poppr (version 2.3.0)

mlg.filter: MLG definitions based on genetic distance

Description

Multilocus genotypes are initially defined by naive string matching, but this definition does not take into account missing data or genotyping error, casting these as unique genotypes. Defining multilocus genotypes by genetic distance allows you to incorporate genotypes that have missing data o genotyping error into their parent clusters.

Usage

mlg.filter(pop, threshold = 0, missing = "asis", memory = FALSE, algorithm = "farthest_neighbor", distance = "diss.dist", threads = 0, stats = "MLGs", ...)
mlg.filter(pop, missing = "asis", memory = FALSE, algorithm = "farthest_neighbor", distance = "diss.dist", threads = 0, ...) <- value

Arguments

pop
a genclone, snpclone, or genind object.
threshold
a number indicating the minimum distance two MLGs must be separated by to be considered different. Defaults to 0, which will reflect the original (naive) MLG definition.
missing
any method to be used by missingno: "mean", "zero", "loci", "genotype", or "asis" (default).
memory
whether this function should remember the last distance matrix it generated. TRUE will attempt to reuse the last distance matrix if the other parameters are the same. (default) FALSE will ignore any stored matrices and not store any it generates.
algorithm
determines the type of clustering to be done.
distance
a character or function defining the distance to be applied to pop. Defaults to diss.dist for genclone objects and bitwise.dist for snpclone objects. A matrix or table containing distances between individuals (such as the output of rogers.dist) is also accepted for this parameter.
threads
The maximum number of parallel threads to be used within this function. A value of 0 (default) will attempt to use as many threads as there are available cores/CPUs. In most cases this is ideal. A value of 1 will force the function to run serially, which may increase stability on some systems. Other values may be specified, but should be used with caution.
stats
a character vector specifying which statistics should be returned (details below). Choices are "MLG", "THRESHOLDS", "DISTANCES", "SIZES", or "ALL". If choosing "ALL" or more than one, a named list will be returned.
...
any parameters to be passed off to the distance method.
value
the threshold at which genotypes should be collapsed.

Value

Default, a vector of collapsed multilocus genotypes. Otherwise, any combination of the following: MLGs a numeric vector defining the multilocus genotype cluster of each individual in the dataset. Each genotype cluster is separated from every other genotype cluster by at least the defined threshold value, as calculated by the selected algorithm.THRESHOLDS A numeric vector representing the thresholds beyond which clusters of multilocus genotypes were collapsed.DISTANCES A square matrix representing the distances between each cluster.SIZES The sizes of the multilocus genotype clusters in order.

Details

This function will take in any distance matrix or function and collapse multilocus genotypes below a given threshold. If you use this function as the assignment method (mlg.filter(myData, distance = myDist) <- 0.5), the distance function or matrix will be remembered by the object. This means that if you define your own distance matrix or function, you must keep it in memory to further utilize mlg.filter.

See Also

filter_stats, cutoff_predictor, mll, genclone, snpclone, diss.dist, bruvo.dist

Examples

Run this code

data(partial_clone)
pc <- as.genclone(partial_clone, threads = 1L) # convert to genclone object

# Basic Use ---------------------------------------------------------------


# Show MLGs at threshold 0.05
mlg.filter(pc, threshold = 0.05, distance = "nei.dist", threads = 1L)
pc # 26 mlgs

# Set MLGs at threshold 0.05
mlg.filter(pc, distance = "nei.dist", threads = 1L) <- 0.05
pc # 25 mlgs

## Not run: 
# 
# # The distance definition is persistant
# mlg.filter(pc) <- 0.1
# pc # 24 mlgs
# 
# # But you can still change the definition
# mlg.filter(pc, distance = "diss.dist", percent = TRUE) <- 0.1
# pc
# 
# # Choosing a threshold ----------------------------------------------------
# 
# 
# # Thresholds for collapsing multilocus genotypes should not be arbitrary. It
# # is important to consider what threshold is suitable. One method of choosing
# # a threshold is to find a gap in the distance distribution that represents
# # clonal groups. You can look at this by analyzing the distribution of all
# # possible thresholds with the function "cutoff_predictor".
# 
# # For this example, we'll use Bruvo's distance to predict the cutoff for
# # P. infestans.
# 
# data(Pinf)
# Pinf
# # Repeat lengths are necessary for Bruvo's distance
# (pinfreps <- fix_replen(Pinf, c(2, 2, 6, 2, 2, 2, 2, 2, 3, 3, 2)))
# 
# # Now we can collect information of the thresholds. We can set threshold = 1
# # because we know that this will capture the maximum possible distance:
# (thresholds <- mlg.filter(Pinf, distance = bruvo.dist, stats = "THRESHOLDS",
#                           replen = pinfreps, threshold = 1))
# # We can use these thresholds to find an appropriate cutoff
# (pcut <- cutoff_predictor(thresholds))
# mlg.filter(Pinf, distance = bruvo.dist, replen = pinfreps) <- pcut
# Pinf
# 
# # This can also be visualized with the "filter_stats" function.
# 
# # Special case: threshold = 0 ---------------------------------------------
# 
# 
# # It's important to remember that a threshold of 0 is equal to the original
# # MLG definition. This example will show a data set that contains genotypes
# # with missing data that share all alleles with other genotypes except for 
# # the missing one.
# 
# data(monpop)
# monpop # 264 mlg
# mlg.filter(monpop) <- 0
# nmll(monpop) # 264 mlg
# 
# # In order to merge these genotypes with missing data, we should set the 
# # threshold to be slightly higher than 0. We will use the smallest fraction 
# # the computer can store.
# 
# mlg.filter(monpop) <- .Machine$double.eps ^ 0.5
# nmll(monpop) # 236 mlg
# 
# # Custom distance ---------------------------------------------------------
# 
# # Custom genetic distances can be used either in functions from other
# # packages or user-defined functions
# 
# data(Pinf)
# Pinf
# mlg.filter(Pinf, distance = function(x) dist(tab(x))) <- 3
# Pinf
# mlg.filter(Pinf) <- 4
# Pinf
# 
# # genlight / snpclone objects ---------------------------------------------
# 
# 
# set.seed(999)
# gc <- as.snpclone(glSim(100, 0, n.snp.struc = 1e3, ploidy = 2))
# gc # 100 mlgs
# mlg.filter(gc) <- 0.25
# gc # 82 mlgs
# 
# ## End(Not run)

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