Abstract
Gene expression data from high-throughput assays, such as
microarray, are often used to predict cancer survival. Available datasets
consist of a small number of samples (n patients) and a large number of
genes (p predictors). Therefore, the main challenge is to cope with the
high-dimensionality. Moreover, genes are co-regulated and their expression
levels are expected to be highly correlated. In order to face these
two issues, network based approaches can be applied. In our analysis,
we compared the most recent network penalized Cox models for highdimensional
survival data aimed to determine pathway structures and
biomarkers involved into cancer progression.
Using these network-based models, we show how to obtain a deeper
understanding of the gene-regulatory networks and investigate the gene
signatures related to prognosis and survival in different types of tumors.
Comparisons are carried out on three real different cancer datasets.
Anno
2015
Autori IAC
Tipo pubblicazione
Altri Autori
A. Iuliano, A. Occhipinti, C. Angelini, I. De Feis, P.Li.
Editore
Springer
Rivista
Lecture notes in computer science