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SynBot is an open-source image analysis software for automated quantification of synapses.
Savage, Justin T; Ramirez, Juan J; Risher, W Christopher; Wang, Yizhi; Irala, Dolores; Eroglu, Cagla.
Affiliation
  • Savage JT; Department of Neurobiology, Duke University Medical Center, Durham, NC 27710, USA.
  • Ramirez JJ; Department of Neurobiology, Duke University Medical Center, Durham, NC 27710, USA.
  • Risher WC; Department of Biomedical Sciences, Joan C. Edwards School of Medicine at Marshall University, Huntington, WV 25755, USA.
  • Wang Y; Bradley Department of Electrical and Computer Engineering, Virginia Polytechnic Institute and State University, Arlington, VA 22203, USA.
  • Irala D; Department of Cell Biology, Duke University Medical Center, Durham, NC 27710, USA. Electronic address: dolores.irala@duke.edu.
  • Eroglu C; Department of Neurobiology, Duke University Medical Center, Durham, NC 27710, USA; Department of Cell Biology, Duke University Medical Center, Durham, NC 27710, USA; Howard Hughes Medical Institute, Duke University Medical Center, Durham, NC 27710, USA; Aligning Science Across Parkinson's (ASAP) Col
Cell Rep Methods ; : 100861, 2024 Sep 05.
Article in En | MEDLINE | ID: mdl-39255792
ABSTRACT
The formation of precise numbers of neuronal connections, known as synapses, is crucial for brain function. Therefore, synaptogenesis mechanisms have been one of the main focuses of neuroscience. Immunohistochemistry is a common tool for visualizing synapses. Thus, quantifying the numbers of synapses from light microscopy images enables screening the impacts of experimental manipulations on synapse development. Despite its utility, this approach is paired with low-throughput analysis methods that are challenging to learn, and the results are variable between experimenters, especially when analyzing noisy images of brain tissue. We developed an open-source ImageJ-based software, SynBot, to address these technical bottlenecks by automating the analysis. SynBot incorporates the advanced algorithms ilastik and SynQuant for accurate thresholding for synaptic puncta identification, and the code can easily be modified by users. The use of this software will allow for rapid and reproducible screening of synaptic phenotypes in healthy and diseased nervous systems.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Cell Rep Methods Year: 2024 Document type: Article Affiliation country: Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Cell Rep Methods Year: 2024 Document type: Article Affiliation country: Country of publication: