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Exploring the Use of Genomic and Routinely Collected Data: Narrative Literature Review and Interview Study
BACKGROUND: Advancing the use of genomic data with routinely collected health data holds great promise for health care and research. Increasing the use of these data is a high priority to understand and address the causes of disease. OBJECTIVE: This study aims to provide an outline of the use of gen...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
JMIR Publications
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8501405/ https://www.ncbi.nlm.nih.gov/pubmed/34559060 http://dx.doi.org/10.2196/15739 |
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author | Daniels, Helen Jones, Kerina Helen Heys, Sharon Ford, David Vincent |
author_facet | Daniels, Helen Jones, Kerina Helen Heys, Sharon Ford, David Vincent |
author_sort | Daniels, Helen |
collection | PubMed |
description | BACKGROUND: Advancing the use of genomic data with routinely collected health data holds great promise for health care and research. Increasing the use of these data is a high priority to understand and address the causes of disease. OBJECTIVE: This study aims to provide an outline of the use of genomic data alongside routinely collected data in health research to date. As this field prepares to move forward, it is important to take stock of the current state of play in order to highlight new avenues for development, identify challenges, and ensure that adequate data governance models are in place for safe and socially acceptable progress. METHODS: We conducted a literature review to draw information from past studies that have used genomic and routinely collected data and conducted interviews with individuals who use these data for health research. We collected data on the following: the rationale of using genomic data in conjunction with routinely collected data, types of genomic and routinely collected data used, data sources, project approvals, governance and access models, and challenges encountered. RESULTS: The main purpose of using genomic and routinely collected data was to conduct genome-wide and phenome-wide association studies. Routine data sources included electronic health records, disease and death registries, health insurance systems, and deprivation indices. The types of genomic data included polygenic risk scores, single nucleotide polymorphisms, and measures of genetic activity, and biobanks generally provided these data. Although the literature search showed that biobanks released data to researchers, the case studies revealed a growing tendency for use within a data safe haven. Challenges of working with these data revolved around data collection, data storage, technical, and data privacy issues. CONCLUSIONS: Using genomic and routinely collected data holds great promise for progressing health research. Several challenges are involved, particularly in terms of privacy. Overcoming these barriers will ensure that the use of these data to progress health research can be exploited to its full potential. |
format | Online Article Text |
id | pubmed-8501405 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | JMIR Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-85014052021-11-01 Exploring the Use of Genomic and Routinely Collected Data: Narrative Literature Review and Interview Study Daniels, Helen Jones, Kerina Helen Heys, Sharon Ford, David Vincent J Med Internet Res Original Paper BACKGROUND: Advancing the use of genomic data with routinely collected health data holds great promise for health care and research. Increasing the use of these data is a high priority to understand and address the causes of disease. OBJECTIVE: This study aims to provide an outline of the use of genomic data alongside routinely collected data in health research to date. As this field prepares to move forward, it is important to take stock of the current state of play in order to highlight new avenues for development, identify challenges, and ensure that adequate data governance models are in place for safe and socially acceptable progress. METHODS: We conducted a literature review to draw information from past studies that have used genomic and routinely collected data and conducted interviews with individuals who use these data for health research. We collected data on the following: the rationale of using genomic data in conjunction with routinely collected data, types of genomic and routinely collected data used, data sources, project approvals, governance and access models, and challenges encountered. RESULTS: The main purpose of using genomic and routinely collected data was to conduct genome-wide and phenome-wide association studies. Routine data sources included electronic health records, disease and death registries, health insurance systems, and deprivation indices. The types of genomic data included polygenic risk scores, single nucleotide polymorphisms, and measures of genetic activity, and biobanks generally provided these data. Although the literature search showed that biobanks released data to researchers, the case studies revealed a growing tendency for use within a data safe haven. Challenges of working with these data revolved around data collection, data storage, technical, and data privacy issues. CONCLUSIONS: Using genomic and routinely collected data holds great promise for progressing health research. Several challenges are involved, particularly in terms of privacy. Overcoming these barriers will ensure that the use of these data to progress health research can be exploited to its full potential. JMIR Publications 2021-09-24 /pmc/articles/PMC8501405/ /pubmed/34559060 http://dx.doi.org/10.2196/15739 Text en ©Helen Daniels, Kerina Helen Jones, Sharon Heys, David Vincent Ford. Originally published in the Journal of Medical Internet Research (https://www.jmir.org), 24.09.2021. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work, first published in the Journal of Medical Internet Research, is properly cited. The complete bibliographic information, a link to the original publication on https://www.jmir.org/, as well as this copyright and license information must be included. |
spellingShingle | Original Paper Daniels, Helen Jones, Kerina Helen Heys, Sharon Ford, David Vincent Exploring the Use of Genomic and Routinely Collected Data: Narrative Literature Review and Interview Study |
title | Exploring the Use of Genomic and Routinely Collected Data: Narrative Literature Review and Interview Study |
title_full | Exploring the Use of Genomic and Routinely Collected Data: Narrative Literature Review and Interview Study |
title_fullStr | Exploring the Use of Genomic and Routinely Collected Data: Narrative Literature Review and Interview Study |
title_full_unstemmed | Exploring the Use of Genomic and Routinely Collected Data: Narrative Literature Review and Interview Study |
title_short | Exploring the Use of Genomic and Routinely Collected Data: Narrative Literature Review and Interview Study |
title_sort | exploring the use of genomic and routinely collected data: narrative literature review and interview study |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8501405/ https://www.ncbi.nlm.nih.gov/pubmed/34559060 http://dx.doi.org/10.2196/15739 |
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