APPLaUD: access for patients and participants to individual level uninterpreted genomic data

APPLaUD: access for patients and participants to individual level uninterpreted genomic data

Abstract Background There is a growing support for the stance that patients and research participants should have better and easier access to their raw (uninterpreted) genomic sequence data in both clinical and research contexts. Main body We review legal frameworks and literature on the benefits, r...

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Bibliographic Details
Main Authors: Adrian Thorogood, Jason Bobe, Barbara Prainsack, Anna Middleton, Erick Scott, Sarah Nelson, Manuel Corpas, Natasha Bonhomme, Laura Lyman Rodriguez, Madeleine Murtagh, Erika Kleiderman, on behalf of the Participant Values Task Team of the Global Alliance for Genomics and Health
Format: Article
Language:English
Published: BMC 2018-02-01
Series:Human Genomics
Subjects:
Ethics
Law
Genomic data
Individual access
Whole genome sequencing
Direct-to-consumer
Online Access:http://link.springer.com/article/10.1186/s40246-018-0139-5

Internet

http://link.springer.com/article/10.1186/s40246-018-0139-5

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