Mass data exploration in oncology: An information synthesis approach

New technologies and equipment allow for mass treatment of samples and research teams share acquired data on an always larger scale. In this context scientists are facing a major data exploitation problem. More precisely, using these data sets through data mining tools or introducing them in a classical experimental approach require a preliminary understanding of the information space, in order to direct the process. But acquiring this grasp on the data is a complex activity, which is seldom supported by current software tools. The goal of this paper is to introduce a solution to this scientific data grasp problem. Illustrated in the Tissue MicroArrays application domain, the proposal is based on the synthesis notion, which is inspired by Information Retrieval paradigms. The envisioned synthesis model gives a central role to the study the researcher wants to conduct, through the task notion. It allows for the implementation of a task-oriented Information Retrieval prototype system. Cases studies and user studies were used to validate this prototype system. It opens interesting prospects for the extension of the model or extensions towards other application domains

Gene prioritization and clustering by multi-view text mining

<p>Abstract</p> <p>Background</p> <p>Text mining has become a useful tool for biologists trying to understand the genetics of diseases. In particular, it can help identify the most interesting candidate genes for a disease for further experimental analysis. Many text mining approaches have been introduced, but the effect of disease-gene identification varies in different text mining models. Thus, the idea of incorporating more text mining models may be beneficial to obtain more refined and accurate knowledge. However, how to effectively combine these models still remains a challenging question in machine learning. In particular, it is a non-trivial issue to guarantee that the integrated model performs better than the best individual model.</p> <p>Results</p> <p>We present a multi-view approach to retrieve biomedical knowledge using different controlled vocabularies. These controlled vocabularies are selected on the basis of nine well-known bio-ontologies and are applied to index the vast amounts of gene-based free-text information available in the MEDLINE repository. The text mining result specified by a vocabulary is considered as a view and the obtained multiple views are integrated by multi-source learning algorithms. We investigate the effect of integration in two fundamental computational disease gene identification tasks: gene prioritization and gene clustering. The performance of the proposed approach is systematically evaluated and compared on real benchmark data sets. In both tasks, the multi-view approach demonstrates significantly better performance than other comparing methods.</p> <p>Conclusions</p> <p>In practical research, the relevance of specific vocabulary pertaining to the task is usually unknown. In such case, multi-view text mining is a superior and promising strategy for text-based disease gene identification.</p

From Text to Knowledge

The global information space provided by the World Wide Web has changed dramatically the way knowledge is shared all over the world. To make this unbelievable huge information space accessible, search engines index the uploaded contents and provide efficient algorithmic machinery for ranking the importance of documents with respect to an input query. All major search engines such as Google, Yahoo or Bing are keyword-based, which is indisputable a very powerful tool for accessing information needs centered around documents. However, this unstructured, document-oriented paradigm of the World Wide Web has serious drawbacks, when searching for specific knowledge about real-world entities. When asking for advanced facts about entities, today's search engines are not very good in providing accurate answers. Hand-built knowledge bases such as Wikipedia or its structured counterpart DBpedia are excellent sources that provide common facts. However, these knowledge bases are far from being complete and most of the knowledge lies still buried in unstructured documents. Statistical machine learning methods have the great potential to help to bridge the gap between text and knowledge by (semi-)automatically transforming the unstructured representation of the today's World Wide Web to a more structured representation. This thesis is devoted to reduce this gap with Probabilistic Graphical Models. Probabilistic Graphical Models play a crucial role in modern pattern recognition as they merge two important fields of applied mathematics: Graph Theory and Probability Theory. The first part of the thesis will present a novel system called Text2SemRel that is able to (semi-)automatically construct knowledge bases from textual document collections. The resulting knowledge base consists of facts centered around entities and their relations. Essential part of the system is a novel algorithm for extracting relations between entity mentions that is based on Conditional Random Fields, which are Undirected Probabilistic Graphical Models. In the second part of the thesis, we will use the power of Directed Probabilistic Graphical Models to solve important knowledge discovery tasks in semantically annotated large document collections. In particular, we present extensions of the Latent Dirichlet Allocation framework that are able to learn in an unsupervised way the statistical semantic dependencies between unstructured representations such as documents and their semantic annotations. Semantic annotations of documents might refer to concepts originating from a thesaurus or ontology but also to user-generated informal tags in social tagging systems. These forms of annotations represent a first step towards the conversion to a more structured form of the World Wide Web. In the last part of the thesis, we prove the large-scale applicability of the proposed fact extraction system Text2SemRel. In particular, we extract semantic relations between genes and diseases from a large biomedical textual repository. The resulting knowledge base contains far more potential disease genes exceeding the number of disease genes that are currently stored in curated databases. Thus, the proposed system is able to unlock knowledge currently buried in the literature. The literature-derived human gene-disease network is subject of further analysis with respect to existing curated state of the art databases. We analyze the derived knowledge base quantitatively by comparing it with several curated databases with regard to size of the databases and properties of known disease genes among other things. Our experimental analysis shows that the facts extracted from the literature are of high quality