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pro vyhledávání: '"Robert Anthony Rebres"'
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
Publikováno v:
BMC Genomics
BMC Genomics, Vol 18, Iss S5, Pp 15-23 (2017)
BMC Genomics, Vol 18, Iss S5, Pp 15-23 (2017)
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 consuming. A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a2ac75658f6cc28421dac50a8923830b
https://doi.org/10.1186/s12864-017-3910-4
https://doi.org/10.1186/s12864-017-3910-4