估计芬兰生物库和医院收集的生物样本的使用情况。

IF 3.7 2区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Aaro Tupasela, Tom Southerington, Johanna Mäkelä, Lila Kallio, Merja Perälä, Veli-Matti Kosma, Arto Mannermaa, Tiina Jokela, Kimmo Pitkänen, Mika Kontro, Tiina Vesterinen, Eero Punkka, Theresa Knopp, Minna Ruddock, Raisa Serpi, Anne-Mari Moilanen, Leena Viiri, Sanna Siltanen, Enni Makkonen, Päivi Ingalsuo
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引用次数: 0

摘要

自2010年代初以来,芬兰一直在稳步发展其生物银行基础设施。本文系统概述了自2013年《芬兰生物银行法案》生效以来提供的用于研究的生物样本数量。利用来自各个生物库和Fimea(以前的Valvira)颁发的许可证的数据,我们在国家层面上提供了最新和完整的样本使用情况。2014年至2023年间,通过998个样本请求,共提供了1,474,881个样本。更好地了解国家一级生物样本的使用可以帮助突出生物库作为支持研究的基础设施的重要影响。我们认为,制定标准可以帮助制定国家生物银行战略,并确定生物银行可以进一步发展的领域。我们还得出结论,灵活有效地结合组织样本和健康数据的能力是必不可少的,也需要在欧洲健康数据空间(EHDS)的背景下得到保障。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Estimating the use of biological samples in Finnish biobanks and hospital collections.

Finland has steadily developed its biobanking infrastructures since the early 2010s. This article presents a systematic overview of the number of biological samples that have been provided for research since 2013 when the Finnish Biobank Act came into force. Using data from individual biobanks and from permits issued by Fimea (formerly Valvira), we present the most up-to-date and complete account of sample use at a national level. Between 2014 and 2023 a total of 1,474,881 samples were provided through 998 sample requests. A better understanding of the use of biological samples at the national level can help highlight the important impact biobanking has as an infrastructure for supporting research. We argue that developing standards can help in developing national biobanking strategies and identify areas where biobanking can be further developed. We also conclude that the ability to combine tissue samples and health data flexibly and efficiently is essential and needs to be secured also within the context of the European Health Data Space (EHDS).

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来源期刊
European Journal of Human Genetics
European Journal of Human Genetics 生物-生化与分子生物学
CiteScore
9.90
自引率
5.80%
发文量
216
审稿时长
2 months
期刊介绍: The European Journal of Human Genetics is the official journal of the European Society of Human Genetics, publishing high-quality, original research papers, short reports and reviews in the rapidly expanding field of human genetics and genomics. It covers molecular, clinical and cytogenetics, interfacing between advanced biomedical research and the clinician, and bridging the great diversity of facilities, resources and viewpoints in the genetics community. Key areas include: -Monogenic and multifactorial disorders -Development and malformation -Hereditary cancer -Medical Genomics -Gene mapping and functional studies -Genotype-phenotype correlations -Genetic variation and genome diversity -Statistical and computational genetics -Bioinformatics -Advances in diagnostics -Therapy and prevention -Animal models -Genetic services -Community genetics
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