Alessandro Verri
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Alessandro Verri has a total of 35 co-authors. Here are the top co-authors by number of shared publications:
- Annalisa Barla
Università di Genova
3 shared publications - Margherita Squillario
IRCCS Ospedale Policlinico San Martino, 16131 Genova, Italy
3 shared publications - Silvia Villa
Dipartimento di Matematica Università di Genova via Dodecaneso 35 16146 Genova Italy
3 shared publications - Sofia Mosci
DIBRIS, Università di Genova, Genoa, Italy
3 shared publications - Alessandra Staglianò
Università degli Studi di Genova
2 shared publications - Lorenzo Rosasco
Malga -DIBRIS University of Genova IT
2 shared publications
Latest Publications
- Open Access
- 1 June 2020
- Published by MDPI AG in Journal of Clinical Medicine
- Vol. 9 (6) , 1670
Transplantation Induces Profound Changes in the Transcriptional Asset of Hematopoietic Stem Cells: Identification of Specific Signatures Using Machine Learning Techniques
During the phase of proliferation needed for hematopoietic reconstitution following transplantation, hematopoietic stem/progenitor cells (HSPC) must express genes involved in stem cell self-renewal. We investigated the expression of genes relevant for self-renewal and expansion of HSPC (operationally defined as CD34+ cells) in steady state and after transplantation. Specifically, we evaluated the expression of ninety-one genes that were analyzed by real-time PCR in CD34+ cells isolated from (i) 12 samples from umbilical cord blood (UCB); (ii) 15 samples from bone marrow healthy donors; (iii) 13 samples from bone marrow after umbilical cord blood transplant (UCBT); and (iv) 29 samples from patients after transplantation with adult hematopoietic cells. The results show that transplanted CD34+ cells from adult cells acquire an asset very different from transplanted CD34+ cells from cord blood. Multivariate machine learning analysis (MMLA) showed that four specific gene signatures can be obtained by comparing the four types of CD34+ cells. In several, but not all cases, transplanted HSPC from UCB overexpress reprogramming genes. However, these remarkable changes do not alter the commitment to hematopoietic lineage. Overall, these results reveal undisclosed aspects of transplantation biology.
- 1 June 2020
- Published by MDPI AG in Journal of Clinical Medicine
- Vol. 9 (6) , 1670
Open AccessTransplantation Induces Profound Changes in the Transcriptional Asset of Hematopoietic Stem Cells: Identification of Specific Signatures Using Machine Learning Techniques
During the phase of proliferation needed for hematopoietic reconstitution following transplantation, hematopoietic stem/progenitor cells (HSPC) must express genes involved in stem cell self-renewal. We investigated the expression of genes relevant for self-renewal and expansion of HSPC (operationally defined as CD34+ cells) in steady state and after transplantation. Specifically, we evaluated the expression of ninety-one genes that were analyzed by real-time PCR in CD34+ cells isolated from (i) 12 samples from umbilical cord blood (UCB); (ii) 15 samples from bone marrow healthy donors; (iii) 13 samples from bone marrow after umbilical cord blood transplant (UCBT); and (iv) 29 samples from patients after transplantation with adult hematopoietic cells. The results show that transplanted CD34+ cells from adult cells acquire an asset very different from transplanted CD34+ cells from cord blood. Multivariate machine learning analysis (MMLA) showed that four specific gene signatures can be obtained by comparing the four types of CD34+ cells. In several, but not all cases, transplanted HSPC from UCB overexpress reprogramming genes. However, these remarkable changes do not alter the commitment to hematopoietic lineage. Overall, these results reveal undisclosed aspects of transplantation biology.
- Open Access
Enhancing Interpretability of Gene Signatures with Prior Biological Knowledge
Biological interpretability is a key requirement for the output of microarray data analysis pipelines. The most used pipeline first identifies a gene signature from the acquired measurements and then uses gene enrichment analysis as a tool for functionally characterizing the obtained results. Recently Knowledge Driven Variable Selection (KDVS), an alternative approach which performs both steps at the same time, has been proposed. In this paper, we assess the effectiveness of KDVS against standard approaches on a Parkinson’s Disease (PD) dataset. The presented quantitative analysis is made possible by the construction of a reference list of genes and gene groups associated to PD. Our work shows that KDVS is much more effective than the standard approach in enhancing the interpretability of the obtained results.
Open AccessEnhancing Interpretability of Gene Signatures with Prior Biological Knowledge
Biological interpretability is a key requirement for the output of microarray data analysis pipelines. The most used pipeline first identifies a gene signature from the acquired measurements and then uses gene enrichment analysis as a tool for functionally characterizing the obtained results. Recently Knowledge Driven Variable Selection (KDVS), an alternative approach which performs both steps at the same time, has been proposed. In this paper, we assess the effectiveness of KDVS against standard approaches on a Parkinson’s Disease (PD) dataset. The presented quantitative analysis is made possible by the construction of a reference list of genes and gene groups associated to PD. Our work shows that KDVS is much more effective than the standard approach in enhancing the interpretability of the obtained results.
- 1 March 2014
- Published by Elsevier in Artificial Intelligence in Medicine
- Vol. 61 (1) , 53-61
Unsupervised tissue segmentation from dynamic contrast-enhanced magnetic resonance imaging
- 1 March 2014
- Published by Elsevier in Artificial Intelligence in Medicine
- Vol. 61 (1) , 53-61
Unsupervised tissue segmentation from dynamic contrast-enhanced magnetic resonance imaging
- 21 December 2013
- Published by Springer Nature in Computational Optimization and Applications
- Vol. 58 (2) , 381-407
Proximal methods for the latent group lasso penalty
- 21 December 2013
- Published by Springer Nature in Computational Optimization and Applications
- Vol. 58 (2) , 381-407
Proximal methods for the latent group lasso penalty
- Open Access
- 9 January 2013
- Published by Springer Nature in Source Code for Biology and Medicine
- Vol. 8 (1) , 2
Knowledge Driven Variable Selection (KDVS) – a new approach to enrichment analysis of gene signatures obtained from high–throughput data
High–throughput (HT) technologies provide huge amount of gene expression data that can be used to identify biomarkers useful in the clinical practice. The most frequently used approaches first select a set of genes (i.e. gene signature) able to characterize differences between two or more phenotypical conditions, and then provide a functional assessment of the selected genes with an a posteriori enrichment analysis, based on biological knowledge. However, this approach comes with some drawbacks. First, gene selection procedure often requires tunable parameters that affect the outcome, typically producing many false hits. Second, a posteriori enrichment analysis is based on mapping between biological concepts and gene expression measurements, which is hard to compute because of constant changes in biological knowledge and genome analysis. Third, such mapping is typically used in the assessment of the coverage of gene signature by biological concepts, that is either score–based or requires tunable parameters as well, limiting its power.
- 9 January 2013
- Published by Springer Nature in Source Code for Biology and Medicine
- Vol. 8 (1) , 2
Open AccessKnowledge Driven Variable Selection (KDVS) – a new approach to enrichment analysis of gene signatures obtained from high–throughput data
High–throughput (HT) technologies provide huge amount of gene expression data that can be used to identify biomarkers useful in the clinical practice. The most frequently used approaches first select a set of genes (i.e. gene signature) able to characterize differences between two or more phenotypical conditions, and then provide a functional assessment of the selected genes with an a posteriori enrichment analysis, based on biological knowledge. However, this approach comes with some drawbacks. First, gene selection procedure often requires tunable parameters that affect the outcome, typically producing many false hits. Second, a posteriori enrichment analysis is based on mapping between biological concepts and gene expression measurements, which is hard to compute because of constant changes in biological knowledge and genome analysis. Third, such mapping is typically used in the assessment of the coverage of gene signature by biological concepts, that is either score–based or requires tunable parameters as well, limiting its power.
- Open Access
Proximal methods for the latent group lasso penalty
We consider a regularized least squares problem, with regularization by structured sparsity-inducing norms, which extend the usual $\ell_1$ and the group lasso penalty, by allowing the subsets to overlap. Such regularizations lead to nonsmooth problems that are difficult to optimize, and we propose in this paper a suitable version of an accelerated proximal method to solve them. We prove convergence of a nested procedure, obtained composing an accelerated proximal method with an inner algorithm for computing the proximity operator. By exploiting the geometrical properties of the penalty, we devise a new active set strategy, thanks to which the inner iteration is relatively fast, thus guaranteeing good computational performances of the overall algorithm. Our approach allows to deal with high dimensional problems without pre-processing for dimensionality reduction, leading to better computational and prediction performances with respect to the state-of-the art methods, as shown empirically both on toy and real data.Open AccessProximal methods for the latent group lasso penalty
We consider a regularized least squares problem, with regularization by structured sparsity-inducing norms, which extend the usual $\ell_1$ and the group lasso penalty, by allowing the subsets to overlap. Such regularizations lead to nonsmooth problems that are difficult to optimize, and we propose in this paper a suitable version of an accelerated proximal method to solve them. We prove convergence of a nested procedure, obtained composing an accelerated proximal method with an inner algorithm for computing the proximity operator. By exploiting the geometrical properties of the penalty, we devise a new active set strategy, thanks to which the inner iteration is relatively fast, thus guaranteeing good computational performances of the overall algorithm. Our approach allows to deal with high dimensional problems without pre-processing for dimensionality reduction, leading to better computational and prediction performances with respect to the state-of-the art methods, as shown empirically both on toy and real data. - Open Access
Nonparametric sparsity and regularization
In this work we are interested in the problems of supervised learning and variable selection when the input-output dependence is described by a nonlinear function depending on a few variables. Our goal is to consider a sparse nonparametric model, hence avoiding linear or additive models. The key idea is to measure the importance of each variable in the model by making use of partial derivatives. Based on this intuition we propose a new notion of nonparametric sparsity and a corresponding least squares regularization scheme. Using concepts and results from the theory of reproducing kernel Hilbert spaces and proximal methods, we show that the proposed learning algorithm corresponds to a minimization problem which can be provably solved by an iterative procedure. The consistency properties of the obtained estimator are studied both in terms of prediction and selection performance. An extensive empirical analysis shows that the proposed method performs favorably with respect to the state-of-the-art methods.
Open AccessNonparametric sparsity and regularization
In this work we are interested in the problems of supervised learning and variable selection when the input-output dependence is described by a nonlinear function depending on a few variables. Our goal is to consider a sparse nonparametric model, hence avoiding linear or additive models. The key idea is to measure the importance of each variable in the model by making use of partial derivatives. Based on this intuition we propose a new notion of nonparametric sparsity and a corresponding least squares regularization scheme. Using concepts and results from the theory of reproducing kernel Hilbert spaces and proximal methods, we show that the proposed learning algorithm corresponds to a minimization problem which can be provably solved by an iterative procedure. The consistency properties of the obtained estimator are studied both in terms of prediction and selection performance. An extensive empirical analysis shows that the proposed method performs favorably with respect to the state-of-the-art methods.
- 18 January 2011
- Published by IGI Global Scientific Publishing
Image Classification and Retrieval with Kernel Methods
Image Classification and Retrieval with Kernel Methods: 10.4018/978-1-59904-042-4.ch014: In this chapter we review some kernel methods useful for image classification and retrieval applications. Starting from the problem of constructing
- 18 January 2011
- Published by IGI Global Scientific Publishing
Image Classification and Retrieval with Kernel Methods
Image Classification and Retrieval with Kernel Methods: 10.4018/978-1-59904-042-4.ch014: In this chapter we review some kernel methods useful for image classification and retrieval applications. Starting from the problem of constructing
- 1 January 2007
- Published by INSTICC
- p. 45-52
FITTING 3D MORPHABLE MODELS USING IMPLICIT REPRESENTATIONS
- 1 January 2007
- Published by INSTICC
- p. 45-52
FITTING 3D MORPHABLE MODELS USING IMPLICIT REPRESENTATIONS