Chung RH, Tsai WY, Hsieh CH, Hung KY, Hsiung CA, Hauser ER,
SeqSIMLA2: simulating correlated quantitative traits accounting for shared environmental effects in user-specified pedigree structure.,
Genet Epidemiol,
01-01-2015,
Primary Citation
[Pubmed ID: 23782512],
Chung RH, Shih CC,
SeqSIMLA: a sequence and phenotype simulation tool for complex disease studies.,
BMC Bioinformatics,
06-20-2013,
https://www.ncbi.nlm.nih.gov/pubmed/?term=23782512,Primary Citation
[Pubmed ID: 25250827],
Chung RH, Tsai WY, Hsieh CH, Hung KY, Hsiung CA, Hauser ER,
SeqSIMLA2: simulating correlated quantitative traits accounting for shared environmental effects in user-specified pedigree structure.,
Genet Epidemiol,
01-01-2015,
https://www.ncbi.nlm.nih.gov/pubmed/?term=25250827,Primary Citation
[Pubmed ID: 30271589],
Baron RV, Stickel JR, Weeks DE,
The Mega2R package: R tools for accessing and processing genetic data in common formats.,
F1000Res,
08-29-2018,
https://www.ncbi.nlm.nih.gov/pubmed/?term=30271589,, Application
[Pubmed ID: 30669967],
Zhang X, Basile AO, Pendergrass SA, Ritchie MD,
Real world scenarios in rare variant association analysis: the impact of imbalance and sample size on the power in silico.,
BMC Bioinformatics,
01-22-2019,
https://www.ncbi.nlm.nih.gov/pubmed/?term=30669967,, Application