Introduction to the Obesity ML Competition with Caroline and Melina @broadinstitute

Uploaded November 2025 | Updated September 2026, 2 weeks ago

The Eric and Wendy Schmidt Center at the Broad Institute and the Broad Diabetes Initiative are proud to launch our new machine learning challenge: the Obesity Machine Learning Challenge: Tackling Metabolic Diseases. This challenge is developed in partnership with Massachusetts General Hospital, Beth Israel Deaconess Medical Center, and Crunch DAO.

Obesity affects more than 890 million people worldwide and dramatically increases risks of type 2 diabetes, cardiovascular diseases, and certain cancers. You will predict how gene perturbations made using CRISPR/Cas9 influence the fate of adipocytes, the pivotal cells in our body related to obesity. Adipocytes are specialized cells storing our body’s fat that can differentiate into energy-storing or energy-burning cells. Top predictions will be experimentally validated in Broad Institute labs.

This lecture series will give you the necessary biology background, along with technology and data details, to participate in the challenge.

The challenge will run from December 2025 - April 2026.

Learn more and register at broad.io/MLC-2025.

Copyright Broad Institute, 2025. All rights reserved.

Introduction to the Obesity ML Competition with Caroline and Melina

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$MIA: Lorin Crawford, Rethinking scale in single-cell foundation models; Primer: Davide DAscenzo Models, Inference and Algorithms September 24, 2025 Broad Institute of MIT and Harvard Meeting: When more isn’t better: rethinking scale in single-cell foundation models Lorin Crawford Microsoft Research New England (MSR) The success of transformer-based foundation models on natural language and images has motivated their use in single-cell biology. Single-cell foundation models have been trained on increasingly larger transcriptomic datasets, scaling from initial studies with 1 million cells to newer atlases with over 100 million cells. In this talk, we will investigate the role of pre-training dataset size and diversity on the performance of single-cell foundation models on both zero-shot and fine-tuned tasks. In the first half, we use a large corpus of 22.2 million cells to pre-train a total of 400 models and evaluate over 6,400 experiments. We show that current methods tend to plateau in performance with pre-training datasets that are only a fraction of the size. This will lead us to the second half of the talk where we evaluate training data composition on model performance. Focusing on a tractable biological system (human hematopoiesis), we train and analyze deep generative models with a variety of training datasets, including cells from adult and developing tissues, disease states, and perturbation atlases. From the performance across these models, we observe that (1) deep generative models generalize poorly to unseen cell types, (2) addition of malignant cells to a healthy cell training corpus does not necessarily improve modeling of unseen malignant cells, and (3) inclusion of an embryonic stem cell transcription factor differentiation atlas in training data improves performance on out-of-distribution tasks. Our results highlight the distinct contributions of different training data types and point towards strategies for optimizing future single cell foundation models. Primer: Infrastructure and modeling challenges in single-cell omics Davide DAscenzo Polytechnic University of Turin Deep learning is expected to play a major role in advancing the analysis of single-cell omics data, but a number of practical challenges have so far limited its impact. In this talk, we will focus on two such challenges, one at the level of data infrastructure and one at the level of model design. With the rise of very large-scale single-cell experiments, we are now able to use datasets of hundreds of millions of cells. Model training on these datasets is often bottlenecked by the data-loading process of moving data from disk to GPU. To address this, we developed scDataset, a scalable and efficient data-loading solution for quasi-random sampling of single-cell data from disk [1]. We present block sampling and batched fetching strategies that balance I/O efficiency with memory consumption and minibatch diversity, demonstrating how to achieve increased throughput while maintaining sampling quality comparable to true random shuffling. Moving to biological tasks, we focus on cell type annotation. We find that both simple linear models and more complex transformer-based architectures struggle to generalize in out-of-distribution settings. To mitigate this, we introduce a hierarchical cross-entropy loss that incorporates the structure of cell type ontologies [2]. Across model classes, this leads to consistent improvements in performance, suggesting that structured biological priors may be more useful than scaling up model parameters.[1] Davide D’Ascenzo and Sebastiano Cultrera di Montesano. scDataset: Scalable data loading for deep learning on large-scale single-cell omics. arXiv, 2025. [2] Sebastiano Cultrera di Montesano, Davide D’Ascenzo, Srivatsan Raghavan, Ava P. Amini, Peter S. Winter, and Lorin Crawford. Hierarchical cross-entropy loss improves atlas-scale single-cell annotation models. bioRxiv, 2025. For more information visit: https://www.broadinstitute.org/talks/spring-2025/mia Copyright Broad Institute, 2025. All rights reserved.$