Focuses on large-scale inference for detecting QTL hotspots in sparse regression models, emphasizing the need to use genomics to understand variation in phenotypes and disease susceptibility.
Explores the analysis of genotypes and variants data through a Genome-Wide Association Study, focusing on the association between genetic variants and phenotypes like height.
Explores genetic traits inheritance, family tree analysis, and various modes of genetic trait transmission in humans, including specific genetic disorders.
