2025 Beddington Medal Winner: Rory Maizels

The Beddington Medal is the BSDB’s major commendation to promising young biologists, awarded for the best PhD thesis in Developmental Biology defended in the year previous to the award. Rosa Beddington was one of the greatest talents and inspirational leaders in the field of developmental biology. Rosa made an enormous contribution to the field in general and to the BSDB in particular, so it seemed entirely appropriate that the Society should establish a lasting memorial to her. The design of the medal, mice on a stylised DNA helix, is from artwork by Rosa herself.

Like many years, it was a tough decision for the BSBD committee to choose a winner for the 2025 Beddington medal. We are pleased to announce that this goes to Rory Maizels, for his PhD work at the Crick Institute on differential signal interpretation and cell fate decisions in the developing neural tube.

I am writing to enthusiastically support Rory Maizels’s nomination for the Beddington Medal. His PhD work represents a remarkable achievement that advances our field’s long-standing goal: developing dynamical models that capture the full complexity of developmental systems. The central challenge in developmental biology is to understand how complex, multicellular tissues emerge from the coordinated actions of individual cells. While we have made great strides in identifying key molecular players and mapping gene regulatory networks, we still lack the ability to create predictive dynamical models that capture development in its full complexity. Rory’s work represents a critical step toward addressing this fundamental challenge. What sets Rory’s contribution apart is both its comprehensive scope and meticulous execution. Rather than pursuing flashy but superficial advances, he focused on building robust foundations – developing and rigorously validating new experimental and computational approaches that together enable dynamic modelling of development at scale. Remarkably, Rory personally drove every aspect of the project: from optimising molecular biology protocols and establishing automated laboratory workflows, to designing novel machine learning frameworks for analysing the resulting data. This rare combination of experimental and computational expertise allowed him to iterate between theory and practice in a uniquely effective way.

Prior to his PhD, Rory built a strong foundation through diverse research experience: molecular biology at LMCB UCL, developing computational tools for mitochondrial research at Oxford (resulting in an eLife publication), and completing the prestigious Frank Knox Fellowship at Harvard in Computational Science and Engineering. It is important to emphasise that this fellowship was not simply a bioinformatics MSc but a computational course aimed at engineers and data scientists. This unique background prepared him perfectly for tackling the emerging challenges in single-cell genomics and developmental biology. At the Crick, he quickly demonstrated exceptional independence and scientific maturity, showing deep knowledge of the field while working autonomously and effectively communicating complex ideas to others.

In the first months in the lab (during the COVID pandemic), Rory led the computational analysis of a major single-cell RNA sequencing study of human neural development, analysing data from multiple stages of embryonic spinal cord tissue to identify distinct cell types and map differentiation pathways. His analysis not only revealed the diversity of neural cell types and their developmental trajectories but also provided important comparative insights between human and mouse development, demonstrating both his technical capabilities and his ability to collaborate effectively on complex projects. This work is published.

In his main PhD project, Rory developed novel experimental and computational methods. This delivered three major technical innovations that together advance our ability to study developmental dynamics. First, he developed sci-FATE2, an optimized and semi-automated protocol for metabolic labelling and single-cell RNA sequencing that matches commercial platforms in quality while being simpler to implement. This is published as a methods paper. Second, he created Velvet, a deep learning framework that improves upon existing methods for inferring cell state transitions from RNA data by integrating neighbourhood information into its velocity calculations. Finally, he extended this work with VelvetSDE, a cutting-edge neural stochastic differential equation system that can predict long-term cell fate trajectories and identify key decision points in development, while capturing the inherent variability in cellular decision-making. Applying this to data from the neural tube led to the realisation that expression of Shh modulators are crucial for differential signal interpretation and cell fate decision in the developing neural tube. This combination of experimental and computational advances provides a robust framework for studying the complex dynamics of development at unprecedented scale and resolution. The work recasts single-cell analyses from descriptions of observed data to models of the dynamics that generated them, providing a framework for investigating developmental fate decisions. This work is published.

Rory’s unique combination of creativity, determination, and technical expertise is responsible for the success of the project. His exceptional strengths in both experimental and computational approaches, spanning molecular biology to machine learning, gives him an ability to tackle complex biological problems from multiple angles. But his ability is not limited to technical skills. He is a deep thinker and has developed a clear and far-reaching view of the future of developmental biology. These scholarly capabilities are evidenced by his invited review on single-cell transcriptomics, which he authored independently following a well-received presentation at the Royal Society. We are also completing an article that sets out a vision for developmental biology in the single cell genomics era. In short, Rory is both a thinker and a doer.

The impact of Rory’s work is already evident in the catalytic effect it is having in the field. It has attracted substantial funding (three grants: CRUK Development, Crick I2I Funding, BBSRC project grant) and underpins five new projects in the lab, including single-cell screening of glioma transcription factors, timeresolved sequencing of organoids, and targeted sequencing approaches. Beyond our group, it has enabled new collaborations in cancer screening, neurodegeneration research, and immunology with leading labs. Most notably, this work formed the foundation for Rory’s successful fellowship application for post-doc at EBI and Sanger, where he will further develop these approaches.

Rory exemplifies the qualities we hope to cultivate in our field: deep theoretical understanding combined with practical capability, rigorous methodology alongside creative vision, and the ability to both conceive and execute transformative research. He is not just technically accomplished but a profound thinker about the future of developmental biology and a clear communicator. His work demonstrates both the insight to identify fundamental challenges and the skill to address them systematically.

Given the extraordinary breadth and depth of his contributions, his proven ability to execute complex interdisciplinary projects, and the clear impact his work is already having on the field, I believe Rory Maizels is an outstanding recipient of the Beddington Medal. He represents the kind of scientist who will help lead our field into its next phase, where we can finally begin to build a comprehensive understanding of development.

James Briscoe

 

Papers:

Maizels, R. J., and Briscoe, J. (2025). Gene regulatory networks: from correlaCve models to causal explanaCons. In prepara(on.

Maizels, R. J. (2024). A dynamical perspecCve: moving towards mechanism in single-cell transcriptomics. Philos. Trans. R. Soc. B

Maizels, R. J., Snell, D. M., and Briscoe, J. (2024). ReconstrucCng developmental trajectories using latent dynamical systems and Cme-resolved transcriptomics. Cell Systems

Maizels, R. J., Snell, D. M., and Briscoe, J. (2024). A protocol for Cme-resolved transcriptomics through metabolic labeling and combinatorial indexing. STAR Protocols

Rayon, T., Maizels, R. J., Barrington, C., and Briscoe, J. (2021). Single-cell transcriptome profiling of the human developing spinal cord reveals a conserved genetic programme with human-specific features. Development

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