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1.
Chin J Integr Med ; 2016 Apr 04.
Article in English | MEDLINE | ID: mdl-27041330

ABSTRACT

OBJECTIVE: To design a face gloss classification model and to provide an automatic and quantitative approach for the diagnosis of Chinese medicine (CM) based on the face images. METHODS: To classify the face gloss images into two groups (gloss and non-gloss), feature extraction methods were applied to the original images. The original images were supposed to obtain a more ideal representation in which gloss information was better revealed in four color spaces [including red, green, blue (RGB), hue, saturation, value (HSV), Gray and Lab]. Principal component analysis (PCA), 2-dimensional PCA (2DPCA), 2-directional 2-dimensional PCA [(2D)2PCA], linear discriminant analysis (LDA), 2-dimensional LDA (2DLDA), and partial least squares (PLS) were used as the feature extraction methods of face gloss. k nearest neighbor was used as the classifification method. RESULTS: All the six feature extraction methods were useful in extracting information of face gloss, especially LDA, which had the best prediction accuracy in the 4 color spaces. The average accuracy of LDA in the Lab was 7%-10% higher than that of PCA, 2DPCA, (2D)2PCA and 2DLDA P<0.05). The prediction accuracy of LDA reached 98% in the Lab color space and showed practical usage in clinical diagnosis. The consistent rate between the CM experts and the facial diagnosis system was 81%. CONCLUSION: A computer-assisted classifification model was designed to provide an automatic and quantitative approach for the gloss diagnosis of CM based on the face images.

2.
IEEE Trans Nanobioscience ; 11(3): 237-43, 2012 Sep.
Article in English | MEDLINE | ID: mdl-22987129

ABSTRACT

Protein subcellular localization aims at predicting the location of a protein within a cell using computational methods. Knowledge of subcellular localization of proteins indicates protein functions and helps in identifying drug targets. Prediction of protein subcellular localization is an important but challenging problem, particularly when proteins may simultaneously exist at, or move between, two or more different subcellular location sites. Most of the existing protein subcellular localization methods are only used to deal with the single-location proteins. To better reflect the characteristics of multiplex proteins, we formulate prediction of subcellular localization of multiplex proteins as a multilabel learning problem. We present and compare two multilabel learning approaches, which exploit correlations between labels and leverage label-specific features, respectively, to induce a high quality prediction model. Experimental results on six protein data sets under various organisms show that our described methods achieve significantly higher performance than any of the existing methods. Among the different multilabel learning methods, we find that methods exploiting label correlations performs better than those leveraging label-specific features.


Subject(s)
Artificial Intelligence , Computational Biology/methods , Intracellular Space/chemistry , Models, Biological , Models, Statistical , Proteins/chemistry , Algorithms , Databases, Protein , Humans
3.
Int J Data Min Bioinform ; 5(4): 383-401, 2011.
Article in English | MEDLINE | ID: mdl-21954671

ABSTRACT

Analysis of clinical records contributes to the Traditional Chinese Medicine (TCM) experience expansion and techniques promotion. More than two diagnostic classes (diagnostic syndromes) in the clinical records raise a popular data mining problem: multi-value classification. In this paper, we propose a novel multi-class classifier, named Multiple Asymmetric Partial Least Squares Classifier (MAPLSC). MAPLSC attempts to be robust facing imbalanced data distribution in the multi-value classification. Elaborated comparisons with other seven state-of-the-art methods on two TCM clinical datasets and four public microarray datasets demonstrate MAPLSC's remarkable improvements.


Subject(s)
Diagnosis , Medicine, Chinese Traditional , Algorithms , Diagnosis, Differential , Humans , Least-Squares Analysis , Oligonucleotide Array Sequence Analysis/classification , Oligonucleotide Array Sequence Analysis/methods , Software , Syndrome
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