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列维标度:应用于DNA序列的扩散熵分析。

Lévy scaling: the diffusion entropy analysis applied to DNA sequences.

作者信息

Scafetta Nicola, Latora Vito, Grigolini Paolo

机构信息

Pratt School EE Department, Duke University, P.O. Box 90291, Durham, North Carolina 27708, USA.

出版信息

Phys Rev E Stat Nonlin Soft Matter Phys. 2002 Sep;66(3 Pt 1):031906. doi: 10.1103/PhysRevE.66.031906. Epub 2002 Sep 20.

Abstract

We address the problem of the statistical analysis of a time series generated by complex dynamics with the diffusion entropy analysis (DEA) [N. Scafetta, P. Hamilton, and P. Grigolini, Fractals 9, 193 (2001)]. This method is based on the evaluation of the Shannon entropy of the diffusion process generated by the time series imagined as a physical source of fluctuations, rather than on the measurement of the variance of this diffusion process, as done with the traditional methods. We compare the DEA to the traditional methods of scaling detection and prove that the DEA is the only method that always yields the correct scaling value, if the scaling condition applies. Furthermore, DEA detects the real scaling of a time series without requiring any form of detrending. We show that the joint use of DEA and variance method allows to assess whether a time series is characterized by Lévy or Gauss statistics. We apply the DEA to the study of DNA sequences and prove that their large-time scales are characterized by Lévy statistics, regardless of whether they are coding or noncoding sequences. We show that the DEA is a reliable technique and, at the same time, we use it to confirm the validity of the dynamic approach to the DNA sequences, proposed in earlier work.

摘要

我们利用扩散熵分析(DEA)[N. 斯卡费塔、P. 汉密尔顿和P. 格里戈利尼,《分形》9,193(2001)]来解决由复杂动力学产生的时间序列的统计分析问题。该方法基于对由时间序列所产生的扩散过程的香农熵的评估,此时间序列被视为波动的物理源,而不是像传统方法那样基于对该扩散过程方差的测量。我们将DEA与传统的标度检测方法进行比较,并证明如果标度条件适用,DEA是唯一总能得出正确标度值的方法。此外,DEA无需任何形式的去趋势处理就能检测时间序列的真实标度。我们表明,联合使用DEA和方差方法能够评估一个时间序列是由 Lévy 统计还是高斯统计所表征。我们将DEA应用于DNA序列的研究,并证明其长时间尺度由 Lévy 统计表征,无论它们是编码序列还是非编码序列。我们表明DEA是一种可靠的技术,同时我们用它来证实早期工作中提出的DNA序列动态方法的有效性。

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