domingo, 4 de agosto de 2019

Low coverage whole genome sequencing enables accurate assessment of common variants and calculation of genome-wide polygenic scores JR Homburger et al, BioxRIV preprints, July 31, 2019

Main|Search|PHGKB

a doctor looking at a tablet with data swirling around


Last Posted: Aug 02, 2019


No hay comentarios:

Publicar un comentario