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Results for “Hidden variables”

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At least 19 recordsLinked to original sources

Using a state-space model with hidden variables to infer transcription factor activities.

MOTIVATION: In a gene regulatory network, genes are typically regulated by transcription factors (TFs). Transcription factor activity (TFA) is more difficult to measure than gene expression levels are. Other models have extracted information about TFA from gene expression data, but without explicitly modeling feedback from the genes. We present a state-space model (SSM) with hidden variables. The hidden variables include regulatory motifs in the gene network, such as feedback loops and auto-regulation, making SSM a useful complement to existing models. RESULTS: A gene regulatory network incorporating, for example, feed-forward loops, auto-regulation and multiple-inputs was constructed with an SSM model. First, the gene expression data were simulated by SSM and used to infer the TFAs. The ability of SSM to infer TFAs was evaluated by comparing the profiles of the inferred and simulated TFAs. Second, SSM was applied to gene expression data obtained from Escherichia coli K12 undergoing a carbon source transition and from the Saccharomyces cerevisiae cell cycle. The inferred activity profile for each TF was validated either by measurement or by activity information from the literature. The SSM model provides a probabilistic framework to simulate gene regulatory networks and to infer activity profiles of hidden variables. AVAILABILITY: Supplementary data and Matlab code will be made available at the URL below. SUPPLEMENTARY INFORMATION: http://www.chems.msu.edu/groups/chan/ssm.zip.

Algorithms↗

Class of correlated random networks with hidden variables.

We study a class of models of correlated random networks in which vertices are characterized by hidden variables controlling the establishment of edges between pairs of vertices. We find analytical expressions for the main topological properties of these models as a function of the distribution of hidden variables and the probability of connecting vertices. The expressions obtained are checked by means of numerical simulations in a particular example. The general model is extended to describe a practical algorithm to generate random networks with an a priori specified correlation structure. We also present an extension of the class, to map nonequilibrium growing networks to networks with hidden variables that represent the time at which each vertex was introduced in the system.

Journal Article↗

Experiments towards falsification of noncontextual hidden variable theories

We present two experiments testing the hypothesis of noncontextual hidden variables. The first one is based on observation of two-photon pseudo-Greenberger-Horne-Zeilinger correlations, with two of the originally three particles mimicked by the polarization degree of freedom and the spatial degree of freedom of a single photon. The second one, a single-photon experiment, utilizes the same trick to emulate two particle correlations, and is an "event ready" test of a Bell-like inequality, derived from the noncontextuality assumption. Modulo fair sampling, the data falsify noncontextual hidden variables.

Journal Article↗

Hidden-variable theorems for real experiments.

It has recently been questioned whether the Kochen-Specker theorem is relevant to real experiments, which by necessity only have finite precision. We give an affirmative answer to this question by showing how to derive hidden-variable theorems that apply to real experiments, so that noncontextual hidden variables can indeed be experimentally disproved. The essential point is that for the derivation of hidden-variable theorems one does not have to know which observables are really measured by the apparatus. Predictions can be derived for observables that are defined in an entirely operational way.

Journal Article↗

Ranked prediction of p53 targets using hidden variable dynamic modeling.

Full exploitation of microarray data requires hidden information that cannot be extracted using current analysis methodologies. We present a new approach, hidden variable dynamic modeling (HVDM), which derives the hidden profile of a transcription factor from time series microarray data, and generates a ranked list of predicted targets. We applied HVDM to the p53 network, validating predictions experimentally using small interfering RNA. HVDM can be applied in many systems biology contexts to predict regulation of gene activity quantitatively.

Cell Line, Tumor↗

Symmetric extensions of quantum States and local hidden variable theories.

While all bipartite pure entangled states violate some Bell inequality, the relationship between entanglement and nonlocality for mixed quantum states is not well understood. We introduce a simple and efficient algorithmic approach for the problem of constructing local hidden variable theories for quantum states. The method is based on constructing a so-called symmetric quasiextension of the quantum state that gives rise to a local hidden variable model with a certain number of settings for the observers Alice and Bob.

Journal Article↗

Complex networks emerging from fluctuating random graphs: analytic formula for the hidden variable distribution.

In analogy to superstatistics, which connects Boltzmann-Gibbs statistical mechanics to its generalizations through temperature fluctuations, complex networks are constructed from fluctuating Erdös-Rényi random graphs. Using a quantum-mechanical method, the exact analytic formula for the hidden variable distribution is presented which describes the nature of the fluctuations and generates a generic degree distribution through the Poisson transformation. As an example, a static scale-free network is discussed and the corresponding hidden variable distribution is found to decay as a power law and to diverge at the origin.

Algorithms↗

Fundamental radar properties: hidden variables in space-time.

A derivation of the properties of pulsed radiative imaging systems is presented with examples drawn from conventional, synthetic aperture, and interferometric radar. A geometric construction of the space and time components of a radar observation yields a simple underlying structural equivalence among many of the properties of radar, including resolution, range ambiguity, azimuth aliasing, signal strength, speckle, layover, Doppler shifts, obliquity and slant range resolution, finite antenna size, atmospheric delays, and beam- and pulse-limited configurations. The same simple structure is shown to account for many interferometric properties of radar: height resolution, image decorrelation, surface velocity detection, and surface deformation measurement. What emerges is a simple, unified description of the complex phenomena of radar observations. The formulation comes from fundamental physical concepts in relativistic field theory, of which the essential elements are presented. In the terminology of physics, radar properties are projections of hidden variables--curved worldlines from a broken symmetry in Minkowski space-time--onto a time-serial receiver.

Journal Article↗

[The neurophysiological aspects of the recurrent functioning of the "hidden" variables of the speech apparatus].

The "hidden" recurrent structure is established of temporal organization of acoustic speech signal. Such "hidden" recurrence can be revealed only due to experimentally established existence of two qualitatively different modes in the temporal organization of stutterers' speech. A theoretical model of speech generation is developed with a logistical property of "hidden" parameters in order to explain this phenomenon. This model is stated in terms of chaotic dynamics and is based on the neurophysiological striopallidal mechanisms which are realized under conditions of polysensory afferent impulsation. The effects of speech memory and actualization of its traces are explained on the basis of our earlier concept of perception of the rhythmical speech sequence. This concept allowed us to discuss the experimentally observed phenomenon of inhibitory modulation under conditions of both ipsi- and contralateral global negative feedback.

Adolescent↗

Control of metabolic rate is a hidden variable in the allometric scaling of homeotherms.

The allometric scaling exponent of the relationship between standard metabolic rate (SMR) and body mass for homeotherms has a long history and has been subject to much debate. Provided the external and internal conditions required to measure SMR are met, it is tacitly assumed that the metabolic rate (B) converges to SMR. If SMR does indeed represent a local minimum, then short-term regulatory control mechanisms should not operate to sustain it. This is a hidden assumption in many published articles aiming to explain the scaling exponent in terms of physical and morphological constraints. This paper discusses the findings of a minimalist body temperature (Tb) control model in which short-term controlling operations, related to the difference between Tb and the set-point temperatures by specific gains and time delays in the control loops, are described by a system of differential equations of Tb, B and thermal conductance. We found that because the gains in the control loops tend to increase as body size decreases (i.e. changes in B and thermal conductance are speeded-up in small homeotherms), the equilibrium point of the system potentially changes from asymptotically stable to a centre, transforming B and Tb in oscillating variables. Under these specific circumstances the very concept of SMR no longer makes sense. A series of empirical reports of metabolic rate in very small homeotherms supports this theoretical prediction, because in these animals B seems not to converge to a SMR value. We conclude that the unrestricted use of allometric equations to relate metabolic rate to body size might be misleading because metabolic control itself experiences size effects that are overlooked in ordinary allometric analysis.

Animals↗

Hidden variables: unstable Abeta chain genes encoding antigen recognition structures in tumor survivors.

Novel single exon genes Abeta4-7 comprising the Abeta6 gene family have been cloned from mouse mutants surviving transplantable metastatic tumors. Their protein coding sequences are similar to H2-Ab cDNA which encodes antigen-binding molecules of antigen presenting cells (APC); their promoters and/or signal sequences are unrelated to Ab sequences but found in other eukaryotic genes. Abeta4(b) protein was demonstrated on macrophages and B cells that are APC. The Abeta6(w302) appears to be an ancient gene ancestral to major histocompatibility complex (MHC) class II beta genes. However, unlike the MHC class II, the Abeta4-7 genes are not involved in skin graft rejection. Despite inbreeding, the Abeta6(w302) locus remains unfixed in several strains of mice. The number of Abeta genes and their alleles varied between individual mice; they do not map into the H2 region but appear to be scattered over the genome. The Abeta6 gene family is molecularly unstable in Abeta6(w302)-positive (but not in Abeta6(w302)-negative) mice which are somatic mosaics for these genes. Biological features of Abeta4-7 genes make them remarkably different from the classical MHC gene system. All available evidence strongly suggests that these genes control susceptibility/resistance to the spread of metastatic tumors.

Animals↗

Revealing Hidden Variables in DESI-Based Spatial Metabolomics: Solvent Composition and Tissue Type as Critical Drivers.

In the development of a desorption electrospray ionization (DESI) workflow for spatial metabolomics, we investigated the impact of two commonly used solvent systems, 90% acetonitrile (ACN) and 90% methanol (MeOH), on the spatial metabolomic profiling of various murine tissues. The performance of both solvents was evaluated across several metabolite classes (central carbon metabolites, amino acids, and fatty acids). Although the ACN-based solvent system led to higher signal intensities for small polar metabolites involved in glycolysis, the tricarboxylic acid (TCA) cycle, and amino acid metabolism, the MeOH-based solvent system provided superior signal intensities for fatty acids. These findings demonstrate that the solvent composition differentially influences metabolite extraction and ionization processes in DESI and should be carefully matched to the biological questions and metabolite classes of interest. As a proof-of-principle, the ACN solvent system was applied to a pilot study based on a rat model of renal ischemic injury, revealing region-specific metabolic changes between normoxic and ischemic conditions. Together, these results demonstrate the importance of solvent selection in DESI-based spatial metabolomics and showcase the ability of this approach to uncover spatially resolved metabolic adaptations associated with tissue injury.

Animals↗