Developing a system for advanced monitoring and intelligent drug administration in critical care units using ontologies

Selected paper of the 16th International Conference on Knowledge-Based and Intelligent Information & Engineering Systems, 2012 September 10-12, San Sebastian, Spain[Abstract] When a patient enters an intensive care unit (ICU), either after surgery or due to a serious clinical condition, his vital signs are continually changing, forcing the medical experts to make rapid and complex decisions, which frequently imply modifications on the dosage of drugs being administered. Life of patients at critical units depends largely on the wisdom of such decisions. However, the human factor is sometimes a source of mistakes that lead to incorrect or inaccurate actions. This work presents an expert system based on a domain ontology that acquires the vital parameters from the patient monitor, analyzes them and provides the expert with a recommendation regarding the treatment that should be administered. If the expert agrees, the system modifies the drug infusion rates being supplied at the infusion pumps in order to improve the patient's physiological status. The system is being developed at the IMEDIR Center (A Coruña, Spain) and it is being tested at the cardiac intensive care unit (CICU) of the Meixoeiro Hospital (Vigo, Spain), which is a specific type of ICU exclusively aimed to treat patients who have underwent heart surgery or that are affected by a serious coronary disorder.Instituto de Salud Carlos III; FIS-PI10/02180Programa Iberoamericano de Ciencia y Tecnología para el Desarrollo; ref. 209RT0366Galicia. Consellería de Cultura, Educación e Ordenación Universitaria; CN2012/217Galicia. Consellería de Cultura, Educación e Ordenación Universitaria; CN2011/034Galcia. Consellería de Cultura, Educación e Ordenación Universitaria; CN2012/21

Local matching learning of large scale biomedical ontologies

Les larges ontologies biomédicales décrivent généralement le même domaine d'intérêt, mais en utilisant des modèles de modélisation et des vocabulaires différents. Aligner ces ontologies qui sont complexes et hétérogènes est une tâche fastidieuse. Les systèmes de matching doivent fournir des résultats de haute qualité en tenant compte de la grande taille de ces ressources. Les systèmes de matching d'ontologies doivent résoudre deux problèmes: (i) intégrer la grande taille d'ontologies, (ii) automatiser le processus d'alignement. Le matching d'ontologies est une tâche difficile en raison de la large taille des ontologies. Les systèmes de matching d'ontologies combinent différents types de matcher pour résoudre ces problèmes. Les principaux problèmes de l'alignement de larges ontologies biomédicales sont: l'hétérogénéité conceptuelle, l'espace de recherche élevé et la qualité réduite des alignements résultants. Les systèmes d'alignement d'ontologies combinent différents matchers afin de réduire l'hétérogénéité. Cette combinaison devrait définir le choix des matchers à combiner et le poids. Différents matchers traitent différents types d'hétérogénéité. Par conséquent, le paramétrage d'un matcher devrait être automatisé par les systèmes d'alignement d'ontologies afin d'obtenir une bonne qualité de correspondance. Nous avons proposé une approche appele "local matching learning" pour faire face à la fois à la grande taille des ontologies et au problème de l'automatisation. Nous divisons un gros problème d'alignement en un ensemble de problèmes d'alignement locaux plus petits. Chaque problème d'alignement local est indépendamment aligné par une approche d'apprentissage automatique. Nous réduisons l'énorme espace de recherche en un ensemble de taches de recherche de corresondances locales plus petites. Nous pouvons aligner efficacement chaque tache de recherche de corresondances locale pour obtenir une meilleure qualité de correspondance. Notre approche de partitionnement se base sur une nouvelle stratégie à découpes multiples générant des partitions non volumineuses et non isolées. Par conséquence, nous pouvons surmonter le problème de l'hétérogénéité conceptuelle. Le nouvel algorithme de partitionnement est basé sur le clustering hiérarchique par agglomération (CHA). Cette approche génère un ensemble de tâches de correspondance locale avec un taux de couverture suffisant avec aucune partition isolée. Chaque tâche d'alignement local est automatiquement alignée en se basant sur les techniques d'apprentissage automatique. Un classificateur local aligne une seule tâche d'alignement local. Les classificateurs locaux sont basés sur des features élémentaires et structurelles. L'attribut class de chaque set de donne d'apprentissage " training set" est automatiquement étiqueté à l'aide d'une base de connaissances externe. Nous avons appliqué une technique de sélection de features pour chaque classificateur local afin de sélectionner les matchers appropriés pour chaque tâche d'alignement local. Cette approche réduit la complexité d'alignement et augmente la précision globale par rapport aux méthodes d'apprentissage traditionnelles. Nous avons prouvé que l'approche de partitionnement est meilleure que les approches actuelles en terme de précision, de taux de couverture et d'absence de partitions isolées. Nous avons évalué l'approche d'apprentissage d'alignement local à l'aide de diverses expériences basées sur des jeux de données d'OAEI 2018. Nous avons déduit qu'il est avantageux de diviser une grande tâche d'alignement d'ontologies en un ensemble de tâches d'alignement locaux. L'espace de recherche est réduit, ce qui réduit le nombre de faux négatifs et de faux positifs. L'application de techniques de sélection de caractéristiques à chaque classificateur local augmente la valeur de rappel pour chaque tâche d'alignement local.Although a considerable body of research work has addressed the problem of ontology matching, few studies have tackled the large ontologies used in the biomedical domain. We introduce a fully automated local matching learning approach that breaks down a large ontology matching task into a set of independent local sub-matching tasks. This approach integrates a novel partitioning algorithm as well as a set of matching learning techniques. The partitioning method is based on hierarchical clustering and does not generate isolated partitions. The matching learning approach employs different techniques: (i) local matching tasks are independently and automatically aligned using their local classifiers, which are based on local training sets built from element level and structure level features, (ii) resampling techniques are used to balance each local training set, and (iii) feature selection techniques are used to automatically select the appropriate tuning parameters for each local matching context. Our local matching learning approach generates a set of combined alignments from each local matching task, and experiments show that a multiple local classifier approach outperforms conventional, state-of-the-art approaches: these use a single classifier for the whole ontology matching task. In addition, focusing on context-aware local training sets based on local feature selection and resampling techniques significantly enhances the obtained results

Doctor of Philosophy

dissertationOver 40 years ago, the first computer simulation of a protein was reported: the atomic motions of a 58 amino acid protein were simulated for few picoseconds. With today's supercomputers, simulations of large biomolecular systems with hundreds of thousands of atoms can reach biologically significant timescales. Through dynamics information biomolecular simulations can provide new insights into molecular structure and function to support the development of new drugs or therapies. While the recent advances in high-performance computing hardware and computational methods have enabled scientists to run longer simulations, they also created new challenges for data management. Investigators need to use local and national resources to run these simulations and store their output, which can reach terabytes of data on disk. Because of the wide variety of computational methods and software packages available to the community, no standard data representation has been established to describe the computational protocol and the output of these simulations, preventing data sharing and collaboration. Data exchange is also limited due to the lack of repositories and tools to summarize, index, and search biomolecular simulation datasets. In this dissertation a common data model for biomolecular simulations is proposed to guide the design of future databases and APIs. The data model was then extended to a controlled vocabulary that can be used in the context of the semantic web. Two different approaches to data management are also proposed. The iBIOMES repository offers a distributed environment where input and output files are indexed via common data elements. The repository includes a dynamic web interface to summarize, visualize, search, and download published data. A simpler tool, iBIOMES Lite, was developed to generate summaries of datasets hosted at remote sites where user privileges and/or IT resources might be limited. These two informatics-based approaches to data management offer new means for the community to keep track of distributed and heterogeneous biomolecular simulation data and create collaborative networks

STRUCTURAL AND LEXICAL METHODS FOR AUDITING BIOMEDICAL TERMINOLOGIES

Biomedical terminologies serve as knowledge sources for a wide variety of biomedical applications including information extraction and retrieval, data integration and management, and decision support. Quality issues of biomedical terminologies, if not addressed, could affect all downstream applications that use them as knowledge sources. Therefore, Terminology Quality Assurance (TQA) has become an integral part of the terminology management lifecycle. However, identification of potential quality issues is challenging due to the ever-growing size and complexity of biomedical terminologies. It is time-consuming and labor-intensive to manually audit them and hence, automated TQA methods are highly desirable. In this dissertation, systematic and scalable methods to audit biomedical terminologies utilizing their structural as well as lexical information are proposed. Two inference-based methods, two non-lattice-based methods and a deep learning-based method are developed to identify potentially missing hierarchical (or is-a) relations, erroneous is-a relations, and missing concepts in biomedical terminologies including the Gene Ontology (GO), the National Cancer Institute thesaurus (NCIt), and SNOMED CT. In the first inference-based method, the GO concept names are represented using set-of-words model and sequence-of-words model, respectively. Inconsistencies derived between hierarchical linked and unlinked concept pairs are leveraged to detect potentially missing or erroneous is-a relations. The set-of-words model detects a total of 5,359 potential inconsistencies in the 03/28/2017 release of GO and the sequence-of-words model detects 4,959. Domain experts’ evaluation shows that the set-of-words model achieves a precision of 53.78% (128 out of 238) and the sequence-of-words model achieves a precision of 57.55% (122 out of 212) in identifying inconsistencies. In the second inference-based method, a Subsumption-based Sub-term Inference Framework (SSIF) is developed by introducing a novel term-algebra on top of a sequence-based representation of GO concepts. The sequence-based representation utilizes the part of speech of concept names, sub-concepts (concept names appearing inside another concept name), and antonyms appearing in concept names. Three conditional rules (monotonicity, intersection, and sub-concept rules) are developed for backward subsumption inference. Applying SSIF to the 10/03/2018 release of GO suggests 1,938 potentially missing is-a relations. Domain experts’ evaluation of randomly selected 210 potentially missing is-a relations shows that SSIF achieves a precision of 60.61%, 60.49%, and 46.03% for the monotonicity, intersection, and sub-concept rules, respectively. In the first non-lattice-based method, lexical patterns of concepts in Non-Lattice Subgraphs (NLSs: graph fragments with a higher tendency to contain quality issues), are mined to detect potentially missing is-a relations and missing concepts in NCIt. Six lexical patterns: containment, union, intersection, union-intersection, inference-contradiction, and inference-union are leveraged. Each pattern indicates a potential specific type of error and suggests a potential type of remediation. This method identifies 809 NLSs exhibiting these patterns in the 16.12d version of NCIt, achieving a precision of 66% (33 out of 50). In the second non-lattice-based method, enriched lexical attributes from concept ancestors are leveraged to identify potentially missing is-a relations in NLSs. The lexical attributes of a concept are inherited in two ways: from ancestors within the NLS, and from all the ancestors. For a pair of concepts without a hierarchical relation, if the lexical attributes of one concept is a subset of that of the other, a potentially missing is-a relation between the two concepts is suggested. This method identifies a total of 1,022 potentially missing is-a relations in the 19.01d release of NCIt with a precision of 84.44% (76 out of 90) for inheriting lexical attributes from ancestors within the NLS and 89.02% (73 out of 82) for inheriting from all the ancestors. For the non-lattice-based methods, similar NLSs may contain similar quality issues, and thus exhaustive examination of NLSs would involve redundant work. A hybrid method is introduced to identify similar NLSs to avoid redundant analyses. Given an input NLS, a graph isomorphism algorithm is used to obtain its structurally identical NLSs. A similarity score between the input NLS and each of its structurally identical NLSs is computed based on semantic similarity between their corresponding concept names. To compute the similarity between concept names, the concept names are converted to vectors using the Doc2Vec document embedding model and then the cosine similarity of the two vectors is computed. All the structurally identical NLSs with a similarity score above 0.85 is considered to be similar to the input NLS. Applying this method to 10 different structures of NLSs in the 02/12/2018 release of GO reveals that 38.43% of these NLSs have at least one similar NLS. Finally, a deep learning-based method is explored to facilitate the suggestion of missing is-a relations in NCIt and SNOMED CT. Concept pairs exhibiting a containment pattern is the focus here. The problem is framed as a binary classification task, where given a pair of concepts, the deep learning model learns to predict whether the two concepts have an is-a relation or not. Positive training samples are existing is-a relations in the terminology exhibiting containment pattern. Negative training samples are concept-pairs without is-a relations that are also exhibiting containment pattern. A graph neural network model is constructed for this task and trained with subgraphs generated enclosing the pairs of concepts in the samples. To evaluate each model trained by the two terminologies, two evaluation sets are created considering newer releases of each terminology as a partial reference standard. The model trained on NCIt achieves a precision of 0.5, a recall of 0.75, and an F1 score of 0.6. The model trained on SNOMED CT achieves a precision of 0.51, a recall of 0.64 and an F1 score of 0.56

An ontology-based approach for modelling and querying Alzheimer’s disease data

Background The recent advances in biotechnology and computer science have led to an ever-increasing availability of public biomedical data distributed in large databases worldwide. However, these data collections are far from being "standardized" so to be harmonized or even integrated, making it impossible to fully exploit the latest machine learning technologies for the analysis of data themselves. Hence, facing this huge flow of biomedical data is a challenging task for researchers and clinicians due to their complexity and high heterogeneity. This is the case of neurodegenerative diseases and the Alzheimer's Disease (AD) in whose context specialized data collections such as the one by the Alzheimer's Disease Neuroimaging Initiative (ADNI) are maintained.Methods Ontologies are controlled vocabularies that allow the semantics of data and their relationships in a given domain to be represented. They are often exploited to aid knowledge and data management in healthcare research. Computational Ontologies are the result of the combination of data management systems and traditional ontologies. Our approach is i) to define a computational ontology representing a logic-based formal conceptual model of the ADNI data collection and ii) to provide a means for populating the ontology with the actual data in the Alzheimer Disease Neuroimaging Initiative (ADNI). These two components make it possible to semantically query the ADNI database in order to support data extraction in a more intuitive manner.Results We developed: i) a detailed computational ontology for clinical multimodal datasets from the ADNI repository in order to simplify the access to these data; ii) a means for populating this ontology with the actual ADNI data. Such computational ontology immediately makes it possible to facilitate complex queries to the ADNI files, obtaining new diagnostic knowledge about Alzheimer's disease.Conclusions The proposed ontology will improve the access to the ADNI dataset, allowing queries to extract multivariate datasets to perform multidimensional and longitudinal statistical analyses. Moreover, the proposed ontology can be a candidate for supporting the design and implementation of new information systems for the collection and management of AD data and metadata, and for being a reference point for harmonizing or integrating data residing in different sources

OM-2017: Proceedings of the Twelfth International Workshop on Ontology Matching

shvaiko2017aInternational audienceOntology matching is a key interoperability enabler for the semantic web, as well as auseful tactic in some classical data integration tasks dealing with the semantic heterogeneityproblem. It takes ontologies as input and determines as output an alignment,that is, a set of correspondences between the semantically related entities of those ontologies.These correspondences can be used for various tasks, such as ontology merging,data translation, query answering or navigation on the web of data. Thus, matchingontologies enables the knowledge and data expressed with the matched ontologies tointeroperate

Ontology Matching: OM-2018: Proceedings of the ISWC Workshop

International audienceno abstrac

A framework for analyzing changes in health care lexicons and nomenclatures

Ontologies play a crucial role in current web-based biomedical applications for capturing contextual knowledge in the domain of life sciences. Many of the so-called bio-ontologies and controlled vocabularies are known to be seriously defective from both terminological and ontological perspectives, and do not sufficiently comply with the standards to be considered formai ontologies. Therefore, they are continuously evolving in order to fix the problems and provide valid knowledge. Moreover, many problems in ontology evolution often originate from incomplete knowledge about the given domain. As our knowledge improves, the related definitions in the ontologies will be altered. This problem is inadequately addressed by available tools and algorithms, mostly due to the lack of suitable knowledge representation formalisms to deal with temporal abstract notations, and the overreliance on human factors. Also most of the current approaches have been focused on changes within the internal structure of ontologies, and interactions with other existing ontologies have been widely neglected. In this research, alter revealing and classifying some of the common alterations in a number of popular biomedical ontologies, we present a novel agent-based framework, RLR (Represent, Legitimate, and Reproduce), to semi-automatically manage the evolution of bio-ontologies, with emphasis on the FungalWeb Ontology, with minimal human intervention. RLR assists and guides ontology engineers through the change management process in general, and aids in tracking and representing the changes, particularly through the use of category theory. Category theory has been used as a mathematical vehicle for modeling changes in ontologies and representing agents' interactions, independent of any specific choice of ontology language or particular implementation. We have also employed rule-based hierarchical graph transformation techniques to propose a more specific semantics for analyzing ontological changes and transformations between different versions of an ontology, as well as tracking the effects of a change in different levels of abstractions. Thus, the RLR framework enables one to manage changes in ontologies, not as standalone artifacts in isolation, but in contact with other ontologies in an openly distributed semantic web environment. The emphasis upon the generality and abstractness makes RLR more feasible in the multi-disciplinary domain of biomedical Ontology change management

The Foundational Model of Anatomy Ontology

Anatomy is the structure of biological organisms. The term also denotes the scientific discipline devoted to the study of anatomical entities and the structural and developmental relations that obtain among these entities during the lifespan of an organism. Anatomical entities are the independent continuants of biomedical reality on which physiological and disease processes depend, and which, in response to etiological agents, can transform themselves into pathological entities. For these reasons, hard copy and in silico information resources in virtually all fields of biology and medicine, as a rule, make extensive reference to anatomical entities. Because of the lack of a generalizable, computable representation of anatomy, developers of computable terminologies and ontologies in clinical medicine and biomedical research represented anatomy from their own more or less divergent viewpoints. The resulting heterogeneity presents a formidable impediment to correlating human anatomy not only across computational resources but also with the anatomy of model organisms used in biomedical experimentation. The Foundational Model of Anatomy (FMA) is being developed to fill the need for a generalizable anatomy ontology, which can be used and adapted by any computer-based application that requires anatomical information. Moreover it is evolving into a standard reference for divergent views of anatomy and a template for representing the anatomy of animals. A distinction is made between the FMA ontology as a theory of anatomy and the implementation of this theory as the FMA artifact. In either sense of the term, the FMA is a spatial-structural ontology of the entities and relations which together form the phenotypic structure of the human organism at all biologically salient levels of granularity. Making use of explicit ontological principles and sound methods, it is designed to be understandable by human beings and navigable by computers. The FMA’s ontological structure provides for machine-based inference, enabling powerful computational tools of the future to reason with biomedical data