FHIR基因组学——一项支持国家基因组医学战略的可行性研究。

IF 4.8 2区 医学 Q1 GENETICS & HEREDITY
Nina Haffer, Caroline Stellmach, Julian Sass, Michael R Muzoora, Adam S L Graefe, Sylvia Thun, Carina N Vorisek
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引用次数: 0

摘要

德国基因组医学国家战略旨在将基因组测序整合到标准医疗保健中。然而,整合来自研究和医疗保健的基因组学数据仍然具有挑战性。本研究分析了如何将基因组数据集映射到国际标准:基因组学报告快速医疗互操作性资源®(FHIR®)实施指南(IG) 2.0.0,全球基因组学与健康联盟(GA4GH)的表型包模式,以及德国国家分子基因组学报告IG医学信息学倡议(MII)。创建并验证了示例FHIR®包和必要的搜索查询。大多数数据集元素可以使用现有的FHIR配置文件来表示,而未映射的元素则通过分析和扩展来解决。该研究强调,基因组数据集可以在很大程度上映射到现有的国际标准,并有可能扩展这些标准以适应缺失的元素,从而提高医疗保健领域基因组数据的互操作性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Genomics on FHIR - a feasibility study to support a National Strategy for Genomic Medicine.

Genomics on FHIR - a feasibility study to support a National Strategy for Genomic Medicine.

The German National Strategy for Genomic Medicine (genomDE) aims to integrate genome sequencing into standard healthcare. However, integrating genomics data from research and healthcare remains challenging. This study analyzed how the genomDE dataset could be mapped to international standards: the Genomics Reporting Fast Healthcare Interoperability Resources® (FHIR®) Implementation Guide (IG) 2.0.0, the Global Alliance for Genomics and Health (GA4GH)'s Phenopacket Schema, and the German national molecular genomics report IG of the Medical Informatics Initiative (MII). Sample FHIR® bundles and necessary search queries were created and validated. Most dataset elements could be represented using existing FHIR profiles, while unmapped elements were addressed through profiling and extensions. The study highlights that the genomDE dataset can largely be mapped to existing international standards, with the potential to extend these standards to accommodate missing elements, thereby improving genomic data interoperability in healthcare.

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来源期刊
NPJ Genomic Medicine
NPJ Genomic Medicine Biochemistry, Genetics and Molecular Biology-Molecular Biology
CiteScore
9.40
自引率
1.90%
发文量
67
审稿时长
17 weeks
期刊介绍: npj Genomic Medicine is an international, peer-reviewed journal dedicated to publishing the most important scientific advances in all aspects of genomics and its application in the practice of medicine. The journal defines genomic medicine as "diagnosis, prognosis, prevention and/or treatment of disease and disorders of the mind and body, using approaches informed or enabled by knowledge of the genome and the molecules it encodes." Relevant and high-impact papers that encompass studies of individuals, families, or populations are considered for publication. An emphasis will include coupling detailed phenotype and genome sequencing information, both enabled by new technologies and informatics, to delineate the underlying aetiology of disease. Clinical recommendations and/or guidelines of how that data should be used in the clinical management of those patients in the study, and others, are also encouraged.
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