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Cruz, D. A.

Publications and source records attributed to Cruz, D. A..

2 recordsLinked to original sources

Ensemble Kalman filter methods for agent-based medical digital twins

Digital twin technology, pioneered for engineering applications, is being adapted to biomedicine and healthcare; however, several problems need to be solved in the process. One major problem is that of dynamically calibrating a computational model to an individual patient, using data collected from that patient over time. This kind of calibration is crucial for improving model-based forecasts and realizing personalized medicine. The underlying computational model often focuses on a particular part of human biology, combines different modeling paradigms at different scales, and is both stochastic and spatially heterogeneous. A commonly used modeling framework is that of an agent-based model, a computational model for simulating autonomous agents such as cells, which captures how system-level properties are affected by local interactions. There are no standard personalization methods that can be readily applied to such models. The key challenge for any such algorithm is to bridge the gap between the clinically measurable quantities (the macrostate) and the fine-grained data at different physiological scales which are required to run the model (the microstate). In this paper we develop an algorithm which applies a classic data assimilation technique, the ensemble Kalman filter, at the macrostate level. We then link the Kalman update at the macrostate level to an update at the microstate level that produces microstates which are not only compatible with desired macrostates but also highly likely with respect to model dynamics. Significance StatementTo realize the promise of personalized medicine, we need to be able to integrate different types of data collected from a given patient into a computational framework that enables decision making about optimal interventions to help this patient to either maintain or regain health. Digital twins represent such a framework, once the technology is sufficiently developed. A fundamental problem that currently does not have a widely applicable solution is how to calibrate a generic computational model of human biology to a given patient at a given time. This paper presents a solution to this problem for the agent-based model framework, commonly used to capture stochastic and spatially heterogeneous biological processes, such as tumor growth or immune system dynamics.

systems biology↗

Topological data analysis of pattern formation of human induced pluripotent stem cell colonies

Understanding the multicellular organization of stem cells is vital for determining the mechanisms that coordinate cell fate decision-making during differentiation; these mechanisms range from neighbor-to-neighbor communication to tissue-level biochemical gradients. Current methods for quantifying multicellular patterning cannot capture the spatial properties of cell colonies across all scales and typically rely on human annotation or a priori selection of parameters. We present a computational pipeline that utilizes topological data analysis to generate quantitative, multiscale descriptors which capture the shape of data extracted from multichannel microscopy images. By applying our pipeline to certain stem cell colonies, we detected subtle differences in patterning that reflect distinct biological markers and progressive stages of differentiation. These results yield insight into directed cellular movement and morphogen-mediated, neighbor-to-neighbor signaling. Because of its broad applicability to immunofluorescence microscopy images, our pipeline is well-positioned to serve as a general-purpose tool for the quantitative study of multicellular pattern formation.

developmental biology↗