## Pereira, Fernando C.N.

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Now showing 1 - 9 of 9

Publication Spanning Tree Methods for Discriminative Training of Dependency Parsers(2006-01-01) McDonald, Ryan; Crammer, Koby; Pereira, Fernando C.N.Untyped dependency parsing can be viewed as the problem of finding maximum spanning trees (MSTs) in directed graphs. Using this representation, the Eisner (1996) parsing algorithm is sufficient for searching the space of projective trees. More importantly, the representation is extended naturally to non-projective parsing using Chu-Liu-Edmonds (Chu and Liu, 1965; Edmonds, 1967) MST algorithm. These efficient parse search methods support large-margin discriminative training methods for learning dependency parsers. We evaluate these methods experimentally on the English and Czech treebanks.Publication Conditional Random Fields: Probabilistic Models for Segmenting and Labeling Sequence Data(2001-06-28) Lafferty, John; McCallum, Andrew; Pereira, Fernando C.N.We present conditional random fields, a framework for building probabilistic models to segment and label sequence data. Conditional random fields offer several advantages over hidden Markov models and stochastic grammars for such tasks, including the ability to relax strong independence assumptions made in those models. Conditional random fields also avoid a fundamental limitation of maximum entropy Markov models (MEMMs) and other discriminative Markov models based on directed graphical models, which can be biased towards states with few successor states. We present iterative parameter estimation algorithms for conditional random fields and compare the performance of the resulting models to HMMs and MEMMs on synthetic and natural-language data.Publication An Automated Procedure to Identify Biomedical Articles that Contain Cancer-associated Gene Variants(2006-09-01) McDonald, Ryan; Winters, Raymond Scott; Ankuda, Claire K; Murphy, Joan A; Rogers, Amy E; Pereira, Fernando C.N.; Greenblatt, Mark S; White, Peter SThe proliferation of biomedical literature makes it increasingly difficult for researchers to find and manage relevant information. However, identifying research articles containing mutation data, a requisite first step in integrating large and complex mutation data sets, is currently tedious, time-consuming and imprecise. More effective mechanisms for identifying articles containing mutation information would be beneficial both for the curation of mutation databases and for individual researchers. We developed an automated method that uses information extraction, classifier, and relevance ranking techniques to determine the likelihood of MEDLINE abstracts containing information regarding genomic variation data suitable for inclusion in mutation databases. We targeted the CDKN2A (p16) gene and the procedure for document identification currently used by CDKN2A Database curators as a measure of feasibility. A set of abstracts was manually identified from a MEDLINE search as potentially containing specific CDKN2A mutation events. A subset of these abstracts was used as a training set for a maximum entropy classifier to identify text features distinguishing "relevant" from "not relevant" abstracts. Each document was represented as a set of indicative word, word pair, and entity tagger-derived genomic variation features. When applied to a test set of 200 candidate abstracts, the classifier predicted 88 articles as being relevant; of these, 29 of 32 manuscripts in which manual curation found CDKN2A sequence variants were positively predicted. Thus, the set of potentially useful articles that a manual curator would have to review was reduced by 56%, maintaining 91% recall (sensitivity) and more than doubling precision (positive predictive value). Subsequent expansion of the training set to 494 articles yielded similar precision and recall rates, and comparison of the original and expanded trials demonstrated that the average precision improved with the larger data set. Our results show that automated systems can effectively identify article subsets relevant to a given task and may prove to be powerful tools for the broader research community. This procedure can be readily adapted to any or all genes, organisms, or sets of documents.Publication Identifying gene and protein mentions in text using conditional random fields(2005-05-24) McDonald, Ryan; Pereira, Fernando C.N.We present a model for tagging gene and protein mentions from text using the probabilistic sequence tagging framework of conditional random fields (CRFs). Conditional random fields model the probability P(t|o) of a tag sequence given an observation sequence directly, and have previously been employed successfully for other tagging tasks. The mechanics of CRFs and their relationship to maximum entropy are discussed in detail. We employ a diverse feature set containing standard orthographic features combined with expert features in the form of gene and biological term lexicons to achieve a precision of 86.4% and recall of 78.7%. An analysis of the contribution of the various features of the model is provided.Publication Global Discriminative Learning for Higher-Accuracy Computational Gene Prediction(2007-03-16) Bernal, Axel; Crammer, Koby; Hatzigeorgiou, Artemis; Pereira, Fernando C.N.Most ab initio gene predictors use a probabilistic sequence model, typically a hidden Markov model, to combine separately trained models of genomic signals and content. By combining separate models of relevant genomic features, such gene predictors can exploit small training sets and incomplete annotations, and can be trained fairly efficiently. However, that type of piecewise training does not optimize prediction accuracy and has difficulty in accounting for statistical dependencies among different parts of the gene model. With genomic information being created at an ever-increasing rate, it is worth investigating alternative approaches in which many different types of genomic evidence, with complex statistical dependencies, can be integrated by discriminative learning to maximize annotation accuracy. Among discriminative learning methods, large-margin classifiers have become prominent because of the success of support vector machines (SVM) in many classification tasks. We describe CRAIG, a new program for ab initio gene prediction based on a conditional random field model with semi-Markov structure that is trained with an online large-margin algorithm related to multiclass SVMs. Our experiments on benchmark vertebrate datasets and on regions from the ENCODE project show significant improvements in prediction accuracy over published gene predictors that use intrinsic features only, particularly at the gene level and on genes with long introns.Publication Hierarchical Distributed Representations for Statistical Language Modeling(2004-12-13) Blitzer, John; Saul, Lawrence K; Weinberger, Kilian Q; Pereira, Fernando C.N.Statistical language models estimate the probability of a word occurring in a given context. The most common language models rely on a discrete enumeration of predictive contexts (e.g., n-grams) and consequently fail to capture and exploit statistical regularities across these contexts. In this paper, we show how to learn hierarchical, distributed representations of word contexts that maximize the predictive value of a statistical language model. The representations are initialized by unsupervised algorithms for linear and nonlinear dimensionality reduction [14], then fed as input into a hierarchical mixture of experts, where each expert is a multinomial distribution over predicted words [12]. While the distributed representations in our model are inspired by the neural probabilistic language model of Bengio et al. [2, 3], our particular architecture enables us to work with significantly larger vocabularies and training corpora. For example, on a large-scale bigram modeling task involving a sixty thousand word vocabulary and a training corpus of three million sentences, we demonstrate consistent improvement over class-based bigram models [10, 13]. We also discuss extensions of our approach to longer multiword contexts.Publication Weighted Finite-State Transducers in Speech Recognition(2001-10-01) Mohri, Mehryar; Pereira, Fernando; Riley, MichaelWe survey the use of weighted finite-state transducers (WFSTs) in speech recognition. We show that WFSTs provide a common and natural representation for hidden Markov models (HMMs), context-dependency, pronunciation dictionaries, grammars, and alternative recognition outputs. Furthermore, general transducer operations combine these representations flexibly and efficiently. Weighted determinization and minimization algorithms optimize their time and space requirements, and a weight pushing algorithm distributes the weights along the paths of a weighted transducer optimally for speech recognition. As an example, we describe a North American Business News (NAB) recognition system built using these techniques that combines the HMMs, full cross-word triphones, a lexicon of 40 000 words, and a large trigram grammar into a single weighted transducer that is only somewhat larger than the trigram word grammar and that runs NAB in real-time on a very simple decoder. In another example, we show that the same techniques can be used to optimize lattices for second-pass recognition. In a third example, we show how general automata operations can be used to assemble lattices from different recognizers to improve recognition performance.Publication Automated Recognition of Malignancy Mentions in Biomedical Literature(2006-11-07) Jin, Yang; McDonald, Ryan T; Lerman, Kevin; Mandel, Mark A; Carroll, Steven; Liberman, Mark Y; Pereira, Fernando C.N.; Winters, Raymond S; White, Peter SThe rapid proliferation of biomedical text makes it increasingly difficult for researchers to identify, synthesize, and utilize developed knowledge in their fields of interest. Automated information extraction procedures can assist in the acquisition and management of this knowledge. Previous efforts in biomedical text mining have focused primarily upon named entity recognition of well-defined molecular objects such as genes, but less work has been performed to identify disease-related objects and concepts. Furthermore, promise has been tempered by an inability to efficiently scale approaches in ways that minimize manual efforts and still perform with high accuracy. Here, we have applied a machine-learning approach previously successful for identifying molecular entities to a disease concept to determine if the underlying probabilistic model effectively generalizes to unrelated concepts with minimal manual intervention for model retraining.Publication Case-Factor Diagrams for Structured Probabilistic Modeling(2004-07-07) McAllester, David; Collins, Michael; Pereira, Fernando C.N.We introduce a probabilistic formalism subsuming Markov random fields of bounded tree width and probabilistic context free grammars. Our models are based on a representation of Boolean formulas that we call case-factor diagrams (CFDs). CFDs are similar to binary decision diagrams (BDDs) but are concise for circuits of bounded tree width (unlike BDDs) and can concisely represent the set of parse trees over a given string under a given context free grammar (also unlike BDDs). A probabilistic model consists of a CFD defining a feasible set of Boolean assignments and a weight (or cost) for each individual Boolean variable. We give an inside-outside algorithm for simultaneously computing the marginal of each Boolean variable, and a Viterbi algorithm for finding the mininum cost variable assignment. Both algorithms run in time proportional to the size of the CFD.