The penetrance model is fitted to family data with a specified baseline hazard distribution,
$$ h(t|x_s, x_g) = h_0(t) \exp(\beta_s x_s+\beta_g x_g) $$
where \(h_0(t)\) is the baseline hazards function specified by base.dist
, which depends on the shape and scale parameters, \(\lambda\) and \(\rho\); \(x_s\) indicates male (1) and female (0) and \(x_g\) indicates carrier (1) or non-carrier (0) of a gene of interest (major gene).
For family data arising from population- or clinic-based study designs (design="pop", "pop+"
, "cli"
, or "cli+"
), the parameters of the penetrance model are estimated from the ascertainment-corrected prospective likelihood approach (Choi, Kopciuk and Briollais, 2008).
For family data arising from a two-stage study design (design="twostage"
), model parameters are estimated based on the composite likelihood approach (Choi and Briollais, 2011)
Transformed baseline parameters (\(\lambda, \rho\)) were used for estimation; log tranformation was applied to both scale and shape parameters for "Weibull"
, "loglogistic"
, "Gompertz"
and "gamma"
baseline distributions. For "lognormal"
baseline distribution, the log transformation was applied only to shape parameter \(\rho\), not to \(\lambda\) which represents the location parameter in log-normal distribution.
Calculations of standard errors and 95% confidence intervals for penetrance estimates by age 70 were based on the penetrances obtained from 1000 Monte-Carlo simulations of the estimated penetrance model; for more details, see penci
.