recrisk.single.ascertain {fam.recrisk} | R Documentation |
Familial recurrence risk assuming single proband
Description
Estimate familial recurrence risk, assuming there is a single identified proband in a family
Usage
recrisk.single.ascertain(s, a)
Arguments
s |
vector of sizes of families |
a |
vector of number of affected members |
Details
When affected subjects (i.e., probands) attend a clinic independent of their family size and independent of their family history, and if the family history provided by probands is complete (i.e., reporting of family history does not depend on the number of affected members), then we can view the probands and their families as sampled under complete ascertainment. This function estimates the disease recurrence risk when there is a single identified proband per family.
Value
A list with the following values
phat |
disease recurrence risk |
var.phat |
variance of phat |
Author(s)
Schaid DJ, Sinnwell JP.
References
Schaid DJ, McDonnell SK, Thibodeau SN. Familial recurrence risk with varying amount of family history. Under review at Genetic Epidemiology, 2018.
Examples
s <- c(4, 8, 6, 6, 10, 8, 7, 8, 5, 6, 10, 4, 4, 8, 6, 8, 4, 5, 9,
9, 5, 4, 4, 7, 3, 3, 9, 5, 3, 3, 4, 6, 8, 3, 5, 8, 6, 8, 9, 3)
a <- c(3, 4, 2, 5, 4, 5, 3, 4, 3, 3, 8, 2, 0, 3, 4, 5, 2, 3, 4, 2, 1, 1,
1, 1, 1, 0, 0, 0, 0, 0, 1, 0, 2, 0, 0, 1, 0, 2, 3, 0)
recrisk.single.ascertain(s,a)