paramlink (version 1.1-5)

lod: 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 linkdat object.

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 breakLoops.

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 optimize as its tolerance parameter.

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.

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.

See Also

likelihood, optimize, breakLoops

Examples

# NOT RUN {
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)))

# }