Above are papers related to the following paper: [Paper_ID] Paper #10531. 	[Title] Using Dirichlet Mixture Priors to Derive Hidden Markov Models for Protein Families [Abstract] A Bayesian method for estimating the amino acid distributions in the states of a hidden Markov model (HMM) for a protein family or the columns of a multiple alignment of that family is introduced. This method uses Dirichlet mixture densities as priors over amino acid distributions. These mixture densities are determined from examination of previously constructed HMMs or multiple alignments. It is shown that this Bayesian method can improve the quality of HMMs produced from small training sets. Specific experiments on the EF-hand motif are reported, for which these priors are shown to produce HMMs with higher likelihood on unseen data, and fewer false positives and false negatives in a database search task. Please summarise all the given information.

Above are papers related to the following paper: [Paper_ID] Paper #1135746. 	[Title] Learning Markov chains with variable memory length from noisy output [Abstract] The problem of modeling complicated data sequences, such as DNA or speech, often arises in practice. Most of the algorithms select a hypothesis from within a model class assuming that the observed sequence is the direct output of the underlying generation process. In this paper we consider the case when the output passes through a memoryless noisy channel before observation. In particular, we show that in the class of Markov chains with variable memory length, learning is affected by factors, which, despite being super-polynomial, are still small in some practical cases. Markov models with variable memory length, or probabilistic finite suffix automata, were introduced in learning theory by Ron, Singer and Tishby who also described a polynomial time learning algorithm [11, 12]. We present a modification of the algorithm which uses a noise-corrupted sample and has knowledge of the noise structure. The same algorithm is still viable if the noise is not known exactly but a good estimation is available. Finally, some experimental results are presented for removing noise from corrupted English text, and to measure how the performance of the learning algorithm is affected by the size of the noisy sample and the noise rate. Please summarise all the given information.

Above are papers related to the following paper: [Paper_ID] Paper #1102850. 	[Title] Optimal Alignments in Linear Space using Automaton-derived Cost Functions (Extended Abstract) Submitted to CPM'96 [Abstract] In a previous paper [SM95], we showed how finite automata could be used to define objective functions for assessing the quality of an alignment of two (or more) sequences. In this paper, we show some results of using such cost functions. We also show how to extend Hischberg's linear space algorithm [Hir75] to this setting, thus generalizing a result of Myers and Miller [MM88b]. Please summarise all the given information.

Above are papers related to the following paper: [Paper_ID] Paper #12165. 	[Title] The Power of Team Exploration: Two Robots Can Learn Unlabeled Directed Graphs [Abstract] We show that two cooperating robots can learn exactly any strongly-connected directed graph with n indistinguishable nodes in expected time polynomial in n. We introduce a new type of homing sequence for two robots, which helps the robots recognize certain previously-seen nodes. We then present an algorithm in which the robots learn the graph and the homing sequence simultaneously by actively wandering through the graph. Unlike most previous learning results using homing sequences, our algorithm does not require a teacher to provide counterexamples. Furthermore, the algorithm can use efficiently any additional information available that distinguishes nodes. We also present an algorithm in which the robots learn by taking random walks. The rate at which a random walk on a graph converges to the stationary distribution is characterized by the conductance of the graph. Our random-walk algorithm learns in expected time polynomial in n and in the inverse of the conductance and is more efficient than the homing-sequence algorithm for high-conductance graphs. Please summarise all the given information.

Above are papers related to the following paper: [Paper_ID] Paper #1152904. 	[Title] GIBBS-MARKOV MODELS [Abstract] In this paper we present a framework for building probabilistic automata parameterized by context-dependent probabilities. Gibbs distributions are used to model state transitions and output generation, and parameter estimation is carried out using an EM algorithm where the M-step uses a generalized iterative scaling procedure. We discuss relations with certain classes of stochastic feedforward neural networks, a geometric interpretation for parameter estimation, and a simple example of a statistical language model constructed using this methodology. Please summarise all the given information.

Above are papers related to the following paper: [Paper_ID] Paper #1129608. 	[Title] A New Look at Tree Models for Multiple Sequence Alignment [Abstract] Evolutionary trees are frequently used as the underlying model in the design of algorithms, optimization criteria and software packages for multiple sequence alignment (MSA). In this paper, we reexamine the suitability of trees as a universal model for MSA in light of the broad range of biological questions that MSA's are used to address. A tree model consists of a tree topology and a model of accepted mutations along the branches. After surveying the major applications of MSA, examples from the molecular biology literature are used to illustrate situations in which this tree model fails. This occurs when the relationship between residues in a column cannot be described by a tree; for example, in some structural and functional applications of MSA. It also occurs in situations, such as lateral gene transfer, where an entire gene cannot be modeled by a unique tree. In cases of nonparsimonous data or convergent evolution, it may be difficult to find a consistent mutational model. We hope that this survey will promote dialogue between biologists and computer scientists, leading to more biologically realistic research on MSA. Please summarise all the given information.

Above are papers related to the following paper: [Paper_ID] Paper #1130634. 	[Title] Protein Secondary Structure Modelling with Probabilistic Networks (Extended Abstract) [Abstract] In this paper we study the performance of probabilistic networks in the context of protein sequence analysis in molecular biology. Specifically, we report the results of our initial experiments applying this framework to the problem of protein secondary structure prediction. One of the main advantages of the probabilistic approach we describe here is our ability to perform detailed experiments where we can experiment with different models. We can easily perform local substitutions (mutations) and measure (probabilistically) their effect on the global structure. Window-based methods do not support such experimentation as readily. Our method is efficient both during training and during prediction, which is important in order to be able to perform many experiments with different networks. We believe that probabilistic methods are comparable to other methods in prediction quality. In addition, the predictions generated by our methods have precise quantitative semantics which is not shared by other classification methods. Specifically, all the causal and statistical independence assumptions are made explicit in our networks thereby allowing biologists to study and experiment with different causal models in a convenient manner. Please summarise all the given information.

Above are papers related to the following paper: [Paper_ID] Paper #36620. 	[Title] Towards a Better Understanding of Memory-Based Reasoning Systems [Abstract] We quantify both experimentally and analytically the performance of memory-based reasoning (MBR) algorithms. To start gaining insight into the capabilities of MBR algorithms, we compare an MBR algorithm using a value difference metric to a popular Bayesian classifier. These two approaches are similar in that they both make certain independence assumptions about the data. However, whereas MBR uses specific cases to perform classification, Bayesian methods summarize the data probabilistically. We demonstrate that a particular MBR system called Pebls works comparatively well on a wide range of domains using both real and artificial data. With respect to the artificial data, we consider distributions where the concept classes are separated by functional discriminants, as well as time-series data generated by Markov models of varying complexity. Finally, we show formally that Pebls can learn (in the limit) natural concept classes that the Bayesian classifier cannot learn, and that it will attain perfect accuracy whenever Please summarise all the given information.

Above are papers related to the following paper: [Paper_ID] Paper #1152272. 	[Title] GIBBS-MARKOV MODELS [Abstract] In this paper we present a framework for building probabilistic automata parameterized by context-dependent probabilities. Gibbs distributions are used to model state transitions and output generation, and parameter estimation is carried out using an EM algorithm where the M-step uses a generalized iterative scaling procedure. We discuss relations with certain classes of stochastic feedforward neural networks, a geometric interpretation for parameter estimation, and a simple example of a statistical language model constructed using this methodology. Please summarise all the given information.

Above are papers related to the following paper: [Paper_ID] Paper #3220. 	[Title] A Weighted Nearest Neighbor Algorithm for Learning with Symbolic Features [Abstract] In the past, nearest neighbor algorithms for learning from examples have worked best in domains in which all features had numeric values. In such domains, the examples can be treated as points and distance metrics can use standard definitions. In symbolic domains, a more sophisticated treatment of the feature space is required. We introduce a nearest neighbor algorithm for learning in domains with symbolic features. Our algorithm calculates distance tables that allow it to produce real-valued distances between instances, and attaches weights to the instances to further modify the structure of feature space. We show that this technique produces excellent classification accuracy on three problems that have been studied by machine learning researchers: predicting protein secondary structure, identifying DNA promoter sequences, and pronouncing English text. Direct experimental comparisons with the other learning algorithms show that our nearest neighbor algorithm is comparable or superior in all three domains. In addition, our algorithm has advantages in training speed, simplicity, and perspicuity. We conclude that experimental evidence favors the use and continued development of nearest neighbor algorithms for domains such as the ones studied here. Please summarise all the given information.

Above are papers related to the following paper: [Paper_ID] Paper #1152162. 	[Title] GIBBS-MARKOV MODELS [Abstract] In this paper we present a framework for building probabilistic automata parameterized by context-dependent probabilities. Gibbs distributions are used to model state transitions and output generation, and parameter estimation is carried out using an EM algorithm where the M-step uses a generalized iterative scaling procedure. We discuss relations with certain classes of stochastic feedforward neural networks, a geometric interpretation for parameter estimation, and a simple example of a statistical language model constructed using this methodology. Please summarise all the given information.

Above are papers related to the following paper: [Paper_ID] Paper #12195. 	[Title] Efficient Learning of Typical Finite Automata from Random Walks (Extended Abstract) [Abstract] This paper describes new and efficient algorithms for learning deterministic finite automata. Our approach is primarily distinguished by two features: (1) the adoption of an average-case setting to model the "typical" labeling of a finite automaton, while retaining a worst-case model for the underlying graph of the automaton, along with (2) a learning model in which the learner is not provided with the means to experiment with the machine, but rather must learn solely by observing the automaton's output behavior on a random input sequence. The main contribution of this paper is in presenting the first efficient algorithms for learning non-trivial classes of automata in an entirely passive learning model. We adopt an on-line learning model in which the learner is asked to predict the output of the next state, given the next symbol of the random input sequence; the goal of the learner is to make as few prediction mistakes as possible. Assuming the learner has a means of resetting the target machine to a fixed start state, we first present an efficient algorithm that makes an expected polynomial number of mistakes in this model. Next, we show how this first algorithm can be used as a subroutine by a second algorithm that also makes a polynomial number of mistakes even in the absence of a reset. Along the way, we prove a number of combinatorial results for randomly labeled automata. We also show that the labeling of the states and the bits of the input sequence need not be truly random, but merely semi-random. Finally, we discuss an extension of our results to a model in which automata are used to represent distributions over binary strings. Please summarise all the given information.

Above are papers related to the following paper: [Paper_ID] Paper #3240. 	[Title] An Analysis of Bayesian Classifiers (1988), involves the formulation of average-case models for specific algorithms [Abstract] In this paper we present an average-case analysis of the Bayesian classifier, a simple induction algorithm that fares remarkably well on many learning tasks. Our analysis assumes a monotone conjunctive target concept, and independent, noise-free Boolean attributes. We calculate the probability that the algorithm will induce an arbitrary pair of concept descriptions and then use this to compute the probability of correct classification over the instance space. The analysis takes into account the number of training instances, the number of attributes, the distribution of these attributes, and the level of class noise. We also explore the behavioral implications of the analysis by presenting predicted learning curves for artificial domains, and give experimental results on these domains as a check on our reasoning. One goal of research in machine learning is to discover principles that relate algorithms and domain characteristics to behavior. To this end, many researchers have carried out systematic experimentation with natural and artificial domains in search of empirical regularities (e.g., Kibler & Langley, 1988). Others have focused on theoretical analyses, often within the paradigm of probably approximately correct learning (e.g., Haus-sler, 1990). However, most experimental studies are based only on informal analyses of the learning task, whereas most formal analyses address the worst case, and thus bear little relation to empirical results. ber of attributes, and the class and attribute frequencies, they obtain predictions about the behavior of induction algorithms and used experiments to check their analyses. 1 However, their research does not focus on algorithms typically used by the experimental and practical sides of machine learning, and it is important that average-case analyses be extended to such methods. Recently, there has been growing interest in probabilistic approaches to inductive learning. For example, Fisher (1987) has described Cobweb, an incremental algorithm for conceptual clustering that draws heavily on Bayesian ideas, and the literature reports a number of systems that build on this work (e.g., Allen & Lang-ley, 1990; Iba & Gennari, 1991; Thompson & Langley, 1991). Cheeseman et al. (1988) have outlined Auto-Class, a nonincremental system that uses Bayesian methods to cluster instances into groups, and other researchers have focused on the induction of Bayesian inference networks (e.g., Cooper & Kerskovits, 1991). These recent Bayesian learning algorithms are complex and not easily amenable to analysis, but they share a common ancestor that is simpler and more tractable. This supervised algorithm, which we refer to simply as a Bayesian classifier, comes originally from work in pattern recognition (Duda & Hart, 1973). The method stores a probabilistic summary for each class; this summary contains the conditional probability of each attribute value given the class, as well as the probability (or base rate) of the class. This data structure approximates the representational power of a perceptron; it describes a single decision boundary through the instance space. When the algorithm encounters a new instance, it updates the probabilities stored with the specified class. Neither the order of training instances nor the occurrence of classification errors have any effect on this process. When given a test instance, the classifier uses an evaluation function (which we describe in detail later) to rank the alter Please summarise all the given information.

Above are papers related to the following paper: [Paper_ID] Paper #43698. 	[Title] Dirichlet Mixtures: A Method for Improving Detection of Weak but Significant Protein Sequence Homology [Abstract] UCSC Technical Report UCSC-CRL-96-09 Abstract This paper presents the mathematical foundations of Dirichlet mixtures, which have been used to improve database search results for homologous sequences, when a variable number of sequences from a protein family or domain are known. We present a method for condensing the information in a protein database into a mixture of Dirichlet densities. These mixtures are designed to be combined with observed amino acid frequencies, to form estimates of expected amino acid probabilities at each position in a profile, hidden Markov model, or other statistical model. These estimates give a statistical model greater generalization capacity, such that remotely related family members can be more reliably recognized by the model. Dirichlet mixtures have been shown to outperform substitution matrices and other methods for computing these expected amino acid distributions in database search, resulting in fewer false positives and false negatives for the families tested. This paper corrects a previously published formula for estimating these expected probabilities, and contains complete derivations of the Dirichlet mixture formulas, methods for optimizing the mixtures to match particular databases, and suggestions for efficient implementation. Please summarise all the given information.

Above are papers related to the following paper: [Paper_ID] Paper #189620. 	[Title] Logarithmic-Time Updates and Queries in Probabilistic Networks [Abstract] Traditional databases commonly support efficient query and update procedures that operate in time which is sublinear in the size of the database. Our goal in this paper is to take a first step toward dynamic reasoning in probabilistic databases with comparable efficiency. We propose a dynamic data structure that supports efficient algorithms for updating and querying singly connected Bayesian networks. In the conventional algorithm, new evidence is absorbed in time O(1) and queries are processed in time O(N ), where N is the size of the network. We propose an algorithm which, after a preprocessing phase, allows us to answer queries in time O(log N ) at the expense of O(log N ) time per evidence absorption. The usefulness of sub-linear processing time manifests itself in applications requiring (near) real-time response over large probabilistic databases. We briefly discuss a potential application of dynamic probabilistic reasoning in computational biology. Please summarise all the given information.

Above are papers related to the following paper: [Paper_ID] Paper #31927. 	[Title] A Generalized Hidden Markov Model for the Recognition of Human Genes in DNA [Abstract] We present a statistical model of genes in DNA. A Generalized Hidden Markov Model (GHMM) provides the framework for describing the grammar of a legal parse of a DNA sequence (Stormo & Haussler 1994). Probabilities are assigned to transitions between states in the GHMM and to the generation of each nucleotide base given a particular state. Machine learning techniques are applied to optimize these probabilities using a standardized training set. Given a new candidate sequence, the best parse is deduced from the model using a dynamic programming algorithm to identify the path through the model with maximum probability. The GHMM is flexible and modular, so new sensors and additional states can be inserted easily. In addition, it provides simple solutions for integrating cardinality constraints, reading frame constraints, "indels", and homology searching. The description and results of an implementation of such a gene-finding model, called Genie, is presented. The exon sensor is a codon frequency model conditioned on windowed nucleotide frequency and the preceding codon. Two neural networks are used, as in (Brunak, Engelbrecht, & Knudsen 1991), for splice site prediction. We show that this simple model performs quite well. For a cross-validated standard test set of 304 genes [ftp://www-hgc.lbl.gov/pub/genesets] in human DNA, our gene-finding system identified up to 85% of protein-coding bases correctly with a specificity of 80%. 58% of exons were exactly identified with a specificity of 51%. Genie is shown to perform favorably compared with several other gene-finding systems. Please summarise all the given information.

Above are papers related to the following paper: [Paper_ID] Paper #194617. 	[Title] Finding Genes in DNA with a Hidden Markov Model [Abstract] This study describes a new Hidden Markov Model (HMM) system for segmenting uncharacterized genomic DNA sequences into exons, introns, and intergenic regions. Separate HMM modules were designed and trained for specific regions of DNA: exons, introns, intergenic regions, and splice sites. The models were then tied together to form a biologically feasible topology. The integrated HMM was trained further on a set of eukaryotic DNA sequences, and tested by using it to segment a separate set of sequences. The resulting HMM system, which is called VEIL (Viterbi Exon-Intron Locator), obtains an overall accuracy on test data of 92% of total bases correctly labelled, with a correlation coefficient of 0.73. Using the more stringent test of exact exon prediction, VEIL correctly located both ends of 53% of the coding exons, and 49% of the exons it predicts are exactly correct. These results compare favorably to the best previous results for gene structure prediction, and demonstrate the benefits of using HMMs for this problem. Please summarise all the given information.

Above are papers related to the following paper: [Paper_ID] Paper #31932. 	[Title] A Decision Tree System for Finding Genes in DNA [Abstract] MORGAN is an integrated system for finding genes in vertebrate DNA sequences. MORGAN uses a variety of techniques to accomplish this task, the most distinctive of which is a decision tree classifier. The decision tree system is combined with new methods for identifying start codons, donor sites, and acceptor sites, and these are brought together in a frame-sensitive dynamic programming algorithm that finds the optimal segmentation of a DNA sequence into coding and noncoding regions (exons and introns). The optimal segmentation is dependent on a separate scoring function that takes a subsequence and assigns to it a score reflecting the probability that the sequence is an exon. The scoring functions in MORGAN are sets of decision trees that are combined to give a probability estimate. Experimental results on a database of 570 vertebrate DNA sequences show that MORGAN has excellent performance by many different measures. On a separate test set, it achieves an overall accuracy of 95%, with a correlation coefficient of 0.78 and a sensitivity and specificity for coding bases of 83% and 79%. In addition, MORGAN identifies 58% of coding exons exactly; i.e., both the beginning and end of the coding regions are predicted correctly. This paper describes the MORGAN system, including its decision tree routines and the algorithms for site recognition, and its performance on a benchmark database of vertebrate DNA. Please summarise all the given information.

Above are papers related to the following paper: [Paper_ID] Paper #686532. 	[Title] Homology Detection via Family Pairwise Search a straightforward generalization of pairwise sequence comparison algorithms to [Abstract] The function of an unknown biological sequence can often be accurately inferred by identifying sequences homologous to the original sequence. Given a query set of known homologs, there exist at least three general classes of techniques for finding additional homologs: pairwise sequence comparisons, motif analysis, and hidden Markov modeling. Pairwise sequence comparisons are typically employed when only a single query sequence is known. Hidden Markov models (HMMs), on the other hand, are usually trained with sets of more than 100 sequences. Motif-based methods fall in between these two extremes. Please summarise all the given information.

Above are papers related to the following paper: [Paper_ID] Paper #12238. 	[Title] Exactly Learning Automata with Small Cover Time [Abstract] We present algorithms for exactly learning unknown environments that can be described by deterministic finite automata. The learner performs a walk on the target automaton, where at each step it observes the output of the state it is at, and chooses a labeled edge to traverse to the next state. We assume that the learner has no means of a reset, and we also assume that the learner does not have access to a teacher that answers equivalence queries and gives the learner counterexamples to its hypotheses. We present two algorithms, one assumes that the outputs observed by the learner are always correct and the other assumes that the outputs might be erroneous. The running times of both algorithms are polynomial in the cover time of the underlying graph of the target automaton. Please summarise all the given information.

Above are papers related to the following paper: [Paper_ID] Paper #39130. 	[Title] Average-Case Analysis of a Nearest Neighbor Algorithm [Abstract] In this paper we present an average-case analysis of the nearest neighbor algorithm, a simple induction method that has been studied by many researchers. Our analysis assumes a conjunctive target concept, noise-free Boolean attributes, and a uniform distribution over the instance space. We calculate the probability that the algorithm will encounter a test instance that is distance d from the prototype of the concept, along with the probability that the nearest stored training case is distance e from this test instance. From this we compute the probability of correct classification as a function of the number of observed training cases, the number of relevant attributes, and the number of irrelevant attributes. We also explore the behavioral implications of the analysis by presenting predicted learning curves for artificial domains, and give experimental results on these domains as a check on our reasoning. Please summarise all the given information.

Above are papers related to the following paper: [Paper_ID] Paper #1063773. 	[Title] A Gentle Guide to Multiple Alignment Version Please send comments, critique, flames and praise Instructions [Abstract] Prerequisites. An understanding of the dynamic programming (edit distance) approach to pairwise sequence alignment is useful for parts 1.3, 1.4, and 2. Also, familiarity with the use of Internet resources would be helpful for part 3. For the former, see Chapters 1.1 - 1.3, and for the latter, see Chapter 2 of the Hypertext Book of the GNA-VSNS Biocomputing Course at http://www.techfak.uni-bielefeld.de/bcd/Curric/welcome.html. General Rationale. You will understand why Multiple Alignment is considered a challenging problem, you will study approaches that try to reduce the number of steps needed to calculate the optimal solution, and you will study fast heuristics. In a case study involving immunoglobulin sequences, you will study multiple alignments obtained from WWW servers, recapitulating results from an original paper. Revision History. Version 1.01 on 17 Sep 1995. Expanded Ex.9. Updated Ex.46. Revised Solution Sheet -re- Ex.3+12. Marked more Exercises by "A" (to be submitted to the Instructor). Various minor clarifications in content Please summarise all the given information.

Above are papers related to the following paper: [Paper_ID] Paper #686559. 	[Title] Parameterization studies for the SAM and HMMER methods of hidden Markov model generation [Abstract] Multiple sequence alignment of distantly related viral proteins remains a challenge to all currently available alignment methods. The hidden Markov model approach offers a new, flexible method for the generation of multiple sequence alignments. The results of studies attempting to infer appropriate parameter constraints for the generation of de novo HMMs for globin, kinase, aspartic acid protease, and ribonuclease H sequences by both the SAM and HMMER methods are described. Please summarise all the given information.

Above are papers related to the following paper: [Paper_ID] Paper #1129442. 	[Title] Minimum-Risk Profiles of Protein Families Based on Statistical Decision Theory [Abstract] Statistical decision theory provides a principled way to estimate amino acid frequencies in conserved positions of a protein family. The goal is to minimize the risk function, or the expected squared-error distance between the estimates and the true population frequencies. The minimum-risk estimates are obtained by adding an optimal number of pseudocounts to the observed data. Two formulas are presented, one for pseudocounts based on marginal amino acid frequencies and one for pseudocounts based on the observed data. Experimental results show that profiles constructed using minimal-risk estimates are more discriminating than those constructed using existing methods. Please summarise all the given information.

Above are papers related to the following paper: [Paper_ID] Paper #286562. 	[Title] Hidden Markov Model Analysis of Motifs in Steroid Dehydrogenases and their Homologs [Abstract]  Please summarise all the given information.

Above are papers related to the following paper: [Paper_ID] Paper #1129572. 	[Title] Non-Deterministic, Constraint-Based Parsing of Human Genes [Abstract]  Please summarise all the given information.

Above are papers related to the following paper: [Paper_ID] Paper #120039. 	[Title] EXPLORING A FRAMEWORK FOR INSTANCE BASED LEARNING AND NAIVE BAYESIAN CLASSIFIERS [Abstract] The relative performance of different methods for classifier learning varies across domains. Some recent Instance Based Learning (IBL) methods, such as IB1-MVDM* 10 , use similarity measures based on conditional class probabilities. These probabilities are a key component of Naive Bayes methods. Given this commonality of approach, it is of interest to consider how the differences between the two methods are linked to their relative performance in different domains. Here we interpret Naive Bayes in an IBL like framework, identifying differences between Naive Bayes and IB1-MVDM* in this framework. Experiments on variants of IB1-MVDM* that lie between it and Naive Bayes in the framework are conducted on sixteen domains. The results strongly suggest that the relative performance of Naive Bayes and IB1-MVDM* is linked to the extent to which each class can be satisfactorily represented by a single instance in the IBL framework. However, this is not the only factor that appears significant. Please summarise all the given information.

Above are papers related to the following paper: [Paper_ID] Paper #215912. 	[Title] A Method for Identifying Splice Sites and Translational Start Sites in [Abstract] This paper describes a new method for determining the consensus sequences that signal the start of translation and the boundaries between exons and introns (donor and acceptor sites) in eukaryotic mRNA. The method takes into account the dependencies between adjacent bases, in contrast to the usual technique of considering each position independently. When coupled with a dynamic program to compute the most likely sequence, new consensus sequences emerge. The consensus sequence information is summarized in conditional probability matrices which, when used to locate signals in uncharacter-ized genomic DNA, have greater sensitivity and specificity than conventional matrices. Species-specific versions of these matrices are especially effective at distinguishing true and false sites. Please summarise all the given information.

Above are papers related to the following paper: [Paper_ID] Paper #31336. 	[Title] The megaprior heuristic for discovering protein sequence patterns [Abstract] Several computer algorithms for discovering patterns in groups of protein sequences are in use that are based on fitting the parameters of a statistical model to a group of related sequences. These include hidden Markov model (HMM) algorithms for multiple sequence alignment, and the MEME and Gibbs sampler algorithms for discovering motifs. These algorithms are sometimes prone to producing models that are incorrect because two or more patterns have been combined. The statistical model produced in this situation is a convex combination (weighted average) of two or more different models. This paper presents a solution to the problem of convex combinations in the form of a heuristic based on using extremely low variance Dirichlet mixture priors as part of the statistical model. This heuristic, which we call the megaprior heuristic, increases the strength (i.e., decreases the variance) of the prior in proportion to the size of the sequence dataset. This causes each column in the final model to strongly resemble the mean of a single component of the prior, regardless of the size of the dataset. We describe the cause of the convex combination problem, analyze it mathematically, motivate and describe the implementation of the megaprior heuristic, and show how it can effectively eliminate the problem of convex combinations in protein sequence pattern discovery. Please summarise all the given information.

Above are papers related to the following paper: [Paper_ID] Paper #1124844. 	[Title] Stochastic Decomposition of DNA Sequences Using Hidden Markov Models [Abstract] This work presents an application of a machine learning for characterizing an important property of natural DNA sequences compositional inhomogeneity. Compositional segments often correspond to meaningful biological units. Taking into account such inhomogeneity is a prerequisite of successful recognition of functional features in DNA sequences, especially, protein-coding genes. Here we present a technique for DNA segmentation using hidden Markov models. A DNA sequence is represented by a chain of homogeneous segments, each described by one of a few statistically discriminated hidden states, whose contents form a first-order Markov chain. The technique is used to describe and compare chromosomes I and IV of the completely sequenced Saccharomyces cerevisiae (yeast) genome. Our results indicate the existence of a few well separated states, which gives support to the isochore theory. We also explore the model's likelihood landscape and analyze the dynamics of the optimization process, thus addressing the problem of reliability of the obtained optima and efficiency of the algorithms. Please summarise all the given information.

Above are papers related to the following paper: [Paper_ID] Paper #1128430. 	[Title] On Reasoning from Data [Abstract]  Please summarise all the given information.

Above are papers related to the following paper: [Paper_ID] Paper #1107567. 	[Title] Learning Algorithms with Applications to Robot Navigation and Protein Folding [Abstract]  Please summarise all the given information.

Above are papers related to the following paper: [Paper_ID] Paper #31349. 	[Title] Meta-MEME: Motif-based Hidden Markov Models of Protein Families [Abstract]  Please summarise all the given information.

Above are papers related to the following paper: [Paper_ID] Paper #1123576. 	[Title] Density Networks and their Application to Protein Modelling [Abstract] I define a latent variable model in the form of a neural network for which only target outputs are specified; the inputs are unspecified. Although the inputs are missing, it is still possible to train this model by placing a simple probability distribution on the unknown inputs and maximizing the probability of the data given the parameters. The model can then discover for itself a description of the data in terms of an underlying latent variable space of lower dimensionality. I present preliminary results of the application of these models to protein data. Please summarise all the given information.

Above are papers related to the following paper: [Paper_ID] Paper #31353. 	[Title] Hidden Markov Models in Computational Biology: Applications to Protein Modeling UCSC-CRL-93-32 Keywords: Hidden Markov Models, [Abstract] Hidden Markov Models (HMMs) are applied to the problems of statistical modeling, database searching and multiple sequence alignment of protein families and protein domains. These methods are demonstrated on the globin family, the protein kinase catalytic domain, and the EF-hand calcium binding motif. In each case the parameters of an HMM are estimated from a training set of unaligned sequences. After the HMM is built, it is used to obtain a multiple alignment of all the training sequences. It is also used to search the SWISS-PROT 22 database for other sequences that are members of the given protein family, or contain the given domain. The HMM produces multiple alignments of good quality that agree closely with the alignments produced by programs that incorporate three-dimensional structural information. When employed in discrimination tests (by examining how closely the sequences in a database fit the globin, kinase and EF-hand HMMs), the HMM is able to distinguish members of these families from non-members with a high degree of accuracy. Both the HMM and PRO-FILESEARCH (a technique used to search for relationships between a protein sequence and multiply aligned sequences) perform better in these tests than PROSITE (a dictionary of sites and patterns in proteins). The HMM appears to have a slight advantage Please summarise all the given information.

Paper #10531 has the title `Using Dirichlet Mixture Priors to Derive Hidden Markov Models for Protein Families  
` and the abstract `A Bayesian method for estimating the amino acid distributions in the states of a hidden Markov model (HMM) for a protein family or the columns of a multiple alignment of that family is introduced. This method uses Dirichlet mixture densities as priors over amino acid distributions. These mixture densities are determined from examination of previously constructed HMMs or multiple alignments. It is shown that this Bayesian method can improve the quality of HMMs produced from small training sets. Specific experiments on the EF-hand motif are reported, for which these priors are shown to produce HMMs with higher likelihood on unseen data, and fewer false positives and false negatives in a database search task. 
`.
Question: Which category should Paper #10531 be classified as ?
You can select one from ['Neural_Networks', 'Case_Based', 'Theory', 'Reinforcement_Learning', 'Probabilistic_Methods', 'Rule_Learning', 'Genetic_Algorithms'].


Paper #10531 has the title `Using Dirichlet Mixture Priors to Derive Hidden Markov Models for Protein Families  
` and the abstract `A Bayesian method for estimating the amino acid distributions in the states of a hidden Markov model (HMM) for a protein family or the columns of a multiple alignment of that family is introduced. This method uses Dirichlet mixture densities as priors over amino acid distributions. These mixture densities are determined from examination of previously constructed HMMs or multiple alignments. It is shown that this Bayesian method can improve the quality of HMMs produced from small training sets. Specific experiments on the EF-hand motif are reported, for which these priors are shown to produce HMMs with higher likelihood on unseen data, and fewer false positives and false negatives in a database search task. 
`.
Question: Which category should Paper #10531 be classified as ?
You can select one from ['Neural_Networks', 'Case_Based', 'Theory', 'Reinforcement_Learning', 'Probabilistic_Methods', 'Rule_Learning', 'Genetic_Algorithms'].

This paper should be classified into: Neural_Networks