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The clinical implementation of whole genome sequencing: a conversation with seven scientific experts
Author(s) -
LernerEllis Jordan P.
Publication year - 2012
Publication title -
journal of inherited metabolic disease
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.462
H-Index - 102
eISSN - 1573-2665
pISSN - 0141-8955
DOI - 10.1007/s10545-012-9463-4
Subject(s) - timeline , conversation , human genetics , medical genetics , precision medicine , medical education , medicine , data science , psychology , genetics , computer science , biology , pathology , history , communication , archaeology , gene
This commentary is based on the key note address given by Jordan Lerner‐Ellis at the annual symposium of the Society for the Study of Inborn Errors of Metabolism, held in Geneva, Switzerland in August 2011. The content of the address was developed from a series of discussions with seven clinicians and medical geneticists, all having a long‐time interest in genetic testing and genomic medicine (the interviews were not intended to be a forum for the introduction of new data). All participants were asked to offer their views on five questions: the benefits of using whole genome sequencing (WGS) in the clinic; the corresponding risks; the limitations on its wider use; the interviewees’ particular interests in using WGS in their practice; and projected timelines for successful adoption in clinical medicine.