Autor(es):
Esteves, Luísa ; Caramelo, Francisco ; Ribeiro, Ilda Patrícia ; Carreira, Isabel M. ; Melo, Joana Barbosa de
Data: 2020
Identificador Persistente: https://hdl.handle.net/10316/106713
Origem: Estudo Geral - Universidade de Coimbra
Assunto(s): Algorithms; Cohort Studies; Comparative Genomic Hybridization; DNA Copy Number Variations; Gene Dosage; Gene Expression; Gene Expression Profiling; Genome; Genomics; Humans; Models, Theoretical; Neoplasms; Probability; Prognosis; Sequence Analysis, DNA
Descrição
Copy number alterations (CNAs) comprise deletions or amplifications of fragments of genomic material that are particularly common in cancer and play a major contribution in its development and progression. High resolution microarray-based genome-wide technologies have been widely used to detect CNAs, generating complex datasets that require further steps to allow for the determination of meaningful results. In this work, we propose a methodology to determine common regions of CNAs from these datasets, that in turn are used to infer the probability distribution of disease profiles in the population. This methodology was validated using simulated data and assessed using real data from Head and Neck Squamous Cell Carcinoma and Lung Adenocarcinoma, from the TCGA platform. Probability distribution profiles were produced allowing for the distinction between different phenotypic groups established within that cohort. This method may be used to distinguish between groups in the diseased population, within well-established degrees of confidence. The application of such methods may be of greater value in the clinical context both as a diagnostic or prognostic tool and, even as a useful way for helping to establish the most adequate treatment and care plans.
