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Unique Mechanisms From Finite Two-State Trajectories 有限双态轨迹的独特机制
Pub Date : 2007-06-15 DOI: 10.1142/9789812793492_0010
O. Flomenbom, R. Silbey
Single molecule data made of on and off events are ubiquitous. Famous examples include enzyme turnover, probed via fluorescence, and opening and closing of ion-channel, probed via the flux of ions. The data reflects the dynamics in the underlying multi-substate on-off kinetic scheme (KS) of the process, but the determination of the underlying KS is difficult, and sometimes even impossible, due to the loss of information in the mapping of the mutli-dimensional KS onto two dimensions. A way to deal with this problem considers canonical (unique) forms. (Unique canonical form is constructed from an infinitely long trajectory, but many KSs.) Here we introduce canonical forms of reduced dimensions that can handle any KS (i.e. also KSs with symmetry and irreversible transitions). We give the mapping of KSs into reduced dimensions forms, which is based on topology of KSs, and the tools for extracting the reduced dimensions form from finite data. The canonical forms of reduced dimensions constitute a powerful tool in discriminating between KSs.
由开与关事件构成的单分子数据无处不在。著名的例子包括通过荧光探测的酶周转,以及通过离子通量探测的离子通道的打开和关闭。数据反映了该过程中潜在的多亚态开关动力学方案(KS)的动力学,但由于在将多维KS映射到二维时丢失了信息,确定潜在的KS是困难的,有时甚至是不可能的。处理这个问题的一种方法是考虑规范(唯一)形式。(唯一的规范形式是由无限长的轨迹构造的,但有许多KSs。)在这里,我们介绍了可以处理任何KS(即具有对称和不可逆转换的KS)的规范降维形式。基于KSs的拓扑结构,给出了KSs的降维映射,并给出了从有限数据中提取降维形式的工具。降维的规范形式构成了区分KSs的有力工具。
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引用次数: 0
Granger Causality: Basic Theory and Application to Neuroscience 格兰杰因果关系:神经科学的基础理论与应用
Pub Date : 2006-08-23 DOI: 10.1002/9783527609970.CH17
M. Ding, Yonghong Chen, S. Bressler
Multi-electrode neurophysiological recordings produce massive quantities of data. Multivariate time series analysis provides the basic framework for analyzing the patterns of neural interactions in these data. It has long been recognized that neural interactions are directional. Being able to assess the directionality of neuronal interactions is thus a highly desired capability for understanding the cooperative nature of neural computation. Research over the last few years has shown that Granger causality is a key technique to furnish this capability. The main goal of this article is to provide an expository introduction to the concept of Granger causality. Mathematical frameworks for both bivariate Granger causality and conditional Granger causality are developed in detail with particular emphasis on their spectral representations. The technique is demonstrated in numerical examples where the exact answers of causal influences are known. It is then applied to analyze multichannel local field potentials recorded from monkeys performing a visuomotor task. Our results are shown to be physiologically interpretable and yield new insights into the dynamical organization of large-scale oscillatory cortical networks.
多电极神经生理记录产生大量的数据。多元时间序列分析为分析这些数据中的神经交互模式提供了基本框架。人们早就认识到神经相互作用是有方向性的。因此,能够评估神经元相互作用的方向性是理解神经计算的合作性质的高度期望的能力。过去几年的研究表明,格兰杰因果关系是提供这种能力的关键技术。本文的主要目的是为格兰杰因果关系的概念提供一个说明性的介绍。对二元格兰杰因果关系和条件格兰杰因果关系的数学框架进行了详细的研究,特别强调了它们的谱表示。在已知因果影响的确切答案的数值例子中,该技术得到了证明。然后将其应用于分析执行视觉运动任务的猴子所记录的多通道局部场电位。我们的结果被证明是生理学上可解释的,并为大规模振荡皮层网络的动态组织提供了新的见解。
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引用次数: 636
Kernel Methods in Genomics and Computational Biology 基因组学和计算生物学中的核方法
Pub Date : 2005-10-17 DOI: 10.4018/978-1-59904-042-4.CH002
Jean-Philippe Vert
Support vector machines and kernel methods are increasingly popular in genomics and computational biology, due to their good performance in real-world applications and strong modularity that makes them suitable to a wide range of problems, from the classification of tumors to the automatic annotation of proteins. Their ability to work in high dimension, to process non-vectorial data, and the natural framework they provide to integrate heterogeneous data are particularly relevant to various problems arising in computational biology. In this chapter we survey some of the most prominent applications published so far, highlighting the particular developments in kernel methods triggered by problems in biology, and mention a few promising research directions likely to expand in the future.
支持向量机和核方法在基因组学和计算生物学中越来越受欢迎,因为它们在实际应用中的良好性能和强大的模块化使它们适用于从肿瘤分类到蛋白质自动注释的广泛问题。它们在高维上工作、处理非矢量数据的能力,以及它们提供的整合异构数据的自然框架,与计算生物学中出现的各种问题特别相关。在本章中,我们概述了迄今为止发表的一些最突出的应用,突出了由生物学问题引发的核方法的特殊发展,并提到了一些有希望的研究方向,可能在未来扩大。
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引用次数: 30
PCA and K-Means Decipher Genome PCA和K-Means解码基因组
Pub Date : 2005-04-08 DOI: 10.1007/978-3-540-73750-6_14
Alexander N Gorban, A. Zinovyev
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引用次数: 6
Evolution at the Edge of Chaos: A Paradigm for the Maturation of the Humoral Immune Response 混沌边缘的进化:体液免疫反应成熟的范例
Pub Date : 2004-06-06 DOI: 10.1007/978-3-642-55606-7_3
P. Theodosopoulos, T. Theodosopoulos
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引用次数: 5
Material Forces in the Context of Biotissue Remodelling 生物组织重塑中的物质力
Pub Date : 2003-11-30 DOI: 10.1007/0-387-26261-X_8
K. Garikipati, H. Narayanan, E. Arruda, K. Grosh, S. Calve
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引用次数: 20
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arXiv: Quantitative Methods
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