arXiv subjects

Filippo Utro

Publications and source records attributed to Filippo Utro.

14 recordsLinked to original sources

arXiv2026

Quantum Kernel Estimation for the Discovery of Early Lung Cancer Detection

Lung cancer screening with low-dose chest computed tomography reduces mortality, but its impact is limited by uptake, adherence, and management challenges. Blood-based cell-free DNA (cfDNA) biomarkers offer a complementary approach, although early detection remains difficult because of lung cancer heterogeneity and high-dimensional, nonlinear molecular signals. We evaluated quantum-classical hybrid machine learning for lung cancer detection using DNA fragmentomics and DNA methylation. After feature selection, models were trained using 20- and 40-feature subsets. Features were encoded into quantum Hilbert space using angle and dense-angle feature maps with multiple entanglement strategies. Fidelity-based quantum kernels were computed with exact statevector simulation and integrated with precomputed-kernel SVM and kernel-PCA logistic regression and compared with an SVM model trained on the original features. This framework enabled systematic evaluation of how encoding and entanglement design affect classification. Across repeated held-out evaluations, quantum-kernel models achieved competitive performance on both datasets. For fragmentomics, several 20-feature configurations improved AUC relative to a classical SVM baseline, suggesting effective capture of nonlinear cfDNA fragmentation structure. For methylation, the classical SVM achieved the highest AUC, although selected quantum models remained competitive and improved specificity in some cases. Increasing features from 20 to 40 did not consistently improve performance and often increased variability. Overall, these results support quantum kernel methods as a promising approach for cfDNA-based lung cancer detection.

cs.LG↗

arXiv2026

A Quantum Reservoir for Neurodynamical Forecasting

Forecasting neural activity from short recordings remains a fundamental challenge. Reservoir computing may offer an efficient paradigm for temporal prediction, however classical reservoirs typically underperform in small-data regimes. Here we investigate whether quantum reservoir computing (QRC) can help overcome this limitation. Building on recent advances, we introduce a quantum reservoir based on a transverse-field Ising model, combined with heterogeneous quantum measurements and polynomial ridge regression. On a standard benchmark task, results show that the quantum reservoir outperforms a classical counterpart overall, with prediction accuracy strongly dependent on reservoir parameters. We further demonstrate feasibility by running the same task on quantum hardware. To assess performance on biological signals, we evaluate QRC on simulated human electroencephalography (EEG) data with a parallel reservoir architecture. On this challenging task, the tested quantum reservoir did not match the performance of the classical one, but it produced stable, convergent predictions. This is a meaningful first step toward forecasting of biologically realistic neural data using a quantum reservoir. Overall, our findings indicate that although current quantum hardware and parallel reservoir architectures do not yet surpass classical methods on complex neural signals, QRC can be executed on near-term devices and does converge with realistic EEG-like data. This work establishes a practical baseline for future algorithmic and hardware developments aimed at clinical time-series forecasting with quantum systems.

quant-ph↗

arXiv2026

Experimental implementation of a discrete-time quantum walk on biological networks

Quantum walks provide a versatile framework for probing the structural and dynamical properties of complex systems ranging from biological networks to synthetic materials. However, their realization on current noisy pre-fault-tolerant quantum computers is fundamentally limited by decoherence. Conventional dense encodings of graph structures require prohibitively deep circuits, making them incompatible with existing hardware. Here we introduce an algorithm that leverages symmetry-sector encoding and trades circuit depth for the number of qubits, while integrating symmetry-respecting postselection as an effective noise-mitigation strategy. This combination enables us to execute practical quantum-walk circuits for biological network motifs on actual quantum hardware. We benchmark the proposed methodology against known state-of-the-art circuit architectures, highlighting significant reduction of circuit depth in our approach at the cost of moderate qubit overhead. Utilizing 40 qubits, we implement quantum walks on complex graphs containing up to 17 nodes and 20 edges -- the largest experiment on superconducting hardware to date, with the Hellinger fidelity exceeding 87% throughout 7 steps. We present a proof-of-principle case study that illustrates how experimentally obtained quantum-walk dynamics on a protein-protein-interaction network can be applied to prioritizing disease-associated genes. We discuss the framework scalability in the pre-fault-tolerant era and its potential for studying larger biological networks.

quant-ph↗

arXiv2026

Data complexity signature predicts quantum projected learning benefit for antibiotic resistance

This study presents the first large-scale empirical evaluation of quantum machine learning for predicting antibiotic resistance in clinical urine cultures. Antibiotic resistance is amongst the top threats to humanity, and inappropriate antibiotic use is a main driver of resistance. We developed a Quantum Projective Learning (QPL) approach and executed 60 qubit experiments on IBM Eagle and Heron quantum processing units. While QPL did not consistently outperform classical baselines, potentially reflecting current quantum hardware limitations, it did achieve parity or superiority in specific scenarios, notably for the antibiotic nitrofurantoin and selected data splits, revealing that quantum advantage may be data-dependent. Analysis of data complexity measures uncovered a multivariate signature, which comprised Shannon entropy, Fisher Discriminant Ratio, standard deviation of kurtosis, number of low-variance features, and total correlations. The multivariate model accurately (AUC = 0.88, $p$-value = 0.03) distinguished cases wherein QPL executed on quantum hardware would outperform classical models. This signature suggests that quantum kernels excel in feature spaces with high entropy and structural complexity. These findings point to complexity-driven adaptive model selection as a promising strategy for optimizing hybrid quantum-classical workflows in healthcare. Overall, this investigation marks the first application of quantum machine learning in urology, and in antibiotic resistance prediction. Further, this work highlights conditional quantum utility and introduces a principled approach for leveraging data complexity signatures to guide quantum machine learning deployment in biomedical applications.

q-bio.OT↗

arXiv2025

Enhanced Prediction of CAR T-Cell Cytotoxicity with Quantum-Kernel Methods

Chimeric antigen receptor (CAR) T-cells are T-cells engineered to recognize and kill specific tumor cells. Through their extracellular domains, CAR T-cells bind tumor cell antigens which triggers CAR T activation and proliferation. These processes are regulated by co-stimulatory domains present in the intracellular region of the CAR T-cell. Through integrating novel signaling components into the co-stimulatory domains, it is possible to modify CAR T-cell phenotype. Identifying and experimentally testing new CAR constructs based on libraries of co-stimulatory domains is nontrivial given the vast combinatorial space defined by such libraries. This leads to a highly data constrained, poorly explored combinatorial problem, where the experiments undersample all possible combinations. We propose a quantum approach using a Projected Quantum Kernel (PQK) to address this challenge. PQK operates by embedding classical data into a high dimensional Hilbert space and employs a kernel method to measure sample similarity. Using 61 qubits on a gate-based quantum computer, we demonstrate the largest PQK application to date and an enhancement in the classification performance over purely classical machine learning methods for CAR T cytotoxicity prediction. Importantly, we show improved learning for specific signaling domains and domain positions, particularly where there was lower information highlighting the potential for quantum computing in data-constrained problems.

cs.LG↗

arXiv2025

On Quantum Random Walks in Biomolecular Networks

Biomolecular networks, such as protein-protein interactions, gene-gene associations, and cell-cell interactions, offer valuable insights into the complex organization of biological systems. These networks are key to understanding cellular functions, disease mechanisms, and identifying therapeutic targets. However, their analysis is challenged by the high dimensionality, heterogeneity, and sparsity of multi-omics data. Random walk algorithms are widely used to propagate information through disease modules, helping to identify disease-associated genes and uncover relevant biological pathways. In this work, we investigate the limitations of classical random walks and explore the potential of quantum random walks (QRWs) for biomolecular network analysis. We evaluate QRWs in two network-based applications. First, in a gene-gene interaction network associated with asthma, autism, and schizophrenia, QRWs more accurately rank disease-associated genes compared to classical methods. Second, in a structured multi-partite cell-cell interaction network derived from mouse brown adipose tissue, QRWs identify key driver genes in malignant cells that are overlooked by classical random walks. Our findings suggest that quantum random walks offer a promising alternative to classical approaches, with improved sensitivity to network structure and better performance in identifying biologically relevant features. This highlights their potential in advancing network medicine and systems biology.

quant-ph↗

arXiv2025

Quantum Ensembling Methods for Healthcare and Life Science

Learning on small data is a challenge frequently encountered in many real-world applications. In this work we study how effective quantum ensemble models are when trained on small data problems in healthcare and life sciences. We constructed multiple types of quantum ensembles for binary classification using up to 26 qubits in simulation and 56 qubits on quantum hardware. Our ensemble designs use minimal trainable parameters but require long-range connections between qubits. We tested these quantum ensembles on synthetic datasets and gene expression data from renal cell carcinoma patients with the task of predicting patient response to immunotherapy. From the performance observed in simulation and initial hardware experiments, we demonstrate how quantum embedding structure affects performance and discuss how to extract informative features and build models that can learn and generalize effectively. We present these exploratory results in order to assist other researchers in the design of effective learning on small data using ensembles. Incorporating quantum computing in these data constrained problems offers hope for a wide range of studies in healthcare and life sciences where biological samples are relatively scarce given the feature space to be explored.

cs.LG↗

arXiv2025

Quantum machine learning framework for longitudinal biomedical studies

Longitudinal biomedical studies play a vital role in tracking disease progression, treatment response, and the emergence of resistance mechanisms, particularly in complex disorders such as cancer and neurodegenerative diseases. However, the high dimensionality of biological data, combined with the limited size of longitudinal cohorts, presents significant challenges for traditional machine learning approaches. In this work, we explore the potential of quantum machine learning (QML) for longitudinal biomarker discovery. We propose a novel modification to the instantaneous quantum polynomial time (IQP) feature map, designed to encode temporal dependencies across multiple time points in biomedical datasets. Through numerical simulations on both synthetic and real-world datasets - including studies on follicular lymphoma and Alzheimer's disease - we demonstrate that our longitudinal IQP feature map improves the ability of quantum kernels to capture intra-subject temporal patterns, offering a promising direction for QML in clinical research.

q-bio.QM↗

arXiv2025

Quantum Doubly Stochastic Transformers

At the core of the Transformer, the softmax normalizes the attention matrix to be right stochastic. Previous research has shown that this often de-stabilizes training and that enforcing the attention matrix to be doubly stochastic (through Sinkhorn's algorithm) consistently improves performance across different tasks, domains and Transformer flavors. However, Sinkhorn's algorithm is iterative, approximative, non-parametric and thus inflexible w.r.t. the obtained doubly stochastic matrix (DSM). Recently, it has been proven that DSMs can be obtained with a parametric quantum circuit, yielding a novel quantum inductive bias for DSMs with no known classical analogue. Motivated by this, we demonstrate the feasibility of a hybrid classical-quantum doubly stochastic Transformer (QDSFormer) that replaces the softmax in the self-attention layer with a variational quantum circuit. We study the expressive power of the circuit and find that it yields more diverse DSMs that better preserve information than classical operators. Across multiple small-scale object recognition tasks, we find that our QDSFormer consistently surpasses both a standard ViT and other doubly stochastic Transformers. Beyond the Sinkformer, this comparison includes a novel quantum-inspired doubly stochastic Transformer (based on QR decomposition) that can be of independent interest. Our QDSFormer also shows improved training stability and lower performance variation suggesting that it may mitigate the notoriously unstable training of ViTs on small-scale data.

cs.LG↗

arXiv2024

How quantum computing can enhance biomarker discovery

Biomarkers play a central role in medicine's gradual progress towards proactive, personalized precision diagnostics and interventions. However, finding biomarkers that provide very early indicators of a change in health status, for example for multi-factorial diseases, has been challenging. Discovery of such biomarkers stands to benefit significantly from advanced information processing and means to detect complex correlations, which quantum computing offers. In this perspective paper, quantum algorithms, particularly in machine learning, are mapped to key applications in biomarker discovery. The opportunities and challenges associated with the algorithms and applications are discussed. The analysis is structured according to different data types - multi-dimensional, time series, and erroneous data - and covers key data modalities in healthcare - electronic health records (EHRs), omics, and medical images. An outlook is provided concerning open research challenges.

q-bio.OT↗

arXiv2023

Probing omics data via harmonic persistent homology

Identifying molecular signatures from complex disease patients with underlying symptomatic similarities is a significant challenge in the analysis of high dimensional multi-omics data. Topological data analysis (TDA) provides a way of extracting such information from the geometric structure of the data and identifying multiway higher-order relationships. Here, we propose an application of Harmonic persistent homology, which overcomes the limitations of ambiguous assignment of the topological information to the original elements in a representative topological cycle from the data. When applied to multi-omics data, this leads to the discovery of hidden patterns highlighting the relationships between different omic profiles, while allowing for common tasks in multi-omics analyses, such as disease subtyping, and most importantly biomarker identification for similar latent biological pathways that are associated with complex diseases. Our experiments on multiple cancer data show that harmonic persistent homology effectively dissects multi-omics data to identify biomarkers by detecting representative cycles predictive of disease subtypes.

q-bio.GN↗

arXiv2023

Towards quantum-enabled cell-centric therapeutics

In recent years, there has been tremendous progress in the development of quantum computing hardware, algorithms and services leading to the expectation that in the near future quantum computers will be capable of performing simulations for natural science applications, operations research, and machine learning at scales mostly inaccessible to classical computers. Whereas the impact of quantum computing has already started to be recognized in fields such as cryptanalysis, natural science simulations, and optimization among others, very little is known about the full potential of quantum computing simulations and machine learning in the realm of healthcare and life science (HCLS). Herein, we discuss the transformational changes we expect from the use of quantum computation for HCLS research, more specifically in the field of cell-centric therapeutics. Moreover, we identify and elaborate open problems in cell engineering, tissue modeling, perturbation modeling, and bio-topology while discussing candidate quantum algorithms for research on these topics and their potential advantages over classical computational approaches.

quant-ph↗

arXiv2012

The Chromatin Organization of an Eukaryotic Genome : Sequence Specific+ Statistical=Combinatorial (Extended Abstract)

Nucleosome organization in eukaryotic genomes has a deep impact on gene function. Although progress has been recently made in the identification of various concurring factors influencing nucleosome positioning, it is still unclear whether nucleosome positions are sequence dictated or determined by a random process. It has been postulated for a long time that,in the proximity of TSS, a barrier determines the position of the +1 nucleosome and then geometric constraints alter the random positioning process determining nucleosomal phasing. Such a pattern fades out as one moves away from the barrier to become again a random positioning process. Although this statistical model is widely accepted,the molecular nature of the barrier is still unknown. Moreover,we are far from the identification of a set of sequence rules able:to account for the genome-wide nucleosome organization;to explain the nature of the barriers on which the statistical mechanism hinges;to allow for a smooth transition from sequence-dictated to statistical positioning and back. We show that sequence complexity,quantified via various methods, can be the rule able to at least partially account for all the above.In particular, we have conducted our analyses on 4 high resolution nucleosomal maps of the model eukaryotes and found that nucleosome depleted regions can be well distinguished from nucleosome enriched regions by sequence complexity measures.In particular, (a) the depleted regions are less complex than the enriched ones, (b) around TSS complexity measures alone are in striking agreement with in vivo nucleosome occupancy,in particular precisely indicating the positions of the +1 and -1 nucleosomes. Those findings indicate that the intrinsic richness of subsequences within sequences plays a role in nucleosomal formation in genomes, and that sequence complexity constitutes the molecular nature of nucleosome barrier.

q-bio.GN↗

arXiv2011

Algorithms for Internal Validation Clustering Measures in the Post Genomic Era

Inferring cluster structure in microarray datasets is a fundamental task for the -omic sciences. A fundamental question in Statistics, Data Analysis and Classification, is the prediction of the number of clusters in a dataset, usually established via internal validation measures. Despite the wealth of internal measures available in the literature, new ones have been recently proposed, some of them specifically for microarray data. In this dissertation, a study of internal validation measures is given, paying particular attention to the stability based ones. Indeed, this class of measures is particularly prominent and promising in order to have a reliable estimate the number of clusters in a dataset. For those measures, a new general algorithmic paradigm is proposed here that highlights the richness of measures in this class and accounts for the ones already available in the literature. Moreover, some of the most representative validation measures are also considered. Experiments on 12 benchmark datasets are performed in order to assess both the intrinsic ability of a measure to predict the correct number of clusters in a dataset and its merit relative to the other measures. The main result is a hierarchy of internal validation measures in terms of precision and speed, highlighting some of their merits and limitations not reported before in the literature. This hierarchy shows that the faster the measure, the less accurate it is. In order to reduce the time performance gap between the fastest and the most precise measures, the technique of designing fast approximation algorithms is systematically applied. The end result is a speed-up of many of the measures studied here that brings the gap between the fastest and the most precise within one order of magnitude in time, with no degradation in their prediction power. Prior to this work, the time gap was at least two orders of magnitude.

cs.DS↗