Jonathan Warrell
Jonathan Warrell is a Researcher in the Machine Learning Department at NEC Laboratories America. He received his BA in Music from the University of Cambridge, his Master’s as well as his PhD in Music Theory and Analysis from King’s College London, an MS in Computer Science (Distinction) from the University College London, and he went on to postdoctoral work in computational genomics and neuroscience in Yale’s Department of Molecular Biophysics and Biochemistry.

His research focuses particularly on computational biology, spatial genomics, and optimization theory.  At NEC, Dr. Warrell contributes to projects involving molecular design, large-scale genomic reasoning, compositionality of diffusion models, biomarker discovery, reinforcement learning, and variational methods. His work leverages hybrid approaches that combine symbolic and neural methods, particularly for solving discrete optimization problems in genomics. He collaborates closely with NEC Bio, NEC OncoImmunity, and NEC’s Biometric Research Laboratories on developing interpretable and efficient methods for solving biological and medical problems.  He has published widely in high impact journals such as Science, Cell, Nature Genetics and Nature Machine Intelligence.

Posts

Variational methods for Learning Multilevel Genetic Algorithms using the Kantorovich Monad

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Levels of selection and multilevel evolutionary processes are essential concepts in evolutionary theory, and yet there is a lack of common mathematical models for these core ideas. Here, we propose a unified mathematical framework for formulating and optimizing multilevel evolutionary processes and genetic algorithms over arbitrarily many levels based on concepts from category theory and population genetics. We formulate a multilevel version of the Wright-Fisher process using this approach, and we show that this model can be analyzed to clarify key features of multilevel selection. Particularly, we derive an extended multilevel probabilistic version of Price’s Equation via the Kantorovich Monad, and we use this to characterize regimes of parameter space within which selection acts antagonistically or cooperatively across levels. Finally, we show how our framework can provide a unified setting for learning genetic algorithms (GAs), and we show how we can use a Variational Optimization and a multi-level analogue of coalescent analysis to fit multilevel GAs to simulated data.

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Predicting Spatially Resolved Gene Expression via Tissue Morphology using Adaptive Spatial GNNs (ECCB)

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Spatial transcriptomics technologies, which generate a spatial map of gene activity, can deepen the understanding of tissue architecture and its molecular underpinnings in health and disease. However, the high cost makes these technologies difficult to use in practice. Histological images co-registered with targeted tissues are more affordable and routinely generated in many research and clinical studies. Hence, predicting spatial gene expression from the morphological clues embedded in tissue histological images provides a scalable alternative approach to decoding tissue complexity.

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Spatially Informed Gene Signatures for Response to Immunotherapy in Melanoma

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We aim to improve the prediction of response or resistance to immunotherapies in patients with melanoma. This goal is based on the hypothesis that current gene signatures predicting immunotherapy outcomes show only modest accuracy due to the lack of spatial information about cellular functions and molecular processes within tumors and their microenvironment.

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zeta-QVAE: A Quantum Variational Autoencoder utilizing Regularized Mixed-state Latent Representations

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A major challenge in near-term quantum computing is its application to large real-world datasets due to scarce quantum hardware resources. One approach to enabling tractable quantum models for such datasets involves compressing the original data to manageable dimensions while still representing essential information for downstream analysis. In classical machine learning, variational autoencoders (VAEs) facilitate efficient data compression, representation learning for subsequent tasks, and novel data generation. However, no model has been proposed that exactly captures all of these features for direct application to quantum data on quantum computers. Some existing quantum models for data compression lack regularization of latent representations, thus preventing direct use for generation and control of generalization. Others are hybrid models with only some internal quantum components, impeding direct training on quantum data. To bridge this gap, we present a fully quantum framework, ?-QVAE, which encompasses all the capabilities of classical VAEs and can be directly applied for both classical and quantum data compression. Our model utilizes regularized mixed states to attain optimal latent representations. It accommodates various divergences for reconstruction and regularization. Furthermore, by accommodating mixed states at every stage, it can utilize the full-data density matrix and allow for a “global” training objective. Doing so, in turn, makes efficient optimization possible and has potential implications for private and federated learning. In addition to exploring the theoretical properties of ?-QVAE, we demonstrate its performance on representative genomics and synthetic data. Our results consistently indicate that ?-QVAE exhibits similar or better performance compared to matched classical models.

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Predicting Spatially Resolved Gene Expression via Tissue Morphology using Adaptive Spatial GNNs

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Motivation Spatial transcriptomics technologies, which generate a spatial map of gene activity, can deepen the understanding of tissue architecture and its molecular underpinnings in health and disease. However, the high cost makes these technologies difficult to use in practice. Histological images co-registered with targeted tissues are more affordable and routinely generated in many research and clinical studies. Hence, predicting spatial gene expression from the morphological clues embedded in tissue histological images, provides a scalable alternative approach to decoding tissue complexity

Read more