| Literature DB >> 32006677 |
Florian Levet1, Jan Tønnesen2, U Valentin Nägerl2, Jean-Baptiste Sibarita3.
Abstract
Super-resolution microscopy provides diffraction-unlimited optical access to the intricate morphology of neurons in living brain tissue, resolving their finest structural details, which are critical for neuronal function. However, as existing image analysis software tools have been developed for diffraction-limited images, they are generally not well suited for quantifying nanoscale structures like dendritic spines. We present SpineJ, a semi-automatic ImageJ plugin that is specifically designed for this purpose. SpineJ offers an intuitive and user-friendly graphical user interface, facilitating fast, accurate, and unbiased analysis of spine morphology.Entities:
Year: 2020 PMID: 32006677 DOI: 10.1016/j.ymeth.2020.01.020
Source DB: PubMed Journal: Methods ISSN: 1046-2023 Impact factor: 3.608