inst/app/tools/bioCancer/rbindna.R

rbind.na <- function (..., deparse.level = 1)
{
  na <- nargs() - (!missing(deparse.level))
  deparse.level <- as.integer(deparse.level)
  stopifnot(0 <= deparse.level, deparse.level <= 2)
  argl <- list(...)
  while (na > 0 && is.null(argl[[na]])) {
    argl <- argl[-na]
    na <- na - 1
  }
  if (na == 0)
    return(NULL)
  if (na == 1) {
    if (isS4(..1))
      return(rbind2(..1))
    else return(matrix(..., nrow = 1)) ##.Internal(rbind(deparse.level, ...)))
  }
  if (deparse.level) {
    symarg <- as.list(sys.call()[-1L])[1L:na]
    Nms <- function(i) {
      if (is.null(r <- names(symarg[i])) || r == "") {
        if (is.symbol(r <- symarg[[i]]) || deparse.level ==
            2)
          deparse(r)
      }
      else r
    }
  }
  
  ## deactivated, otherwise no fill in with two arguments
  if (na == 0) {
    r <- argl[[2]]
    fix.na <- FALSE
  }
  else {
    nrs <- unname(lapply(argl, ncol))
    iV <- sapply(nrs, is.null)
    fix.na <- identical(nrs[(na - 1):na], list(NULL, NULL))
    ## deactivated, otherwise data will be recycled
    #if (fix.na) {
    #    nr <- max(if (all(iV)) sapply(argl, length) else unlist(nrs[!iV]))
    #    argl[[na]] <- rbind(rep(argl[[na]], length.out = nr),
    #        deparse.level = 0)
    #}
    if (deparse.level) {
      if (fix.na)
        fix.na <- !is.null(Nna <- Nms(na))
      if (!is.null(nmi <- names(argl)))
        iV <- iV & (nmi == "")
      ii <- if (fix.na)
        2:(na - 1)
      else 2:na
      if (any(iV[ii])) {
        for (i in ii[iV[ii]]) if (!is.null(nmi <- Nms(i)))
          names(argl)[i] <- nmi
      }
    }
    
    ## filling with NA's to maximum occuring ncols
    nCol <- as.numeric(sapply(argl, function(x) if (is.null(ncol(x))) length(x)
                              else ncol(x)))
    maxCol <- max(nCol, na.rm = TRUE)
    argl <- lapply(argl, function(x)  if (is.null(ncol(x))) c(x, rep(NA, maxCol - length(x)))
                   else cbind(x, matrix(, nrow(x), maxCol - ncol(x))))
    
    ## create a common name vector from the
    ## column names of all 'argl' items
    namesVEC <- rep(NA, maxCol)
    for (i in 1:length(argl)) {
      CN <- colnames(argl[[i]])
      m <- !(CN %in% namesVEC)
      namesVEC[m] <- CN[m]
    }
    
    ## make all column names from common 'namesVEC'
    for (j in 1:length(argl)) {
      if (!is.null(ncol(argl[[j]]))) colnames(argl[[j]]) <- namesVEC
    }
    
    r <- do.call(rbind, c(argl[-1L], list(deparse.level = deparse.level)))
  }
  
  d2 <- dim(r)
  
  ## make all column names from common 'namesVEC'
  colnames(r) <- colnames(argl[[1]])
  
  r <- rbind2(argl[[1]], r)
  
  if (deparse.level == 0)
    return(r)
  ism1 <- !is.null(d1 <- dim(..1)) && length(d1) == 2L
  ism2 <- !is.null(d2) && length(d2) == 2L && !fix.na
  if (ism1 && ism2)
    return(r)
  Nrow <- function(x) {
    d <- dim(x)
    if (length(d) == 2L)
      d[1L]
    else as.integer(length(x) > 0L)
  }
  nn1 <- !is.null(N1 <- if ((l1 <- Nrow(..1)) && !ism1) Nms(1))
  nn2 <- !is.null(N2 <- if (na == 2 && Nrow(..2) && !ism2) Nms(2))
  if (nn1 || nn2 || fix.na) {
    if (is.null(rownames(r)))
      rownames(r) <- rep.int("", nrow(r))
    setN <- function(i, nams) rownames(r)[i] <- if (is.null(nams))
      ""
    else nams
    if (nn1)
      setN(1, N1)
    if (nn2)
      setN(1 + l1, N2)
    if (fix.na)
      setN(nrow(r), Nna)
  }
  r
}

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bioCancer documentation built on Nov. 8, 2020, 6:26 p.m.