Corrmotif Analysis
Last updated: 2025-02-27
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Knit directory: CX5461_Project/
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| File | Version | Author | Date | Message |
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| Rmd | 4e8a4bc | sayanpaul01 | 2025-02-24 | Commit |
| html | 4e8a4bc | sayanpaul01 | 2025-02-24 | Commit |
| Rmd | 2862c42 | sayanpaul01 | 2025-02-24 | Commit |
| html | 2862c42 | sayanpaul01 | 2025-02-24 | Commit |
| Rmd | ebfddcd | sayanpaul01 | 2025-02-23 | Commit |
| html | ebfddcd | sayanpaul01 | 2025-02-23 | Commit |
| html | b557095 | sayanpaul01 | 2025-02-23 | Added CX_DOX shared late response (SVIP) boxplot |
| Rmd | 1cd333a | sayanpaul01 | 2025-02-23 | Added CX_DOX shared late response (SVIP) boxplot |
| html | e73d731 | sayanpaul01 | 2025-02-23 | Build site. |
| Rmd | c4ed3e0 | sayanpaul01 | 2025-02-23 | Updated Corrmotif analysis and index file |
| html | b56a62a | sayanpaul01 | 2025-02-21 | Build site. |
| Rmd | bf0c4a3 | sayanpaul01 | 2025-02-21 | Published updated Index and Corrmotif analysis with new |
📌 Fit Limma Model Functions
## Fit limma model using code as it is found in the original cormotif code. It has
## only been modified to add names to the matrix of t values, as well as the
## limma fits
limmafit.default <- function(exprs,groupid,compid) {
limmafits <- list()
compnum <- nrow(compid)
genenum <- nrow(exprs)
limmat <- matrix(0,genenum,compnum)
limmas2 <- rep(0,compnum)
limmadf <- rep(0,compnum)
limmav0 <- rep(0,compnum)
limmag1num <- rep(0,compnum)
limmag2num <- rep(0,compnum)
rownames(limmat) <- rownames(exprs)
colnames(limmat) <- rownames(compid)
names(limmas2) <- rownames(compid)
names(limmadf) <- rownames(compid)
names(limmav0) <- rownames(compid)
names(limmag1num) <- rownames(compid)
names(limmag2num) <- rownames(compid)
for(i in 1:compnum) {
selid1 <- which(groupid == compid[i,1])
selid2 <- which(groupid == compid[i,2])
eset <- new("ExpressionSet", exprs=cbind(exprs[,selid1],exprs[,selid2]))
g1num <- length(selid1)
g2num <- length(selid2)
designmat <- cbind(base=rep(1,(g1num+g2num)), delta=c(rep(0,g1num),rep(1,g2num)))
fit <- lmFit(eset,designmat)
fit <- eBayes(fit)
limmat[,i] <- fit$t[,2]
limmas2[i] <- fit$s2.prior
limmadf[i] <- fit$df.prior
limmav0[i] <- fit$var.prior[2]
limmag1num[i] <- g1num
limmag2num[i] <- g2num
limmafits[[i]] <- fit
# log odds
# w<-sqrt(1+fit$var.prior[2]/(1/g1num+1/g2num))
# log(0.99)+dt(fit$t[1,2],g1num+g2num-2+fit$df.prior,log=TRUE)-log(0.01)-dt(fit$t[1,2]/w, g1num+g2num-2+fit$df.prior, log=TRUE)+log(w)
}
names(limmafits) <- rownames(compid)
limmacompnum<-nrow(compid)
result<-list(t = limmat,
v0 = limmav0,
df0 = limmadf,
s20 = limmas2,
g1num = limmag1num,
g2num = limmag2num,
compnum = limmacompnum,
fits = limmafits)
}
limmafit.counts <-
function (exprs, groupid, compid, norm.factor.method = "TMM", voom.normalize.method = "none")
{
limmafits <- list()
compnum <- nrow(compid)
genenum <- nrow(exprs)
limmat <- matrix(NA,genenum,compnum)
limmas2 <- rep(0,compnum)
limmadf <- rep(0,compnum)
limmav0 <- rep(0,compnum)
limmag1num <- rep(0,compnum)
limmag2num <- rep(0,compnum)
rownames(limmat) <- rownames(exprs)
colnames(limmat) <- rownames(compid)
names(limmas2) <- rownames(compid)
names(limmadf) <- rownames(compid)
names(limmav0) <- rownames(compid)
names(limmag1num) <- rownames(compid)
names(limmag2num) <- rownames(compid)
for (i in 1:compnum) {
message(paste("Running limma for comparision",i,"/",compnum))
selid1 <- which(groupid == compid[i, 1])
selid2 <- which(groupid == compid[i, 2])
# make a new count data frame
counts <- cbind(exprs[, selid1], exprs[, selid2])
# remove NAs
not.nas <- which(apply(counts, 1, function(x) !any(is.na(x))) == TRUE)
# runn voom/limma
d <- DGEList(counts[not.nas,])
d <- calcNormFactors(d, method = norm.factor.method)
g1num <- length(selid1)
g2num <- length(selid2)
designmat <- cbind(base = rep(1, (g1num + g2num)), delta = c(rep(0,
g1num), rep(1, g2num)))
y <- voom(d, designmat, normalize.method = voom.normalize.method)
fit <- lmFit(y, designmat)
fit <- eBayes(fit)
limmafits[[i]] <- fit
limmat[not.nas, i] <- fit$t[, 2]
limmas2[i] <- fit$s2.prior
limmadf[i] <- fit$df.prior
limmav0[i] <- fit$var.prior[2]
limmag1num[i] <- g1num
limmag2num[i] <- g2num
}
limmacompnum <- nrow(compid)
names(limmafits) <- rownames(compid)
result <- list(t = limmat,
v0 = limmav0,
df0 = limmadf,
s20 = limmas2,
g1num = limmag1num,
g2num = limmag2num,
compnum = limmacompnum,
fits = limmafits)
}
limmafit.list <-
function (fitlist, cmp.idx=2)
{
compnum <- length(fitlist)
genes <- c()
for (i in 1:compnum) genes <- unique(c(genes, rownames(fitlist[[i]])))
genenum <- length(genes)
limmat <- matrix(NA,genenum,compnum)
limmas2 <- rep(0,compnum)
limmadf <- rep(0,compnum)
limmav0 <- rep(0,compnum)
limmag1num <- rep(0,compnum)
limmag2num <- rep(0,compnum)
rownames(limmat) <- genes
colnames(limmat) <- names(fitlist)
names(limmas2) <- names(fitlist)
names(limmadf) <- names(fitlist)
names(limmav0) <- names(fitlist)
names(limmag1num) <- names(fitlist)
names(limmag2num) <- names(fitlist)
for (i in 1:compnum) {
this.t <- fitlist[[i]]$t[,cmp.idx]
limmat[names(this.t),i] <- this.t
limmas2[i] <- fitlist[[i]]$s2.prior
limmadf[i] <- fitlist[[i]]$df.prior
limmav0[i] <- fitlist[[i]]$var.prior[cmp.idx]
limmag1num[i] <- sum(fitlist[[i]]$design[,cmp.idx]==0)
limmag2num[i] <- sum(fitlist[[i]]$design[,cmp.idx]==1)
}
limmacompnum <- compnum
result <- list(t = limmat,
v0 = limmav0,
df0 = limmadf,
s20 = limmas2,
g1num = limmag1num,
g2num = limmag2num,
compnum = limmacompnum,
fits = limmafits)
}
## Rank genes based on statistics
generank<-function(x) {
xcol<-ncol(x)
xrow<-nrow(x)
result<-matrix(0,xrow,xcol)
z<-(1:1:xrow)
for(i in 1:xcol) {
y<-sort(x[,i],decreasing=TRUE,na.last=TRUE)
result[,i]<-match(x[,i],y)
result[,i]<-order(result[,i])
}
result
}
## Log-likelihood for moderated t under H0
modt.f0.loglike<-function(x,df) {
a<-dt(x, df, log=TRUE)
result<-as.vector(a)
flag<-which(is.na(result)==TRUE)
result[flag]<-0
result
}
## Log-likelihood for moderated t under H1
## param=c(df,g1num,g2num,v0)
modt.f1.loglike<-function(x,param) {
df<-param[1]
g1num<-param[2]
g2num<-param[3]
v0<-param[4]
w<-sqrt(1+v0/(1/g1num+1/g2num))
dt(x/w, df, log=TRUE)-log(w)
a<-dt(x/w, df, log=TRUE)-log(w)
result<-as.vector(a)
flag<-which(is.na(result)==TRUE)
result[flag]<-0
result
}
## Correlation Motif Fit
cmfit.X<-function(x, type, K=1, tol=1e-3, max.iter=100) {
## initialize
xrow <- nrow(x)
xcol <- ncol(x)
loglike0 <- list()
loglike1 <- list()
p <- rep(1, K)/K
q <- matrix(runif(K * xcol), K, xcol)
q[1, ] <- rep(0.01, xcol)
for (i in 1:xcol) {
f0 <- type[[i]][[1]]
f0param <- type[[i]][[2]]
f1 <- type[[i]][[3]]
f1param <- type[[i]][[4]]
loglike0[[i]] <- f0(x[, i], f0param)
loglike1[[i]] <- f1(x[, i], f1param)
}
condlike <- list()
for (i in 1:xcol) {
condlike[[i]] <- matrix(0, xrow, K)
}
loglike.old <- -1e+10
for (i.iter in 1:max.iter) {
if ((i.iter%%50) == 0) {
print(paste("We have run the first ", i.iter, " iterations for K=",
K, sep = ""))
}
err <- tol + 1
clustlike <- matrix(0, xrow, K)
#templike <- matrix(0, xrow, 2)
templike1 <- rep(0, xrow)
templike2 <- rep(0, xrow)
for (j in 1:K) {
for (i in 1:xcol) {
templike1 <- log(q[j, i]) + loglike1[[i]]
templike2 <- log(1 - q[j, i]) + loglike0[[i]]
tempmax <- Rfast::Pmax(templike1, templike2)
templike1 <- exp(templike1 - tempmax)
templike2 <- exp(templike2 - tempmax)
tempsum <- templike1 + templike2
clustlike[, j] <- clustlike[, j] + tempmax +
log(tempsum)
condlike[[i]][, j] <- templike1/tempsum
}
clustlike[, j] <- clustlike[, j] + log(p[j])
}
#tempmax <- apply(clustlike, 1, max)
tempmax <- Rfast::rowMaxs(clustlike, value=TRUE)
for (j in 1:K) {
clustlike[, j] <- exp(clustlike[, j] - tempmax)
}
#tempsum <- apply(clustlike, 1, sum)
tempsum <- Rfast::rowsums(clustlike)
for (j in 1:K) {
clustlike[, j] <- clustlike[, j]/tempsum
}
#p.new <- (apply(clustlike, 2, sum) + 1)/(xrow + K)
p.new <- (Rfast::colsums(clustlike) + 1)/(xrow + K)
q.new <- matrix(0, K, xcol)
for (j in 1:K) {
clustpsum <- sum(clustlike[, j])
for (i in 1:xcol) {
q.new[j, i] <- (sum(clustlike[, j] * condlike[[i]][,
j]) + 1)/(clustpsum + 2)
}
}
err.p <- max(abs(p.new - p)/p)
err.q <- max(abs(q.new - q)/q)
err <- max(err.p, err.q)
loglike.new <- (sum(tempmax + log(tempsum)) + sum(log(p.new)) +
sum(log(q.new) + log(1 - q.new)))/xrow
p <- p.new
q <- q.new
loglike.old <- loglike.new
if (err < tol) {
break
}
}
clustlike <- matrix(0, xrow, K)
for (j in 1:K) {
for (i in 1:xcol) {
templike1 <- log(q[j, i]) + loglike1[[i]]
templike2 <- log(1 - q[j, i]) + loglike0[[i]]
tempmax <- Rfast::Pmax(templike1, templike2)
templike1 <- exp(templike1 - tempmax)
templike2 <- exp(templike2 - tempmax)
tempsum <- templike1 + templike2
clustlike[, j] <- clustlike[, j] + tempmax + log(tempsum)
condlike[[i]][, j] <- templike1/tempsum
}
clustlike[, j] <- clustlike[, j] + log(p[j])
}
#tempmax <- apply(clustlike, 1, max)
tempmax <- Rfast::rowMaxs(clustlike, value=TRUE)
for (j in 1:K) {
clustlike[, j] <- exp(clustlike[, j] - tempmax)
}
#tempsum <- apply(clustlike, 1, sum)
tempsum <- Rfast::rowsums(clustlike)
for (j in 1:K) {
clustlike[, j] <- clustlike[, j]/tempsum
}
p.post <- matrix(0, xrow, xcol)
for (j in 1:K) {
for (i in 1:xcol) {
p.post[, i] <- p.post[, i] + clustlike[, j] * condlike[[i]][,
j]
}
}
loglike.old <- loglike.old - (sum(log(p)) + sum(log(q) +
log(1 - q)))/xrow
loglike.old <- loglike.old * xrow
result <- list(p.post = p.post, motif.prior = p, motif.q = q,
loglike = loglike.old, clustlike=clustlike, condlike=condlike)
}
## Fit using (0,0,...,0) and (1,1,...,1)
cmfitall<-function(x, type, tol=1e-3, max.iter=100) {
## initialize
xrow<-nrow(x)
xcol<-ncol(x)
loglike0<-list()
loglike1<-list()
p<-0.01
## compute loglikelihood
L0<-matrix(0,xrow,1)
L1<-matrix(0,xrow,1)
for(i in 1:xcol) {
f0<-type[[i]][[1]]
f0param<-type[[i]][[2]]
f1<-type[[i]][[3]]
f1param<-type[[i]][[4]]
loglike0[[i]]<-f0(x[,i],f0param)
loglike1[[i]]<-f1(x[,i],f1param)
L0<-L0+loglike0[[i]]
L1<-L1+loglike1[[i]]
}
## EM algorithm to get MLE of p and q
loglike.old <- -1e10
for(i.iter in 1:max.iter) {
if((i.iter%%50) == 0) {
print(paste("We have run the first ", i.iter, " iterations",sep=""))
}
err<-tol+1
## compute posterior cluster membership
clustlike<-matrix(0,xrow,2)
clustlike[,1]<-log(1-p)+L0
clustlike[,2]<-log(p)+L1
tempmax<-apply(clustlike,1,max)
for(j in 1:2) {
clustlike[,j]<-exp(clustlike[,j]-tempmax)
}
tempsum<-apply(clustlike,1,sum)
## update motif occurrence rate
for(j in 1:2) {
clustlike[,j]<-clustlike[,j]/tempsum
}
p.new<-(sum(clustlike[,2])+1)/(xrow+2)
## evaluate convergence
err<-abs(p.new-p)/p
## evaluate whether the log.likelihood increases
loglike.new<-(sum(tempmax+log(tempsum))+log(p.new)+log(1-p.new))/xrow
loglike.old<-loglike.new
p<-p.new
if(err<tol) {
break;
}
}
## compute posterior p
clustlike<-matrix(0,xrow,2)
clustlike[,1]<-log(1-p)+L0
clustlike[,2]<-log(p)+L1
tempmax<-apply(clustlike,1,max)
for(j in 1:2) {
clustlike[,j]<-exp(clustlike[,j]-tempmax)
}
tempsum<-apply(clustlike,1,sum)
for(j in 1:2) {
clustlike[,j]<-clustlike[,j]/tempsum
}
p.post<-matrix(0,xrow,xcol)
for(i in 1:xcol) {
p.post[,i]<-clustlike[,2]
}
## return
#calculate back loglikelihood
loglike.old<-loglike.old-(log(p)+log(1-p))/xrow
loglike.old<-loglike.old*xrow
result<-list(p.post=p.post, motif.prior=p, loglike=loglike.old)
}
## Fit each dataset separately
cmfitsep<-function(x, type, tol=1e-3, max.iter=100) {
## initialize
xrow<-nrow(x)
xcol<-ncol(x)
loglike0<-list()
loglike1<-list()
p<-0.01*rep(1,xcol)
loglike.final<-rep(0,xcol)
## compute loglikelihood
for(i in 1:xcol) {
f0<-type[[i]][[1]]
f0param<-type[[i]][[2]]
f1<-type[[i]][[3]]
f1param<-type[[i]][[4]]
loglike0[[i]]<-f0(x[,i],f0param)
loglike1[[i]]<-f1(x[,i],f1param)
}
p.post<-matrix(0,xrow,xcol)
## EM algorithm to get MLE of p
for(coli in 1:xcol) {
loglike.old <- -1e10
for(i.iter in 1:max.iter) {
if((i.iter%%50) == 0) {
print(paste("We have run the first ", i.iter, " iterations",sep=""))
}
err<-tol+1
## compute posterior cluster membership
clustlike<-matrix(0,xrow,2)
clustlike[,1]<-log(1-p[coli])+loglike0[[coli]]
clustlike[,2]<-log(p[coli])+loglike1[[coli]]
tempmax<-apply(clustlike,1,max)
for(j in 1:2) {
clustlike[,j]<-exp(clustlike[,j]-tempmax)
}
tempsum<-apply(clustlike,1,sum)
## evaluate whether the log.likelihood increases
loglike.new<-sum(tempmax+log(tempsum))/xrow
## update motif occurrence rate
for(j in 1:2) {
clustlike[,j]<-clustlike[,j]/tempsum
}
p.new<-(sum(clustlike[,2]))/(xrow)
## evaluate convergence
err<-abs(p.new-p[coli])/p[coli]
loglike.old<-loglike.new
p[coli]<-p.new
if(err<tol) {
break;
}
}
## compute posterior p
clustlike<-matrix(0,xrow,2)
clustlike[,1]<-log(1-p[coli])+loglike0[[coli]]
clustlike[,2]<-log(p[coli])+loglike1[[coli]]
tempmax<-apply(clustlike,1,max)
for(j in 1:2) {
clustlike[,j]<-exp(clustlike[,j]-tempmax)
}
tempsum<-apply(clustlike,1,sum)
for(j in 1:2) {
clustlike[,j]<-clustlike[,j]/tempsum
}
p.post[,coli]<-clustlike[,2]
loglike.final[coli]<-loglike.old
}
## return
loglike.final<-loglike.final*xrow
result<-list(p.post=p.post, motif.prior=p, loglike=loglike.final)
}
## Fit the full model
cmfitfull<-function(x, type, tol=1e-3, max.iter=100) {
## initialize
xrow<-nrow(x)
xcol<-ncol(x)
loglike0<-list()
loglike1<-list()
K<-2^xcol
p<-rep(1,K)/K
pattern<-rep(0,xcol)
patid<-matrix(0,K,xcol)
## compute loglikelihood
for(i in 1:xcol) {
f0<-type[[i]][[1]]
f0param<-type[[i]][[2]]
f1<-type[[i]][[3]]
f1param<-type[[i]][[4]]
loglike0[[i]]<-f0(x[,i],f0param)
loglike1[[i]]<-f1(x[,i],f1param)
}
L<-matrix(0,xrow,K)
for(i in 1:K)
{
patid[i,]<-pattern
for(j in 1:xcol) {
if(pattern[j] < 0.5) {
L[,i]<-L[,i]+loglike0[[j]]
} else {
L[,i]<-L[,i]+loglike1[[j]]
}
}
if(i < K) {
pattern[xcol]<-pattern[xcol]+1
j<-xcol
while(pattern[j] > 1) {
pattern[j]<-0
j<-j-1
pattern[j]<-pattern[j]+1
}
}
}
## EM algorithm to get MLE of p and q
loglike.old <- -1e10
for(i.iter in 1:max.iter) {
if((i.iter%%50) == 0) {
print(paste("We have run the first ", i.iter, " iterations",sep=""))
}
err<-tol+1
## compute posterior cluster membership
clustlike<-matrix(0,xrow,K)
for(j in 1:K) {
clustlike[,j]<-log(p[j])+L[,j]
}
tempmax<-apply(clustlike,1,max)
for(j in 1:K) {
clustlike[,j]<-exp(clustlike[,j]-tempmax)
}
tempsum<-apply(clustlike,1,sum)
## update motif occurrence rate
for(j in 1:K) {
clustlike[,j]<-clustlike[,j]/tempsum
}
p.new<-(apply(clustlike,2,sum)+1)/(xrow+K)
## evaluate convergence
err<-max(abs(p.new-p)/p)
## evaluate whether the log.likelihood increases
loglike.new<-(sum(tempmax+log(tempsum))+sum(log(p.new)))/xrow
loglike.old<-loglike.new
p<-p.new
if(err<tol) {
break;
}
}
## compute posterior p
clustlike<-matrix(0,xrow,K)
for(j in 1:K) {
clustlike[,j]<-log(p[j])+L[,j]
}
tempmax<-apply(clustlike,1,max)
for(j in 1:K) {
clustlike[,j]<-exp(clustlike[,j]-tempmax)
}
tempsum<-apply(clustlike,1,sum)
for(j in 1:K) {
clustlike[,j]<-clustlike[,j]/tempsum
}
p.post<-matrix(0,xrow,xcol)
for(j in 1:K) {
for(i in 1:xcol) {
if(patid[j,i] > 0.5) {
p.post[,i]<-p.post[,i]+clustlike[,j]
}
}
}
## return
#calculate back loglikelihood
loglike.old<-loglike.old-sum(log(p))/xrow
loglike.old<-loglike.old*xrow
result<-list(p.post=p.post, motif.prior=p, loglike=loglike.old)
}
generatetype<-function(limfitted)
{
jtype<-list()
df<-limfitted$g1num+limfitted$g2num-2+limfitted$df0
for(j in 1:limfitted$compnum)
{
jtype[[j]]<-list(f0=modt.f0.loglike, f0.param=df[j], f1=modt.f1.loglike, f1.param=c(df[j],limfitted$g1num[j],limfitted$g2num[j],limfitted$v0[j]))
}
jtype
}
cormotiffit <- function(exprs, groupid=NULL, compid=NULL, K=1, tol=1e-3,
max.iter=100, BIC=TRUE, norm.factor.method="TMM",
voom.normalize.method = "none", runtype=c("logCPM","counts","limmafits"), each=3)
{
# first I want to do some typechecking. Input can be either a normalized
# matrix, a count matrix, or a list of limma fits. Dispatch the correct
# limmafit accordingly.
# todo: add some typechecking here
limfitted <- list()
if (runtype=="counts") {
limfitted <- limmafit.counts(exprs,groupid,compid, norm.factor.method, voom.normalize.method)
} else if (runtype=="logCPM") {
limfitted <- limmafit.default(exprs,groupid,compid)
} else if (runtype=="limmafits") {
limfitted <- limmafit.list(exprs)
} else {
stop("runtype must be one of 'logCPM', 'counts', or 'limmafits'")
}
jtype<-generatetype(limfitted)
fitresult<-list()
ks <- rep(K, each = each)
fitresult <- bplapply(1:length(ks), function(i, x, type, ks, tol, max.iter) {
cmfit.X(x, type, K = ks[i], tol = tol, max.iter = max.iter)
}, x=limfitted$t, type=jtype, ks=ks, tol=tol, max.iter=max.iter)
best.fitresults <- list()
for (i in 1:length(K)) {
w.k <- which(ks==K[i])
this.bic <- c()
for (j in w.k) this.bic[j] <- -2 * fitresult[[j]]$loglike + (K[i] - 1 + K[i] * limfitted$compnum) * log(dim(limfitted$t)[1])
w.min <- which(this.bic == min(this.bic, na.rm = TRUE))[1]
best.fitresults[[i]] <- fitresult[[w.min]]
}
fitresult <- best.fitresults
bic <- rep(0, length(K))
aic <- rep(0, length(K))
loglike <- rep(0, length(K))
for (i in 1:length(K)) loglike[i] <- fitresult[[i]]$loglike
for (i in 1:length(K)) bic[i] <- -2 * fitresult[[i]]$loglike + (K[i] - 1 + K[i] * limfitted$compnum) * log(dim(limfitted$t)[1])
for (i in 1:length(K)) aic[i] <- -2 * fitresult[[i]]$loglike + 2 * (K[i] - 1 + K[i] * limfitted$compnum)
if(BIC==TRUE) {
bestflag=which(bic==min(bic))
}
else {
bestflag=which(aic==min(aic))
}
result<-list(bestmotif=fitresult[[bestflag]],bic=cbind(K,bic),
aic=cbind(K,aic),loglike=cbind(K,loglike), allmotifs=fitresult)
}
cormotiffitall<-function(exprs,groupid,compid, tol=1e-3, max.iter=100)
{
limfitted<-limmafit(exprs,groupid,compid)
jtype<-generatetype(limfitted)
fitresult<-cmfitall(limfitted$t,type=jtype,tol=1e-3,max.iter=max.iter)
}
cormotiffitsep<-function(exprs,groupid,compid, tol=1e-3, max.iter=100)
{
limfitted<-limmafit(exprs,groupid,compid)
jtype<-generatetype(limfitted)
fitresult<-cmfitsep(limfitted$t,type=jtype,tol=1e-3,max.iter=max.iter)
}
cormotiffitfull<-function(exprs,groupid,compid, tol=1e-3, max.iter=100)
{
limfitted<-limmafit(exprs,groupid,compid)
jtype<-generatetype(limfitted)
fitresult<-cmfitfull(limfitted$t,type=jtype,tol=1e-3,max.iter=max.iter)
}
plotIC<-function(fitted_cormotif)
{
oldpar<-par(mfrow=c(1,2))
plot(fitted_cormotif$bic[,1], fitted_cormotif$bic[,2], type="b",xlab="Motif Number", ylab="BIC", main="BIC")
plot(fitted_cormotif$aic[,1], fitted_cormotif$aic[,2], type="b",xlab="Motif Number", ylab="AIC", main="AIC")
}
plotMotif<-function(fitted_cormotif,title="")
{
layout(matrix(1:2,ncol=2))
u<-1:dim(fitted_cormotif$bestmotif$motif.q)[2]
v<-1:dim(fitted_cormotif$bestmotif$motif.q)[1]
image(u,v,t(fitted_cormotif$bestmotif$motif.q),
col=gray(seq(from=1,to=0,by=-0.1)),xlab="Study",yaxt = "n",
ylab="Corr. Motifs",main=paste(title,"pattern",sep=" "))
axis(2,at=1:length(v))
for(i in 1:(length(u)+1))
{
abline(v=(i-0.5))
}
for(i in 1:(length(v)+1))
{
abline(h=(i-0.5))
}
Ng=10000
if(is.null(fitted_cormotif$bestmotif$p.post)!=TRUE)
Ng=nrow(fitted_cormotif$bestmotif$p.post)
genecount=floor(fitted_cormotif$bestmotif$motif.p*Ng)
NK=nrow(fitted_cormotif$bestmotif$motif.q)
plot(0,0.7,pch=".",xlim=c(0,1.2),ylim=c(0.75,NK+0.25),
frame.plot=FALSE,axes=FALSE,xlab="No. of genes",ylab="", main=paste(title,"frequency",sep=" "))
segments(0,0.7,fitted_cormotif$bestmotif$motif.p[1],0.7)
rect(0,1:NK-0.3,fitted_cormotif$bestmotif$motif.p,1:NK+0.3,
col="dark grey")
mtext(1:NK,at=1:NK,side=2,cex=0.8)
text(fitted_cormotif$bestmotif$motif.p+0.15,1:NK,
labels=floor(fitted_cormotif$bestmotif$motif.p*Ng))
}📌 Load Required Libraries
library(tidyverse)
library(ggplot2)
library(tidyr)
library(dplyr)
library(reshape2)
library(clusterProfiler)
library(AnnotationDbi)
library(org.Hs.eg.db)
library(RColorBrewer)
library(gprofiler2)
library(pheatmap)
library(ggpubr)
library(corrplot)
library(Cormotif)
library(Rfast)
library(BiocParallel)📌 Load Corrmotif Data
# Read the Corrmotif Results
Corrmotif <- read.csv("data/Corrmotif/CX5461.csv")
Corrmotif_df <- data.frame(Corrmotif)
rownames(Corrmotif_df) <- Corrmotif_df$Gene
exprs.corrmotif <- as.matrix(Corrmotif_df[,2:109])
# Read group and comparison IDs
groupid_df <- read.csv("data/Corrmotif/groupid.csv")
compid_df <- read.csv("data/Corrmotif/Compid.csv")📌 Fit Corrmotif Model (K=1:8)
set.seed(11111)
# Fit Corrmotif Model (K = 1 to 8)
set.seed(11111)
motif.fitted <- cormotiffit(
exprs = exprs.corrmotif,
groupid = groupid_df,
compid = compid_df,
K = 1:8,
max.iter = 1000,
BIC = TRUE,
runtype = "logCPM"
)
gene_prob_all <- motif.fitted$bestmotif$p.post
rownames(gene_prob_all) <- rownames(Corrmotif_df)
motif_prob <- motif.fitted$bestmotif$clustlike
rownames(motif_prob) <- rownames(gene_prob_all)
write.csv(motif_prob,"data/cormotif_probability_genelist_all.csv")📌 Plot motif
cormotif_all <- readRDS("data/Corrmotif/cormotif_all.RDS")
cormotif_all$bic K bic
[1,] 1 643837.2
[2,] 2 632515.2
[3,] 3 626572.5
[4,] 4 624577.2
[5,] 5 624656.6
[6,] 6 624667.6
[7,] 7 624660.0
[8,] 8 624786.5plotIC(cormotif_all)
plotMotif(cormotif_all)
📌 Extract Gene Probabilities
# Extract posterior probabilities for genes
gene_prob_all <- cormotif_all$bestmotif$p.post
rownames(gene_prob_all) <- rownames(Corrmotif_df)
# Define gene probability groups
prob_all_1 <- rownames(gene_prob_all[(gene_prob_all[,1] <0.5 & gene_prob_all[,2] <0.5 & gene_prob_all[,3] <0.5 & gene_prob_all[,4] <0.5 & gene_prob_all[,5] < 0.5 & gene_prob_all[,6]<0.5 & gene_prob_all[,7]<0.5 & gene_prob_all[,8]<0.5 & gene_prob_all[,9]<0.5 & gene_prob_all[,10]<0.5 & gene_prob_all[,11]<0.5 & gene_prob_all[,12]<0.5),])
length(prob_all_1)
prob_all_2 <- rownames(gene_prob_all[(gene_prob_all[,1] <0.5 & gene_prob_all[,2] <0.5 & gene_prob_all[,3] >0.5 & gene_prob_all[,4] >0.5 & gene_prob_all[,5] > 0.5 & gene_prob_all[,6]>0.5 & gene_prob_all[,7]<0.5 & gene_prob_all[,8]<0.5 & gene_prob_all[,9]>0.5 & gene_prob_all[,10]>0.1 & gene_prob_all[,11]>0.5 & gene_prob_all[,12]>0.1),])
length(prob_all_2)
prob_all_3 <- rownames(gene_prob_all[(gene_prob_all[,1] <0.5 & gene_prob_all[,2] <0.5 & gene_prob_all[,3] <0.5 & gene_prob_all[,4] <0.5 & gene_prob_all[,5] < 0.5 & gene_prob_all[,6]<0.5 & gene_prob_all[,7]<0.5 & gene_prob_all[,8]>=0.02 & gene_prob_all[,9]>0.5 & gene_prob_all[,10]>0.5 & gene_prob_all[,11]>0.5 & gene_prob_all[,12]>0.5),])
length(prob_all_3)
prob_all_4 <- rownames(gene_prob_all[(gene_prob_all[,1] <0.5 & gene_prob_all[,2] <0.5 & gene_prob_all[,3] <0.5 & gene_prob_all[,4] <0.5 & gene_prob_all[,5] < 0.5 & gene_prob_all[,6]<0.5 & gene_prob_all[,7]<0.5 & gene_prob_all[,8]<0.5 & gene_prob_all[,9]<0.5 & gene_prob_all[,10]>0.5 & gene_prob_all[,11]<0.5 & gene_prob_all[,12]>0.5),])
length(prob_all_4)📌 Distribution of Gene Clusters Identified by Corrmotif
# Load necessary library
library(ggplot2)
# Data
data <- data.frame(
Category = c("Non response", "CX_DOX shared late response",
"Dox specific response", "Late high dose DOX specific response"),
Value = c(7031, 414, 1531, 4874)
)
# Define custom colors
custom_colors <- c("Non response" = "#FF9999",
"CX_DOX shared late response" = "#66B2FF",
"Dox specific response" = "#99FF99",
"Late high dose DOX specific response" = "#FFD700")
# Create pie chart
ggplot(data, aes(x = "", y = Value, fill = Category)) +
geom_bar(width = 1, stat = "identity") +
coord_polar("y", start = 0) +
geom_text(aes(label = Value),
position = position_stack(vjust = 0.5),
size = 4, color = "black") +
labs(title = "Distribution of Gene Clusters Identified by Corrmotif", x = NULL, y = NULL) +
theme_void() +
scale_fill_manual(values = custom_colors)
| Version | Author | Date |
|---|---|---|
| b56a62a | sayanpaul01 | 2025-02-21 |
📌 Corr-motif Boxplots
📌 Non response (MRPL20)
# Load the dataset from the data folder
# Load the dataset from the data folder
boxplot1 <- read.csv("data/boxplot1.csv", check.names = FALSE)
boxplot1 <- as.data.frame(boxplot1)
# Print first few column names to check structure
print(colnames(boxplot1)) [1] "" "ENTREZID" "SYMBOL"
[4] "GENENAME" "17.3_CX.5461_0.1_3" "17.3_DOX_0.5_24"
[7] "87.1_DOX_0.5_24" "87.1_VEH_0.1_24" "87.1_VEH_0.5_24"
[10] "87.1_CX.5461_0.1_48" "87.1_CX.5461_0.5_48" "87.1_DOX_0.1_48"
[13] "87.1_DOX_0.5_48" "87.1_VEH_0.1_48" "87.1_VEH_0.5_48"
[16] "17.3_VEH_0.1_24" "17.3_VEH_0.5_24" "17.3_CX.5461_0.1_48"
[19] "17.3_CX.5461_0.5_48" "17.3_DOX_0.1_48" "17.3_DOX_0.5_48"
[22] "17.3_VEH_0.1_48" "17.3_VEH_0.5_48" "84.1_CX.5461_0.1_3"
[25] "17.3_CX.5461_0.5_3" "84.1_CX.5461_0.5_3" "84.1_DOX_0.1_3"
[28] "84.1_DOX_0.5_3" "84.1_VEH_0.1_3" "84.1_VEH_0.5_3"
[31] "84.1_CX.5461_0.1_24" "84.1_CX.5461_0.5_24" "84.1_DOX_0.1_24"
[34] "84.1_DOX_0.5_24" "84.1_VEH_0.1_24" "17.3_DOX_0.1_3"
[37] "84.1_VEH_0.5_24" "84.1_CX.5461_0.1_48" "84.1_CX.5461_0.5_48"
[40] "84.1_DOX_0.1_48" "84.1_DOX_0.5_48" "84.1_VEH_0.1_48"
[43] "84.1_VEH_0.5_48" "90.1_CX.5461_0.1_3" "90.1_CX.5461_0.5_3"
[46] "90.1_DOX_0.1_3" "17.3_DOX_0.5_3" "90.1_DOX_0.5_3"
[49] "90.1_VEH_0.1_3" "90.1_VEH_0.5_3" "90.1_CX.5461_0.1_24"
[52] "90.1_CX.5461_0.5_24" "90.1_DOX_0.1_24" "90.1_DOX_0.5_24"
[55] "90.1_VEH_0.1_24" "90.1_VEH_0.5_24" "90.1_CX.5461_0.1_48"
[58] "17.3_VEH_0.1_3" "90.1_CX.5461_0.5_48" "90.1_DOX_0.1_48"
[61] "90.1_DOX_0.5_48" "90.1_VEH_0.1_48" "90.1_VEH_0.5_48"
[64] "75.1_CX.5461_0.1_3" "75.1_CX.5461_0.5_3" "75.1_DOX_0.1_3"
[67] "75.1_DOX_0.5_3" "75.1_VEH_0.1_3" "17.3_VEH_0.5_3"
[70] "75.1_VEH_0.5_3" "75.1_CX.5461_0.1_24" "75.1_CX.5461_0.5_24"
[73] "75.1_DOX_0.1_24" "75.1_DOX_0.5_24" "75.1_VEH_0.1_24"
[76] "75.1_VEH_0.5_24" "75.1_CX.5461_0.1_48" "75.1_CX.5461_0.5_48"
[79] "75.1_DOX_0.1_48" "17.3_CX.5461_0.1_24" "75.1_DOX_0.5_48"
[82] "75.1_VEH_0.1_48" "75.1_VEH_0.5_48" "78.1_CX.5461_0.1_3"
[85] "78.1_CX.5461_0.5_3" "78.1_DOX_0.1_3" "78.1_DOX_0.5_3"
[88] "78.1_VEH_0.1_3" "78.1_VEH_0.5_3" "78.1_CX.5461_0.1_24"
[91] "17.3_CX.5461_0.5_24" "78.1_CX.5461_0.5_24" "78.1_DOX_0.1_24"
[94] "78.1_DOX_0.5_24" "78.1_VEH_0.1_24" "78.1_VEH_0.5_24"
[97] "78.1_CX.5461_0.1_48" "78.1_CX.5461_0.5_48" "78.1_DOX_0.1_48"
[100] "78.1_DOX_0.5_48" "78.1_VEH_0.1_48" "17.3_DOX_0.1_24"
[103] "78.1_VEH_0.5_48" "87.1_CX.5461_0.1_3" "87.1_CX.5461_0.5_3"
[106] "87.1_DOX_0.1_3" "87.1_DOX_0.5_3" "87.1_VEH_0.1_3"
[109] "87.1_VEH_0.5_3" "87.1_CX.5461_0.1_24" "87.1_CX.5461_0.5_24"
[112] "87.1_DOX_0.1_24" # Print first few rows to check format
print(head(boxplot1[, 1:10])) ENTREZID SYMBOL GENENAME
1 1 653635 WASH7P WASP family homolog 7, pseudogene
2 2 729737 LOC729737 uncharacterized LOC729737
3 3 102723897 LOC102723897 WAS protein family homolog 9, pseudogene
4 4 100132287 LOC100132287 uncharacterized LOC100132287
5 5 102465432 <NA> <NA>
6 6 100133331 <NA> <NA>
17.3_CX.5461_0.1_3 17.3_DOX_0.5_24 87.1_DOX_0.5_24 87.1_VEH_0.1_24
1 3.499737 3.777758 4.051060 3.631547
2 4.018739 3.087263 2.799033 3.631547
3 3.581464 3.765087 4.210151 3.707275
4 3.229725 2.970710 1.422530 2.309608
5 6.910839 6.896427 5.596078 5.581451
6 3.044515 2.902929 1.971919 2.674101
87.1_VEH_0.5_24 87.1_CX.5461_0.1_48
1 3.758155 3.982758
2 4.399176 4.292059
3 3.679166 4.047012
4 2.553616 2.748309
5 5.117157 5.156085
6 2.861516 2.903876# Filter data for the gene with Entrez ID: 55052
gene_data <- boxplot1[boxplot1$ENTREZID == 55052, ]
# Check if gene_data is empty
if(nrow(gene_data) == 0) {
stop("No data found for the selected gene ENTIREZID 55052.")
}
# Reshape data from wide to long format
gene_data_long <- melt(gene_data,
id.vars = c("ENTREZID", "SYMBOL", "GENENAME"),
variable.name = "Sample",
value.name = "log2CPM")
# Print some sample names for debugging
print(unique(gene_data_long$Sample)) [1] 17.3_CX.5461_0.1_3 17.3_DOX_0.5_24
[4] 87.1_DOX_0.5_24 87.1_VEH_0.1_24 87.1_VEH_0.5_24
[7] 87.1_CX.5461_0.1_48 87.1_CX.5461_0.5_48 87.1_DOX_0.1_48
[10] 87.1_DOX_0.5_48 87.1_VEH_0.1_48 87.1_VEH_0.5_48
[13] 17.3_VEH_0.1_24 17.3_VEH_0.5_24 17.3_CX.5461_0.1_48
[16] 17.3_CX.5461_0.5_48 17.3_DOX_0.1_48 17.3_DOX_0.5_48
[19] 17.3_VEH_0.1_48 17.3_VEH_0.5_48 84.1_CX.5461_0.1_3
[22] 17.3_CX.5461_0.5_3 84.1_CX.5461_0.5_3 84.1_DOX_0.1_3
[25] 84.1_DOX_0.5_3 84.1_VEH_0.1_3 84.1_VEH_0.5_3
[28] 84.1_CX.5461_0.1_24 84.1_CX.5461_0.5_24 84.1_DOX_0.1_24
[31] 84.1_DOX_0.5_24 84.1_VEH_0.1_24 17.3_DOX_0.1_3
[34] 84.1_VEH_0.5_24 84.1_CX.5461_0.1_48 84.1_CX.5461_0.5_48
[37] 84.1_DOX_0.1_48 84.1_DOX_0.5_48 84.1_VEH_0.1_48
[40] 84.1_VEH_0.5_48 90.1_CX.5461_0.1_3 90.1_CX.5461_0.5_3
[43] 90.1_DOX_0.1_3 17.3_DOX_0.5_3 90.1_DOX_0.5_3
[46] 90.1_VEH_0.1_3 90.1_VEH_0.5_3 90.1_CX.5461_0.1_24
[49] 90.1_CX.5461_0.5_24 90.1_DOX_0.1_24 90.1_DOX_0.5_24
[52] 90.1_VEH_0.1_24 90.1_VEH_0.5_24 90.1_CX.5461_0.1_48
[55] 17.3_VEH_0.1_3 90.1_CX.5461_0.5_48 90.1_DOX_0.1_48
[58] 90.1_DOX_0.5_48 90.1_VEH_0.1_48 90.1_VEH_0.5_48
[61] 75.1_CX.5461_0.1_3 75.1_CX.5461_0.5_3 75.1_DOX_0.1_3
[64] 75.1_DOX_0.5_3 75.1_VEH_0.1_3 17.3_VEH_0.5_3
[67] 75.1_VEH_0.5_3 75.1_CX.5461_0.1_24 75.1_CX.5461_0.5_24
[70] 75.1_DOX_0.1_24 75.1_DOX_0.5_24 75.1_VEH_0.1_24
[73] 75.1_VEH_0.5_24 75.1_CX.5461_0.1_48 75.1_CX.5461_0.5_48
[76] 75.1_DOX_0.1_48 17.3_CX.5461_0.1_24 75.1_DOX_0.5_48
[79] 75.1_VEH_0.1_48 75.1_VEH_0.5_48 78.1_CX.5461_0.1_3
[82] 78.1_CX.5461_0.5_3 78.1_DOX_0.1_3 78.1_DOX_0.5_3
[85] 78.1_VEH_0.1_3 78.1_VEH_0.5_3 78.1_CX.5461_0.1_24
[88] 17.3_CX.5461_0.5_24 78.1_CX.5461_0.5_24 78.1_DOX_0.1_24
[91] 78.1_DOX_0.5_24 78.1_VEH_0.1_24 78.1_VEH_0.5_24
[94] 78.1_CX.5461_0.1_48 78.1_CX.5461_0.5_48 78.1_DOX_0.1_48
[97] 78.1_DOX_0.5_48 78.1_VEH_0.1_48 17.3_DOX_0.1_24
[100] 78.1_VEH_0.5_48 87.1_CX.5461_0.1_3 87.1_CX.5461_0.5_3
[103] 87.1_DOX_0.1_3 87.1_DOX_0.5_3 87.1_VEH_0.1_3
[106] 87.1_VEH_0.5_3 87.1_CX.5461_0.1_24 87.1_CX.5461_0.5_24
[109] 87.1_DOX_0.1_24
109 Levels: 17.3_CX.5461_0.1_3 17.3_DOX_0.5_24 ... 87.1_DOX_0.1_24# Extract details from sample names
gene_data_long <- gene_data_long %>%
mutate(
Time = sub(".*_(\\d+)$", "\\1", Sample),
Concentration = sub(".*_(0\\.\\d)_\\d+$", "\\1", Sample),
Drug = sub(".*_(CX\\.5461|DOX|VEH)_.*", "\\1", Sample),
Indv = sub("^([0-9]+\\.[0-9]+)_.*", "\\1", Sample) # Ensure correct pattern extraction
)
# Print extracted `Indv` column for debugging
print(unique(gene_data_long$Indv))[1] "" "17.3" "87.1" "84.1" "90.1" "75.1" "78.1"# Convert extracted columns to factors
gene_data_long$Time <- factor(gene_data_long$Time, levels = c("3", "24", "48"))
gene_data_long$Concentration <- factor(gene_data_long$Concentration, levels = c("0.1", "0.5"))
# Ensure each concentration facet only shows relevant data
gene_data_long <- gene_data_long %>%
group_by(Concentration) %>%
filter(all(Concentration == "0.1") | all(Concentration == "0.5")) %>%
ungroup()
# Map individual IDs
indv_mapping <- c("75.1" = "1", "78.1" = "2", "87.1" = "3", "17.3" = "4", "84.1" = "5", "90.1" = "6")
# Ensure `Indv` values match the keys in `indv_mapping`
gene_data_long <- gene_data_long %>%
mutate(
Indv = ifelse(Indv %in% names(indv_mapping), indv_mapping[Indv], NA)
)
# Print `Indv` column again to confirm mapping worked
print(unique(gene_data_long$Indv))[1] "4" "3" "5" "6" "1" "2"# Check for missing values and handle them
gene_data_long <- gene_data_long %>%
mutate(Indv = ifelse(is.na(Indv), "Unknown", Indv)) # Assign "Unknown" to unidentified individuals
# Define drug colors
drug_palette <- c("CX.5461" = "blue", "DOX" = "red", "VEH" = "green")
# Extract the gene symbol for labeling
gene_symbol <- unique(gene_data_long$SYMBOL)[1]
# Create the boxplot
ggplot(gene_data_long, aes(x = Drug, y = log2CPM, fill = Drug)) +
geom_boxplot(outlier.shape = NA) +
scale_fill_manual(values = drug_palette) +
facet_grid(Concentration ~ Time, labeller = label_both) +
geom_point(aes(color = Indv), size = 2, alpha = 0.5,
position = position_jitter(width = -0.3, height = 0)) +
ggtitle("Non response") +
labs(
title = "Non response",
x = "Drugs",
y = paste(gene_symbol, " log2CPM")
) +
ylim(0, NA) +
theme_bw() +
theme(
plot.title = element_text(size = rel(1.5), hjust = 0.5),
axis.title = element_text(size = 15, color = "black"),
axis.ticks = element_line(linewidth = 1.5),
axis.line = element_line(linewidth = 1.5),
axis.text.y = element_text(size = 10, color = "black"),
axis.text.x = element_text(size = 10, color = "black", angle = 45, hjust = 1),
strip.text = element_text(size = 12, face = "bold")
)
| Version | Author | Date |
|---|---|---|
| e73d731 | sayanpaul01 | 2025-02-23 |
📌 Non response (FAAP20)
# Load the dataset from the data folder
# Load the dataset from the data folder
# Filter data for the gene with Entrez ID: 199990
gene_data <- boxplot1[boxplot1$ENTREZID == 199990, ]
# Check if gene_data is empty
if(nrow(gene_data) == 0) {
stop("No data found for the selected gene ENTIREZID 199990.")
}
# Reshape data from wide to long format
gene_data_long <- melt(gene_data,
id.vars = c("ENTREZID", "SYMBOL", "GENENAME"),
variable.name = "Sample",
value.name = "log2CPM")
# Print some sample names for debugging
print(unique(gene_data_long$Sample)) [1] 17.3_CX.5461_0.1_3 17.3_DOX_0.5_24
[4] 87.1_DOX_0.5_24 87.1_VEH_0.1_24 87.1_VEH_0.5_24
[7] 87.1_CX.5461_0.1_48 87.1_CX.5461_0.5_48 87.1_DOX_0.1_48
[10] 87.1_DOX_0.5_48 87.1_VEH_0.1_48 87.1_VEH_0.5_48
[13] 17.3_VEH_0.1_24 17.3_VEH_0.5_24 17.3_CX.5461_0.1_48
[16] 17.3_CX.5461_0.5_48 17.3_DOX_0.1_48 17.3_DOX_0.5_48
[19] 17.3_VEH_0.1_48 17.3_VEH_0.5_48 84.1_CX.5461_0.1_3
[22] 17.3_CX.5461_0.5_3 84.1_CX.5461_0.5_3 84.1_DOX_0.1_3
[25] 84.1_DOX_0.5_3 84.1_VEH_0.1_3 84.1_VEH_0.5_3
[28] 84.1_CX.5461_0.1_24 84.1_CX.5461_0.5_24 84.1_DOX_0.1_24
[31] 84.1_DOX_0.5_24 84.1_VEH_0.1_24 17.3_DOX_0.1_3
[34] 84.1_VEH_0.5_24 84.1_CX.5461_0.1_48 84.1_CX.5461_0.5_48
[37] 84.1_DOX_0.1_48 84.1_DOX_0.5_48 84.1_VEH_0.1_48
[40] 84.1_VEH_0.5_48 90.1_CX.5461_0.1_3 90.1_CX.5461_0.5_3
[43] 90.1_DOX_0.1_3 17.3_DOX_0.5_3 90.1_DOX_0.5_3
[46] 90.1_VEH_0.1_3 90.1_VEH_0.5_3 90.1_CX.5461_0.1_24
[49] 90.1_CX.5461_0.5_24 90.1_DOX_0.1_24 90.1_DOX_0.5_24
[52] 90.1_VEH_0.1_24 90.1_VEH_0.5_24 90.1_CX.5461_0.1_48
[55] 17.3_VEH_0.1_3 90.1_CX.5461_0.5_48 90.1_DOX_0.1_48
[58] 90.1_DOX_0.5_48 90.1_VEH_0.1_48 90.1_VEH_0.5_48
[61] 75.1_CX.5461_0.1_3 75.1_CX.5461_0.5_3 75.1_DOX_0.1_3
[64] 75.1_DOX_0.5_3 75.1_VEH_0.1_3 17.3_VEH_0.5_3
[67] 75.1_VEH_0.5_3 75.1_CX.5461_0.1_24 75.1_CX.5461_0.5_24
[70] 75.1_DOX_0.1_24 75.1_DOX_0.5_24 75.1_VEH_0.1_24
[73] 75.1_VEH_0.5_24 75.1_CX.5461_0.1_48 75.1_CX.5461_0.5_48
[76] 75.1_DOX_0.1_48 17.3_CX.5461_0.1_24 75.1_DOX_0.5_48
[79] 75.1_VEH_0.1_48 75.1_VEH_0.5_48 78.1_CX.5461_0.1_3
[82] 78.1_CX.5461_0.5_3 78.1_DOX_0.1_3 78.1_DOX_0.5_3
[85] 78.1_VEH_0.1_3 78.1_VEH_0.5_3 78.1_CX.5461_0.1_24
[88] 17.3_CX.5461_0.5_24 78.1_CX.5461_0.5_24 78.1_DOX_0.1_24
[91] 78.1_DOX_0.5_24 78.1_VEH_0.1_24 78.1_VEH_0.5_24
[94] 78.1_CX.5461_0.1_48 78.1_CX.5461_0.5_48 78.1_DOX_0.1_48
[97] 78.1_DOX_0.5_48 78.1_VEH_0.1_48 17.3_DOX_0.1_24
[100] 78.1_VEH_0.5_48 87.1_CX.5461_0.1_3 87.1_CX.5461_0.5_3
[103] 87.1_DOX_0.1_3 87.1_DOX_0.5_3 87.1_VEH_0.1_3
[106] 87.1_VEH_0.5_3 87.1_CX.5461_0.1_24 87.1_CX.5461_0.5_24
[109] 87.1_DOX_0.1_24
109 Levels: 17.3_CX.5461_0.1_3 17.3_DOX_0.5_24 ... 87.1_DOX_0.1_24# Extract details from sample names
gene_data_long <- gene_data_long %>%
mutate(
Time = sub(".*_(\\d+)$", "\\1", Sample),
Concentration = sub(".*_(0\\.\\d)_\\d+$", "\\1", Sample),
Drug = sub(".*_(CX\\.5461|DOX|VEH)_.*", "\\1", Sample),
Indv = sub("^([0-9]+\\.[0-9]+)_.*", "\\1", Sample) # Ensure correct pattern extraction
)
# Print extracted `Indv` column for debugging
print(unique(gene_data_long$Indv))[1] "" "17.3" "87.1" "84.1" "90.1" "75.1" "78.1"# Convert extracted columns to factors
gene_data_long$Time <- factor(gene_data_long$Time, levels = c("3", "24", "48"))
gene_data_long$Concentration <- factor(gene_data_long$Concentration, levels = c("0.1", "0.5"))
# Ensure each concentration facet only shows relevant data
gene_data_long <- gene_data_long %>%
group_by(Concentration) %>%
filter(all(Concentration == "0.1") | all(Concentration == "0.5")) %>%
ungroup()
# Map individual IDs
indv_mapping <- c("75.1" = "1", "78.1" = "2", "87.1" = "3", "17.3" = "4", "84.1" = "5", "90.1" = "6")
# Ensure `Indv` values match the keys in `indv_mapping`
gene_data_long <- gene_data_long %>%
mutate(
Indv = ifelse(Indv %in% names(indv_mapping), indv_mapping[Indv], NA)
)
# Print `Indv` column again to confirm mapping worked
print(unique(gene_data_long$Indv))[1] "4" "3" "5" "6" "1" "2"# Check for missing values and handle them
gene_data_long <- gene_data_long %>%
mutate(Indv = ifelse(is.na(Indv), "Unknown", Indv)) # Assign "Unknown" to unidentified individuals
# Define drug colors
drug_palette <- c("CX.5461" = "blue", "DOX" = "red", "VEH" = "green")
# Extract the gene symbol for labeling
gene_symbol <- unique(gene_data_long$SYMBOL)[1]
# Create the boxplot
ggplot(gene_data_long, aes(x = Drug, y = log2CPM, fill = Drug)) +
geom_boxplot(outlier.shape = NA) +
scale_fill_manual(values = drug_palette) +
facet_grid(Concentration ~ Time, labeller = label_both) +
geom_point(aes(color = Indv), size = 2, alpha = 0.5,
position = position_jitter(width = -0.3, height = 0)) +
ggtitle("Non response") +
labs(
title = "Non response",
x = "Drugs",
y = paste(gene_symbol, " log2CPM")
) +
ylim(0, NA) +
theme_bw() +
theme(
plot.title = element_text(size = rel(1.5), hjust = 0.5),
axis.title = element_text(size = 15, color = "black"),
axis.ticks = element_line(linewidth = 1.5),
axis.line = element_line(linewidth = 1.5),
axis.text.y = element_text(size = 10, color = "black"),
axis.text.x = element_text(size = 10, color = "black", angle = 45, hjust = 1),
strip.text = element_text(size = 12, face = "bold")
)
| Version | Author | Date |
|---|---|---|
| e73d731 | sayanpaul01 | 2025-02-23 |
📌 CX_DOX shared late response (MPHOSPH9)
# Load the dataset from the data folder
# Load the dataset from the data folder
# Filter data for the gene with Entrez ID: 10198
gene_data <- boxplot1[boxplot1$ENTREZID == 10198, ]
# Check if gene_data is empty
if(nrow(gene_data) == 0) {
stop("No data found for the selected gene ENTIREZID 10198.")
}
# Reshape data from wide to long format
gene_data_long <- melt(gene_data,
id.vars = c("ENTREZID", "SYMBOL", "GENENAME"),
variable.name = "Sample",
value.name = "log2CPM")
# Print some sample names for debugging
print(unique(gene_data_long$Sample)) [1] 17.3_CX.5461_0.1_3 17.3_DOX_0.5_24
[4] 87.1_DOX_0.5_24 87.1_VEH_0.1_24 87.1_VEH_0.5_24
[7] 87.1_CX.5461_0.1_48 87.1_CX.5461_0.5_48 87.1_DOX_0.1_48
[10] 87.1_DOX_0.5_48 87.1_VEH_0.1_48 87.1_VEH_0.5_48
[13] 17.3_VEH_0.1_24 17.3_VEH_0.5_24 17.3_CX.5461_0.1_48
[16] 17.3_CX.5461_0.5_48 17.3_DOX_0.1_48 17.3_DOX_0.5_48
[19] 17.3_VEH_0.1_48 17.3_VEH_0.5_48 84.1_CX.5461_0.1_3
[22] 17.3_CX.5461_0.5_3 84.1_CX.5461_0.5_3 84.1_DOX_0.1_3
[25] 84.1_DOX_0.5_3 84.1_VEH_0.1_3 84.1_VEH_0.5_3
[28] 84.1_CX.5461_0.1_24 84.1_CX.5461_0.5_24 84.1_DOX_0.1_24
[31] 84.1_DOX_0.5_24 84.1_VEH_0.1_24 17.3_DOX_0.1_3
[34] 84.1_VEH_0.5_24 84.1_CX.5461_0.1_48 84.1_CX.5461_0.5_48
[37] 84.1_DOX_0.1_48 84.1_DOX_0.5_48 84.1_VEH_0.1_48
[40] 84.1_VEH_0.5_48 90.1_CX.5461_0.1_3 90.1_CX.5461_0.5_3
[43] 90.1_DOX_0.1_3 17.3_DOX_0.5_3 90.1_DOX_0.5_3
[46] 90.1_VEH_0.1_3 90.1_VEH_0.5_3 90.1_CX.5461_0.1_24
[49] 90.1_CX.5461_0.5_24 90.1_DOX_0.1_24 90.1_DOX_0.5_24
[52] 90.1_VEH_0.1_24 90.1_VEH_0.5_24 90.1_CX.5461_0.1_48
[55] 17.3_VEH_0.1_3 90.1_CX.5461_0.5_48 90.1_DOX_0.1_48
[58] 90.1_DOX_0.5_48 90.1_VEH_0.1_48 90.1_VEH_0.5_48
[61] 75.1_CX.5461_0.1_3 75.1_CX.5461_0.5_3 75.1_DOX_0.1_3
[64] 75.1_DOX_0.5_3 75.1_VEH_0.1_3 17.3_VEH_0.5_3
[67] 75.1_VEH_0.5_3 75.1_CX.5461_0.1_24 75.1_CX.5461_0.5_24
[70] 75.1_DOX_0.1_24 75.1_DOX_0.5_24 75.1_VEH_0.1_24
[73] 75.1_VEH_0.5_24 75.1_CX.5461_0.1_48 75.1_CX.5461_0.5_48
[76] 75.1_DOX_0.1_48 17.3_CX.5461_0.1_24 75.1_DOX_0.5_48
[79] 75.1_VEH_0.1_48 75.1_VEH_0.5_48 78.1_CX.5461_0.1_3
[82] 78.1_CX.5461_0.5_3 78.1_DOX_0.1_3 78.1_DOX_0.5_3
[85] 78.1_VEH_0.1_3 78.1_VEH_0.5_3 78.1_CX.5461_0.1_24
[88] 17.3_CX.5461_0.5_24 78.1_CX.5461_0.5_24 78.1_DOX_0.1_24
[91] 78.1_DOX_0.5_24 78.1_VEH_0.1_24 78.1_VEH_0.5_24
[94] 78.1_CX.5461_0.1_48 78.1_CX.5461_0.5_48 78.1_DOX_0.1_48
[97] 78.1_DOX_0.5_48 78.1_VEH_0.1_48 17.3_DOX_0.1_24
[100] 78.1_VEH_0.5_48 87.1_CX.5461_0.1_3 87.1_CX.5461_0.5_3
[103] 87.1_DOX_0.1_3 87.1_DOX_0.5_3 87.1_VEH_0.1_3
[106] 87.1_VEH_0.5_3 87.1_CX.5461_0.1_24 87.1_CX.5461_0.5_24
[109] 87.1_DOX_0.1_24
109 Levels: 17.3_CX.5461_0.1_3 17.3_DOX_0.5_24 ... 87.1_DOX_0.1_24# Extract details from sample names
gene_data_long <- gene_data_long %>%
mutate(
Time = sub(".*_(\\d+)$", "\\1", Sample),
Concentration = sub(".*_(0\\.\\d)_\\d+$", "\\1", Sample),
Drug = sub(".*_(CX\\.5461|DOX|VEH)_.*", "\\1", Sample),
Indv = sub("^([0-9]+\\.[0-9]+)_.*", "\\1", Sample) # Ensure correct pattern extraction
)
# Print extracted `Indv` column for debugging
print(unique(gene_data_long$Indv))[1] "" "17.3" "87.1" "84.1" "90.1" "75.1" "78.1"# Convert extracted columns to factors
gene_data_long$Time <- factor(gene_data_long$Time, levels = c("3", "24", "48"))
gene_data_long$Concentration <- factor(gene_data_long$Concentration, levels = c("0.1", "0.5"))
# Ensure each concentration facet only shows relevant data
gene_data_long <- gene_data_long %>%
group_by(Concentration) %>%
filter(all(Concentration == "0.1") | all(Concentration == "0.5")) %>%
ungroup()
# Map individual IDs
indv_mapping <- c("75.1" = "1", "78.1" = "2", "87.1" = "3", "17.3" = "4", "84.1" = "5", "90.1" = "6")
# Ensure `Indv` values match the keys in `indv_mapping`
gene_data_long <- gene_data_long %>%
mutate(
Indv = ifelse(Indv %in% names(indv_mapping), indv_mapping[Indv], NA)
)
# Print `Indv` column again to confirm mapping worked
print(unique(gene_data_long$Indv))[1] "4" "3" "5" "6" "1" "2"# Check for missing values and handle them
gene_data_long <- gene_data_long %>%
mutate(Indv = ifelse(is.na(Indv), "Unknown", Indv)) # Assign "Unknown" to unidentified individuals
# Define drug colors
drug_palette <- c("CX.5461" = "blue", "DOX" = "red", "VEH" = "green")
# Extract the gene symbol for labeling
gene_symbol <- unique(gene_data_long$SYMBOL)[1]
# Create the boxplot
ggplot(gene_data_long, aes(x = Drug, y = log2CPM, fill = Drug)) +
geom_boxplot(outlier.shape = NA) +
scale_fill_manual(values = drug_palette) +
facet_grid(Concentration ~ Time, labeller = label_both) +
geom_point(aes(color = Indv), size = 2, alpha = 0.5,
position = position_jitter(width = -0.3, height = 0)) +
ggtitle("CX_DOX shared late response") +
labs(
title = "CX_DOX shared late response",
x = "Drugs",
y = paste(gene_symbol, " log2CPM")
) +
ylim(0, NA) +
theme_bw() +
theme(
plot.title = element_text(size = rel(1.5), hjust = 0.5),
axis.title = element_text(size = 15, color = "black"),
axis.ticks = element_line(linewidth = 1.5),
axis.line = element_line(linewidth = 1.5),
axis.text.y = element_text(size = 10, color = "black"),
axis.text.x = element_text(size = 10, color = "black", angle = 45, hjust = 1),
strip.text = element_text(size = 12, face = "bold")
)
📌 CX_DOX shared late response (SVIP)
# Load the dataset from the data folder
# Load the dataset from the data folder
# Filter data for the gene with Entrez ID: 258010
gene_data <- boxplot1[boxplot1$ENTREZID == 258010, ]
# Check if gene_data is empty
if(nrow(gene_data) == 0) {
stop("No data found for the selected gene ENTIREZID 258010.")
}
# Reshape data from wide to long format
gene_data_long <- melt(gene_data,
id.vars = c("ENTREZID", "SYMBOL", "GENENAME"),
variable.name = "Sample",
value.name = "log2CPM")
# Print some sample names for debugging
print(unique(gene_data_long$Sample)) [1] 17.3_CX.5461_0.1_3 17.3_DOX_0.5_24
[4] 87.1_DOX_0.5_24 87.1_VEH_0.1_24 87.1_VEH_0.5_24
[7] 87.1_CX.5461_0.1_48 87.1_CX.5461_0.5_48 87.1_DOX_0.1_48
[10] 87.1_DOX_0.5_48 87.1_VEH_0.1_48 87.1_VEH_0.5_48
[13] 17.3_VEH_0.1_24 17.3_VEH_0.5_24 17.3_CX.5461_0.1_48
[16] 17.3_CX.5461_0.5_48 17.3_DOX_0.1_48 17.3_DOX_0.5_48
[19] 17.3_VEH_0.1_48 17.3_VEH_0.5_48 84.1_CX.5461_0.1_3
[22] 17.3_CX.5461_0.5_3 84.1_CX.5461_0.5_3 84.1_DOX_0.1_3
[25] 84.1_DOX_0.5_3 84.1_VEH_0.1_3 84.1_VEH_0.5_3
[28] 84.1_CX.5461_0.1_24 84.1_CX.5461_0.5_24 84.1_DOX_0.1_24
[31] 84.1_DOX_0.5_24 84.1_VEH_0.1_24 17.3_DOX_0.1_3
[34] 84.1_VEH_0.5_24 84.1_CX.5461_0.1_48 84.1_CX.5461_0.5_48
[37] 84.1_DOX_0.1_48 84.1_DOX_0.5_48 84.1_VEH_0.1_48
[40] 84.1_VEH_0.5_48 90.1_CX.5461_0.1_3 90.1_CX.5461_0.5_3
[43] 90.1_DOX_0.1_3 17.3_DOX_0.5_3 90.1_DOX_0.5_3
[46] 90.1_VEH_0.1_3 90.1_VEH_0.5_3 90.1_CX.5461_0.1_24
[49] 90.1_CX.5461_0.5_24 90.1_DOX_0.1_24 90.1_DOX_0.5_24
[52] 90.1_VEH_0.1_24 90.1_VEH_0.5_24 90.1_CX.5461_0.1_48
[55] 17.3_VEH_0.1_3 90.1_CX.5461_0.5_48 90.1_DOX_0.1_48
[58] 90.1_DOX_0.5_48 90.1_VEH_0.1_48 90.1_VEH_0.5_48
[61] 75.1_CX.5461_0.1_3 75.1_CX.5461_0.5_3 75.1_DOX_0.1_3
[64] 75.1_DOX_0.5_3 75.1_VEH_0.1_3 17.3_VEH_0.5_3
[67] 75.1_VEH_0.5_3 75.1_CX.5461_0.1_24 75.1_CX.5461_0.5_24
[70] 75.1_DOX_0.1_24 75.1_DOX_0.5_24 75.1_VEH_0.1_24
[73] 75.1_VEH_0.5_24 75.1_CX.5461_0.1_48 75.1_CX.5461_0.5_48
[76] 75.1_DOX_0.1_48 17.3_CX.5461_0.1_24 75.1_DOX_0.5_48
[79] 75.1_VEH_0.1_48 75.1_VEH_0.5_48 78.1_CX.5461_0.1_3
[82] 78.1_CX.5461_0.5_3 78.1_DOX_0.1_3 78.1_DOX_0.5_3
[85] 78.1_VEH_0.1_3 78.1_VEH_0.5_3 78.1_CX.5461_0.1_24
[88] 17.3_CX.5461_0.5_24 78.1_CX.5461_0.5_24 78.1_DOX_0.1_24
[91] 78.1_DOX_0.5_24 78.1_VEH_0.1_24 78.1_VEH_0.5_24
[94] 78.1_CX.5461_0.1_48 78.1_CX.5461_0.5_48 78.1_DOX_0.1_48
[97] 78.1_DOX_0.5_48 78.1_VEH_0.1_48 17.3_DOX_0.1_24
[100] 78.1_VEH_0.5_48 87.1_CX.5461_0.1_3 87.1_CX.5461_0.5_3
[103] 87.1_DOX_0.1_3 87.1_DOX_0.5_3 87.1_VEH_0.1_3
[106] 87.1_VEH_0.5_3 87.1_CX.5461_0.1_24 87.1_CX.5461_0.5_24
[109] 87.1_DOX_0.1_24
109 Levels: 17.3_CX.5461_0.1_3 17.3_DOX_0.5_24 ... 87.1_DOX_0.1_24# Extract details from sample names
gene_data_long <- gene_data_long %>%
mutate(
Time = sub(".*_(\\d+)$", "\\1", Sample),
Concentration = sub(".*_(0\\.\\d)_\\d+$", "\\1", Sample),
Drug = sub(".*_(CX\\.5461|DOX|VEH)_.*", "\\1", Sample),
Indv = sub("^([0-9]+\\.[0-9]+)_.*", "\\1", Sample) # Ensure correct pattern extraction
)
# Print extracted `Indv` column for debugging
print(unique(gene_data_long$Indv))[1] "" "17.3" "87.1" "84.1" "90.1" "75.1" "78.1"# Convert extracted columns to factors
gene_data_long$Time <- factor(gene_data_long$Time, levels = c("3", "24", "48"))
gene_data_long$Concentration <- factor(gene_data_long$Concentration, levels = c("0.1", "0.5"))
# Ensure each concentration facet only shows relevant data
gene_data_long <- gene_data_long %>%
group_by(Concentration) %>%
filter(all(Concentration == "0.1") | all(Concentration == "0.5")) %>%
ungroup()
# Map individual IDs
indv_mapping <- c("75.1" = "1", "78.1" = "2", "87.1" = "3", "17.3" = "4", "84.1" = "5", "90.1" = "6")
# Ensure `Indv` values match the keys in `indv_mapping`
gene_data_long <- gene_data_long %>%
mutate(
Indv = ifelse(Indv %in% names(indv_mapping), indv_mapping[Indv], NA)
)
# Print `Indv` column again to confirm mapping worked
print(unique(gene_data_long$Indv))[1] "4" "3" "5" "6" "1" "2"# Check for missing values and handle them
gene_data_long <- gene_data_long %>%
mutate(Indv = ifelse(is.na(Indv), "Unknown", Indv)) # Assign "Unknown" to unidentified individuals
# Define drug colors
drug_palette <- c("CX.5461" = "blue", "DOX" = "red", "VEH" = "green")
# Extract the gene symbol for labeling
gene_symbol <- unique(gene_data_long$SYMBOL)[1]
# Create the boxplot
ggplot(gene_data_long, aes(x = Drug, y = log2CPM, fill = Drug)) +
geom_boxplot(outlier.shape = NA) +
scale_fill_manual(values = drug_palette) +
facet_grid(Concentration ~ Time, labeller = label_both) +
geom_point(aes(color = Indv), size = 2, alpha = 0.5,
position = position_jitter(width = -0.3, height = 0)) +
ggtitle("CX_DOX shared late response") +
labs(
title = "CX_DOX shared late response",
x = "Drugs",
y = paste(gene_symbol, " log2CPM")
) +
ylim(0, NA) +
theme_bw() +
theme(
plot.title = element_text(size = rel(1.5), hjust = 0.5),
axis.title = element_text(size = 15, color = "black"),
axis.ticks = element_line(linewidth = 1.5),
axis.line = element_line(linewidth = 1.5),
axis.text.y = element_text(size = 10, color = "black"),
axis.text.x = element_text(size = 10, color = "black", angle = 45, hjust = 1),
strip.text = element_text(size = 12, face = "bold")
)
| Version | Author | Date |
|---|---|---|
| ebfddcd | sayanpaul01 | 2025-02-23 |
📌 DOX-Specific Response (ESPN)
# Load the dataset from the data folder
# Load the dataset from the data folder
# Filter data for the gene with Entrez ID: 83715
gene_data <- boxplot1[boxplot1$ENTREZID == 83715, ]
# Check if gene_data is empty
if(nrow(gene_data) == 0) {
stop("No data found for the selected gene ENTIREZID
83715.")
}
# Reshape data from wide to long format
gene_data_long <- melt(gene_data,
id.vars = c("ENTREZID", "SYMBOL", "GENENAME"),
variable.name = "Sample",
value.name = "log2CPM")
# Print some sample names for debugging
print(unique(gene_data_long$Sample)) [1] 17.3_CX.5461_0.1_3 17.3_DOX_0.5_24
[4] 87.1_DOX_0.5_24 87.1_VEH_0.1_24 87.1_VEH_0.5_24
[7] 87.1_CX.5461_0.1_48 87.1_CX.5461_0.5_48 87.1_DOX_0.1_48
[10] 87.1_DOX_0.5_48 87.1_VEH_0.1_48 87.1_VEH_0.5_48
[13] 17.3_VEH_0.1_24 17.3_VEH_0.5_24 17.3_CX.5461_0.1_48
[16] 17.3_CX.5461_0.5_48 17.3_DOX_0.1_48 17.3_DOX_0.5_48
[19] 17.3_VEH_0.1_48 17.3_VEH_0.5_48 84.1_CX.5461_0.1_3
[22] 17.3_CX.5461_0.5_3 84.1_CX.5461_0.5_3 84.1_DOX_0.1_3
[25] 84.1_DOX_0.5_3 84.1_VEH_0.1_3 84.1_VEH_0.5_3
[28] 84.1_CX.5461_0.1_24 84.1_CX.5461_0.5_24 84.1_DOX_0.1_24
[31] 84.1_DOX_0.5_24 84.1_VEH_0.1_24 17.3_DOX_0.1_3
[34] 84.1_VEH_0.5_24 84.1_CX.5461_0.1_48 84.1_CX.5461_0.5_48
[37] 84.1_DOX_0.1_48 84.1_DOX_0.5_48 84.1_VEH_0.1_48
[40] 84.1_VEH_0.5_48 90.1_CX.5461_0.1_3 90.1_CX.5461_0.5_3
[43] 90.1_DOX_0.1_3 17.3_DOX_0.5_3 90.1_DOX_0.5_3
[46] 90.1_VEH_0.1_3 90.1_VEH_0.5_3 90.1_CX.5461_0.1_24
[49] 90.1_CX.5461_0.5_24 90.1_DOX_0.1_24 90.1_DOX_0.5_24
[52] 90.1_VEH_0.1_24 90.1_VEH_0.5_24 90.1_CX.5461_0.1_48
[55] 17.3_VEH_0.1_3 90.1_CX.5461_0.5_48 90.1_DOX_0.1_48
[58] 90.1_DOX_0.5_48 90.1_VEH_0.1_48 90.1_VEH_0.5_48
[61] 75.1_CX.5461_0.1_3 75.1_CX.5461_0.5_3 75.1_DOX_0.1_3
[64] 75.1_DOX_0.5_3 75.1_VEH_0.1_3 17.3_VEH_0.5_3
[67] 75.1_VEH_0.5_3 75.1_CX.5461_0.1_24 75.1_CX.5461_0.5_24
[70] 75.1_DOX_0.1_24 75.1_DOX_0.5_24 75.1_VEH_0.1_24
[73] 75.1_VEH_0.5_24 75.1_CX.5461_0.1_48 75.1_CX.5461_0.5_48
[76] 75.1_DOX_0.1_48 17.3_CX.5461_0.1_24 75.1_DOX_0.5_48
[79] 75.1_VEH_0.1_48 75.1_VEH_0.5_48 78.1_CX.5461_0.1_3
[82] 78.1_CX.5461_0.5_3 78.1_DOX_0.1_3 78.1_DOX_0.5_3
[85] 78.1_VEH_0.1_3 78.1_VEH_0.5_3 78.1_CX.5461_0.1_24
[88] 17.3_CX.5461_0.5_24 78.1_CX.5461_0.5_24 78.1_DOX_0.1_24
[91] 78.1_DOX_0.5_24 78.1_VEH_0.1_24 78.1_VEH_0.5_24
[94] 78.1_CX.5461_0.1_48 78.1_CX.5461_0.5_48 78.1_DOX_0.1_48
[97] 78.1_DOX_0.5_48 78.1_VEH_0.1_48 17.3_DOX_0.1_24
[100] 78.1_VEH_0.5_48 87.1_CX.5461_0.1_3 87.1_CX.5461_0.5_3
[103] 87.1_DOX_0.1_3 87.1_DOX_0.5_3 87.1_VEH_0.1_3
[106] 87.1_VEH_0.5_3 87.1_CX.5461_0.1_24 87.1_CX.5461_0.5_24
[109] 87.1_DOX_0.1_24
109 Levels: 17.3_CX.5461_0.1_3 17.3_DOX_0.5_24 ... 87.1_DOX_0.1_24# Extract details from sample names
gene_data_long <- gene_data_long %>%
mutate(
Time = sub(".*_(\\d+)$", "\\1", Sample),
Concentration = sub(".*_(0\\.\\d)_\\d+$", "\\1", Sample),
Drug = sub(".*_(CX\\.5461|DOX|VEH)_.*", "\\1", Sample),
Indv = sub("^([0-9]+\\.[0-9]+)_.*", "\\1", Sample) # Ensure correct pattern extraction
)
# Print extracted `Indv` column for debugging
print(unique(gene_data_long$Indv))[1] "" "17.3" "87.1" "84.1" "90.1" "75.1" "78.1"# Convert extracted columns to factors
gene_data_long$Time <- factor(gene_data_long$Time, levels = c("3", "24", "48"))
gene_data_long$Concentration <- factor(gene_data_long$Concentration, levels = c("0.1", "0.5"))
# Ensure each concentration facet only shows relevant data
gene_data_long <- gene_data_long %>%
group_by(Concentration) %>%
filter(all(Concentration == "0.1") | all(Concentration == "0.5")) %>%
ungroup()
# Map individual IDs
indv_mapping <- c("75.1" = "1", "78.1" = "2", "87.1" = "3", "17.3" = "4", "84.1" = "5", "90.1" = "6")
# Ensure `Indv` values match the keys in `indv_mapping`
gene_data_long <- gene_data_long %>%
mutate(
Indv = ifelse(Indv %in% names(indv_mapping), indv_mapping[Indv], NA)
)
# Print `Indv` column again to confirm mapping worked
print(unique(gene_data_long$Indv))[1] "4" "3" "5" "6" "1" "2"# Check for missing values and handle them
gene_data_long <- gene_data_long %>%
mutate(Indv = ifelse(is.na(Indv), "Unknown", Indv)) # Assign "Unknown" to unidentified individuals
# Define drug colors
drug_palette <- c("CX.5461" = "blue", "DOX" = "red", "VEH" = "green")
# Extract the gene symbol for labeling
gene_symbol <- unique(gene_data_long$SYMBOL)[1]
# Create the boxplot
ggplot(gene_data_long, aes(x = Drug, y = log2CPM, fill = Drug)) +
geom_boxplot(outlier.shape = NA) +
scale_fill_manual(values = drug_palette) +
facet_grid(Concentration ~ Time, labeller = label_both) +
geom_point(aes(color = Indv), size = 2, alpha = 0.5,
position = position_jitter(width = -0.3, height = 0)) +
ggtitle("DOX-Specific Response") +
labs(
title = "DOX-Specific Response",
x = "Drugs",
y = paste(gene_symbol, " log2CPM")
) +
ylim(0, NA) +
theme_bw() +
theme(
plot.title = element_text(size = rel(1.5), hjust = 0.5),
axis.title = element_text(size = 15, color = "black"),
axis.ticks = element_line(linewidth = 1.5),
axis.line = element_line(linewidth = 1.5),
axis.text.y = element_text(size = 10, color = "black"),
axis.text.x = element_text(size = 10, color = "black", angle = 45, hjust = 1),
strip.text = element_text(size = 12, face = "bold")
)
| Version | Author | Date |
|---|---|---|
| ebfddcd | sayanpaul01 | 2025-02-23 |
📌 DOX-Specific Response (FBXO2)
# Load the dataset from the data folder
# Load the dataset from the data folder
# Filter data for the gene with Entrez ID: 26232
gene_data <- boxplot1[boxplot1$ENTREZID == 26232, ]
# Check if gene_data is empty
if(nrow(gene_data) == 0) {
stop("No data found for the selected gene ENTIREZID
26232.")
}
# Reshape data from wide to long format
gene_data_long <- melt(gene_data,
id.vars = c("ENTREZID", "SYMBOL", "GENENAME"),
variable.name = "Sample",
value.name = "log2CPM")
# Print some sample names for debugging
print(unique(gene_data_long$Sample)) [1] 17.3_CX.5461_0.1_3 17.3_DOX_0.5_24
[4] 87.1_DOX_0.5_24 87.1_VEH_0.1_24 87.1_VEH_0.5_24
[7] 87.1_CX.5461_0.1_48 87.1_CX.5461_0.5_48 87.1_DOX_0.1_48
[10] 87.1_DOX_0.5_48 87.1_VEH_0.1_48 87.1_VEH_0.5_48
[13] 17.3_VEH_0.1_24 17.3_VEH_0.5_24 17.3_CX.5461_0.1_48
[16] 17.3_CX.5461_0.5_48 17.3_DOX_0.1_48 17.3_DOX_0.5_48
[19] 17.3_VEH_0.1_48 17.3_VEH_0.5_48 84.1_CX.5461_0.1_3
[22] 17.3_CX.5461_0.5_3 84.1_CX.5461_0.5_3 84.1_DOX_0.1_3
[25] 84.1_DOX_0.5_3 84.1_VEH_0.1_3 84.1_VEH_0.5_3
[28] 84.1_CX.5461_0.1_24 84.1_CX.5461_0.5_24 84.1_DOX_0.1_24
[31] 84.1_DOX_0.5_24 84.1_VEH_0.1_24 17.3_DOX_0.1_3
[34] 84.1_VEH_0.5_24 84.1_CX.5461_0.1_48 84.1_CX.5461_0.5_48
[37] 84.1_DOX_0.1_48 84.1_DOX_0.5_48 84.1_VEH_0.1_48
[40] 84.1_VEH_0.5_48 90.1_CX.5461_0.1_3 90.1_CX.5461_0.5_3
[43] 90.1_DOX_0.1_3 17.3_DOX_0.5_3 90.1_DOX_0.5_3
[46] 90.1_VEH_0.1_3 90.1_VEH_0.5_3 90.1_CX.5461_0.1_24
[49] 90.1_CX.5461_0.5_24 90.1_DOX_0.1_24 90.1_DOX_0.5_24
[52] 90.1_VEH_0.1_24 90.1_VEH_0.5_24 90.1_CX.5461_0.1_48
[55] 17.3_VEH_0.1_3 90.1_CX.5461_0.5_48 90.1_DOX_0.1_48
[58] 90.1_DOX_0.5_48 90.1_VEH_0.1_48 90.1_VEH_0.5_48
[61] 75.1_CX.5461_0.1_3 75.1_CX.5461_0.5_3 75.1_DOX_0.1_3
[64] 75.1_DOX_0.5_3 75.1_VEH_0.1_3 17.3_VEH_0.5_3
[67] 75.1_VEH_0.5_3 75.1_CX.5461_0.1_24 75.1_CX.5461_0.5_24
[70] 75.1_DOX_0.1_24 75.1_DOX_0.5_24 75.1_VEH_0.1_24
[73] 75.1_VEH_0.5_24 75.1_CX.5461_0.1_48 75.1_CX.5461_0.5_48
[76] 75.1_DOX_0.1_48 17.3_CX.5461_0.1_24 75.1_DOX_0.5_48
[79] 75.1_VEH_0.1_48 75.1_VEH_0.5_48 78.1_CX.5461_0.1_3
[82] 78.1_CX.5461_0.5_3 78.1_DOX_0.1_3 78.1_DOX_0.5_3
[85] 78.1_VEH_0.1_3 78.1_VEH_0.5_3 78.1_CX.5461_0.1_24
[88] 17.3_CX.5461_0.5_24 78.1_CX.5461_0.5_24 78.1_DOX_0.1_24
[91] 78.1_DOX_0.5_24 78.1_VEH_0.1_24 78.1_VEH_0.5_24
[94] 78.1_CX.5461_0.1_48 78.1_CX.5461_0.5_48 78.1_DOX_0.1_48
[97] 78.1_DOX_0.5_48 78.1_VEH_0.1_48 17.3_DOX_0.1_24
[100] 78.1_VEH_0.5_48 87.1_CX.5461_0.1_3 87.1_CX.5461_0.5_3
[103] 87.1_DOX_0.1_3 87.1_DOX_0.5_3 87.1_VEH_0.1_3
[106] 87.1_VEH_0.5_3 87.1_CX.5461_0.1_24 87.1_CX.5461_0.5_24
[109] 87.1_DOX_0.1_24
109 Levels: 17.3_CX.5461_0.1_3 17.3_DOX_0.5_24 ... 87.1_DOX_0.1_24# Extract details from sample names
gene_data_long <- gene_data_long %>%
mutate(
Time = sub(".*_(\\d+)$", "\\1", Sample),
Concentration = sub(".*_(0\\.\\d)_\\d+$", "\\1", Sample),
Drug = sub(".*_(CX\\.5461|DOX|VEH)_.*", "\\1", Sample),
Indv = sub("^([0-9]+\\.[0-9]+)_.*", "\\1", Sample) # Ensure correct pattern extraction
)
# Print extracted `Indv` column for debugging
print(unique(gene_data_long$Indv))[1] "" "17.3" "87.1" "84.1" "90.1" "75.1" "78.1"# Convert extracted columns to factors
gene_data_long$Time <- factor(gene_data_long$Time, levels = c("3", "24", "48"))
gene_data_long$Concentration <- factor(gene_data_long$Concentration, levels = c("0.1", "0.5"))
# Ensure each concentration facet only shows relevant data
gene_data_long <- gene_data_long %>%
group_by(Concentration) %>%
filter(all(Concentration == "0.1") | all(Concentration == "0.5")) %>%
ungroup()
# Map individual IDs
indv_mapping <- c("75.1" = "1", "78.1" = "2", "87.1" = "3", "17.3" = "4", "84.1" = "5", "90.1" = "6")
# Ensure `Indv` values match the keys in `indv_mapping`
gene_data_long <- gene_data_long %>%
mutate(
Indv = ifelse(Indv %in% names(indv_mapping), indv_mapping[Indv], NA)
)
# Print `Indv` column again to confirm mapping worked
print(unique(gene_data_long$Indv))[1] "4" "3" "5" "6" "1" "2"# Check for missing values and handle them
gene_data_long <- gene_data_long %>%
mutate(Indv = ifelse(is.na(Indv), "Unknown", Indv)) # Assign "Unknown" to unidentified individuals
# Define drug colors
drug_palette <- c("CX.5461" = "blue", "DOX" = "red", "VEH" = "green")
# Extract the gene symbol for labeling
gene_symbol <- unique(gene_data_long$SYMBOL)[1]
# Create the boxplot
ggplot(gene_data_long, aes(x = Drug, y = log2CPM, fill = Drug)) +
geom_boxplot(outlier.shape = NA) +
scale_fill_manual(values = drug_palette) +
facet_grid(Concentration ~ Time, labeller = label_both) +
geom_point(aes(color = Indv), size = 2, alpha = 0.5,
position = position_jitter(width = -0.3, height = 0)) +
ggtitle("DOX-Specific Response") +
labs(
title = "DOX-Specific Response",
x = "Drugs",
y = paste(gene_symbol, " log2CPM")
) +
ylim(0, NA) +
theme_bw() +
theme(
plot.title = element_text(size = rel(1.5), hjust = 0.5),
axis.title = element_text(size = 15, color = "black"),
axis.ticks = element_line(linewidth = 1.5),
axis.line = element_line(linewidth = 1.5),
axis.text.y = element_text(size = 10, color = "black"),
axis.text.x = element_text(size = 10, color = "black", angle = 45, hjust = 1),
strip.text = element_text(size = 12, face = "bold")
)
| Version | Author | Date |
|---|---|---|
| ebfddcd | sayanpaul01 | 2025-02-23 |
📌 Late high dose DOX-specific response (EPHX1)
# Load the dataset from the data folder
# Load the dataset from the data folder
# Filter data for the gene with Entrez ID: 2052
gene_data <- boxplot1[boxplot1$ENTREZID == 2052, ]
# Check if gene_data is empty
if(nrow(gene_data) == 0) {
stop("No data found for the selected gene ENTIREZID
2052.")
}
# Reshape data from wide to long format
gene_data_long <- melt(gene_data,
id.vars = c("ENTREZID", "SYMBOL", "GENENAME"),
variable.name = "Sample",
value.name = "log2CPM")
# Print some sample names for debugging
print(unique(gene_data_long$Sample)) [1] 17.3_CX.5461_0.1_3 17.3_DOX_0.5_24
[4] 87.1_DOX_0.5_24 87.1_VEH_0.1_24 87.1_VEH_0.5_24
[7] 87.1_CX.5461_0.1_48 87.1_CX.5461_0.5_48 87.1_DOX_0.1_48
[10] 87.1_DOX_0.5_48 87.1_VEH_0.1_48 87.1_VEH_0.5_48
[13] 17.3_VEH_0.1_24 17.3_VEH_0.5_24 17.3_CX.5461_0.1_48
[16] 17.3_CX.5461_0.5_48 17.3_DOX_0.1_48 17.3_DOX_0.5_48
[19] 17.3_VEH_0.1_48 17.3_VEH_0.5_48 84.1_CX.5461_0.1_3
[22] 17.3_CX.5461_0.5_3 84.1_CX.5461_0.5_3 84.1_DOX_0.1_3
[25] 84.1_DOX_0.5_3 84.1_VEH_0.1_3 84.1_VEH_0.5_3
[28] 84.1_CX.5461_0.1_24 84.1_CX.5461_0.5_24 84.1_DOX_0.1_24
[31] 84.1_DOX_0.5_24 84.1_VEH_0.1_24 17.3_DOX_0.1_3
[34] 84.1_VEH_0.5_24 84.1_CX.5461_0.1_48 84.1_CX.5461_0.5_48
[37] 84.1_DOX_0.1_48 84.1_DOX_0.5_48 84.1_VEH_0.1_48
[40] 84.1_VEH_0.5_48 90.1_CX.5461_0.1_3 90.1_CX.5461_0.5_3
[43] 90.1_DOX_0.1_3 17.3_DOX_0.5_3 90.1_DOX_0.5_3
[46] 90.1_VEH_0.1_3 90.1_VEH_0.5_3 90.1_CX.5461_0.1_24
[49] 90.1_CX.5461_0.5_24 90.1_DOX_0.1_24 90.1_DOX_0.5_24
[52] 90.1_VEH_0.1_24 90.1_VEH_0.5_24 90.1_CX.5461_0.1_48
[55] 17.3_VEH_0.1_3 90.1_CX.5461_0.5_48 90.1_DOX_0.1_48
[58] 90.1_DOX_0.5_48 90.1_VEH_0.1_48 90.1_VEH_0.5_48
[61] 75.1_CX.5461_0.1_3 75.1_CX.5461_0.5_3 75.1_DOX_0.1_3
[64] 75.1_DOX_0.5_3 75.1_VEH_0.1_3 17.3_VEH_0.5_3
[67] 75.1_VEH_0.5_3 75.1_CX.5461_0.1_24 75.1_CX.5461_0.5_24
[70] 75.1_DOX_0.1_24 75.1_DOX_0.5_24 75.1_VEH_0.1_24
[73] 75.1_VEH_0.5_24 75.1_CX.5461_0.1_48 75.1_CX.5461_0.5_48
[76] 75.1_DOX_0.1_48 17.3_CX.5461_0.1_24 75.1_DOX_0.5_48
[79] 75.1_VEH_0.1_48 75.1_VEH_0.5_48 78.1_CX.5461_0.1_3
[82] 78.1_CX.5461_0.5_3 78.1_DOX_0.1_3 78.1_DOX_0.5_3
[85] 78.1_VEH_0.1_3 78.1_VEH_0.5_3 78.1_CX.5461_0.1_24
[88] 17.3_CX.5461_0.5_24 78.1_CX.5461_0.5_24 78.1_DOX_0.1_24
[91] 78.1_DOX_0.5_24 78.1_VEH_0.1_24 78.1_VEH_0.5_24
[94] 78.1_CX.5461_0.1_48 78.1_CX.5461_0.5_48 78.1_DOX_0.1_48
[97] 78.1_DOX_0.5_48 78.1_VEH_0.1_48 17.3_DOX_0.1_24
[100] 78.1_VEH_0.5_48 87.1_CX.5461_0.1_3 87.1_CX.5461_0.5_3
[103] 87.1_DOX_0.1_3 87.1_DOX_0.5_3 87.1_VEH_0.1_3
[106] 87.1_VEH_0.5_3 87.1_CX.5461_0.1_24 87.1_CX.5461_0.5_24
[109] 87.1_DOX_0.1_24
109 Levels: 17.3_CX.5461_0.1_3 17.3_DOX_0.5_24 ... 87.1_DOX_0.1_24# Extract details from sample names
gene_data_long <- gene_data_long %>%
mutate(
Time = sub(".*_(\\d+)$", "\\1", Sample),
Concentration = sub(".*_(0\\.\\d)_\\d+$", "\\1", Sample),
Drug = sub(".*_(CX\\.5461|DOX|VEH)_.*", "\\1", Sample),
Indv = sub("^([0-9]+\\.[0-9]+)_.*", "\\1", Sample) # Ensure correct pattern extraction
)
# Print extracted `Indv` column for debugging
print(unique(gene_data_long$Indv))[1] "" "17.3" "87.1" "84.1" "90.1" "75.1" "78.1"# Convert extracted columns to factors
gene_data_long$Time <- factor(gene_data_long$Time, levels = c("3", "24", "48"))
gene_data_long$Concentration <- factor(gene_data_long$Concentration, levels = c("0.1", "0.5"))
# Ensure each concentration facet only shows relevant data
gene_data_long <- gene_data_long %>%
group_by(Concentration) %>%
filter(all(Concentration == "0.1") | all(Concentration == "0.5")) %>%
ungroup()
# Map individual IDs
indv_mapping <- c("75.1" = "1", "78.1" = "2", "87.1" = "3", "17.3" = "4", "84.1" = "5", "90.1" = "6")
# Ensure `Indv` values match the keys in `indv_mapping`
gene_data_long <- gene_data_long %>%
mutate(
Indv = ifelse(Indv %in% names(indv_mapping), indv_mapping[Indv], NA)
)
# Print `Indv` column again to confirm mapping worked
print(unique(gene_data_long$Indv))[1] "4" "3" "5" "6" "1" "2"# Check for missing values and handle them
gene_data_long <- gene_data_long %>%
mutate(Indv = ifelse(is.na(Indv), "Unknown", Indv)) # Assign "Unknown" to unidentified individuals
# Define drug colors
drug_palette <- c("CX.5461" = "blue", "DOX" = "red", "VEH" = "green")
# Extract the gene symbol for labeling
gene_symbol <- unique(gene_data_long$SYMBOL)[1]
# Create the boxplot
ggplot(gene_data_long, aes(x = Drug, y = log2CPM, fill = Drug)) +
geom_boxplot(outlier.shape = NA) +
scale_fill_manual(values = drug_palette) +
facet_grid(Concentration ~ Time, labeller = label_both) +
geom_point(aes(color = Indv), size = 2, alpha = 0.5,
position = position_jitter(width = -0.3, height = 0)) +
ggtitle("Late high dose DOX-specific response") +
labs(
title = "Late high dose DOX-specific response",
x = "Drugs",
y = paste(gene_symbol, " log2CPM")
) +
ylim(0, NA) +
theme_bw() +
theme(
plot.title = element_text(size = rel(1.5), hjust = 0.5),
axis.title = element_text(size = 15, color = "black"),
axis.ticks = element_line(linewidth = 1.5),
axis.line = element_line(linewidth = 1.5),
axis.text.y = element_text(size = 10, color = "black"),
axis.text.x = element_text(size = 10, color = "black", angle = 45, hjust = 1),
strip.text = element_text(size = 12, face = "bold")
)
| Version | Author | Date |
|---|---|---|
| ebfddcd | sayanpaul01 | 2025-02-23 |
📌 Late high dose DOX-specific response (OBSCN)
# Load the dataset from the data folder
# Load the dataset from the data folder
# Filter data for the gene with Entrez ID: 84033
gene_data <- boxplot1[boxplot1$ENTREZID == 84033, ]
# Check if gene_data is empty
if(nrow(gene_data) == 0) {
stop("No data found for the selected gene ENTIREZID
84033.")
}
# Reshape data from wide to long format
gene_data_long <- melt(gene_data,
id.vars = c("ENTREZID", "SYMBOL", "GENENAME"),
variable.name = "Sample",
value.name = "log2CPM")
# Print some sample names for debugging
print(unique(gene_data_long$Sample)) [1] 17.3_CX.5461_0.1_3 17.3_DOX_0.5_24
[4] 87.1_DOX_0.5_24 87.1_VEH_0.1_24 87.1_VEH_0.5_24
[7] 87.1_CX.5461_0.1_48 87.1_CX.5461_0.5_48 87.1_DOX_0.1_48
[10] 87.1_DOX_0.5_48 87.1_VEH_0.1_48 87.1_VEH_0.5_48
[13] 17.3_VEH_0.1_24 17.3_VEH_0.5_24 17.3_CX.5461_0.1_48
[16] 17.3_CX.5461_0.5_48 17.3_DOX_0.1_48 17.3_DOX_0.5_48
[19] 17.3_VEH_0.1_48 17.3_VEH_0.5_48 84.1_CX.5461_0.1_3
[22] 17.3_CX.5461_0.5_3 84.1_CX.5461_0.5_3 84.1_DOX_0.1_3
[25] 84.1_DOX_0.5_3 84.1_VEH_0.1_3 84.1_VEH_0.5_3
[28] 84.1_CX.5461_0.1_24 84.1_CX.5461_0.5_24 84.1_DOX_0.1_24
[31] 84.1_DOX_0.5_24 84.1_VEH_0.1_24 17.3_DOX_0.1_3
[34] 84.1_VEH_0.5_24 84.1_CX.5461_0.1_48 84.1_CX.5461_0.5_48
[37] 84.1_DOX_0.1_48 84.1_DOX_0.5_48 84.1_VEH_0.1_48
[40] 84.1_VEH_0.5_48 90.1_CX.5461_0.1_3 90.1_CX.5461_0.5_3
[43] 90.1_DOX_0.1_3 17.3_DOX_0.5_3 90.1_DOX_0.5_3
[46] 90.1_VEH_0.1_3 90.1_VEH_0.5_3 90.1_CX.5461_0.1_24
[49] 90.1_CX.5461_0.5_24 90.1_DOX_0.1_24 90.1_DOX_0.5_24
[52] 90.1_VEH_0.1_24 90.1_VEH_0.5_24 90.1_CX.5461_0.1_48
[55] 17.3_VEH_0.1_3 90.1_CX.5461_0.5_48 90.1_DOX_0.1_48
[58] 90.1_DOX_0.5_48 90.1_VEH_0.1_48 90.1_VEH_0.5_48
[61] 75.1_CX.5461_0.1_3 75.1_CX.5461_0.5_3 75.1_DOX_0.1_3
[64] 75.1_DOX_0.5_3 75.1_VEH_0.1_3 17.3_VEH_0.5_3
[67] 75.1_VEH_0.5_3 75.1_CX.5461_0.1_24 75.1_CX.5461_0.5_24
[70] 75.1_DOX_0.1_24 75.1_DOX_0.5_24 75.1_VEH_0.1_24
[73] 75.1_VEH_0.5_24 75.1_CX.5461_0.1_48 75.1_CX.5461_0.5_48
[76] 75.1_DOX_0.1_48 17.3_CX.5461_0.1_24 75.1_DOX_0.5_48
[79] 75.1_VEH_0.1_48 75.1_VEH_0.5_48 78.1_CX.5461_0.1_3
[82] 78.1_CX.5461_0.5_3 78.1_DOX_0.1_3 78.1_DOX_0.5_3
[85] 78.1_VEH_0.1_3 78.1_VEH_0.5_3 78.1_CX.5461_0.1_24
[88] 17.3_CX.5461_0.5_24 78.1_CX.5461_0.5_24 78.1_DOX_0.1_24
[91] 78.1_DOX_0.5_24 78.1_VEH_0.1_24 78.1_VEH_0.5_24
[94] 78.1_CX.5461_0.1_48 78.1_CX.5461_0.5_48 78.1_DOX_0.1_48
[97] 78.1_DOX_0.5_48 78.1_VEH_0.1_48 17.3_DOX_0.1_24
[100] 78.1_VEH_0.5_48 87.1_CX.5461_0.1_3 87.1_CX.5461_0.5_3
[103] 87.1_DOX_0.1_3 87.1_DOX_0.5_3 87.1_VEH_0.1_3
[106] 87.1_VEH_0.5_3 87.1_CX.5461_0.1_24 87.1_CX.5461_0.5_24
[109] 87.1_DOX_0.1_24
109 Levels: 17.3_CX.5461_0.1_3 17.3_DOX_0.5_24 ... 87.1_DOX_0.1_24# Extract details from sample names
gene_data_long <- gene_data_long %>%
mutate(
Time = sub(".*_(\\d+)$", "\\1", Sample),
Concentration = sub(".*_(0\\.\\d)_\\d+$", "\\1", Sample),
Drug = sub(".*_(CX\\.5461|DOX|VEH)_.*", "\\1", Sample),
Indv = sub("^([0-9]+\\.[0-9]+)_.*", "\\1", Sample) # Ensure correct pattern extraction
)
# Print extracted `Indv` column for debugging
print(unique(gene_data_long$Indv))[1] "" "17.3" "87.1" "84.1" "90.1" "75.1" "78.1"# Convert extracted columns to factors
gene_data_long$Time <- factor(gene_data_long$Time, levels = c("3", "24", "48"))
gene_data_long$Concentration <- factor(gene_data_long$Concentration, levels = c("0.1", "0.5"))
# Ensure each concentration facet only shows relevant data
gene_data_long <- gene_data_long %>%
group_by(Concentration) %>%
filter(all(Concentration == "0.1") | all(Concentration == "0.5")) %>%
ungroup()
# Map individual IDs
indv_mapping <- c("75.1" = "1", "78.1" = "2", "87.1" = "3", "17.3" = "4", "84.1" = "5", "90.1" = "6")
# Ensure `Indv` values match the keys in `indv_mapping`
gene_data_long <- gene_data_long %>%
mutate(
Indv = ifelse(Indv %in% names(indv_mapping), indv_mapping[Indv], NA)
)
# Print `Indv` column again to confirm mapping worked
print(unique(gene_data_long$Indv))[1] "4" "3" "5" "6" "1" "2"# Check for missing values and handle them
gene_data_long <- gene_data_long %>%
mutate(Indv = ifelse(is.na(Indv), "Unknown", Indv)) # Assign "Unknown" to unidentified individuals
# Define drug colors
drug_palette <- c("CX.5461" = "blue", "DOX" = "red", "VEH" = "green")
# Extract the gene symbol for labeling
gene_symbol <- unique(gene_data_long$SYMBOL)[1]
# Create the boxplot
ggplot(gene_data_long, aes(x = Drug, y = log2CPM, fill = Drug)) +
geom_boxplot(outlier.shape = NA) +
scale_fill_manual(values = drug_palette) +
facet_grid(Concentration ~ Time, labeller = label_both) +
geom_point(aes(color = Indv), size = 2, alpha = 0.5,
position = position_jitter(width = -0.3, height = 0)) +
ggtitle("Late high dose DOX-specific response") +
labs(
title = "Late high dose DOX-specific response",
x = "Drugs",
y = paste(gene_symbol, " log2CPM")
) +
ylim(0, NA) +
theme_bw() +
theme(
plot.title = element_text(size = rel(1.5), hjust = 0.5),
axis.title = element_text(size = 15, color = "black"),
axis.ticks = element_line(linewidth = 1.5),
axis.line = element_line(linewidth = 1.5),
axis.text.y = element_text(size = 10, color = "black"),
axis.text.x = element_text(size = 10, color = "black", angle = 45, hjust = 1),
strip.text = element_text(size = 12, face = "bold")
)
| Version | Author | Date |
|---|---|---|
| ebfddcd | sayanpaul01 | 2025-02-23 |
📌 Corr-motif set Abs logFC boxplots
📌 Read and Process DEG Data
# Load DEGs Data
CX_0.1_3 <- read.csv("data/DEGs/Toptable_CX_0.1_3.csv")
CX_0.1_24 <- read.csv("data/DEGs/Toptable_CX_0.1_24.csv")
CX_0.1_48 <- read.csv("data/DEGs/Toptable_CX_0.1_48.csv")
CX_0.5_3 <- read.csv("data/DEGs/Toptable_CX_0.5_3.csv")
CX_0.5_24 <- read.csv("data/DEGs/Toptable_CX_0.5_24.csv")
CX_0.5_48 <- read.csv("data/DEGs/Toptable_CX_0.5_48.csv")
DOX_0.1_3 <- read.csv("data/DEGs/Toptable_DOX_0.1_3.csv")
DOX_0.1_24 <- read.csv("data/DEGs/Toptable_DOX_0.1_24.csv")
DOX_0.1_48 <- read.csv("data/DEGs/Toptable_DOX_0.1_48.csv")
DOX_0.5_3 <- read.csv("data/DEGs/Toptable_DOX_0.5_3.csv")
DOX_0.5_24 <- read.csv("data/DEGs/Toptable_DOX_0.5_24.csv")
DOX_0.5_48 <- read.csv("data/DEGs/Toptable_DOX_0.5_48.csv")
Toptable_CX_0.1_3_df<- data.frame(CX_0.1_3)
Toptable_CX_0.1_24_df<- data.frame(CX_0.1_24)
Toptable_CX_0.1_48_df<- data.frame(CX_0.1_48)
Toptable_CX_0.5_3_df<- data.frame(CX_0.5_3)
Toptable_CX_0.5_24_df<- data.frame(CX_0.5_24)
Toptable_CX_0.5_48_df<- data.frame(CX_0.5_48)
Toptable_DOX_0.1_3_df<- data.frame(DOX_0.1_3)
Toptable_DOX_0.1_24_df<- data.frame(DOX_0.1_24)
Toptable_DOX_0.1_48_df<- data.frame(DOX_0.1_48)
Toptable_DOX_0.5_3_df<- data.frame(DOX_0.5_3)
Toptable_DOX_0.5_24_df<- data.frame(DOX_0.5_24)
Toptable_DOX_0.5_48_df<- data.frame(DOX_0.5_48)📌 Non response abs logFC boxplots
# Extract Entrez_IDs from set1
non_response_entrez_ids <- prob_all_1
all_toptables <- bind_rows(
Toptable_CX_0.1_3_df %>% mutate(Drug = "CX.5461", Concentration = 0.1, Timepoint = "3"),
Toptable_CX_0.1_24_df %>% mutate(Drug = "CX.5461", Concentration = 0.1, Timepoint = "24"),
Toptable_CX_0.1_48_df %>% mutate(Drug = "CX.5461", Concentration = 0.1, Timepoint = "48"),
Toptable_CX_0.5_3_df %>% mutate(Drug = "CX.5461", Concentration = 0.5, Timepoint = "3"),
Toptable_CX_0.5_24_df %>% mutate(Drug = "CX.5461", Concentration = 0.5, Timepoint = "24"),
Toptable_CX_0.5_48_df %>% mutate(Drug = "CX.5461", Concentration = 0.5, Timepoint = "48"),
Toptable_DOX_0.1_3_df %>% mutate(Drug = "DOX", Concentration = 0.1, Timepoint = "3"),
Toptable_DOX_0.1_24_df %>% mutate(Drug = "DOX", Concentration = 0.1, Timepoint = "24"),
Toptable_DOX_0.1_48_df %>% mutate(Drug = "DOX", Concentration = 0.1, Timepoint = "48"),
Toptable_DOX_0.5_3_df %>% mutate(Drug = "DOX", Concentration = 0.5, Timepoint = "3"),
Toptable_DOX_0.5_24_df %>% mutate(Drug = "DOX", Concentration = 0.5, Timepoint = "24"),
Toptable_DOX_0.5_48_df %>% mutate(Drug = "DOX", Concentration = 0.5, Timepoint = "48")
)
# Filter and visualize data for shared late response genes
filtered_toptables <- all_toptables %>%
filter(Entrez_ID %in% non_response_entrez_ids)
# Filter and visualize data with exact same font size and bold styling for concentration and timepoints
filtered_toptables %>%
mutate(absFC = abs(logFC)) %>% # Compute absolute log fold change
mutate(
Drug = factor(Drug, levels = c("CX.5461", "DOX")), # Factorize Drug with CX.5461 first
Timepoint = factor(Timepoint, levels = c("3", "24", "48"), labels = c("Timepoint: 3 hours", "Timepoint: 24 hours", "Timepoint: 48 hours")),
Concentration = factor(Concentration, levels = c(0.1, 0.5), labels = c("Concentration: 0.1", "Concentration: 0.5"))
) %>%
ggplot(aes(x = Drug, y = absFC)) +
geom_boxplot(aes(fill = Drug)) +
scale_fill_manual(values = c("CX.5461" = "blue", "DOX" = "red")) + # Updated color palette
guides(fill = guide_legend(title = "Treatment")) +
facet_grid(Concentration ~ Timepoint) + # Facet by Concentration and Timepoint
theme_bw() +
xlab("Drugs") +
ylab("|Log Fold Change|") +
ggtitle("|Log Fold| for Non-Response Genes") +
theme(
plot.title = element_text(size = rel(1.5), hjust = 0.5),
axis.title = element_text(size = 15, color = "black"),
axis.line = element_line(linewidth = 1.5),
strip.background = element_rect(fill = "gray"), # Set strip background to gray
strip.text = element_text(size = 12, color = "black", face = "bold"), # Unified styling for all facet labels
axis.text.x = element_text(size = 8, color = "black", angle = 15)
)
| Version | Author | Date |
|---|---|---|
| 2862c42 | sayanpaul01 | 2025-02-24 |
📌 CX_DOX shared late response abs logFC boxplots
# Extract Entrez_IDs from set2
shared_late_response_entrez_ids <- prob_all_2
# Combine all subset_toptables into a single data frame with additional metadata columns
all_toptables <- bind_rows(
Toptable_CX_0.1_3_df %>% mutate(Drug = "CX.5461", Concentration = 0.1, Timepoint = "3"),
Toptable_CX_0.1_24_df %>% mutate(Drug = "CX.5461", Concentration = 0.1, Timepoint = "24"),
Toptable_CX_0.1_48_df %>% mutate(Drug = "CX.5461", Concentration = 0.1, Timepoint = "48"),
Toptable_CX_0.5_3_df %>% mutate(Drug = "CX.5461", Concentration = 0.5, Timepoint = "3"),
Toptable_CX_0.5_24_df %>% mutate(Drug = "CX.5461", Concentration = 0.5, Timepoint = "24"),
Toptable_CX_0.5_48_df %>% mutate(Drug = "CX.5461", Concentration = 0.5, Timepoint = "48"),
Toptable_DOX_0.1_3_df %>% mutate(Drug = "DOX", Concentration = 0.1, Timepoint = "3"),
Toptable_DOX_0.1_24_df %>% mutate(Drug = "DOX", Concentration = 0.1, Timepoint = "24"),
Toptable_DOX_0.1_48_df %>% mutate(Drug = "DOX", Concentration = 0.1, Timepoint = "48"),
Toptable_DOX_0.5_3_df %>% mutate(Drug = "DOX", Concentration = 0.5, Timepoint = "3"),
Toptable_DOX_0.5_24_df %>% mutate(Drug = "DOX", Concentration = 0.5, Timepoint = "24"),
Toptable_DOX_0.5_48_df %>% mutate(Drug = "DOX", Concentration = 0.5, Timepoint = "48")
)
# Filter and visualize data for shared late response genes
filtered_toptables <- all_toptables %>%
filter(Entrez_ID %in% shared_late_response_entrez_ids)
filtered_toptables %>%
mutate(absFC = abs(logFC)) %>% # Compute absolute log fold change
mutate(
Drug = factor(Drug, levels = c("CX.5461", "DOX")), # Factorize Drug with CX.5461 first
Timepoint = factor(Timepoint, levels = c("3", "24", "48"), labels = c("Timepoint: 3 hours", "Timepoint: 24 hours", "Timepoint: 48 hours")),
Concentration = factor(Concentration, levels = c(0.1, 0.5), labels = c("Concentration: 0.1", "Concentration: 0.5"))
) %>%
ggplot(aes(x = Drug, y = absFC)) +
geom_boxplot(aes(fill = Drug)) +
scale_fill_manual(values = c("CX.5461" = "blue", "DOX" = "red")) + # Updated color palette
guides(fill = guide_legend(title = "Treatment")) +
facet_grid(Concentration ~ Timepoint) + # Facet by Concentration and Timepoint
theme_bw() +
xlab("Drugs") +
ylab("|Log Fold Change|") +
ggtitle("|Log Fold| for CX_DOX shared late response Genes") +
theme(
plot.title = element_text(size = rel(1.5), hjust = 0.5),
axis.title = element_text(size = 15, color = "black"),
axis.line = element_line(linewidth = 1.5),
strip.background = element_rect(fill = "gray"), # Set strip background to gray
strip.text = element_text(size = 12, color = "black", face = "bold"), # Unified styling for all facet labels
axis.text.x = element_text(size = 8, color = "black", angle = 15)
)
| Version | Author | Date |
|---|---|---|
| 2862c42 | sayanpaul01 | 2025-02-24 |
📌 DOX Specific response abs logFC boxplots
# Extract Entrez_IDs from set3
dox_specific_response_entrez_ids <- prob_all_3
# Combine all subset_toptables into a single data frame with additional metadata columns
all_toptables <- bind_rows(
Toptable_CX_0.1_3_df %>% mutate(Drug = "CX.5461", Concentration = 0.1, Timepoint = "3"),
Toptable_CX_0.1_24_df %>% mutate(Drug = "CX.5461", Concentration = 0.1, Timepoint = "24"),
Toptable_CX_0.1_48_df %>% mutate(Drug = "CX.5461", Concentration = 0.1, Timepoint = "48"),
Toptable_CX_0.5_3_df %>% mutate(Drug = "CX.5461", Concentration = 0.5, Timepoint = "3"),
Toptable_CX_0.5_24_df %>% mutate(Drug = "CX.5461", Concentration = 0.5, Timepoint = "24"),
Toptable_CX_0.5_48_df %>% mutate(Drug = "CX.5461", Concentration = 0.5, Timepoint = "48"),
Toptable_DOX_0.1_3_df %>% mutate(Drug = "DOX", Concentration = 0.1, Timepoint = "3"),
Toptable_DOX_0.1_24_df %>% mutate(Drug = "DOX", Concentration = 0.1, Timepoint = "24"),
Toptable_DOX_0.1_48_df %>% mutate(Drug = "DOX", Concentration = 0.1, Timepoint = "48"),
Toptable_DOX_0.5_3_df %>% mutate(Drug = "DOX", Concentration = 0.5, Timepoint = "3"),
Toptable_DOX_0.5_24_df %>% mutate(Drug = "DOX", Concentration = 0.5, Timepoint = "24"),
Toptable_DOX_0.5_48_df %>% mutate(Drug = "DOX", Concentration = 0.5, Timepoint = "48")
)
# Filter and visualize data for DOX-specific response genes
filtered_toptables <- all_toptables %>%
filter(Entrez_ID %in% dox_specific_response_entrez_ids)
filtered_toptables %>%
mutate(absFC = abs(logFC)) %>% # Compute absolute log fold change
mutate(
Drug = factor(Drug, levels = c("CX.5461", "DOX")), # Factorize Drug with CX.5461 first
Timepoint = factor(Timepoint, levels = c("3", "24", "48"), labels = c("Timepoint: 3 hours", "Timepoint: 24 hours", "Timepoint: 48 hours")),
Concentration = factor(Concentration, levels = c(0.1, 0.5), labels = c("Concentration: 0.1", "Concentration: 0.5"))
) %>%
ggplot(aes(x = Drug, y = absFC)) +
geom_boxplot(aes(fill = Drug)) +
scale_fill_manual(values = c("CX.5461" = "blue", "DOX" = "red")) + # Updated color palette
guides(fill = guide_legend(title = "Treatment")) +
facet_grid(Concentration ~ Timepoint) + # Facet by Concentration and Timepoint
theme_bw() +
xlab("Drugs") +
ylab("|Log Fold Change|") +
ggtitle("|Log Fold| for DOX-Specific Response Genes") +
theme(
plot.title = element_text(size = rel(1.5), hjust = 0.5),
axis.title = element_text(size = 15, color = "black"),
axis.line = element_line(linewidth = 1.5),
strip.background = element_rect(fill = "gray"), # Set strip background to gray
strip.text = element_text(size = 12, color = "black", face = "bold"), # Unified styling for all facet labels
axis.text.x = element_text(size = 8, color = "black", angle = 15)
)
| Version | Author | Date |
|---|---|---|
| 2862c42 | sayanpaul01 | 2025-02-24 |
📌 Late high dose DOX-specific response abs logFC boxplots
# Extract Entrez_IDs from set4
late_high_dose_dox_entrez_ids <- prob_all_4
# Combine all subset_toptables into a single data frame with additional metadata columns
all_toptables <- bind_rows(
Toptable_CX_0.1_3_df %>% mutate(Drug = "CX.5461", Concentration = 0.1, Timepoint = "3"),
Toptable_CX_0.1_24_df %>% mutate(Drug = "CX.5461", Concentration = 0.1, Timepoint = "24"),
Toptable_CX_0.1_48_df %>% mutate(Drug = "CX.5461", Concentration = 0.1, Timepoint = "48"),
Toptable_CX_0.5_3_df %>% mutate(Drug = "CX.5461", Concentration = 0.5, Timepoint = "3"),
Toptable_CX_0.5_24_df %>% mutate(Drug = "CX.5461", Concentration = 0.5, Timepoint = "24"),
Toptable_CX_0.5_48_df %>% mutate(Drug = "CX.5461", Concentration = 0.5, Timepoint = "48"),
Toptable_DOX_0.1_3_df %>% mutate(Drug = "DOX", Concentration = 0.1, Timepoint = "3"),
Toptable_DOX_0.1_24_df %>% mutate(Drug = "DOX", Concentration = 0.1, Timepoint = "24"),
Toptable_DOX_0.1_48_df %>% mutate(Drug = "DOX", Concentration = 0.1, Timepoint = "48"),
Toptable_DOX_0.5_3_df %>% mutate(Drug = "DOX", Concentration = 0.5, Timepoint = "3"),
Toptable_DOX_0.5_24_df %>% mutate(Drug = "DOX", Concentration = 0.5, Timepoint = "24"),
Toptable_DOX_0.5_48_df %>% mutate(Drug = "DOX", Concentration = 0.5, Timepoint = "48")
)
# Filter and visualize data for late high dose DOX-specific response genes
filtered_toptables <- all_toptables %>%
filter(Entrez_ID %in% late_high_dose_dox_entrez_ids)
filtered_toptables %>%
mutate(absFC = abs(logFC)) %>% # Compute absolute log fold change
mutate(
Drug = factor(Drug, levels = c("CX.5461", "DOX")), # Factorize Drug with CX.5461 first
Timepoint = factor(Timepoint, levels = c("3", "24", "48"), labels = c("Timepoint: 3 hours", "Timepoint: 24 hours", "Timepoint: 48 hours")),
Concentration = factor(Concentration, levels = c(0.1, 0.5), labels = c("Concentration: 0.1", "Concentration: 0.5"))
) %>%
ggplot(aes(x = Drug, y = absFC)) +
geom_boxplot(aes(fill = Drug)) +
scale_fill_manual(values = c("CX.5461" = "blue", "DOX" = "red")) + # Updated color palette
guides(fill = guide_legend(title = "Treatment")) +
facet_grid(Concentration ~ Timepoint) + # Facet by Concentration and Timepoint
theme_bw() +
xlab("Drugs") +
ylab("|Log Fold Change|") +
ggtitle("|Log Fold| for Late High Dose DOX-Specific Response Genes") +
theme(
plot.title = element_text(size = rel(1.5), hjust = 0.5),
axis.title = element_text(size = 15, color = "black"),
axis.line = element_line(linewidth = 1.5),
strip.background = element_rect(fill = "gray"), # Set strip background to gray
strip.text = element_text(size = 12, color = "black", face = "bold"), # Unified styling for all facet labels
axis.text.x = element_text(size = 8, color = "black", angle = 15)
)
| Version | Author | Date |
|---|---|---|
| 2862c42 | sayanpaul01 | 2025-02-24 |
📌 Corr-motif set mean (Abs logFC) across timepoints
all_toptables <- bind_rows(
Toptable_CX_0.1_3_df %>% mutate(Drug = "CX.5461", Concentration = 0.1, Timepoint = "3"),
Toptable_CX_0.1_24_df %>% mutate(Drug = "CX.5461", Concentration = 0.1, Timepoint = "24"),
Toptable_CX_0.1_48_df %>% mutate(Drug = "CX.5461", Concentration = 0.1, Timepoint = "48"),
Toptable_CX_0.5_3_df %>% mutate(Drug = "CX.5461", Concentration = 0.5, Timepoint = "3"),
Toptable_CX_0.5_24_df %>% mutate(Drug = "CX.5461", Concentration = 0.5, Timepoint = "24"),
Toptable_CX_0.5_48_df %>% mutate(Drug = "CX.5461", Concentration = 0.5, Timepoint = "48"),
Toptable_DOX_0.1_3_df %>% mutate(Drug = "DOX", Concentration = 0.1, Timepoint = "3"),
Toptable_DOX_0.1_24_df %>% mutate(Drug = "DOX", Concentration = 0.1, Timepoint = "24"),
Toptable_DOX_0.1_48_df %>% mutate(Drug = "DOX", Concentration = 0.1, Timepoint = "48"),
Toptable_DOX_0.5_3_df %>% mutate(Drug = "DOX", Concentration = 0.5, Timepoint = "3"),
Toptable_DOX_0.5_24_df %>% mutate(Drug = "DOX", Concentration = 0.5, Timepoint = "24"),
Toptable_DOX_0.5_48_df %>% mutate(Drug = "DOX", Concentration = 0.5, Timepoint = "48")
)
# Convert Entrez_ID in `all_toptables` to character for proper matching
all_toptables <- all_toptables %>% mutate(Entrez_ID = as.character(Entrez_ID))
# Define datasets for filtering (lists of Entrez IDs)
data_sets <- list(
"Non Response" = prob_all_1,
"CX_DOX Shared\nLate Response" = prob_all_2,
"DOX-Specific Response" = prob_all_3,
"Late High Dose\nDOX-Specific Response" = prob_all_4
)
# Filter datasets and add labels
data_combined <- bind_rows(lapply(names(data_sets), function(label) {
all_toptables %>%
filter(Entrez_ID %in% data_sets[[label]]) %>% # Use list directly for filtering
mutate(Dataset = label)
}))
# Ensure `logFC` column exists before computing mean absolute logFC
if (!"logFC" %in% colnames(data_combined)) {
stop("Column `logFC` is missing in `data_combined`. Ensure that `all_toptables` has `logFC`.")
}
# Compute mean absolute logFC grouped by Dataset, Drug, Concentration, and Timepoint
data_summary <- data_combined %>%
mutate(abs_logFC = abs(logFC)) %>% # Take absolute log fold change
group_by(Dataset, Drug, Concentration, Timepoint) %>%
dplyr::summarize(mean_abs_logFC = mean(abs_logFC, na.rm = TRUE), .groups = "drop") %>%
as.data.frame()
# Convert factors for plotting
data_summary <- data_summary %>%
mutate(
Timepoint = factor(Timepoint, levels = c("3", "24", "48"), labels = c("3 hours", "24 hours", "48 hours")),
Concentration = factor(Concentration, levels = c(0.1, 0.5)),
Dataset = factor(Dataset, levels = c("Non Response", "CX_DOX Shared\nLate Response", "DOX-Specific Response", "Late High Dose\nDOX-Specific Response"))
)
# Define custom drug palette
drug_palette <- c("CX.5461" = "blue", "DOX" = "red")
# Plot the data for absolute logFC
ggplot(data_summary, aes(x = Timepoint, y = mean_abs_logFC, group = Drug, color = Drug)) +
geom_point(size = 3) +
geom_line(size = 1.2) +
scale_color_manual(values = drug_palette) +
ylim(0, 2) + # Adjust the Y-axis for better visualization
facet_grid(Dataset ~ Concentration) +
theme_bw() +
labs(
x = "Timepoints",
y = "Mean |Log Fold Change|",
title = "Average |Log Fold Change| Across Motifs and Concentrations",
color = "Drug"
) +
theme(
plot.title = element_text(size = rel(1.5), hjust = 0.5),
axis.title = element_text(size = 15, color = "black"),
axis.text = element_text(size = 12, color = "black"),
strip.text = element_text(size = 12, color = "black", face = "bold"),
legend.title = element_text(size = 14),
legend.text = element_text(size = 12)
)
| Version | Author | Date |
|---|---|---|
| 2862c42 | sayanpaul01 | 2025-02-24 |
📌 Corr-motif set logFC boxplots
📌 Non response logFC boxplots
# Extract Entrez_IDs from set1
non_response_entrez_ids <- prob_all_1
# Combine all subset_toptables into a single data frame with additional metadata columns
all_toptables <- bind_rows(
Toptable_CX_0.1_3_df %>% mutate(Drug = "CX.5461", Concentration = 0.1, Timepoint = "3"),
Toptable_CX_0.1_24_df %>% mutate(Drug = "CX.5461", Concentration = 0.1, Timepoint = "24"),
Toptable_CX_0.1_48_df %>% mutate(Drug = "CX.5461", Concentration = 0.1, Timepoint = "48"),
Toptable_CX_0.5_3_df %>% mutate(Drug = "CX.5461", Concentration = 0.5, Timepoint = "3"),
Toptable_CX_0.5_24_df %>% mutate(Drug = "CX.5461", Concentration = 0.5, Timepoint = "24"),
Toptable_CX_0.5_48_df %>% mutate(Drug = "CX.5461", Concentration = 0.5, Timepoint = "48"),
Toptable_DOX_0.1_3_df %>% mutate(Drug = "DOX", Concentration = 0.1, Timepoint = "3"),
Toptable_DOX_0.1_24_df %>% mutate(Drug = "DOX", Concentration = 0.1, Timepoint = "24"),
Toptable_DOX_0.1_48_df %>% mutate(Drug = "DOX", Concentration = 0.1, Timepoint = "48"),
Toptable_DOX_0.5_3_df %>% mutate(Drug = "DOX", Concentration = 0.5, Timepoint = "3"),
Toptable_DOX_0.5_24_df %>% mutate(Drug = "DOX", Concentration = 0.5, Timepoint = "24"),
Toptable_DOX_0.5_48_df %>% mutate(Drug = "DOX", Concentration = 0.5, Timepoint = "48")
)
# Filter and visualize data for shared late response genes
filtered_toptables <- all_toptables %>%
filter(Entrez_ID %in% non_response_entrez_ids)
# Visualization of logFC for non-response genes
filtered_toptables %>%
mutate(
Drug = factor(Drug, levels = c("CX.5461", "DOX")), # Factorize Drug with CX.5461 first
Timepoint = factor(Timepoint, levels = c("3", "24", "48"), labels = c("Timepoint: 3 hours", "Timepoint: 24 hours", "Timepoint: 48 hours")),
Concentration = factor(Concentration, levels = c(0.1, 0.5), labels = c("Concentration: 0.1", "Concentration: 0.5"))
) %>%
ggplot(aes(x = Drug, y = logFC)) + # Plot logFC directly
geom_boxplot(aes(fill = Drug)) +
scale_fill_manual(values = c("CX.5461" = "blue", "DOX" = "red")) + # Updated color palette
guides(fill = guide_legend(title = "Treatment")) +
facet_grid(Concentration ~ Timepoint) + # Facet by Concentration and Timepoint
theme_bw() +
xlab("Drugs") +
ylab("Log Fold Change") + # Updated y-axis label
ggtitle("Log Fold Change for Non-Response Genes") +
theme(
plot.title = element_text(size = rel(1.5), hjust = 0.5),
axis.title = element_text(size = 15, color = "black"),
axis.line = element_line(linewidth = 1.5),
strip.background = element_rect(fill = "gray"), # Set strip background to gray
strip.text = element_text(size = 12, color = "black", face = "bold"), # Unified styling for all facet labels
axis.text.x = element_text(size = 8, color = "black", angle = 15)
)
| Version | Author | Date |
|---|---|---|
| 2862c42 | sayanpaul01 | 2025-02-24 |
📌 CX_DOX Shared Late Response logFC boxplots
# Extract Entrez_IDs from set2
cx_dox_shared_entrez_ids <- prob_all_2
# Combine all subset_toptables into a single data frame with additional metadata columns
all_toptables <- bind_rows(
Toptable_CX_0.1_3_df %>% mutate(Drug = "CX.5461", Concentration = 0.1, Timepoint = "3"),
Toptable_CX_0.1_24_df %>% mutate(Drug = "CX.5461", Concentration = 0.1, Timepoint = "24"),
Toptable_CX_0.1_48_df %>% mutate(Drug = "CX.5461", Concentration = 0.1, Timepoint = "48"),
Toptable_CX_0.5_3_df %>% mutate(Drug = "CX.5461", Concentration = 0.5, Timepoint = "3"),
Toptable_CX_0.5_24_df %>% mutate(Drug = "CX.5461", Concentration = 0.5, Timepoint = "24"),
Toptable_CX_0.5_48_df %>% mutate(Drug = "CX.5461", Concentration = 0.5, Timepoint = "48"),
Toptable_DOX_0.1_3_df %>% mutate(Drug = "DOX", Concentration = 0.1, Timepoint = "3"),
Toptable_DOX_0.1_24_df %>% mutate(Drug = "DOX", Concentration = 0.1, Timepoint = "24"),
Toptable_DOX_0.1_48_df %>% mutate(Drug = "DOX", Concentration = 0.1, Timepoint = "48"),
Toptable_DOX_0.5_3_df %>% mutate(Drug = "DOX", Concentration = 0.5, Timepoint = "3"),
Toptable_DOX_0.5_24_df %>% mutate(Drug = "DOX", Concentration = 0.5, Timepoint = "24"),
Toptable_DOX_0.5_48_df %>% mutate(Drug = "DOX", Concentration = 0.5, Timepoint = "48")
)
# Filter and visualize data for CX_DOX shared late response genes
filtered_toptables <- all_toptables %>%
filter(Entrez_ID %in% cx_dox_shared_entrez_ids)
# Visualization of logFC for CX_DOX shared late response genes
filtered_toptables %>%
mutate(
Drug = factor(Drug, levels = c("CX.5461", "DOX")), # Factorize Drug with CX.5461 first
Timepoint = factor(Timepoint, levels = c("3", "24", "48"), labels = c("Timepoint: 3 hours", "Timepoint: 24 hours", "Timepoint: 48 hours")),
Concentration = factor(Concentration, levels = c(0.1, 0.5), labels = c("Concentration: 0.1", "Concentration: 0.5"))
) %>%
ggplot(aes(x = Drug, y = logFC)) + # Plot logFC directly
geom_boxplot(aes(fill = Drug)) +
scale_fill_manual(values = c("CX.5461" = "blue", "DOX" = "red")) + # Updated color palette
guides(fill = guide_legend(title = "Treatment")) +
facet_grid(Concentration ~ Timepoint) + # Facet by Concentration and Timepoint
theme_bw() +
theme_bw() +
xlab("Drugs") +
ylab("Log Fold Change") + # Updated y-axis label
ggtitle("Log Fold Change for CX_DOX Shared Late Response Genes") +
theme(
plot.title = element_text(size = rel(1.5), hjust = 0.5),
axis.title = element_text(size = 15, color = "black"),
axis.line = element_line(linewidth = 1.5),
strip.background = element_rect(fill = "gray"), # Set strip background to gray
strip.text = element_text(size = 12, color = "black", face = "bold"), # Unified styling for all facet labels
axis.text.x = element_text(size = 8, color = "black", angle = 15)
)
| Version | Author | Date |
|---|---|---|
| 2862c42 | sayanpaul01 | 2025-02-24 |
📌 DOX-Specific Response logFC boxplots
# Extract Entrez_IDs from set3
dox_specific_entrez_ids <- prob_all_3
# Combine all subset_toptables into a single data frame with additional metadata columns
all_toptables <- bind_rows(
Toptable_CX_0.1_3_df %>% mutate(Drug = "CX.5461", Concentration = 0.1, Timepoint = "3"),
Toptable_CX_0.1_24_df %>% mutate(Drug = "CX.5461", Concentration = 0.1, Timepoint = "24"),
Toptable_CX_0.1_48_df %>% mutate(Drug = "CX.5461", Concentration = 0.1, Timepoint = "48"),
Toptable_CX_0.5_3_df %>% mutate(Drug = "CX.5461", Concentration = 0.5, Timepoint = "3"),
Toptable_CX_0.5_24_df %>% mutate(Drug = "CX.5461", Concentration = 0.5, Timepoint = "24"),
Toptable_CX_0.5_48_df %>% mutate(Drug = "CX.5461", Concentration = 0.5, Timepoint = "48"),
Toptable_DOX_0.1_3_df %>% mutate(Drug = "DOX", Concentration = 0.1, Timepoint = "3"),
Toptable_DOX_0.1_24_df %>% mutate(Drug = "DOX", Concentration = 0.1, Timepoint = "24"),
Toptable_DOX_0.1_48_df %>% mutate(Drug = "DOX", Concentration = 0.1, Timepoint = "48"),
Toptable_DOX_0.5_3_df %>% mutate(Drug = "DOX", Concentration = 0.5, Timepoint = "3"),
Toptable_DOX_0.5_24_df %>% mutate(Drug = "DOX", Concentration = 0.5, Timepoint = "24"),
Toptable_DOX_0.5_48_df %>% mutate(Drug = "DOX", Concentration = 0.5, Timepoint = "48")
)
# Filter and visualize data for DOX-specific response genes
filtered_toptables <- all_toptables %>%
filter(Entrez_ID %in% dox_specific_entrez_ids)
# Visualization of logFC for DOX-specific response genes
filtered_toptables %>%
mutate(
Drug = factor(Drug, levels = c("CX.5461", "DOX")), # Factorize Drug with CX.5461 first
Timepoint = factor(Timepoint, levels = c("3", "24", "48"), labels = c("Timepoint: 3 hours", "Timepoint: 24 hours", "Timepoint: 48 hours")),
Concentration = factor(Concentration, levels = c(0.1, 0.5), labels = c("Concentration: 0.1", "Concentration: 0.5"))
) %>%
ggplot(aes(x = Drug, y = logFC)) + # Plot logFC directly
geom_boxplot(aes(fill = Drug)) +
scale_fill_manual(values = c("CX.5461" = "blue", "DOX" = "red")) + # Updated color palette
guides(fill = guide_legend(title = "Treatment")) +
facet_grid(Concentration ~ Timepoint) + # Facet by Concentration and Timepoint
theme_bw() +
xlab("Drugs") +
ylab("Log Fold Change") + # Updated y-axis label
ggtitle("Log Fold Change for DOX-Specific Response Genes") +
theme(
plot.title = element_text(size = rel(1.5), hjust = 0.5),
axis.title = element_text(size = 15, color = "black"),
axis.line = element_line(linewidth = 1.5),
strip.background = element_rect(fill = "gray"), # Set strip background to gray
strip.text = element_text(size = 12, color = "black", face = "bold"), # Unified styling for all facet labels
axis.text.x = element_text(size = 8, color = "black", angle = 15)
)
| Version | Author | Date |
|---|---|---|
| 2862c42 | sayanpaul01 | 2025-02-24 |
📌 Late High Dose DOX-Specific Response logFC boxplots
# Extract Entrez_IDs from set4
late_high_dose_dox_specific_entrez_ids <- prob_all_4
# Combine all subset_toptables into a single data frame with additional metadata columns
all_toptables <- bind_rows(
Toptable_CX_0.1_3_df %>% mutate(Drug = "CX.5461", Concentration = 0.1, Timepoint = "3"),
Toptable_CX_0.1_24_df %>% mutate(Drug = "CX.5461", Concentration = 0.1, Timepoint = "24"),
Toptable_CX_0.1_48_df %>% mutate(Drug = "CX.5461", Concentration = 0.1, Timepoint = "48"),
Toptable_CX_0.5_3_df %>% mutate(Drug = "CX.5461", Concentration = 0.5, Timepoint = "3"),
Toptable_CX_0.5_24_df %>% mutate(Drug = "CX.5461", Concentration = 0.5, Timepoint = "24"),
Toptable_CX_0.5_48_df %>% mutate(Drug = "CX.5461", Concentration = 0.5, Timepoint = "48"),
Toptable_DOX_0.1_3_df %>% mutate(Drug = "DOX", Concentration = 0.1, Timepoint = "3"),
Toptable_DOX_0.1_24_df %>% mutate(Drug = "DOX", Concentration = 0.1, Timepoint = "24"),
Toptable_DOX_0.1_48_df %>% mutate(Drug = "DOX", Concentration = 0.1, Timepoint = "48"),
Toptable_DOX_0.5_3_df %>% mutate(Drug = "DOX", Concentration = 0.5, Timepoint = "3"),
Toptable_DOX_0.5_24_df %>% mutate(Drug = "DOX", Concentration = 0.5, Timepoint = "24"),
Toptable_DOX_0.5_48_df %>% mutate(Drug = "DOX", Concentration = 0.5, Timepoint = "48")
)
# Filter and visualize data for Late High Dose DOX-Specific Response Genes
filtered_toptables <- all_toptables %>%
filter(Entrez_ID %in% late_high_dose_dox_specific_entrez_ids)
# Visualization of logFC for Late High Dose DOX-Specific Response Genes
filtered_toptables %>%
mutate(
Drug = factor(Drug, levels = c("CX.5461", "DOX")), # Factorize Drug with CX.5461 first
Timepoint = factor(Timepoint, levels = c("3", "24", "48"), labels = c("Timepoint: 3 hours", "Timepoint: 24 hours", "Timepoint: 48 hours")),
Concentration = factor(Concentration, levels = c(0.1, 0.5), labels = c("Concentration: 0.1", "Concentration: 0.5"))
) %>%
ggplot(aes(x = Drug, y = logFC)) + # Plot logFC directly
geom_boxplot(aes(fill = Drug)) +
scale_fill_manual(values = c("CX.5461" = "blue", "DOX" = "red")) + # Updated color palette
guides(fill = guide_legend(title = "Treatment")) +
facet_grid(Concentration ~ Timepoint) + # Facet by Concentration and Timepoint
theme_bw() +
xlab("Drugs") +
ylab("Log Fold Change") + # Updated y-axis label
ggtitle("Log Fold Change for Late High Dose DOX-Specific Response Genes") +
theme(
plot.title = element_text(size = rel(1.5), hjust = 0.5),
axis.title = element_text(size = 15, color = "black"),
axis.line = element_line(linewidth = 1.5),
strip.background = element_rect(fill = "gray"), # Set strip background to gray
strip.text = element_text(size = 12, color = "black", face = "bold"), # Unified styling for all facet labels
axis.text.x = element_text(size = 8, color = "black", angle = 15)
)
| Version | Author | Date |
|---|---|---|
| 2862c42 | sayanpaul01 | 2025-02-24 |
📌 Corr-motif set mean logFC across timepoints
# Combine all subset_toptables into a single data frame with additional metadata columns
all_toptables <- bind_rows(
Toptable_CX_0.1_3_df %>% mutate(Drug = "CX.5461", Concentration = 0.1, Timepoint = "3"),
Toptable_CX_0.1_24_df %>% mutate(Drug = "CX.5461", Concentration = 0.1, Timepoint = "24"),
Toptable_CX_0.1_48_df %>% mutate(Drug = "CX.5461", Concentration = 0.1, Timepoint = "48"),
Toptable_CX_0.5_3_df %>% mutate(Drug = "CX.5461", Concentration = 0.5, Timepoint = "3"),
Toptable_CX_0.5_24_df %>% mutate(Drug = "CX.5461", Concentration = 0.5, Timepoint = "24"),
Toptable_CX_0.5_48_df %>% mutate(Drug = "CX.5461", Concentration = 0.5, Timepoint = "48"),
Toptable_DOX_0.1_3_df %>% mutate(Drug = "DOX", Concentration = 0.1, Timepoint = "3"),
Toptable_DOX_0.1_24_df %>% mutate(Drug = "DOX", Concentration = 0.1, Timepoint = "24"),
Toptable_DOX_0.1_48_df %>% mutate(Drug = "DOX", Concentration = 0.1, Timepoint = "48"),
Toptable_DOX_0.5_3_df %>% mutate(Drug = "DOX", Concentration = 0.5, Timepoint = "3"),
Toptable_DOX_0.5_24_df %>% mutate(Drug = "DOX", Concentration = 0.5, Timepoint = "24"),
Toptable_DOX_0.5_48_df %>% mutate(Drug = "DOX", Concentration = 0.5, Timepoint = "48")
)
# Convert Entrez_ID in `all_toptables` to character for proper matching
all_toptables <- all_toptables %>% mutate(Entrez_ID = as.character(Entrez_ID))
# Define datasets for filtering (lists of Entrez IDs)
data_sets <- list(
"Non Response" = prob_all_1,
"CX_DOX Shared\nLate Response" = prob_all_2,
"DOX-Specific Response" = prob_all_3,
"Late High Dose\nDOX-Specific Response" = prob_all_4
)
# Filter datasets and add labels
data_combined <- bind_rows(lapply(names(data_sets), function(label) {
all_toptables %>%
filter(Entrez_ID %in% data_sets[[label]]) %>% # Use list directly for filtering
mutate(Dataset = label)
}))
# Ensure `logFC` column exists before computing mean
if (!"logFC" %in% colnames(data_combined)) {
stop("Column `logFC` is missing in `data_combined`. Ensure that `all_toptables` has `logFC`.")
}
# Calculate the average logFC grouped by Dataset, Drug, Concentration, and Timepoint
data_summary <- data_combined %>%
group_by(Dataset, Drug, Concentration, Timepoint) %>%
dplyr::summarize(avg_logFC = mean(logFC, na.rm = TRUE), .groups = "drop") %>%
as.data.frame()
# Convert factors for plotting
data_summary <- data_summary %>%
mutate(
Timepoint = factor(Timepoint, levels = c("3", "24", "48"), labels = c("3 hours", "24 hours", "48 hours")),
Concentration = factor(Concentration, levels = c(0.1, 0.5)),
Dataset = factor(Dataset, levels = c("Non Response", "CX_DOX Shared\nLate Response", "DOX-Specific Response", "Late High Dose\nDOX-Specific Response"))
)
# Define custom drug palette
drug_palette <- c("CX.5461" = "blue", "DOX" = "red")
# Plot the data
ggplot(data_summary, aes(x = Timepoint, y = avg_logFC, group = Drug, color = Drug)) +
geom_point(size = 3) +
geom_line(size = 1.2) +
scale_color_manual(values = drug_palette) +
ylim(-2, 2) + # Set the Y-axis scale
facet_grid(Dataset ~ Concentration) +
theme_bw() +
labs(
x = "Timepoints",
y = "Mean Log Fold Change",
title = "Average Log Fold Change Across Motifs and Concentrations",
color = "Drug"
) +
theme(
plot.title = element_text(size = rel(1.5), hjust = 0.5),
axis.title = element_text(size = 15, color = "black"),
axis.text = element_text(size = 12, color = "black"),
strip.text = element_text(size = 12, color = "black", face = "bold"),
legend.title = element_text(size = 14),
legend.text = element_text(size = 12)
)
| Version | Author | Date |
|---|---|---|
| 2862c42 | sayanpaul01 | 2025-02-24 |
📌 Save Corr-motif datasets for Gene Ontology analysis
write.csv(data.frame(Entrez_ID = prob_all_1), "data/prob_all_1.csv", row.names = FALSE)
write.csv(data.frame(Entrez_ID = prob_all_2), "data/prob_all_2.csv", row.names = FALSE)
write.csv(data.frame(Entrez_ID = prob_all_3), "data/prob_all_3.csv", row.names = FALSE)
write.csv(data.frame(Entrez_ID = prob_all_4), "data/prob_all_4.csv", row.names = FALSE)
sessionInfo()R version 4.3.0 (2023-04-21 ucrt)
Platform: x86_64-w64-mingw32/x64 (64-bit)
Running under: Windows 11 x64 (build 22631)
Matrix products: default
locale:
[1] LC_COLLATE=English_United States.utf8
[2] LC_CTYPE=English_United States.utf8
[3] LC_MONETARY=English_United States.utf8
[4] LC_NUMERIC=C
[5] LC_TIME=English_United States.utf8
time zone: America/Chicago
tzcode source: internal
attached base packages:
[1] stats4 stats graphics grDevices utils datasets methods
[8] base
other attached packages:
[1] BiocParallel_1.36.0 Rfast_2.1.0 RcppParallel_5.1.9
[4] RcppZiggurat_0.1.6 Rcpp_1.0.12 Cormotif_1.48.0
[7] limma_3.58.1 affy_1.80.0 corrplot_0.95
[10] ggpubr_0.6.0 pheatmap_1.0.12 gprofiler2_0.2.3
[13] RColorBrewer_1.1-3 org.Hs.eg.db_3.18.0 AnnotationDbi_1.64.1
[16] IRanges_2.36.0 S4Vectors_0.40.1 Biobase_2.62.0
[19] BiocGenerics_0.48.1 clusterProfiler_4.10.1 reshape2_1.4.4
[22] lubridate_1.9.3 forcats_1.0.0 stringr_1.5.1
[25] dplyr_1.1.4 purrr_1.0.2 readr_2.1.5
[28] tidyr_1.3.1 tibble_3.2.1 ggplot2_3.5.1
[31] tidyverse_2.0.0 workflowr_1.7.1
loaded via a namespace (and not attached):
[1] rstudioapi_0.17.1 jsonlite_1.8.9 magrittr_2.0.3
[4] farver_2.1.2 rmarkdown_2.29 fs_1.6.3
[7] zlibbioc_1.48.0 vctrs_0.6.5 memoise_2.0.1
[10] RCurl_1.98-1.13 ggtree_3.10.1 rstatix_0.7.2
[13] htmltools_0.5.8.1 broom_1.0.7 Formula_1.2-5
[16] gridGraphics_0.5-1 sass_0.4.9 bslib_0.8.0
[19] htmlwidgets_1.6.4 plyr_1.8.9 plotly_4.10.4
[22] cachem_1.0.8 whisker_0.4.1 igraph_2.1.1
[25] lifecycle_1.0.4 pkgconfig_2.0.3 Matrix_1.6-1.1
[28] R6_2.5.1 fastmap_1.1.1 gson_0.1.0
[31] GenomeInfoDbData_1.2.11 digest_0.6.34 aplot_0.2.3
[34] enrichplot_1.22.0 colorspace_2.1-0 patchwork_1.3.0
[37] ps_1.8.1 rprojroot_2.0.4 RSQLite_2.3.3
[40] labeling_0.4.3 timechange_0.3.0 abind_1.4-8
[43] httr_1.4.7 polyclip_1.10-7 compiler_4.3.0
[46] bit64_4.0.5 withr_3.0.2 backports_1.5.0
[49] carData_3.0-5 viridis_0.6.5 DBI_1.2.3
[52] ggforce_0.4.2 ggsignif_0.6.4 MASS_7.3-60
[55] HDO.db_0.99.1 tools_4.3.0 ape_5.8
[58] scatterpie_0.2.4 httpuv_1.6.15 glue_1.7.0
[61] callr_3.7.6 nlme_3.1-166 GOSemSim_2.28.1
[64] promises_1.3.0 grid_4.3.0 shadowtext_0.1.4
[67] getPass_0.2-4 fgsea_1.28.0 generics_0.1.3
[70] gtable_0.3.6 tzdb_0.4.0 preprocessCore_1.64.0
[73] data.table_1.14.10 hms_1.1.3 car_3.1-3
[76] tidygraph_1.3.1 XVector_0.42.0 ggrepel_0.9.6
[79] pillar_1.10.1 yulab.utils_0.1.8 later_1.3.2
[82] splines_4.3.0 tweenr_2.0.3 treeio_1.26.0
[85] lattice_0.22-5 bit_4.0.5 tidyselect_1.2.1
[88] GO.db_3.18.0 Biostrings_2.70.1 knitr_1.49
[91] git2r_0.35.0 gridExtra_2.3 xfun_0.50
[94] graphlayouts_1.2.0 statmod_1.5.0 stringi_1.8.3
[97] lazyeval_0.2.2 ggfun_0.1.8 yaml_2.3.10
[100] evaluate_1.0.3 codetools_0.2-20 ggraph_2.2.1
[103] qvalue_2.34.0 BiocManager_1.30.25 affyio_1.72.0
[106] ggplotify_0.1.2 cli_3.6.1 munsell_0.5.1
[109] processx_3.8.5 jquerylib_0.1.4 GenomeInfoDb_1.38.8
[112] png_0.1-8 parallel_4.3.0 blob_1.2.4
[115] DOSE_3.28.2 bitops_1.0-7 viridisLite_0.4.2
[118] tidytree_0.4.6 scales_1.3.0 crayon_1.5.3
[121] rlang_1.1.3 cowplot_1.1.3 fastmatch_1.1-4
[124] KEGGREST_1.42.0