34,216 research outputs found
Chi-square-based scoring function for categorization of MEDLINE citations
Objectives: Text categorization has been used in biomedical informatics for
identifying documents containing relevant topics of interest. We developed a
simple method that uses a chi-square-based scoring function to determine the
likelihood of MEDLINE citations containing genetic relevant topic. Methods: Our
procedure requires construction of a genetic and a nongenetic domain document
corpus. We used MeSH descriptors assigned to MEDLINE citations for this
categorization task. We compared frequencies of MeSH descriptors between two
corpora applying chi-square test. A MeSH descriptor was considered to be a
positive indicator if its relative observed frequency in the genetic domain
corpus was greater than its relative observed frequency in the nongenetic
domain corpus. The output of the proposed method is a list of scores for all
the citations, with the highest score given to those citations containing MeSH
descriptors typical for the genetic domain. Results: Validation was done on a
set of 734 manually annotated MEDLINE citations. It achieved predictive
accuracy of 0.87 with 0.69 recall and 0.64 precision. We evaluated the method
by comparing it to three machine learning algorithms (support vector machines,
decision trees, na\"ive Bayes). Although the differences were not statistically
significantly different, results showed that our chi-square scoring performs as
good as compared machine learning algorithms. Conclusions: We suggest that the
chi-square scoring is an effective solution to help categorize MEDLINE
citations. The algorithm is implemented in the BITOLA literature-based
discovery support system as a preprocessor for gene symbol disambiguation
process.Comment: 34 pages, 2 figure
Using Neural Networks for Relation Extraction from Biomedical Literature
Using different sources of information to support automated extracting of
relations between biomedical concepts contributes to the development of our
understanding of biological systems. The primary comprehensive source of these
relations is biomedical literature. Several relation extraction approaches have
been proposed to identify relations between concepts in biomedical literature,
namely, using neural networks algorithms. The use of multichannel architectures
composed of multiple data representations, as in deep neural networks, is
leading to state-of-the-art results. The right combination of data
representations can eventually lead us to even higher evaluation scores in
relation extraction tasks. Thus, biomedical ontologies play a fundamental role
by providing semantic and ancestry information about an entity. The
incorporation of biomedical ontologies has already been proved to enhance
previous state-of-the-art results.Comment: Artificial Neural Networks book (Springer) - Chapter 1
Mining Images in Biomedical Publications: Detection and Analysis of Gel Diagrams
Authors of biomedical publications use gel images to report experimental
results such as protein-protein interactions or protein expressions under
different conditions. Gel images offer a concise way to communicate such
findings, not all of which need to be explicitly discussed in the article text.
This fact together with the abundance of gel images and their shared common
patterns makes them prime candidates for automated image mining and parsing. We
introduce an approach for the detection of gel images, and present a workflow
to analyze them. We are able to detect gel segments and panels at high
accuracy, and present preliminary results for the identification of gene names
in these images. While we cannot provide a complete solution at this point, we
present evidence that this kind of image mining is feasible.Comment: arXiv admin note: substantial text overlap with arXiv:1209.148
Extraction of Transcript Diversity from Scientific Literature
Transcript diversity generated by alternative splicing and associated mechanisms contributes heavily to the functional complexity of biological systems. The numerous examples of the mechanisms and functional implications of these events are scattered throughout the scientific literature. Thus, it is crucial to have a tool that can automatically extract the relevant facts and collect them in a knowledge base that can aid the interpretation of data from high-throughput methods. We have developed and applied a composite text-mining method for extracting information on transcript diversity from the entire MEDLINE database in order to create a database of genes with alternative transcripts. It contains information on tissue specificity, number of isoforms, causative mechanisms, functional implications, and experimental methods used for detection. We have mined this resource to identify 959 instances of tissue-specific splicing. Our results in combination with those from EST-based methods suggest that alternative splicing is the preferred mechanism for generating transcript diversity in the nervous system. We provide new annotations for 1,860 genes with the potential for generating transcript diversity. We assign the MeSH term “alternative splicing” to 1,536 additional abstracts in the MEDLINE database and suggest new MeSH terms for other events. We have successfully extracted information about transcript diversity and semiautomatically generated a database, LSAT, that can provide a quantitative understanding of the mechanisms behind tissue-specific gene expression. LSAT (Literature Support for Alternative Transcripts) is publicly available at http://www.bork.embl.de/LSAT/
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