Quantum machine learning (QML) algorithms have demonstrated the power of quantum computing for solving complex problems and big data in certain tasks. In this study, we explore the capabilities of QML for the classification of real-world biological large datasets including ten different cancer types based on gene expression values. By comparing the classification results obtained from the quantum algorithm with those from classical approaches, we disclose that the QML algorithm overall achieves comparable and reliable results. Moreover, we identify novel biomarkers that can contribute to the understanding of cancer biology. Some of these biomarkers are consistent with DNA promoter methylation. Our findings highlight the potential of QML in cancer classification and biomarker discovery, paving the way for future advancements in other disease research and clinical applications.
Quantum machine learning (QML) algorithms have demonstrated the power of quantum computing for solving complex problems and big data in certain tasks. In this study, we explore the capabilities of QML for the classification of real-world biological large datasets including ten different cancer types based on gene expression values. By comparing the classification results obtained from the quantum algorithm with those from classical approaches, we disclose that the QML algorithm overall achieves comparable and reliable results. Moreover, we identify novel biomarkers that can contribute to the understanding of cancer biology. Some of these biomarkers are consistent with DNA promoter methylation. Our findings highlight the potential of QML in cancer classification and biomarker discovery, paving the way for future advancements in other disease research and clinical applications.
Abstract Quantum machine learning algorithms using the power of quantum computing provide fast- developing approaches for solving complicated problems and speeding-up calculations for big data. As such, they could effectively operate better than the classical algorithms. Herein, we demonstrate for the first time the classification of eleven cancers based on the gene expression values with 4495 samples using quantum machine learning. In addition, we compare the obtained quantum classification results with the classical outcomes. By implementing a dimensional reduction method, we introduce significant biomarkers for each cancer. In this research, we express that some of the identified gene biomarkers are consistent with DNA promotor methylation, and some other ones can be applied for the survival determination of patients.
Quantum machine learning offers a promising new paradigm for computational biology by leveraging quantum mechanical principles to enhance cancer classification, biomarker discovery, and bioinformatics diagnostics. In this study, we apply QML to identify subtype specific biomarkers for lung adenocarcinoma (LUAD) and lung squamous cell carcinoma (LUSC), the two predominant forms of non-small cell lung cancer. Our methodology involves a two-phase process: in Phase 1, differential expression analysis and methylation analysis between tumor and normal samples allows us to identify LUAD-specific and LUSC-specific genes, revealing potential prognostic biomarkers for cancer subtypes. Phase 2 focuses on developing a quantum classifier capable of distinguishing between LUAD and LUSC tumors, as well as between tumor and normal samples. This classifier not only enhances diagnostic precision but also demonstrates the quantum advantage in processing large-scale multiomic datasets. Our results consistently demonstrated that Sample3, representing the combined gene set, achieved the highest overall predictive performance in all metrics. These results demonstrate that QML provides an effective and scalable approach for biomarker discovery and subtype specific cancer classification. GO enrichment analysis highlighted the significant involvement of genes in synaptic signaling, ion channel regulation, and neuronal development. In the quantum phase, KEGG analysis further identified enrichment in cancer-associated pathways, including neurotrophin, MAPK, Ras, and PI3KAkt signaling, with key genes such as NGFR, NTRK2, and NTF3 suggesting a central role in neurotrophinmediated oncogenic processes. Our findings highlight the growing potential of quantum computing to advance precision oncology and next-generation biomedical analytics.
Quantum machine learning (QML) presents novel opportunities for resolving, accelerating, and refining computational biology challenges. In biomedical research and personalized medicine, multi-omics integration offers a comprehensive understanding of complex biological systems, bridging the gap between basic research and clinical applications. Recent advancements in quantum computing could enhance multi-omics integration by leveraging unique quantum principles, potentially revealing intricate patterns in multi-omics datasets and offering new insights into the molecular landscape of lung cancer. This study focuses on the integration, feature selection, diagnostic classification, and biomarker identification of lung cancer types-LUAD primary tumor and solid tissue normal-using QML. Given the heterogeneity and high dimensionality of the data, we aim to assess the performance of QML in feature selection, reduction, encoding, and diagnostic classification in integrated multi-omics cancer datasets. We demonstrate the efficacy of Quantum Neural Networks (QNNs) for classifying multi-omics lung cancer data from The Cancer Genome Atlas, comparing our framework with 16 and 64 dimensions of feature using QML. Our results show that the Multi-omic Quantum Machine Learning (MQML) framework achieves superior classification performance with smaller training datasets, as determined by significant and non-significant p-values. This study provides empirical evidence for the potential application of unconventional computing approaches in biomed-ical sciences, particularly in oncology research, including cancer subtype diagnostic, survival, and stage classification. Key results include the identification of sixteen genes and thirty-two genes with the hybrid quantum-classical neural net-work model, with notable genes such as MIR632, CYP19A1, RP11-108K3.1, C14orf39, THUMPD1, ACSM3, GSC, MIR92a-2, DYRK1B, DNAJA1, IRX1, FMR1, POU2F2, MIR9-2, ZNF274, MIR196a-1, MIR3653, MIR33b, MIR301a, MIR182, MIR520a, PYGO2, EMX2OS, EMX2, RP11-550F7.1, RPS11, MIR20a, EIF4G2, IGLV1-47, RP11-180M15.7, SCYL3, AC107081.5, C2orf47, FST, MIR7-1, SLC22A18, CLDN5, and AC007879.7 identified as having significant and non-significant p-values asso-ciated with LUAD patient predictions.
The rapid advancements in genomics and the availability of large-scale genetic datasets have revolutionized our understanding of genetic diseases. However, the complexity and high dimensionality of genomic data pose significant computational challenges for classical machine learning (ML) algorithms. Quantum machine learning (QML), an emerging interdisciplinary field that combines quantum computing with ML techniques, offers a promising solution to address these challenges. This paper explores the application of QML algorithms for diagnosing genetic diseases by leveraging the unique properties of quantum computing, such as superposition, entanglement, and quantum parallelism. A novel hybrid quantum-classical approach is proposed to enhance the accuracy and efficiency of disease diagnosis using genomic datasets. The methodology involves encoding genetic data into quantum states, applying quantum-enhanced feature selection and classification algorithms, and validating the results on publicly available datasets, such as the UK Biobank and the Cancer Genome Atlas (TCGA). Experimental results demonstrate that the proposed QML framework achieves higher classification accuracy and faster computation times compared to classical counterparts. Equations, tables, and charts are used to illustrate the effectiveness of the approach. This research highlights the transformative potential of QML in precision medicine and lays the groundwork for future investigations into quantum-enabled healthcare solutions.
Quantum Machine Learning (QML) has emerged as a paradigm that combines the computational advantages of quantum computing with the predictive capabilities of machine learning to address complex data classification problems. As data dimensionality increases rapidly and classical learning algorithms face scalability constraints, QML leverages quantum parallelism, entanglement, and high-dimensional Hilbert space representations to enhance learning performance. This paper reviews and analyses advanced QML algorithms, including Quantum Support Vector Machines (QSVM), Variational Quantum Circuits (VQC), Quantum Neural Networks (QNN), and Quantum Kernel Estimation, for optimizing both binary and multi-class classification tasks under high-complexity conditions. The proposed QML framework is evaluated on benchmark datasets like MNIST, the Breast Cancer Wisconsin (BCW) dataset, and synthetic nonlinear datasets, and is compared against classical machine learning baselines, including Support Vector Machines (SVM), Random Forests (RF), and Deep Neural Networks (DNN). The results demonstrate notable improvements in classification accuracy (up to 96.8%), decision margins, and computational efficiency in quantum-suitable data regimes, while also highlighting current limitations related to noise, circuit depth, and hardware constraints. Overall, the study presents a unified QML framework, theoretical formulations, and experimental evaluations that illustrate the potential of quantum algorithms for next-generation classification tasks.
Quantum computing has reintroduced itself as a breakthrough technology for machine learning, especially in the analysis of massive datasets, especially the genomic ones. The present research focuses on using QML, namely QSVM, to parse sequences, discover features relating to multiple genetic alterations, biomarkers, and gene expression patterns. The data type under consideration, namely genomic data, is high-dimensional and complex, which presents some problems to the computational methods originating from traditional mathematics. QSVM is designed to work with the mathematical foundations of quantum mechanics including superposition and entanglement and for this reason, it solves problems associated with large scale genomic data more efficiently and accurately. The application of QSVM in MEPs confirms its superiority over classical counterparts in classifying gene mutations, clustering of expression profiles or prediction of disease susceptibility. In addition, through feature mapping, QSVM offers better insights into biological information contained on genomic data, as compared to linear correlations. Furthermore, the ability of QML frameworks to expand to fit the increasing amount of data produced by next-generation sequencing technologies is assessed. Leveraging on this research QSVM has been recognised to redefine precision medicine by rapidly diagnosing diseases and providing unique therapeutic options. The results re-echo the potential of QML in transforming CG and promoting future innovations in biomedicine and health.