lapadj(reg.formula, loc.right, marker.distances, state.matrix,
marker.names=dimnames(state.matrix)[[2]], rparm=NULL, casewt=NULL,
tol=9.9e-09, return.hess=F, mode.names=NULL, mode.mat=NULL,
nc = 1), method="BC1", maxit=100, nem=1, start.parm=NULL, ...)
y~add.X.3+dom.X.3+add.x.45*add.x.72
make.analysis.obj
, which returns
objects like this. It is a matrix of pointers to the next marker with a
known state on the current chromosome (if any).-log(lambda)/2
is the Haldane map
distance. Linkage groups are separated by values of 0.0.make.analysis.obj
, which returns
objects like this. An n by k by q array. q is 2 for method="BC1" and
3 for method="F2". Each element encodes the probability of the
allele state conA scalar that will be used as the ridge parameter for all design terms except for the intercept ridge parameter which is set to zero
A vector who named elements can be matched by the design term
dimnames(mode.mat)[[2]]
mode.mat
is
not given by the user,
ana.obj$mode.mat
is used.