Biomedical subjects

Nicola Ancona

Publications and source records attributed to Nicola Ancona.

4 recordsLinked to original sources

PubMed2006

Selection of relevant genes in cancer diagnosis based on their prediction accuracy.

MOTIVATIONS: One of the main problems in cancer diagnosis by using DNA microarray data is selecting genes relevant for the pathology by analyzing their expression profiles in tissues in two different phenotypical conditions. The question we pose is the following: how do we measure the relevance of a single gene in a given pathology? METHODS: A gene is relevant for a particular disease if we are able to correctly predict the occurrence of the pathology in new patients on the basis of its expression level only. In other words, a gene is informative for the disease if its expression levels are useful for training a classifier able to generalize, that is, able to correctly predict the status of new patients. In this paper we present a selection bias free, statistically well founded method for finding relevant genes on the basis of their classification ability. RESULTS: We applied the method on a colon cancer data set and produced a list of relevant genes, ranked on the basis of their prediction accuracy. We found, out of more than 6500 available genes, 54 overexpressed in normal tissues and 77 overexpressed in tumor tissues having prediction accuracy greater than 70% with p-value <or=0.05. CONCLUSIONS: The relevance of the selected genes was assessed (a) statistically, evaluating the p-value of the estimate prediction accuracy of each gene; (b) biologically, confirming the involvement of many genes in generic carcinogenic processes and in particular for the colon; (c) comparatively, verifying the presence of these genes in other studies on the same data-set.

Biomarkers, Tumor↗

PubMed2006

An invariance property of predictors in kernel-induced hypothesis spaces.

We consider kernel-based learning methods for regression and analyze what happens to the risk minimizer when new variables, statistically independent of input and target variables, are added to the set of input variables. This problem arises, for example, in the detection of causality relations between two time series. We find that the risk minimizer remains unchanged if we constrain the risk minimization to hypothesis spaces induced by suitable kernel functions. We show that not all kernel-induced hypothesis spaces enjoy this property. We present sufficient conditions ensuring that the risk minimizer does not change and show that they hold for inhomogeneous polynomial and gaussian radial basis function kernels. We also provide examples of kernel-induced hypothesis spaces whose risk minimizer changes if independent variables are added as input.

Journal Article↗

PubMed2005

Regularized Least Squares Cancer classifiers from DNA microarray data.

BACKGROUND: The advent of the technology of DNA microarrays constitutes an epochal change in the classification and discovery of different types of cancer because the information provided by DNA microarrays allows an approach to the problem of cancer analysis from a quantitative rather than qualitative point of view. Cancer classification requires well founded mathematical methods which are able to predict the status of new specimens with high significance levels starting from a limited number of data. In this paper we assess the performances of Regularized Least Squares (RLS) classifiers, originally proposed in regularization theory, by comparing them with Support Vector Machines (SVM), the state-of-the-art supervised learning technique for cancer classification by DNA microarray data. The performances of both approaches have been also investigated with respect to the number of selected genes and different gene selection strategies. RESULTS: We show that RLS classifiers have performances comparable to those of SVM classifiers as the Leave-One-Out (LOO) error evaluated on three different data sets shows. The main advantage of RLS machines is that for solving a classification problem they use a linear system of order equal to either the number of features or the number of training examples. Moreover, RLS machines allow to get an exact measure of the LOO error with just one training. CONCLUSION: RLS classifiers are a valuable alternative to SVM classifiers for the problem of cancer classification by gene expression data, due to their simplicity and low computational complexity. Moreover, RLS classifiers show generalization ability comparable to the ones of SVM classifiers also in the case the classification of new specimens involves very few gene expression levels.

Algorithms↗

PubMed2004

Radial basis function approach to nonlinear Granger causality of time series.

We consider an extension of Granger causality to nonlinear bivariate time series. In this frame, if the prediction error of the first time series is reduced by including measurements from the second time series, then the second time series is said to have a causal influence on the first one. Not all the nonlinear prediction schemes are suitable to evaluate causality; indeed, not all of them allow one to quantify how much knowledge of the other time series counts to improve prediction error. We present an approach with bivariate time series modeled by a generalization of radial basis functions and show its application to a pair of unidirectionally coupled chaotic maps and to physiological examples.

Adaptation, Physiological↗