Literature DB >> 32425102

A Scenario-Based Methodology for Analyzing the Ethical, Legal, and Social Issues in Genomic Data Sharing.

Rebekah McWhirter1, Lisa Eckstein1, Don Chalmers1, Christine Critchley1,2, Jane Nielsen1, Margaret Otlowski1, Dianne Nicol1.   

Abstract

Sharing of genomic and associated data is essential to clinical practice and biomedical research, and is increasingly encouraged by journals and funding bodies. Grappling with the range of legal and ethical issues raised by genomic data sharing presents a significant challenge, given the diversity of practices: from defined sharing of individual patient data, to broad-scale public sharing of research data, to uploading of direct-to-consumer test data by community members. Most commentary to date has discussed these issues in broad terms, but the debate can only progress if we engage with more granularity, grounded in jurisdictional and contextual specifics. We developed an empirical approach, creating a set of prototypical scenarios that capture the diversity of current genomic data sharing practices, which allows legal and ethical analysis of key issues at a granular level. The specificity of this approach provides a strong foundation for developing useful and relevant regulatory recommendations.

Entities:  

Keywords:  ELSI; data sharing; ethics; genomics; law

Year:  2020        PMID: 32425102     DOI: 10.1177/1556264620920460

Source DB:  PubMed          Journal:  J Empir Res Hum Res Ethics        ISSN: 1556-2646            Impact factor:   1.742


  1 in total

1.  Italian public's views on sharing genetic information and medical information: findings from the 'Your DNA, Your Say' study.

Authors:  Virginia Romano; Richard Milne; Deborah Mascalzoni
Journal:  Wellcome Open Res       Date:  2021-07-12
  1 in total

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