From Rosalind Franklin to Barack Obama: Data Sharing Challenges and Solutions in Genomics and Personalised Medicine†. Issue 1 (2nd January 2017)

• Record Type: Journal Article
• Authors: Lawler, Mark; Maughan, Tim
• Is Part Of: New bioethics. Volume 23:Issue 1(2017)
• Page Start: 64
• Page End: 73
• Publication Date: 2017-01-02
• Subjects: personalised medicine -- big data -- data sharing -- genomics -- cancer -- bioethics; Bioethics -- Periodicals; Medical genetics -- Moral and ethical aspects -- Periodicals; 174.2
• DOI: 10.1080/20502877.2017.1314883
• Languages: English
• ISSNs: 2050-2877

Abstract

Abstract : The collection, storage and use of genomic and clinical data from patients and healthy individuals is a key component of personalised medicine enterprises such as the Precision Medicine Initiative, the Cancer Moonshot and the 100, 000 Genomes Project. In order to maximise the value of this data, it is important to embed a culture within the scientific, medical and patient communities that supports the appropriate sharing of genomic and clinical information. However, this aspiration raises a number of ethical, legal and regulatory challenges that need to be addressed. The Global Alliance for Genomics and Health, a worldwide coalition of researchers, healthcare professionals, patients and industry partners, is developing innovative solutions to support the responsible and effective sharing of genomic and clinical data. This article identifies the challenges that a data sharing culture poses and highlights a series of practical solutions that will benefit patients, researchers and society.