TY - JOUR
T1 - Analysis-Synthesis Learning with Shared Features
T2 - Algorithms for Histology Image Classification
AU - Li, Xuelu
AU - Monga, Vishal
AU - Rao, U. K.Arvind
N1 - Funding Information:
The work of U. K. A. Rao was supported in part by the American Cancer Society under Grant RSG-16-005-01 and in part by the National Cancer Institute under Grant R01CA21495501A1.
Publisher Copyright:
© 1964-2012 IEEE.
PY - 2020/4
Y1 - 2020/4
N2 - Objective: The diversity of tissue structure in histopathological images makes feature extraction for classification a challenging task. Dictionary learning within a sparse representation-based classification (SRC) framework has been shown to be successful for feature discovery. However, there exist stiff practical challenges: 1) computational complexity of SRC can be onerous in the decision stage since it involves solving a sparsity constrained optimization problem and often over a large number of image patches; and 2) images from distinct classes continue to share several geometric features. We propose a novel analysis-synthesis model learning with shared features algorithm (ALSF) for classifying such images more effectively. Methods: In the ALSF, a joint analysis and synthesis learning model is introduced to learn the classifier and the feature extractor at the same time. Unlike SRC, no explicit optimization is needed in the inference phase leading to much reduced computation. Crucially, we introduce the learning of a low-rank shared dictionary and a shared analysis operator, which more accurately represents both similarities and differences in histopathological images from distinct classes. We also develop an extension of ALSF with a sparsity constraint, whose presence or absence facilitates a cost-performance tradeoff. Results: The ALSF is evaluated on three challenging and well-known datasets: 1) spleen tissue images; 2) brain tumor images; and 3) breast cancer tissue dataset, provided by different organizations. Conclusion: Experimental results demonstrate both complexity and performance benefits of the ALSF over state-of-the-art alternatives. Significance: Modeling shared features with appropriate quantitative constraints lead to significantly improved classification in histopathology.
AB - Objective: The diversity of tissue structure in histopathological images makes feature extraction for classification a challenging task. Dictionary learning within a sparse representation-based classification (SRC) framework has been shown to be successful for feature discovery. However, there exist stiff practical challenges: 1) computational complexity of SRC can be onerous in the decision stage since it involves solving a sparsity constrained optimization problem and often over a large number of image patches; and 2) images from distinct classes continue to share several geometric features. We propose a novel analysis-synthesis model learning with shared features algorithm (ALSF) for classifying such images more effectively. Methods: In the ALSF, a joint analysis and synthesis learning model is introduced to learn the classifier and the feature extractor at the same time. Unlike SRC, no explicit optimization is needed in the inference phase leading to much reduced computation. Crucially, we introduce the learning of a low-rank shared dictionary and a shared analysis operator, which more accurately represents both similarities and differences in histopathological images from distinct classes. We also develop an extension of ALSF with a sparsity constraint, whose presence or absence facilitates a cost-performance tradeoff. Results: The ALSF is evaluated on three challenging and well-known datasets: 1) spleen tissue images; 2) brain tumor images; and 3) breast cancer tissue dataset, provided by different organizations. Conclusion: Experimental results demonstrate both complexity and performance benefits of the ALSF over state-of-the-art alternatives. Significance: Modeling shared features with appropriate quantitative constraints lead to significantly improved classification in histopathology.
UR - https://www.scopus.com/pages/publications/85082342523
UR - https://www.scopus.com/pages/publications/85082342523#tab=citedBy
U2 - 10.1109/TBME.2019.2928997
DO - 10.1109/TBME.2019.2928997
M3 - Article
C2 - 31329103
AN - SCOPUS:85082342523
SN - 0018-9294
VL - 67
SP - 1061
EP - 1073
JO - IEEE Transactions on Biomedical Engineering
JF - IEEE Transactions on Biomedical Engineering
IS - 4
M1 - 8764410
ER -