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Automatic Dendritic Length Quantification for High Throughput Screening of Mature Neurons

Automatic Dendritic Length Quantification for High Throughput Screening of Mature Neurons High-throughput automated fluorescent imaging and screening are important for studying neuronal development, functions, and pathogenesis. An automatic approach of analyzing images acquired in automated fashion, and quantifying dendritic characteristics is critical for making such screens high-throughput. However, automatic and effective algorithms and tools, especially for the images of mature mammalian neurons with complex arbors, have been lacking. Here, we present algorithms and a tool for quantifying dendritic length that is fundamental for analyzing growth of neuronal network. We employ a divide-and-conquer framework that tackles the challenges of high-throughput images of neurons and enables the integration of multiple automatic algorithms. Within this framework, we developed algorithms that adapt to local properties to detect faint branches. We also developed a path search that can preserve the curvature change to accurately measure dendritic length with arbor branches and turns. In addition, we proposed an ensemble strategy of three estimation algorithms to further improve the overall efficacy. We tested our tool on images for cultured mouse hippocampal neurons immunostained with a dendritic marker for high-throughput screen. Results demonstrate the effectiveness of our proposed method when comparing the accuracy with previous methods. The software has been implemented as an ImageJ plugin and available for use. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Neuroinformatics Springer Journals

Automatic Dendritic Length Quantification for High Throughput Screening of Mature Neurons

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Publisher
Springer Journals
Copyright
Copyright © 2015 by Springer Science+Business Media New York
Subject
Biomedicine; Neurosciences; Bioinformatics; Computational Biology/Bioinformatics; Computer Appl. in Life Sciences; Neurology
ISSN
1539-2791
eISSN
1559-0089
DOI
10.1007/s12021-015-9267-4
pmid
25854493
Publisher site
See Article on Publisher Site

Abstract

High-throughput automated fluorescent imaging and screening are important for studying neuronal development, functions, and pathogenesis. An automatic approach of analyzing images acquired in automated fashion, and quantifying dendritic characteristics is critical for making such screens high-throughput. However, automatic and effective algorithms and tools, especially for the images of mature mammalian neurons with complex arbors, have been lacking. Here, we present algorithms and a tool for quantifying dendritic length that is fundamental for analyzing growth of neuronal network. We employ a divide-and-conquer framework that tackles the challenges of high-throughput images of neurons and enables the integration of multiple automatic algorithms. Within this framework, we developed algorithms that adapt to local properties to detect faint branches. We also developed a path search that can preserve the curvature change to accurately measure dendritic length with arbor branches and turns. In addition, we proposed an ensemble strategy of three estimation algorithms to further improve the overall efficacy. We tested our tool on images for cultured mouse hippocampal neurons immunostained with a dendritic marker for high-throughput screen. Results demonstrate the effectiveness of our proposed method when comparing the accuracy with previous methods. The software has been implemented as an ImageJ plugin and available for use.

Journal

NeuroinformaticsSpringer Journals

Published: Apr 9, 2015

References