Allen, Andrew S.; Satten, Glen A.; Tsiatis, Anastasios A. - In: Biometrika 92 (2005) 3, pp. 559-571
Modelling human genetic variation is critical to understanding the genetic basis of complex disease. The Human Genome Project has discovered millions of binary DNA sequence variants, called single nucleotide polymorphisms, and millions more may exist. As coding for proteins takes place along...