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首页> 外文期刊>BMC Bioinformatics >Overview of the ID, EPI and REL tasks of BioNLP Shared Task 2011
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Overview of the ID, EPI and REL tasks of BioNLP Shared Task 2011

机译:Bionlp共享任务的ID,EPI和Rel任务概述2011

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We present the preparation, resources, results and analysis of three tasks of the BioNLP Shared Task 2011: the main tasks on Infectious Diseases (ID) and Epigenetics and Post-translational Modifications (EPI), and the supporting task on Entity Relations (REL). The two main tasks represent extensions of the event extraction model introduced in the BioNLP Shared Task 2009 (ST'09) to two new areas of biomedical scientific literature, each motivated by the needs of specific biocuration tasks. The ID task concerns the molecular mechanisms of infection, virulence and resistance, focusing in particular on the functions of a class of signaling systems that are ubiquitous in bacteria. The EPI task is dedicated to the extraction of statements regarding chemical modifications of DNA and proteins, with particular emphasis on changes relating to the epigenetic control of gene expression. By contrast to these two application-oriented main tasks, the REL task seeks to support extraction in general by separating challenges relating to part-of relations into a subproblem that can be addressed by independent systems. Seven groups participated in each of the two main tasks and four groups in the supporting task. The participating systems indicated advances in the capability of event extraction methods and demonstrated generalization in many aspects: from abstracts to full texts, from previously considered subdomains to new ones, and from the ST'09 extraction targets to other entities and events. The highest performance achieved in the supporting task REL, 58% F-score, is broadly comparable with levels reported for other relation extraction tasks. For the ID task, the highest-performing system achieved 56% F-score, comparable to the state-of-the-art performance at the established ST'09 task. In the EPI task, the best result was 53% F-score for the full set of extraction targets and 69% F-score for a reduced set of core extraction targets, approaching a level of performance sufficient for user-facing applications. In this study, we extend on previously reported results and perform further analyses of the outputs of the participating systems. We place specific emphasis on aspects of system performance relating to real-world applicability, considering alternate evaluation metrics and performing additional manual analysis of system outputs. We further demonstrate that the strengths of extraction systems can be combined to improve on the performance achieved by any system in isolation. The manually annotated corpora, supporting resources, and evaluation tools for all tasks are available from http://www.bionlp-st.org and the tasks continue as open challenges for all interested parties.
机译:我们提出了三项任务的准备,资源,结果和分析2011年的三项任务:传染病(ID)和表观遗传学和翻译后修改(EPI)的主要任务以及实体关系的支持任务(rel) 。这两个主要任务代表了在Bionlp共享任务2009(ST'09)中引入的事件提取模型的扩展,每个生物医学科学文献的两个新的领域,每个都是通过特定的酶任务的需求激励。 ID任务涉及感染,毒力和抗性的分子机制,特别是对细菌中普遍存在的一类信号系统的功能。 EPI任务致力于提取关于DNA和蛋白的化学修饰的陈述,特别强调与基因表达的表观遗传控制有关的变化。与这两个面向应用导向的主要任务相比,Rel任务通过将与独立系统可以解决的子问题分离为子问题,通过将挑战分开,以支持提取。七组参加了两个主要任务中的每一个和四组支持任务。参与系统指示事件提取方法的能力的进步,并在许多方面展示了概括:从摘要到全文,从以前认为的子域名到新的子项,并从ST'09提取目标到其他实体和事件。支持任务中实现的最高性能,58%F分数,与其他关系提取任务报告的水平相比广泛可比较。对于ID任务,最高性能的系统实现了56%的F分,与已建立的ST'09任务的最先进的性能相当。在EPI任务中,最佳结果为全套提取目标的53%F分,以及减少一组核心提取目标的69%F分,接近足以用于面向用户的应用的性能水平。在本研究中,我们在先前报告的结果上延伸,并进一步分析了参与系统的产出。考虑备用评估指标并对系统输出进行额外的手动分析,我们对系统性能有关的特定强调系统性能方面。我们进一步证明,可以组合提取系统的强度以改善任何系统中任何系统所达到的性能。用于所有任务的手动注释的Corpora,支持资源和评估工具可从http://www.bionlp -st.org获得,并且任务继续作为所有有关方面的开放挑战。

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