1,720,979 research outputs found
Learning Bayesian networks: a copula approach for mixed-type data
Estimating dependence relationships between variables is a crucial issue in
many applied domains, such as medicine, social sciences and psychology. When
several variables are entertained, these can be organized into a network which
encodes their set of conditional dependence relations. Typically however, the
underlying network structure is completely unknown or can be partially drawn
only; accordingly it should be learned from the available data, a process known
as structure learning. In addition, data arising from social and psychological
studies are often of different types, as they can include categorical, discrete
and continuous measurements. In this paper we develop a novel Bayesian
methodology for structure learning of directed networks which applies to mixed
data, i.e. possibly containing continuous, discrete, ordinal and binary
variables simultaneously. Whenever available, our method can easily incorporate
known dependence structures among variables represented by paths or edge
directions that can be postulated in advance based on the specific problem
under consideration. We evaluate the proposed method through extensive
simulation studies, with appreciable performances in comparison with current
state-of-the-art alternative methods. Finally, we apply our methodology to
well-being data from a social survey promoted by the United Nations, and mental
health data collected from a cohort of medical students
Objective Bayes model selection of Gaussian interventional essential graphs for the identification of signaling pathways
A signalling pathway is a sequence of chemical reactions initiated by a stimulus which in turn affects a receptor, and then through some intermediate steps cascades down to the final cell response. Based on the technique of flow cytometry, samples of cell-by-cell measurements are collected under each experimental condition, resulting in a collection of interventional data (assuming no latent variables are involved). Usually several external interventions are applied at different points of the pathway, the ultimate aim being the structural recovery of the underlying signalling network which we model as a causal Directed Acyclic Graph (DAG) using intervention calculus. The advantage of using interventional data, rather than purely observational one, is that identifiability of the true data generating DAG is enhanced. More technically a Markov equivalence class of DAGs, whose members are statistically indistinguishable based on observational data alone, can be further decomposed, using additional interventional data, into smaller distinct Interventional Markov equivalence classes. We present a Bayesian methodology for structural learning of Interventional Markov equivalence classes based on observational and interventional samples of multivariate Gaussian observations. Our approach is objective, meaning that it is based on default parameter priors requiring no personal elicitation; some flexibility is however allowed through a tuning parameter which regulates sparsity in the prior on model space. Based on an analytical expression for the marginal likelihood of a given Interventional Essential Graph, and a suitable MCMC scheme, our analysis produces an approximate posterior distribution on the space of Interventional Markov equivalence classes, which can be used to provide uncertainty quantification for features of substantive scientific interest, such as the posterior probability of inclusion of selected edges, or paths
Discovering causal structures in Bayesian Gaussian directed acyclic graph models
Causal directed acyclic graphs (DAGs) are naturally tailored to represent biological signalling pathways. However, a causal DAG is only identifiable up to Markov equivalence if only observational data are available. Interventional data, based on exogenous perturbations of the system, can greatly improve identifiability. Since the gain of an intervention crucially depends on the intervened variables, a natural issue is devising efficient strategies for optimal causal discovery. We present a Bayesian active learning procedure for Gaussian DAGs which requires no subjective specification on the side of the user, explicitly takes into account the uncertainty on the space of equivalence classes (through the posterior distribution) and sequentially proposes the choice of the optimal intervention variable. In simulation experiments our method, besides surpassing designs based on a random choice of intervention nodes, shows decisive improvements over currently available algorithms and is competitive with the best alternative benchmarks. An important reason behind this strong performance is that, unlike non-Bayesian algorithms, our utility function naturally incorporates graph estimation uncertainty through the posterior edge inclusion probability. We also reanalyse the Sachs data on protein signalling pathways from an active learning perspective and show that DAG identification can be achieved by using only a subset of the available intervention samples
Bayesian inference of graph-based dependencies from mixed-type data
Mixed data comprise measurements of different types, with both categorical and continuous variables, and can be found in various areas, such as in life science or industrial processes. Inferring conditional independencies from the data is crucial to understand how these variables relate to each other. To this end, graphical models provide an effective framework, which adopts a graph-based representation of the joint distribution to encode such dependence relations. This framework has been extensively studied in the Gaussian and categorical settings separately; on the other hand, the literature addressing this problem in presence of mixed data is still narrow. We propose a Bayesian model for the analysis of mixed data based on the notion of Conditional Gaussian (CG) distribution. Our method is based on a canonical parameterization of the CG distribution, which allows for posterior inference of parameters indexing the (marginal) distributions of continuous and categorical variables, as well as expressing the interactions between the two types of variables. We derive the limiting Gaussian distributions, centered on the correct unknown value and with vanishing variance, for the Bayesian estimators of the canonical parameters expressing continuous, discrete and mixed interactions. In addition, we implement the proposed method for structure learning purposes, namely to infer the underlying graph of conditional independencies. When compared to alternative frequentist methods, our approach shows favorable results both in a simulation setting and in real-data applications, besides allowing for a coherent uncertainty quantification around parameter estimates
Joint structure learning and causal effect estimation for categorical graphical models
The scope of this paper is a multivariate setting involving categorical variables. Following an external manipulation of one variable, the goal is to evaluate the causal effect on an outcome of interest. A typical scenario involves a system of variables representing lifestyle, physical and mental features, symptoms, and risk factors, with the outcome being the presence or absence of a disease. These variables are interconnected in complex ways, allowing the effect of an intervention to propagate through multiple paths. A distinctive feature of our approach is the estimation of causal effects while accounting for uncertainty in both the dependence structure, which we represent through a directed acyclic graph (DAG), and the DAG-model parameters. Specifically, we propose a Markov chain Monte Carlo algorithm that targets the joint posterior over DAGs and parameters, based on an efficient reversible-jump proposal scheme. We validate our method through extensive simulation studies and demonstrate that it outperforms current state-of-the-art procedures in terms of estimation accuracy. Finally, we apply our methodology to analyze a dataset on depression and anxiety in undergraduate students
Going Beyond Counting First Authors in Author Co-citation Analysis
The present study examines one of the fundamental aspects of author co-citation analysis (ACA) - the way co-citation
counts are defined. Co-citation counting provides the data on which all subsequent statistical analyses and mappings
are based, and we compare ACA results based on two different types of co-citation counting - the traditional type that
only counts the first one among a cited work's authors on the one hand and a non-traditional type that takes into
account the first 5 authors of a cited work on the other hand. Results indicate that the picture produced through this non-traditional author co-citation counting contains more coherent author groups and is therefore considerably clearer. However, this picture represents fewer specialties in the research field being studied than that produced through the traditional first-author co-citation counting when the same number of top-ranked authors is selected and analyzed. Reasons for these effects are discussed
Variations on the Author
“Variations on the Author” discusses two of Eduardo Coutinho’s recent films (Um Dia na Vida, from 2010, and Últimas Conversas, posthumously released in 2015) and their contribution to the general question of documentary authorship. The director’s filmography is characterized by a consistent yet self-effacing form of authorial self-inscription: Coutinho often features as an interviewer that rather than express opinions propels discourses; an interviewer that is good at listening. This mode of self-inscription characterizes him as an author who is not expressive but who is nonetheless markedly present on the screen. In Um Dia na Vida, however, Coutinho is completely absent form the image, while Últimas Conversas, on the contrary, includes a confessional prologue that moves the director from the margins to the center of his films. This article examines the ways in which these works stand out in the filmography of a director who offers new insights into the notion of cinematic authorship
Appropriate Similarity Measures for Author Cocitation Analysis
We provide a number of new insights into the methodological discussion about author cocitation analysis. We first argue that the use of the Pearson correlation for measuring the similarity between authors’ cocitation profiles is not very satisfactory. We then discuss what kind of similarity measures may be used as an alternative to the Pearson correlation. We consider three similarity measures in particular. One is the well-known cosine. The other two similarity measures have not been used before in the bibliometric literature. Finally, we show by means of an example that our findings have a high practical relevance.information science;Pearson correlation;cosine;similarity measure;author cocitation analysis
Bayesian learning of multiple essential graphs
L’apprendimento strutturale di modelli grafici e` un approccio consolidato all’identificazione di dipendenze complesse in reti biologiche. Presentiamo qui una metodologia bayesiana per l’apprendimento di reti orientate da dati osservazionali quando si osservino sottogruppi distinti di una popolazione.Structural learning of graphical models is a well-established approach to the identification of complex dependencies in biological networks. We here present a Bayesian methodology for learning directed networks from observational data when distinct subgroups of a population are observed
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