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dc.contributor.authorCorpas, Manuel (1)
dc.contributor.authorBeck, Stephan
dc.contributor.authorGlusman, Gustavo
dc.contributor.authorShabani, Mahsa
dc.date2021
dc.date.accessioned2022-01-18T13:07:04Z
dc.date.available2022-01-18T13:07:04Z
dc.identifier.issn1664-8021
dc.identifier.urihttps://reunir.unir.net/handle/123456789/12332
dc.description.abstractOver the past few years we have witnessed a number of advances in the personal genomics space including (a) more affordable sequencing technology, (b) mainstreaming of genomics in healthcare systems, (c) augmented sharing of genomic data, and (d) increased demand for direct-to-consumer genetic testing. All of these developments have brought us closer to the long-awaited genomics revolution. This genomics revolution is not exempt from challenges, in part amplified by lack of standards (ethical, legal, and technological), slow translation of knowledge to the clinic, and unequal access of personal genome benefits for all.es_ES
dc.language.isoenges_ES
dc.publisherFrontiers in Geneticses_ES
dc.relation.ispartofseries;vol. 12
dc.relation.urihttps://www.frontiersin.org/articles/10.3389/fgene.2021.687584/fulles_ES
dc.rightsopenAccesses_ES
dc.subjectpersonal genomeses_ES
dc.subjectWOS(2)es_ES
dc.subjectScopus(2)es_ES
dc.titleEditorial: Personal Genomes: Accessing, Sharing, and Interpretationes_ES
dc.typearticlees_ES
reunir.tag~ARIes_ES
dc.identifier.doihttps://doi.org/10.3389/fgene.2021.687584


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