Computing Network of Diseases and Pharmacological Entities through the Integration of Distributed Literature Mining and Ontology Mapping

The proliferation of -omics (such as, Genomics, Proteomics) and -ology (such as, System Biology, Cell Biology, Pharmacology) have spawned new frontiers of research in drug discovery and personalized medicine. A vast amount (21 million) of published research results are archived in the PubMed and are continually growing in size. To improve the accessibility and utility of such a large number of literatures, it is critical to develop a suit of semantic sensitive technology that is capable of discovering knowledge and can also infer possible new relationships based on statistical co-occurrences of meaningful terms or concepts. In this context, this thesis presents a unified framework to mine a large number of literatures through the integration of latent semantic analysis (LSA) and ontology mapping. In particular, a parameter optimized, robust, scalable, and distributed LSA (DiLSA) technique was designed and implemented on a carefully selected 7.4 million PubMed records related to pharmacology. The DiLSA model was integrated with MeSH to make the model effective and efficient for a specific domain. An optimized multi-gram dictionary was customized by mapping the MeSH to build the DiLSA model. A fully integrated web-based application, called PharmNet, was developed to bridge the gap between biological knowledge and clinical practices. Preliminary analysis using the PharmNet shows an improved performance over global LSA model. A limited expert evaluation was performed to validate the retrieved results and network with biological literatures. A thorough performance evaluation and validation of results is in progress

Enhancing Automatic Construction of Gene Subnetworks by Integrating Multiple Sources of Information

We present an approach to extracting information from textual documents of biological knowledge and demonstrate how cellular gene pathways may be inferred. Natural language processing techniques are used to represent title and abstract fields of publications to derive a gene similarity vectors which are subject to cluster analysis. Gene interactions are derived by parsing sentences in the abstracts to infer causal relationships. We show how high throughput transcriptome data may then be used to enhance the construction of gene pathways from information derived from text. Subnetworks constructed by integrating information automatically derived from literature with gene expression data is validated by comparing biological processes defined in the Gene Ontology 2(GO) database. We find that precision increases in $$58\%$$ of the clusters when enhanced in this manner while a decrease in precision is observed in a relatively small number of clusters. These results are compared to similar attempts at the same problem and appear to be better in terms of precision of network construction. We also show an example of a subnetwork found by this analysis that overlaps a known gene pathway in KEGG and MIPS databases

Combining heterogeneous sources of data for the reverse-engineering of gene regulatory networks

This thesis was submitted for the degree of Doctor of Philosophy and awarded by Brunel University.Gene Regulatory Networks (GRNs) represent how genes interact in various cellular processes by describing how the expression level, or activity, of genes can affect the expression of the other genes. Reverse-engineering GRN models can help biologists understand and gain insight into genetic conditions and diseases. Recently, the increasingly widespread use of DNA microarrays, a high-throughput technology that allows the expression of thousands of genes to be measured simultaneously in biological experiments, has led to many datasets of gene expression measurements becoming publicly available and a subsequent explosion of research in the reverse-engineering of GRN models. However, microarray technology has a number of limitations as a data source for the modelling of GRNs, due to concerns over its reliability and the reproducibility of experimental results. The underlying theme of the research presented in this thesis is the incorporation of multiple sources and different types of data into techniques for reverse-engineering or learning GRNs from data. By drawing on many data sources, the resulting network models should be more robust, accurate and reliable than models that have been learnt using a single data source. This is achieved by focusing on two main strands of research. First, the thesis presents some of the earliest work in the incorporation of prior knowledge that has been generated from a large body of scientific papers, for Bayesian network based GRN models. Second, novel methods for the use of multiple microarray datasets to produce Bayesian network based GRN models are introduced. Empirical evaluations are used to show that the incorporation of literature-based prior knowledge and combining multiple microarray datasets can provide an improvement, when compared to the use of a single microarray dataset, for the reverse-engineering of Bayesian network based GRN models

Combining heterogeneous sources of data for the reverse-engineering of gene regulatory networks

Gene Regulatory Networks (GRNs) represent how genes interact in various cellular processes by describing how the expression level, or activity, of genes can affect the expression of the other genes. Reverse-engineering GRN models can help biologists understand and gain insight into genetic conditions and diseases. Recently, the increasingly widespread use of DNA microarrays, a high-throughput technology that allows the expression of thousands of genes to be measured simultaneously in biological experiments, has led to many datasets of gene expression measurements becoming publicly available and a subsequent explosion of research in the reverse-engineering of GRN models. However, microarray technology has a number of limitations as a data source for the modelling of GRNs, due to concerns over its reliability and the reproducibility of experimental results. The underlying theme of the research presented in this thesis is the incorporation of multiple sources and different types of data into techniques for reverse-engineering or learning GRNs from data. By drawing on many data sources, the resulting network models should be more robust, accurate and reliable than models that have been learnt using a single data source. This is achieved by focusing on two main strands of research. First, the thesis presents some of the earliest work in the incorporation of prior knowledge that has been generated from a large body of scientific papers, for Bayesian network based GRN models. Second, novel methods for the use of multiple microarray datasets to produce Bayesian network based GRN models are introduced. Empirical evaluations are used to show that the incorporation of literature-based prior knowledge and combining multiple microarray datasets can provide an improvement, when compared to the use of a single microarray dataset, for the reverse-engineering of Bayesian network based GRN models.EThOS - Electronic Theses Online ServiceGBUnited Kingdo