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    Using varying negative examples to improve computational predictions of transcription factor binding sites

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    The identification of transcription factor binding sites (TFBSs) is a non-trivial problem as the existing computational predictors produce a lot of false predictions. Though it is proven that combining these predictions with a meta-classifier, like Support Vector Machines (SVMs), can improve the overall results, this improvement is not as significant as expected. The reason for this is that the predictors are not reliable for the negative examples from non-binding sites in the promoter region. Therefore, using negative examples from different sources during training an SVM can be one of the solutions to this problem. In this study, we used different types of negative examples during training the classifier. These negative examples can be far away from the promoter regions or produced by randomisation or from the intronic region of genes. By using these negative examples during training, we observed their effect in improving predictions of TFBSs in the yeast. We also used a modified cross-validation method for this type of problem. Thus we observed substantial improvement in the classifier performance that could constitute a model for predicting TFBSs. Therefore, the major contribution of the analysis is that for the yeast genome, the position of binding sites could be predicted with high confidence using our technique and the predictions are of much higher quality than the predictions of the original prediction algorithms.</p

    Improving transcription factor binding site predictions by using randomised negative examples

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    It is known that much of the genetic change underlying morphological evolution takes place in cis-regulatory regions, rather than in the coding regions of genes. Identifying these sites in a genome is a non-trivial problem. Experimental methods for finding binding sites exist with some limitations regarding their applicability, accuracy, availability or cost. On the other hand predicting algorithms perform rather poorly. The aim of this research is to develop and improve computational approaches for the prediction of transcription factor binding sites (TFBSs) by integrating the results of computational algorithms and other sources of complementary biological evidence, with particular emphasis on the use of the Support Vector Machine (SVM). Data from two organisms, yeast and mouse, were used in this study. The initial results were not particularly encouraging, as still giving predictions of low quality. However, when the vectors labelled as non-binding sites in the training set were replaced by randomised training vectors, a significant improvement in performance was observed. This gave substantial improvement over the yeast genome and even greater improvement for the mouse data. In fact the resulting classifier was finding over 80% of the binding sites in the test set and moreover 80% of the predictions were correct.</p

    Effect of using varying negative examples in transcription factor binding site predictions

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    Identifying transcription factor binding sites computationally is a hard problem as it produces many false predictions. Combining the predictions from existing predictors can improve the overall predictions by using classification methods like Support Vector Machines (SVM). But conventional negative examples (that is, example of non-binding sites) in this type of problem are highly unreliable. In this study, we have used different types of negative examples. One class of the negative examples has been taken from far away from the promoter regions, where the occurrence of binding sites is very low, and another one has been produced by randomization. Thus we observed the effect of using different negative examples in predicting transcription factor binding sites in mouse. We have also devised a novel cross-validation technique for this type of biological problem.</p

    Using randomised vectors in transcription factor binding site predictions

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    Finding the location of binding sites in DNA is a difficult problem. Although the location of some binding sites have been experimentally identified, other parts of the genome may or may not contain binding sites. This poses problems with negative data in a trainable classifier. Here we show that using randomized negative data gives a large boost in classifier performance when compared to the original labeled data.</p

    Going Beyond Counting First Authors in Author Co-citation Analysis

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    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

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    “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

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    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

    Dispelling the Myths Behind First-author Citation Counts

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    We conducted a full-scale evaluative citation analysis study of scholars in the XML research field to explore just how different from each other author rankings resulting from different citation counting methods actually are, and to demonstrate the capability of emerging data and tools on the Web in supporting more realistic citation counting methods. Our results contest some common arguments for the continued use of first-author citation counts in the evaluation of scholars, such as high correlations between author rankings by first-author citation counts and other citation counting methods, and high costs of using more realistic citation counting methods that are not well-supported by the ISI databases. It is argued that increasingly available digital full text research papers make it possible for citation analysis studies to go beyond what the ISI databases have directly supported and to employ more sophisticated methods
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