Health data collected in cohort studies are valuable sources for knowledge generation and the advance of biomedical research. However, the use of these data for research projects beyond the initial purpose raises several ethical, legal, and societal questions regarding the sensitivity of genomic data sourced from vulnerable and ethnic groups, such as African genetic data and material. Federated data infrastructures have become a key approach to make population-scale genomic and biomolecular data accessible across international borders. While the FAIR principles have become a guiding technical resource for data sharing, legal and socio-ethical considerations are equally important for a fair data ecosystem for further uses of genomic data. T...
This document outlines Points to Consider (PtC) for the responsible sharing of human genomic and he...
Data sharing models designed to facilitate global business provide insights for improving transborde...
This deliverable (D.5.2) allows clinical researchers to access and reuse existing data from public o...
Health data collected in cohort studies are valuable sources for knowledge generation and the advanc...
Health data collected in cohort studies are valuable sources for knowledge generation and the advanc...
The goal of CINECA is to enable the exchange of population scale health data across international bo...
The CINECA consortium was formed in response to the EU call ‘Better Health and care, economic growth...
The overarching purpose of CINECA is to achieve federated human data interoperability between 10 exi...
* p>Genomics research promises better health at the global level and GlobalCollaborative Researc h ...
The overarching purpose of CINECA is to achieve federated human data interoperability between 10 exi...
To support human cohort genomic and other omic data discovery and analysis across jurisdictions, bas...
nticipating and addressing the ethical, legal, and social implica-tions (ELSI) of scientifi c develo...
We need an international infrastructure for the ethical, legal, and social implications of genomic r...
Genomics is the study of the genetic material that constitutes the genomes of organisms. This geneti...
Remaining liberties that GDPR provides to EU Member States as well as remaining ambiguities on GDPR ...
This document outlines Points to Consider (PtC) for the responsible sharing of human genomic and he...
Data sharing models designed to facilitate global business provide insights for improving transborde...
This deliverable (D.5.2) allows clinical researchers to access and reuse existing data from public o...
Health data collected in cohort studies are valuable sources for knowledge generation and the advanc...
Health data collected in cohort studies are valuable sources for knowledge generation and the advanc...
The goal of CINECA is to enable the exchange of population scale health data across international bo...
The CINECA consortium was formed in response to the EU call ‘Better Health and care, economic growth...
The overarching purpose of CINECA is to achieve federated human data interoperability between 10 exi...
* p>Genomics research promises better health at the global level and GlobalCollaborative Researc h ...
The overarching purpose of CINECA is to achieve federated human data interoperability between 10 exi...
To support human cohort genomic and other omic data discovery and analysis across jurisdictions, bas...
nticipating and addressing the ethical, legal, and social implica-tions (ELSI) of scientifi c develo...
We need an international infrastructure for the ethical, legal, and social implications of genomic r...
Genomics is the study of the genetic material that constitutes the genomes of organisms. This geneti...
Remaining liberties that GDPR provides to EU Member States as well as remaining ambiguities on GDPR ...
This document outlines Points to Consider (PtC) for the responsible sharing of human genomic and he...
Data sharing models designed to facilitate global business provide insights for improving transborde...
This deliverable (D.5.2) allows clinical researchers to access and reuse existing data from public o...