logit_run: Simulated disease endpoints
In cnfoley/Sun-et-al-2021-protein-coding-variants-in-human-disease: Computing and predicting gains in power owing to allelic heterogenity between population cohorts
Description
Usage
Arguments
Value
Description
Simulated disease endpoints
Usage
1
logit_run(n, maf, pi_y, bta)
Arguments
n
sample size
maf
minor allele frequency
pi_y
disease prevalence
bta
genetic effect size
Value
Return simulated disease endpoint.
cnfoley/Sun-et-al-2021-protein-coding-variants-in-human-disease documentation built on Dec. 19, 2021, 5:19 p.m.
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Description Usage Arguments Value
Description
Simulated disease endpoints
Usage
1 | logit_run(n, maf, pi_y, bta)
|
Arguments
n |
sample size |
maf |
minor allele frequency |
pi_y |
disease prevalence |
bta |
genetic effect size |
Value
Return simulated disease endpoint.
R Package Documentation
Browse R Packages
We want your feedback!
Note that we can't provide technical support on individual packages. You should contact the package authors for that.
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