Desiderata for digital consent in genomic research.

Herein, we describe the characterization of a Digital Consent (DC) System to support current ethical-legal issues associated with challenges posed by informed consent for genomic research. A potential solution to support ongoing interaction with patients and allow control over how their data and sam...

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Main Authors: Parra-Calderón, CL, Kaye, J, Moreno-Conde, A, Teare, HJA, Nuñez-Benjumea, F
Formato: Journal article
Idioma:English
Publicado: Springer 2018
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author Parra-Calderón, CL
Kaye, J
Moreno-Conde, A
Teare, HJA
Nuñez-Benjumea, F
author_facet Parra-Calderón, CL
Kaye, J
Moreno-Conde, A
Teare, HJA
Nuñez-Benjumea, F
author_sort Parra-Calderón, CL
collection OXFORD
description Herein, we describe the characterization of a Digital Consent (DC) System to support current ethical-legal issues associated with challenges posed by informed consent for genomic research. A potential solution to support ongoing interaction with patients and allow control over how their data and samples are being used in genomic research can be Digital Consent based. But there are other challenges that need to be addressed, such as incidental findings when analyzing the results of genomic tests (not expected). This paper addresses security and privacy recommendations for the development of precision medicine, and the interoperability references of Health Information Standardization Organizations such as HL7 and IHE, as well as recent research in the field of ethics in Genomic Medicine. As a result of this work, ten key features that need to be further explored have been identified in order to support the realization of DC in Genomic Research.
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spelling oxford-uuid:ff1213a4-5d16-4a5e-bd3d-64f25edfb8fc2022-03-27T13:41:41ZDesiderata for digital consent in genomic research.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:ff1213a4-5d16-4a5e-bd3d-64f25edfb8fcEnglishSymplectic Elements at OxfordSpringer2018Parra-Calderón, CLKaye, JMoreno-Conde, ATeare, HJANuñez-Benjumea, FHerein, we describe the characterization of a Digital Consent (DC) System to support current ethical-legal issues associated with challenges posed by informed consent for genomic research. A potential solution to support ongoing interaction with patients and allow control over how their data and samples are being used in genomic research can be Digital Consent based. But there are other challenges that need to be addressed, such as incidental findings when analyzing the results of genomic tests (not expected). This paper addresses security and privacy recommendations for the development of precision medicine, and the interoperability references of Health Information Standardization Organizations such as HL7 and IHE, as well as recent research in the field of ethics in Genomic Medicine. As a result of this work, ten key features that need to be further explored have been identified in order to support the realization of DC in Genomic Research.
spellingShingle Parra-Calderón, CL
Kaye, J
Moreno-Conde, A
Teare, HJA
Nuñez-Benjumea, F
Desiderata for digital consent in genomic research.
title Desiderata for digital consent in genomic research.
title_full Desiderata for digital consent in genomic research.
title_fullStr Desiderata for digital consent in genomic research.
title_full_unstemmed Desiderata for digital consent in genomic research.
title_short Desiderata for digital consent in genomic research.
title_sort desiderata for digital consent in genomic research
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