lod {paramlink} | R Documentation |
Two-point LOD score
Description
Calculates the two-point LOD scores of a pedigree for the specified markers. The recombination ratio between the disease and marker loci can be either fixed at specific values, or optimized.
Usage
lod(
x,
markers = seq_len(x$nMark),
theta = 0,
loop_breakers = NULL,
max.only = FALSE,
verbose = FALSE,
tol = 0.01
)
Arguments
x |
a |
markers |
an integer vector denoting which markers to use. |
theta |
either a numeric containing specific recombination ratio(s), or the word 'max', indicating that the recombination ratio should be optimized by the program. |
loop_breakers |
a numeric containing IDs of individuals to be used as
loop breakers. Relevant only if the pedigree has loops. See
|
max.only |
a logical indicating whether only the maximum LOD score should be returned. |
verbose |
a logical: verbose output or not. |
tol |
a numeric passed on to |
Details
The LOD score of a marker is defined as
LOD(\theta) =
\log[10]\frac{L(\theta)}{L(0.5)}
where L(\theta)
denotes the
likelihood of the observed marker genotypes given a recombination ratio
\theta
between the marker and the disease locus.
Value
If max.only=TRUE
, the highest computed LOD score is returned,
as a single number.
Otherwise a linkres
object, which is essentially a matrix containing
the LOD scores. The details depend on the other parameters:
If theta
is numeric, the matrix has dimensions length(theta) *
length(markers)
, and the entry in row t
, column m
is the lod
score of the pedigree for marker m
assuming a recombination rate of
t
.
If theta='max'
, the linkres
matrix has one column per marker
and two rows: The first containing the LOD score and the second the optimal
recombination ratio for each marker.
If a marker has incompatible values (i.e. if a child of homozygous 1/1
parents has a 2 allele), the corresponding output entries are NaN
.
See Also
likelihood
, optimize
,
breakLoops
Examples
x = linkdat(toyped, model=1)
res = lod(x)
res_theta = lod(x, theta=c(0, 0.1, 0.2, 0.5))
res_max = lod(x, theta='max')
stopifnot(all(0.3 == round(c(res, res_theta['0',], res_max['LOD',]), 1)))
# bigger pedigree with several markers
y = linkdat(dominant)
y = setModel(y, model=1, penetrances=c(.001, .9, .99))
lod(y, markers=305:310)
lod(y, markers=305:310, theta='max')
# Example with pedigree with loops:
z = linkdat(twoloops, model=2) # fully penetrant autosomal recessive model.
# add SNP for which individuals 15 and 16 are homozygous for the rare allele.
m = marker(z, 15:16, c(1,1), alleles=1:2, afreq=c(0.001, 0.999))
z = addMarker(z, m)
res1 = lod(z)
# manual specification of loop breakers gives same result
res2 = lod(z, loop_breakers=c(8,12))
# making the marker triallelic and adding some genotypes.
z = modifyMarker(z, marker=1, ids=c(7,9,11,13), genotype=3, alleles=1:3, afreq=c(0.001, 0.499, 0.5))
plot(z, 1)
res3 = lod(z)
z = modifyMarker(z, marker=1, alleles=1:4, afreq=c(0.001, 0.499, 0.25, 0.25))
res4 = lod(z)
stopifnot(all(3 == round(c(res1, res2, res3, res4), 1)))