cluster/hvtn/HVTNclusterFinalIsh.R

library(flowReMix)
library(magrittr)
require(dplyr)
library(ggplot2)
cpus <- 2
print(cpus)

args <- commandArgs(TRUE)
eval(parse(text=args[[1]]))
setting <- as.numeric(setting)

getExpression <- function(str) {
  first <- substr(str, 1, 7)
  second <- substr(str, 8, nchar(str))
  second <- strsplit(second, "")[[1]]
  seperators <- c(0, which(second %in% c("-", "+")))
  expressed <- list()
  for(i in 2:length(seperators)) {
    if(second[seperators[i]] == "+") {
      expressed[[i]] <- paste(second[(seperators[(i - 1)] + 1) : seperators[i]], collapse = '')
    }
  }

  expressed <- paste(unlist(expressed), collapse = '')
  expressed <- paste(first, expressed, sep = '')
  return(expressed)
}

# Loading Data --------------------------------
# hvtn <- read.csv(file = "data/merged_505_stats.csv")
# names(hvtn) <- tolower(names(hvtn))
# hvtn <- subset(hvtn, !is.na(ptid))
# saveRDS(hvtn, file = "data/505_stats.rds")

# Getting marginals -----------------------------
library(flowReMix)
hvtn <- readRDS(file = "data/505_stats.rds")
length(unique(hvtn$name))
length(unique(hvtn$ptid))
length(unique(hvtn$population))
unique(hvtn$population)
unique(hvtn$stim)
nchars <- nchar(as.character(unique(hvtn$population)))
#marginals <- unique(hvtn$population)[nchars < 26]
marginals <- unique(hvtn$population)[nchars == 26]
marginals <- subset(hvtn, population %in% marginals)
marginals <- subset(marginals, stim %in% c("negctrl", "VRC ENV A",
                                           "VRC ENV B", "VRC ENV C",
                                           "VRC GAG B", "VRC NEF B",
                                           "VRC POL 1 B", "VRC POL 2 B"))
                                           # "Empty Ad5 (VRC)"))
marginals <- subset(marginals, !(population %in% c("4+", "8+")))
marginals <- subset(marginals, !(population %in% c("8+/107a-154-IFNg-IL2-TNFa-", "4+/107a-154-IFNg-IL2-TNFa-")))
marginals$stim <- factor(as.character(marginals$stim))
marginals$population <- factor(as.character(marginals$population))

# Descriptives -------------------------------------
marginals$prop <- marginals$count / marginals$parentcount
# ggplot(marginals) + geom_boxplot(aes(x = population, y = log(prop), col = stim))

negctrl <- subset(marginals, stim == "negctrl")
negctrl <- summarize(group_by(negctrl, ptid, population), negprop = mean(prop))
negctrl <- as.data.frame(negctrl)
marginals <- merge(marginals, negctrl, all.x = TRUE)

# ggplot(subset(marginals, stim != "negctrl" & parent == "4+")) +
#   geom_point(aes(x = log(negprop), y = log(prop)), size = 0.25) +
#   facet_grid(stim ~ population, scales = "free") +
#   theme_bw() +
#   geom_abline(intercept = 0, slope = 1)

# Converting subset names ------------------
subsets <- as.character(unique(marginals$population))
expressed <- sapply(subsets, getExpression)
map <- cbind(subsets, expressed)
marginals$population <- as.character(marginals$population)
for(i in 1:nrow(map)) {
  marginals$population[which(marginals$population == map[i, 1])] <- map[i, 2]
}
marginals$population <- factor(marginals$population)
# nfunctions <- marginals$population %>% as.character %>%
#   strsplit(split = "/") %>%
#   sapply(function(x) x[[2]]) %>% strsplit("+", fixed = TRUE) %>%
#   unlist() %>% unique()


# Setting up data for analysis ---------------------------
subsetDat <- stimulationModel(marginals,
                              cell_type = population,
                              stim_var = stim,
                              stim_groups = list(gag = "VRC GAG B",
                                                 pol = c("VRC POL 1 B", "VRC POL 2 B"),
                                                 env = c("VRC ENV C", "VRC ENV B", "VRC ENV A"),
                                                 nef = "VRC NEF B"),
                                                 # Ad5 = "Empty Ad5 (VRC)"),
                              controls = c("negctrl"))
subsetDat$subset <- subsetDat$stimCellType
subsetDat$stimCellType <- NULL

# Getting outcomes -------------------------------
# treatmentdat <- read.csv(file = "data/rx_v2.csv")
# names(treatmentdat) <- tolower(names(treatmentdat))
# treatmentdat$ptid <- factor(gsub("-", "", (treatmentdat$ptid)))
# treatmentdat <- subset(treatmentdat, ptid %in% unique(subsetDat$ptid))

# Finding problematic subsets?
keep <- by(subsetDat, list(subsetDat$subset), function(x) mean(x$count > 1) > 0.02)
keep <- names(keep[sapply(keep, function(x) x)])
subsetDat <- subset(subsetDat, subset %in% keep)
subsetDat$subset <- factor(as.character(subsetDat$subset))

keep <- by(marginals, list(marginals$population), function(x) mean(x$count > 1) > 0.02)
keep <- names(keep[sapply(keep, function(x) x)])
marginals <- subset(marginals, population %in% keep)
marginals$population <- factor(as.character(marginals$population))

configurations <- expand.grid(method = c("MC"),
                              seed = 1:30,
                              maxdisp = c(50),
                              niter = c(20),
                              includeBatch = FALSE)
config <- configurations[setting, ]
print(config)
niter <- config[["niter"]]
seed <- config[["seed"]]
prior <- 0
maxdisp <- config[["maxdisp"]]
method <- config[["method"]]
includeBatch <- config[["includeBatch"]]
if(method == "MC") {
  npost <- 1
  lag <- round(niter / 3)
  keepeach <- 5
  mcEM <- TRUE
}

# Fitting the model ------------------------------
control <- flowReMix_control(updateLag = lag, nsamp = 50,
                             keepEach = keepeach, initMHcoef = 2.5,
                             nPosteriors = npost, centerCovariance = FALSE,
                             maxDispersion = maxdisp * 1000, minDispersion = 10^7,
                             randomAssignProb = 10^-8, intSampSize = 50,
                             seed = seed, zeroPosteriorProbs = FALSE,
                             ncores = cpus, preAssignCoefs = 1,
                             prior = prior, isingWprior = FALSE,
                             markovChainEM = mcEM,
                             initMethod = "robust",
                             threads = cpus * 2,
                             learningRate = 0.6, keepWeightPercent = 0.9)

subsetDat$batch <- factor(subsetDat$batch..)
subsetDat$stimGroup <- factor(subsetDat$stimGroup)
subsetDat <- subsetDat %>% group_by(ptid,population,stim,stimGroup,parent) %>%
  filter(collection.num==max(collection.num)) %>% data.frame()
marginals <- marginals %>% group_by(ptid, population, stim ,parent) %>%
  filter(collection.num==max(collection.num)) %>% data.frame()
# preAssign <- by(subsetDat, subsetDat$ptid, assign)
# preAssign <- do.call("rbind", preAssign)
subsetDat$batch <- factor(as.character(subsetDat$batch), levels = unique(as.character(subsetDat$batch)))
# unique(data.frame(subsetDat$ptid, subsetDat$batch))
# by(subsetDat, subsetDat$subset, function(x) table(x$batch))

fit <- flowReMix(cbind(count, parentcount - count) ~ stim,
                 subject_id = ptid,
                 cell_type = subset,
                 cluster_variable = stim,
                 data = subsetDat,
                 covariance = "sparse",
                 ising_model = "sparse",
                 regression_method = "robust",
                 iterations = niter,
                 parallel = TRUE, keepSamples = TRUE,
                 cluster_assignment = TRUE,
                 verbose = TRUE, control = control)

file <- paste("results/hvtn_robJoint_A",
              "_maxdisp", maxdisp,
              "_niter", niter,
              "npost", npost,
              "seed", seed,
              "prior", prior,
              method, ".rds", sep = "")
print(file)
saveRDS(object = fit, file = file)
stab <- stabilityGraph(fit, type = "ising", cpus = cpus, AND = TRUE,
                       gamma = 0.25, reps = 50, cv = FALSE)
fit$stabilityGraph <- stab
fit$randomEffectSamp <- NULL
fit$assignmentList <- NULL
fit$data <- NULL
saveRDS(object = fit, file = file)
RGLab/flowReMix documentation built on May 8, 2019, 5:55 a.m.