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A novel method for estimating the common signals for consensus across multiple ranked lists

机译:一种估算跨多个排名列表共识的共同信号的新方法

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Abstract The ranking of objects, such as journals, institutions or biological entities, is broadly used to assess the relative quality or relevance of such objects. A multiple ranking is performed by a number of assessors (humans or machines) and inference about the nature of the observed rankings is desirable for evaluation, business or scientific purposes. The assessors’ decisions are based on some inherent metric scale and depend on judgement and discriminatory ability, data to which we usually do not have access. An indirect inference approach is proposed that allows one to estimate those signal parameters that might be causal for the observed rankings obtained from several assessors, some of which may not necessarily provide the same decision quality. The order of the values represents a consensus ranking across the observed individual rankings. The standard errors of the estimated signal parameters are obtained through a non-parametric bootstrap. Hence, the signal variability can be evaluated object-wise for the purpose of quantifying the stability of the associated rank positions. As a result, such signal estimates can be used in the meta-analysis of conceptually similar evaluation exercises, studies or experiments, and in any data integration task where measurements on the metric scale are either unavailable, or not directly comparable. The suggested approach is validated on simulated rank data as well as on experimental rank data from current molecular medicine. The proposed algorithms were implemented and all calculations performed in the R environment. The source code is provided.
机译:<![cdata [ Abstract 广泛地用于评估这些物体的相对质量或相关性等物体的排名。通过许多评估员(人或机器)进行多次排名,并对观察排名的性质推断是可取的评估,商业或科学目的的理想。评估员的决定基于一些固有的公制量表,依赖于判断和歧视性能力,我们通常无法访问的数据。提出了一种间接推理方法,其允许一个人估计可能是从几个评估员获得的观察排名的因果的那些信号参数,其中一些可能不一定提供相同的决策质量。值的顺序代表了观察到的个体排名中的共识。通过非参数释放启动获得估计信号参数的标准误差。因此,为了量化相关等级位置的稳定性,可以评估信号变异性。结果,这种信号估计可以用于概念上类似的评估练习,研究或实验的元分析,以及在公制刻度上测量的任何数据集成任务中,或者不可直接可比较。建议的方法在模拟等级数据以及来自当前分子药物的实验级数据上验证。实施了所提出的算法,并在 r 环境中进行所有计算。提供源代码。

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