/data.id.l) * (tn/data.o.l) *
(x.factor.p^2)
x.val <- x.val * exprs.max + exprs.min
x.split.p <- data.frame(gene, x.val, x.margin, x.margin.adj,
tp, fp, tn, fn, "+", fp.string)
# Negative direction final score calculation
x.split <- gene.prauc.n[1, ]
x.val <- x.split[, 1]
x.margin <- x.split[, 2]
tp <- sum(data.id$exp < x.val)
fp <- sum(data.other$exp < x.val)
tn <- sum(data.other$exp >= x.val)
fn <- sum(data.id$exp >= x.val)
# get top 5 false positive resources
fp.pro <- subset(data.other, exp < x.val)
fp.pro <- as.data.frame(table(fp.pro$id))
fp.pro <- fp.pro[order(fp.pro$Freq, decreasing = T), ]
if (nrow(fp.pro) >= 5) {
fp.pro <- fp.pro[1:5, ]
}
fp.string <- paste(fp.pro$Var1, fp.pro$Freq)
fp.string <- toString(fp.string)
x.factor.n <- round(1/x.factor.p, 1)
x.margin.adj <- x.margin * (tp/data.id.l) * (tn/data.o.l) *
(x.factor.n^2)
x.val <- x.val * exprs.max + exprs.min
if (tn/data.o.l < min.tnr) {
x.margin.adj <- 0
}
x.split.n <- data.frame(gene, x.val, x.margin, x.margin.adj,
tp, fp, tn, fn, "-", fp.string)
return(rbind(x.split.p, x.split.n))
}
#' Get Antibody information table
#' @param markers.list makers list from Detect single markers function
#' @param rm.noab whether to remove genes without antibody information. Default TRUE.
#' @param self.db User provided database
#' @param self.db.only Bolean, whether to only use the user provided database
#' @return list of markers with antibody information
#' @export
#'
get_antibody <- function(markers.list, rm.noab = T, org = "human",
self.db = NULL, self.db.only = F, return_matrix = F,...){
# markers.list <- markers.list[markers.list$gene %in% intersect.ignorecase(markers$gene, union(ICC$Gene, IHC$Gene)),]
markers.list$gene <- toupper(markers.list$gene)
markers.list$antibody <- "NULL"
markers.list$x.margin <- round(markers.list$x.margin, 2)
markers.list$x.margin.adj <- round(markers.list$x.margin.adj, 2)
flow_mouse$Gene <- toupper(flow_mouse$Gene)
if (org == "human") {
IHC$Gene <- toupper(IHC$Gene)
ICC$Gene <- toupper(ICC$Gene)
markers.list$Reliability <- "Validated"
for (i in 1:nrow(markers.list)) {
gene.i <- markers.list[i,]$gene
if (gene.i %in% IHC$Gene) {
markers.list[i,]$antibody <- IHC[IHC$Gene == gene.i, ]$Antibody.RRID[1]
}
if (gene.i %in% ICC$Gene) {
markers.list[i,]$antibody <- ICC[ICC$Gene == gene.i, ]$Antibody.RRID[1]
}
}
}
if (org == "mouse") {
IHC_mouse$Gene <- toupper(IHC_mouse$Gene)
ICC_mouse$Gene <- toupper(ICC_mouse$Gene)
markers.list$Reliability <- "Homology"
for (i in 1:nrow(markers.list)) {
gene.i <- markers.list[i,]$gene
if (gene.i %in% IHC_mouse$Gene) {
markers.list[i,]$antibody <- IHC_mouse[IHC_mouse$Gene == gene.i, ]$Antibody.RRID[1]
markers.list[i,]$Reliability <- IHC_mouse[IHC_mouse$Gene == gene.i, ]$Reliability[1]
}
if (gene.i %in% ICC_mouse$Gene) {
markers.list[i,]$antibody <- ICC_mouse[ICC_mouse$Gene == gene.i, ]$Antibody.RRID[1]
markers.list[i,]$Reliability <- ICC_mouse[ICC_mouse$Gene == gene.i, ]$Reliability[1]
}
if (gene.i %in% toupper(flow_mouse$Gene)) {
markers.list[i,]$antibody <- flow_mouse[flow_mouse$Gene == gene.i, ]$Antibody.RRID[1]
markers.list[i,]$Reliability <- flow_mouse[flow_mouse$Gene == gene.i, ]$Reliability_1[1]
}
}
}
if (!is.null(self.db)){
self.db.table <- utils::read.csv(self.db)
self.db.table[,1] <- toupper(self.db.table[,1])
if(self.db.only){
markers.list <- markers.list[markers.list$gene %in% self.db.table$Gene, ]
}
for (i in 1:nrow(markers.list)) {
gene.i <- markers.list[i,]$gene
if (gene.i %in% toupper(self.db.table$Gene)) {
markers.list[i,]$antibody <- self.db.table[self.db.table$Gene == gene.i, ]$Antibody[1]
markers.list[i,]$Reliability <- self.db.table[self.db.table$Gene == gene.i, ]$Reliability[1]
}
}
}
markers.list <- markers.list[, -3]
markers.list[,2] <- round(markers.list[,2], 3)
colnames(markers.list)[2] <- "Alpha"
colnames(markers.list)[3] <- "Score"
if (rm.noab) {
markers.list <- markers.list[markers.list$antibody != "NULL",]
}
rownames(markers.list) <- 1:nrow(markers.list)
if (return_matrix) {
return(markers.list)
}else{
DT::datatable(markers.list,
extensions = 'Buttons',
options = list(dom = 'Bfrtip',
buttons = c('copy',
'csv',
'excel'
),
autoWidth = FALSE),
escape = F)
}
}
#' RidgePlot of selected genes, with split value
#' @param scrna seurat obj to be used
#' @param genes genes to plot
#' @param id interested cell group
#' @param step quantile steps
#' @param show_split whether to show the split line
#' @param aggr.other whether to aggregate other cell clusters
#' @return Ridge plot
#' @export
#'
plot_ridge <- function(scrna, id, genes, ncol = 1, step = 0.01, show_split = T, assay = "RNA", slot = "data", aggr.other = F){
Seurat::DefaultAssay(scrna) <- assay
require(ggplot2)
df.all <-data.frame()
df.split <-data.frame()
if (aggr.other) {
for (gene in genes) {
# get the alpha split value
df.g <- get_gene_score(Seurat::FetchData(scrna, vars = c(gene, "ident")), celltype = id, gene = gene)
df.g <- df.g[order(df.g$x.margin, decreasing = T),]
df.g <- df.g[1,]
df.c <-Seurat::FetchData(scrna, vars = c(gene, "ident"))
df.c$ident <- ifelse(df.c$ident == id, id, "Other")
df.c$gene <- paste(gene)
colnames(df.c) <- c("Exprs", "Ident", "Gene")
df.all <- rbind(df.all,df.c)
df.g <- df.g[,c(1,2)]
colnames(df.g) <- c("Gene", "Split")
df.split <- rbind(df.split,df.g)
}
df.s <- reshape2::melt(df.all)
df.s[df.s == -Inf] <- 0
df.s$Gene <- factor(df.s$Gene, levels = as.character(genes))
df.split$Gene <- factor(df.split$Gene, levels = c(genes))
g <- ggplot2::ggplot(df.s, aes(x=value, y=variable, color=Ident, point_color=Ident, fill=Ident)) +
ggridges::geom_density_ridges_gradient(scale = 3, size = 0.3, rel_min_height = 0.01) +
scale_fill_manual(values = c("#CB181D80", "#2171B580")) +
scale_discrete_manual("point_color", values = c("#CB181D80", "#2171B580"), guide = "none") +
guides(fill = guide_legend(
override.aes = list(
fill = c("#CB181D80", "#2171B580"),
color = NA, point_color = NA))
) +
ggridges::theme_ridges(grid = FALSE) +
ylab("") +
theme(
plot.title = element_text(hjust = 0.5),
plot.subtitle = element_text(hjust = 0.5)
)
df.split$Gene <- factor(df.split$Gene, levels = c(genes))
g <- g + facet_wrap(~Gene, ncol = ncol) +
geom_vline(data = df.split, aes(xintercept = Split), linetype="dotted",
color = "red", size=1.5) + labs(fill = "Expression")
# return()
}else{
for (gene in genes) {
# get the alpha split value
df.g <- get_gene_score(Seurat::FetchData(scrna, vars = c(gene, "ident")), celltype = id, gene = gene)
df.g <- df.g[order(df.g$x.margin, decreasing = T),]
df.g <- df.g[1,]
df.c <-Seurat::FetchData(scrna, vars = c(gene, "ident"))
df.c$gene <- paste(gene)
colnames(df.c) <- c("Exprs", "Ident", "Gene")
df.all <- rbind(df.all,df.c)
df.g <- df.g[,c(1,2)]
colnames(df.g) <- c("Gene", "Split")
df.split <- rbind(df.split,df.g)
}
df.split$Gene <- factor(df.split$Gene, levels = c(genes))
df.all$Gene <- factor(df.all$Gene, levels = c(genes))
g <- ggplot2::ggplot(df.all, aes(y=reorder(Ident, Exprs , mean),x=Exprs, fill = stat(x))) +
ggridges::geom_density_ridges_gradient()+
scale_fill_viridis_c(option = "D")+
theme(legend.position = "none")+
theme(
plot.title = element_text(hjust = 0.5),
plot.subtitle = element_text(hjust = 0.5)
) + ylab("") + xlab("")
g <- g +
geom_vline(data = df.split, aes(xintercept = Split), linetype="dotted",
color = "red", size=1.5) +
facet_wrap(~Gene, ncol = ncol)
# return()
}
g <- g + theme_bw() +
theme(panel.border = element_blank(), panel.grid.major = element_blank(),
panel.grid.minor = element_blank(), axis.line = element_line(colour = "black")) + labs(fill = "Expression")
print(g)
# return(g)
}
#' Calculate gene positive specific score with FBeta (Hypergate like approach)
#'
#' Calculate gene FBeta score with positive direction
#' @param scrna obj to use
#' @param id interested cell id
#' @param gene gene to use
#' @param step quantile step
#' @param assay which assay to use in obj, default RNA
#' @param slot which slot to use, default data
#' @param panel ID panel in metadata of obj
#' @export
#' @examples
#' @return seurat obj with re-set Idents
#'
get_gene_score_pos.fbeta <- function(scrna, gene, id, step = 0.01, assay = "RNA", slot = "data") {
Seurat::DefaultAssay(scrna) <- assay
# scrna@active.assay <- assay
data.mat.surf <- Seurat::FetchData(scrna, vars = c(gene, "ident"), slot = slot)
colnames(data.mat.surf) <- c("exp", "id")
colnames(data.mat.surf) <- c("exp", "id")
x.max <- max(data.mat.surf$exp)
x.min <- min(data.mat.surf$exp)
data.mat.surf$exp <- normalize(data.mat.surf$exp)
gene.prauc <- data.frame(x.val <- c(),
margin <- c())
data.id <- data.mat.surf[data.mat.surf$id == id,]
data.other <- data.mat.surf[data.mat.surf$id != id,]
data.id.l <- nrow(data.id)
data.o.l <- nrow(data.other)
data.all.l <- nrow(data.mat.surf)
for (x.val in seq(0, 1, step)) {
am <- data.id[data.id$exp > x.val, ]
cm <- data.other[data.other$exp > x.val, ]
bm <- data.id[data.id$exp <= x.val, ]
dm <- data.other[data.other$exp <= x.val, ]
x.pr <- nrow(am)/(nrow(am) + nrow(cm))
x.re <- nrow(am)/(nrow(am) + nrow(bm))
x.margin <- x.pr*x.re/(x.pr + x.re)
de <- data.frame(x.val, x.margin)
gene.prauc <- rbind(gene.prauc, de)
}
gene.prauc <- gene.prauc[order(gene.prauc$x.margin, decreasing = T),]
x.split <- gene.prauc[1,]
x.val <- x.split[,1]
x.margin <- x.split[,2]
tp <- sum(data.id$exp > x.val)
fp <- sum(data.other$exp > x.val)
fn <- sum(data.id$exp <= x.val)
tn <- sum(data.other$exp <= x.val)
x.margin.adj <- x.margin
x.val <- x.val*x.max + x.min
x.split <- data.frame(gene, x.val, x.margin, x.margin.adj, tp, fp, "+")
return(x.split)
}
#' Calculate gene positive specific score with FBeta (Hypergate like approach)
#'
#' Calculate gene FBeta score with negative direction
#' @param scrna obj to use
#' @param id interested cell id
#' @param gene gene to use
#' @param step quantile step
#' @param assay which assay to use in obj, default RNA
#' @param slot which slot to use, default data
#' @param panel ID panel in metadata of obj
#' @export
#' @examples
#' @return seurat obj with re-set Idents
#'
get_gene_score_neg.fbeta <- function(scrna, gene, id, step = 0.01, assay = "RNA", slot = "data") {
Seurat::DefaultAssay(scrna) <- assay
# scrna@active.assay <- assay
data.mat.surf <- Seurat::FetchData(scrna, vars = c(gene, "ident"), slot = slot)
colnames(data.mat.surf) <- c("exp", "id")
data.mat.surf$exp <- normalize(data.mat.surf$exp)
gene.prauc <- data.frame(x.val <- c(),
margin <- c())
data.id <- data.mat.surf[data.mat.surf$id == id,]
data.other <- data.mat.surf[data.mat.surf$id != id,]
data.id.l <- nrow(data.id)
data.o.l <- nrow(data.other)
data.all.l <- nrow(data.mat.surf)
for (x.val in seq(0, 1, step)) {
am <- data.id[data.id$exp < x.val, ]
cm <- data.other[data.other$exp < x.val, ]
bm <- data.id[data.id$exp >= x.val, ]
dm <- data.other[data.other$exp >= x.val, ]
x.pr <- nrow(am)/(nrow(am) + nrow(cm))
x.re <- nrow(am)/(nrow(am) + nrow(bm))
x.margin <- x.pr*x.re/(x.pr + x.re)
de <- data.frame(x.val, x.margin)
gene.prauc <- rbind(gene.prauc, de)
}
gene.prauc <- gene.prauc[order(gene.prauc$x.margin, decreasing = T),]
x.split <- gene.prauc[1,]
x.val <- x.split[,1]
x.margin <- x.split[,2]
tp <- sum(data.id$exp < x.val)
fp <- sum(data.other$exp < x.val)
fn <- sum(data.id$exp >= x.val)
tn <- sum(data.other$exp >= x.val)
x.margin.adj <- x.margin
x.split <- data.frame(gene, x.val, x.margin, x.margin.adj, tp, fp, "-")
return(x.split)
}
#' Intersect 2 list ignoring the cases and return the elements in list1
#' @param list1 list 1 of genes
#' @param list2 list 2 of genes
#' @export
#' @return Ridge plot
#'
intersect.ignorecase <- function(list1, list2){
list1.u <- toupper(list1)
list2.u <- toupper(list2)
list12.u <- intersect(list1.u, list2.u)
list.r <- list1[match(list12.u, list1.u)]
return(list.r)
}
#' Detect single markers of all cell groups
#' @param scrna seurat obj to be used
#' @param geneset custom genes to test, all genes in obj to use if NULL
#' @param id interested cell group
#' @param test.use Denotes which test to use. Available options are:
#' \itemize{
#' \item{"IHC"} : use genes with valid antibody for IHC in human protein atlas
#' \item{"ICC"} : use genes with valid antibody for ICC in human protein atlas
#' \item{"ICC.IHC"} : use genes with valid antibody for ICC or IHC in human protein atlas
#' \item{"Flow"} : Only use cell surface genes with at least one valid antibody(ICC or IHC)
#' }
#' @param assay indicate the assay to compute
#' @param slot indicate the slot of data to compute
#' @param step quantile steps
#' @param min.pct only test genes that are detected in a minimum fraction of cells in interested cell types. Default is 0.15
#' @param use.all Don't do any filter on input geneset
#' @param clusters_to_detect set of clusters for compupation
#' @param geneset custom genes to test
#' @param org Choose database for human or mouse
#' @param self.db self defined antibody database
#' @param self.db.only Bolean. Only use the self deifned antibody database or not
#' @return list of markers performance
#' @export
#'
#'
Detect_single_marker_all <- function (scrna, step = 0.1, slot = "data", category = NULL,
clusters_to_detect = NULL, geneset = NULL, assay = "RNA",
do.fast = F, min.pct = 0.15, min.fc = 0.25, use.all = F,
do.f1score = F, pseudo.count = 0.01, min.tnr = 0.65, org="mouse",
self.db = NULL, self.db.only=F, ...)
{
all.list <- vector("list")
if (length(clusters_to_detect) == 0) {
for (id in unique(Seurat::Idents(scrna))) {
message(paste("Calculating Markers for", id))
df.s <- Detect_single_marker(scrna = scrna, id = id,
step = step, slot = slot, assay = assay, min.pct = min.pct,
min.fc = min.fc, min.tnr = min.tnr, pseudo.count = pseudo.count,
use.all = use.all, do.f1score = do.f1score, category = category,
geneset = geneset, do.fast = do.fast, org = org, self.db = self.db,
self.db.only = self.db.only, ...)
all.list[[id]] <- df.s
}
}
else {
cluster.in <- intersect(clusters_to_detect, unique(Seurat::Idents(scrna)))
cluster.out <- setdiff(clusters_to_detect, unique(Seurat::Idents(scrna)))
cat(paste("These clusters are detected\n"))
cat(cluster.in)
cat(paste("\n"))
if (length(cluster.out) > 0) {
cat(paste("\nThese clusters are not in the obj\n"))
cat(cluster.out)
}
for (id in cluster.in) {
message(paste("Calculating Markers for", id))
df.s <- Detect_single_marker(scrna = scrna, id = id,
step = step, slot = slot, assay = assay, min.pct = min.pct,
min.fc = min.fc, min.tnr = min.tnr, pseudo.count = pseudo.count,
use.all = use.all, do.f1score = do.f1score, category = category,
geneset = geneset, do.fast = do.fast, org = org, self.db = self.db,
self.db.only = self.db.only, ...)
all.list[[id]] <- df.s
}
}
return(all.list)
}
#' generate html report for single markers of all cell groups
#' @param scrna seurat obj to be used
#' @param markers.list results of Detect_single_marker_all()
#' @param aggr.other whether to aggregate other celltypes
#' @param ridge_ncol
#' @param fpath Path to generate the report
#' @param fname file name. Default NULL
#' @return list of markers performance
#' @export
#'
#'
generate_report <- function(scrna, markers.list,
fpath = ".", aggr.other = F, fname = NULL,
top_n_genes = 6, ridge_ncol = 3, assay = "RNA", slot = "data", org = "human",
...){
markers.list <- markers.list
saveRDS(markers.list, file = file.path(fpath, "sc2marker.allmarkers.intermediate.rds"))
saveRDS(scrna, file = file.path(fpath, "sc2marker.scrna.intermediate.rds"))
generate_report_rmd(scrna = scrna, markers.list = markers.list, fpath = fpath,
aggr.other = aggr.other,
top_n_genes = top_n_genes,
fname = fname,
assay = assay,
slot = slot,
ridge_ncol = ridge_ncol, org = org,...)
if (is.null(fname)) {
fname.rmd <- "sc2marker.report.Rmd"
}else{
fname.rmd <- paste(fname, ".sc2marker.report.Rmd", sep = "")
}
rmarkdown::render(file.path(fpath, fname.rmd))
unlink(file.path(fpath, "sc2marker.allmarkers.intermediate.rds"))
unlink(file.path(fpath, "sc2marker.scrna.intermediate.rds"))
}
#' generate html report for single markers of all cell groups
#' @param scrna seurat obj to be used
#' @param markers.list results from Detect_single_marker_all()
#' @param top_n_genes top number of genes for RidgePlot
#' @param sc2marker_ncol number of col of Ridgeplot
#' @param fname file name. Default NULL
#' @param fpath Path to generate report
#' @return list of markers performance
#' @export
#'
#'
generate_report_rmd <- function(scrna, markers.list, aggr.other = F, top_n_genes = 6, ridge_ncol = 3,
fname = NULL, fpath = ".", assay = "RNA", slot = "data", org = "human"){
if (is.null(fname)) {
fname.rmd <- "sc2marker.report.Rmd"
}else{
fname.rmd <- paste(fname, ".sc2marker.report.Rmd", sep = "")
}
write(setup.template, file = file.path(fpath, fname.rmd))
for (id in unique(names(markers.list))) {
chunk.template.s <- chunk.template
chunk.template.s <- gsub("sc2marker_celltype", paste("\"",id, "\"", sep = ""), chunk.template.s)
chunk.template.s <- gsub("sc2marker_aggrother", aggr.other, chunk.template.s)
chunk.template.s <- gsub("sc2marker_ncol", ridge_ncol, chunk.template.s)
chunk.template.s <- gsub("sc2marker_org", paste("\"",org, "\"", sep = ""), chunk.template.s)
chunk.template.s <- gsub("top_n_genes", top_n_genes, chunk.template.s)
chunk.template.s <- gsub("sc2marker_slot", paste("\"",slot, "\"", sep = ""), chunk.template.s)
chunk.template.s <- gsub("sc2marker_assay", paste("\"",assay, "\"", sep = ""), chunk.template.s)
write(chunk.template.s, file = file.path(fpath, fname.rmd), append = T)
}
}
#########________________________________________
######### code for next version (developing)
#########________________________________________
Detect_combine_markers <- function(scrna, id, step = 0.1, category = NULL,
geneset = NULL, assay = "RNA", slot = "data",
do.fast = F, min.pct = 0.1, use.all = F, pseudo.count = 0.01){
if (is.null(geneset)) {
geneset <- rownames(scrna[[assay]])
}else{
geneset <- intersect(rownames(scrna[[assay]]), geneset)
}
if (use.all) {
geneset <- intersect(rownames(scrna[[assay]]), geneset)
de <- Seurat::FoldChange(scrna, ident.1 = id, features = geneset)
de$gene <- rownames(de)
}
if (!use.all) {
if (do.fast) {
de <- Seurat::FindMarkers(scrna, ident.1 = id, features = geneset)
de <- subset(de, p_val_adj < 0.05)
}else{
de <- Seurat::FoldChange(scrna, ident.1 = id, features = geneset)
de$gene <- rownames(de)
de <- de[de$pct.1 > min.pct, ]
}
}
de.genes.p <- subset(de, avg_log2FC > 0)
de.genes.n <- subset(de, avg_log2FC < 0)
gene.combn <- t(combn(de.genes.p$gene, 2))
gene.combn.prauc <- data.frame()
star_time <- Sys.time()
for (gene.iter in 1:nrow(gene.combn)) {
genes <- gene.combn[gene.iter,]
gene1 <- genes[1]
gene2 <- genes[2]
de <- get_split_pos_pos(scrna, gene1, gene2, id, step = step, assay = assay, slot = slot)
colnames(de) <- c("Gene1", "Gene2", "Gene1.split", "Gene2.split", "x.margin", "x.margin.adj", "TP", "FP", "Direction1", "Direction2")
gene.combn.prauc <- rbind(gene.combn.prauc, de)
}
for (gene1 in de.genes.p$gene) {
for (gene2 in de.genes.n$gene) {
de <- get_split_pos_neg(scrna, gene1, gene2, id, step = step, assay = assay, slot = slot)
colnames(de) <- c("Gene1", "Gene2", "Gene1.split", "Gene2.split", "x.margin", "x.margin.adj", "TP", "FP", "Direction1", "Direction2")
gene.combn.prauc <- rbind(gene.combn.prauc, de)
}
}
gene.combn <- t(combn(de.genes.n$gene, 2))
for (gene.iter in 1:nrow(gene.combn)) {
genes <- gene.combn[gene.iter,]
gene1 <- genes[1]
gene2 <- genes[2]
de <- get_split_neg_neg(scrna, gene1, gene2, id, step = step, assay = assay, slot = slot)
colnames(de) <- c("Gene1", "Gene2", "Gene1.split", "Gene2.split", "x.margin", "x.margin.adj", "TP", "FP", "Direction1", "Direction2")
gene.combn.prauc <- rbind(gene.combn.prauc, de)
}
end_time <- Sys.time()
# close(pb)
run_time <- end_time - star_time
print(run_time)
gene.combn.prauc <- gene.combn.prauc[order(gene.combn.prauc$x.margin.adj, decreasing = T),]
return(gene.combn.prauc)
}
#' UmapPlot based on results from Markers Greedy Search
#' @param scrna seurat objects
#' @param df.split results from Greedy Search
#' @param id cell groups to identify
#' @return
#'
# Combine_marker_umap <- function(scrna, df.split, id){
# idents.c <- Seurat::Idents(scrna)
# gene1 <- df.split$gene[1]
# gene2 <- df.split$gene[2]
# gene1.split <- df.split$split.value[1]
# gene2.split <- df.split$split.value[2]
#
# cells.1 <- GetCellNames(cbmc, gene1, gene1.split, df.split$direction[1])
# cells.2 <- GetCellNames(cbmc, gene2, gene2.split, df.split$direction[2])
# cells.1.2 <- intersect(cells.1, cells.2)
#
# Seurat::Idents(scrna) <- "other"
# Seurat::Idents(scrna, cells = cells.1) <- paste(gene1, "filter")
# p1 <- UMAPPlot(scrna, cols = c('red', "grey"))
#
# Seurat::Idents(scrna) <- "other"
# Seurat::Idents(scrna, cells = cells.2) <- paste(gene2, "filter")
# p2 <- UMAPPlot(scrna, cols = c('blue', "grey"))
#
# Seurat::Idents(scrna) <- "other"
# Seurat::Idents(scrna, cells = cells.1.2) <- paste(gene1, "+", gene2)
# p3 <- UMAPPlot(scrna, cols = c('black', "grey"))
#
# Seurat::Idents(scrna) <- idents.c
# scrna <- makeid(scrna, id)
# p4 <- UMAPPlot(scrna)
#
# plot_grid(p1, p2, p3, p4)
# }
#
# GetCellNames <- function(scrna, gene, value, direction, assay = "RNA", slot = "data"){
# # if (do.magic) {
# # df <- data.frame(exp = scrna@assays$MAGIC_RNA@data[gene,])
# # }else{
# # df <- data.frame(exp = scrna@assays$RNA@data[gene,])
# # }
# scrna@active.assay <- assay
# df <- Seurat::FetchData(scrna, vars = c(gene), slot = slot)
#
# colnames(df) <- "exp"
#
# if (direction == "+") {
# df <- subset(df, exp > value)
# }else{
# df <- subset(df, exp < value)
# }
# return(rownames(df))
# }
get_split_pos_pos <- function(scrna, gene1, gene2, id, step = 0.01, assay = "RNA", slot = "data") {
DefaultAssay(scrna) <- assay
data.mat.surf <- FetchData(scrna, vars = c(gene1, gene2, "ident"), slot = slot)
colnames(data.mat.surf) <- c("exp1", "exp2", "id")
data.mat.surf$exp1 <- normalize(data.mat.surf$exp1)
data.mat.surf$exp2 <- normalize(data.mat.surf$exp2)
sp1 = boxplot.stats(data.mat.surf$exp1)$out
sp2 = boxplot.stats(data.mat.surf$exp2)$out
`%notin%` <- Negate(`%in%`)
data.mat.surf <- data.mat.surf[data.mat.surf$exp2 %notin% sp2 & data.mat.surf$exp1 %notin% sp1, ]
gene.prauc <- data.frame(x.val <- c(),
margin <- c())
data.id <- data.mat.surf[data.mat.surf$id == id,]
data.other <- data.mat.surf[data.mat.surf$id != id,]
data.id.l <- nrow(data.id)
data.o.l <- nrow(data.other)
data.all.l <- nrow(data.mat.surf)
# size.factor <- nrow(data.mat.surf)/nrow(data.id)
size.factor <- nrow(data.mat.surf)/nrow(data.other)
# size.factor <- ifelse(size.factor < 3, 3, size.factor)
for (x.val in seq(0.01, 1, step)) {
for (y.val in seq(0.01, 1, step)) {
data.i.a <- data.id[data.id$exp1 > x.val & data.id$exp2 > y.val, ]
tp <- nrow(data.i.a)
data.o.a <- data.other[data.other$exp1 > x.val & data.other$exp2 > y.val, ]
fp <- nrow(data.o.a)
# x.margin <- tp*size.factor - fp#*size.factor
x.margin <- tp - fp*size.factor
# x.margin <- tp*nrow(data.other) - fp*nrow(data.id)
x.margin <- x.margin/data.all.l
de <- data.frame(gene1, gene2, x.val, y.val, x.margin)
gene.prauc <- rbind(gene.prauc, de)
}
}
gene.prauc <- gene.prauc[order(gene.prauc$x.margin, decreasing = T),]
x.split <- gene.prauc[1,]
x.val <- x.split[,3]
y.val <- x.split[,4]
x.margin <- x.split[,5]
data.i.a <- data.id[data.id$exp1 > x.val & data.id$exp2 > y.val, ]
tp <- nrow(data.i.a)
data.o.a <- data.other[data.other$exp1 > x.val & data.other$exp2 > y.val, ]
fp <- nrow(data.o.a)
data.o.b <- data.other[data.other$exp1 <= x.val | data.other$exp2 <= y.val, ]
tn <- nrow(data.o.b)
x.margin.a <- sum((data.i.a$exp1 - x.val))*nrow(data.o.a) + sum((data.i.a$exp2 - y.val))*nrow(data.o.a) -#+
# sum((x.val -data.o.b$exp1))*nrow(data.id) + sum((y.val -data.o.b$exp2))*nrow(data.id) -
sum((data.o.a$exp1 - x.val))*nrow(data.i.a) - sum((data.o.a$exp2 - y.val))*nrow(data.i.a)
x.margin.a <- ifelse(x.margin.a > 1, x.margin.a, 1)
# x.margin.a2 <- ifelse(x.margin.a2 > 1, x.margin.a2, 1)
x.margin.a <- log(x.margin.a)
x.margin.adj <- x.margin*(tp/data.id.l)*(tn/data.o.l)*x.margin.a#*x.margin.a2
# x.margin.adj <- x.margin.a
x.split <- data.frame(gene1, gene2, x.val, y.val, x.margin, x.margin.adj, tp, fp, "+", "+", x.margin.a)
return(x.split)
}
get_split_pos_neg <- function(scrna, gene1, gene2, id, step = 0.01, assay = "RNA", slot = "data") {
Seurat::DefaultAssay(scrna) <- assay
data.mat.surf <- Seurat::FetchData(scrna, vars = c(gene1, gene2, "ident"), slot = slot)
colnames(data.mat.surf) <- c("exp1", "exp2", "id")
data.mat.surf$exp1 <- normalize(data.mat.surf$exp1)
data.mat.surf$exp2 <- normalize(data.mat.surf$exp2)
sp1 = boxplot.stats(data.mat.surf$exp1)$out
sp2 = boxplot.stats(data.mat.surf$exp2)$out
`%notin%` <- Negate(`%in%`)
data.mat.surf <- data.mat.surf[data.mat.surf$exp2 %notin% sp2 & data.mat.surf$exp1 %notin% sp1, ]
if(max(data.mat.surf$exp2) == 0 | max(data.mat.surf$exp1) == 0){
x.split <- data.frame(gene1, gene2, 0, 0, 0, 0, 0, 0, "+", "-")
return(x.split)
}
gene.prauc <- data.frame(x.val <- c(),
margin <- c())
data.id <- data.mat.surf[data.mat.surf$id == id,]
data.other <- data.mat.surf[data.mat.surf$id != id,]
data.id.l <- nrow(data.id)
data.o.l <- nrow(data.other)
data.all.l <- nrow(data.mat.surf)
size.factor <- nrow(data.mat.surf)/nrow(data.other)
for (x.val in seq(0.01, 1, 0.1)) {
for (y.val in seq(0.01, 1, 0.1)) {
data.i.a <- data.id[data.id$exp1 > x.val & data.id$exp2 < y.val, ]
tp <- nrow(data.i.a)
data.o.a <- data.other[data.other$exp1 > x.val & data.other$exp2 < y.val, ]
fp <- nrow(data.o.a)
# x.margin <- tp*size.factor - fp
x.margin <- tp - fp*size.factor
# x.margin <- tp*nrow(data.other) - fp*nrow(data.id)
x.margin <- x.margin/data.all.l
de <- data.frame(gene1, gene2, x.val, y.val, x.margin)
gene.prauc <- rbind(gene.prauc, de)
}
}
gene.prauc <- gene.prauc[order(gene.prauc$x.margin, decreasing = T),]
x.split <- gene.prauc[1,]
x.val <- x.split[,3]
y.val <- x.split[,4]
x.margin <- x.split[,5]
data.i.a <- data.id[data.id$exp1 > x.val & data.id$exp2 < y.val, ]
tp <- nrow(data.i.a)
data.o.a <- data.other[data.other$exp1 > x.val & data.other$exp2 < y.val, ]
fp <- nrow(data.o.a)
data.o.b <- data.other[data.other$exp1 <= x.val | data.other$exp2 >= y.val, ]
tn <- nrow(data.o.b)
x.margin.a <- sum((data.i.a$exp1 - x.val))*nrow(data.o.a) + sum((y.val - data.i.a$exp2))*nrow(data.o.a) -#+
# sum((x.val - data.o.b$exp1))*nrow(data.id) + sum((data.o.b$exp2 - y.val))*nrow(data.id) -
sum((data.o.a$exp1 - x.val))*nrow(data.i.a) - sum((y.val - data.o.a$exp2))*nrow(data.i.a)
# x.margin.a <- x.margin.a/(nrow(data.i.a) + nrow(data.o.a))
x.margin.a2 <- sum((x.val - data.o.b$exp1))*nrow(data.id) + sum((data.o.b$exp2 - y.val))*nrow(data.id)
x.margin.a <- ifelse(x.margin.a > 1, x.margin.a, 1)
x.margin.a2 <- ifelse(x.margin.a2 > 1, x.margin.a2, 1)
x.margin.a <- log(x.margin.a)
x.margin.a2 <- log(x.margin.a2)
x.margin.a2 <- ifelse(x.margin.a2 > 1, x.margin.a2, 1)
# x.margin.a <- dist.i.a*nrow(data.other) - dist.o.a*nrow(data.id)# + dist.o.b*nrow(data.id)
x.margin.adj <- x.margin*(tp/data.id.l)*(tn/data.o.l)*x.margin.a#*x.margin.a2
# x.margin.adj <- x.margin.a
x.split <- data.frame(gene1, gene2, x.val, y.val, x.margin, x.margin.adj, tp, fp, "+", "-")
return(x.split)
}
get_split_neg_neg <- function(scrna, gene1, gene2, id, step = 0.01, assay = "RNA", slot = "data") {
Seurat::DefaultAssay(scrna) <- assay
# scrna@active.assay <- assay
data.mat.surf <- Seurat::FetchData(scrna, vars = c(gene1, gene2, "ident"), slot = slot)
colnames(data.mat.surf) <- c("exp1", "exp2", "id")
data.mat.surf$exp1 <- normalize(data.mat.surf$exp1)
data.mat.surf$exp2 <- normalize(data.mat.surf$exp2)
sp1 = boxplot.stats(data.mat.surf$exp1)$out
sp2 = boxplot.stats(data.mat.surf$exp2)$out
`%notin%` <- Negate(`%in%`)
data.mat.surf <- data.mat.surf[data.mat.surf$exp2 %notin% sp2 & data.mat.surf$exp1 %notin% sp1, ]
if(max(data.mat.surf$exp2) == 0 | max(data.mat.surf$exp1) == 0){
x.split <- data.frame(gene1, gene2, 0, 0, 0, 0, 0, 0, "-", "-")
return(x.split)
}
gene.prauc <- data.frame(x.val <- c(),
margin <- c())
data.id <- data.mat.surf[data.mat.surf$id == id,]
data.other <- data.mat.surf[data.mat.surf$id != id,]
data.id.l <- nrow(data.id)
data.o.l <- nrow(data.other)
data.all.l <- nrow(data.mat.surf)
size.factor <- nrow(data.mat.surf)/nrow(data.other)
for (x.val in seq(0.01, 1, step)) {
for (y.val in seq(0.01, 1, step)) {
data.i.a <- data.id[data.id$exp1 < x.val & data.id$exp2 < y.val, ]
tp <- nrow(data.i.a)
data.o.a <- data.other[data.other$exp1 < x.val & data.other$exp2 < y.val, ]
fp <- nrow(data.o.a)
x.margin <- tp - fp*size.factor
# x.margin <- tp*nrow(data.other) - fp*nrow(data.id)
x.margin <- x.margin/data.all.l
de <- data.frame(gene1, gene2, x.val, y.val, x.margin)
gene.prauc <- rbind(gene.prauc, de)
}
}
gene.prauc <- gene.prauc[order(gene.prauc$x.margin, decreasing = T),]
x.split <- gene.prauc[1,]
x.val <- x.split[,3]
y.val <- x.split[,4]
x.margin <- x.split[,5]
data.i.a <- data.id[data.id$exp1 < x.val & data.id$exp2 < y.val, ]
tp <- nrow(data.i.a)
data.o.a <- data.other[data.other$exp1 < x.val & data.other$exp2 < y.val, ]
fp <- nrow(data.o.a)
data.o.b <- data.other[data.other$exp1 >= x.val | data.other$exp2 >= y.val, ]
tn <- nrow(data.o.b)
x.margin.a <- sum((x.val - data.i.a$exp1))/nrow(data.o.a) + sum((y.val - data.i.a$exp2))*nrow(data.o.a) -#+
# sum((data.o.b$exp1 - x.val))*nrow(data.id) + sum((data.o.b$exp2 - y.val))*nrow(data.id) -
sum((x.val - data.o.a$exp1))*nrow(data.i.a) - sum((y.val - data.o.a$exp2))*nrow(data.i.a)
x.margin.a <- ifelse(x.margin.a > 1, x.margin.a, 1)
x.margin.a <- log(x.margin.a)
x.margin.adj <- x.margin*(tp/data.id.l)*(tn/data.o.l)*x.margin.a#*x.margin.a2
# x.margin.adj <- x.margin.a
x.split <- data.frame(gene1, gene2, x.val, y.val, x.margin, x.margin.adj, tp, fp, "-", "-")
return(x.split)
}
#
# marker_stepbystep <- function(scrna, cellgroup, depth = 2, geneset = NULL, step = 0.01){
# if (is.null(geneset)) {
# geneset <- rownames(scrna)
# }
# geneset <- intersect(rownames(scrna[["RNA"]]), geneset)
# len.id <- sum(Seurat::Idents(scrna) == cellgroup)
# len.other <- sum(Seurat::Idents(scrna) != cellgroup)
# df.split <- data.frame()
#
# for (variable in seq(depth)) {
# markers <- FindMarkers(scrna, ident.1 = cellgroup, features = geneset)
# markers <- subset(markers, p_val_adj < 0.05)
#
# markers.pos <- subset(markers, avg_log2FC > 0)
# markers.neg <- subset(markers, avg_log2FC < 0)
#
# gene.prauc <- data.frame()
#
# for (genes in rownames(markers.pos)) {
# de <- data.frame(genes, get_split_pos(scrna, genes, cellgroup, step))
# names(de)<-c("gene", "split.value","filtered.adj", "direction")
# gene.prauc <- rbind(gene.prauc, de)
# }
# for (genes in rownames(markers.neg)) {
# de <- data.frame(genes, get_split_neg(scrna, genes, cellgroup, step))
# names(de)<-c("gene", "split.value","filtered.adj", "direction")
# gene.prauc <- rbind(gene.prauc, de)
# }
# gene.prauc <- gene.prauc[order(gene.prauc$filtered.adj, decreasing = T),]
#
# df.split <- rbind(df.split, gene.prauc[1,])
#
# left.cells <- GetCellNames(scrna, gene.prauc[1,1], gene.prauc[1,2], gene.prauc[1,4])
# scrna <- subset(scrna, cells = left.cells)
# }
# return(df.split)
# }
# marker_stepbystep.2 <- function(scrna, cellgroup, depth = 2, geneset = NULL, step = 0.01, assay = "RNA", slot = "data", max.recall = T){
# if (is.null(geneset)) {
# geneset <- rownames(scrna[["RNA"]])
# }
# geneset <- intersect(rownames(scrna[["RNA"]]), geneset)
# len.id <- sum(Seurat::Idents(scrna) == cellgroup)
# len.other <- sum(Seurat::Idents(scrna) != cellgroup)
# df.split <- data.frame()
#
# suppressWarnings(
# for (variable in seq(depth)) {
# df.fc <- FoldChange(scrna, ident.1 = cellgroup, features = geneset)
#
# markers.pos <- subset(df.fc, avg_log2FC > 0)
# markers.neg <- subset(df.fc, avg_log2FC < 0)
#
# gene.prauc <- data.frame()
#
# for (genes in rownames(markers.pos)) {
# de <- data.frame(get_gene_score_pos(scrna, genes, cellgroup, step, assay = assay, slot = slot))
# names(de)<-c("gene", "split.value","x.margin", "x.margin.adj", "tp", "fp", "direction")
# gene.prauc <- rbind(gene.prauc, de)
# }
# for (genes in rownames(markers.neg)) {
# de <- data.frame(get_gene_score_neg(scrna, genes, cellgroup, step, assay = assay, slot = slot))
# names(de)<-c("gene", "split.value","x.margin", "x.margin.adj", "tp", "fp", "direction")
# gene.prauc <- rbind(gene.prauc, de)
# }
# gene.prauc <- gene.prauc[order(gene.prauc$x.margin.adj, decreasing = T),]
#
# df <- gene.prauc[1,]
# if (df$direction == "+") {
# split.step <- get_split_pos(scrna, df$gene, cellgroup, assay = assay, slot = slot, max.recall = T)
# }else{
# split.step <- get_split_neg(scrna, df$gene, cellgroup, assay = assay, slot = slot, max.recall = T)
# }
#
# names(split.step) <- c("Gene", "split.value", "direction")
#
# df.split <- rbind(df.split, split.step)
# left.cells <- GetCellNames(scrna = scrna, gene = df$gene, value = df.split$split.value, direction = df.split$direction, assay = assay, slot = slot)
# scrna <- subset(scrna, cells = left.cells)
# geneset <- setdiff(geneset, df$gene)
# }
# )
# return(df.split)
# }
plot_combine_PRAUC <- function(scrna, gene1, gene2, id, step = 0.01, return.obj = F){
x.df <- get_PRAUC_matrix_combine_markers(scrna, gene1, gene2, id = id, step = step)
g <- ggplot() + geom_line(x.df, mapping = aes(x.rec, x.pre)) + xlim(c(0,1)) + ylim(c(0,1))
if (!return.obj) {
print(g)
}else{
return(g)
}
}
get_split_pos_tp <- function(scrna, gene, id, step = 0.01) {
data.mat.surf <- data.frame(exp = scrna@assays$RNA@data[gene,],
id = as.character(Seurat::Idents(makeid(scrna, id))))
gene.prauc <- data.frame(x.val <- c(),
margin <- c())
data.id <- data.mat.surf[data.mat.surf$id == id,]
data.other <- data.mat.surf[data.mat.surf$id != id,]
x.factor <- length(data.other$id)/length(data.id$id)
x.max <- max(data.id$exp)
x.min <- min(data.id$exp)
for (x.val in seq(x.min + (x.max - x.min)/100, x.max, (x.max - x.min)/100)) {
tp <- sum(data.id$exp >= x.val)
fp <- sum(data.other$exp >= x.val)
tn <- sum(data.other$exp < x.val)
fn <- sum(data.id$exp < x.val)
if (length(data.id$id) <= length(data.other$id)) {
x.margin <- tp*x.factor - fp
}
else{
x.margin <- tp - fp
}
de <- data.frame(x.val, x.margin, "+")
gene.prauc <- rbind(gene.prauc, de)
}
gene.prauc <- gene.prauc[order(gene.prauc$x.margin, decreasing = T),]
x.split <- gene.prauc[1,]
rownames(x.split) <- paste(gene)
return(x.split)
}
get_split_neg_tp <- function(scrna, gene, id, step = 0.01) {
data.mat.surf <- data.frame(exp = scrna@assays$RNA@data[gene,],
id = as.character(Seurat::Idents(makeid(scrna, id))))
gene.prauc <- data.frame(x.val <- c(),
margin <- c())
data.id <- data.mat.surf[data.mat.surf$id == id,]
data.other <- data.mat.surf[data.mat.surf$id != id,]
x.factor <- length(data.other$id)/length(data.id$id)
x.max <- max(data.id$exp)
x.min <- min(data.id$exp)
for (x.val in seq(x.min, x.max, (x.max - x.min)/100)) {
tp <- sum(data.id$exp < x.val)
fp <- sum(data.other$exp < x.val)
tn <- sum(data.other$exp >= x.val)
fn <- sum(data.id$exp >= x.val)
if (length(data.id$id) <= length(data.other$id)) {
x.margin <- tp*x.factor - fp
}
else{
x.margin <- tp - fp
}
de <- data.frame(x.val, x.margin, "-")
gene.prauc <- rbind(gene.prauc, de)
}
gene.prauc <- gene.prauc[order(gene.prauc$x.margin, decreasing = T),]
x.split <- gene.prauc[1,]
rownames(x.split) <- paste(gene)
return(x.split)
}
get_PRAUC_matrix_combine_markers_neg_pos <- function(scrna, gene1, gene2, id, step = 0.01){
data.mat.surf <- data.frame(gene1 = scrna@assays$RNA@data[gene1,],
gene2 = scrna@assays$RNA@data[gene2,],
id = as.character(Seurat::Idents(makeid(scrna, id))))
gene.prauc <- data.frame(x.pre <- c(),
x.rec <- c())
data.id <- data.mat.surf[data.mat.surf$id == id,]
data.other <- data.mat.surf[data.mat.surf$id != id,]
gene1.min <- min(data.id$gene1)
gene2.max <- max(data.id$gene2)
gene1.range <- max(data.id$gene1) - gene1.min
gene2.range <- gene2.max - min(data.id$gene2)
for (x.seq in seq(0.05, 0.95, step)) {
x.val <- gene1.min + x.seq*gene1.range
y.val <- gene2.max - x.seq*gene2.range
tp <- sum(data.id$gene1 >= x.val & data.id$gene2 <= y.val)
fp <- sum(data.other$gene1 >= x.val & data.other$gene2 <= y.val)
# tn <- sum(data.other$gene1 < x.val | data.other$gene2 < y.val)
fn <- sum(data.id$gene1 < x.val | data.id$gene2 > y.val)
x.pre <- tp/(tp + fp)
x.rec <- tp/(tp + fn)
de <- data.frame(x.pre, x.rec)
gene.prauc <- rbind(gene.prauc, de)
}
gene.prauc <- gene.prauc[complete.cases(gene.prauc), ]
gene.prauc <- gene.prauc[order(gene.prauc$x.rec), ]
return(gene.prauc)
}
get_PRAUC_matrix_combine_markers_neg <- function(scrna, gene1, gene2, id, step = 0.01){
data.mat.surf <- data.frame(gene1 = scrna@assays$RNA@data[gene1,],
gene2 = scrna@assays$RNA@data[gene2,],
id = as.character(Seurat::Idents(makeid(scrna, id))))
gene.prauc <- data.frame(x.pre <- c(),
x.rec <- c())
data.id <- data.mat.surf[data.mat.surf$id == id,]
data.other <- data.mat.surf[data.mat.surf$id != id,]
for (x.seq in seq(0.05, 1, step)) {
x.val = quantile(data.id$gene1, x.seq)
y.val = quantile(data.id$gene2, x.seq)
tp <- sum(data.id$gene1 < x.val & data.id$gene2 < y.val)
fp <- sum(data.other$gene1 < x.val & data.other$gene2 < y.val)
# tn <- sum(data.other$gene1 < x.val | data.other$gene2 < y.val)
fn <- sum(data.id$gene1 >= x.val | data.id$gene2 >= y.val)
x.pre <- tp/(tp + fp)
x.rec <- tp/(tp + fn)
de <- data.frame(x.pre, x.rec)
gene.prauc <- rbind(gene.prauc, de)
}
gene.prauc <- gene.prauc[complete.cases(gene.prauc), ]
gene.prauc <- gene.prauc[order(gene.prauc$x.rec), ]
return(gene.prauc)
}
get_PRAUC_matrix_combine_markers <- function(scrna, gene1, gene2, id, step = 0.01){
data.mat.surf <- data.frame(gene1 = scrna@assays$RNA@data[gene1,],
gene2 = scrna@assays$RNA@data[gene2,],
id = as.character(Seurat::Idents(makeid(scrna, id))))
gene.prauc <- data.frame(x.pre <- c(),
x.rec <- c())
data.id <- data.mat.surf[data.mat.surf$id == id,]
data.other <- data.mat.surf[data.mat.surf$id != id,]
for (x.seq in seq(0, 0.95, step)) {
x.val = quantile(data.id$gene1, x.seq)
y.val = quantile(data.id$gene2, x.seq)
tp <- sum(data.id$gene1 >= x.val & data.id$gene2 >= y.val)
fp <- sum(data.other$gene1 >= x.val & data.other$gene2 >= y.val)
# tn <- sum(data.other$gene1 < x.val | data.other$gene2 < y.val)
fn <- sum(data.id$gene1 < x.val | data.id$gene2 < y.val)
x.pre <- tp/(tp + fp)
x.rec <- tp/(tp + fn)
de <- data.frame(x.pre, x.rec)
gene.prauc <- rbind(gene.prauc, de)
}
gene.prauc <- gene.prauc[complete.cases(gene.prauc), ]
gene.prauc <- gene.prauc[order(gene.prauc$x.rec), ]
return(gene.prauc)
}
#' Detect greedy step by step filters for cell group identification
#' @param scrna seurat object
#' @param cellgroup, interested cell group
#' @param depth how much steps to filter
#' @param geneset Gene set to be used
#' @return
plot_filter_stepbystep_first2 <- function(scrna, df.split, id, step = 0.01){
gene1 <- df.split$gene[1]
gene2 <- df.split$gene[2]
df <- data.frame(exp1 = scrna@assays$RNA@data[gene1,],
exp2 = scrna@assays$RNA@data[gene2,],
id = as.character(Seurat::Idents(makeid(scrna, id))))
x.split <- df.split$split.value[1]
y.split <- df.split$split.value[2]
ggplot(df)+
geom_point(aes(exp1, exp2, color = id)) +
geom_segment(aes(x = x.split, y = y.split, xend = max(exp1), yend = y.split), linetype = 2)+
geom_segment(aes(x = x.split, y = y.split, xend = x.split, yend = max(exp2)), linetype = 2)+
xlab(paste(gene1)) + ylab(paste(gene2))
}
plot_filter_combination_first2 <- function(scrna, df.split, id, step = 0.01){
gene1 <- df.split$gene[1]
gene2 <- df.split$gene[2]
df <- data.frame(exp1 = scrna@assays$RNA@data[gene1,],
exp2 = scrna@assays$RNA@data[gene2,],
ID = as.character(Seurat::Idents(makeid(scrna, id))))
x.split <- df.split$split.value[1]
y.split <- df.split$split.value[2]
g <- ggplot(df)+
geom_point(aes(exp1, exp2, color = ID))
if (df.split$direction[2] == "+") {
g <- g + geom_segment(aes(x = x.split, y = y.split, xend = x.split, yend = max(exp2)), linetype = 2)
}else{
g <- g + geom_segment(aes(x = x.split, y = y.split, xend = x.split, yend = min(exp2)), linetype = 2)
}
if(df.split$direction[1] == "+") {
g <- g + geom_segment(aes(x = x.split, y = y.split, xend = max(exp1), yend = y.split), linetype = 2)
}else{
g <- g + geom_segment(aes(x = x.split, y = y.split, xend = min(exp1), yend = y.split), linetype = 2)
}
g <- g + xlab(paste(gene1)) + ylab(paste(gene2))
print(g)
}
#
# Combine_markers_point_plot <- function(scrna, c.markers, id, ranking = 1, assay = "RNA", slot = "data", return.obj = F, step = 0.01, max.recall = F){
# scrna@active.assay = assay
# markers.c <- c.markers[ranking, ]
# scrna@active.assay = assay
# df <- Seurat::FetchData(scrna, vars = c(markers.c$Gene1, markers.c$Gene2, "ident"))
# gene1 <- markers.c$Gene1
# gene2 <- markers.c$Gene2
# colnames(df) <- c("exp1", "exp2", "id")
# gene1.direc = markers.c$Direction1
# gene2.direc = markers.c$Direction2
# if (max.recall) {
# if (gene1.direc == "+") {
# x.split <- get_split_pos(scrna, gene1, id, step = step, assay = assay, slot = slot, max.recall = max.recall)$split.value
# }else{
# x.split <- get_split_neg(scrna, gene1, id, step = step, assay = assay, slot = slot, max.recall = max.recall)$split.value
# }
# left.cells <- GetCellNames(scrna, markers.c$Gene1, x.split, markers.c$Direction1, assay = assay, slot = slot)
# scrna.left <- subset(scrna, cells = left.cells)
#
# if (gene2.direc == "+") {
# y.split <- get_split_pos(scrna.left, gene2, id, step = step, assay = assay, slot = slot, max.recall = max.recall)$split.value
# }else{
# y.split <- get_split_neg(scrna.left, gene2, id, step = step, assay = assay, slot = slot, max.recall = max.recall)$split.value
# }
#
# left.cells <- GetCellNames(scrna, markers.c$Gene2, y.split, markers.c$Direction2, assay = assay, slot = slot)
# scrna.left <- subset(scrna.left, cells = left.cells)
#
#
# left.cells <- GetCellNames(scrna, markers.c$Gene2, y.split, markers.c$Direction2, assay = assay, slot = slot)
# scrna.left <- subset(scrna.left, cells = left.cells)
# }else {
# if (gene1.direc == "+" & gene2.direc == "+") {
# df.c <-get_split_pos_pos(scrna, gene1 = gene1, gene2 = gene2, id = id, assay = assay, slot = slot, step = step)
# colnames(df.c) <- c("Gene1", "Gene2", "Gene1.split", "Gene2.split", "x.margin", "x.margin.adj", "TP", "FP", "Direction1", "Direction2")
# }
# if (gene1.direc == "+" & gene2.direc == "-") {
# df.c <-get_split_pos_neg(scrna, gene1 = gene1, gene2 = gene2, id = id, assay = assay, slot = slot, step = step)
# colnames(df.c) <- c("Gene1", "Gene2", "Gene1.split", "Gene2.split", "x.margin", "x.margin.adj", "TP", "FP", "Direction1", "Direction2")
# }
# if (gene1.direc == "-" & gene2.direc == "-") {
# df.c <-get_split_neg_neg(scrna, gene1 = gene1, gene2 = gene2, id = id, assay = assay, slot = slot, step = step)
# colnames(df.c) <- c("Gene1", "Gene2", "Gene1.split", "Gene2.split", "x.margin", "x.margin.adj", "TP", "FP", "Direction1", "Direction2")
# }
#
# x.split <- df.c$Gene1.split*max(df$exp1) + min(df$exp1)
# y.split <- df.c$Gene2.split*max(df$exp2) + min(df$exp2)
#
# left.cells <- GetCellNames(scrna, markers.c$Gene1, x.split, markers.c$Direction1, assay = assay, slot = slot)
# scrna.left <- subset(scrna, cells = left.cells)
# left.cells <- GetCellNames(scrna, markers.c$Gene2, y.split, markers.c$Direction2, assay = assay, slot = slot)
# scrna.left <- subset(scrna.left, cells = left.cells)
#
# }
#
# tp <- sum(Seurat::Idents(scrna.left) == id)
# fp <- sum(Seurat::Idents(scrna.left) != id)
# x.pre <- tp/(tp+fp)
# x.pre <- round(x.pre, 3)
# x.rec <- sum(Seurat::Idents(scrna.left) == id)/sum(Seurat::Idents(scrna.left) == id)
# x.rec <- round(x.rec, 3)
#
# g <- ggplot(df)+
# geom_point(aes(exp1, exp2, color = id))
#
# if (gene2.direc == "+") {
# g <- g + geom_segment(aes(x = x.split, y = y.split, xend = x.split, yend = max(exp2)), linetype = 2)
# }else{
# g <- g + geom_segment(aes(x = x.split, y = y.split, xend = x.split, yend = min(exp2)), linetype = 2)
# }
#
# if(gene1.direc == "+") {
# g <- g + geom_segment(aes(x = x.split, y = y.split, xend = max(exp1), yend = y.split), linetype = 2)
# }else{
# g <- g + geom_segment(aes(x = x.split, y = y.split, xend = min(exp1), yend = y.split), linetype = 2)
# }
#
# g <- g + xlab(paste(markers.c$Gene1, "--Recall: ", x.rec,"; Precision: ", x.pre, sep = "")) + ylab(paste(markers.c$Gene2))
# if (return.obj) {
# return(g)
# }
# print(g)
# }
#
# GetCellNames <- function(scrna, gene, value, direction){
# df <- data.frame(exp = scrna@assays$RNA@data[gene,])
# if (direction == "+") {
# df <- subset(df, exp >= value)
# }else{
# df <- subset(df, exp <= value)
# }
# return(rownames(df))
# }
#
# grid_plot <- function(scrna, df.split, cellgroup){
# x.len <- length(df.split$gene)
# plots = list()
# # scrna.id <- Idents(scrna)
# scrna <- makeid(scrna, cellgroup)
# scrna.left <- scrna
# for (gene in df.split$gene) {
# plots[[gene]] <- VlnPlot(scrna.left, features = gene) + geom_hline(yintercept=df.split[df.split$gene == gene, ]$split.value, linetype = 1)
# left.cells <- GetCellNames(scrna.left, gene, df.split[df.split$gene == gene, ]$split.value, df.split[df.split$gene == gene, ]$direction)
# scrna.left <- subset(scrna.left, cells = left.cells)
# tp <- sum(Seurat::Idents(scrna.left) == cellgroup)
# fp <- sum(Seurat::Idents(scrna.left) != cellgroup)
# x.pre <- round(tp/(tp+fp), 3)
# x.rec <- sum(Seurat::Idents(scrna.left) == cellgroup)/sum(Seurat::Idents(scrna) == cellgroup)
# x.rec <- round(x.rec, 3)
# plots[[gene]] <- plots[[gene]] + xlab(paste("Precision:", x.pre, " Recall:", x.rec, sep = ""))
# plots[[gene]] <- plots[[gene]] + ggtitle(paste(gene, df.split[df.split$gene == gene, ]$direction))
# }
# plot_grid(plotlist=plots)
# }
#' Get cell names which meet cutoff
#' @param scrna seurat obj to be used
#' @param geneset custom genes to test, all genes in obj to use if NULL
#' @param id interested cell group
#' @param category indicate the ICC/IHC/Flow, if NULL use all genes.
#' @param assay indicate the assay to compute
#' @param slot indicate the slot of data to compute
#' @param step quantile steps
#' @param min.pct only test genes that are detected in a minimum fraction of min.pct cells in either of the two populations. Meant to speed up the function by not testing genes that are very infrequently expressed. Default is 0.1
#' @param use.all Don't do any filter on input geneset
#' @return list of markers performance
#'
# GetGenes <- function(scrna, slot = "data", category = NULL, geneset = NULL,
# assay = "RNA", min.pct = 0.1, use.all = F, species = "Human"){
# if (category == "IHC") {
# genes.touse <- IHC$Gene
# }else if (category == "ICC") {
# genes.touse <- ICC$Gene
# }else if (category == "Flow") {
# genes.touse <- surface.genes
# }
#
# if (!is.null(category) & is.null(geneset)) {
# print("Use self define genes should set the category to NULL")
# return(NULL)
# }
#
# if (is.null(category) & is.null(geneset)) {
# genes.touse <- rownames(scrna[[assay]])
# }else if (is.null(category) & !is.null(geneset)){
# genes.touse <- intersect(rownames(scrna[[assay]]), geneset)
# }
#
# if (length(genes.touse) == 0) {
# print("Find none of genes in the obj")
# return(NULL)
# }
#
# if (use.all) {
# geneset <- intersect(rownames(scrna[[assay]]), geneset)
# de <- Seurat::FoldChange(scrna, ident.1 = id, features = geneset)
# }
# if (!use.all) {
# if (do.fast) {
# de <- Seurat::FindMarkers(scrna, ident.1 = id, features = geneset)
# de <- subset(de, p_val_adj < 0.05)
# }else{
# de <- Seurat::FoldChange(scrna, ident.1 = id, features = geneset)
# de <- de[de$pct.1 > min.pct, ]
# }
# }
#
#
# de$gene <- rownames(de)
# markers.pos <- de
# markers.neg <- de
#
# gene.rank.list <- data.frame()
#
# for (genes in rownames(markers.pos)) {
# de <- data.frame(get_gene_score_pos(scrna, genes, id, step, assay = assay, slot = slot))
# names(de)<-c("gene", "split.value","x.margin", "x.margin.adj", "tp", "fp", "direction")
# gene.rank.list <- rbind(gene.rank.list, de)
# }
# for (genes in rownames(markers.neg)) {
# de <- data.frame(get_gene_score_neg(scrna, genes, id, step, assay = assay, slot = slot))
# names(de)<-c("gene", "split.value","x.margin", "x.margin.adj", "tp", "fp", "direction")
# gene.rank.list <- rbind(gene.rank.list, de)
# }
# gene.rank.list <- gene.rank.list[order(gene.rank.list$x.margin.adj, decreasing = T),]
# rownames(gene.rank.list) <- seq(nrow(gene.rank.list))
# return(gene.rank.list)
# }
#' Calculate gene positive specific score
#'
#' Calculate gene specific score in positive direction
#' @param scrna obj to use
#' @param id interested cell id
#' @param gene gene to use
#' @param step quantile step
#' @param assay which assay to use in obj, default RNA
#' @param slot which slot to use, default data
#' @export
#' @examples
#' @return seurat obj with re-set Idents
#'
get_gene_score_pos <- function(scrna, gene, id, step = 0.01, assay = "RNA", slot = "data", pseudo.count = 0.01) {
scrna@active.assay <- assay
exprs.matrix <- Seurat::FetchData(scrna, vars = c(gene, "ident"), slot = slot)
colnames(exprs.matrix) <- c("exp", "id")
# exprs.matrix$
exprs.matrix <- data.table::as.data.table(exprs.matrix)
exprs.max <- max(exprs.matrix$exp)
exprs.min <- min(exprs.matrix$exp)
exprs.matrix$exp <- normalize(exprs.matrix$exp)
exprs.matrix$exp <- round(exprs.matrix$exp, 3)
gene.prauc.p <- data.frame(x.val <- c(),
margin <- c())
celltype.in <- id
data.id <- subset(exprs.matrix, id == celltype.in)
data.other <- subset(exprs.matrix, id != celltype.in)
data.id.l <- nrow(data.id)
data.o.l <- nrow(data.other)
data.all.l <- nrow(exprs.matrix)
for (x.val in seq(0.01, 0.99, step)) {
data.i.a <- subset(data.id, exp > x.val)
data.o.a <- subset(data.other, exp > x.val)
data.i.b <- subset(data.id, exp <= x.val)
data.o.b <- subset(data.other, exp <= x.val)
x.margin.p <- sum((data.i.a$exp - x.val))*nrow(data.o.b) +
sum((x.val - data.o.b$exp))*nrow(data.i.a) -
sum((data.o.a$exp - x.val))*nrow(data.i.b)# +
x.margin.p <- x.margin.p/data.all.l
de.p <- data.frame(x.val, x.margin.p)
gene.prauc.p <- rbind(gene.prauc.p, de.p)
}
gene.prauc.p <- gene.prauc.p[order(gene.prauc.p$x.margin, decreasing = T),]
# gene.prauc.n <- gene.prauc.n[order(gene.prauc.n$x.margin, decreasing = T),]
# pos
x.split <- gene.prauc.p[1,]
x.val <- x.split[,1]
x.margin <- x.split[,2]
tp <- sum(data.id$exp > x.val)
fp <- sum(data.other$exp > x.val)
fn <- sum(data.id$exp <= x.val)
tn <- sum(data.other$exp <= x.val)
fp.pro <- subset(data.other, exp > x.val)
fp.pro <- as.data.frame(table(fp.pro$id))
fp.pro <- fp.pro[order(fp.pro$Freq, decreasing = T),]
if (nrow(fp.pro) >= 5) {
fp.pro <- fp.pro[1:5,]
}
fp.string <- paste(fp.pro$Var1, fp.pro$Freq)
fp.string <- toString(fp.string)
x.factor.p <- (mean(data.id$exp) + pseudo.count)/(mean(data.other$exp) + pseudo.count)
# x.factor.p <- (mean(data.id$exp) + pseudo.count)/(mean(data.other$exp) + pseudo.count)
x.margin.adj <- x.margin*(tp/data.id.l)*(tn/data.o.l)*(x.factor.p**2)
x.val <- x.val*exprs.max + exprs.min
x.split.p <- data.frame(gene, x.val, x.margin, x.margin.adj, tp, fp, tn, fn, "+", fp.string)
return(x.split.p)
}
#' Calculate gene negative specific score
#'
#' Calculate gene specific score in negative direction
#' @param scrna obj to use
#' @param id interested cell id
#' @param gene gene to use
#' @param step quantile step
#' @param assay which assay to use in obj, default RNA
#' @param slot which slot to use, default data
#' @export
#' @examples
#' @return seurat obj with re-set Idents
#'
#'
get_gene_score_neg <- function(scrna, gene, id, step = 0.01, assay = "RNA", slot = "data", pseudo.count = 0.01) {
scrna@active.assay <- assay
exprs.matrix <- Seurat::FetchData(scrna, vars = c(gene, "ident"), slot = slot)
colnames(exprs.matrix) <- c("exp", "id")
# exprs.matrix$
exprs.matrix <- data.table::as.data.table(exprs.matrix)
exprs.max <- max(exprs.matrix$exp)
exprs.min <- min(exprs.matrix$exp)
exprs.matrix$exp <- normalize(exprs.matrix$exp)
exprs.matrix$exp <- round(exprs.matrix$exp, 3)
exprs.matrix$exp.n <- 0 - exprs.matrix$exp
gene.prauc.n <- data.frame(x.val <- c(),
margin <- c())
celltype.in <- id
data.id <- subset(exprs.matrix, id == celltype.in)
data.other <- subset(exprs.matrix, id != celltype.in)
data.id.l <- nrow(data.id)
data.o.l <- nrow(data.other)
data.all.l <- nrow(exprs.matrix)
for (x.val in seq(0.01, 0.99, step)) {
x.val.n <- 0 - x.val
data.i.a <- subset(data.id, exp.n > x.val.n)
data.o.a <- subset(data.other, exp.n > x.val.n)
data.i.b <- subset(data.id, exp.n <= x.val.n)
data.o.b <- subset(data.other, exp.n <= x.val.n)
x.margin.n <- sum((data.i.a$exp.n - x.val.n))*nrow(data.o.b) +
sum((x.val.n -data.o.b$exp.n))*nrow(data.i.a) -
sum((data.o.a$exp.n - x.val.n))*nrow(data.i.b)
x.margin.n <- x.margin.n/data.all.l
de.n <- data.frame(x.val, x.margin.n)
gene.prauc.n <- rbind(gene.prauc.n, de.n)
}
gene.prauc.n <- gene.prauc.n[order(gene.prauc.n$x.margin, decreasing = T),]
x.factor.p <- (mean(data.id$exp) + pseudo.count)/(mean(data.other$exp) + pseudo.count)
x.split <- gene.prauc.n[1,]
x.val <- x.split[,1]
x.margin <- x.split[,2]
tp <- sum(data.id$exp < x.val)
fp <- sum(data.other$exp < x.val)
tn <- sum(data.other$exp >= x.val)
fn <- sum(data.id$exp >= x.val)
fp.pro <- subset(data.other, exp < x.val)
fp.pro <- as.data.frame(table(fp.pro$id))
fp.pro <- fp.pro[order(fp.pro$Freq, decreasing = T),]
if (nrow(fp.pro) >= 5) {
fp.pro <- fp.pro[1:5,]
}
fp.string <- paste(fp.pro$Var1, fp.pro$Freq)
fp.string <- toString(fp.string)
x.factor.n <- round(1/x.factor.p, 1)
x.margin.adj <- x.margin*(tp/data.id.l)*(tn/data.o.l)*(x.factor.n**2)
x.val <- x.val*exprs.max + exprs.min
x.split.n <- data.frame(gene, x.val, x.margin, x.margin.adj, tp, fp, tn, fn, "-", fp.string)
return(x.split.n)
}
get_split_pos <- function(scrna, gene, id, step = 0.01, assay = "RNA", slot = "data", max.recall = F) {
scrna@active.assay <- assay
df <- FetchData(scrna, vars = c(gene, "ident"))
colnames(df) <- c("exp", "id")
gene.prauc <- data.frame(x.val <- c(),
margin <- c())
data.id <- df[df$id == id,]
data.other <- df[df$id != id,]
x.max <- max(data.id$exp)
x.min <- min(data.id$exp)
x.min <- 0
x.num <- 1/step
x.factor <- as.numeric(length(df$id)/length(data.id$id))
x.factor <- ifelse(x.factor > 5, x.factor, 5)
for (x.val in seq(x.min, x.max, (x.max - x.min)/x.num)) {
tp <- sum(data.id$exp > x.val)
fp <- sum(data.other$exp > x.val)
tn <- sum(data.other$exp <= x.val)
fn <- sum(data.id$exp <= x.val)
if (max.recall) {
x.margin <- tn - fn*x.factor
}else{
x.margin <- tn - fn#*x.factor
}
de <- data.frame(gene, x.val, x.margin, "+")
gene.prauc <- rbind(gene.prauc, de)
}
gene.prauc <- gene.prauc[order(gene.prauc$x.margin, decreasing = T),]
colnames(gene.prauc) <- c("Gene", "split.value", "split.margin", "direction")
x.split <- gene.prauc[1,c(1,2,4)]
rownames(x.split) <- paste(gene)
return(x.split)
}
get_split_neg <- function(scrna, gene, id, step = 0.01, assay = "RNA", slot = "data", max.recall = F) {
scrna@active.assay <- assay
df <- FetchData(scrna, vars = c(gene, "ident"))
colnames(df) <- c("exp", "id")
gene.prauc <- data.frame(x.val <- c(),
margin <- c())
data.id <- df[df$id == id,]
data.other <- df[df$id != id,]
x.max <- max(df$exp)
# x.min <- min(df[df$exp != 0, ]$exp)
x.min <- min(df$exp)
x.min <- 0
x.num <- 1/step
x.factor <- as.numeric(length(df$id)/length(data.id$id))
x.factor <- ifelse(x.factor > 5, x.factor, 5)
for (x.val in seq(x.min, x.max, (x.max - x.min)/x.num)) {
tp <- sum(data.id$exp <= x.val)
fp <- sum(data.other$exp <= x.val)
tn <- sum(data.other$exp > x.val)
fn <- sum(data.id$exp > x.val)
if (max.recall) {
x.margin <- tn - fn*x.factor
}else{
x.margin <- tn - fn#*x.factor
}
de <- data.frame(gene, x.val, x.margin, "-")
gene.prauc <- rbind(gene.prauc, de)
}
# colnames(gene.prauc) <- c("Gene", "split.value", "direction")
gene.prauc <- gene.prauc[order(gene.prauc$x.margin, decreasing = T),]
colnames(gene.prauc) <- c("Gene", "split.value", "split.margin", "direction")
x.split <- gene.prauc[1,c(1,2,4)]
rownames(x.split) <- paste(gene)
return(x.split)
}
CostaLab/sc2marker documentation built on May 12, 2022, 6:05 a.m.
R Package Documentation
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Defines functions get_split_neg get_split_pos get_gene_score_neg get_gene_score_pos plot_filter_combination_first2 plot_filter_stepbystep_first2 get_PRAUC_matrix_combine_markers get_PRAUC_matrix_combine_markers_neg get_PRAUC_matrix_combine_markers_neg_pos get_split_neg_tp get_split_pos_tp plot_combine_PRAUC get_split_neg_neg get_split_pos_neg get_split_pos_pos Detect_combine_markers generate_report_rmd generate_report intersect.ignorecase get_gene_score_neg.fbeta get_gene_score_pos.fbeta plot_ridge get_antibody Detect_single_marker normalize makeid firstup get_original_alpha
Documented in Detect_single_marker firstup generate_report generate_report_rmd get_antibody get_gene_score_neg get_gene_score_neg.fbeta get_gene_score_pos get_gene_score_pos.fbeta get_original_alpha get_split_pos_pos intersect.ignorecase makeid normalize plot_filter_stepbystep_first2 plot_ridge
#' Calculate gene negative specific score
#'
#' Calculate gene specific score in negative direction
#' @param scrna obj to use
#' @param gene gene to use
#' @param assay which assay to use in obj, default RNA
#' @param slot which slot to use, default data
#' @export
#' @examples
#' @return alpha before normalization
#'
get_original_alpha <- function(scrna, gene, x.alpha, assay = "RNA", slot = "data"){
Seurat::DefaultAssay(scrna) <- assay
g.exprs <- FetchData(scrna, gene, slot = slot)
g.max <- max(g.exprs[,1])
g.min <- min(g.exprs[,1])
alpha.ori <- x.alpha*g.max + g.min
return(alpha.ori)
}
#' Firstup character
#'
#' @param x character
#' @return up case first letter
#' @export
#'
firstup <- function(x) {
x <- tolower(x)
substr(x, 1, 1) <- toupper(substr(x, 1, 1))
x
}
#' make id for plotting
#'
#' Reset active.ident of obj for plotting.
#' @param scrna obj to use
#' @param id interested cell id
#' @param panel ID panel in metadata of obj
#' @export
#' @examples
#' @return seurat obj with re-set Idents
#'
makeid <- function(scrna, id, panel = "seurat_clusters"){
levels(Seurat::Idents(scrna)) <- c(levels(Seurat::Idents(scrna)), "other")
Seurat::Idents(scrna)[Seurat::Idents(scrna) != id] <- 'other'
return(scrna)
}
#' Min-Max Normalization
#'
#' Normalize scRNA sequencing data.
#' @param x Gene expression
#' @export
#' @examples
#' @return Normalized expression data
#'
normalize <- function(x, ...) {
return((x - min(x, ...)) /(max(x, ...) - min(x, ...)))
}
#' Detect single markers of specific cell groups
#' @param scrna seurat obj to be used
#' @param geneset custom genes to test, all genes in obj to use if NULL
#' @param id interested cell group
#' @param category Denotes which experiment to use. Available options are:
#' \itemize{
#' \item{"IHC"} : use genes with valid antibody for IHC in human protein atlas
#' \item{"ICC"} : use genes with valid antibody for ICC in human protein atlas
#' \item{"ICC.IHC"} : use genes with valid antibody for ICC or IHC in human protein atlas
#' \item{"Flow"} : Only use cell surface genes with at least one valid antibody(ICC or IHC)
#' }
#' @param assay indicate the assay to compute
#' @param slot indicate the slot of data to compute
#' @param step quantile steps
#' @param min.pct only test genes that are detected in a minimum fraction of cells in interested cell types. Default is 0.15
#' @param use.all Don't do any filter on input geneset
#' @param geneset custom genes to test
#' @param self.db self defined antibody database
#' @param self.db.only Bolean. Only use the self deifned antibody database or not
#' @return list of markers performance
#' @export
#'
#'
Detect_single_marker <- function(scrna, id, step = 0.1, slot = "data", category = NULL,
geneset = NULL, assay = "RNA", do.fast = F, min.pct = 0.15, min.fc = 0.25,
use.all = F, do.f1score = F, pseudo.count = 0.01, min.tnr = 0.65, org = "human",
self.db = NULL, self.db.only = F,...){
genes.to.use <- NULL
SeuratObject::DefaultAssay(scrna) <- assay
## get application and org
if (org == "human") {
if (!is.null(category)) {
if (!(category %in% c("ICC.IHC", "ICC", "IHC", "Flow", "FlowComet"))) {
print("category not found, it should be one of ICC, IHC, ICC.IHC, FlowComet or Flow.")
return(NULL)
}
if (category == "ICC.IHC") {
genes.to.use <- unique(union(ICC$Gene, IHC$Gene))
}else if(category == "ICC"){
genes.to.use <- ICC$Gene
}else if(category == "IHC"){
genes.to.use <- IHC$Gene
}else if(category == "Flow"){
genes.to.use <- surface.genes
}
}
if (!is.null(category)){
if(category == "FlowComet"){
genes.to.use <- intersect(firstup(comet_human), rownames(scrna[[assay]]))
}
}
}
if (org == "mouse") {
if (!is.null(category)) {
if (!(category %in% c("ICC.IHC", "ICC", "IHC", "Flow", "FlowComet"))) {
print("category not found, it should be one of ICC, IHC, ICC.IHC, FlowComet or Flow.")
return(NULL)
}
if (category == "ICC.IHC") {
genes.to.use <- unique(union(ICC_mouse$Gene, IHC_mouse$Gene))
genes.to.use <- c(genes.to.use, flow_mouse$Gene)
}else if(category == "ICC"){
genes.to.use <- ICC_mouse$Gene
genes.to.use <- c(genes.to.use, flow_mouse$Gene)
}else if(category == "IHC"){
genes.to.use <- IHC_mouse$Gene
genes.to.use <- c(genes.to.use, flow_mouse$Gene)
}else if(category == "Flow"){
genes.to.use <- flow_mouse$Gene
}
}
genes.to.use <- unique(genes.to.use)
if (!is.null(category)){
if(category == "FlowComet"){
genes.to.use <- intersect(firstup(comet_genes), rownames(scrna[[assay]]))
}
}
}
if (!is.null(self.db)){
self.db.table <- utils::read.csv(self.db)
if(self.db.only){
genes.to.use <- self.db.table[,1]
}else{
genes.to.use <- c(genes.to.use, self.db.table[,1])
}
}
genes.to.use <- c(genes.to.use, geneset)
if (!is.null(genes.to.use)) {
genes.to.use <- intersect.ignorecase(rownames(scrna[[assay]]), genes.to.use)
geneset.in <- intersect.ignorecase(geneset, rownames(scrna[[assay]]))
geneset.out <- setdiff(geneset, geneset.in)
if (length(geneset.out) > 0) {
cat(paste("\nThese genes are not in the obj. Please check! \n"))
cat(geneset.out)
cat(paste("\n"))
}
}else{
cat(paste("\n Using all genes as input."))
cat(paste("\n"))
genes.to.use <- rownames(scrna[[assay]])
}
if (use.all) {
de <- Seurat::FoldChange(scrna, ident.1 = id, features = genes.to.use)
}
if (!use.all) {
de <- Seurat::FoldChange(scrna, ident.1 = id, features = genes.to.use)
de <- de[de$pct.1 > min.pct, ]
de$avg_log2FC <- abs(de$avg_log2FC)
de <- de[de$avg_log2FC > min.fc, ]
}
de <- na.omit(de)
markers <- de
gene.rank.list <- data.frame()
Seurat::DefaultAssay(scrna) <- assay
exprs.matrix <- Seurat::FetchData(scrna, vars = c(rownames(markers), "ident"), slot = slot)
# Ids.totest <- Idents(scrna)
gene.list <- rownames(markers)
gene.list <- intersect.ignorecase(rownames(scrna[[assay]]), gene.list)
pb <- utils::txtProgressBar(min = 0, max = length(gene.list), style = 3, file = stderr())
i = 1
for (genes in gene.list) {
tryCatch({
# exprs.matrix <- Seurat::FetchData(scrna, vars = c(genes, "ident"), slot = slot)
df.input <- exprs.matrix[, c(genes, "ident")]
de <- data.frame(get_gene_score(df.input, gene = genes, celltype = id,
step = step, pseudo.count = pseudo.count, min.tnr = min.tnr))
names(de)<-c("gene", "split.value","x.margin", "x.margin.adj", "TP", "FP", "TN", "FN", "direction", "FP details")
gene.rank.list <- rbind(gene.rank.list, de)
}, error=function(e){cat("Warning :",conditionMessage(e), "\n")})
setTxtProgressBar(pb = pb, value = i)
i = i + 1
}
close(con = pb)
gene.rank.list <- gene.rank.list[order(gene.rank.list$x.margin.adj, decreasing = T),]
rownames(gene.rank.list) <- seq(nrow(gene.rank.list))
gene.rank.list <- dplyr::distinct(gene.rank.list, gene, .keep_all = TRUE)
return(gene.rank.list)
}
#' Calculate gene specific score in both direction
#' @param exprs.matrix exprs matrix with ident panel
#' @param id interested cell id
#' @param gene gene to use
#' @param step quantile step
#' @export
#' @examples
#' @return gene score in both direction
#'
#'
get_gene_score <- function (exprs.matrix, celltype, gene, step = 0.01, pseudo.count = 0.01,
min.tnr = 0.65)
{
colnames(exprs.matrix) <- c("exp", "id")
exprs.matrix <- data.table::as.data.table(exprs.matrix)
exprs.max <- max(exprs.matrix$exp)
exprs.min <- min(exprs.matrix$exp)
# Min-max normalization
exprs.matrix$exp <- normalize(exprs.matrix$exp)
exprs.matrix$exp <- round(exprs.matrix$exp, 3)
exprs.matrix$exp.n <- 0 - exprs.matrix$exp
gene.prauc.p <- data.frame(x.val <- c(), margin <- c())
gene.prauc.n <- data.frame(x.val <- c(), margin <- c())
celltype.in <- celltype
data.id <- subset(exprs.matrix, id == celltype.in)
data.other <- subset(exprs.matrix, id != celltype.in)
data.id.l <- nrow(data.id)
data.o.l <- nrow(data.other)
data.all.l <- nrow(exprs.matrix)
# grid search for optimal cutoff
for (x.val in seq(0.001, 0.99, step)) {
# Positive direction
# get subset for TP, FP, TN, FN
data.i.a <- subset(data.id, exp > x.val)
data.o.a <- subset(data.other, exp > x.val)
data.i.b <- subset(data.id, exp <= x.val)
data.o.b <- subset(data.other, exp <= x.val)
# get the margin
x.margin.p <- sum((data.i.a$exp - x.val)) * nrow(data.o.b) +
sum((x.val - data.o.b$exp)) * nrow(data.i.a) - sum((data.o.a$exp -
x.val)) * nrow(data.i.b)
x.margin.p <- x.margin.p/data.all.l
de.p <- data.frame(x.val, x.margin.p)
gene.prauc.p <- rbind(gene.prauc.p, de.p)
# Negative direction
# get subset for TP, FP, TN, FN
x.val.n <- 0 - x.val
data.i.a <- subset(data.id, exp.n > x.val.n)
data.o.a <- subset(data.other, exp.n > x.val.n)
data.i.b <- subset(data.id, exp.n <= x.val.n)
data.o.b <- subset(data.other, exp.n <= x.val.n)
# get the margin
x.margin.n <- sum((data.i.a$exp.n - x.val.n)) * nrow(data.o.b) +
sum((x.val.n - data.o.b$exp.n)) * nrow(data.i.a) -
sum((data.o.a$exp.n - x.val.n)) * nrow(data.i.b)
x.margin.n <- x.margin.n/data.all.l
de.n <- data.frame(x.val, x.margin.n)
gene.prauc.n <- rbind(gene.prauc.n, de.n)
}
# get the max margin
gene.prauc.p <- gene.prauc.p[order(gene.prauc.p$x.margin,
decreasing = T), ]
gene.prauc.n <- gene.prauc.n[order(gene.prauc.n$x.margin,
decreasing = T), ]
# Positive direction final score calculation
x.split <- gene.prauc.p[1, ]
x.val <- x.split[, 1]
x.margin <- x.split[, 2]
tp <- sum(data.id$exp > x.val)
fp <- sum(data.other$exp > x.val)
fn <- sum(data.id$exp <= x.val)
tn <- sum(data.other$exp <= x.val)
# get top 5 false positive resources
fp.pro <- subset(data.other, exp > x.val)
fp.pro <- as.data.frame(table(fp.pro$id))
fp.pro <- fp.pro[order(fp.pro$Freq, decreasing = T), ]
if (nrow(fp.pro) >= 5) {
fp.pro <- fp.pro[1:5, ]
}
fp.string <- paste(fp.pro$Var1, fp.pro$Freq)
fp.string <- toString(fp.string)
x.factor.p <- (mean(data.id$exp) + pseudo.count)/(mean(data.other$exp) +
pseudo.count)
# get the score
x.margin.adj <- x.margin * (tp/data.id.l) * (tn/data.o.l) *
(x.factor.p^2)
x.val <- x.val * exprs.max + exprs.min
x.split.p <- data.frame(gene, x.val, x.margin, x.margin.adj,
tp, fp, tn, fn, "+", fp.string)
# Negative direction final score calculation
x.split <- gene.prauc.n[1, ]
x.val <- x.split[, 1]
x.margin <- x.split[, 2]
tp <- sum(data.id$exp < x.val)
fp <- sum(data.other$exp < x.val)
tn <- sum(data.other$exp >= x.val)
fn <- sum(data.id$exp >= x.val)
# get top 5 false positive resources
fp.pro <- subset(data.other, exp < x.val)
fp.pro <- as.data.frame(table(fp.pro$id))
fp.pro <- fp.pro[order(fp.pro$Freq, decreasing = T), ]
if (nrow(fp.pro) >= 5) {
fp.pro <- fp.pro[1:5, ]
}
fp.string <- paste(fp.pro$Var1, fp.pro$Freq)
fp.string <- toString(fp.string)
x.factor.n <- round(1/x.factor.p, 1)
x.margin.adj <- x.margin * (tp/data.id.l) * (tn/data.o.l) *
(x.factor.n^2)
x.val <- x.val * exprs.max + exprs.min
if (tn/data.o.l < min.tnr) {
x.margin.adj <- 0
}
x.split.n <- data.frame(gene, x.val, x.margin, x.margin.adj,
tp, fp, tn, fn, "-", fp.string)
return(rbind(x.split.p, x.split.n))
}
#' Get Antibody information table
#' @param markers.list makers list from Detect single markers function
#' @param rm.noab whether to remove genes without antibody information. Default TRUE.
#' @param self.db User provided database
#' @param self.db.only Bolean, whether to only use the user provided database
#' @return list of markers with antibody information
#' @export
#'
get_antibody <- function(markers.list, rm.noab = T, org = "human",
self.db = NULL, self.db.only = F, return_matrix = F,...){
# markers.list <- markers.list[markers.list$gene %in% intersect.ignorecase(markers$gene, union(ICC$Gene, IHC$Gene)),]
markers.list$gene <- toupper(markers.list$gene)
markers.list$antibody <- "NULL"
markers.list$x.margin <- round(markers.list$x.margin, 2)
markers.list$x.margin.adj <- round(markers.list$x.margin.adj, 2)
flow_mouse$Gene <- toupper(flow_mouse$Gene)
if (org == "human") {
IHC$Gene <- toupper(IHC$Gene)
ICC$Gene <- toupper(ICC$Gene)
markers.list$Reliability <- "Validated"
for (i in 1:nrow(markers.list)) {
gene.i <- markers.list[i,]$gene
if (gene.i %in% IHC$Gene) {
markers.list[i,]$antibody <- IHC[IHC$Gene == gene.i, ]$Antibody.RRID[1]
}
if (gene.i %in% ICC$Gene) {
markers.list[i,]$antibody <- ICC[ICC$Gene == gene.i, ]$Antibody.RRID[1]
}
}
}
if (org == "mouse") {
IHC_mouse$Gene <- toupper(IHC_mouse$Gene)
ICC_mouse$Gene <- toupper(ICC_mouse$Gene)
markers.list$Reliability <- "Homology"
for (i in 1:nrow(markers.list)) {
gene.i <- markers.list[i,]$gene
if (gene.i %in% IHC_mouse$Gene) {
markers.list[i,]$antibody <- IHC_mouse[IHC_mouse$Gene == gene.i, ]$Antibody.RRID[1]
markers.list[i,]$Reliability <- IHC_mouse[IHC_mouse$Gene == gene.i, ]$Reliability[1]
}
if (gene.i %in% ICC_mouse$Gene) {
markers.list[i,]$antibody <- ICC_mouse[ICC_mouse$Gene == gene.i, ]$Antibody.RRID[1]
markers.list[i,]$Reliability <- ICC_mouse[ICC_mouse$Gene == gene.i, ]$Reliability[1]
}
if (gene.i %in% toupper(flow_mouse$Gene)) {
markers.list[i,]$antibody <- flow_mouse[flow_mouse$Gene == gene.i, ]$Antibody.RRID[1]
markers.list[i,]$Reliability <- flow_mouse[flow_mouse$Gene == gene.i, ]$Reliability_1[1]
}
}
}
if (!is.null(self.db)){
self.db.table <- utils::read.csv(self.db)
self.db.table[,1] <- toupper(self.db.table[,1])
if(self.db.only){
markers.list <- markers.list[markers.list$gene %in% self.db.table$Gene, ]
}
for (i in 1:nrow(markers.list)) {
gene.i <- markers.list[i,]$gene
if (gene.i %in% toupper(self.db.table$Gene)) {
markers.list[i,]$antibody <- self.db.table[self.db.table$Gene == gene.i, ]$Antibody[1]
markers.list[i,]$Reliability <- self.db.table[self.db.table$Gene == gene.i, ]$Reliability[1]
}
}
}
markers.list <- markers.list[, -3]
markers.list[,2] <- round(markers.list[,2], 3)
colnames(markers.list)[2] <- "Alpha"
colnames(markers.list)[3] <- "Score"
if (rm.noab) {
markers.list <- markers.list[markers.list$antibody != "NULL",]
}
rownames(markers.list) <- 1:nrow(markers.list)
if (return_matrix) {
return(markers.list)
}else{
DT::datatable(markers.list,
extensions = 'Buttons',
options = list(dom = 'Bfrtip',
buttons = c('copy',
'csv',
'excel'
),
autoWidth = FALSE),
escape = F)
}
}
#' RidgePlot of selected genes, with split value
#' @param scrna seurat obj to be used
#' @param genes genes to plot
#' @param id interested cell group
#' @param step quantile steps
#' @param show_split whether to show the split line
#' @param aggr.other whether to aggregate other cell clusters
#' @return Ridge plot
#' @export
#'
plot_ridge <- function(scrna, id, genes, ncol = 1, step = 0.01, show_split = T, assay = "RNA", slot = "data", aggr.other = F){
Seurat::DefaultAssay(scrna) <- assay
require(ggplot2)
df.all <-data.frame()
df.split <-data.frame()
if (aggr.other) {
for (gene in genes) {
# get the alpha split value
df.g <- get_gene_score(Seurat::FetchData(scrna, vars = c(gene, "ident")), celltype = id, gene = gene)
df.g <- df.g[order(df.g$x.margin, decreasing = T),]
df.g <- df.g[1,]
df.c <-Seurat::FetchData(scrna, vars = c(gene, "ident"))
df.c$ident <- ifelse(df.c$ident == id, id, "Other")
df.c$gene <- paste(gene)
colnames(df.c) <- c("Exprs", "Ident", "Gene")
df.all <- rbind(df.all,df.c)
df.g <- df.g[,c(1,2)]
colnames(df.g) <- c("Gene", "Split")
df.split <- rbind(df.split,df.g)
}
df.s <- reshape2::melt(df.all)
df.s[df.s == -Inf] <- 0
df.s$Gene <- factor(df.s$Gene, levels = as.character(genes))
df.split$Gene <- factor(df.split$Gene, levels = c(genes))
g <- ggplot2::ggplot(df.s, aes(x=value, y=variable, color=Ident, point_color=Ident, fill=Ident)) +
ggridges::geom_density_ridges_gradient(scale = 3, size = 0.3, rel_min_height = 0.01) +
scale_fill_manual(values = c("#CB181D80", "#2171B580")) +
scale_discrete_manual("point_color", values = c("#CB181D80", "#2171B580"), guide = "none") +
guides(fill = guide_legend(
override.aes = list(
fill = c("#CB181D80", "#2171B580"),
color = NA, point_color = NA))
) +
ggridges::theme_ridges(grid = FALSE) +
ylab("") +
theme(
plot.title = element_text(hjust = 0.5),
plot.subtitle = element_text(hjust = 0.5)
)
df.split$Gene <- factor(df.split$Gene, levels = c(genes))
g <- g + facet_wrap(~Gene, ncol = ncol) +
geom_vline(data = df.split, aes(xintercept = Split), linetype="dotted",
color = "red", size=1.5) + labs(fill = "Expression")
# return()
}else{
for (gene in genes) {
# get the alpha split value
df.g <- get_gene_score(Seurat::FetchData(scrna, vars = c(gene, "ident")), celltype = id, gene = gene)
df.g <- df.g[order(df.g$x.margin, decreasing = T),]
df.g <- df.g[1,]
df.c <-Seurat::FetchData(scrna, vars = c(gene, "ident"))
df.c$gene <- paste(gene)
colnames(df.c) <- c("Exprs", "Ident", "Gene")
df.all <- rbind(df.all,df.c)
df.g <- df.g[,c(1,2)]
colnames(df.g) <- c("Gene", "Split")
df.split <- rbind(df.split,df.g)
}
df.split$Gene <- factor(df.split$Gene, levels = c(genes))
df.all$Gene <- factor(df.all$Gene, levels = c(genes))
g <- ggplot2::ggplot(df.all, aes(y=reorder(Ident, Exprs , mean),x=Exprs, fill = stat(x))) +
ggridges::geom_density_ridges_gradient()+
scale_fill_viridis_c(option = "D")+
theme(legend.position = "none")+
theme(
plot.title = element_text(hjust = 0.5),
plot.subtitle = element_text(hjust = 0.5)
) + ylab("") + xlab("")
g <- g +
geom_vline(data = df.split, aes(xintercept = Split), linetype="dotted",
color = "red", size=1.5) +
facet_wrap(~Gene, ncol = ncol)
# return()
}
g <- g + theme_bw() +
theme(panel.border = element_blank(), panel.grid.major = element_blank(),
panel.grid.minor = element_blank(), axis.line = element_line(colour = "black")) + labs(fill = "Expression")
print(g)
# return(g)
}
#' Calculate gene positive specific score with FBeta (Hypergate like approach)
#'
#' Calculate gene FBeta score with positive direction
#' @param scrna obj to use
#' @param id interested cell id
#' @param gene gene to use
#' @param step quantile step
#' @param assay which assay to use in obj, default RNA
#' @param slot which slot to use, default data
#' @param panel ID panel in metadata of obj
#' @export
#' @examples
#' @return seurat obj with re-set Idents
#'
get_gene_score_pos.fbeta <- function(scrna, gene, id, step = 0.01, assay = "RNA", slot = "data") {
Seurat::DefaultAssay(scrna) <- assay
# scrna@active.assay <- assay
data.mat.surf <- Seurat::FetchData(scrna, vars = c(gene, "ident"), slot = slot)
colnames(data.mat.surf) <- c("exp", "id")
colnames(data.mat.surf) <- c("exp", "id")
x.max <- max(data.mat.surf$exp)
x.min <- min(data.mat.surf$exp)
data.mat.surf$exp <- normalize(data.mat.surf$exp)
gene.prauc <- data.frame(x.val <- c(),
margin <- c())
data.id <- data.mat.surf[data.mat.surf$id == id,]
data.other <- data.mat.surf[data.mat.surf$id != id,]
data.id.l <- nrow(data.id)
data.o.l <- nrow(data.other)
data.all.l <- nrow(data.mat.surf)
for (x.val in seq(0, 1, step)) {
am <- data.id[data.id$exp > x.val, ]
cm <- data.other[data.other$exp > x.val, ]
bm <- data.id[data.id$exp <= x.val, ]
dm <- data.other[data.other$exp <= x.val, ]
x.pr <- nrow(am)/(nrow(am) + nrow(cm))
x.re <- nrow(am)/(nrow(am) + nrow(bm))
x.margin <- x.pr*x.re/(x.pr + x.re)
de <- data.frame(x.val, x.margin)
gene.prauc <- rbind(gene.prauc, de)
}
gene.prauc <- gene.prauc[order(gene.prauc$x.margin, decreasing = T),]
x.split <- gene.prauc[1,]
x.val <- x.split[,1]
x.margin <- x.split[,2]
tp <- sum(data.id$exp > x.val)
fp <- sum(data.other$exp > x.val)
fn <- sum(data.id$exp <= x.val)
tn <- sum(data.other$exp <= x.val)
x.margin.adj <- x.margin
x.val <- x.val*x.max + x.min
x.split <- data.frame(gene, x.val, x.margin, x.margin.adj, tp, fp, "+")
return(x.split)
}
#' Calculate gene positive specific score with FBeta (Hypergate like approach)
#'
#' Calculate gene FBeta score with negative direction
#' @param scrna obj to use
#' @param id interested cell id
#' @param gene gene to use
#' @param step quantile step
#' @param assay which assay to use in obj, default RNA
#' @param slot which slot to use, default data
#' @param panel ID panel in metadata of obj
#' @export
#' @examples
#' @return seurat obj with re-set Idents
#'
get_gene_score_neg.fbeta <- function(scrna, gene, id, step = 0.01, assay = "RNA", slot = "data") {
Seurat::DefaultAssay(scrna) <- assay
# scrna@active.assay <- assay
data.mat.surf <- Seurat::FetchData(scrna, vars = c(gene, "ident"), slot = slot)
colnames(data.mat.surf) <- c("exp", "id")
data.mat.surf$exp <- normalize(data.mat.surf$exp)
gene.prauc <- data.frame(x.val <- c(),
margin <- c())
data.id <- data.mat.surf[data.mat.surf$id == id,]
data.other <- data.mat.surf[data.mat.surf$id != id,]
data.id.l <- nrow(data.id)
data.o.l <- nrow(data.other)
data.all.l <- nrow(data.mat.surf)
for (x.val in seq(0, 1, step)) {
am <- data.id[data.id$exp < x.val, ]
cm <- data.other[data.other$exp < x.val, ]
bm <- data.id[data.id$exp >= x.val, ]
dm <- data.other[data.other$exp >= x.val, ]
x.pr <- nrow(am)/(nrow(am) + nrow(cm))
x.re <- nrow(am)/(nrow(am) + nrow(bm))
x.margin <- x.pr*x.re/(x.pr + x.re)
de <- data.frame(x.val, x.margin)
gene.prauc <- rbind(gene.prauc, de)
}
gene.prauc <- gene.prauc[order(gene.prauc$x.margin, decreasing = T),]
x.split <- gene.prauc[1,]
x.val <- x.split[,1]
x.margin <- x.split[,2]
tp <- sum(data.id$exp < x.val)
fp <- sum(data.other$exp < x.val)
fn <- sum(data.id$exp >= x.val)
tn <- sum(data.other$exp >= x.val)
x.margin.adj <- x.margin
x.split <- data.frame(gene, x.val, x.margin, x.margin.adj, tp, fp, "-")
return(x.split)
}
#' Intersect 2 list ignoring the cases and return the elements in list1
#' @param list1 list 1 of genes
#' @param list2 list 2 of genes
#' @export
#' @return Ridge plot
#'
intersect.ignorecase <- function(list1, list2){
list1.u <- toupper(list1)
list2.u <- toupper(list2)
list12.u <- intersect(list1.u, list2.u)
list.r <- list1[match(list12.u, list1.u)]
return(list.r)
}
#' Detect single markers of all cell groups
#' @param scrna seurat obj to be used
#' @param geneset custom genes to test, all genes in obj to use if NULL
#' @param id interested cell group
#' @param test.use Denotes which test to use. Available options are:
#' \itemize{
#' \item{"IHC"} : use genes with valid antibody for IHC in human protein atlas
#' \item{"ICC"} : use genes with valid antibody for ICC in human protein atlas
#' \item{"ICC.IHC"} : use genes with valid antibody for ICC or IHC in human protein atlas
#' \item{"Flow"} : Only use cell surface genes with at least one valid antibody(ICC or IHC)
#' }
#' @param assay indicate the assay to compute
#' @param slot indicate the slot of data to compute
#' @param step quantile steps
#' @param min.pct only test genes that are detected in a minimum fraction of cells in interested cell types. Default is 0.15
#' @param use.all Don't do any filter on input geneset
#' @param clusters_to_detect set of clusters for compupation
#' @param geneset custom genes to test
#' @param org Choose database for human or mouse
#' @param self.db self defined antibody database
#' @param self.db.only Bolean. Only use the self deifned antibody database or not
#' @return list of markers performance
#' @export
#'
#'
Detect_single_marker_all <- function (scrna, step = 0.1, slot = "data", category = NULL,
clusters_to_detect = NULL, geneset = NULL, assay = "RNA",
do.fast = F, min.pct = 0.15, min.fc = 0.25, use.all = F,
do.f1score = F, pseudo.count = 0.01, min.tnr = 0.65, org="mouse",
self.db = NULL, self.db.only=F, ...)
{
all.list <- vector("list")
if (length(clusters_to_detect) == 0) {
for (id in unique(Seurat::Idents(scrna))) {
message(paste("Calculating Markers for", id))
df.s <- Detect_single_marker(scrna = scrna, id = id,
step = step, slot = slot, assay = assay, min.pct = min.pct,
min.fc = min.fc, min.tnr = min.tnr, pseudo.count = pseudo.count,
use.all = use.all, do.f1score = do.f1score, category = category,
geneset = geneset, do.fast = do.fast, org = org, self.db = self.db,
self.db.only = self.db.only, ...)
all.list[[id]] <- df.s
}
}
else {
cluster.in <- intersect(clusters_to_detect, unique(Seurat::Idents(scrna)))
cluster.out <- setdiff(clusters_to_detect, unique(Seurat::Idents(scrna)))
cat(paste("These clusters are detected\n"))
cat(cluster.in)
cat(paste("\n"))
if (length(cluster.out) > 0) {
cat(paste("\nThese clusters are not in the obj\n"))
cat(cluster.out)
}
for (id in cluster.in) {
message(paste("Calculating Markers for", id))
df.s <- Detect_single_marker(scrna = scrna, id = id,
step = step, slot = slot, assay = assay, min.pct = min.pct,
min.fc = min.fc, min.tnr = min.tnr, pseudo.count = pseudo.count,
use.all = use.all, do.f1score = do.f1score, category = category,
geneset = geneset, do.fast = do.fast, org = org, self.db = self.db,
self.db.only = self.db.only, ...)
all.list[[id]] <- df.s
}
}
return(all.list)
}
#' generate html report for single markers of all cell groups
#' @param scrna seurat obj to be used
#' @param markers.list results of Detect_single_marker_all()
#' @param aggr.other whether to aggregate other celltypes
#' @param ridge_ncol
#' @param fpath Path to generate the report
#' @param fname file name. Default NULL
#' @return list of markers performance
#' @export
#'
#'
generate_report <- function(scrna, markers.list,
fpath = ".", aggr.other = F, fname = NULL,
top_n_genes = 6, ridge_ncol = 3, assay = "RNA", slot = "data", org = "human",
...){
markers.list <- markers.list
saveRDS(markers.list, file = file.path(fpath, "sc2marker.allmarkers.intermediate.rds"))
saveRDS(scrna, file = file.path(fpath, "sc2marker.scrna.intermediate.rds"))
generate_report_rmd(scrna = scrna, markers.list = markers.list, fpath = fpath,
aggr.other = aggr.other,
top_n_genes = top_n_genes,
fname = fname,
assay = assay,
slot = slot,
ridge_ncol = ridge_ncol, org = org,...)
if (is.null(fname)) {
fname.rmd <- "sc2marker.report.Rmd"
}else{
fname.rmd <- paste(fname, ".sc2marker.report.Rmd", sep = "")
}
rmarkdown::render(file.path(fpath, fname.rmd))
unlink(file.path(fpath, "sc2marker.allmarkers.intermediate.rds"))
unlink(file.path(fpath, "sc2marker.scrna.intermediate.rds"))
}
#' generate html report for single markers of all cell groups
#' @param scrna seurat obj to be used
#' @param markers.list results from Detect_single_marker_all()
#' @param top_n_genes top number of genes for RidgePlot
#' @param sc2marker_ncol number of col of Ridgeplot
#' @param fname file name. Default NULL
#' @param fpath Path to generate report
#' @return list of markers performance
#' @export
#'
#'
generate_report_rmd <- function(scrna, markers.list, aggr.other = F, top_n_genes = 6, ridge_ncol = 3,
fname = NULL, fpath = ".", assay = "RNA", slot = "data", org = "human"){
if (is.null(fname)) {
fname.rmd <- "sc2marker.report.Rmd"
}else{
fname.rmd <- paste(fname, ".sc2marker.report.Rmd", sep = "")
}
write(setup.template, file = file.path(fpath, fname.rmd))
for (id in unique(names(markers.list))) {
chunk.template.s <- chunk.template
chunk.template.s <- gsub("sc2marker_celltype", paste("\"",id, "\"", sep = ""), chunk.template.s)
chunk.template.s <- gsub("sc2marker_aggrother", aggr.other, chunk.template.s)
chunk.template.s <- gsub("sc2marker_ncol", ridge_ncol, chunk.template.s)
chunk.template.s <- gsub("sc2marker_org", paste("\"",org, "\"", sep = ""), chunk.template.s)
chunk.template.s <- gsub("top_n_genes", top_n_genes, chunk.template.s)
chunk.template.s <- gsub("sc2marker_slot", paste("\"",slot, "\"", sep = ""), chunk.template.s)
chunk.template.s <- gsub("sc2marker_assay", paste("\"",assay, "\"", sep = ""), chunk.template.s)
write(chunk.template.s, file = file.path(fpath, fname.rmd), append = T)
}
}
#########________________________________________
######### code for next version (developing)
#########________________________________________
Detect_combine_markers <- function(scrna, id, step = 0.1, category = NULL,
geneset = NULL, assay = "RNA", slot = "data",
do.fast = F, min.pct = 0.1, use.all = F, pseudo.count = 0.01){
if (is.null(geneset)) {
geneset <- rownames(scrna[[assay]])
}else{
geneset <- intersect(rownames(scrna[[assay]]), geneset)
}
if (use.all) {
geneset <- intersect(rownames(scrna[[assay]]), geneset)
de <- Seurat::FoldChange(scrna, ident.1 = id, features = geneset)
de$gene <- rownames(de)
}
if (!use.all) {
if (do.fast) {
de <- Seurat::FindMarkers(scrna, ident.1 = id, features = geneset)
de <- subset(de, p_val_adj < 0.05)
}else{
de <- Seurat::FoldChange(scrna, ident.1 = id, features = geneset)
de$gene <- rownames(de)
de <- de[de$pct.1 > min.pct, ]
}
}
de.genes.p <- subset(de, avg_log2FC > 0)
de.genes.n <- subset(de, avg_log2FC < 0)
gene.combn <- t(combn(de.genes.p$gene, 2))
gene.combn.prauc <- data.frame()
star_time <- Sys.time()
for (gene.iter in 1:nrow(gene.combn)) {
genes <- gene.combn[gene.iter,]
gene1 <- genes[1]
gene2 <- genes[2]
de <- get_split_pos_pos(scrna, gene1, gene2, id, step = step, assay = assay, slot = slot)
colnames(de) <- c("Gene1", "Gene2", "Gene1.split", "Gene2.split", "x.margin", "x.margin.adj", "TP", "FP", "Direction1", "Direction2")
gene.combn.prauc <- rbind(gene.combn.prauc, de)
}
for (gene1 in de.genes.p$gene) {
for (gene2 in de.genes.n$gene) {
de <- get_split_pos_neg(scrna, gene1, gene2, id, step = step, assay = assay, slot = slot)
colnames(de) <- c("Gene1", "Gene2", "Gene1.split", "Gene2.split", "x.margin", "x.margin.adj", "TP", "FP", "Direction1", "Direction2")
gene.combn.prauc <- rbind(gene.combn.prauc, de)
}
}
gene.combn <- t(combn(de.genes.n$gene, 2))
for (gene.iter in 1:nrow(gene.combn)) {
genes <- gene.combn[gene.iter,]
gene1 <- genes[1]
gene2 <- genes[2]
de <- get_split_neg_neg(scrna, gene1, gene2, id, step = step, assay = assay, slot = slot)
colnames(de) <- c("Gene1", "Gene2", "Gene1.split", "Gene2.split", "x.margin", "x.margin.adj", "TP", "FP", "Direction1", "Direction2")
gene.combn.prauc <- rbind(gene.combn.prauc, de)
}
end_time <- Sys.time()
# close(pb)
run_time <- end_time - star_time
print(run_time)
gene.combn.prauc <- gene.combn.prauc[order(gene.combn.prauc$x.margin.adj, decreasing = T),]
return(gene.combn.prauc)
}
#' UmapPlot based on results from Markers Greedy Search
#' @param scrna seurat objects
#' @param df.split results from Greedy Search
#' @param id cell groups to identify
#' @return
#'
# Combine_marker_umap <- function(scrna, df.split, id){
# idents.c <- Seurat::Idents(scrna)
# gene1 <- df.split$gene[1]
# gene2 <- df.split$gene[2]
# gene1.split <- df.split$split.value[1]
# gene2.split <- df.split$split.value[2]
#
# cells.1 <- GetCellNames(cbmc, gene1, gene1.split, df.split$direction[1])
# cells.2 <- GetCellNames(cbmc, gene2, gene2.split, df.split$direction[2])
# cells.1.2 <- intersect(cells.1, cells.2)
#
# Seurat::Idents(scrna) <- "other"
# Seurat::Idents(scrna, cells = cells.1) <- paste(gene1, "filter")
# p1 <- UMAPPlot(scrna, cols = c('red', "grey"))
#
# Seurat::Idents(scrna) <- "other"
# Seurat::Idents(scrna, cells = cells.2) <- paste(gene2, "filter")
# p2 <- UMAPPlot(scrna, cols = c('blue', "grey"))
#
# Seurat::Idents(scrna) <- "other"
# Seurat::Idents(scrna, cells = cells.1.2) <- paste(gene1, "+", gene2)
# p3 <- UMAPPlot(scrna, cols = c('black', "grey"))
#
# Seurat::Idents(scrna) <- idents.c
# scrna <- makeid(scrna, id)
# p4 <- UMAPPlot(scrna)
#
# plot_grid(p1, p2, p3, p4)
# }
#
# GetCellNames <- function(scrna, gene, value, direction, assay = "RNA", slot = "data"){
# # if (do.magic) {
# # df <- data.frame(exp = scrna@assays$MAGIC_RNA@data[gene,])
# # }else{
# # df <- data.frame(exp = scrna@assays$RNA@data[gene,])
# # }
# scrna@active.assay <- assay
# df <- Seurat::FetchData(scrna, vars = c(gene), slot = slot)
#
# colnames(df) <- "exp"
#
# if (direction == "+") {
# df <- subset(df, exp > value)
# }else{
# df <- subset(df, exp < value)
# }
# return(rownames(df))
# }
get_split_pos_pos <- function(scrna, gene1, gene2, id, step = 0.01, assay = "RNA", slot = "data") {
DefaultAssay(scrna) <- assay
data.mat.surf <- FetchData(scrna, vars = c(gene1, gene2, "ident"), slot = slot)
colnames(data.mat.surf) <- c("exp1", "exp2", "id")
data.mat.surf$exp1 <- normalize(data.mat.surf$exp1)
data.mat.surf$exp2 <- normalize(data.mat.surf$exp2)
sp1 = boxplot.stats(data.mat.surf$exp1)$out
sp2 = boxplot.stats(data.mat.surf$exp2)$out
`%notin%` <- Negate(`%in%`)
data.mat.surf <- data.mat.surf[data.mat.surf$exp2 %notin% sp2 & data.mat.surf$exp1 %notin% sp1, ]
gene.prauc <- data.frame(x.val <- c(),
margin <- c())
data.id <- data.mat.surf[data.mat.surf$id == id,]
data.other <- data.mat.surf[data.mat.surf$id != id,]
data.id.l <- nrow(data.id)
data.o.l <- nrow(data.other)
data.all.l <- nrow(data.mat.surf)
# size.factor <- nrow(data.mat.surf)/nrow(data.id)
size.factor <- nrow(data.mat.surf)/nrow(data.other)
# size.factor <- ifelse(size.factor < 3, 3, size.factor)
for (x.val in seq(0.01, 1, step)) {
for (y.val in seq(0.01, 1, step)) {
data.i.a <- data.id[data.id$exp1 > x.val & data.id$exp2 > y.val, ]
tp <- nrow(data.i.a)
data.o.a <- data.other[data.other$exp1 > x.val & data.other$exp2 > y.val, ]
fp <- nrow(data.o.a)
# x.margin <- tp*size.factor - fp#*size.factor
x.margin <- tp - fp*size.factor
# x.margin <- tp*nrow(data.other) - fp*nrow(data.id)
x.margin <- x.margin/data.all.l
de <- data.frame(gene1, gene2, x.val, y.val, x.margin)
gene.prauc <- rbind(gene.prauc, de)
}
}
gene.prauc <- gene.prauc[order(gene.prauc$x.margin, decreasing = T),]
x.split <- gene.prauc[1,]
x.val <- x.split[,3]
y.val <- x.split[,4]
x.margin <- x.split[,5]
data.i.a <- data.id[data.id$exp1 > x.val & data.id$exp2 > y.val, ]
tp <- nrow(data.i.a)
data.o.a <- data.other[data.other$exp1 > x.val & data.other$exp2 > y.val, ]
fp <- nrow(data.o.a)
data.o.b <- data.other[data.other$exp1 <= x.val | data.other$exp2 <= y.val, ]
tn <- nrow(data.o.b)
x.margin.a <- sum((data.i.a$exp1 - x.val))*nrow(data.o.a) + sum((data.i.a$exp2 - y.val))*nrow(data.o.a) -#+
# sum((x.val -data.o.b$exp1))*nrow(data.id) + sum((y.val -data.o.b$exp2))*nrow(data.id) -
sum((data.o.a$exp1 - x.val))*nrow(data.i.a) - sum((data.o.a$exp2 - y.val))*nrow(data.i.a)
x.margin.a <- ifelse(x.margin.a > 1, x.margin.a, 1)
# x.margin.a2 <- ifelse(x.margin.a2 > 1, x.margin.a2, 1)
x.margin.a <- log(x.margin.a)
x.margin.adj <- x.margin*(tp/data.id.l)*(tn/data.o.l)*x.margin.a#*x.margin.a2
# x.margin.adj <- x.margin.a
x.split <- data.frame(gene1, gene2, x.val, y.val, x.margin, x.margin.adj, tp, fp, "+", "+", x.margin.a)
return(x.split)
}
get_split_pos_neg <- function(scrna, gene1, gene2, id, step = 0.01, assay = "RNA", slot = "data") {
Seurat::DefaultAssay(scrna) <- assay
data.mat.surf <- Seurat::FetchData(scrna, vars = c(gene1, gene2, "ident"), slot = slot)
colnames(data.mat.surf) <- c("exp1", "exp2", "id")
data.mat.surf$exp1 <- normalize(data.mat.surf$exp1)
data.mat.surf$exp2 <- normalize(data.mat.surf$exp2)
sp1 = boxplot.stats(data.mat.surf$exp1)$out
sp2 = boxplot.stats(data.mat.surf$exp2)$out
`%notin%` <- Negate(`%in%`)
data.mat.surf <- data.mat.surf[data.mat.surf$exp2 %notin% sp2 & data.mat.surf$exp1 %notin% sp1, ]
if(max(data.mat.surf$exp2) == 0 | max(data.mat.surf$exp1) == 0){
x.split <- data.frame(gene1, gene2, 0, 0, 0, 0, 0, 0, "+", "-")
return(x.split)
}
gene.prauc <- data.frame(x.val <- c(),
margin <- c())
data.id <- data.mat.surf[data.mat.surf$id == id,]
data.other <- data.mat.surf[data.mat.surf$id != id,]
data.id.l <- nrow(data.id)
data.o.l <- nrow(data.other)
data.all.l <- nrow(data.mat.surf)
size.factor <- nrow(data.mat.surf)/nrow(data.other)
for (x.val in seq(0.01, 1, 0.1)) {
for (y.val in seq(0.01, 1, 0.1)) {
data.i.a <- data.id[data.id$exp1 > x.val & data.id$exp2 < y.val, ]
tp <- nrow(data.i.a)
data.o.a <- data.other[data.other$exp1 > x.val & data.other$exp2 < y.val, ]
fp <- nrow(data.o.a)
# x.margin <- tp*size.factor - fp
x.margin <- tp - fp*size.factor
# x.margin <- tp*nrow(data.other) - fp*nrow(data.id)
x.margin <- x.margin/data.all.l
de <- data.frame(gene1, gene2, x.val, y.val, x.margin)
gene.prauc <- rbind(gene.prauc, de)
}
}
gene.prauc <- gene.prauc[order(gene.prauc$x.margin, decreasing = T),]
x.split <- gene.prauc[1,]
x.val <- x.split[,3]
y.val <- x.split[,4]
x.margin <- x.split[,5]
data.i.a <- data.id[data.id$exp1 > x.val & data.id$exp2 < y.val, ]
tp <- nrow(data.i.a)
data.o.a <- data.other[data.other$exp1 > x.val & data.other$exp2 < y.val, ]
fp <- nrow(data.o.a)
data.o.b <- data.other[data.other$exp1 <= x.val | data.other$exp2 >= y.val, ]
tn <- nrow(data.o.b)
x.margin.a <- sum((data.i.a$exp1 - x.val))*nrow(data.o.a) + sum((y.val - data.i.a$exp2))*nrow(data.o.a) -#+
# sum((x.val - data.o.b$exp1))*nrow(data.id) + sum((data.o.b$exp2 - y.val))*nrow(data.id) -
sum((data.o.a$exp1 - x.val))*nrow(data.i.a) - sum((y.val - data.o.a$exp2))*nrow(data.i.a)
# x.margin.a <- x.margin.a/(nrow(data.i.a) + nrow(data.o.a))
x.margin.a2 <- sum((x.val - data.o.b$exp1))*nrow(data.id) + sum((data.o.b$exp2 - y.val))*nrow(data.id)
x.margin.a <- ifelse(x.margin.a > 1, x.margin.a, 1)
x.margin.a2 <- ifelse(x.margin.a2 > 1, x.margin.a2, 1)
x.margin.a <- log(x.margin.a)
x.margin.a2 <- log(x.margin.a2)
x.margin.a2 <- ifelse(x.margin.a2 > 1, x.margin.a2, 1)
# x.margin.a <- dist.i.a*nrow(data.other) - dist.o.a*nrow(data.id)# + dist.o.b*nrow(data.id)
x.margin.adj <- x.margin*(tp/data.id.l)*(tn/data.o.l)*x.margin.a#*x.margin.a2
# x.margin.adj <- x.margin.a
x.split <- data.frame(gene1, gene2, x.val, y.val, x.margin, x.margin.adj, tp, fp, "+", "-")
return(x.split)
}
get_split_neg_neg <- function(scrna, gene1, gene2, id, step = 0.01, assay = "RNA", slot = "data") {
Seurat::DefaultAssay(scrna) <- assay
# scrna@active.assay <- assay
data.mat.surf <- Seurat::FetchData(scrna, vars = c(gene1, gene2, "ident"), slot = slot)
colnames(data.mat.surf) <- c("exp1", "exp2", "id")
data.mat.surf$exp1 <- normalize(data.mat.surf$exp1)
data.mat.surf$exp2 <- normalize(data.mat.surf$exp2)
sp1 = boxplot.stats(data.mat.surf$exp1)$out
sp2 = boxplot.stats(data.mat.surf$exp2)$out
`%notin%` <- Negate(`%in%`)
data.mat.surf <- data.mat.surf[data.mat.surf$exp2 %notin% sp2 & data.mat.surf$exp1 %notin% sp1, ]
if(max(data.mat.surf$exp2) == 0 | max(data.mat.surf$exp1) == 0){
x.split <- data.frame(gene1, gene2, 0, 0, 0, 0, 0, 0, "-", "-")
return(x.split)
}
gene.prauc <- data.frame(x.val <- c(),
margin <- c())
data.id <- data.mat.surf[data.mat.surf$id == id,]
data.other <- data.mat.surf[data.mat.surf$id != id,]
data.id.l <- nrow(data.id)
data.o.l <- nrow(data.other)
data.all.l <- nrow(data.mat.surf)
size.factor <- nrow(data.mat.surf)/nrow(data.other)
for (x.val in seq(0.01, 1, step)) {
for (y.val in seq(0.01, 1, step)) {
data.i.a <- data.id[data.id$exp1 < x.val & data.id$exp2 < y.val, ]
tp <- nrow(data.i.a)
data.o.a <- data.other[data.other$exp1 < x.val & data.other$exp2 < y.val, ]
fp <- nrow(data.o.a)
x.margin <- tp - fp*size.factor
# x.margin <- tp*nrow(data.other) - fp*nrow(data.id)
x.margin <- x.margin/data.all.l
de <- data.frame(gene1, gene2, x.val, y.val, x.margin)
gene.prauc <- rbind(gene.prauc, de)
}
}
gene.prauc <- gene.prauc[order(gene.prauc$x.margin, decreasing = T),]
x.split <- gene.prauc[1,]
x.val <- x.split[,3]
y.val <- x.split[,4]
x.margin <- x.split[,5]
data.i.a <- data.id[data.id$exp1 < x.val & data.id$exp2 < y.val, ]
tp <- nrow(data.i.a)
data.o.a <- data.other[data.other$exp1 < x.val & data.other$exp2 < y.val, ]
fp <- nrow(data.o.a)
data.o.b <- data.other[data.other$exp1 >= x.val | data.other$exp2 >= y.val, ]
tn <- nrow(data.o.b)
x.margin.a <- sum((x.val - data.i.a$exp1))/nrow(data.o.a) + sum((y.val - data.i.a$exp2))*nrow(data.o.a) -#+
# sum((data.o.b$exp1 - x.val))*nrow(data.id) + sum((data.o.b$exp2 - y.val))*nrow(data.id) -
sum((x.val - data.o.a$exp1))*nrow(data.i.a) - sum((y.val - data.o.a$exp2))*nrow(data.i.a)
x.margin.a <- ifelse(x.margin.a > 1, x.margin.a, 1)
x.margin.a <- log(x.margin.a)
x.margin.adj <- x.margin*(tp/data.id.l)*(tn/data.o.l)*x.margin.a#*x.margin.a2
# x.margin.adj <- x.margin.a
x.split <- data.frame(gene1, gene2, x.val, y.val, x.margin, x.margin.adj, tp, fp, "-", "-")
return(x.split)
}
#
# marker_stepbystep <- function(scrna, cellgroup, depth = 2, geneset = NULL, step = 0.01){
# if (is.null(geneset)) {
# geneset <- rownames(scrna)
# }
# geneset <- intersect(rownames(scrna[["RNA"]]), geneset)
# len.id <- sum(Seurat::Idents(scrna) == cellgroup)
# len.other <- sum(Seurat::Idents(scrna) != cellgroup)
# df.split <- data.frame()
#
# for (variable in seq(depth)) {
# markers <- FindMarkers(scrna, ident.1 = cellgroup, features = geneset)
# markers <- subset(markers, p_val_adj < 0.05)
#
# markers.pos <- subset(markers, avg_log2FC > 0)
# markers.neg <- subset(markers, avg_log2FC < 0)
#
# gene.prauc <- data.frame()
#
# for (genes in rownames(markers.pos)) {
# de <- data.frame(genes, get_split_pos(scrna, genes, cellgroup, step))
# names(de)<-c("gene", "split.value","filtered.adj", "direction")
# gene.prauc <- rbind(gene.prauc, de)
# }
# for (genes in rownames(markers.neg)) {
# de <- data.frame(genes, get_split_neg(scrna, genes, cellgroup, step))
# names(de)<-c("gene", "split.value","filtered.adj", "direction")
# gene.prauc <- rbind(gene.prauc, de)
# }
# gene.prauc <- gene.prauc[order(gene.prauc$filtered.adj, decreasing = T),]
#
# df.split <- rbind(df.split, gene.prauc[1,])
#
# left.cells <- GetCellNames(scrna, gene.prauc[1,1], gene.prauc[1,2], gene.prauc[1,4])
# scrna <- subset(scrna, cells = left.cells)
# }
# return(df.split)
# }
# marker_stepbystep.2 <- function(scrna, cellgroup, depth = 2, geneset = NULL, step = 0.01, assay = "RNA", slot = "data", max.recall = T){
# if (is.null(geneset)) {
# geneset <- rownames(scrna[["RNA"]])
# }
# geneset <- intersect(rownames(scrna[["RNA"]]), geneset)
# len.id <- sum(Seurat::Idents(scrna) == cellgroup)
# len.other <- sum(Seurat::Idents(scrna) != cellgroup)
# df.split <- data.frame()
#
# suppressWarnings(
# for (variable in seq(depth)) {
# df.fc <- FoldChange(scrna, ident.1 = cellgroup, features = geneset)
#
# markers.pos <- subset(df.fc, avg_log2FC > 0)
# markers.neg <- subset(df.fc, avg_log2FC < 0)
#
# gene.prauc <- data.frame()
#
# for (genes in rownames(markers.pos)) {
# de <- data.frame(get_gene_score_pos(scrna, genes, cellgroup, step, assay = assay, slot = slot))
# names(de)<-c("gene", "split.value","x.margin", "x.margin.adj", "tp", "fp", "direction")
# gene.prauc <- rbind(gene.prauc, de)
# }
# for (genes in rownames(markers.neg)) {
# de <- data.frame(get_gene_score_neg(scrna, genes, cellgroup, step, assay = assay, slot = slot))
# names(de)<-c("gene", "split.value","x.margin", "x.margin.adj", "tp", "fp", "direction")
# gene.prauc <- rbind(gene.prauc, de)
# }
# gene.prauc <- gene.prauc[order(gene.prauc$x.margin.adj, decreasing = T),]
#
# df <- gene.prauc[1,]
# if (df$direction == "+") {
# split.step <- get_split_pos(scrna, df$gene, cellgroup, assay = assay, slot = slot, max.recall = T)
# }else{
# split.step <- get_split_neg(scrna, df$gene, cellgroup, assay = assay, slot = slot, max.recall = T)
# }
#
# names(split.step) <- c("Gene", "split.value", "direction")
#
# df.split <- rbind(df.split, split.step)
# left.cells <- GetCellNames(scrna = scrna, gene = df$gene, value = df.split$split.value, direction = df.split$direction, assay = assay, slot = slot)
# scrna <- subset(scrna, cells = left.cells)
# geneset <- setdiff(geneset, df$gene)
# }
# )
# return(df.split)
# }
plot_combine_PRAUC <- function(scrna, gene1, gene2, id, step = 0.01, return.obj = F){
x.df <- get_PRAUC_matrix_combine_markers(scrna, gene1, gene2, id = id, step = step)
g <- ggplot() + geom_line(x.df, mapping = aes(x.rec, x.pre)) + xlim(c(0,1)) + ylim(c(0,1))
if (!return.obj) {
print(g)
}else{
return(g)
}
}
get_split_pos_tp <- function(scrna, gene, id, step = 0.01) {
data.mat.surf <- data.frame(exp = scrna@assays$RNA@data[gene,],
id = as.character(Seurat::Idents(makeid(scrna, id))))
gene.prauc <- data.frame(x.val <- c(),
margin <- c())
data.id <- data.mat.surf[data.mat.surf$id == id,]
data.other <- data.mat.surf[data.mat.surf$id != id,]
x.factor <- length(data.other$id)/length(data.id$id)
x.max <- max(data.id$exp)
x.min <- min(data.id$exp)
for (x.val in seq(x.min + (x.max - x.min)/100, x.max, (x.max - x.min)/100)) {
tp <- sum(data.id$exp >= x.val)
fp <- sum(data.other$exp >= x.val)
tn <- sum(data.other$exp < x.val)
fn <- sum(data.id$exp < x.val)
if (length(data.id$id) <= length(data.other$id)) {
x.margin <- tp*x.factor - fp
}
else{
x.margin <- tp - fp
}
de <- data.frame(x.val, x.margin, "+")
gene.prauc <- rbind(gene.prauc, de)
}
gene.prauc <- gene.prauc[order(gene.prauc$x.margin, decreasing = T),]
x.split <- gene.prauc[1,]
rownames(x.split) <- paste(gene)
return(x.split)
}
get_split_neg_tp <- function(scrna, gene, id, step = 0.01) {
data.mat.surf <- data.frame(exp = scrna@assays$RNA@data[gene,],
id = as.character(Seurat::Idents(makeid(scrna, id))))
gene.prauc <- data.frame(x.val <- c(),
margin <- c())
data.id <- data.mat.surf[data.mat.surf$id == id,]
data.other <- data.mat.surf[data.mat.surf$id != id,]
x.factor <- length(data.other$id)/length(data.id$id)
x.max <- max(data.id$exp)
x.min <- min(data.id$exp)
for (x.val in seq(x.min, x.max, (x.max - x.min)/100)) {
tp <- sum(data.id$exp < x.val)
fp <- sum(data.other$exp < x.val)
tn <- sum(data.other$exp >= x.val)
fn <- sum(data.id$exp >= x.val)
if (length(data.id$id) <= length(data.other$id)) {
x.margin <- tp*x.factor - fp
}
else{
x.margin <- tp - fp
}
de <- data.frame(x.val, x.margin, "-")
gene.prauc <- rbind(gene.prauc, de)
}
gene.prauc <- gene.prauc[order(gene.prauc$x.margin, decreasing = T),]
x.split <- gene.prauc[1,]
rownames(x.split) <- paste(gene)
return(x.split)
}
get_PRAUC_matrix_combine_markers_neg_pos <- function(scrna, gene1, gene2, id, step = 0.01){
data.mat.surf <- data.frame(gene1 = scrna@assays$RNA@data[gene1,],
gene2 = scrna@assays$RNA@data[gene2,],
id = as.character(Seurat::Idents(makeid(scrna, id))))
gene.prauc <- data.frame(x.pre <- c(),
x.rec <- c())
data.id <- data.mat.surf[data.mat.surf$id == id,]
data.other <- data.mat.surf[data.mat.surf$id != id,]
gene1.min <- min(data.id$gene1)
gene2.max <- max(data.id$gene2)
gene1.range <- max(data.id$gene1) - gene1.min
gene2.range <- gene2.max - min(data.id$gene2)
for (x.seq in seq(0.05, 0.95, step)) {
x.val <- gene1.min + x.seq*gene1.range
y.val <- gene2.max - x.seq*gene2.range
tp <- sum(data.id$gene1 >= x.val & data.id$gene2 <= y.val)
fp <- sum(data.other$gene1 >= x.val & data.other$gene2 <= y.val)
# tn <- sum(data.other$gene1 < x.val | data.other$gene2 < y.val)
fn <- sum(data.id$gene1 < x.val | data.id$gene2 > y.val)
x.pre <- tp/(tp + fp)
x.rec <- tp/(tp + fn)
de <- data.frame(x.pre, x.rec)
gene.prauc <- rbind(gene.prauc, de)
}
gene.prauc <- gene.prauc[complete.cases(gene.prauc), ]
gene.prauc <- gene.prauc[order(gene.prauc$x.rec), ]
return(gene.prauc)
}
get_PRAUC_matrix_combine_markers_neg <- function(scrna, gene1, gene2, id, step = 0.01){
data.mat.surf <- data.frame(gene1 = scrna@assays$RNA@data[gene1,],
gene2 = scrna@assays$RNA@data[gene2,],
id = as.character(Seurat::Idents(makeid(scrna, id))))
gene.prauc <- data.frame(x.pre <- c(),
x.rec <- c())
data.id <- data.mat.surf[data.mat.surf$id == id,]
data.other <- data.mat.surf[data.mat.surf$id != id,]
for (x.seq in seq(0.05, 1, step)) {
x.val = quantile(data.id$gene1, x.seq)
y.val = quantile(data.id$gene2, x.seq)
tp <- sum(data.id$gene1 < x.val & data.id$gene2 < y.val)
fp <- sum(data.other$gene1 < x.val & data.other$gene2 < y.val)
# tn <- sum(data.other$gene1 < x.val | data.other$gene2 < y.val)
fn <- sum(data.id$gene1 >= x.val | data.id$gene2 >= y.val)
x.pre <- tp/(tp + fp)
x.rec <- tp/(tp + fn)
de <- data.frame(x.pre, x.rec)
gene.prauc <- rbind(gene.prauc, de)
}
gene.prauc <- gene.prauc[complete.cases(gene.prauc), ]
gene.prauc <- gene.prauc[order(gene.prauc$x.rec), ]
return(gene.prauc)
}
get_PRAUC_matrix_combine_markers <- function(scrna, gene1, gene2, id, step = 0.01){
data.mat.surf <- data.frame(gene1 = scrna@assays$RNA@data[gene1,],
gene2 = scrna@assays$RNA@data[gene2,],
id = as.character(Seurat::Idents(makeid(scrna, id))))
gene.prauc <- data.frame(x.pre <- c(),
x.rec <- c())
data.id <- data.mat.surf[data.mat.surf$id == id,]
data.other <- data.mat.surf[data.mat.surf$id != id,]
for (x.seq in seq(0, 0.95, step)) {
x.val = quantile(data.id$gene1, x.seq)
y.val = quantile(data.id$gene2, x.seq)
tp <- sum(data.id$gene1 >= x.val & data.id$gene2 >= y.val)
fp <- sum(data.other$gene1 >= x.val & data.other$gene2 >= y.val)
# tn <- sum(data.other$gene1 < x.val | data.other$gene2 < y.val)
fn <- sum(data.id$gene1 < x.val | data.id$gene2 < y.val)
x.pre <- tp/(tp + fp)
x.rec <- tp/(tp + fn)
de <- data.frame(x.pre, x.rec)
gene.prauc <- rbind(gene.prauc, de)
}
gene.prauc <- gene.prauc[complete.cases(gene.prauc), ]
gene.prauc <- gene.prauc[order(gene.prauc$x.rec), ]
return(gene.prauc)
}
#' Detect greedy step by step filters for cell group identification
#' @param scrna seurat object
#' @param cellgroup, interested cell group
#' @param depth how much steps to filter
#' @param geneset Gene set to be used
#' @return
plot_filter_stepbystep_first2 <- function(scrna, df.split, id, step = 0.01){
gene1 <- df.split$gene[1]
gene2 <- df.split$gene[2]
df <- data.frame(exp1 = scrna@assays$RNA@data[gene1,],
exp2 = scrna@assays$RNA@data[gene2,],
id = as.character(Seurat::Idents(makeid(scrna, id))))
x.split <- df.split$split.value[1]
y.split <- df.split$split.value[2]
ggplot(df)+
geom_point(aes(exp1, exp2, color = id)) +
geom_segment(aes(x = x.split, y = y.split, xend = max(exp1), yend = y.split), linetype = 2)+
geom_segment(aes(x = x.split, y = y.split, xend = x.split, yend = max(exp2)), linetype = 2)+
xlab(paste(gene1)) + ylab(paste(gene2))
}
plot_filter_combination_first2 <- function(scrna, df.split, id, step = 0.01){
gene1 <- df.split$gene[1]
gene2 <- df.split$gene[2]
df <- data.frame(exp1 = scrna@assays$RNA@data[gene1,],
exp2 = scrna@assays$RNA@data[gene2,],
ID = as.character(Seurat::Idents(makeid(scrna, id))))
x.split <- df.split$split.value[1]
y.split <- df.split$split.value[2]
g <- ggplot(df)+
geom_point(aes(exp1, exp2, color = ID))
if (df.split$direction[2] == "+") {
g <- g + geom_segment(aes(x = x.split, y = y.split, xend = x.split, yend = max(exp2)), linetype = 2)
}else{
g <- g + geom_segment(aes(x = x.split, y = y.split, xend = x.split, yend = min(exp2)), linetype = 2)
}
if(df.split$direction[1] == "+") {
g <- g + geom_segment(aes(x = x.split, y = y.split, xend = max(exp1), yend = y.split), linetype = 2)
}else{
g <- g + geom_segment(aes(x = x.split, y = y.split, xend = min(exp1), yend = y.split), linetype = 2)
}
g <- g + xlab(paste(gene1)) + ylab(paste(gene2))
print(g)
}
#
# Combine_markers_point_plot <- function(scrna, c.markers, id, ranking = 1, assay = "RNA", slot = "data", return.obj = F, step = 0.01, max.recall = F){
# scrna@active.assay = assay
# markers.c <- c.markers[ranking, ]
# scrna@active.assay = assay
# df <- Seurat::FetchData(scrna, vars = c(markers.c$Gene1, markers.c$Gene2, "ident"))
# gene1 <- markers.c$Gene1
# gene2 <- markers.c$Gene2
# colnames(df) <- c("exp1", "exp2", "id")
# gene1.direc = markers.c$Direction1
# gene2.direc = markers.c$Direction2
# if (max.recall) {
# if (gene1.direc == "+") {
# x.split <- get_split_pos(scrna, gene1, id, step = step, assay = assay, slot = slot, max.recall = max.recall)$split.value
# }else{
# x.split <- get_split_neg(scrna, gene1, id, step = step, assay = assay, slot = slot, max.recall = max.recall)$split.value
# }
# left.cells <- GetCellNames(scrna, markers.c$Gene1, x.split, markers.c$Direction1, assay = assay, slot = slot)
# scrna.left <- subset(scrna, cells = left.cells)
#
# if (gene2.direc == "+") {
# y.split <- get_split_pos(scrna.left, gene2, id, step = step, assay = assay, slot = slot, max.recall = max.recall)$split.value
# }else{
# y.split <- get_split_neg(scrna.left, gene2, id, step = step, assay = assay, slot = slot, max.recall = max.recall)$split.value
# }
#
# left.cells <- GetCellNames(scrna, markers.c$Gene2, y.split, markers.c$Direction2, assay = assay, slot = slot)
# scrna.left <- subset(scrna.left, cells = left.cells)
#
#
# left.cells <- GetCellNames(scrna, markers.c$Gene2, y.split, markers.c$Direction2, assay = assay, slot = slot)
# scrna.left <- subset(scrna.left, cells = left.cells)
# }else {
# if (gene1.direc == "+" & gene2.direc == "+") {
# df.c <-get_split_pos_pos(scrna, gene1 = gene1, gene2 = gene2, id = id, assay = assay, slot = slot, step = step)
# colnames(df.c) <- c("Gene1", "Gene2", "Gene1.split", "Gene2.split", "x.margin", "x.margin.adj", "TP", "FP", "Direction1", "Direction2")
# }
# if (gene1.direc == "+" & gene2.direc == "-") {
# df.c <-get_split_pos_neg(scrna, gene1 = gene1, gene2 = gene2, id = id, assay = assay, slot = slot, step = step)
# colnames(df.c) <- c("Gene1", "Gene2", "Gene1.split", "Gene2.split", "x.margin", "x.margin.adj", "TP", "FP", "Direction1", "Direction2")
# }
# if (gene1.direc == "-" & gene2.direc == "-") {
# df.c <-get_split_neg_neg(scrna, gene1 = gene1, gene2 = gene2, id = id, assay = assay, slot = slot, step = step)
# colnames(df.c) <- c("Gene1", "Gene2", "Gene1.split", "Gene2.split", "x.margin", "x.margin.adj", "TP", "FP", "Direction1", "Direction2")
# }
#
# x.split <- df.c$Gene1.split*max(df$exp1) + min(df$exp1)
# y.split <- df.c$Gene2.split*max(df$exp2) + min(df$exp2)
#
# left.cells <- GetCellNames(scrna, markers.c$Gene1, x.split, markers.c$Direction1, assay = assay, slot = slot)
# scrna.left <- subset(scrna, cells = left.cells)
# left.cells <- GetCellNames(scrna, markers.c$Gene2, y.split, markers.c$Direction2, assay = assay, slot = slot)
# scrna.left <- subset(scrna.left, cells = left.cells)
#
# }
#
# tp <- sum(Seurat::Idents(scrna.left) == id)
# fp <- sum(Seurat::Idents(scrna.left) != id)
# x.pre <- tp/(tp+fp)
# x.pre <- round(x.pre, 3)
# x.rec <- sum(Seurat::Idents(scrna.left) == id)/sum(Seurat::Idents(scrna.left) == id)
# x.rec <- round(x.rec, 3)
#
# g <- ggplot(df)+
# geom_point(aes(exp1, exp2, color = id))
#
# if (gene2.direc == "+") {
# g <- g + geom_segment(aes(x = x.split, y = y.split, xend = x.split, yend = max(exp2)), linetype = 2)
# }else{
# g <- g + geom_segment(aes(x = x.split, y = y.split, xend = x.split, yend = min(exp2)), linetype = 2)
# }
#
# if(gene1.direc == "+") {
# g <- g + geom_segment(aes(x = x.split, y = y.split, xend = max(exp1), yend = y.split), linetype = 2)
# }else{
# g <- g + geom_segment(aes(x = x.split, y = y.split, xend = min(exp1), yend = y.split), linetype = 2)
# }
#
# g <- g + xlab(paste(markers.c$Gene1, "--Recall: ", x.rec,"; Precision: ", x.pre, sep = "")) + ylab(paste(markers.c$Gene2))
# if (return.obj) {
# return(g)
# }
# print(g)
# }
#
# GetCellNames <- function(scrna, gene, value, direction){
# df <- data.frame(exp = scrna@assays$RNA@data[gene,])
# if (direction == "+") {
# df <- subset(df, exp >= value)
# }else{
# df <- subset(df, exp <= value)
# }
# return(rownames(df))
# }
#
# grid_plot <- function(scrna, df.split, cellgroup){
# x.len <- length(df.split$gene)
# plots = list()
# # scrna.id <- Idents(scrna)
# scrna <- makeid(scrna, cellgroup)
# scrna.left <- scrna
# for (gene in df.split$gene) {
# plots[[gene]] <- VlnPlot(scrna.left, features = gene) + geom_hline(yintercept=df.split[df.split$gene == gene, ]$split.value, linetype = 1)
# left.cells <- GetCellNames(scrna.left, gene, df.split[df.split$gene == gene, ]$split.value, df.split[df.split$gene == gene, ]$direction)
# scrna.left <- subset(scrna.left, cells = left.cells)
# tp <- sum(Seurat::Idents(scrna.left) == cellgroup)
# fp <- sum(Seurat::Idents(scrna.left) != cellgroup)
# x.pre <- round(tp/(tp+fp), 3)
# x.rec <- sum(Seurat::Idents(scrna.left) == cellgroup)/sum(Seurat::Idents(scrna) == cellgroup)
# x.rec <- round(x.rec, 3)
# plots[[gene]] <- plots[[gene]] + xlab(paste("Precision:", x.pre, " Recall:", x.rec, sep = ""))
# plots[[gene]] <- plots[[gene]] + ggtitle(paste(gene, df.split[df.split$gene == gene, ]$direction))
# }
# plot_grid(plotlist=plots)
# }
#' Get cell names which meet cutoff
#' @param scrna seurat obj to be used
#' @param geneset custom genes to test, all genes in obj to use if NULL
#' @param id interested cell group
#' @param category indicate the ICC/IHC/Flow, if NULL use all genes.
#' @param assay indicate the assay to compute
#' @param slot indicate the slot of data to compute
#' @param step quantile steps
#' @param min.pct only test genes that are detected in a minimum fraction of min.pct cells in either of the two populations. Meant to speed up the function by not testing genes that are very infrequently expressed. Default is 0.1
#' @param use.all Don't do any filter on input geneset
#' @return list of markers performance
#'
# GetGenes <- function(scrna, slot = "data", category = NULL, geneset = NULL,
# assay = "RNA", min.pct = 0.1, use.all = F, species = "Human"){
# if (category == "IHC") {
# genes.touse <- IHC$Gene
# }else if (category == "ICC") {
# genes.touse <- ICC$Gene
# }else if (category == "Flow") {
# genes.touse <- surface.genes
# }
#
# if (!is.null(category) & is.null(geneset)) {
# print("Use self define genes should set the category to NULL")
# return(NULL)
# }
#
# if (is.null(category) & is.null(geneset)) {
# genes.touse <- rownames(scrna[[assay]])
# }else if (is.null(category) & !is.null(geneset)){
# genes.touse <- intersect(rownames(scrna[[assay]]), geneset)
# }
#
# if (length(genes.touse) == 0) {
# print("Find none of genes in the obj")
# return(NULL)
# }
#
# if (use.all) {
# geneset <- intersect(rownames(scrna[[assay]]), geneset)
# de <- Seurat::FoldChange(scrna, ident.1 = id, features = geneset)
# }
# if (!use.all) {
# if (do.fast) {
# de <- Seurat::FindMarkers(scrna, ident.1 = id, features = geneset)
# de <- subset(de, p_val_adj < 0.05)
# }else{
# de <- Seurat::FoldChange(scrna, ident.1 = id, features = geneset)
# de <- de[de$pct.1 > min.pct, ]
# }
# }
#
#
# de$gene <- rownames(de)
# markers.pos <- de
# markers.neg <- de
#
# gene.rank.list <- data.frame()
#
# for (genes in rownames(markers.pos)) {
# de <- data.frame(get_gene_score_pos(scrna, genes, id, step, assay = assay, slot = slot))
# names(de)<-c("gene", "split.value","x.margin", "x.margin.adj", "tp", "fp", "direction")
# gene.rank.list <- rbind(gene.rank.list, de)
# }
# for (genes in rownames(markers.neg)) {
# de <- data.frame(get_gene_score_neg(scrna, genes, id, step, assay = assay, slot = slot))
# names(de)<-c("gene", "split.value","x.margin", "x.margin.adj", "tp", "fp", "direction")
# gene.rank.list <- rbind(gene.rank.list, de)
# }
# gene.rank.list <- gene.rank.list[order(gene.rank.list$x.margin.adj, decreasing = T),]
# rownames(gene.rank.list) <- seq(nrow(gene.rank.list))
# return(gene.rank.list)
# }
#' Calculate gene positive specific score
#'
#' Calculate gene specific score in positive direction
#' @param scrna obj to use
#' @param id interested cell id
#' @param gene gene to use
#' @param step quantile step
#' @param assay which assay to use in obj, default RNA
#' @param slot which slot to use, default data
#' @export
#' @examples
#' @return seurat obj with re-set Idents
#'
get_gene_score_pos <- function(scrna, gene, id, step = 0.01, assay = "RNA", slot = "data", pseudo.count = 0.01) {
scrna@active.assay <- assay
exprs.matrix <- Seurat::FetchData(scrna, vars = c(gene, "ident"), slot = slot)
colnames(exprs.matrix) <- c("exp", "id")
# exprs.matrix$
exprs.matrix <- data.table::as.data.table(exprs.matrix)
exprs.max <- max(exprs.matrix$exp)
exprs.min <- min(exprs.matrix$exp)
exprs.matrix$exp <- normalize(exprs.matrix$exp)
exprs.matrix$exp <- round(exprs.matrix$exp, 3)
gene.prauc.p <- data.frame(x.val <- c(),
margin <- c())
celltype.in <- id
data.id <- subset(exprs.matrix, id == celltype.in)
data.other <- subset(exprs.matrix, id != celltype.in)
data.id.l <- nrow(data.id)
data.o.l <- nrow(data.other)
data.all.l <- nrow(exprs.matrix)
for (x.val in seq(0.01, 0.99, step)) {
data.i.a <- subset(data.id, exp > x.val)
data.o.a <- subset(data.other, exp > x.val)
data.i.b <- subset(data.id, exp <= x.val)
data.o.b <- subset(data.other, exp <= x.val)
x.margin.p <- sum((data.i.a$exp - x.val))*nrow(data.o.b) +
sum((x.val - data.o.b$exp))*nrow(data.i.a) -
sum((data.o.a$exp - x.val))*nrow(data.i.b)# +
x.margin.p <- x.margin.p/data.all.l
de.p <- data.frame(x.val, x.margin.p)
gene.prauc.p <- rbind(gene.prauc.p, de.p)
}
gene.prauc.p <- gene.prauc.p[order(gene.prauc.p$x.margin, decreasing = T),]
# gene.prauc.n <- gene.prauc.n[order(gene.prauc.n$x.margin, decreasing = T),]
# pos
x.split <- gene.prauc.p[1,]
x.val <- x.split[,1]
x.margin <- x.split[,2]
tp <- sum(data.id$exp > x.val)
fp <- sum(data.other$exp > x.val)
fn <- sum(data.id$exp <= x.val)
tn <- sum(data.other$exp <= x.val)
fp.pro <- subset(data.other, exp > x.val)
fp.pro <- as.data.frame(table(fp.pro$id))
fp.pro <- fp.pro[order(fp.pro$Freq, decreasing = T),]
if (nrow(fp.pro) >= 5) {
fp.pro <- fp.pro[1:5,]
}
fp.string <- paste(fp.pro$Var1, fp.pro$Freq)
fp.string <- toString(fp.string)
x.factor.p <- (mean(data.id$exp) + pseudo.count)/(mean(data.other$exp) + pseudo.count)
# x.factor.p <- (mean(data.id$exp) + pseudo.count)/(mean(data.other$exp) + pseudo.count)
x.margin.adj <- x.margin*(tp/data.id.l)*(tn/data.o.l)*(x.factor.p**2)
x.val <- x.val*exprs.max + exprs.min
x.split.p <- data.frame(gene, x.val, x.margin, x.margin.adj, tp, fp, tn, fn, "+", fp.string)
return(x.split.p)
}
#' Calculate gene negative specific score
#'
#' Calculate gene specific score in negative direction
#' @param scrna obj to use
#' @param id interested cell id
#' @param gene gene to use
#' @param step quantile step
#' @param assay which assay to use in obj, default RNA
#' @param slot which slot to use, default data
#' @export
#' @examples
#' @return seurat obj with re-set Idents
#'
#'
get_gene_score_neg <- function(scrna, gene, id, step = 0.01, assay = "RNA", slot = "data", pseudo.count = 0.01) {
scrna@active.assay <- assay
exprs.matrix <- Seurat::FetchData(scrna, vars = c(gene, "ident"), slot = slot)
colnames(exprs.matrix) <- c("exp", "id")
# exprs.matrix$
exprs.matrix <- data.table::as.data.table(exprs.matrix)
exprs.max <- max(exprs.matrix$exp)
exprs.min <- min(exprs.matrix$exp)
exprs.matrix$exp <- normalize(exprs.matrix$exp)
exprs.matrix$exp <- round(exprs.matrix$exp, 3)
exprs.matrix$exp.n <- 0 - exprs.matrix$exp
gene.prauc.n <- data.frame(x.val <- c(),
margin <- c())
celltype.in <- id
data.id <- subset(exprs.matrix, id == celltype.in)
data.other <- subset(exprs.matrix, id != celltype.in)
data.id.l <- nrow(data.id)
data.o.l <- nrow(data.other)
data.all.l <- nrow(exprs.matrix)
for (x.val in seq(0.01, 0.99, step)) {
x.val.n <- 0 - x.val
data.i.a <- subset(data.id, exp.n > x.val.n)
data.o.a <- subset(data.other, exp.n > x.val.n)
data.i.b <- subset(data.id, exp.n <= x.val.n)
data.o.b <- subset(data.other, exp.n <= x.val.n)
x.margin.n <- sum((data.i.a$exp.n - x.val.n))*nrow(data.o.b) +
sum((x.val.n -data.o.b$exp.n))*nrow(data.i.a) -
sum((data.o.a$exp.n - x.val.n))*nrow(data.i.b)
x.margin.n <- x.margin.n/data.all.l
de.n <- data.frame(x.val, x.margin.n)
gene.prauc.n <- rbind(gene.prauc.n, de.n)
}
gene.prauc.n <- gene.prauc.n[order(gene.prauc.n$x.margin, decreasing = T),]
x.factor.p <- (mean(data.id$exp) + pseudo.count)/(mean(data.other$exp) + pseudo.count)
x.split <- gene.prauc.n[1,]
x.val <- x.split[,1]
x.margin <- x.split[,2]
tp <- sum(data.id$exp < x.val)
fp <- sum(data.other$exp < x.val)
tn <- sum(data.other$exp >= x.val)
fn <- sum(data.id$exp >= x.val)
fp.pro <- subset(data.other, exp < x.val)
fp.pro <- as.data.frame(table(fp.pro$id))
fp.pro <- fp.pro[order(fp.pro$Freq, decreasing = T),]
if (nrow(fp.pro) >= 5) {
fp.pro <- fp.pro[1:5,]
}
fp.string <- paste(fp.pro$Var1, fp.pro$Freq)
fp.string <- toString(fp.string)
x.factor.n <- round(1/x.factor.p, 1)
x.margin.adj <- x.margin*(tp/data.id.l)*(tn/data.o.l)*(x.factor.n**2)
x.val <- x.val*exprs.max + exprs.min
x.split.n <- data.frame(gene, x.val, x.margin, x.margin.adj, tp, fp, tn, fn, "-", fp.string)
return(x.split.n)
}
get_split_pos <- function(scrna, gene, id, step = 0.01, assay = "RNA", slot = "data", max.recall = F) {
scrna@active.assay <- assay
df <- FetchData(scrna, vars = c(gene, "ident"))
colnames(df) <- c("exp", "id")
gene.prauc <- data.frame(x.val <- c(),
margin <- c())
data.id <- df[df$id == id,]
data.other <- df[df$id != id,]
x.max <- max(data.id$exp)
x.min <- min(data.id$exp)
x.min <- 0
x.num <- 1/step
x.factor <- as.numeric(length(df$id)/length(data.id$id))
x.factor <- ifelse(x.factor > 5, x.factor, 5)
for (x.val in seq(x.min, x.max, (x.max - x.min)/x.num)) {
tp <- sum(data.id$exp > x.val)
fp <- sum(data.other$exp > x.val)
tn <- sum(data.other$exp <= x.val)
fn <- sum(data.id$exp <= x.val)
if (max.recall) {
x.margin <- tn - fn*x.factor
}else{
x.margin <- tn - fn#*x.factor
}
de <- data.frame(gene, x.val, x.margin, "+")
gene.prauc <- rbind(gene.prauc, de)
}
gene.prauc <- gene.prauc[order(gene.prauc$x.margin, decreasing = T),]
colnames(gene.prauc) <- c("Gene", "split.value", "split.margin", "direction")
x.split <- gene.prauc[1,c(1,2,4)]
rownames(x.split) <- paste(gene)
return(x.split)
}
get_split_neg <- function(scrna, gene, id, step = 0.01, assay = "RNA", slot = "data", max.recall = F) {
scrna@active.assay <- assay
df <- FetchData(scrna, vars = c(gene, "ident"))
colnames(df) <- c("exp", "id")
gene.prauc <- data.frame(x.val <- c(),
margin <- c())
data.id <- df[df$id == id,]
data.other <- df[df$id != id,]
x.max <- max(df$exp)
# x.min <- min(df[df$exp != 0, ]$exp)
x.min <- min(df$exp)
x.min <- 0
x.num <- 1/step
x.factor <- as.numeric(length(df$id)/length(data.id$id))
x.factor <- ifelse(x.factor > 5, x.factor, 5)
for (x.val in seq(x.min, x.max, (x.max - x.min)/x.num)) {
tp <- sum(data.id$exp <= x.val)
fp <- sum(data.other$exp <= x.val)
tn <- sum(data.other$exp > x.val)
fn <- sum(data.id$exp > x.val)
if (max.recall) {
x.margin <- tn - fn*x.factor
}else{
x.margin <- tn - fn#*x.factor
}
de <- data.frame(gene, x.val, x.margin, "-")
gene.prauc <- rbind(gene.prauc, de)
}
# colnames(gene.prauc) <- c("Gene", "split.value", "direction")
gene.prauc <- gene.prauc[order(gene.prauc$x.margin, decreasing = T),]
colnames(gene.prauc) <- c("Gene", "split.value", "split.margin", "direction")
x.split <- gene.prauc[1,c(1,2,4)]
rownames(x.split) <- paste(gene)
return(x.split)
}
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