Papers: 10.1186/s13073-019-0682-2

https://doi.org/10.1186/s13073-019-0682-2

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

Cited by: 59
Author(s): Julian R. Homburger, Cynthia L. Neben, Gilad Mishne, Alicia Y. Zhou, Sekar Kathiresan, Amit V. Khera
Published: over 5 years ago

Software Mentions 1