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Jasmin Saric

Bio: Jasmin Saric is an academic researcher from Boehringer Ingelheim. The author has contributed to research in topics: Information extraction & Ontology (information science). The author has an hindex of 12, co-authored 17 publications receiving 1209 citations.

Papers
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Journal ArticleDOI
TL;DR: This work states that literature mining is also becoming useful for both hypothesis generation and biological discovery, however, the latter will require the integration of literature and high-throughput data, which should encourage close collaborations between biologists and computational linguists.
Abstract: For the average biologist, hands-on literature mining currently means a keyword search in PubMed. However, methods for extracting biomedical facts from the scientific literature have improved considerably, and the associated tools will probably soon be used in many laboratories to automatically annotate and analyse the growing number of system-wide experimental data sets. Owing to the increasing body of text and the open-access policies of many journals, literature mining is also becoming useful for both hypothesis generation and biological discovery. However, the latter will require the integration of literature and high-throughput data, which should encourage close collaborations between biologists and computational linguists.

661 citations

Journal ArticleDOI
TL;DR: An organism-specific resource of gene/protein names considerably larger than those used in most other biology related information extraction approaches is made use, to capture both new types of linguistic constructs as well as new type of biological information.
Abstract: Motivation: We have previously developed a rule-based approach for extracting information on the regulation of gene expression in yeast. The biomedical literature, however, contains information on several other equally important regulatory mechanisms, in particular phosphorylation, which we now expanded for our rule-based system also to extract. Results: This paper presents new results for extraction of relational information from biomedical text. We have improved our system, STRING-IE, to capture both new types of linguistic constructs as well as new types of biological information [i.e. (de-)phosphorylation]. The precision remains stable with a slight increase in recall. From almost one million PubMed abstracts related to four model organisms, we manage to extract regulatory networks and binary phosphorylations comprising 3319 relation chunks. The accuracy is 83--90% and 86--95% for gene expression and (de-)phosphorylation relations, respectively. To achieve this, we made use of an organism-specific resource of gene/protein names considerably larger than those used in most other biology related information extraction approaches. These names were included in the lexicon when retraining the part-of-speech (POS) tagger on the GENIA corpus. For the domain in question, an accuracy of 96.4% was attained on POS tags. It should be noted that the rules were developed for yeast and successfully applied to both abstracts and full-text articles related to other organisms with comparable accuracy. Availability: The revised GENIA corpus, the POS tagger, the extraction rules and the full sets of extracted relations are available from http://www.bork.embl.de/Docu/STRING-IE Contact: [email protected]

158 citations

Proceedings Article
30 Jul 2005
TL;DR: An in-depth analysis of the output of the system shows that the model is accurate and has good potentials for text mining and ontology building applications.
Abstract: In this paper we present an unsupervised model for learning arbitrary relations between concepts of a molecular biology ontology for the purpose of supporting text mining and manual ontology building. Relations between named-entities are learned from the GENIA corpus by means of several standard natural language processing techniques. An in-depth analysis of the output of the system shows that the model is accurate and has good potentials for text mining and ontology building applications.

129 citations

Book ChapterDOI
20 Jul 2006
TL;DR: SABIO-RK is a curated database with information about biochemical reactions and their kinetic properties, which contains and merges information about reactions such as reactants and modifiers, organism, tissue and cellular location, as well as the kinetic properties of the reactions.
Abstract: Simulating networks of biochemical reactions require reliable kinetic data. In order to facilitate the access to such kinetic data we have developed SABIO-RK, a curated database with information about biochemical reactions and their kinetic properties. The data are manually extracted from literature and verified by curators, concerning standards, formats and controlled vocabularies. This process is supported by tools in a semi-automatic manner. SABIO-RK contains and merges information about reactions such as reactants and modifiers, organism, tissue and cellular location, as well as the kinetic properties of the reactions. The type of the kinetic mechanism, modes of inhibition or activation, and corresponding rate equations are presented together with their parameters and measured values, specifying the experimental conditions under which these were determined. Links to other databases enable the user to gather further information and to refer to the original publication. Information about reactions and their kinetic data can be exported to an SBML file, allowing users to employ the information as the basis for their simulation models.

69 citations

Journal ArticleDOI
01 Oct 2005
TL;DR: A novel approach to discourse analysis within information extraction systems that makes use of DRT as formal representation of the linguistic context as well as of a domain-specific ontology as a basis to compute conceptual relations between extracted events thus establishing discourse coherence.
Abstract: This paper presents a novel approach to discourse analysis within information extraction systems. It makes use of DRT as formal representation of the linguistic context as well as of a domain-specific ontology as a basis to compute conceptual relations between extracted events thus establishing discourse coherence. The approach has been implemented within GenIE, an information extraction system with the aim of extracting information about biochemical pathways, about sequences, structures and functions of genomes and proteins. The approach is evaluated against a semantically hand-annotated set of Swiss-Prot protein function descriptions and shows very promising results.

44 citations


Cited by
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Journal ArticleDOI
TL;DR: A basic taxonomy of feature selection techniques is provided, providing their use, variety and potential in a number of both common as well as upcoming bioinformatics applications.
Abstract: Feature selection techniques have become an apparent need in many bioinformatics applications. In addition to the large pool of techniques that have already been developed in the machine learning and data mining fields, specific applications in bioinformatics have led to a wealth of newly proposed techniques. In this article, we make the interested reader aware of the possibilities of feature selection, providing a basic taxonomy of feature selection techniques, and discussing their use, variety and potential in a number of both common as well as upcoming bioinformatics applications. Contact: yvan.saeys@psb.ugent.be Supplementary information: http://bioinformatics.psb.ugent.be/supplementary_data/yvsae/fsreview

4,706 citations

Journal ArticleDOI
TL;DR: The update to version 9.1 of STRING is described, introducing several improvements, including extending the automated mining of scientific texts for interaction information, to now also include full-text articles, and providing users with statistical information on any functional enrichment observed in their networks.
Abstract: Complete knowledge of all direct and indirect interactions between proteins in a given cell would represent an important milestone towards a comprehensive description of cellular mechanisms and functions. Although this goal is still elusive, considerable progress has been made-particularly for certain model organisms and functional systems. Currently, protein interactions and associations are annotated at various levels of detail in online resources, ranging from raw data repositories to highly formalized pathway databases. For many applications, a global view of all the available interaction data is desirable, including lower-quality data and/or computational predictions. The STRING database (http://string-db.org/) aims to provide such a global perspective for as many organisms as feasible. Known and predicted associations are scored and integrated, resulting in comprehensive protein networks covering >1100 organisms. Here, we describe the update to version 9.1 of STRING, introducing several improvements: (i) we extend the automated mining of scientific texts for interaction information, to now also include full-text articles; (ii) we entirely re-designed the algorithm for transferring interactions from one model organism to the other; and (iii) we provide users with statistical information on any functional enrichment observed in their networks.

3,900 citations

Journal ArticleDOI
TL;DR: This work has mapped reads from short RNA deep-sequencing experiments to microRNAs in miRBase and developed web interfaces to view these mappings, which can be used as a proxy for relative expression levels of microRNA sequences, provide detailed evidence for microRNA annotations and alternative isoforms of mature micro RNAs, and allow us to revisit previous annotations.
Abstract: miRBase is the primary online repository for all microRNA sequences and annotation. The current release (miRBase 16) contains over 15,000 microRNA gene loci in over 140 species, and over 17,000 distinct mature microRNA sequences. Deep-sequencing technologies have delivered a sharp rise in the rate of novel microRNA discovery. We have mapped reads from short RNA deep-sequencing experiments to microRNAs in miRBase and developed web interfaces to view these mappings. The user can view all read data associated with a given microRNA annotation, filter reads by experiment and count, and search for microRNAs by tissue- and stage-specific expression. These data can be used as a proxy for relative expression levels of microRNA sequences, provide detailed evidence for microRNA annotations and alternative isoforms of mature microRNAs, and allow us to revisit previous annotations. miRBase is available online at: http://www.mirbase.org/.

3,618 citations

Journal ArticleDOI
TL;DR: The most important new developments in STRING 8 over previous releases include a URL-based programming interface, improved interaction prediction via genomic neighborhood in prokaryotes, and the inclusion of protein structures.
Abstract: Functional partnerships between proteins are at the core of complex cellular phenotypes, and the networks formed by interacting proteins provide researchers with crucial scaffolds for modeling, data reduction and annotation. STRING is a database and web resource dedicated to protein–protein interactions, including both physical and functional interactions. It weights and integrates information from numerous sources, including experimental repositories, computational prediction methods and public text collections, thus acting as a metadatabase that maps all interaction evidence onto a common set of genomes and proteins. The most important new developments in STRING 8 over previous releases include a URL-based programming interface, which can be used to query STRING from other resources, improved interaction prediction via genomic neighborhood in prokaryotes, and the inclusion of protein structures. Version 8.0 of STRING covers about 2.5 million proteins from 630 organisms, providing the most comprehensive view on protein–protein interactions currently available. STRING can be reached at http://string-db.org/.

2,394 citations