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J Neurophysiol 100: 2422-2429, 2008. First published August 13, 2008; doi:10.1152/jn.90627.2008
0022-3077/08 $8.00
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INNOVATIVE METHODOLOGY

Live Neuron Morphology Automatically Reconstructed From Multiphoton and Confocal Imaging Data

Bradley E. Losavio1, Yong Liang2, Alberto Santamaría-Pang3, Ioannis A. Kakadiaris3, Costa M. Colbert2,4 and Peter Saggau1

1Department of Neuroscience, Baylor College of Medicine; 2Department of Biology and Biochemistry and 3Department of Computer Science, University of Houston, Houston, Texas; and 4Evolved Machines, Palo Alto, California

Submitted 30 May 2008; accepted in final form 7 August 2008

We have developed a fully automated procedure for extracting dendritic morphology from multiple three-dimensional image stacks produced by laser scanning microscopy. By eliminating human intervention, we ensure that the results are objective, quickly generated, and accurate. The software suite accounts for typical experimental conditions by reducing background noise, removing pipette artifacts, and aligning multiple overlapping image stacks. The output morphology is appropriate for simulation in compartmental simulation environments. In this report, we validate the utility of this procedure by comparing its performance on live neurons and test specimens with other fully and semiautomated reconstruction tools.


Address for reprint requests and other correspondence: P. Saggau, Dept. of Neuroscience, Baylor College of Medicine, One Baylor Plaza, Houston, TX 77030 (E-mail: psaggau{at}bcm.edu)







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