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Träfflista för sökning "WFRF:(Koski Timo) "

Sökning: WFRF:(Koski Timo)

  • Resultat 1-10 av 96
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1.
  • Armerin, Fredrik, 1971-, et al. (författare)
  • Forecasting Ranking in Harness Racing Using Probabilities Induced by Expected Positions
  • 2019
  • Ingår i: Applied Artificial Intelligence. - : TAYLOR & FRANCIS INC. - 0883-9514 .- 1087-6545. ; 33:2, s. 171-189
  • Tidskriftsartikel (refereegranskat)abstract
    • Ranked events are pivotal in many important AI-applications such as Question Answering and recommendations systems. This paper studies ranked events in the setting of harness racing. For each horse there exists a probability distribution over its possible rankings. In the paper, it is shown that a set of expected positions (and more generally, higher moments) for the horses induces this probability distribution. The main contribution of the paper is a method, which extracts this induced probability distribution from a set of expected positions. An algorithm is proposed where the extraction of the induced distribution is given by the estimated expectations. MATLAB code is provided for the methodology. This approach gives freedom to model the horses in many different ways without the restrictions imposed by for instance logistic regression. To illustrate this point, we employ a neural network and ordinary ridge regression. The method is applied to predicting the distribution of the finishing positions for horses in harness racing. It outperforms both multinomial logistic regression and the market odds. The ease of use combined with fine results from the suggested approach constitutes a relevant addition to the increasingly important field of ranked events.
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2.
  • Austin, Brian, et al. (författare)
  • Sliding window discretization : A new method for multiple band matching of bacterial genotyping fingerprints
  • 2004
  • Ingår i: Bulletin of Mathematical Biology. - : Springer Science and Business Media LLC. - 0092-8240 .- 1522-9602. ; 66:6, s. 1575-1596
  • Tidskriftsartikel (refereegranskat)abstract
    • Microbiologists have traditionally applied hierarchical clustering algorithms as their mathematical tool of choice to unravel the taxonomic relationships between micro-organisms. However, the interpretation of such hierarchical classifications suffers from being subjective, in that a variety of ad hoc choices must be made during their construction. On the other hand, the application of more profound and objective mathematical methods - such as the minimization of stochastic complexity - for the classification of bacterial genotyping fingerprints data is hampered by the prerequisite that such methods only act upon vectorized data. In this paper we introduce a new method, coined sliding window discretization, for the transformation of genotypic fingerprint patterns into binary vector format. In the context of an extensive amplified fragment length polymorphism (AFLP) data set of 507 strains from the Vibrionaceae family that has previously been analysed, we demonstrate by comparison with a number of other discretization methods that this new discretization method results in minimal loss of the original information content captured in the banding patterns. Finally, we investigate the implications of the different discretization methods on the classification of bacterial genotyping fingerprints by minimization of stochastic complexity, as it is implemented in the BinClass software package for probabilistic clustering of binary vectors. The new taxonomic insights learned from the resulting classification of the AFLP patterns will prove the value of combining sliding window discretization with minimization of stochastic complexity, as an alternative classification algorithm for bacterial genotyping fingerprints.
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3.
  • Berglund, Daniel, et al. (författare)
  • Measures of Additive Interactionand Effect Direction
  • Annan publikation (övrigt vetenskapligt/konstnärligt)abstract
    • Measures for additive interaction are defined using risk ratios. These ratios need to be modeled so that all combinations of the exposures are harmful, as the scale between protective and harmful factors differs. This remodeling is referred to as recoding. Previously, recoding has been thought of as random. In this paper, we will examine and discuss the impact of recoding in studies with small effect sizes, such as genome wide association studies, and the impact recoding has on significance testing.
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4.
  • Berglund, Daniel (författare)
  • Models for Additive and Sufficient Cause Interaction
  • 2019
  • Licentiatavhandling (övrigt vetenskapligt/konstnärligt)abstract
    • The aim of this thesis is to develop and explore models in, and related to, the sufficient cause framework, and additive interaction. Additive interaction is closely connected with public health interventions and can be used to make inferences about the sufficient causes in order to find the mechanisms behind an outcome, for instance a disease.In paper A we extend the additive interaction, and interventions, to include continuous exposures. We show that there does not exist a model that does not lead to inconsistent conclusions about the interaction.The sufficient cause framework can also be expressed using Boolean functions, which is expanded upon in paper B. In this paper we define a new model based on the multifactor potential outcome model (MFPO) and independence of causal influence models (ICI).In paper C we discuss the modeling and estimation of additive interaction in relation to if the exposures are harmful or protective conditioned on some other exposure. If there is uncertainty about the effects direction there can be errors in the testing of the interaction effect.
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5.
  • Berglund, Daniel, et al. (författare)
  • On Probabilistic Multifactor Potential Outcome Models
  • Annan publikation (övrigt vetenskapligt/konstnärligt)abstract
    • The sufficient cause framework describes how sets of sufficient causes are responsible for causing some event or outcome. It is known that it is closely connected with Boolean functions. In this paper we define this relation formally, and show how it can be used together with Fourier expansion of the Boolean functions to lead to new insights. The main result is a probibalistic version of the multifactor potential outcome model based on independence of causal influence models and Bayesian networks.
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6.
  • Berglund, Daniel, et al. (författare)
  • On the Existence of Suitable Models for Additive Interaction with Continuous Exposures
  • Annan publikation (övrigt vetenskapligt/konstnärligt)abstract
    • Additive interaction can be of importance for public health interventions and it is commonly defined using binary exposures. There has been expansions of the models to also include continuous exposures, which could lead to better and more precise estimations of the effect of interventions. In this paper we define the intervention for a continuous exposure as a monotonic function. Based on this function for the interventions we prove that there is no model for estimating additive interactions with continuous exposures for which it holds that; (i) both exposures have marginal effects and no additive interaction on the exposure level for both exposures, (ii) neither exposure has marginal effect and there is additive interaction between the exposures. We also show that a logistic regression model for continuous exposures will always produce additive interaction if both exposures have marginal effects.
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7.
  • Corander, Jukka, et al. (författare)
  • A bayesian random fragment insertion model for de novo detection of DNA regulatory binding regions
  • 2007
  • Annan publikation (övrigt vetenskapligt/konstnärligt)abstract
    • Identification of regulatory binding motifs within DNA sequences is a commonly occurring problem in computationnl bioinformatics. A wide variety of statistical approaches have been proposed in the literature to either scan for previously known motif types or to attempt de novo identification of a fixed number (typically one) of putative motifs. Most approaches assume the existence of reliable biodatabasc information to build probabilistic a priori description of the motif classes. No method has been previously proposed for finding the number of putative de novo motif types and their positions within a set of DNA sequences. As the number of sequenced genomes from a wide variety of organisms is constantly increasing, there is a clear need for such methods. Here we introduce a Bayesian unsupervised approach for this purpose by using recent advances in the theory of predictive classification and Markov chain Monte Carlo computation. Our modelling framework enables formal statistical inference in a large-scale sequence screening and we illustrate it by a set of examples.
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8.
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9.
  • Corander, Jukka, et al. (författare)
  • Bayesian Block-Diagonal Predictive Classifier for Gaussian Data
  • 2013
  • Ingår i: Synergies of Soft Computing and Statistics for Intelligent Data Analysis. - Berlin, Heidelberg : Springer Berlin/Heidelberg. - 9783642330414 - 9783642330421 ; , s. 543-551
  • Bokkapitel (refereegranskat)abstract
    • The paper presents a method for constructing Bayesian predictive classifier in a high-dimensional setting. Given that classes are represented by Gaussian distributions with block-structured covariance matrix, a closed form expression for the posterior predictive distribution of the data is established. Due to factorization of this distribution, the resulting Bayesian predictive and marginal classifier provides an efficient solution to the high-dimensional problem by splitting it into smaller tractable problems. In a simulation study we show that the suggested classifier outperforms several alternative algorithms such as linear discriminant analysis based on block-wise inverse covariance estimators and the shrunken centroids regularized discriminant analysis.
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10.
  • Corander, Jukka, et al. (författare)
  • Bayesian model learning based on a parallel MCMC strategy
  • 2006
  • Ingår i: Statistics and computing. - : Springer Science and Business Media LLC. - 0960-3174 .- 1573-1375. ; 16:4, s. 355-362
  • Tidskriftsartikel (refereegranskat)abstract
    • We introduce a novel Markov chain Monte Carlo algorithm for estimation of posterior probabilities over discrete model spaces. Our learning approach is applicable to families of models for which the marginal likelihood can be analytically calculated, either exactly or approximately, given any fixed structure. It is argued that for certain model neighborhood structures, the ordinary reversible Metropolis-Hastings algorithm does not yield an appropriate solution to the estimation problem. Therefore, we develop an alternative, non-reversible algorithm which can avoid the scaling effect of the neighborhood. To efficiently explore a model space, a finite number of interacting parallel stochastic processes is utilized. Our interaction scheme enables exploration of several local neighborhoods of a model space simultaneously, while it prevents the absorption of any particular process to a relatively inferior state. We illustrate the advantages of our method by an application to a classification model. In particular, we use an extensive bacterial database and compare our results with results obtained by different methods for the same data.
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