海军航空大学,山东 烟台 264001
[ "吕佳朋(1994—),男,博士研究生,研究方向为可诊断性评价与设计、故障诊断。E-mail:lvjiapeng001@163.com;" ]
史贤俊(1968—),男,教授,博士生导师,研究方向为飞行器智能检测与故障诊断、测试性设计与评估等。E-mail:sxjaa@sina.com
[ "聂新华(1985—),男,讲师,博士,研究方向为智能检测与故障诊断。E-mail:nxhylng@163.com;" ]
[ "秦玉峰(1995—),男,博士,研究方向为故障可诊断性评价与设计。E-mail:hy_qyf082@163.com;" ]
[ "龙玉峰(1982—),男,工程师,博士,研究方向为系统建模、基于模型的诊断。E-mail:47314226@qq.com" ]
收稿:2021-11-22,
纸质出版:2023-03-28
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吕佳朋, 史贤俊, 聂新华, 等. 基于递归图和张量分解的故障可诊断性评价方法[J]. 兵工学报, 2023,44(3):763-772.
Jiapeng LÜ, Xianjun SHI, Xinhua NIE, et al. Evaluation Method of Fault Diagnosability Based on Recursive Plot and Tensor Decomposition[J]. Acta Armamentarii, 2023, 44(3): 763-772.
吕佳朋, 史贤俊, 聂新华, 等. 基于递归图和张量分解的故障可诊断性评价方法[J]. 兵工学报, 2023,44(3):763-772. DOI: 10.12382/bgxb.2021.0790.
Jiapeng LÜ, Xianjun SHI, Xinhua NIE, et al. Evaluation Method of Fault Diagnosability Based on Recursive Plot and Tensor Decomposition[J]. Acta Armamentarii, 2023, 44(3): 763-772. DOI: 10.12382/bgxb.2021.0790.
可诊断性反映了系统故障诊断的难易程度,对系统进行可诊断性评价是开展故障诊断工作的前提条件。针对可诊断性评价问题,将测点信号考虑在内,提出了一种基于递归图和张量分解的故障可诊断性评价方法。利用相空间重构技术对装备在不同状态下的测点信号进行图形化表示,形成递归图;对递归图进行分析以提取其中的特征,并将该特征视为原信号特征;通过张量分解的方法,计算不同状态下信号特征之间的相似程度,作为故障诊断难易程度的基本度量。通过仿真实验对所提出的方法与仅考虑系统模型的D矩阵的可诊断性评价方法进行对比,结果表明该方法在评价可诊断性方面具有准确性和客观性。
Diagnosability reflects the difficulty of diagnosing system faults
so diagnosability evaluation of the system is a prerequisite for fault diagnosis. Taking the signals of test points into consideration
a fault diagnosability evaluation method based on a recurrence plot and tensor decomposition is proposed. The phase space reconstruction technique is used to graphically represent the signals of measured points in different states to form a recurrence plot. Features are extracted through analyzing the recurrence plot
which are then regarded as the original signal features. Through tensor decomposition
the similarity between signal features in different states is calculated as a basic measure of fault diagnosis difficulty. Simulation experiments show that
compared with the previous D-matrix diagnosability evaluation method that only considers the system model
the newly proposed method has effectiveness and objectivity.
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BORZOU A , YOUSEFI R , SADYGOV R G . Another look at matrix correlations [J ] . Bioinformatics , 2019 , 35 ( 22 ): 4748 - 4753 . DOI: 10.1093/bioinformatics/btz281 http://doi.org/10.1093/bioinformatics/btz281 High throughput technologies are widely employed in modern biomedical research. They yield measurements of a large number of biomolecules in a single experiment. The number of experiments usually is much smaller than the number of measurements in each experiment. The simultaneous measurements of biomolecules provide a basis for a comprehensive, systems view for describing relevant biological processes. Often it is necessary to determine correlations between the data matrices under different conditions or pathways. However, the techniques for analyzing the data with a low number of samples for possible correlations within or between conditions are still in development. Earlier developed correlative measures, such as the RV coefficient, use the trace of the product of data matrices as the most relevant characteristic. However, a recent study has shown that the RV coefficient consistently overestimates the correlations in the case of low sample numbers. To correct for this bias, it was suggested to discard the diagonal elements of the outer products of each data matrix. In this work, a principled approach based on the matrix decomposition generates three trace-independent parts for every matrix. These components are unique, and they are used to determine different aspects of correlations between the original datasets.Simulations show that the decomposition results in the removal of high correlation bias and the dependence on the sample number intrinsic to the RV coefficient. We then use the correlations to analyze a real proteomics dataset.The python code can be downloaded from http://dynamic-proteome.utmb.edu/MatrixCorrelations.aspx.Supplementary data are available at Bioinformatics online.© The Author(s) 2019. Published by Oxford University Press. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.
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