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迈向公平基因组之路:荷兰二代测序数据生成与共享的差距分析

Road to FAIR genomes: a gap analysis of NGS data generation and sharing in the Netherlands.

作者信息

Belien Jeroen A M, Kip Anke E, Swertz Morris A

机构信息

Pathology, Amsterdam UMC, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.

Lygature, Utrecht, The Netherlands.

出版信息

BMJ Open Sci. 2022 Apr 12;6(1):e100268. doi: 10.1136/bmjos-2021-100268. eCollection 2022.

Abstract

OBJECTIVE

This study investigates current standards and operational gaps in the management and sharing of next generation sequencing (NGS) data within the healthcare and research setting and according to Findable, Accessible, Interoperable and Reusable (FAIR) principles.

METHODS

The analysis was performed as the basis from which to bridge identified gaps and develop widely accepted working standards that ensure optimal reusability of genomic data in healthcare and research settings in the Netherlands. This work is part of the 'Rational Pharmacotherapy Program' led by ZonMw, The Netherlands Organisation for Health Research and Development, which aims to promote the efficient implementation of NGS and personalised medicine within Dutch healthcare, with an initial focus on oncology and rare diseases.

RESULTS

Based on this analysis and as part of this programme, a consortium was formed to develop an instruction manual for FAIR genomic data in clinical care and research based on an inventory of commonly used workflows and standards in the (inter)national field of genome analysis.

CONCLUSIONS

The gap analysis presented and discussed in this paper represents the starting point for this inventory and is a possible contribution from the Netherlands to the European 1+ Million Genomes Initiative. This paper addresses the topics of data generation, data quality, (meta)data standards, data storage and archiving and data integration and exchange.

摘要

目的

本研究调查了医疗保健和研究环境中下一代测序(NGS)数据管理与共享方面的现行标准和操作差距,并依据可查找、可访问、可互操作和可重复使用(FAIR)原则进行了研究。

方法

进行该分析是为了弥补已识别的差距,并制定被广泛接受的工作标准,以确保荷兰医疗保健和研究环境中基因组数据的最佳可重复使用性。这项工作是由荷兰卫生研究与发展组织(ZonMw)牵头的“合理药物治疗计划”的一部分,该计划旨在促进荷兰医疗保健领域中NGS和个性化医疗的有效实施,最初侧重于肿瘤学和罕见病。

结果

基于此分析并作为该计划的一部分,成立了一个联盟,以根据基因组分析(国际)领域常用工作流程和标准清单,制定临床护理和研究中FAIR基因组数据的操作手册。

结论

本文提出并讨论的差距分析是该清单的起点,也是荷兰对欧洲100万基因组计划的一项可能贡献。本文涉及数据生成、数据质量、(元)数据标准、数据存储与存档以及数据整合与交换等主题。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/02c1/9014103/1a7b85e818d6/bmjos-2021-100268f01.jpg

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