Generative moment matching networks for genotype simulation
Polygenic risk score portability for common diseases across genetically diverse populations
Predicting dog phenotypes from genotypes
Adversarial learning for feature shift detection and correction
Advances in biomedical missing data imputation: A survey
Genomic databases homogenization with machine learning
Feature Shift Localization Network
Analysis of a deeply-phenotyped familial hypercholesterolemia cohort from Mexico shows a role for both rare and common alleles across known dyslipidemia genes and reveals …
P310: Polygenic and rare variant contributions to the genetic architecture of familial hypercholesterolemia in a Mexican registry cohort
