Towards knowledge-based gene expression data mining

The field of gene expression data analysis has grown in the past few years from being purely data-centric to integrative, aiming at complementing microarray analysis with data and knowledge from diverse available sources. In this review, we report on the plethora of gene expression data mining techniques and focus on their evolution toward knowledge-based data analysis approaches. In particular, we discuss recent developments in gene expression-based analysis methods used in association and classification studies, phenotyping and reverse engineering of gene networks

Multivariate time series classification with temporal abstractions

The increase in the number of complex temporal datasets collected today has prompted the development of methods that extend classical machine learning and data mining methods to time-series data. This work focuses on methods for multivariate time-series classification. Time series classification is a challenging problem mostly because the number of temporal features that describe the data and are potentially useful for classification is enormous. We study and develop a temporal abstraction framework for generating multivariate time series features suitable for classification tasks. We propose the STF-Mine algorithm that automatically mines discriminative temporal abstraction patterns from the time series data and uses them to learn a classification model. Our experimental evaluations, carried out on both synthetic and real world medical data, demonstrate the benefit of our approach in learning accurate classifiers for time-series datasets. Copyright © 2009, Assocation for the Advancement of ArtdicaI Intelligence (www.aaai.org). All rights reserved

The emergence of the postgenomic gene

The identity and the existence of genes has been challenged by postgenomic discoveries. Specifically, the consideration of molecular and cellular phenomena in which genes are embedded has proved relevant for their understanding. In response to these challenges, I will argue that the complexity of genetic phenomena supports the weak emergence of genes from the DNA. In Section 2, I will expose what genes are taken to be in the postgenomic world. In Section 3, I will present the relevant account of emergence. I consider weak emergence as in Franklin and Knox (Studies for the History and Philosophy of Modern Physics, 64, 68–78, 2018), for which a phenomenon is emergent when it displays novelty and robustness. In Section 4, I will argue that genes are weakly emergent since they are novel, improving explanations, and robust in respect to some perturbations. Then, I will conclude in Section 5 that genes’ emergence is a way to allow genes’ flexibility and context dependency, without compromising their existence

Phenotypic and genotypic data integration and exploration through a web-service architecture

<p>Abstract</p> <p>Background</p> <p>Linking genotypic and phenotypic information is one of the greatest challenges of current genetics research. The definition of an Information Technology infrastructure to support this kind of studies, and in particular studies aimed at the analysis of complex traits, which require the definition of multifaceted phenotypes and the integration genotypic information to discover the most prevalent diseases, is a paradigmatic goal of Biomedical Informatics. This paper describes the use of Information Technology methods and tools to develop a system for the management, inspection and integration of phenotypic and genotypic data.</p> <p>Results</p> <p>We present the design and architecture of the Phenotype Miner, a software system able to flexibly manage phenotypic information, and its extended functionalities to retrieve genotype information from external repositories and to relate it to phenotypic data. For this purpose we developed a module to allow customized data upload by the user and a SOAP-based communications layer to retrieve data from existing biomedical knowledge management tools. In this paper we also demonstrate the system functionality by an example application of the system in which we analyze two related genomic datasets.</p> <p>Conclusion</p> <p>In this paper we show how a comprehensive, integrated and automated workbench for genotype and phenotype integration can facilitate and improve the hypothesis generation process underlying modern genetic studies.</p

An automated reasoning framework for translational research

AbstractIn this paper we propose a novel approach to the design and implementation of knowledge-based decision support systems for translational research, specifically tailored to the analysis and interpretation of data from high-throughput experiments. Our approach is based on a general epistemological model of the scientific discovery process that provides a well-founded framework for integrating experimental data with preexisting knowledge and with automated inference tools.In order to demonstrate the usefulness and power of the proposed framework, we present its application to Genome-Wide Association Studies, and we use it to reproduce a portion of the initial analysis performed on the well-known WTCCC dataset. Finally, we describe a computational system we are developing, aimed at assisting translational research. The system, based on the proposed model, will be able to automatically plan and perform knowledge discovery steps, to keep track of the inferences performed, and to explain the obtained results

Filtering and Mapping Public Health Data with an Innovative Kriging Approach, Accounting for Single Observation Variance

AbstractThe main scope of the paper is performing appropriate kriging interpolation of the diabetes prevalence data coming from the Pavia (Italy) Local Health Care Agency (ASL). The original dataset is analyzed, the Bayesian regularization is evaluated, which is applied by other authors and finally prevalence data are simulated by means of random fields, in order to tune and evaluate kriging interpolation

Thirty years of artificial intelligence in medicine (AIME) conferences: A review of research themes

Over the past 30 years, the international conference on Artificial Intelligence in MEdicine (AIME) has been organized at different venues across Europe every 2 years, establishing a forum for scientific exchange and creating an active research community. The Artificial Intelligence in Medicine journal has published theme issues with extended versions of selected AIME papers since 1998