Biomathematics Oriented Machine Learning System for Reconstructing Temporal Profiles of Biological or Clinical Markers

Ronen Tal-Botzer, Nir Hadaya, Rachel S. Levy-Drummer, Ariel Feiglin, David H. Shalom, A. Neumann
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引用次数: 1

Abstract

Time series reconstruction algorithms are widely used to create temporal profiles from data series. However, in many clinical fields, e.g., viral kinetics, the data is noisy and sparse, making it difficult to use standard algorithms. We developed PROFILASE, which combines advanced multi-objective genetic algorithm search with machine learning architecture to harvest experts' decision-making considerations. Furthermore, PROFILASE implements additional scoring considerations, more biological in nature, thus further exploits domain expertise. We tested our system against a standard bottom-up algorithm by reconstruction of time series sparsely sampled with noise from simulated profiles. PROFILASE obtained RMS distance 2.5 fold lower (P<0.0001) than the standard algorithm, 93% correct identification rate of segment number and 88% correct profile classification rate (versus 68%). The additional considerations were found to have a significant effect on the success of reconstruction. Finally, PROFILASE was generalized to evaluate additional considerations from different fields, thus allowing better understanding of other diseases
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面向生物数学的机器学习系统,用于重建生物或临床标记物的时间剖面
时间序列重构算法被广泛用于从数据序列中创建时间剖面。然而,在许多临床领域,例如病毒动力学,数据是嘈杂和稀疏的,使得很难使用标准算法。我们开发了PROFILASE,它结合了先进的多目标遗传算法搜索和机器学习架构来收集专家的决策考虑。此外,PROFILASE实现了额外的评分考虑,本质上更具有生物学性,因此进一步利用了领域专业知识。我们用标准的自底向上算法对系统进行了测试,方法是对时间序列进行稀疏采样,并从模拟剖面中提取噪声。PROFILASE的RMS距离比标准算法低2.5倍(P<0.0001),对片段数量的正确率为93%,对剖面的正确率为88%(标准算法为68%)。人们发现,这些额外的考虑因素对重建的成功有重大影响。最后,对PROFILASE进行了推广,以评估不同领域的其他考虑因素,从而更好地了解其他疾病
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