Topological data analysis of zebrafish patterns

TL;DR

This paper introduces a novel approach combining topological data analysis and interpretable machine learning to quantify and analyze variability in zebrafish skin patterns, capturing both agent-level and global features.

Contribution

It presents a new methodology for analyzing biological patterns that overcomes limitations of existing methods by incorporating agent-based data and topological analysis.

Findings

Quantifies the impact of stochasticity on pattern formation.

Predicts pattern statistics based on cellular communication.

Differentiates wild-type and mutant zebrafish patterns.

Abstract

Self-organized pattern behavior is ubiquitous throughout nature, from fish schooling to collective cell dynamics during organism development. Qualitatively these patterns display impressive consistency, yet variability inevitably exists within pattern-forming systems on both microscopic and macroscopic scales. Quantifying variability and measuring pattern features can inform the underlying agent interactions and allow for predictive analyses. Nevertheless, current methods for analyzing patterns that arise from collective behavior only capture macroscopic features, or rely on either manual inspection or smoothing algorithms that lose the underlying agent-based nature of the data. Here we introduce methods based on topological data analysis and interpretable machine learning for quantifying both agent-level features and global pattern attributes on a large scale. Because the zebrafish is a model organism for skin pattern formation, we focus specifically on analyzing its skin patterns as a means of illustrating our approach. Using a recent agent-based model, we simulate thousands of wild-type and mutant zebrafish patterns and apply our methodology to better understand pattern variability in zebrafish. Our methodology is able to quantify the differential impact of stochasticity in cell interactions on wild-type and mutant patterns, and we use our methods to predict stripe and spot statistics as a function of varying cellular communication. Our work provides a new approach to automatically quantifying biological patterns and analyzing agent-based dynamics so that we can now answer critical questions in pattern formation at a much larger scale.