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#' @name gl.filter.locmetric
#' @title Filters loci on the basis of numeric information stored in
#' other$loc.metrics in a genlight \{adegenet\} object
#' @family matched filter
#'
#' @description
#' This script uses any field with numeric values stored in $other$loc.metrics
#' to filter loci. The loci to keep can be within the upper and lower thresholds
#' ('within') or outside of the upper and lower thresholds ('outside').
#' @param x Name of the genlight object containing the SNP data [required].
#' @param metric Name of the metric to be used for filtering [required].
#' @param upper Filter upper threshold [required].
#' @param lower Filter lower threshold [required].
#' @param keep Whether keep loci within of upper and lower thresholds or keep
#' loci outside of upper and lower thresholds [within].
#' @param verbose Verbosity: 0, silent or fatal errors; 1, begin and end; 2,
#' progress log; 3, progress and results summary; 5, full report
#' [default 2, unless specified using gl.set.verbosity].
#'
#' @details
#' The fields that are included in dartR, and a short description, are found
#' below. Optionally, the user can also set his/her own filter by adding a
#' vector into $other$loc.metrics as shown in the example.
#' \enumerate{
#' \item SnpPosition - position (zero is position 1) in the sequence tag of the
#' defined SNP variant base.
#' \item CallRate - proportion of samples for which the genotype call is
#' non-missing (that is, not '-' ).
#' \item OneRatioRef - proportion of samples for which the genotype score is 0.
#' \item OneRatioSnp - proportion of samples for which the genotype score is 2.
#' \item FreqHomRef - proportion of samples homozygous for the Reference allele.
#' \item FreqHomSnp - proportion of samples homozygous for the Alternate (SNP)
#' allele.
#' \item FreqHets - proportion of samples which score as heterozygous, that is,
#' scored as 1.
#' \item PICRef - polymorphism information content (PIC) for the Reference
#' allele.
#' \item PICSnp - polymorphism information content (PIC) for the SNP.
#' \item AvgPIC - average of the polymorphism information content (PIC) of the
#' Reference and SNP alleles.
#' \item AvgCountRef - sum of the tag read counts for all samples, divided by
#' the number of samples with non-zero tag read counts, for the Reference allele
#' row.
#' \item AvgCountSnp - sum of the tag read counts for all samples, divided by
#' the number of samples with non-zero tag read counts, for the Alternate (SNP)
#' allele row.
#' \item RepAvg - proportion of technical replicate assay pairs for which the
#' marker score is consistent.
#' }
#'
#' @author Luis Mijangos -- Post to
#' \url{https://groups.google.com/d/forum/dartr}
#'
#' @examples
#' # adding dummy data
#' test <- testset.gl
#' test$other$loc.metrics$test <- 1:nLoc(test)
#' result <- gl.filter.locmetric(x=test, metric= 'test', upper=255,
#' lower=200, keep= 'within', verbose=3)
#'
#' @export
#' @return The reduced genlight dataset.
gl.filter.locmetric <- function(x,
metric,
upper,
lower,
keep = "within",
verbose = NULL) {
# SET VERBOSITY
verbose <- gl.check.verbosity(verbose)
#if(verbose==0){plot.display <- FALSE}
# FLAG SCRIPT START
funname <- match.call()[[1]]
utils.flag.start(func = funname,
build = "v.2023.2",
verbose = verbose)
# CHECK DATATYPE
datatype <- utils.check.datatype(x, verbose = verbose)
# Work around a bug in adegenet if genlight object is created by subsetting
if (nLoc(x) != nrow(x@other$loc.metrics)) {
stop(
error(
"The number of rows in the loc.metrics table does not match the
number of loci in your genlight object!"
)
)
}
# Set a population if none is specified (such as if the genlight object has
#been generated manually)
if (is.null(pop(x)) |
is.na(length(pop(x))) | length(pop(x)) <= 0) {
if (verbose >= 2) {
cat(
report(
" Population assignments not detected, individuals assigned
to a single population labelled 'pop1'\n"
)
)
}
pop(x) <- array("pop1", dim = nInd(x))
pop(x) <- as.factor(pop(x))
}
# Check for monomorphic loci
tmp <- gl.filter.monomorphs(x, verbose = 0)
if ((nLoc(tmp) < nLoc(x)) & verbose >= 2) {
cat(warn(" Warning: genlight object contains monomorphic loci\n"))
}
# FUNCTION SPECIFIC ERROR CHECKING check whether the field exists in the
#genlight object
if (!(metric %in% colnames(x$other$loc.metrics))) {
stop(error("Fatal Error: name of the metric not found\n"))
}
# DO THE JOB
field <- which(colnames(x@other$loc.metrics) == metric)
if (keep == "within") {
index <-
which(x@other$loc.metrics[, field] >= lower &
x@other$loc.metrics[, field] <= upper)
x2 <- x[, index]
x2@other$loc.metrics <- x@other$loc.metrics[index,]
}
if (keep == "outside") {
index <-
which(x@other$loc.metrics[, field] <= lower &
x@other$loc.metrics[, field] >= upper)
x2 <- x[, index]
x2@other$loc.metrics <- x@other$loc.metrics[index,]
}
if (verbose > 2) {
cat(" Initial number of loci:", nLoc(x), "\n")
cat(" Number of loci deleted:", nLoc(x) - nLoc(x2), "\n")
cat(" Final number of loci:", nLoc(x2), "\n")
}
# ADD TO HISTORY
nh <- length(x2@other$history)
x2@other$history[[nh + 1]] <- match.call()
# FLAG SCRIPT END
if (verbose > 0) {
cat(report("Completed:", funname, "\n"))
}
return(x2)
}
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