arXiv subjects

Vincenzo Lagani

Publications and source records attributed to Vincenzo Lagani.

4 recordsLinked to original sources

arXiv2025

Interpretable Causal Representation Learning for Biological Data in the Pathway Space

Predicting the impact of genomic and drug perturbations in cellular function is crucial for understanding gene functions and drug effects, ultimately leading to improved therapies. To this end, Causal Representation Learning (CRL) constitutes one of the most promising approaches, as it aims to identify the latent factors that causally govern biological systems, thus facilitating the prediction of the effect of unseen perturbations. Yet, current CRL methods fail in reconciling their principled latent representations with known biological processes, leading to models that are not interpretable. To address this major issue, we present SENA-discrepancy-VAE, a model based on the recently proposed CRL method discrepancy-VAE, that produces representations where each latent factor can be interpreted as the (linear) combination of the activity of a (learned) set of biological processes. To this extent, we present an encoder, SENA-δ, that efficiently compute and map biological processes' activity levels to the latent causal factors. We show that SENA-discrepancy-VAE achieves predictive performances on unseen combinations of interventions that are comparable with its original, non-interpretable counterpart, while inferring causal latent factors that are biologically meaningful.

cs.LG↗

arXiv2023

IHCV: Discovery of Hidden Time-Dependent Control Variables in Non-Linear Dynamical Systems

Discovering non-linear dynamical models from data is at the core of science. Recent progress hinges upon sparse regression of observables using extensive libraries of candidate functions. However, it remains challenging to model hidden non-observable control variables governing switching between different dynamical regimes. Here we develop a data-efficient derivative-free method, IHCV, for the Identification of Hidden Control Variables. First, the performance and robustness of IHCV against noise are evaluated by benchmarking the IHCV method using well-known bifurcation models (saddle-node, transcritical, pitchfork, Hopf). Next, we demonstrate that IHCV discovers hidden driver variables in the Lorenz, van der Pol, Hodgkin-Huxley, and Fitzhugh-Nagumo models. Finally, IHCV generalizes to the case when only partial observational is given, as demonstrated using the toggle switch model, the genetic repressilator oscillator, and a Waddington landscape model. Our proof-of-principle illustrates that utilizing normal forms could facilitate the data-efficient and scalable discovery of hidden variables controlling transitions between different dynamical regimes and non-linear models.

q-bio.QM↗

arXiv2018

Multiple Equivalent Solutions for the Lasso

Feature selection is an important problem studied in data analytics seeking to identify a minimal-size feature subset that is optimally predictive for an outcome of interest. It is also a powerful tool in Knowledge Discovery as a means for gaining domain insight, e.g., identifying which medical quantities carry unique information for the disease status. It is arguably less recognized however, that the problem may have multiple, equivalent solutions. In that case, it is misleading to domain experts to report only one of them and ignore all other equivalent solutions. In this paper, we extend a well-established single, feature selection algorithm (i.e., reporting a single solution), namely the Lasso algorithm, to the multiple solution problem based on formalized notion of equivalence for both classification and regression tasks. Empirical results are obtained using a fully automated pipeline called Just Add Data Bio or JAD Bio training and selecting multiple, linear as well as nonlinear learners, optimizing hyper-parameter values, and correcting for the bias of multiple inductions (model selection). The results show that multiple solutions do exist in real datasets, as well as the ability of the algorithm to identify a subset of them. A comparison with the Statistical Equivalent Solutions (SES) algorithm shows that Lasso equivalent solutions have better prediction performance at the cost of selecting more features.

math.ST↗

arXiv2016

Feature Selection with the R Package MXM: Discovering Statistically-Equivalent Feature Subsets

The statistically equivalent signature (SES) algorithm is a method for feature selection inspired by the principles of constrained-based learning of Bayesian Networks. Most of the currently available feature-selection methods return only a single subset of features, supposedly the one with the highest predictive power. We argue that in several domains multiple subsets can achieve close to maximal predictive accuracy, and that arbitrarily providing only one has several drawbacks. The SES method attempts to identify multiple, predictive feature subsets whose performances are statistically equivalent. Under that respect SES subsumes and extends previous feature selection algorithms, like the max-min parent children algorithm. SES is implemented in an homonym function included in the R package MXM, standing for mens ex machina, meaning 'mind from the machine' in Latin. The MXM implementation of SES handles several data-analysis tasks, namely classification, regression and survival analysis. In this paper we present the SES algorithm, its implementation, and provide examples of use of the SES function in R. Furthermore, we analyze three publicly available data sets to illustrate the equivalence of the signatures retrieved by SES and to contrast SES against the state-of-the-art feature selection method LASSO. Our results provide initial evidence that the two methods perform comparably well in terms of predictive accuracy and that multiple, equally predictive signatures are actually present in real world data.

stat.ML↗