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sbv IMPROVER Diagnostic Signature Challenge Design and results

机译:sbv IMPROVER诊断签名挑战设计和结果

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The sbv IMPROVER (systems biology verification—Industrial Methodology for Process Verification in Research) process aims to help companies verify component steps or tasks in larger research workflows for industrial applications. IMPROVER is built on challenges posed to the community that draws on the wisdom of crowds to assess the most suitable methods for a given research task. The Diagnostic Signature Challenge, open to the public from Mar. 5 to Jun. 21, 2012, was the first instantiation of the IMPROVER methodology and evaluated a fundamental biological question, specifically, if there is sufficient information in gene expression data to diagnose diseases. Fifty-four teams used publically available data to develop prediction models in four disease areas: multiple sclerosis, lung cancer, psoriasis, and chronic obstructive pulmonary disease. The predictions were scored against unpublished, blinded data provided by the organizers, and the results, including methods of the top performers, presented at a conference in Boston on Oct. 2–3, 2012. This paper offers an overview of the Diagnostic Signature Challenge and the accompanying symposium, and is the first article in a special issue of Systems Biomedicine, providing focused reviews of the submitted methods and general conclusions from the challenge. Overall, it was observed that optimal method choice and performance appeared largely dependent on endpoint, and results indicate the psoriasis and lung cancer subtypes sub-challenges were more accurately predicted, while the remaining classification tasks were much more challenging. Though no one approach was superior for every sub-challenge, there were methods, like linear discriminant analysis, that were found to perform consistently well in all.
机译:sbv IMPROVER(系统生物学验证-用于研究过程验证的工业方法论)过程旨在帮助公司验证更大的工业应用研究工作流程中的组件步骤或任务。 IMPROVER建立在向社区提出的挑战的基础上,该挑战利用人群的智慧来评估针对给定研究任务的最合适方法。 “诊断签名挑战赛”于2012年3月5日至6月21日向公众开放,是IMPROVER方法的首次实例化,并评估了一个基本的生物学问题,特别是基因表达数据中是否有足够的信息可用于诊断疾病。 54个小组使用可公开获得的数据来开发四个疾病领域的预测模型:多发性硬化症,肺癌,牛皮癣和慢性阻塞性肺疾病。预测是根据组织者提供的未发布的盲目数据进行评分的,其结果(包括绩效最高的方法)在2012年10月2日至3日于波士顿举行的会议上进行了介绍。本文概述了诊断签名挑战以及相关的座谈会,这是《系统生物医学》特刊的第一篇文章,重点介绍了所提交的方法以及挑战所得出的一般性结论。总体而言,观察到最佳的方法选择和性能似乎很大程度上取决于终点,结果表明,对银屑病和肺癌亚型亚挑战的预测更为准确,而其余分类任务则更具挑战性。尽管没有任何一种方法能在所有子挑战中均胜出,但还是有一些方法(如线性判别分析)在所有方面都表现良好。

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