Zobrazeno 1 - 1
of 1
pro vyhledávání: '"Daniel Rene Richards"'
Publikováno v:
BMC Genomics, Vol 18, Iss S5, Pp 15-23 (2017)
Abstract Background Next-generation sequencing is widely used to identify disease-causing variants in patients with rare genetic disorders. Identifying those variants from whole-genome or exome data can be both scientifically challenging and time con
Externí odkaz:
https://doaj.org/article/bb3309c3ea1d4fa19799244ab44536fd
