Low coverage whole genome sequencing enables accurate assessment of common variants and calculation of genome-wide polygenic scores

Genome Medicine (2019) - Comment
pubmed: 31771638 doi: 10.1186/s13073-019-0682-2 issn: 1756-994x

Julian R. Homburger, Cynthia L. Neben, Gilad Mishne, Alicia Y. Zhou, Sekar Kathiresan, Amit V. Khera