TY - GEN
T1 - Sparsity reconstruction for bioluminescence tomography based on an augmented Lagrangian method
AU - Guo, Wei
AU - Jia, Kebin
AU - Tian, Jie
AU - Han, Dong
AU - Liu, Xueyan
AU - Liu, Kai
AU - Zhang, Qian
AU - Feng, Jinchao
AU - Qin, Chenghu
PY - 2012
Y1 - 2012
N2 - Bioluminescence imaging (BLI) is an optical molecular imaging modality for monitoring physiological and pathological activities at the molecular level. The information of bioluminescent probe distribution in small animals can be threedimensionally and quantitatively obtained by bioluminescence tomography (BLT). Due to ill-posed nature, BLT may bear multiple solutions and aberrant reconstruction in the presence of measurement noise and optical parameter mismatches. Among different regularization methods, L2-type regularization strategy is the most popular and commonly-applied method, which minimizes the output-least-square formulation incorporated with the l2-norm regularization term to stabilize the problem. However, it often imposes over-smoothing on the reconstruction results. In contrast, for many practical applications, such as early detection of tumors, the volumes of the bioluminescent sources are very small compared with the whole body. In this paper, L1 regularization is used to fully take advantage of the sparsity prior knowledge and improve both efficiency and stability. And then a reconstruction method based on the augmented Lagrangian approach is proposed, which considers the BLT problem as the constrained optimization problem and employs the Bregman iterative method to deal with it. By using "divide and conquer" approach, the optimization problem can be exactly and fast solved by iteratively solving a sequence of unconstrained subproblems. To evaluate the performance of the proposed method in turbid mouse geometry, stimulate experiments with a heterogeneous 3D mouse atlas are conducted. In addition, physical experiments further demonstrate the potential of the proposed algorithm in practical applications.
AB - Bioluminescence imaging (BLI) is an optical molecular imaging modality for monitoring physiological and pathological activities at the molecular level. The information of bioluminescent probe distribution in small animals can be threedimensionally and quantitatively obtained by bioluminescence tomography (BLT). Due to ill-posed nature, BLT may bear multiple solutions and aberrant reconstruction in the presence of measurement noise and optical parameter mismatches. Among different regularization methods, L2-type regularization strategy is the most popular and commonly-applied method, which minimizes the output-least-square formulation incorporated with the l2-norm regularization term to stabilize the problem. However, it often imposes over-smoothing on the reconstruction results. In contrast, for many practical applications, such as early detection of tumors, the volumes of the bioluminescent sources are very small compared with the whole body. In this paper, L1 regularization is used to fully take advantage of the sparsity prior knowledge and improve both efficiency and stability. And then a reconstruction method based on the augmented Lagrangian approach is proposed, which considers the BLT problem as the constrained optimization problem and employs the Bregman iterative method to deal with it. By using "divide and conquer" approach, the optimization problem can be exactly and fast solved by iteratively solving a sequence of unconstrained subproblems. To evaluate the performance of the proposed method in turbid mouse geometry, stimulate experiments with a heterogeneous 3D mouse atlas are conducted. In addition, physical experiments further demonstrate the potential of the proposed algorithm in practical applications.
KW - L1 regularization
KW - augmented Lagrangian approach
KW - bioluminescence tomography
KW - heterogeneous model
UR - https://www.scopus.com/pages/publications/84859042545
U2 - 10.1117/12.907657
DO - 10.1117/12.907657
M3 - 会议稿件
AN - SCOPUS:84859042545
SN - 9780819488688
T3 - Progress in Biomedical Optics and Imaging - Proceedings of SPIE
BT - Imaging, Manipulation, and Analysis of Biomolecules, Cells, and Tissues X
T2 - Imaging, Manipulation, and Analysis of Biomolecules, Cells, and Tissues X
Y2 - 21 January 2012 through 23 January 2012
ER -