#' Stepwise regression based on risk profile concept and raw risk factors
#'
#' \code{stepRPCr} customized stepwise regression with p-value and trend check on raw risk factors which additionally takes into account
#' the order of supplied risk factors per group when selects a candidate for the final regression model. Trend check is performed
#' comparing observed trend between target and analyzed risk factor and trend of the estimated coefficients.
#' Note that procedure checks the column names of supplied \code{db} data frame therefore some
#' renaming (replacement of special characters) is possible to happen. For details, please, check the help example.
#'@param start.model Formula class that represents the starting model. It can include some risk factors, but it can be
#' defined only with intercept (\code{y ~ 1} where \code{y} is target variable).
#'@param risk.profile Data frame with defined risk profile. It has to contain the following columns: \code{rf} and
#' \code{group}. Column \code{group} defines order of groups that will be tested first as a candidate
#' for the regression model. Risk factors selected in each group are kept as a starting variables
#' for the next group testing. Column \code{rf} contains all candidate risk factors supplied for testing.
#'@param p.value Significance level of p-value of the estimated coefficients. For numerical risk factors this value is
#' is directly compared to the p-value of the estimated coefficients, while for categorical risk factors
#' multiple Wald test is employed and its value is used for comparison with selected threshold (\code{p.value}).
#'@param db Modeling data with risk factors and target variable. All risk factors (apart from the risk factors from the starting model)
#' should be categorized and as of character type.
#'@param check.start.model Logical (\code{TRUE} or \code{FALSE}), if risk factors from the starting model should
#' checked for p-value and trend in stepwise process.
#'@param offset.vals This can be used to specify an a priori known component to be included in the linear predictor during fitting.
#' This should be \code{NULL} or a numeric vector of length equal to the number of cases. Default is \code{NULL}.
#'@return The command \code{stepRPCr} returns a list of four objects.\cr
#' The first object (\code{model}), is the final model, an object of class inheriting from \code{"glm"}.\cr
#' The second object (\code{steps}), is the data frame with risk factors selected at each iteration.\cr
#' The third object (\code{warnings}), is the data frame with warnings if any observed.
#' The warnings refer to the following checks: if risk factor has more than 10 modalities or
#' if any of the bins (groups) has less than 5% of observations.\cr
#' The final, fourth, object \code{dev.db} returns the model development database.
#'@examples
#'suppressMessages(library(PDtoolkit))
#'data(loans)
#'#create risk factor priority groups
#'rf.all <- names(loans)[-1]
#'set.seed(6422)
#'rf.pg <- data.frame(rf = rf.all, group = sample(1:3, length(rf.all), rep = TRUE))
#'rf.pg <- rf.pg[order(rf.pg$group), ]
#'head(rf.pg)
#'res <- stepRPCr(start.model = Creditability ~ 1,
#' risk.profile = rf.pg,
#' p.value = 0.05,
#' db = loans)
#'summary(res$model)$coefficients
#'res$steps
#'head(res$dev.db)
#'@importFrom stats formula coef vcov
#'@export
stepRPCr <- function(start.model, risk.profile, p.value = 0.05, db, check.start.model = TRUE, offset.vals = NULL) {
#check arguments
if (!is.data.frame(db)) {
stop("db is not a data frame.")
}
if (!all(c("rf", "group")%in%names(risk.profile))) {
stop("risk.profile data frame has to contain columns: rf and group.")
}
if (!all(risk.profile$rf%in%names(db))) {
rp.rf.miss <- risk.profile$rf[!risk.profile$rf%in%names(db)]
msg <- "Following risk factors from risk.profile are missing in supplied db: "
msg <- paste0(msg, paste0(rp.rf.miss, collapse = ", "), ".")
stop(msg)
}
if (any(is.na(risk.profile$group))) {
stop("Missing value(s) in risk.profile group.")
}
if ((!is.numeric(p.value) | !length(p.value) == 1) |
!(p.value[1] > 0 & p.value[1] < 1)) {
stop("p.value has to be of single numeric value vector greater than 0 and less then 1.")
}
if (!is.logical(check.start.model)) {
stop("check.start.model has to be logical (TRUE or FALSE).")
}
#extract model variables
start.vars <- all.vars(start.model)
target <- start.vars[1]
if (length(start.vars) > 1) {
rf.start <- start.vars[-1]
} else {
rf.start <- NULL
}
#check starting model formula
check <- any(!c(target, rf.start)%in%names(db))
if (check | is.na(target)) {
stop("Formula for start.model not specified correctly.
Check column names and if formula class is passed to start.model.")
}
rf.rest <- unique(risk.profile$rf)
#check supplied risk factors
rf.restl <- length(rf.rest)
if (rf.restl == 0) {
stop("Risk factors are missing. Check risk.profile argument.")
}
#correct names
names.c <- check.names(x = names(db))
names(db) <- unname(names.c[names(db)])
target <- unname(names.c[target])
if (!is.null(rf.start)) {rf.start <- unname(names.c[rf.start])}
rf.rest <- unname(names.c[rf.rest])
risk.profile$rf <- unname(names.c[risk.profile$rf])
#define warning table
warn.tbl <- data.frame()
#check num of modalities per risk factor
num.type <- sapply(db[, rf.rest, drop = FALSE], is.numeric)
num.rf <- names(num.type)[num.type]
unique.mod <- sapply(db[, rf.rest[!rf.rest%in%num.rf], drop = FALSE], function(x) length(unique(x)))
check.mod <- names(unique.mod)[unique.mod > 10]
if (length(check.mod) > 0) {
warn.rep <- data.frame(rf = check.mod, comment = "More than 10 modalities.")
warn.tbl <- bind_rows(warn.tbl, warn.rep)
}
#check for missing values in categorical risk factors
cat.check <- sapply(db[, rf.rest[!rf.rest%in%num.rf], drop = FALSE],
function(x) sum(is.na(x)))
check.miss.cat <- names(cat.check)[cat.check > 0]
if (length(check.miss.cat) > 0) {
warn.rep <- data.frame(rf = cat.check, comment = "Contains missing values.")
warn.tbl <- bind_rows(warn.tbl, warn.rep)
}
#check for missing values in numeric risk factors
num.check <- sapply(db[, rf.rest[rf.rest%in%num.rf], drop = FALSE],
function(x) sum(x%in%c(NA, NaN, Inf, -Inf)))
check.miss.num <- names(num.check)[num.check > 0]
if (length(check.miss.num) > 0) {
warn.rep <- data.frame(rf = check.miss.num, comment = "Contains special cases (NA, NaN, Inf, -Inf),")
warn.tbl <- bind_rows(warn.tbl, warn.rep)
}
#generate summary table for categorical risk factors
rf.a <- c(rf.start, rf.rest)
rf.n <- sapply(db[, rf.a, drop = FALSE], is.numeric)
rf.c <- rf.a[!rf.a%in%names(rf.n)[rf.n]]
rf.cl <- length(rf.c)
rf.cat.o <- vector("list", rf.cl)
if (length(rf.c) > 0) {
for (i in 1:rf.cl) {
rf.c.l <- rf.c[i]
cat.o <- summary_tbl(tbl = db, x = rf.c.l, y = target)
cat.o$bin <- as.character(cat.o$bin)
cat.o <- cbind.data.frame(rf = rf.c.l, cat.o)
pct.check <- any(cat.o$pct.o < 0.05)
cat.o$pct.check <- pct.check
rf.cat.o[[i]] <- cat.o
}
rf.cat.o <- bind_rows(rf.cat.o)
} else {
rf.cat.o <- data.frame()
}
#observed correlation for numerical risk factor
rf.n <- names(rf.n)[rf.n]
rf.nl <- length(rf.n)
if (rf.nl > 0) {
rf.num.o <- vector("list", rf.nl)
for (i in 1:rf.nl) {
rf.n.l <- rf.n[i]
cor.obs <- cor(x = db[!db[, rf.n.l]%in%c(NA, NaN, Inf, -Inf), rf.n.l],
y = db[!db[, rf.n.l]%in%c(NA, NaN, Inf, -Inf), target],
method = "spearman")
num.o <- data.frame(rf = rf.n.l, cor = cor.obs)
rf.num.o[[i]] <- num.o
}
} else {
rf.num.o <- data.frame()
}
rf.num.o <- bind_rows(rf.num.o)
#check pct of obs per bin
check.pct <- unique(rf.cat.o$rf[rf.cat.o$pct.check])
if (length(check.pct) > 0) {
warn.rep <- data.frame(rf = check.pct, comment = "At least one pct per bin less than 5%.")
warn.tbl <- bind_rows(warn.tbl, warn.rep)
}
if (nrow(rf.cat.o) > 0) {
rf.cat.o$mf <- paste0(rf.cat.o$rf, rf.cat.o$bin)
}
#summarize rf groups for priority estimations
if (!is.null(offset.vals)) {
db <- cbind.data.frame(db, offset.vals = offset.vals)
}
rf.mod <- NULL
pg <- unique(risk.profile$group)
pgl <- length(pg)
#run stepwise per group
steps <- vector("list", pgl)
for (i in 1:pgl) {
pg.l <- group.summary.r(db = db,
target = target,
rp.tbl = risk.profile,
g = pg[i],
rf.mod = rf.mod,
rf.start = rf.start,
rf.rest = rf.rest,
p.value = p.value,
rf.cat.o = rf.cat.o,
rf.num.o = rf.num.o,
check.start.model = check.start.model,
offset.vals = offset.vals)
steps[[i]] <- pg.l[["steps"]]
rf.mod <- pg.l[["rf.mod"]]
}
steps <- bind_rows(steps)
if (length(rf.mod) == 0) {rf.mod <- "1"}
frm.f <- paste0(target, " ~ ", paste0(c(rf.start, rf.mod), collapse = " + "))
if (is.null(offset.vals)) {
lr.mod <- glm(formula = as.formula(frm.f), family = "binomial", data = db)
} else {
lr.mod <- glm(formula = as.formula(frm.f), family = "binomial", data = db, offset = offset.vals)
}
res <- list(model = lr.mod,
steps = steps,
warnings = if (nrow(warn.tbl) > 0) {warn.tbl} else {data.frame(comment = "There are no warnings.")},
dev.db = db)
return(res)
}
#group summary
group.summary.r <- function(db, target, rp.tbl, g, rf.mod, rf.start, rf.rest, p.value, rf.cat.o, rf.num.o,
check.start.model, offset.vals) {
rf.g <- rp.tbl$rf[rp.tbl$group%in%g]
rf.g <- rf.g[rf.g%in%rf.rest]
rf.mod <- c(rf.mod, rf.start)
steps <- data.frame()
if (length(rf.g) == 0) {
return(list(rf.mod = rf.mod, steps = steps))
}
#initialte rf table for stepwise
tbl.c <- data.frame(rf = rf.g, checked = FALSE)
iter <- 1
repeat {
message(paste0("Running iteration: ", iter, " for group: ", g))
it.s <- iter.summary.r(target = target,
rf.mod = rf.mod,
rf.start = rf.start,
check.start.model = check.start.model,
tbl.c = tbl.c,
p.value = p.value,
rf.cat.o = rf.cat.o,
rf.num.o = rf.num.o,
db = db,
offset.vals = offset.vals)
step.i <- find.next(it.s = it.s, tbl.c = tbl.c)
tbl.c <- step.i[["tbl.c"]]
rf.mod <- c(rf.mod, step.i[["rf.next"]])
steps <- bind_rows(steps, step.i[["step"]])
if (nrow(tbl.c) == 0 | all(tbl.c$checked)) {
break
}
iter <- iter + 1
}
if (nrow(steps) > 0) {
steps <- cbind.data.frame(group = g, steps)
}
return(list(rf.mod = rf.mod, steps = steps))
}
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