2015 | OriginalPaper | Buchkapitel
HEp-2 Staining Pattern Recognition Using Stacked Fisher Network for Encoding Weber Local Descriptor
verfasst von : Xian-Hua Han, Yen-Wei Chen, Gang Xu
Erschienen in: Machine Learning in Medical Imaging
Aktivieren Sie unsere intelligente Suche um passende Fachinhalte oder Patente zu finden.
Wählen Sie Textabschnitte aus um mit Künstlicher Intelligenz passenden Patente zu finden. powered by
Markieren Sie Textabschnitte, um KI-gestützt weitere passende Inhalte zu finden. powered by
This study addresses the recognition problem of the HEp-2 cell using indirect immunofluorescent (IIF) image analysis, which can indicate the presence of autoimmune diseases by finding antibodies in the patient serum. Generally, the method used for IIF analysis remains subjective, and depends too heavily on the experience and expertise of the physician. This study aims to explore an automatic HEp-2 cell recognition system, in which how to extract highly discriminate visual features plays a key role in this recognition application. In order to realize this purpose, our main efforts include: (1) a transformed excitation domain instead of the raw image domain, which is based on the fact that human perception for disguising a pattern depends not only on the absolute intensity of the stimulus but also on the relative variance of the stimulus; (2) a simple but robust micro-texton without any quantization in the excitation domain, called as Weber local descriptor (WLD); (3) a data-driven coding strategy with a parametric probability process, and the extraction of not only low- but also high-order statistics for image representation called as Fisher vector; (4) the stacking of the Fisher network into deep learning framework for more discriminate feature. Experiments using the open HEp-2 cell dataset released in the ICIP2013 contest validate that the proposed strategy can achieve a much better performance than the state-of-the-art approaches, and that the achieved recognition error rate is even very significantly below the observed intra-laboratory variability