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Content available remote Cell image augmentation for classification task using GANs on Pap smear dataset
EN
One of the solutions to the problem of insufficiently large training datasets in image processing is data augmentation. This process artificially extends the size of training datasets to avoid overfitting. Generative Adversarial Networks yield that become increasingly difficult to differentiate from real images, until the differentiation is no longer possible. Thus, artificial images closely resembling original ones can be generated. Inclusion of artificial images contributes to improving the training process. Medical domain is one of the areas where data acquisition is burdened by many procedures, laws, and prohibitions. As a result the potential size of collected datasets is reduced. This article presents the results of training Convolutional Neural Networks on a artificially extended image datasets. The resulting classification accuracy on a cell classification task of models trained with images generated using the proposed method were increased by up to 12.9% in comparison to that of the model trained only with original dataset from the HErlev Pap smear dataset.
EN
With the advent and great advances of methods based on deep learning in image analysis, it appears that they can be effective in digital pathology to support the work of pathologists. However, a major limitation in the development of computer-aided diagnostic systems for pathology is the cost of data annotation. Evaluation of tissue (histopathological) and cellular (cytological) specimens seems to be a complex challenge. To simplify the laborious process of obtaining a sufficiently large set of data, a number of different systems could be used for image annotation. Some of these systems are reviewed in this paper with a comparison of their capabilities.
EN
Diffuse large B-cell lymphoma (DLBCL) is a fast-growing and aggressive neoplasm originating from B lymphocytes. Evaluation of proliferation index (PI) based on Ki67 immunohistochemical nuclear staining is used to distinguish proliferating (immunopositive) from nonproliferating (immunonegative) lymphoma cells. Human interpretation of PI varies and is time-consuming, therefore automatic computer-assisted approach may facilitate the performance. Herein we propose a new fully automatic proliferation index estimation (FLAPIE) algorithm, dedicated to detection of immunopositive and immunonegative nuclei, and evaluation of PI in digital microscopy images of DAB&H-stained samples from patients with high-grade DLBCL. FLAPIE performs nuclei detection in original RGB colour space and is independent of image brightness due to its textural-statistical approach. Validation of FLAPIE was performed in 61 non-overlapping whole-slide imagefragments and compared to the results of PI estimation by QuPath open-source software, MetPiKi algorithm and manual evaluation by two independent observers. Interobserver agreement was calculated between the nuclei count and PIs by two observers. High concordance was found between both DAB and H-stained nuclei count, and PIs by two observers. Compared to MetPiKi, FLAPIE presented improved results of DAB and H-stained nuclei detection. In contrary to MetPiKi and QuPath, FLAPIE performed nuclei detection in all images and its results closely matched the number of DAB-stained nuclei evaluated by two observers. No significant difference was found between PIs by all computational methods and observers. FLAPIE achieved good results in PI estimation and prospectively aims to serve as a tool for clinical application in support of patients selection and decision to treatment.
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