Selecting the appropriate value for alleleMismatch, cutHeight, or
	matchThreshold is an important task. Use this function to assist in this
	process. Typically the optimal value of any of these parameters is found where the
	number of multiple matches is minimized (the majority of samples are similar to only
	one unique genotype). Usually there is a minimum when these parameters are set to be
	very sensitive to differences among samples (i.e., alleleMismatch or
	cutHeight are 0, matchThreshold is 1). Simulations suggest that the next
	most sensitive minimum in multiple matches is the optimal value. This minimum will
	often be associated with a drop in multiple matches as sensitivity drops. For more
	discussion of this important step, see the Data S1 Supplementary documentation and
	tutorials (PDF) located at <doi:10.1111/j.1755-0998.2012.03137.x>.
	
Using guessOptimum = TRUE will attempt to estimate the location of this minimum
	and add it to the profile plot. Manual assessment of this estimate using the plot is
	strongly recommended.
	
If none of alleleMismatch, cutHeight, or matchThreshold is given,
	the function runs a sequence of values for alleleMismatch as follows:
	seq(from = 0, to = floor(ncol(amDatasetFocal$multilocus) * 0.4), by = 1)
	
multilocusMap is often not required, as amDataset objects will typically
	consist of paired columns of genotypes, where each pair is a separate locus. In cases
	where this is not the case (e.g., gender is given in only one column), a map vector
	must be specified.
	
Example: amDataset consists of gender followed by 4 diploid loci in paired
	columns
	multilocusMap = c(1, 2, 2, 3, 3, 4, 4, 5, 5)
	or equally
	multilocusMap=c("GENDER", "LOC1", "LOC1", "LOC2", "LOC2", "LOC3", "LOC4",
	"LOC4")
	
For more information on selecting consensusMethod see amCluster.
	The default consensusMethod = 1 is typically adequate.