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Emma Lejeune

Publications and source records attributed to Emma Lejeune.

21 records · Page 2Linked to original sources

Learning Mechanically Driven Emergent Behavior with Message Passing Neural Networks

From designing architected materials to connecting mechanical behavior across scales, computational modeling is a critical tool in solid mechanics. Recently, there has been a growing interest in using machine learning to reduce the computational cost of physics-based simulations. Notably, while machine learning approaches that rely on Graph Neural Networks (GNNs) have shown success in learning mechanics, the performance of GNNs has yet to be investigated on a myriad of solid mechanics problems. In this work, we examine the ability of GNNs to predict a fundamental aspect of mechanically driven emergent behavior: the connection between a column's geometric structure and the direction that it buckles. To accomplish this, we introduce the Asymmetric Buckling Columns (ABC) dataset, a dataset comprised of three sub-datasets of asymmetric and heterogeneous column geometries where the goal is to classify the direction of symmetry breaking (left or right) under compression after the onset of instability. Because of complex local geometry, the "image-like" data representations required for implementing standard convolutional neural network based metamodels are not ideal, thus motivating the use of GNNs. In addition to investigating GNN model architecture, we study the effect of different input data representation approaches, data augmentation, and combining multiple models as an ensemble. While we were able to obtain good results, we also showed that predicting solid mechanics based emergent behavior is non-trivial. Because both our model implementation and dataset are distributed under open-source licenses, we hope that future researchers can build on our work to create enhanced mechanics-specific machine learning pipelines for capturing the behavior of complex geometric structures.

cs.LG↗

Sarc-Graph: Automated segmentation, tracking, and analysis of sarcomeres in hiPSC-derived cardiomyocytes

A better fundamental understanding of human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) has the potential to advance applications ranging from drug discovery to cardiac repair. Automated quantitative analysis of beating hiPSC-CMs is an important and fast developing component of the hiPSC-CM research pipeline. Here we introduce "Sarc-Graph," a computational framework to segment, track, and analyze sarcomeres in fluorescently tagged hiPSC-CMs. Our framework includes functions to segment z-discs and sarcomeres, track z-discs and sarcomeres in beating cells, and perform automated spatiotemporal analysis and data visualization. In addition to reporting good performance for sarcomere segmentation and tracking with little to no parameter tuning and a short runtime, we introduce two novel analysis approaches. First, we construct spatial graphs where z-discs correspond to nodes and sarcomeres correspond to edges. This makes measuring the network distance between each sarcomere (i.e., the number of connecting sarcomeres separating each sarcomere pair) straightforward. Second, we treat tracked and segmented components as fiducial markers and use them to compute the approximate deformation gradient of the entire tracked population. This represents a new quantitative descriptor of hiPSC-CM function. We showcase and validate our approach with both synthetic and experimental movies of beating hiPSC-CMs. By publishing Sarc-Graph, we aim to make automated quantitative analysis of hiPSC-CM behavior more accessible to the broader research community.

q-bio.QM↗

Exploring the potential of transfer learning for metamodels of heterogeneous material deformation

From the nano-scale to the macro-scale, biological tissue is spatially heterogeneous. Even when tissue behavior is well understood, the exact subject specific spatial distribution of material properties is often unknown. And, when developing computational models of biological tissue, it is usually prohibitively computationally expensive to simulate every plausible spatial distribution of material properties for each problem of interest. Therefore, one of the major challenges in developing accurate computational models of biological tissue is capturing the potential effects of this spatial heterogeneity. Recently, machine learning based metamodels have gained popularity as a computationally tractable way to overcome this problem because they can make predictions based on a limited number of direct simulation runs. These metamodels are promising, but they often still require a high number of direct simulations to achieve an acceptable performance. Here we show that transfer learning, a strategy where knowledge gained while solving one problem is transferred to solving a different but related problem, can help overcome this limitation. Critically, transfer learning can be used to leverage both low-fidelity simulation data and simulation data that is the outcome of solving a different but related mechanical problem. In this paper, we extend Mechanical MNIST, our open source benchmark dataset of heterogeneous material undergoing large deformation, to include a selection of low-fidelity simulation results that require 2-4 orders of magnitude less CPU time to run. Then, we show that transferring the knowledge stored in metamodels trained on these low-fidelity simulation results can vastly improve the performance of metamodels used to predict the results of high-fidelity simulations.

q-bio.TO↗