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1.
IEEE Trans Image Process ; 27(9): 4345-4356, 2018 Sep.
Article in English | MEDLINE | ID: mdl-29870352

ABSTRACT

Utilizing multiple descriptions/views of an object is often useful in image clustering tasks. Despite many works that have been proposed to effectively cluster multi-view data, there are still unaddressed problems such as the errors introduced by the traditional spectral-based clustering methods due to the two disjoint stages: 1) eigendecomposition and 2) the discretization of new representations. In this paper, we propose a unified clustering framework which jointly learns the two stages together as well as utilizing multiple descriptions of the data. More specifically, two learning methods from this framework are proposed: 1) through a graph construction from different views and 2) through combining multiple graphs. Furthermore, benefiting from the separability and local graph preserving properties of the proposed methods, a novel unsupervised automatic attribute discovery method is proposed. We validate the efficacy of our methods on five data sets, showing that the proposed joint learning clustering methods outperform the recent state-of-the-art methods. We also show that it is possible to derive a novel method to address the unsupervised automatic attribute discovery tasks.

2.
Artif Intell Med ; 65(3): 239-50, 2015 Nov.
Article in English | MEDLINE | ID: mdl-26303104

ABSTRACT

OBJECTIVE: This paper presents benchmarking results of human epithelial type 2 (HEp-2) interphase cell image classification methods on a very large dataset. The indirect immunofluorescence method applied on HEp-2 cells has been the gold standard to identify connective tissue diseases such as systemic lupus erythematosus and Sjögren's syndrome. However, the method suffers from numerous issues such as being subjective, time consuming and labor intensive. This has been the main motivation for the development of various computer-aided diagnosis systems whose main task is to automatically classify a given cell image into one of the predefined classes. METHODS AND MATERIAL: The benchmarking was performed in the form of an international competition held in conjunction with the International Conference of Image Processing in 2013: fourteen teams, composed of practitioners and researchers in this area, took part in the initiative. The system developed by each team was trained and tested on a very large HEp-2 cell dataset comprising over 68,000 images of HEp-2 cell. The dataset contains cells with six different staining patterns and two levels of fluorescence intensity. For each method we provide a brief description highlighting the design choices and an in-depth analysis on the benchmarking results. RESULTS: The staining pattern recognition accuracy attained by the methods varies between 47.91% and slightly above 83.65%. However, the difference between the top performing method and the seventh ranked method is only 5%. In the paper, we also study the performance achieved by fusing the best methods, finding that a recognition rate of 85.60% is reached when the top seven methods are employed. CONCLUSIONS: We found that highest performance is obtained when using a strong classifier (typically a kernelised support vector machine) in conjunction with features extracted from local statistics. Furthermore, the misclassification profiles of the different methods highlight that some staining patterns are intrinsically more difficult to recognize. We also noted that performance is strongly affected by the fluorescence intensity level. Thus, low accuracy is to be expected when analyzing low contrasted images.


Subject(s)
Connective Tissue Diseases/diagnosis , Diagnosis, Computer-Assisted/methods , Epithelial Cells/classification , Image Processing, Computer-Assisted/methods , Pattern Recognition, Automated/methods , Support Vector Machine , Algorithms , Fluorescent Antibody Technique, Indirect , Humans , Interphase , Sensitivity and Specificity
3.
Cytometry A ; 87(6): 549-57, 2015 Jun.
Article in English | MEDLINE | ID: mdl-25492545

ABSTRACT

The antinuclear antibody (ANA) test via indirect immunofluorescence applied on Human Epithelial type 2 (HEp-2) cells is a pathology test commonly used to identify connective tissue diseases (CTDs). Despite its effectiveness, the test is still considered labor intensive and time consuming. Applying image-based computer aided diagnosis (CAD) systems is one of the possible ways to address these issues. Ideally, a CAD system should be able to classify ANA HEp-2 images taken by a camera fitted to a fluorescence microscope. Unfortunately, most prior works have primarily focused on the HEp-2 cell image classification problem which is one of the early essential steps in the system pipeline. In this work we directly tackle the specimen image classification problem. We aim to develop a system that can be easily scaled and has competitive accuracy. ANA HEp-2 images or ANA images are generally comprised of a number of cells. Patterns exhibiting in the cells are then used to make inference on the ANA image pattern. To that end, we adapted a popular approach for general image classification problems, namely a bag of visual words approach. Each specimen is considered as a visual document containing visual vocabularies represented by its cells. A specimen image is then represented by a histogram of visual vocabulary occurrences. We name this approach as the Bag of Cells approach. We studied the performance of the proposed approach on a set of images taken from 262 ANA positive patient sera. The results show the proposed approach has competitive performance compared to the recent state-of-the-art approaches. Our proposal can also be expanded to other tests involving examining patterns of human cells to make inferences.


Subject(s)
Antibodies, Antinuclear/immunology , Cell Nucleus/immunology , Connective Tissue Diseases/diagnosis , Image Processing, Computer-Assisted/methods , Microscopy, Fluorescence/methods , Cell Cycle , Cell Line , Computational Biology/methods , Epithelial Cells/immunology , Fluorescent Antibody Technique, Indirect/methods , Humans
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