Genomic Sequencing Capacity, Data Retention, and Personal Access to Raw Data in Europe-Reference-Cited by-同舟云学术

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Genomic Sequencing Capacity, Data Retention, and Personal Access to Raw Data in Europe

Published:2020-05-06 Issue: Volume:11 Page:
ISSN:1664-8021
Container-title:Frontiers in Genetics
language:
Short-container-title:Front. Genet.

Author:

Narayanasamy Shaman,Markina Varvara,Thorogood Adrian,Blazkova Adriana,Shabani Mahsa,Knoppers Bartha M.,Prainsack Barbara,Koesters Robert

Publisher

Frontiers Media SA

Subject

Genetics(clinical),Genetics,Molecular Medicine

Reference32 articles.

1. DNA data marketplace: an analysis of the ethical concerns regarding the participation of the individuals.;Ahmed;Front. Genet.,2019

2. From fastq data to high-confidence variant calls: the genome analysis toolkit best practices pipeline.;Auwera;Curr. Protoc. Bioinform.,2013

3. The convergence of research and clinical genomics.;Birney;Am. J. Hum. Genet.,2019

4. Genomics in healthcare: GA4GH looks to 2022.;Birney;bioRxiv,2017

5. The scramble conversion tool.;Bonfield;Bioinform. Oxf. Engl.,2014

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2. Future on a Flashdrive: Timely Considerations for the Imminent Adoption of Whole Genome Sequencing in Pediatric Healthcare;Journal of Science Policy & Governance;2023-01-23

3. Ethical and Legal Considerations in Genomic Data Sharing: Evolution of the Discourse and the Road Ahead;Collaborative Bioethics;2023

4. Mapping the Empirical Evidence of the GDPR's (In-)Effectiveness: A Systematic Review;SSRN Electronic Journal;2023

5. A proposal for an international Code of Conduct for data sharing in genomics;Developing World Bioethics;2022-10-21

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