STAR Protoc. 2025 Jan 2;6(1):103515. doi: 10.1016/j.xpro.2024.103515. Online ahead of print.
ABSTRACT
As light sheet fluorescence microscopy (LSFM) becomes widely available, reconstruction of time-lapse imaging will further our understanding of complex biological processes at cellular resolution. Here, we present a comprehensive workflow for in toto capture, processing, and analysis of multi-view LSFM experiments using the ex vivo mouse embryo as a model system of development. Our protocol describes imaging on a commercial LSFM instrument followed by computational analysis in discrete segments, using open-source software. Quantification of migration and morphodynamics is included. For complete details on the use and execution of this protocol, please refer to Dominguez et al.1.
PMID:39754721 | DOI:10.1016/j.xpro.2024.103515
