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Microattribution and nanopublication as means to incentivize the placement of human genome variation data into the public domain

机译:微观归因和纳米出版物是激励人类基因组变异数据进入公共领域的手段

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摘要

The advances in bioinformatics required to annotate human genomic variants and to place them in public data repositories have not kept pace with their discovery. Moreover, a law of diminishing returns has begun to operate both in terms of data publication and submission. Although the continued deposition of such data in the public domain is essential to maximize both their scientific and clinical utility, rewards for data sharing are few, representing a serious practical impediment to data submission. To date, two main strategies have been adopted as a means to encourage the submission of human genomic variant data: (1) database journal linkups involving the affiliation of a scientific journal with a publicly available database and (2) microattribution, involving the unambiguous linkage of data to their contributors via a unique identifier. The latter could in principle lead to the establishment of a microcitation-tracking system that acknowledges individual endeavor and achievement. Both approaches could incentivize potential data contributors, thereby encouraging them to share their data with the scientific community. Here, we summarize and critically evaluate approaches that have been proposed to address current deficiencies in data attribution and discuss ways in which they could become more widely adopted as novel scientific publication modalities.
机译:注释人类基因组变异并将其放置在公共数据存储库中所需的生物信息学进展与他们的发现并不一致。此外,就数据发布和提交而言,收益递减法已开始生效。尽管在公共领域持续存储此类数据对于最大化其科学和临床效用至关重要,但共享数据的奖励却很少,这严重阻碍了数据提交的实际操作。迄今为止,已经采取了两种主要策略来鼓励提交人类基因组变异数据:(1)数据库期刊链接,涉及将科学期刊与可公开获得的数据库联系起来;(2)微属性,涉及明确的链接通过唯一标识符将数据分配给其贡献者。后者原则上可以导致建立一个承认个人努力和成就的微引文跟踪系统。两种方法都可以激励潜在的数据提供者,从而鼓励他们与科学界共享其数据。在这里,我们总结并批判性地评估了为解决当前数据归因不足而提出的方法,并讨论了如何将其更广泛地用作新型科学出版方式。

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