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

机译:用于重建生物或临床标记的时间谱的生物疗法取向机器学习系统

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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 (Ple0.0001) 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.
机译:时间序列重建算法广泛用于从数据系列创建时间配置文件。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,使得难以使用标准算法。我们开发了Profilase,将先进的多目标遗传算法搜索与机器学习架构相结合,以收获专家的决策考虑因素。此外,Profilase实现了额外的评分考虑因素,更生物本质上,从而进一步利用域专业知识。我们通过从模拟配置文件的噪声重建进行时间序列稀疏地采样来测试我们的系统对标准的自下而上算法。 Profilase获得的RMS距离2.5倍(PLE0.0001)比标准算法,93%正确的段数识别率和88%正确的概况分类率(与68%)。发现其他考虑因素对重建的成功产生了重大影响。最后,推广分析酶以评估来自不同领域的其他注意事项,从而允许更好地了解其他疾病。

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