TY - JOUR
T1 - Automatic Morphological Reconstruction of Neurons from Multiphoton and Confocal Microscopy Images Using 3D Tubular Models
AU - Santamaría-Pang, Alberto
AU - Hernandez-Herrera, Paul
AU - Papadakis, Manos
AU - Saggau, Peter
AU - Kakadiaris, Ioannis A.
N1 - Funding Information:
We wish to thank all of the members of the ORION team (Computational Biomedicine Lab ) and especially Costa M. Colbert, Yong Liang, and Bradley E. Losavio. The data were acquired at P. Saggau’s Laboratory in the Department of Neuroscience of the Baylor College of Medicine. This work was supported in part by NIH 5R01EB001048-02, NSF-DMS 0915242, NHARP 003652-0136-2009 and the University of Houston–Eckhard Pfeiffer Endowment Fund. Any opinions, findings, conclusions or recommendations expressed in this material are those of the authors and may not reflect the views of UH, NIH, NHARP, or NSF.
Publisher Copyright:
© 2015, Springer Science+Business Media New York.
PY - 2015/7/17
Y1 - 2015/7/17
N2 - The challenges faced in analyzing optical imaging data from neurons include a low signal-to-noise ratio of the acquired images and the multiscale nature of the tubular structures that range in size from hundreds of microns to hundreds of nanometers. In this paper, we address these challenges and present a computational framework for an automatic, three-dimensional (3D) morphological reconstruction of live nerve cells. The key aspects of this approach are: (i) detection of neuronal dendrites through learning 3D tubular models, and (ii) skeletonization by a new algorithm using a morphology-guided deformable model for extracting the dendritic centerline. To represent the neuron morphology, we introduce a novel representation, the Minimum Shape-Cost (MSC) Tree that approximates the dendrite centerline with sub-voxel accuracy and demonstrate the uniqueness of such a shape representation as well as its computational efficiency. We present extensive quantitative and qualitative results that demonstrate the accuracy and robustness of our method.
AB - The challenges faced in analyzing optical imaging data from neurons include a low signal-to-noise ratio of the acquired images and the multiscale nature of the tubular structures that range in size from hundreds of microns to hundreds of nanometers. In this paper, we address these challenges and present a computational framework for an automatic, three-dimensional (3D) morphological reconstruction of live nerve cells. The key aspects of this approach are: (i) detection of neuronal dendrites through learning 3D tubular models, and (ii) skeletonization by a new algorithm using a morphology-guided deformable model for extracting the dendritic centerline. To represent the neuron morphology, we introduce a novel representation, the Minimum Shape-Cost (MSC) Tree that approximates the dendrite centerline with sub-voxel accuracy and demonstrate the uniqueness of such a shape representation as well as its computational efficiency. We present extensive quantitative and qualitative results that demonstrate the accuracy and robustness of our method.
KW - Confocal microscopy images
KW - Machine learning
KW - Multiphoton microscopy images
KW - Neuron segmentation
KW - Neuronal morphology extraction
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U2 - 10.1007/s12021-014-9253-2
DO - 10.1007/s12021-014-9253-2
M3 - Article
C2 - 25631538
AN - SCOPUS:84931006013
SN - 1539-2791
VL - 13
SP - 297
EP - 320
JO - Neuroinformatics
JF - Neuroinformatics
IS - 3
ER -