9 research outputs found
Spectral analysis of gene expression profiles using gene networks
Microarrays have become extremely useful for analysing genetic phenomena, but
establishing a relation between microarray analysis results (typically a list
of genes) and their biological significance is often difficult. Currently, the
standard approach is to map a posteriori the results onto gene networks to
elucidate the functions perturbed at the level of pathways. However,
integrating a priori knowledge of the gene networks could help in the
statistical analysis of gene expression data and in their biological
interpretation. Here we propose a method to integrate a priori the knowledge of
a gene network in the analysis of gene expression data. The approach is based
on the spectral decomposition of gene expression profiles with respect to the
eigenfunctions of the graph, resulting in an attenuation of the high-frequency
components of the expression profiles with respect to the topology of the
graph. We show how to derive unsupervised and supervised classification
algorithms of expression profiles, resulting in classifiers with biological
relevance. We applied the method to the analysis of a set of expression
profiles from irradiated and non-irradiated yeast strains. It performed at
least as well as the usual classification but provides much more biologically
relevant results and allows a direct biological interpretation
Elucidating regulatory mechanisms downstream of a signaling pathway using informative experiments
Signaling cascades are triggered by environmental stimulation and propagate the signal to regulate transcription. Systematic reconstruction of the underlying regulatory mechanisms requires pathway-targeted, informative experimental data. However, practical experimental design approaches are still in their infancy. Here, we propose a framework that iterates design of experiments and identification of regulatory relationships downstream of a given pathway. The experimental design component, called MEED, aims to minimize the amount of laboratory effort required in this process. To avoid ambiguity in the identification of regulatory relationships, the choice of experiments maximizes diversity between expression profiles of genes regulated through different mechanisms. The framework takes advantage of expert knowledge about the pathways under study, formalized in a predictive logical model. By considering model-predicted dependencies between experiments, MEED is able to suggest a whole set of experiments that can be carried out simultaneously. Our framework was applied to investigate interconnected signaling pathways in yeast. In comparison with other approaches, MEED suggested the most informative experiments for unambiguous identification of transcriptional regulation in this system
Διακλαδώσεις και ευστάθεια λύσεων μοντέλου διαφοροποίησης μεσεγχυματικών στρωματικών/βλαστικών κυττάρων
Εθνικό Μετσόβιο Πολυτεχνείο--Μεταπτυχιακή Εργασία. Διεπιστημονικό-Διατμηματικό Πρόγραμμα Μεταπτυχιακών Σπουδών (Δ.Π.Μ.Σ.) “Εφαρμοσμένη Μηχανική