introgress.data
may either be the list that is returned by the
function prepare.data
, or, if fixed=TRUE
,
introgress.data
may simply be a matrix or array providing counts
of the number of alleles derived from parental population 1 for each
admixed individual. If introgress.data
is a matrix or array, rows
and columns correspond to loci and individuals, respectively.loci.data
is a matrix or array where each row provides
information on one locus. The first column gives a unique locus name
(e.g. "locus3"), and the second column specifies whether the
locus is co-dominant ("C" or "c"), haploid ("H" or
"h"), or dominant ("D" or "d"). These first two
columns in loci.data
are required. The third column, which is
optional, is a numeric value specifying the linkage groups for the
marker. The fourth column, which is also optional, is a numeric value
specifying both the linkage group and location on the linkage group
(e.g. 3.70, for a marker at 70 cM on linkage group 3). These
optional columns can be used for ordering markers for the
mk.image
, genomic.clines
, and clines.plot
functions.
If the parental populations exhibit fixed allelic differences for all
markers scored (i.e. fixed=TRUE
) then p1.allele
and
p2.allele
should give the character used to specify alleles
derived from parental populations one and two, respectively
(e.g. p1.allele="p1"
and p2.allele="p2"
).
est.h
uses a maximum likelihood method to estimate the hybrid
index for each admixed individual. This estimate is simply the
proportion of alleles derived from population 2 if fixed=TRUE
.
In contrast, if populations share alleles (i.e. fixed=FALSE
), the
estimate accounts for uncertainty in the ancestry of alleles, but the
estimate of hybrid index is still an estimate of the proportion of the
genome that is inherited from population 2. For each individual,
est.h
returns a point estimate and 95% confidence interval of
hybrid index.
See Buerkle (2005) for additional details.