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Identification of expression patterns in the progression of disease stages by integration of transcriptomic data

Authors :
Instituto de Salud Carlos III
Consejo Superior de Investigaciones Científicas (España)
European Commission
Junta de Castilla y León
Ministerio de Economía y Competitividad (España)
Aibar, Sara
Abáigar, María
Campos-Laborie, Francisco J.
Sanchez-Santos, Jose Manuel
Hernández, Jesús M.
De Las Rivas, Javier
Instituto de Salud Carlos III
Consejo Superior de Investigaciones Científicas (España)
European Commission
Junta de Castilla y León
Ministerio de Economía y Competitividad (España)
Aibar, Sara
Abáigar, María
Campos-Laborie, Francisco J.
Sanchez-Santos, Jose Manuel
Hernández, Jesús M.
De Las Rivas, Javier
Publication Year :
2016

Abstract

[Background]: In the study of complex diseases using genome-wide expression data from clinical samples, a difficult case is the identification and mapping of the gene signatures associated to the stages that occur in the progression of a disease. The stages usually correspond to different subtypes or classes of the disease, and the difficulty to identify them often comes from patient heterogeneity and sample variability that can hide the biomedical relevant changes that characterize each stage, making standard differential analysis inadequate or inefficient. [Results]: We propose a methodology to study diseases or disease stages ordered in a sequential manner (e.g. from early stages with good prognosis to more acute or serious stages associated to poor prognosis). The methodology is applied to diseases that have been studied obtaining genome-wide expression profiling of cohorts of patients at different stages. The approach allows searching for consistent expression patterns along the progression of the disease through two major steps: (i) identifying genes with increasing or decreasing trends in the progression of the disease; (ii) clustering the increasing/decreasing gene expression patterns using an unsupervised approach to reveal whether there are consistent patterns and find genes altered at specific disease stages. The first step is carried out using Gamma rank correlation to identify genes whose expression correlates with a categorical variable that represents the stages of the disease. The second step is done using a Self Organizing Map (SOM) to cluster the genes according to their progressive profiles and identify specific patterns. Both steps are done after normalization of the genomic data to allow the integration of multiple independent datasets. In order to validate the results and evaluate their consistency and biological relevance, the methodology is applied to datasets of three different diseases: myelodysplastic syndrome, colorectal cancer and Alzhei

Details

Database :
OAIster
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1103438587
Document Type :
Electronic Resource